US20180048040A1 - Capacitor-battery hybrid formed by plasma powder electrode coating - Google Patents
Capacitor-battery hybrid formed by plasma powder electrode coating Download PDFInfo
- Publication number
- US20180048040A1 US20180048040A1 US15/560,206 US201515560206A US2018048040A1 US 20180048040 A1 US20180048040 A1 US 20180048040A1 US 201515560206 A US201515560206 A US 201515560206A US 2018048040 A1 US2018048040 A1 US 2018048040A1
- Authority
- US
- United States
- Prior art keywords
- capacitor
- layer
- lithium
- electrode
- negative electrode
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 238000000576 coating method Methods 0.000 title description 9
- 239000011248 coating agent Substances 0.000 title description 7
- 239000000843 powder Substances 0.000 title description 5
- 239000003990 capacitor Substances 0.000 claims abstract description 237
- 229910001416 lithium ion Inorganic materials 0.000 claims abstract description 107
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 claims abstract description 81
- 238000000034 method Methods 0.000 claims abstract description 28
- 239000011244 liquid electrolyte Substances 0.000 claims abstract description 5
- 239000002245 particle Substances 0.000 claims description 81
- 239000007772 electrode material Substances 0.000 claims description 76
- 239000011888 foil Substances 0.000 claims description 69
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 53
- 239000007774 positive electrode material Substances 0.000 claims description 39
- 239000007773 negative electrode material Substances 0.000 claims description 32
- 239000003792 electrolyte Substances 0.000 claims description 28
- 229910052751 metal Inorganic materials 0.000 claims description 23
- 239000002184 metal Substances 0.000 claims description 23
- 238000000151 deposition Methods 0.000 claims description 21
- 239000000463 material Substances 0.000 claims description 20
- 229910052782 aluminium Inorganic materials 0.000 claims description 16
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 15
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 15
- 229910052744 lithium Inorganic materials 0.000 claims description 15
- 238000004519 manufacturing process Methods 0.000 claims description 14
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 8
- 230000015572 biosynthetic process Effects 0.000 claims description 7
- 229910002804 graphite Inorganic materials 0.000 claims description 6
- 239000010439 graphite Substances 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 6
- 229910002986 Li4Ti5O12 Inorganic materials 0.000 claims description 5
- 239000011889 copper foil Substances 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims 2
- 150000002641 lithium Chemical class 0.000 claims 2
- 239000007921 spray Substances 0.000 abstract description 13
- 238000004146 energy storage Methods 0.000 abstract 1
- 210000004027 cell Anatomy 0.000 description 45
- 230000008021 deposition Effects 0.000 description 16
- 229910052802 copper Inorganic materials 0.000 description 13
- 239000010949 copper Substances 0.000 description 13
- 239000000758 substrate Substances 0.000 description 11
- -1 lithium cations Chemical class 0.000 description 10
- 239000010406 cathode material Substances 0.000 description 7
- 230000000295 complement effect Effects 0.000 description 7
- 239000007789 gas Substances 0.000 description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- 229910052748 manganese Inorganic materials 0.000 description 6
- 239000011572 manganese Substances 0.000 description 6
- 229920000642 polymer Polymers 0.000 description 6
- 229910019142 PO4 Inorganic materials 0.000 description 5
- 239000000919 ceramic Substances 0.000 description 5
- 229910052804 chromium Inorganic materials 0.000 description 5
- 238000005137 deposition process Methods 0.000 description 5
- 229910052742 iron Inorganic materials 0.000 description 5
- 229910052759 nickel Inorganic materials 0.000 description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 5
- 239000011148 porous material Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 239000011651 chromium Substances 0.000 description 3
- 229910003002 lithium salt Inorganic materials 0.000 description 3
- 159000000002 lithium salts Chemical class 0.000 description 3
- 239000002923 metal particle Substances 0.000 description 3
- 235000021317 phosphate Nutrition 0.000 description 3
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 3
- 229910052719 titanium Inorganic materials 0.000 description 3
- 239000010936 titanium Substances 0.000 description 3
- QENGPZGAWFQWCZ-UHFFFAOYSA-N 3-Methylthiophene Chemical compound CC=1C=CSC=1 QENGPZGAWFQWCZ-UHFFFAOYSA-N 0.000 description 2
- 229910052493 LiFePO4 Inorganic materials 0.000 description 2
- 229910001290 LiPF6 Inorganic materials 0.000 description 2
- 229910000857 LiTi2(PO4)3 Inorganic materials 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- 230000001464 adherent effect Effects 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- 239000010405 anode material Substances 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- 239000012159 carrier gas Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000003795 desorption Methods 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 description 2
- 238000007599 discharging Methods 0.000 description 2
- 238000010891 electric arc Methods 0.000 description 2
- JBTWLSYIZRCDFO-UHFFFAOYSA-N ethyl methyl carbonate Chemical compound CCOC(=O)OC JBTWLSYIZRCDFO-UHFFFAOYSA-N 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 229910052732 germanium Inorganic materials 0.000 description 2
- 238000001764 infiltration Methods 0.000 description 2
- 230000008595 infiltration Effects 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 238000009830 intercalation Methods 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 229910021450 lithium metal oxide Inorganic materials 0.000 description 2
- 229910001496 lithium tetrafluoroborate Inorganic materials 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920005596 polymer binder Polymers 0.000 description 2
- 239000002491 polymer binding agent Substances 0.000 description 2
- 239000002861 polymer material Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 238000009718 spray deposition Methods 0.000 description 2
- 229910052721 tungsten Inorganic materials 0.000 description 2
- 238000011144 upstream manufacturing Methods 0.000 description 2
- 229910052720 vanadium Inorganic materials 0.000 description 2
- 229920003026 Acene Polymers 0.000 description 1
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 description 1
- 229910001111 Fine metal Inorganic materials 0.000 description 1
- 229910012648 Li3FeV(PO4)3 Inorganic materials 0.000 description 1
- 229910001367 Li3V2(PO4)3 Inorganic materials 0.000 description 1
- 229910011623 LiCrTiO4 Inorganic materials 0.000 description 1
- 229910010584 LiFeO2 Inorganic materials 0.000 description 1
- 229910001305 LiMPO4 Inorganic materials 0.000 description 1
- 229910013318 LiMSiO4 Inorganic materials 0.000 description 1
- 229910014169 LiMn2-xMxO4 Inorganic materials 0.000 description 1
- 229910014435 LiMn2−xMxO4 Inorganic materials 0.000 description 1
- 229910003327 LiNbO3 Inorganic materials 0.000 description 1
- 229910016127 LiNi1-x-y-zCoxM1yM2zO2 Inorganic materials 0.000 description 1
- 229910014359 LiNi1−x−y−zCoxM1yM2zO2 Inorganic materials 0.000 description 1
- 229910013124 LiNiVO4 Inorganic materials 0.000 description 1
- 229910012616 LiTi2O4 Inorganic materials 0.000 description 1
- 229910002097 Lithium manganese(III,IV) oxide Inorganic materials 0.000 description 1
- 229910016618 LixFe2(SO4)3 Inorganic materials 0.000 description 1
- 229910016839 LixFeyMn1−y Inorganic materials 0.000 description 1
- 229910017286 LixM2O4 Inorganic materials 0.000 description 1
- 229910015530 LixMO2 Inorganic materials 0.000 description 1
- 229910014514 LixNiyM1-yO2 Inorganic materials 0.000 description 1
- 229910014512 LixNiyM1−yO2 Inorganic materials 0.000 description 1
- 229920000265 Polyparaphenylene Polymers 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229910000676 Si alloy Inorganic materials 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- ZVLDJSZFKQJMKD-UHFFFAOYSA-N [Li].[Si] Chemical compound [Li].[Si] ZVLDJSZFKQJMKD-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 210000003850 cellular structure Anatomy 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000003487 electrochemical reaction Methods 0.000 description 1
- 239000008151 electrolyte solution Substances 0.000 description 1
- 230000005672 electromagnetic field Effects 0.000 description 1
- 229910052735 hafnium Inorganic materials 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 238000009396 hybridization Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 230000002687 intercalation Effects 0.000 description 1
- LQJIDIOGYJAQMF-UHFFFAOYSA-N lambda2-silanylidenetin Chemical class [Si].[Sn] LQJIDIOGYJAQMF-UHFFFAOYSA-N 0.000 description 1
- 229910052745 lead Inorganic materials 0.000 description 1
- 229910000625 lithium cobalt oxide Inorganic materials 0.000 description 1
- 229910001540 lithium hexafluoroarsenate(V) Inorganic materials 0.000 description 1
- GELKBWJHTRAYNV-UHFFFAOYSA-K lithium iron phosphate Chemical compound [Li+].[Fe+2].[O-]P([O-])([O-])=O GELKBWJHTRAYNV-UHFFFAOYSA-K 0.000 description 1
- 229910002102 lithium manganese oxide Inorganic materials 0.000 description 1
- FUJCRWPEOMXPAD-UHFFFAOYSA-N lithium oxide Chemical class [Li+].[Li+].[O-2] FUJCRWPEOMXPAD-UHFFFAOYSA-N 0.000 description 1
- 229910001947 lithium oxide Inorganic materials 0.000 description 1
- MHCFAGZWMAWTNR-UHFFFAOYSA-M lithium perchlorate Chemical compound [Li+].[O-]Cl(=O)(=O)=O MHCFAGZWMAWTNR-UHFFFAOYSA-M 0.000 description 1
- SWAIALBIBWIKKQ-UHFFFAOYSA-N lithium titanium Chemical compound [Li].[Ti] SWAIALBIBWIKKQ-UHFFFAOYSA-N 0.000 description 1
- VGYDTVNNDKLMHX-UHFFFAOYSA-N lithium;manganese;nickel;oxocobalt Chemical compound [Li].[Mn].[Ni].[Co]=O VGYDTVNNDKLMHX-UHFFFAOYSA-N 0.000 description 1
- BFZPBUKRYWOWDV-UHFFFAOYSA-N lithium;oxido(oxo)cobalt Chemical compound [Li+].[O-][Co]=O BFZPBUKRYWOWDV-UHFFFAOYSA-N 0.000 description 1
- VLXXBCXTUVRROQ-UHFFFAOYSA-N lithium;oxido-oxo-(oxomanganiooxy)manganese Chemical compound [Li+].[O-][Mn](=O)O[Mn]=O VLXXBCXTUVRROQ-UHFFFAOYSA-N 0.000 description 1
- 229910052960 marcasite Inorganic materials 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 229910001463 metal phosphate Inorganic materials 0.000 description 1
- 229910052976 metal sulfide Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 239000011236 particulate material Substances 0.000 description 1
- 229920000767 polyaniline Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920000128 polypyrrole Polymers 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- NIFIFKQPDTWWGU-UHFFFAOYSA-N pyrite Chemical compound [Fe+2].[S-][S-] NIFIFKQPDTWWGU-UHFFFAOYSA-N 0.000 description 1
- 229910052683 pyrite Inorganic materials 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000002210 silicon-based material Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 229910052596 spinel Inorganic materials 0.000 description 1
- 239000011029 spinel Substances 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M16/00—Structural combinations of different types of electrochemical generators
-
- H01M12/005—
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/04—Hybrid capacitors
- H01G11/06—Hybrid capacitors with one of the electrodes allowing ions to be reversibly doped thereinto, e.g. lithium ion capacitors [LIC]
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/08—Structural combinations, e.g. assembly or connection, of hybrid or EDL capacitors with other electric components, at least one hybrid or EDL capacitor being the main component
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/22—Electrodes
- H01G11/24—Electrodes characterised by structural features of the materials making up or comprised in the electrodes, e.g. form, surface area or porosity; characterised by the structural features of powders or particles used therefor
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/22—Electrodes
- H01G11/26—Electrodes characterised by their structure, e.g. multi-layered, porosity or surface features
- H01G11/28—Electrodes characterised by their structure, e.g. multi-layered, porosity or surface features arranged or disposed on a current collector; Layers or phases between electrodes and current collectors, e.g. adhesives
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/22—Electrodes
- H01G11/30—Electrodes characterised by their material
- H01G11/32—Carbon-based
- H01G11/34—Carbon-based characterised by carbonisation or activation of carbon
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/22—Electrodes
- H01G11/30—Electrodes characterised by their material
- H01G11/46—Metal oxides
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/54—Electrolytes
- H01G11/58—Liquid electrolytes
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/54—Electrolytes
- H01G11/58—Liquid electrolytes
- H01G11/62—Liquid electrolytes characterised by the solute, e.g. salts, anions or cations therein
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/66—Current collectors
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/66—Current collectors
- H01G11/72—Current collectors specially adapted for integration in multiple or stacked hybrid or EDL capacitors
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/78—Cases; Housings; Encapsulations; Mountings
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/84—Processes for the manufacture of hybrid or EDL capacitors, or components thereof
- H01G11/86—Processes for the manufacture of hybrid or EDL capacitors, or components thereof specially adapted for electrodes
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/04—Construction or manufacture in general
- H01M10/0459—Cells or batteries with folded separator between plate-like electrodes
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/052—Li-accumulators
- H01M10/0525—Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/058—Construction or manufacture
- H01M10/0583—Construction or manufacture of accumulators with folded construction elements except wound ones, i.e. folded positive or negative electrodes or separators, e.g. with "Z"-shaped electrodes or separators
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/42—Methods or arrangements for servicing or maintenance of secondary cells or secondary half-cells
- H01M10/425—Structural combination with electronic components, e.g. electronic circuits integrated to the outside of the casing
- H01M10/4264—Structural combination with electronic components, e.g. electronic circuits integrated to the outside of the casing with capacitors
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M12/00—Hybrid cells; Manufacture thereof
- H01M12/02—Details
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/04—Processes of manufacture in general
- H01M4/0402—Methods of deposition of the material
- H01M4/0404—Methods of deposition of the material by coating on electrode collectors
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/64—Carriers or collectors
- H01M4/66—Selection of materials
- H01M4/661—Metal or alloys, e.g. alloy coatings
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/10—Primary casings; Jackets or wrappings
- H01M50/102—Primary casings; Jackets or wrappings characterised by their shape or physical structure
- H01M50/105—Pouches or flexible bags
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
- H01M10/0564—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of organic materials only
- H01M10/0566—Liquid materials
- H01M10/0568—Liquid materials characterised by the solutes
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M2220/00—Batteries for particular applications
- H01M2220/20—Batteries in motive systems, e.g. vehicle, ship, plane
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/36—Selection of substances as active materials, active masses, active liquids
- H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
- H01M4/485—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of mixed oxides or hydroxides for inserting or intercalating light metals, e.g. LiTi2O4 or LiTi2OxFy
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/36—Selection of substances as active materials, active masses, active liquids
- H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
- H01M4/50—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese
- H01M4/505—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/10—Primary casings; Jackets or wrappings
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/13—Energy storage using capacitors
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02T—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
- Y02T10/00—Road transport of goods or passengers
- Y02T10/60—Other road transportation technologies with climate change mitigation effect
- Y02T10/70—Energy storage systems for electromobility, e.g. batteries
Definitions
- a combination of a lithium-utilizing capacitor and a lithium-ion battery is made in which each member of the combination comprises porous electrode layers prepared by using atmospheric plasma coating devices and processes.
- the layered, electrochemical, capacitor and battery are assembled in a common pouch and electrically interconnected as a hybridized capacitor-battery, suitable for providing balanced energy and power to electrical load demanding devices.
- Electric powered automotive vehicles use multi-cell batteries to provide electrical energy for providing electrical power for driving the vehicle and for providing electrical energy to many devices on the vehicle.
- Batteries comprising many lithium-ion electrochemical cells are examples of such electrical power sources. And such batteries are used in many non-automotive applications.
- lithium-ion battery with an electrochemical capacitor which also uses lithium ions.
- capacitors may be charged during braking of the vehicle and the stored electrical charge used later in recharging cells of a lithium-ion battery.
- the capacitors include (1) electric double layer capacitors (ELDC), (2) supercapacitors, and (3) hybridcapacitors.
- An ELDC-type capacitor is based on the formation of electric double layers on the surfaces of electrodes, where cations and anions of an electrolyte form Helmholz layers on the surfaces of both electrodes.
- positive ions such as lithium cations in the electrolyte adsorb on one electrode while the negative ions, anions such as (PF 6 ) ⁇ adsorb on the other electrode.
- the fundamental process is adsorption and desorption, which enables the faster rate of charging and discharging.
- Supercapacitors utilize the hybridization of electric double layer capacitance with redox capacitance, where the composite electrode material is prepared to consist of porous carbon and fine metal particles.
- Hybridcapacitors or asymmetric supercapacitors are proposed to get high capacitance and high energy density using different material at the two electrodes, anode and cathode, such as graphitized carbon at the anode and activated carbon at the cathode, where the intercalation/de-intercalation of Li + at the anode and the formation of electric double layers at the cathode are intended to occur.
- the negative electrode (anode) releases lithium ions (de-intercalates lithium ions) during discharging of the cell, and the positive electrode absorbs lithium ions.
- the negative electrode releases electrons to the external circuit and the positive electrode receives them.
- the reverse electrochemical process occurs when the battery is charged.
- the close proximity of the separate capacitor and lithium-ion battery cell structures simplifies electrical connections and facilitates their interaction in providing electrical energy to nearby electrical loads.
- the outline shapes of the respective current collectors, porous electrode material layers, and porous separators may be similar and complementary so as to suggest the simultaneous manufacture of both the capacitor electrodes and the battery electrodes and their interrelated functions.
- the manufacturing process of this invention is particularly useful in making hybrid combinations of a lithium-using capacitor and lithium-ion battery cell.
- atmospheric plasma spray devices and methods are used to form the porous particulate electrodes of both a capacitor and a lithium-ion cell.
- the plasma-spray methods of forming porous layered electrodes of the capacitor are comparable and compatible with plasma-spray methods that may be used for forming the porous layered electrodes of a lithium-ion battery.
- the electrodes and separator for a capacitor and the electrodes and separator for a lithium-ion cell may be prepared contemporaneously, but separately, and a capacitor and a lithium-ion cell may be placed, spaced-apart, in a suitable pouch module or other container and the porous electrodes and separators infiltrated with a lithium-ion transporting, non-aqueous, liquid electrolyte.
- each member of the capacitor and battery may be prepared in a rectangular shape of suitable predetermined dimensions for assembly of the complementary, hybridized members in operating units.
- Pre-formed current collector foils for each of the positive and negative electrodes of the capacitor and battery may serve as substrates for the plasma deposition of porous layers of the respective electrode materials.
- Such current collector foils are typically flat and are sized with opposing rectangular surfaces (faces) of suitable area for the deposit of a suitable layer of selected electrode material on each side (major face) of the foil.
- the foil may have an uncoated tab extending from one side for electrical connection of the electrode material with other electrodes or with an electrical circuit.
- a porous polymer separator may serve as a substrate for the plasma deposition of particulate electrode material.
- a layer of positive capacitor electrode material may be deposited by plasma deposition on one side of a suitably sized, rectangular porous separator and a porous layer of negative capacitor electrode material is deposited by plasma deposition on the other side of the separator.
- the deposited electrode material and its substrate are assembled with other members of the capacitor structure.
- a complementary lithium battery may be made using a like process.
- Atmospheric plasma spray devices are commercially available, and practices for their use in the deposition of capacitor electrode materials and battery electrode materials will be described and illustrated in more detail below.
- the deposition process will be initially described with reference to a capacitor. But substantially the same practices may be used to make the members of the battery.
- a quantity of small particles of electrode material is prepared. Suitable portions are continually introduced into a confined stream of unheated air (or other suitable carrier gas) flowing in a suitable duct or housing.
- the confined air stream is directed through a plasma generator, within the housing, in which the stream-borne particles are momentarily, rapidly heated.
- the energized stream of electrode material particles is passed through a suitable nozzle and directed so as to progressively form an adherent, porous, particulate coating on a major surface of a current collector foil or on a major surface of a separator.
- a porous layer of the particles is formed having a generally predetermined uniform thickness.
- the thickness of the electrode material layer for the capacitor which is often in the range of about 100-200 micrometers, is determined to provide a porous electrode layer for infiltration with a lithium-ion conducting electrolyte, to provide suitable lithium ion transporting properties for the capacitor.
- suitable anode materials for the capacitor include graphite, activated carbon, and lithium-titanium containing oxides and phosphates.
- suitable cathode materials include certain lithium-metal oxides and phosphates, activated carbon, graphite, and additional materials which will be identified below in this specification. It may also be helpful to coat some of the respective electrode material particles with small metal particles (or other binder materials) which are at least partially melted or softened in the plasma and serve to bond the electrode material particles to each other and to their current collector or separator substrate.
- both the capacitor and the lithium-ion battery may have several layers of electrodes (with interspersed porous separators) with their respective current collectors.
- the current collectors are suitably connected so that the capacitor and lithium-ion battery each have two terminals.
- an assembly of like-sized elements of both the capacitor member and the lithium-ion cell member are placed in the pouch, but the capacitor is separated from the battery cell.
- the pores of the electrode members of the capacitor and the lithium-ion cell, and their respective separators are infiltrated with a common lithium ion transporting, non-aqueous lithium electrolyte solution.
- FIG. 1 is a schematic, side view of a positive electrode, porous separator, and negative electrode of a capacitor placed in a common pouch with a positive electrode, porous separator, and negative electrode for a lithium-ion battery cell.
- each of the capacitor and lithium-ion battery would have many layers of electrode materials deposited on current collectors.
- the current collector tabs of the positive electrodes would be suitably interconnected at a positive terminal and the current collector tabs of the negative electrodes would be likewise connected at a negative terminal.
- the illustrations of the capacitor and lithium ion battery have been simplified in FIG. 1 by depicting only one of the seven-layer sets of the electrode and separator elements of each capacitor unit and lithium-ion battery unit.
- FIG. 1 a side of the pouch has been removed to show the layered structures of the capacitor and lithium-ion cell.
- the respective electrode materials have been deposited as porous particulate layers from a plasma spray device onto metal current collector foils.
- Each element is a thin rectangular body.
- the current collector foils have connector tabs extending from their upper sides and are arranged for a series-type electric connection between a hybrid combination of the capacitor and its associated lithium-ion battery cell.
- FIG. 1 there are four separate current collector leads extending from the top of the pouch, representing the four terminals of the hybridized capacitor and lithium-ion battery.
- FIG. 2 is a simplified, schematic side view, with a portion of the pouch container removed, similar to FIG. 1 , of the hybrid combination of a capacitor and lithium-ion cell.
- the capacitor and lithium-ion cell are positioned in a common pouch in an arrangement in which they are in electrical parallel-connection for co-delivery of electrical power to an external circuit.
- FIG. 2 only two terminals emerge from the pouch because the positive electrode tabs of the capacitor and battery have been connected, as have their negative electrode tabs.
- FIG. 3A is a schematic illustration of an atmospheric plasma device, a plasma nozzle supported and adapted to progressively apply particles of cathode material onto the upper side of an aluminum current collector foil.
- the device and coating process may be used in making electrodes for both capacitors and lithium ion cells.
- the aluminum current collector foil is carried on a conveyor belt or the like.
- the particles of cathode material may, for example, be particles of activated carbon for a capacitor cathode or particles of LiMn 2 O 4 for a cathode of a lithium-ion battery.
- the particles of electrode material may be coated with small particles of a metal or of a suitable resin which, when heated in the plasma device, melt and re-solidify to serve as a binder to bond the electrode material particles to each other and to the current collector foil.
- FIG. 3B is an enlarged side view of an aluminum current collector foil which has been coated on both of its opposing sides or faces with a bonded layer of positive electrode (cathode) particles for a lithium-containing capacitor.
- FIG. 3C is an enlarged side view of a copper current collector foil which has been coated on both of its opposing sides or faces with a bonded layer of negative electrode (anode) particles for a lithium-containing capacitor.
- FIG. 4 is an enlarged schematic side view illustration of a seven layer capacitor structure that is produced using the plasma spray process illustrated in FIG. 3A .
- the center layer of the capacitor structure is a porous polymer separator.
- Three layers of materials for the capacitor have been applied, progressively, to each side of the porous plasma separator.
- a layer of capacitor cathode material has been applied to the upper surface of the separator (as it is shown in FIG. 4 ), followed by a current collector foil layer, and a second layer of capacitor cathode material.
- three layers of material for the anode have been applied, progressively, to the bottom side of the capacitor as illustrated in FIG. 4 .
- a lithium-ion battery structure could be prepared and illustrated in a similar manner.
- hybrid electrochemical capacitors are prepared, consisting of a capacitor and a lithium-ion battery which are fabricated by plasma powder electrode coating technology, delivering a balanced energy-power performance. Both the capacitor and the battery will adsorb or intercalate lithium ions and both the capacitor and battery will be combined in a common pouch or other suitable container. Accordingly, electrode members for both the capacitor and the battery may be prepared using atmospheric plasma spray devices or like plasma deposition devices. As stated, a uniform layer of particulate electrode material may be deposited over a selected surface area of a metal foil current collector or over a selected surface area of a porous separator member.
- the formation of electrode layers on current collectors and separator surfaces may be conducted in sequential or complementary steps to accommodate the assembly of positive and negative electrodes on opposite sides of a compatible separator.
- the positive electrode-separator-negative electrode structures for a capacitor and a lithium-ion cell may thus be prepared separately, but contemporaneously, for assembly into a pouch and infiltration with a common volume of a non-aqueous, lithium-ion conducting electrolyte.
- selected electrode materials, for both the electrochemical capacitor positive and negative electrodes be prepared in the form of micrometer size particles for deposition on a selected substrate.
- the selected electrode material compositions are deposited on compatible metal current collector foils, or on a sheet of porous separator material, using one or more atmospheric plasma spray devices.
- the particles of electrode materials, prepared for the plasma deposition may have been coated with smaller particles of a metal or of other suitable binder material.
- Electrode materials for the lithium-ion cell are likewise separately prepared and plasma deposited on selected cell substrates for assembly into lithium-ion cells and placement with a compatible lithium-ion absorbing capacitor in a container.
- Suitable materials for plasma deposition as cathode (positive electrode) particles for the capacitor include:
- Metal oxides MO x , where M is one or more of Pb, Ge, Co, Ni, Cu, Fe, Mn, Ru, Rh, Pd, Cr, Mo, W, and Nb.
- a lithium-metal-oxide including: Li x MO 2 in which M is Co, Ni, Mn, Cr, or V.
- Li x M 2 O 4 in which M is Co, Ni, Mn, Cr, or V.
- Li x Ni y M 1-y O 2 in which m is Fe or Mn.
- LiNi 1-x-y-z Co x M1 y M2 z O 2 in which M1, M2 are different metals selected from Al, Ni, Co, Fe, Mn, V, Cr, Ti, W, Ta, or Mo.
- LiNiVO 4 LiNbO 3 , LiFePO 4 , LiTi 2 (PO 4 ) 3 , or Li 3 V 2 (PO 4 ) 3 .
- a metal sulfide NiS, Ag 4 Hf 3 S 8 , CuS, FeS, and FeS 2 .
- a polymer such as: poly (3-methyl thiophene), polyaniline, polypyrrole, poly (para-phenylene), or polyacene.
- cathode particles for the capacitor are usually plasma-deposited on an aluminum current collector foil or on a porous polymer separator.
- Suitable materials for plasma deposition as anode (negative electrode) particles for the capacitor include:
- Li 4 Ti 5 O 12 LiTi 2 O 4 , LiCrTiO 4 , LiTi 2 (PO 4 ) 3 , and graphite or activated carbon.
- Positive electrode material for the capacitor is preferably plasma deposited on an aluminum current collector foil or on a polymeric separator such as a porous layer of polyethylene, polypropylene, or an ethylene-propylene copolymer.
- the hybrid capacitor and battery undergo a formation cycle and are then degassed.
- the plasma powder coating method can optimize the surface area of the material layers coated on the foil or the separator, and can also control the porosity of the respective electrodes, in order to improve both the energy and power performance of the hybrid capacitor-battery.
- Li 4 Ti 5 O 12 has been demonstrated as a promising negative electrode material for use in combination with activated carbon as the positive electrode material for hybrid capacitor applications.
- the power density depends on the rate capability of the intercalated compound Li 4 Ti 5 O 12 , which is associated with the Li-ion diffusion coefficient and the diffusion distance in the intercalated compound particle.
- plasma powder electrode coating technology can be introduced to develop a nanosize-Li 4 Ti 5 O 12 electrode with well controlled porosity, in which conductive metal particle and no polymer binder will benefit the rate performance.
- the energy density of the capacitor is critically dependent on the energy density of the carbon positive electrode material.
- Plasma powder electrode coating technology can be used to enlarge the surface area of carbon material in the electrode by size and porosity optimization to improve the specific capacity.
- the lithium-ion cell component of this capacitor-cell combination may be formed of like current collector foils and like porous separator materials.
- suitable particulate materials for positive electrodes for lithium-ion cells include lithium manganese nickel cobalt oxide, lithium manganese oxide, lithium cobalt oxide, lithium nickel aluminum cobalt oxide, lithium iron phosphate, and other lithium oxides and phosphates.
- suitable particulate negative electrode materials for lithium-ion cells include lithium titanate, graphite, activated carbon, and silicon-based materials such as silicon, silicon-based alloys, SiOx, silicon-tin composites, and lithium-silicon alloys.
- the common electrolyte for the capacitor cell and the lithium-ion cell may be a lithium salt dissolved in one or more organic liquid solvents.
- salts include lithium hexafluorophosphate (LiPF 6 ), lithium tetrafluoroborate (LiBF 4 ), lithium perchlorate (LiClO 4 ), lithium hexafluoroarsenate (LiAsF 6 ), and lithium trifluoroethanesulfonimide.
- Some examples of solvents that may be used to dissolve the electrolyte salt include ethylene carbonate, dimethyl carbonate, methylethyl carbonate, and propylene carbonate. There are other lithium salts that may be used and other solvents.
- a combination of lithium salt and non-aqueous liquid solvent is selected for providing suitable mobility and transport of lithium ions between the opposing electrodes in the operation of the cell.
- the electrolyte is carefully dispersed into and between closely spaced layers of the electrode elements and separator layers of each of the capacitor cell and the battery cell.
- the electrolyte is not illustrated in the following drawing figures because it is difficult to illustrate the electrolyte between tightly compacted electrode layers pressing on an interposed separator.
- a thin porous separator layer is interposed between the major outer face of the negative electrode material layer and the major outer face of the positive electrode material layer of each of the capacitor and the battery unit.
- the porous separator may be formed of a porous film or of porous interwoven fibers of suitable polymer material, or of ceramic particles, or a polymer material filled with ceramic particles.
- the porous separator layer is filled with a liquid lithium-ion containing electrolyte and enables the transport of lithium ions between the porous electrode members. But the separator layer is used to prevent direct electrical contact between each of the negative and positive electrode material layers in each unit, and is shaped and sized to serve this function.
- FIG. 1 is a schematic illustration of a pouch-contained assembly 10 of the elements of an electrochemical capacitor 12 , a lithium-ion battery cell 14 , and a polymer-coated, metal foil pouch 16 to contain the combined capacitor and cell elements for electrical series connection to each other and/or to other members of an electrical circuit.
- One side of the pouch 16 including the closure seam of its sides, has been cut-away in the figure to show the relative positions of the electrochemical capacitor 12 and the lithium-ion cell 14 .
- each capacitor will be formed of several layers of positive electrodes, negative electrodes, and separators, prepared as described in the following paragraphs.
- the like-charged electrode layers are connected by tabs on their current collectors, respectively, in a positive terminal and a negative terminal for the capacitor.
- the positive and negative tabs for the groups of positive and negative capacitor electrodes may be connected with other devices in an electrical circuit as desired.
- Lithium-ion batteries are also typically formed of many positive electrodes connected to a positive terminal and many negative electrodes connected to a negative terminal. But since the focus of this specification is on the use of plasma deposition methods and devices to make such electrodes and separators, the illustrations of FIGS. 1 and 2 have been simplified to depict the single set of electrodes for capacitor 12 and lithium-ion cell 14 .
- the illustrated electrochemical, capacitor 12 comprises a positive electrode, which in this example comprises a rectangular aluminum foil current collector 18 with a connector tab 18 ′ extending from its top side and through the overlapping surface of pouch 16 .
- the positive electrode of the capacitor further comprises porous particulate layers of electrode material 20 which have been deposited by atmospheric plasma deposition on each face of the aluminum foil current collector 18 .
- the positive electrode material for the capacitor may, for example, be activated carbon.
- the thickness of the current collector foil 18 may be, for example, about ten micrometers and the lengths of the sides of the foil may, for example be in the range of 75 mm to 100 mm, not including the tab 18 ′.
- the porous layers of electrode material 20 may, for example, be about 10 to 500 micrometers in thickness and applied to substantially cover the rectangular faces of current collector foil 18 , but not tab 18 ′.
- the electrochemical capacitor 12 further comprises a negative electrode, which in this example comprises a rectangular copper foil current collector 22 with a connector tab 22 ′ extending from its top side and through the overlying surface of pouch 16 .
- the negative electrode of the capacitor further comprises porous particulate layers of electrode material 24 which have also been deposited by atmospheric plasma deposition on each face of the copper foil current collector 22 , but not on tab 22 ′.
- the negative electrode material for the capacitor may, for example, also be activated carbon.
- the side lengths and thickness of the copper current collector foil 22 are suitably like the dimensions of the positive electrode current collector foil.
- the porous layers of negative electrode material 24 may, for example, be of complementary thickness to that of the positive electrode materials and applied to substantially cover the rectangular faces of current collector foil 22 , but not tab 22 ′.
- Porous separator 26 may be formed, for example, of polyethylene fibers. Separator 26 has a two-dimensional shape and a thickness. In this example, the rectangular shape of separator is determined to cover the contacting surfaces of the respective electrode materials 20 , 24 and to physically separate them. The shape and thickness of the porous separator 26 also serves to retain liquid electrolyte for lithium absorption and desorption by the electrode layers 20 , 24 of the capacitor. In the assembled device, the pores of the electrode materials 20 , 24 are infiltrated with liquid lithium-ion conducting electrolyte, as well as the pores of separator 26 .
- the liquid electrolyte is not illustrated in FIG. 1 , but it is present in the porous electrode layers and the separators of each of the assembled capacitor 12 and battery 14 .
- lithium ions are transported between the electrode materials 20 and 24 through the electrolyte.
- the structure of the lithium-ion cell or battery 14 is similar to that of capacitor 12 and the outline sizes and thickness of the respective current collector foils, electrode material layers and separator of battery 14 are comparable to the similar structural elements of capacitor 12 . But the electrode materials may be different and the electrochemical reactions are different.
- batteryl 4 includes an aluminum positive electrode current collector foil 30 with a connector tab 30 ′ extending through the overlying pouch material 16 .
- Plasma deposited positive electrode layers 32 (e.g., activated carbon) are formed on both major faces of the aluminum current collector foil 30 .
- the positive electrode material 32 for the battery 14 may, for example, be particles of LiFePO 4 .
- a copper negative current collector foil 34 with tab 34 ′ is plasma coated on both of its major faces with layers of negative electrode material 36 .
- the particle layers of negative electrode material 36 may comprise activated carbon or resin-bonded activated carbon.
- the facing porous layers of positive electrode material 32 and of negative electrode material 36 are kept apart by porous polymer separator 38 .
- the pores of separator 38 and of electrode layers 32 and 36 are filled with a suitable non-aqueous, lithium-ion conducting electrolyte.
- the electrolyte may, for example, comprise lithium hexafluorophosphate (LiPF 6 ) dissolved in a mixture of dimethyl carbonate and methylethyl carbonate as solvent.
- the current collector tab leads 18 ′ and 22 ′ for capacitor 12 and the current collector tab leads 30 ′, 34 ′ for battery 14 each extend through the adjoining pouch material and are positioned for serial electrical connections. In a typical hybrid capacitor, these current collector leads would be the four terminal posts for the series-connected assembly in pouchl 6 .
- Such an arrangement offers many possibilities for interconnection of the capacitor electrodes and battery electrodes with each other and with other members of an electrical power-requiring system.
- the electrical connections between capacitor 12 and lithium-ion battery 14 may, for example, be through a DC-DC converter. This type of electrical interconnection could enable the capacitor 12 to store energy, for example, when an automotive vehicle is braking, and to later release energy to the adjacent lithium-ion battery 14 during vehicle starting or acceleration.
- FIG. 2 illustrates a pouch-contained assembly 110 of a capacitor 112 and battery 114 which are arranged and oriented in pouch 116 for parallel electrical connection between capacitor 112 and battery 114 .
- a capacitor and battery would each comprise many connected positive electrodes with current collector tabs connected in a single positive terminal and many negative electrodes with current collector tabs electrically connected in a single negative terminal.
- the electrodes and separator of capacitor 112 may be substantially identical in shapes and compositions with respect to the corresponding elements of capacitor 12 as shown in FIG. 1 .
- the electrodes and separator of battery 114 may be substantially identical in shapes and compositions with respect to the corresponding elements of battery 14 shown in FIG. 1 .
- the corresponding current collector foils, electrode layers and separators of FIG. 2 are identified by numerals 1 xx (or 1 xx′) with respect to the same parts of FIG. 1 which are identified as xx or xx′.
- capacitor 112 and battery 114 are arranged and oriented in pouch 116 for parallel electrical connection between capacitor 112 and battery 114 , and for series connection with these combined elements and electrical power-requiring devices outside pouch 116 . Accordingly, positive electrode tab 118 ′ of capacitor 112 and positive electrode tab 130 ′ of battery 114 are connected as a single positive (+) terminal 140 which extends through the top of pouch 116 . In a similar arrangement, negative electrode tab 122 ′ of capacitor 112 and negative electrode tab 134 ′ of battery 114 are connected as a single negative ( ⁇ ) terminal 142 which extends through the top of pouch 116 .
- the two components may be designed to operate in a common voltage window and to achieve a higher power in their common voltage range.
- FIG. 3A is presented to illustrate the plasma deposition of heated particles of active positive electrode (cathode during capacitor discharge) material for a capacitor onto one major face of an aluminum current collector foil.
- the capacitor elements may be shaped and composed like those of capacitor 12 in FIG. 1 , or capacitor 112 in FIG. 2 , with its aluminum current collector foil 18 and positive electrode material 20 .
- FIG. 3A illustrates the practice of using an atmospheric plasma application device 200 to deposit active positive electrode material particles for a capacitor in a porous layer on a surface of a metal current collector foil.
- the finished capacitor is intended to be like capacitor 12 as illustrated in FIG. 1 .
- FIG. 3A is intended to illustrate the method of applying particles of positive electrode material as electrode material layer 20 on one side of current collector foil 18 .
- the substrate is the upper surface 17 of a copper current collector foil 18 with its connection tab 18 ′. Connection tab 18 ′ is not coated with the electrode material.
- the active positive electrode material is particles of commercially available activated carbon with their extraordinary porosity and surface area.
- the activated carbon particles may be coated with a suitable amount of a polymer binder for bonding of the particles to each other and to surface 17 of the current collector 18 .
- the current collector foil 18 is placed and carried on a movable work surface 202 , such as a conveyor belt, or the like, for locating the current collector foil 18 , with its upper surface 17 , under the plasma application device.
- a movable work surface 202 such as a conveyor belt, or the like, for locating the current collector foil 18 , with its upper surface 17 , under the plasma application device. This process may be conducted in air and in a normal ambient workplace atmosphere.
- the copper current collector foil 18 is illustrated in the form of a thin, square layer of about 100 millimeters length on each side, but the capacitor elements are also often made in other rectangular shapes and dimensions depending on the intended size of the capacitor elements and assembled capacitor modules.
- the copper current collector foil layer 18 is often about ten to twelve micrometers in thickness.
- the substrate 202 is moved and placed in a flat position at ambient conditions under a suitable atmospheric plasma spray generator apparatus 200 with a nozzle for directing its flow stream of electrode material particles.
- the spray device(s) and/or workpiece may be carried on a suitable support and moved under suitable programmable controls for sequential deposition of particulate electrode material on the surface 17 of one or more copper current collectors 18 .
- an atmospheric plasma apparatus 200 may comprise an upstream round flow chamber 204 (shown partly broken-off in FIG. 3 ) for the introduction and conduct of a flowing stream of suitable working gas, such as air, nitrogen, or an inert gas such as helium or argon.
- suitable working gas such as air, nitrogen, or an inert gas such as helium or argon.
- the flow of the working gas would be introduced above the broken-off illustration of flow chamber 204 and proceed in a downward direction.
- this illustrative initial flow chamber 204 is tapered inwardly to smaller round flow chamber 206 .
- Active positive electrode material particles 208 for the capacitor are delivered through opposing supply tubes 210 , 212 into round flow chamber 206 .
- Supply tube 208 is shown partially broken-away to illustrate delivery of the positive capacitor electrode material particles 208 .
- the electrode material particles 208 are suitably introduced from opposing sides of the apparatus 200 into the working gas stream in chamber 206 and then carried into a plasma nozzle 214 in which the air (or other working gas) is converted to a plasma stream at atmospheric pressure.
- the electrode material particles 208 enter the gas stream in chamber 206 they are dispersed and mixed in the stream and carried by it.
- the electrode material particles 208 are heated by the formed plasma of predetermined and controlled energy to a precursor processing temperature.
- the momentary thermal impact on the electrode material particles may be a temperature of from about 300 ° C. up to about 3500 ° C.
- the plasma activated electrode material particles exit nozzle 214 as stream 216 .
- the stream 216 of air-based plasma and suspended, plasma-activated, activated carbon electrode material particles is progressively directed by the nozzle 214 to deposit particles as a layer of electrode material 20 onto the surface of the upper surface 17 of the copper foil current collector 18 .
- the nozzle 214 and stream 216 of suspended electrode material is moved in a suitable path and at a suitable rate such that the particulate activated carbon electrode material 208 is deposited as a porous layer 20 of specified thickness of the electrode particles on the surface 17 of the current collector foil 18 .
- the relative movement of the plasma spray stream 216 and/or the substrate 202 is continues until the entire face 17 of current collector foil 18 (but not tab 18 ′) is covered with a generally uniformly thick layer of capacitor positive electrode material 20 .
- the current collector foil may then be turned over so that its opposing face is likewise coated with a layer of positive electrode material 20 .
- FIG. 3B is a schematic illustration of a representative positive electrode for a capacitor, like capacitor 12 in FIG. 1 or capacitor 112 in FIG. 2 .
- Both major sides of aluminum current collector foil 18 have been coated, using an atmospheric plasma spray device, with substantially identical adherent layers of positive capacitor electrode material 20 .
- Current collector tab 18 ′ remains exposed for desired inter-connection with other capacitor electrodes or with battery electrodes or with other electrical devices.
- FIG. 3C illustrates a negative capacitor electrode that, in this example, consists of a copper current collector foil 22 (with extended tab 22 ′) coated on both major faces with generally uniformly thick layers of plasma deposited negative electrode material 24 .
- the negative electrode material for the capacitor may also be suitably sized particles of a commercially-available activated carbon.
- both the positive electrode and the negative electrode for a capacitor cell were prepared by plasma deposition of particles of the electrode material onto both sides of a suitable metal current collector.
- the assembly of the capacitor elements is then advanced by placing one face of positive electrode material against one side of a porous separator and one face of a negative electrode material against the opposite face of the separator.
- the assembled capacitor is illustrated in FIG. 4 .
- the capacitor is identified by numeral 12 because it is intended to illustrate in perspective view, the capacitor structures illustrated in side view in FIGS. 1 and 2 . As seen in FIG.
- the seven layers of capacitor 12 comprise porous layer 20 of positive capacitor electrode material, copper positive electrode current collector foil 18 with its uncoated connector tab 18 ′, the opposing layer of porous positive electrode material 20 , porous separator 26 , a layer of porous negative capacitor electrode material 24 , aluminum negative electrode current collector foil 22 with its uncoated connector tab 22 ′, and an opposing layer of porous positive electrode material 24 . It is seen that a layer of positive electrode material 20 and a layer negative electrode material 24 are pressed against the corresponding faces of the porous separator 26 .
- capacitor 12 When capacitor 12 has been assembled with a like-shaped and like- made battery (e.g., battery 14 ) in a suitable container, like pouch 16 , both the capacitor and battery will be suitably infiltrated with a shared lithium-ion transporting electrolyte.
- a like-shaped and like- made battery e.g., battery 14
- a suitable container like pouch 16
- both the capacitor and battery will be suitably infiltrated with a shared lithium-ion transporting electrolyte.
- particulate cathode material was plasma coated on both sides of an aluminum current collector foil to form a capacitor cathode, and particulate anode material was plasma coated onto both sides of a copper current collector foil to form a capacitor anode.
- the assembly of the capacitor cell was then completed by placing a cathode on one side of a suitable porous separator and a cathode on the other side of the separator.
- a like plasma deposition process, using suitable electrode materials, may be used to make and assemble a lithium-ion battery cell for the hybrid combination.
- particles of cathode electrode material are deposited on one side of a suitable separator.
- particles of a current collector metal e.g., Al
- a second layer of particulate cathode material may be plasma deposited on the current collector layer.
- Particles of anode electrode material, metal current collector material, and anode electrode material are then sequentially plasma deposited onto the opposite side of the separator. The result of the six layers of plasma-deposited is equivalent to the seven layer capacitor structure illustrated in FIG. 4 .
- either plasma deposition process using appropriate particulate electrode materials and current collector material may be used to make the electrochemical cell structures of either a lithium-ion using capacitor or a lithium-ion battery.
- the plasma deposition process can be conducted, for example, in parallel or other complementary manufacturing lines to simultaneously produce complementary capacitors and batteries for assembly into suitable containers for hybrid combination.
- the porous elements of the combined assembly are then infiltrated or impregnated with a suitable lithium ion containing electrolyte.
- capacitor and battery members of the combination may be charged or otherwise prepared for their respective electrochemical functions.
- the layers of the respective electrode material particles is pre-deposited on a compatible current collector surface or a compatible separator surface using one or more atmospheric plasma nozzles or deposition devices.
- plasma nozzles for this application are commercially available and may also be carried and used on robot arms, under multi-directional computer control, to apply suitable electrode particles to coat the surfaces of each metal current collector foil or separator surface for a lithium-using capacitor and, separately, for a lithium-ion cell.
- Multiple nozzles may be required and arranged in such a way that a desired coating speed may be achieved in terms coated area per unit of time.
- the atmospheric plasma nozzle typically has a metallic tubular housing which provides a flow path of suitable length for receiving the flow of working gas, receiving and dispersing particles of electrode material, and for enabling the formation of the plasma stream in an electromagnetic field established within the flow path of the tubular housing.
- the tubular housing terminates in a conically tapered outlet, shaped to direct a suitably shaped plasma stream toward an intended substrate to be coated.
- An electrically insulating ceramic tube is typically inserted at the inlet of the tubular housing such that it extends along a portion of the flow passage.
- a stream of a working gas, such as air (or nitrogen or argon), and carrying dispersed particles of a specified electrode material, is introduced into the inlet of the nozzle.
- the flow of the air-particle mixture may be caused to swirl turbulently in its flow path by use of a swirl piece with flow openings, also inserted near the inlet end of the nozzle.
- a linear (pin-like) electrode is placed at the ceramic tube site, along the flow axis of the nozzle at the upstream end of the flow tube.
- the electrode is powered by a suitable generator at a frequency in the 0.1 hertz to gigahertz range and to a suitable potential of a few kilovolts.
- Plasma generation technology such as corona discharge, radio wave, and microwave sources, and the like, may be employed.
- the metallic housing of the plasma nozzle is grounded. Thus, an electrical discharge can be generated between the axial pin electrode and the housing. No vacuum chamber is used.
- the frequency of the applied voltage and the dielectric properties of the ceramic tube produce a corona discharge at the stream inlet and the electrode.
- an arc discharge from the electrode tip to the housing is formed.
- This arc discharge is carried by the turbulent flow of the air/particulate electrode material stream to the outlet of the nozzle.
- a reactive plasma of the air (or other carrier gas) and dispersed electrode particles is formed at a relatively low temperature.
- a copper nozzle at the outlet of the plasma container is shaped to direct the plasma stream in a suitably confined path against the surfaces of the current collector substrates for the lithium-ion cell electrode members. The energy of the plasma may be determined and managed for the material to be applied.
Landscapes
- Engineering & Computer Science (AREA)
- Power Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Electric Double-Layer Capacitors Or The Like (AREA)
- Cell Electrode Carriers And Collectors (AREA)
- Secondary Cells (AREA)
- Inorganic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
Abstract
Atmospheric plasma spray devices and methods are used in the making of the electrodes for both a lithium-ion battery and a lithium-ion utilizing capacitor structure, which are to be placed in a common container and infiltrated with a common lithium-ion transporting, liquid electrolyte. The lithium-ion-utilizing capacitor and lithium-ion cell battery are combined such that the respective electrodes may be electrically connected, either in series or parallel connection for in energy storage and management in an automotive vehicle or other electrical power supply application.
Description
- A combination of a lithium-utilizing capacitor and a lithium-ion battery is made in which each member of the combination comprises porous electrode layers prepared by using atmospheric plasma coating devices and processes. The layered, electrochemical, capacitor and battery are assembled in a common pouch and electrically interconnected as a hybridized capacitor-battery, suitable for providing balanced energy and power to electrical load demanding devices.
- Electric powered automotive vehicles use multi-cell batteries to provide electrical energy for providing electrical power for driving the vehicle and for providing electrical energy to many devices on the vehicle. Batteries comprising many lithium-ion electrochemical cells are examples of such electrical power sources. And such batteries are used in many non-automotive applications.
- In some applications it may be useful to combine a lithium-ion battery with an electrochemical capacitor which also uses lithium ions. For example, such capacitors may be charged during braking of the vehicle and the stored electrical charge used later in recharging cells of a lithium-ion battery.
- There is a need for manufacturing practices to jointly prepare cells for lithium-ion batteries and such electrochemical capacitors for efficiency in their mutual interconnection and interaction.
- It is believed that there are applications in electrically powered automotive vehicles (and in non-automotive applications) in which suitable lithium-containing capacitor structures and suitable lithium-ion battery structures may be placed close to each other, as in a common pouch or like container, and share a common volume of a lithium-ion conducting electrolyte, with a suitable amount of electrolyte constituents for both devices. A hybridized combination of capacitor and battery is thus provided. The capacitor and battery each use lithium, and a lithium-ion conducting electrolyte, in its electrochemical function.
- Here the capacitors include (1) electric double layer capacitors (ELDC), (2) supercapacitors, and (3) hybridcapacitors. An ELDC-type capacitor is based on the formation of electric double layers on the surfaces of electrodes, where cations and anions of an electrolyte form Helmholz layers on the surfaces of both electrodes. During cell charge-discharge, positive ions such as lithium cations in the electrolyte adsorb on one electrode while the negative ions, anions such as (PF6)− adsorb on the other electrode. The fundamental process is adsorption and desorption, which enables the faster rate of charging and discharging. Supercapacitors utilize the hybridization of electric double layer capacitance with redox capacitance, where the composite electrode material is prepared to consist of porous carbon and fine metal particles. Hybridcapacitors (or asymmetric supercapacitors) are proposed to get high capacitance and high energy density using different material at the two electrodes, anode and cathode, such as graphitized carbon at the anode and activated carbon at the cathode, where the intercalation/de-intercalation of Li+ at the anode and the formation of electric double layers at the cathode are intended to occur.
- In the lithium-ion battery cell, the negative electrode (anode) releases lithium ions (de-intercalates lithium ions) during discharging of the cell, and the positive electrode absorbs lithium ions. The negative electrode releases electrons to the external circuit and the positive electrode receives them. The reverse electrochemical process occurs when the battery is charged. The close proximity of the separate capacitor and lithium-ion battery cell structures simplifies electrical connections and facilitates their interaction in providing electrical energy to nearby electrical loads.
- In such hybrid applications, the outline shapes of the respective current collectors, porous electrode material layers, and porous separators may be similar and complementary so as to suggest the simultaneous manufacture of both the capacitor electrodes and the battery electrodes and their interrelated functions. The manufacturing process of this invention is particularly useful in making hybrid combinations of a lithium-using capacitor and lithium-ion battery cell.
- In accordance with practices of this invention, atmospheric plasma spray devices and methods are used to form the porous particulate electrodes of both a capacitor and a lithium-ion cell. The plasma-spray methods of forming porous layered electrodes of the capacitor are comparable and compatible with plasma-spray methods that may be used for forming the porous layered electrodes of a lithium-ion battery. In some preferred embodiments of this invention, the electrodes and separator for a capacitor and the electrodes and separator for a lithium-ion cell may be prepared contemporaneously, but separately, and a capacitor and a lithium-ion cell may be placed, spaced-apart, in a suitable pouch module or other container and the porous electrodes and separators infiltrated with a lithium-ion transporting, non-aqueous, liquid electrolyte.
- In an illustrative example, each member of the capacitor and battery may be prepared in a rectangular shape of suitable predetermined dimensions for assembly of the complementary, hybridized members in operating units. Pre-formed current collector foils for each of the positive and negative electrodes of the capacitor and battery may serve as substrates for the plasma deposition of porous layers of the respective electrode materials. Such current collector foils are typically flat and are sized with opposing rectangular surfaces (faces) of suitable area for the deposit of a suitable layer of selected electrode material on each side (major face) of the foil. The foil may have an uncoated tab extending from one side for electrical connection of the electrode material with other electrodes or with an electrical circuit.
- In another embodiment of the invention, a porous polymer separator may serve as a substrate for the plasma deposition of particulate electrode material. A layer of positive capacitor electrode material may be deposited by plasma deposition on one side of a suitably sized, rectangular porous separator and a porous layer of negative capacitor electrode material is deposited by plasma deposition on the other side of the separator. In each embodiment, the deposited electrode material and its substrate are assembled with other members of the capacitor structure. A complementary lithium battery may be made using a like process.
- Atmospheric plasma spray devices are commercially available, and practices for their use in the deposition of capacitor electrode materials and battery electrode materials will be described and illustrated in more detail below. The deposition process will be initially described with reference to a capacitor. But substantially the same practices may be used to make the members of the battery.
- In summary, a quantity of small particles of electrode material is prepared. Suitable portions are continually introduced into a confined stream of unheated air (or other suitable carrier gas) flowing in a suitable duct or housing. The confined air stream is directed through a plasma generator, within the housing, in which the stream-borne particles are momentarily, rapidly heated. The energized stream of electrode material particles is passed through a suitable nozzle and directed so as to progressively form an adherent, porous, particulate coating on a major surface of a current collector foil or on a major surface of a separator. A porous layer of the particles is formed having a generally predetermined uniform thickness. The thickness of the electrode material layer for the capacitor, which is often in the range of about 100-200 micrometers, is determined to provide a porous electrode layer for infiltration with a lithium-ion conducting electrolyte, to provide suitable lithium ion transporting properties for the capacitor.
- Examples of suitable anode materials for the capacitor include graphite, activated carbon, and lithium-titanium containing oxides and phosphates. Examples of suitable cathode materials include certain lithium-metal oxides and phosphates, activated carbon, graphite, and additional materials which will be identified below in this specification. It may also be helpful to coat some of the respective electrode material particles with small metal particles (or other binder materials) which are at least partially melted or softened in the plasma and serve to bond the electrode material particles to each other and to their current collector or separator substrate.
- After the electrode materials for the capacitor have been suitably deposited on and bonded in a porous layer to their current collector foils or separators, the assembly of the elements for formation of a layered capacitor is completed for placement in a suitable pouch or other module container. Both the capacitor and the lithium-ion battery may have several layers of electrodes (with interspersed porous separators) with their respective current collectors. The current collectors are suitably connected so that the capacitor and lithium-ion battery each have two terminals. In preferred embodiments of the invention, an assembly of like-sized elements of both the capacitor member and the lithium-ion cell member are placed in the pouch, but the capacitor is separated from the battery cell. The pores of the electrode members of the capacitor and the lithium-ion cell, and their respective separators, are infiltrated with a common lithium ion transporting, non-aqueous lithium electrolyte solution.
- Other aspects and features of our invention will be further understood following a more detailed description of illustrated examples of forming electrodes for capacitors which are to be used in combination with a lithium-ion cell or group of cells.
-
FIG. 1 is a schematic, side view of a positive electrode, porous separator, and negative electrode of a capacitor placed in a common pouch with a positive electrode, porous separator, and negative electrode for a lithium-ion battery cell. In practice, each of the capacitor and lithium-ion battery would have many layers of electrode materials deposited on current collectors. The current collector tabs of the positive electrodes would be suitably interconnected at a positive terminal and the current collector tabs of the negative electrodes would be likewise connected at a negative terminal. The illustrations of the capacitor and lithium ion battery have been simplified inFIG. 1 by depicting only one of the seven-layer sets of the electrode and separator elements of each capacitor unit and lithium-ion battery unit. - In
FIG. 1 , a side of the pouch has been removed to show the layered structures of the capacitor and lithium-ion cell. The respective electrode materials have been deposited as porous particulate layers from a plasma spray device onto metal current collector foils. Each element is a thin rectangular body. The current collector foils have connector tabs extending from their upper sides and are arranged for a series-type electric connection between a hybrid combination of the capacitor and its associated lithium-ion battery cell. In the series-type connection ofFIG. 1 there are four separate current collector leads extending from the top of the pouch, representing the four terminals of the hybridized capacitor and lithium-ion battery. -
FIG. 2 is a simplified, schematic side view, with a portion of the pouch container removed, similar toFIG. 1 , of the hybrid combination of a capacitor and lithium-ion cell. In this hybrid combination, the capacitor and lithium-ion cell are positioned in a common pouch in an arrangement in which they are in electrical parallel-connection for co-delivery of electrical power to an external circuit. InFIG. 2 , only two terminals emerge from the pouch because the positive electrode tabs of the capacitor and battery have been connected, as have their negative electrode tabs. -
FIG. 3A is a schematic illustration of an atmospheric plasma device, a plasma nozzle supported and adapted to progressively apply particles of cathode material onto the upper side of an aluminum current collector foil. The device and coating process may be used in making electrodes for both capacitors and lithium ion cells. The aluminum current collector foil is carried on a conveyor belt or the like. The particles of cathode material may, for example, be particles of activated carbon for a capacitor cathode or particles of LiMn2O4 for a cathode of a lithium-ion battery. The particles of electrode material may be coated with small particles of a metal or of a suitable resin which, when heated in the plasma device, melt and re-solidify to serve as a binder to bond the electrode material particles to each other and to the current collector foil. -
FIG. 3B is an enlarged side view of an aluminum current collector foil which has been coated on both of its opposing sides or faces with a bonded layer of positive electrode (cathode) particles for a lithium-containing capacitor. -
FIG. 3C is an enlarged side view of a copper current collector foil which has been coated on both of its opposing sides or faces with a bonded layer of negative electrode (anode) particles for a lithium-containing capacitor. -
FIG. 4 is an enlarged schematic side view illustration of a seven layer capacitor structure that is produced using the plasma spray process illustrated inFIG. 3A . The center layer of the capacitor structure is a porous polymer separator. Three layers of materials for the capacitor have been applied, progressively, to each side of the porous plasma separator. A layer of capacitor cathode material has been applied to the upper surface of the separator (as it is shown inFIG. 4 ), followed by a current collector foil layer, and a second layer of capacitor cathode material. Likewise, three layers of material for the anode have been applied, progressively, to the bottom side of the capacitor as illustrated inFIG. 4 . A lithium-ion battery structure could be prepared and illustrated in a similar manner. - 30
- In accordance with practices of this invention, hybrid electrochemical capacitors are prepared, consisting of a capacitor and a lithium-ion battery which are fabricated by plasma powder electrode coating technology, delivering a balanced energy-power performance. Both the capacitor and the battery will adsorb or intercalate lithium ions and both the capacitor and battery will be combined in a common pouch or other suitable container. Accordingly, electrode members for both the capacitor and the battery may be prepared using atmospheric plasma spray devices or like plasma deposition devices. As stated, a uniform layer of particulate electrode material may be deposited over a selected surface area of a metal foil current collector or over a selected surface area of a porous separator member. The formation of electrode layers on current collectors and separator surfaces may be conducted in sequential or complementary steps to accommodate the assembly of positive and negative electrodes on opposite sides of a compatible separator. The positive electrode-separator-negative electrode structures for a capacitor and a lithium-ion cell may thus be prepared separately, but contemporaneously, for assembly into a pouch and infiltration with a common volume of a non-aqueous, lithium-ion conducting electrolyte.
- In accordance with practices of this invention, it is intended that selected electrode materials, for both the electrochemical capacitor positive and negative electrodes be prepared in the form of micrometer size particles for deposition on a selected substrate. The selected electrode material compositions are deposited on compatible metal current collector foils, or on a sheet of porous separator material, using one or more atmospheric plasma spray devices. The particles of electrode materials, prepared for the plasma deposition, may have been coated with smaller particles of a metal or of other suitable binder material. Electrode materials for the lithium-ion cell are likewise separately prepared and plasma deposited on selected cell substrates for assembly into lithium-ion cells and placement with a compatible lithium-ion absorbing capacitor in a container.
- Suitable materials for plasma deposition as cathode (positive electrode) particles for the capacitor include:
- Metal oxides, MOx, where M is one or more of Pb, Ge, Co, Ni, Cu, Fe, Mn, Ru, Rh, Pd, Cr, Mo, W, and Nb.
- A lithium-metal-oxide including: LixMO2 in which M is Co, Ni, Mn, Cr, or V.
- LixM2O4 , in which M is Co, Ni, Mn, Cr, or V.
- LixNiyM1-yO2, in which m is Fe or Mn.
- LiNi1-x-y-zCoxM1yM2zO2, in which M1, M2 are different metals selected from Al, Ni, Co, Fe, Mn, V, Cr, Ti, W, Ta, or Mo.
- LiMn2-xMxO4 in which M is one of Co, Ni, Fe, Cu, Cr, V.
- One of LiNiVO4, LiNbO3, LiFePO4, LiTi2(PO4)3, or Li3V2(PO4)3.
- LiMPO4 in which M is one of Ti, Ge, Zr, Hf.
- One or more of Li3FeV(PO4)3, LiFeNb(PO4)3, Li2FeNb(PO4)3, LixFeyMn1-yPO4, LiMSiO4 (M=Mn, Fe), LixFe2(WO4)3, LixFe2(SO4)3, and LiFeO2.
- A metal sulfide: NiS, Ag4Hf3S8, CuS, FeS, and FeS2.
- Activated carbon.
- A polymer such as: poly (3-methyl thiophene), polyaniline, polypyrrole, poly (para-phenylene), or polyacene.
- As further described in this specification, cathode particles for the capacitor are usually plasma-deposited on an aluminum current collector foil or on a porous polymer separator.
- Suitable materials for plasma deposition as anode (negative electrode) particles for the capacitor include:
- Li4Ti5O12, LiTi2O4, LiCrTiO4, LiTi2(PO4)3, and graphite or activated carbon.
- Positive electrode material for the capacitor is preferably plasma deposited on an aluminum current collector foil or on a polymeric separator such as a porous layer of polyethylene, polypropylene, or an ethylene-propylene copolymer.
- After the assembling of electrodes and separator and filling their pores with the electrolyte, the hybrid capacitor and battery undergo a formation cycle and are then degassed. The plasma powder coating method can optimize the surface area of the material layers coated on the foil or the separator, and can also control the porosity of the respective electrodes, in order to improve both the energy and power performance of the hybrid capacitor-battery.
- Recently, a lithium and titanium containing spinel structure, Li4Ti5O12, listed above, has been demonstrated as a promising negative electrode material for use in combination with activated carbon as the positive electrode material for hybrid capacitor applications. Accordingly, the power density depends on the rate capability of the intercalated compound Li4Ti5O12, which is associated with the Li-ion diffusion coefficient and the diffusion distance in the intercalated compound particle. To obtain a high rate capability, plasma powder electrode coating technology can be introduced to develop a nanosize-Li4Ti5O12 electrode with well controlled porosity, in which conductive metal particle and no polymer binder will benefit the rate performance. In addition, the energy density of the capacitor is critically dependent on the energy density of the carbon positive electrode material. Plasma powder electrode coating technology can be used to enlarge the surface area of carbon material in the electrode by size and porosity optimization to improve the specific capacity.
- The lithium-ion cell component of this capacitor-cell combination may be formed of like current collector foils and like porous separator materials.
- Examples of suitable particulate materials for positive electrodes for lithium-ion cells include lithium manganese nickel cobalt oxide, lithium manganese oxide, lithium cobalt oxide, lithium nickel aluminum cobalt oxide, lithium iron phosphate, and other lithium oxides and phosphates. Examples of particulate negative electrode materials for lithium-ion cells include lithium titanate, graphite, activated carbon, and silicon-based materials such as silicon, silicon-based alloys, SiOx, silicon-tin composites, and lithium-silicon alloys.
- The common electrolyte for the capacitor cell and the lithium-ion cell may be a lithium salt dissolved in one or more organic liquid solvents. Examples of salts include lithium hexafluorophosphate (LiPF6), lithium tetrafluoroborate (LiBF4), lithium perchlorate (LiClO4), lithium hexafluoroarsenate (LiAsF6), and lithium trifluoroethanesulfonimide. Some examples of solvents that may be used to dissolve the electrolyte salt include ethylene carbonate, dimethyl carbonate, methylethyl carbonate, and propylene carbonate. There are other lithium salts that may be used and other solvents. But a combination of lithium salt and non-aqueous liquid solvent is selected for providing suitable mobility and transport of lithium ions between the opposing electrodes in the operation of the cell. The electrolyte is carefully dispersed into and between closely spaced layers of the electrode elements and separator layers of each of the capacitor cell and the battery cell. The electrolyte is not illustrated in the following drawing figures because it is difficult to illustrate the electrolyte between tightly compacted electrode layers pressing on an interposed separator.
- A thin porous separator layer is interposed between the major outer face of the negative electrode material layer and the major outer face of the positive electrode material layer of each of the capacitor and the battery unit. The porous separator may be formed of a porous film or of porous interwoven fibers of suitable polymer material, or of ceramic particles, or a polymer material filled with ceramic particles. In the assembly of the hybrid capacitor and separated lithium-ion cell units, the porous separator layer is filled with a liquid lithium-ion containing electrolyte and enables the transport of lithium ions between the porous electrode members. But the separator layer is used to prevent direct electrical contact between each of the negative and positive electrode material layers in each unit, and is shaped and sized to serve this function.
-
FIG. 1 is a schematic illustration of a pouch-containedassembly 10 of the elements of anelectrochemical capacitor 12, a lithium-ion battery cell 14, and a polymer-coated,metal foil pouch 16 to contain the combined capacitor and cell elements for electrical series connection to each other and/or to other members of an electrical circuit. One side of thepouch 16, including the closure seam of its sides, has been cut-away in the figure to show the relative positions of theelectrochemical capacitor 12 and the lithium-ion cell 14. - As stated above in this specification, in actual practice each capacitor will be formed of several layers of positive electrodes, negative electrodes, and separators, prepared as described in the following paragraphs. The like-charged electrode layers are connected by tabs on their current collectors, respectively, in a positive terminal and a negative terminal for the capacitor. The positive and negative tabs for the groups of positive and negative capacitor electrodes may be connected with other devices in an electrical circuit as desired. Lithium-ion batteries are also typically formed of many positive electrodes connected to a positive terminal and many negative electrodes connected to a negative terminal. But since the focus of this specification is on the use of plasma deposition methods and devices to make such electrodes and separators, the illustrations of
FIGS. 1 and 2 have been simplified to depict the single set of electrodes forcapacitor 12 and lithium-ion cell 14. - The illustrated electrochemical,
capacitor 12 comprises a positive electrode, which in this example comprises a rectangular aluminum foilcurrent collector 18 with aconnector tab 18′ extending from its top side and through the overlapping surface ofpouch 16. The positive electrode of the capacitor further comprises porous particulate layers ofelectrode material 20 which have been deposited by atmospheric plasma deposition on each face of the aluminum foilcurrent collector 18. The positive electrode material for the capacitor may, for example, be activated carbon. The thickness of thecurrent collector foil 18 may be, for example, about ten micrometers and the lengths of the sides of the foil may, for example be in the range of 75 mm to 100 mm, not including thetab 18′. The porous layers ofelectrode material 20 may, for example, be about 10 to 500 micrometers in thickness and applied to substantially cover the rectangular faces ofcurrent collector foil 18, but nottab 18′. - The
electrochemical capacitor 12 further comprises a negative electrode, which in this example comprises a rectangular copper foilcurrent collector 22 with aconnector tab 22′ extending from its top side and through the overlying surface ofpouch 16. The negative electrode of the capacitor further comprises porous particulate layers ofelectrode material 24 which have also been deposited by atmospheric plasma deposition on each face of the copper foilcurrent collector 22, but not ontab 22′. The negative electrode material for the capacitor may, for example, also be activated carbon. The side lengths and thickness of the coppercurrent collector foil 22 are suitably like the dimensions of the positive electrode current collector foil. The porous layers ofnegative electrode material 24 may, for example, be of complementary thickness to that of the positive electrode materials and applied to substantially cover the rectangular faces ofcurrent collector foil 22, but nottab 22′. - As illustrated in
FIG. 1 , the outer surface of one side of thepositive electrode material 20 is placed close against one face of aporous separator layer 26 and the outer surface of one side of the negative electrode material is pressed against the opposite face of theporous separator 26.Porous separator 26 may be formed, for example, of polyethylene fibers.Separator 26 has a two-dimensional shape and a thickness. In this example, the rectangular shape of separator is determined to cover the contacting surfaces of the 20, 24 and to physically separate them. The shape and thickness of therespective electrode materials porous separator 26 also serves to retain liquid electrolyte for lithium absorption and desorption by the electrode layers 20, 24 of the capacitor. In the assembled device, the pores of the 20, 24 are infiltrated with liquid lithium-ion conducting electrolyte, as well as the pores ofelectrode materials separator 26. - The liquid electrolyte is not illustrated in
FIG. 1 , but it is present in the porous electrode layers and the separators of each of the assembledcapacitor 12 andbattery 14. In thecapacitor 12, lithium ions are transported between the 20 and 24 through the electrolyte.electrode materials - The structure of the lithium-ion cell or
battery 14 is similar to that ofcapacitor 12 and the outline sizes and thickness of the respective current collector foils, electrode material layers and separator ofbattery 14 are comparable to the similar structural elements ofcapacitor 12. But the electrode materials may be different and the electrochemical reactions are different. - In this example and simplified illustration, batteryl4 includes an aluminum positive electrode
current collector foil 30 with aconnector tab 30′ extending through theoverlying pouch material 16. Plasma deposited positive electrode layers 32 (e.g., activated carbon) are formed on both major faces of the aluminumcurrent collector foil 30. Thepositive electrode material 32 for thebattery 14 may, for example, be particles of LiFePO4. A copper negativecurrent collector foil 34 withtab 34′ is plasma coated on both of its major faces with layers ofnegative electrode material 36. The particle layers ofnegative electrode material 36 may comprise activated carbon or resin-bonded activated carbon. The facing porous layers ofpositive electrode material 32 and ofnegative electrode material 36 are kept apart byporous polymer separator 38. In the assembledbattery 14, placed inpouch 16, the pores ofseparator 38 and of electrode layers 32 and 36 are filled with a suitable non-aqueous, lithium-ion conducting electrolyte. The electrolyte may, for example, comprise lithium hexafluorophosphate (LiPF6) dissolved in a mixture of dimethyl carbonate and methylethyl carbonate as solvent. - In
FIG. 1 , the current collector tab leads 18′ and 22′ forcapacitor 12 and the current collector tab leads 30′, 34′ forbattery 14, each extend through the adjoining pouch material and are positioned for serial electrical connections. In a typical hybrid capacitor, these current collector leads would be the four terminal posts for the series-connected assembly in pouchl6. Such an arrangement offers many possibilities for interconnection of the capacitor electrodes and battery electrodes with each other and with other members of an electrical power-requiring system. The electrical connections betweencapacitor 12 and lithium-ion battery 14 may, for example, be through a DC-DC converter. This type of electrical interconnection could enable thecapacitor 12 to store energy, for example, when an automotive vehicle is braking, and to later release energy to the adjacent lithium-ion battery 14 during vehicle starting or acceleration. -
FIG. 2 illustrates a pouch-containedassembly 110 of acapacitor 112 andbattery 114 which are arranged and oriented inpouch 116 for parallel electrical connection betweencapacitor 112 andbattery 114. Again, in this simplified illustration only single electrode structures are illustrated for each ofcapacitor 112 andbattery 114. In practice, a capacitor and battery would each comprise many connected positive electrodes with current collector tabs connected in a single positive terminal and many negative electrodes with current collector tabs electrically connected in a single negative terminal. - In this example and illustration, the electrodes and separator of
capacitor 112 may be substantially identical in shapes and compositions with respect to the corresponding elements ofcapacitor 12 as shown inFIG. 1 . And the electrodes and separator ofbattery 114 may be substantially identical in shapes and compositions with respect to the corresponding elements ofbattery 14 shown inFIG. 1 . Accordingly, the corresponding current collector foils, electrode layers and separators ofFIG. 2 are identified by numerals 1xx (or 1xx′) with respect to the same parts ofFIG. 1 which are identified as xx or xx′. - The main difference between
FIG. 1 andFIG. 2 is thatcapacitor 112 andbattery 114 are arranged and oriented inpouch 116 for parallel electrical connection betweencapacitor 112 andbattery 114, and for series connection with these combined elements and electrical power-requiring devices outsidepouch 116. Accordingly,positive electrode tab 118′ ofcapacitor 112 andpositive electrode tab 130′ ofbattery 114 are connected as a single positive (+) terminal 140 which extends through the top ofpouch 116. In a similar arrangement,negative electrode tab 122′ ofcapacitor 112 andnegative electrode tab 134′ ofbattery 114 are connected as a single negative (−) terminal 142 which extends through the top ofpouch 116. - Thus, in the parallel connection arrangement of the electrodes of
capacitor 112 andbattery 114, the two components may be designed to operate in a common voltage window and to achieve a higher power in their common voltage range. -
FIG. 3A is presented to illustrate the plasma deposition of heated particles of active positive electrode (cathode during capacitor discharge) material for a capacitor onto one major face of an aluminum current collector foil. For example, the capacitor elements may be shaped and composed like those ofcapacitor 12 inFIG. 1 , orcapacitor 112 inFIG. 2 , with its aluminumcurrent collector foil 18 andpositive electrode material 20. -
FIG. 3A illustrates the practice of using an atmosphericplasma application device 200 to deposit active positive electrode material particles for a capacitor in a porous layer on a surface of a metal current collector foil. In this embodiment, the finished capacitor is intended to be likecapacitor 12 as illustrated inFIG. 1 .FIG. 3A is intended to illustrate the method of applying particles of positive electrode material aselectrode material layer 20 on one side ofcurrent collector foil 18. Thus, the substrate is theupper surface 17 of a coppercurrent collector foil 18 with itsconnection tab 18′.Connection tab 18′ is not coated with the electrode material. The active positive electrode material is particles of commercially available activated carbon with their extraordinary porosity and surface area. The activated carbon particles may be coated with a suitable amount of a polymer binder for bonding of the particles to each other and to surface 17 of thecurrent collector 18. - In this example, the
current collector foil 18 is placed and carried on amovable work surface 202, such as a conveyor belt, or the like, for locating thecurrent collector foil 18, with itsupper surface 17, under the plasma application device. This process may be conducted in air and in a normal ambient workplace atmosphere. - In this example, the copper
current collector foil 18 is illustrated in the form of a thin, square layer of about 100 millimeters length on each side, but the capacitor elements are also often made in other rectangular shapes and dimensions depending on the intended size of the capacitor elements and assembled capacitor modules. The copper currentcollector foil layer 18 is often about ten to twelve micrometers in thickness. Thesubstrate 202 is moved and placed in a flat position at ambient conditions under a suitable atmospheric plasmaspray generator apparatus 200 with a nozzle for directing its flow stream of electrode material particles. The spray device(s) and/or workpiece may be carried on a suitable support and moved under suitable programmable controls for sequential deposition of particulate electrode material on thesurface 17 of one or more coppercurrent collectors 18. - In practices of this invention, and with reference to
FIG. 3 , anatmospheric plasma apparatus 200 may comprise an upstream round flow chamber 204 (shown partly broken-off inFIG. 3 ) for the introduction and conduct of a flowing stream of suitable working gas, such as air, nitrogen, or an inert gas such as helium or argon. The flow of the working gas would be introduced above the broken-off illustration offlow chamber 204 and proceed in a downward direction. In this embodiment, this illustrativeinitial flow chamber 204 is tapered inwardly to smallerround flow chamber 206. Active positiveelectrode material particles 208 for the capacitor (for example, activated carbon particles) are delivered through opposing 210, 212 intosupply tubes round flow chamber 206.Supply tube 208 is shown partially broken-away to illustrate delivery of the positive capacitorelectrode material particles 208. Theelectrode material particles 208 are suitably introduced from opposing sides of theapparatus 200 into the working gas stream inchamber 206 and then carried into aplasma nozzle 214 in which the air (or other working gas) is converted to a plasma stream at atmospheric pressure. As theelectrode material particles 208 enter the gas stream inchamber 206 they are dispersed and mixed in the stream and carried by it. As the stream flows through the downstream plasma-generator nozzle 214, theelectrode material particles 208 are heated by the formed plasma of predetermined and controlled energy to a precursor processing temperature. The momentary thermal impact on the electrode material particles may be a temperature of from about 300° C. up to about 3500° C. The plasma activated electrode material particles exitnozzle 214 asstream 216. - In this example, the
stream 216 of air-based plasma and suspended, plasma-activated, activated carbon electrode material particles is progressively directed by thenozzle 214 to deposit particles as a layer ofelectrode material 20 onto the surface of theupper surface 17 of the copper foilcurrent collector 18. Thenozzle 214 and stream 216 of suspended electrode material is moved in a suitable path and at a suitable rate such that the particulate activatedcarbon electrode material 208 is deposited as aporous layer 20 of specified thickness of the electrode particles on thesurface 17 of thecurrent collector foil 18. - The relative movement of the
plasma spray stream 216 and/or thesubstrate 202 is continues until theentire face 17 of current collector foil 18 (but nottab 18′) is covered with a generally uniformly thick layer of capacitorpositive electrode material 20. The current collector foil may then be turned over so that its opposing face is likewise coated with a layer ofpositive electrode material 20. -
FIG. 3B is a schematic illustration of a representative positive electrode for a capacitor, likecapacitor 12 inFIG. 1 orcapacitor 112 inFIG. 2 . Both major sides of aluminumcurrent collector foil 18 have been coated, using an atmospheric plasma spray device, with substantially identical adherent layers of positivecapacitor electrode material 20.Current collector tab 18′ remains exposed for desired inter-connection with other capacitor electrodes or with battery electrodes or with other electrical devices. - The above described plasma spray deposition device and method may be used to deposit porous layers of particulate negative capacitor electrode material on a suitable metal foil current collector material. For example,
FIG. 3C illustrates a negative capacitor electrode that, in this example, consists of a copper current collector foil 22 (withextended tab 22′) coated on both major faces with generally uniformly thick layers of plasma depositednegative electrode material 24. For example, the negative electrode material for the capacitor may also be suitably sized particles of a commercially-available activated carbon. - In the above described process, both the positive electrode and the negative electrode for a capacitor cell were prepared by plasma deposition of particles of the electrode material onto both sides of a suitable metal current collector. The assembly of the capacitor elements is then advanced by placing one face of positive electrode material against one side of a porous separator and one face of a negative electrode material against the opposite face of the separator. The assembled capacitor is illustrated in
FIG. 4 . InFIG. 4 , the capacitor is identified by numeral 12 because it is intended to illustrate in perspective view, the capacitor structures illustrated in side view inFIGS. 1 and 2 . As seen inFIG. 4 , and described in downward order from top surface, the seven layers ofcapacitor 12 compriseporous layer 20 of positive capacitor electrode material, copper positive electrodecurrent collector foil 18 with itsuncoated connector tab 18′, the opposing layer of porouspositive electrode material 20,porous separator 26, a layer of porous negativecapacitor electrode material 24, aluminum negative electrodecurrent collector foil 22 with itsuncoated connector tab 22′, and an opposing layer of porouspositive electrode material 24. It is seen that a layer ofpositive electrode material 20 and a layernegative electrode material 24 are pressed against the corresponding faces of theporous separator 26. - When
capacitor 12 has been assembled with a like-shaped and like- made battery (e.g., battery 14) in a suitable container, likepouch 16, both the capacitor and battery will be suitably infiltrated with a shared lithium-ion transporting electrolyte. - In the above described plasma application process, particulate cathode material was plasma coated on both sides of an aluminum current collector foil to form a capacitor cathode, and particulate anode material was plasma coated onto both sides of a copper current collector foil to form a capacitor anode. The assembly of the capacitor cell was then completed by placing a cathode on one side of a suitable porous separator and a cathode on the other side of the separator. A like plasma deposition process, using suitable electrode materials, may be used to make and assemble a lithium-ion battery cell for the hybrid combination.
- In a second plasma deposition process, similar to that illustrated in
FIG. 3a , particles of cathode electrode material are deposited on one side of a suitable separator. Then particles of a current collector metal (e.g., Al) are plasma deposited onto the particulate cathode layer. Then, a second layer of particulate cathode material may be plasma deposited on the current collector layer. Particles of anode electrode material, metal current collector material, and anode electrode material are then sequentially plasma deposited onto the opposite side of the separator. The result of the six layers of plasma-deposited is equivalent to the seven layer capacitor structure illustrated inFIG. 4 . - As stated, either plasma deposition process, using appropriate particulate electrode materials and current collector material may be used to make the electrochemical cell structures of either a lithium-ion using capacitor or a lithium-ion battery. The plasma deposition process can be conducted, for example, in parallel or other complementary manufacturing lines to simultaneously produce complementary capacitors and batteries for assembly into suitable containers for hybrid combination. The porous elements of the combined assembly are then infiltrated or impregnated with a suitable lithium ion containing electrolyte. And capacitor and battery members of the combination may be charged or otherwise prepared for their respective electrochemical functions.
- As stated, the layers of the respective electrode material particles is pre-deposited on a compatible current collector surface or a compatible separator surface using one or more atmospheric plasma nozzles or deposition devices. Such plasma nozzles for this application are commercially available and may also be carried and used on robot arms, under multi-directional computer control, to apply suitable electrode particles to coat the surfaces of each metal current collector foil or separator surface for a lithium-using capacitor and, separately, for a lithium-ion cell. Multiple nozzles may be required and arranged in such a way that a desired coating speed may be achieved in terms coated area per unit of time.
- The atmospheric plasma nozzle typically has a metallic tubular housing which provides a flow path of suitable length for receiving the flow of working gas, receiving and dispersing particles of electrode material, and for enabling the formation of the plasma stream in an electromagnetic field established within the flow path of the tubular housing. The tubular housing terminates in a conically tapered outlet, shaped to direct a suitably shaped plasma stream toward an intended substrate to be coated. An electrically insulating ceramic tube is typically inserted at the inlet of the tubular housing such that it extends along a portion of the flow passage. A stream of a working gas, such as air (or nitrogen or argon), and carrying dispersed particles of a specified electrode material, is introduced into the inlet of the nozzle. The flow of the air-particle mixture may be caused to swirl turbulently in its flow path by use of a swirl piece with flow openings, also inserted near the inlet end of the nozzle. A linear (pin-like) electrode is placed at the ceramic tube site, along the flow axis of the nozzle at the upstream end of the flow tube. During plasma generation the electrode is powered by a suitable generator at a frequency in the 0.1 hertz to gigahertz range and to a suitable potential of a few kilovolts. Plasma generation technology such as corona discharge, radio wave, and microwave sources, and the like, may be employed. The metallic housing of the plasma nozzle is grounded. Thus, an electrical discharge can be generated between the axial pin electrode and the housing. No vacuum chamber is used.
- When the generator voltage is applied, the frequency of the applied voltage and the dielectric properties of the ceramic tube produce a corona discharge at the stream inlet and the electrode. As a result of the corona discharge, an arc discharge from the electrode tip to the housing is formed. This arc discharge is carried by the turbulent flow of the air/particulate electrode material stream to the outlet of the nozzle. A reactive plasma of the air (or other carrier gas) and dispersed electrode particles is formed at a relatively low temperature. A copper nozzle at the outlet of the plasma container is shaped to direct the plasma stream in a suitably confined path against the surfaces of the current collector substrates for the lithium-ion cell electrode members. The energy of the plasma may be determined and managed for the material to be applied.
- Thus, specific examples have been presented for the use of plasma spray deposition devices and methods in the preparation of lithium-ion incorporating capacitors and batteries for assembly into a common container to serve as hybrid electrochemical devices for provision of electrical power in many devices consuming electrical energy. The examples are intended to illustrate practices of the invention and not the scope of the following claims.
Claims (20)
1. A method of forming a hybrid combination of a (i) lithium-ion battery and (ii) a capacitor that both use a common lithium ion conducting electrolyte; the method comprising:
forming porous positive and negative electrode material layers for the capacitor by separately using an atmospheric plasma stream to deposit particles of capacitor positive electrode material as a porous positive electrode layer bonded to a one side of a porous separator member or to a metal positive electrode current collector, and, separately, to deposit particles of capacitor negative electrode material as a porous negative electrode layer bonded to the opposing side of a porous separator member or to a metal negative electrode current collector, at least one of the positive and negative electrode materials being of a composition to work with the electrolyte used with the lithium-ion battery;
assembling one or more pairs of capacitor positive and negative electrodes as a capacitor with each positive electrode layer bonded to a porous separator on one of its layer sides and to a positive electrode current collector on the other of its layer sides, and with one layer side of each negative electrode layer bonded to the opposite side of a porous separator from a positive electrode layer and to a negative electrode current collector on the other of its negative electrode layer sides;
placing the assembled capacitor in a container with a lithium-ion battery comprising one or more pairs of porous layer, positive and negative electrode members with corresponding porous separators ; and
infiltrating the porous electrodes and separators of the capacitor and the porous layer electrodes and separators of the lithium-ion battery with the same lithium ion conducting liquid electrolyte composition.
2. A method of forming a hybrid combination of a (i) lithium-ion battery and (ii) a capacitor as stated in claim 1 in which porous layer electrodes and separators of the lithium-ion battery are formed with like sizes and shapes as the electrodes and separators for the capacitor.
3. A method of forming a hybrid combination of a (i) lithium-ion battery and (ii) as recited in claim 1 in which particles of capacitor positive electrode material are deposited as a positive capacitor electrode layer on one side of a porous separator and particles of a capacitor negative electrode layer are deposited as a negative capacitor electrode layer on the other side of the porous separator layer.
4. A method of forming a hybrid combination of a (i) lithium-ion battery and (ii) as recited in claim 3 in which particles of metal current collector material are deposited on the sides of each of the positive electrode layer and the negative electrode layer that are not bonded to the porous separator.
5. A method of forming a hybrid combination of a (i) lithium-ion battery and (ii) as recited in claim 4 in which a layer of positive electrode material is deposited on the exposed side of the positive electrode current collector and a layer of negative electrode material is deposited on the exposed side of the negative electrode current collector.
6. A method of forming a hybrid combination of a (i) lithium-ion battery and (ii) as recited in claim 1 in which layers of capacitor positive electrode material are deposited on both sides of a positive current collector foil to form a positive capacitor electrode, layers of capacitor negative electrode material are deposited on both sides of a negative current collector foil to form a capacitor negative electrode, and the capacitor electrodes are placed on opposite sides of a porous separator.
7. A method of forming a hybrid combination of a (i) lithium-ion battery and (ii) as recited in claim 6 in which the positive current collector foil is an aluminum foil and the negative current collector foil is a copper foil.
8. A method of forming a hybrid combination of a (i) lithium-ion battery and (ii) as recited in claim 1 in which the capacitor positive electrode material comprises activated carbon or graphite.
9. A method of forming a hybrid combination of a (i) lithium-ion battery and (ii) as recited in claim 1 in which the capacitor negative electrode material comprises activated carbon or graphite.
10. A method of forming a hybrid combination of a (i) lithium-ion battery and (ii) as recited in claim 1 in which the capacitor positive electrode material comprises activated carbon and the capacitor negative electrode material comprises Li4Ti5O12.
11. A method of making a combination of (i) a lithium-ion battery and (ii) a capacitor comprising an electrode that uses the lithium-containing electrolyte composition of the lithium-ion battery, for placement of the capacitor and battery in a common container for use with a common lithium ion conducting electrolyte; the capacitor comprising a plurality of positive capacitor electrode layers and of negative capacitor electrode layers, one side of each positive electrode layer facing one side of a negative electrode layer with the facing sides of the electrode layers being physically separated by a porous separator layer, and the opposing sides of the electrode layers being bonded to current collector foils; the method comprising:
heating particles of positive capacitor electrode material in an atmospheric plasma stream and depositing the heated particles as a porous positive capacitor electrode layer, either on the surface of a metal current collector foil for the positive electrode material or on one surface of a porous capacitor separator with two opposing surfaces;
heating particles of negative capacitor electrode material in an atmospheric plasma stream and depositing the heated particles as a porous negative capacitor electrode layer, either on the surface of a metal current collector foil for the negative electrode material or on the opposing surface of the porous capacitor separator;
completing the formation of the capacitor with a surface of each of the atmospheric plasma-deposited positive and negative electrode layers separated from electrical contact by a porous separator and with the opposite surface of each capacitor electrode being covered and bonded for electrical contact with a metal current collector shaped with a connector tab for electrical contact with another electrode member;
placing the capacitor in a common container with a lithium-ion battery comprising porous battery electrodes and separators, but with the capacitor and lithium-ion battery separated from physical contact with each other; and
infiltrating the electrodes and separators of the capacitor and battery with a common lithium ion-conducting electrolyte.
12. A method of making a combination of (i) a lithium-ion battery and (ii) a capacitor as recited in claim 11 in which particles of capacitor positive electrode material are plasma deposited on both sides of a metal current collector to form a capacitor positive electrode, particles of capacitor negative electrode material are plasma deposited on both sides of a metal current collector to form a capacitor negative electrode, and the positive and negative electrodes are placed on opposite sides of a porous separator.
13. A method of making a combination of (i) a lithium-ion battery and (ii) a capacitor as recited in claim 11 in which particles of capacitor positive electrode material are plasma deposited as a positive electrode layer on one side of a porous capacitor separator, particles of capacitor negative electrode material are plasma deposited as a negative electrode layer on the opposite side of a porous capacitor separator, and metallic current collectors with connector tabs are formed on the exposed sides of the positive electrode layer and the negative electrode layer.
14. A method of making electrode materials for a positive electrode-separator-negative electrode structure of a capacitor which is to be used in combination with a positive electrode-separator-negative electrode structure of a lithium-ion battery, the capacitor electrode materials being compatible with like-made electrode materials for the lithium-ion battery, the capacitor electrode materials and lithium-ion battery electrode materials being made for use with a common lithium-conducting electrolyte and placement in a common container as a hybridized combination, the method comprising:
depositing particles, which are dispersed and heated in an atmospheric plasma stream, as a porous layer of capacitor positive electrode material, deposited, either on a surface of a metal current collector foil for the positive electrode material or on a surface of a porous capacitor separator with two opposing surfaces, to form a porous layer of positive electrode material with one layer side contacting the current collector foil, or the surface of the separator, and with an opposing positive electrode material layer side;
separately depositing particles, which are dispersed and heated in an atmospheric plasma stream, as a layer of capacitor negative electrode material, either on the surface of a metal current collector foil for the negative electrode material or on one surface of a porous capacitor separator with two opposing surfaces, to form a porous layer of negative electrode material with one layer side contacting the negative current collector foil, or the surface of the separator, and an opposing negative electrode material layer side; and
using the plasma deposited layer of capacitor positive electrode material and the plasma deposited layer of capacitor negative electrode material in an assembly of a layered capacitor structure comprising a porous separator with a layer of capacitor positive electrode material on one separator surface and a layer of capacitor negative electrode material on the opposing separator surface, and each of the layers of capacitor electrode material having a current collector foil on their opposing material layer side.
15. A method of making electrode materials for a capacitor as recited in claim 14 in which
a layer of capacitor positive electrode particles are plasma deposited on each side of a metallic current collector foil to form a positive capacitor electrode;
a layer of capacitor negative electrode materials are plasma deposited on each side of a metallic current collector foil to form a negative capacitor electrode; and
the positive capacitor electrode is placed with one of its layers of electrode particles against one side of a porous separator and the negative electrode is placed with one of its layers of electrode particles against the opposite side of the porous separator to form the positive electrode-separator-negative electrode structure of a capacitor.
16. A method of making electrode materials for a capacitor as recited in claim 14 in which
a layer of capacitor positive electrode particles are plasma deposited on one side of a porous separator; a layer of particles of a metallic current collector are deposited on the layer of particles of capacitor positive electrode material, and a layer of capacitor positive electrode particles are plasma deposited on the metallic current collector layer; and
a layer of capacitor negative electrode particles are plasma deposited on the opposite side of the porous separator; a layer of particles of a metallic current collector are deposited on the layer of particles of capacitor negative electrode material, and a layer of capacitor negative electrode particles are plasma deposited on the metallic current collector layer to form the to form the positive electrode-separator-negative electrode structure of a capacitor.
17. A method of making electrode materials for a capacitor as recited in claim 15 and further comprising placing the positive electrode-separator-negative electrode structure of the capacitor into a common container with, but spaced from, the positive electrode-separator-negative electrode structure of a lithium battery and impregnating the electrodes and separators of both the capacitor and lithium-ion battery with a liquid, lithium-conducting electrolyte.
18. A method of making electrode materials for a capacitor as recited in claim 16 and further comprising placing the positive electrode-separator-negative electrode structure of the capacitor into a common container with, but spaced from, the positive electrode-separator-negative electrode structure of a lithium battery and impregnating the electrodes and separators of both the capacitor and lithium-ion battery with a liquid, lithium-conducting electrolyte.
19. A method of making electrode materials for a capacitor as recited in claim 17 in which a plurality of positive electrode-separator-negative electrode structures are placed in the common container with intervening separators and with the positive electrodes connected to a positive electrode terminal and the negative electrodes connected to a negative electrode terminal.
20. A method of making electrode materials for a capacitor as recited in claim 18 in which a plurality of positive electrode-separator-negative electrode structures are placed in the common container with intervening separators and with the positive electrodes connected to a positive electrode terminal and the negative electrodes connected to a negative electrode terminal.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/CN2015/075046 WO2016149919A1 (en) | 2015-03-25 | 2015-03-25 | Capacitor-battery hybrid formed by plasma powder electrode coating |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20180048040A1 true US20180048040A1 (en) | 2018-02-15 |
Family
ID=56975911
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US15/560,206 Abandoned US20180048040A1 (en) | 2015-03-25 | 2015-03-25 | Capacitor-battery hybrid formed by plasma powder electrode coating |
| US15/015,227 Active US10297885B2 (en) | 2015-03-25 | 2016-02-04 | Lithium ion battery and capacitor hybrid system in a single pouch |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US15/015,227 Active US10297885B2 (en) | 2015-03-25 | 2016-02-04 | Lithium ion battery and capacitor hybrid system in a single pouch |
Country Status (4)
| Country | Link |
|---|---|
| US (2) | US20180048040A1 (en) |
| CN (1) | CN107039711A (en) |
| DE (1) | DE102017201561A1 (en) |
| WO (1) | WO2016149919A1 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20170256779A1 (en) * | 2016-03-02 | 2017-09-07 | Asustek Computer Inc. | Method for manufacturing electrode |
| CN110828189A (en) * | 2018-08-08 | 2020-02-21 | 丰田自动车株式会社 | Positive electrode for lithium ion capacitor, lithium ion capacitor using same, and method for producing same |
Families Citing this family (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10964488B2 (en) * | 2016-12-13 | 2021-03-30 | Innocell Aps | Electrochemical and capacitative energy storage device and method of manufacture |
| CN109435672B (en) | 2017-08-24 | 2022-12-02 | 通用汽车环球科技运作有限责任公司 | System and method for monitoring a hybrid energy storage device |
| CN109427489A (en) | 2017-08-24 | 2019-03-05 | 通用汽车环球科技运作有限责任公司 | Supercapacitor control system and method |
| US11501917B2 (en) * | 2018-03-02 | 2022-11-15 | Capacitor Foundry Llc | Capacitors employing dielectric material outside volume enclosed by electrodes |
| WO2019200609A1 (en) * | 2018-04-20 | 2019-10-24 | GM Global Technology Operations LLC | Incorporation of lithium-ion source material into an activated carbon electrode for a capacitor-assisted battery |
| CN112236893B (en) * | 2018-04-23 | 2025-01-10 | 通用汽车环球科技运作有限责任公司 | Hybrid electrode and electrochemical cell and module using the same |
| US20190372186A1 (en) * | 2018-05-30 | 2019-12-05 | GM Global Technology Operations LLC | Sulfone electrolytes for capacitor-assisted batteries |
| US11239469B2 (en) | 2018-06-01 | 2022-02-01 | GM Global Technology Operations LLC | Pre-lithiation of anodes for high performance capacitor assisted battery |
| WO2019241917A1 (en) * | 2018-06-20 | 2019-12-26 | GM Global Technology Operations LLC | Water based hybrid lithium ion capacitor battery having a water-in-salt electrolyte |
| KR102103454B1 (en) * | 2018-07-18 | 2020-04-23 | 삼화콘덴서공업 주식회사 | Battery capacitor with hybrid assembly structure |
| US11205798B2 (en) * | 2018-07-30 | 2021-12-21 | GM Global Technology Operations LLC | Capacitor-assisted solid-state battery |
| US11121375B2 (en) | 2018-10-15 | 2021-09-14 | GM Global Technology Operations LLC | Solid-state electrodes with non-carbon electronic conductive additives |
| US11479080B2 (en) | 2018-10-19 | 2022-10-25 | Systematic Power Manufacturing, Llc | Hybrid energy power module for mobile electrical devices |
| JP7021057B2 (en) * | 2018-11-30 | 2022-02-16 | 本田技研工業株式会社 | Secondary battery and comb-shaped electrode |
| WO2020117672A2 (en) * | 2018-12-04 | 2020-06-11 | Freudenberg-Nok General Partnership | Integrated battery unit |
| CN111477472B (en) * | 2019-01-23 | 2021-04-02 | 清华大学 | Self-charging supercapacitors |
| CN111477459B (en) * | 2019-01-23 | 2021-04-02 | 清华大学 | Self-charging supercapacitors |
| CN111477466B (en) * | 2019-01-23 | 2021-04-02 | 清华大学 | Charging method of self-charging super capacitor |
| US12040654B2 (en) | 2019-03-13 | 2024-07-16 | Systematic Power Manufacturing, Llc | On-board starting module for vehicle engine |
| US12031511B2 (en) | 2019-03-13 | 2024-07-09 | Systematic Power Manufacturing, Llc | On-board starting module for vehicle engine |
| CN109888371B (en) * | 2019-04-15 | 2021-05-04 | 北京理工大学 | A book-structured flexible battery |
| CN111952080B (en) * | 2019-05-17 | 2022-08-16 | 清华大学 | Energy storage device capable of being charged in situ |
| CN111987391A (en) * | 2019-05-22 | 2020-11-24 | 重庆九环新越新能源科技发展有限公司 | Composite power energy storage monomer, module and equipment |
| CN111987369A (en) * | 2019-05-22 | 2020-11-24 | 重庆九环新越新能源科技发展有限公司 | Composite power energy storage battery cell |
| CN112086716A (en) * | 2019-06-13 | 2020-12-15 | 青岛九环新越新能源科技股份有限公司 | All-solid-state composite power storage cells |
| CN112103572A (en) * | 2019-06-18 | 2020-12-18 | 重庆九环新越新能源科技发展有限公司 | Composite power solid-state energy storage battery cell based on composite material electrode |
| CN112447409A (en) * | 2019-09-04 | 2021-03-05 | 通用汽车环球科技运作有限责任公司 | Electrochemical cell comprising a sulfur-containing capacitor |
| CN112736298B (en) | 2019-10-15 | 2024-08-09 | 通用汽车环球科技运作有限责任公司 | Hybrid electrochemical cell design with voltage change |
| CN112670559A (en) | 2019-10-15 | 2021-04-16 | 通用汽车环球科技运作有限责任公司 | Solid electrolyte and method for preparing the same |
| CN112768811B (en) | 2019-11-01 | 2024-09-24 | 通用汽车环球科技运作有限责任公司 | Capacitor-assisted electrochemical device with hybrid architecture |
| CN112820952B (en) * | 2019-11-15 | 2025-02-11 | 通用汽车环球科技运作有限责任公司 | Capacitor-assisted battery modules and systems |
| US11784010B2 (en) | 2019-11-15 | 2023-10-10 | GM Global Technology Operations LLC | Electrode including capacitor material disposed on or intermingled with electroactive material and electrochemical cell including the same |
| US12034131B2 (en) | 2021-06-11 | 2024-07-09 | Systematic Power Manufacturing, Llc | Stand-by power module for vehicle engine |
| CN115842381A (en) | 2021-09-18 | 2023-03-24 | 通用汽车环球科技运作有限责任公司 | Battery system including AC fast rechargeable capacitor auxiliary battery |
| CN113904036B (en) * | 2021-10-08 | 2024-04-30 | 陕西奥林波斯电力能源有限责任公司 | High-capacity single battery and assembly method |
| WO2023122819A1 (en) * | 2021-12-30 | 2023-07-06 | Duvoisin Charles Adriano | Battery with ionisation potential generation and control, and method for generating and controlling ionisation potential in a battery |
| CN116799313A (en) | 2022-03-14 | 2023-09-22 | 通用汽车环球科技运作有限责任公司 | Capacitor auxiliary battery cell |
| CN117497707A (en) | 2022-07-26 | 2024-02-02 | 通用汽车环球科技运作有限责任公司 | Cellulose-based fiber dispersants for hybrid capacitive electrodes |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3218170B2 (en) * | 1995-09-06 | 2001-10-15 | キヤノン株式会社 | Lithium secondary battery and method of manufacturing lithium secondary battery |
| US6631072B1 (en) | 1998-12-05 | 2003-10-07 | Energy Storage Systems Pty Ltd | Charge storage device |
| KR20030014988A (en) * | 2001-08-14 | 2003-02-20 | 한국전자통신연구원 | Hybrid power source device and method for manufacturing the same |
| TW531058U (en) | 2002-01-14 | 2003-05-01 | Yan Jeng Jie | Super battery module for portable electronic device |
| EP1391961B1 (en) | 2002-08-19 | 2006-03-29 | Luxon Energy Devices Corporation | Battery with built-in load leveling |
| WO2006093441A1 (en) * | 2005-03-02 | 2006-09-08 | St. Jude Medical Ab | Metal-vanadium-oxide-product and producing process |
| CN101164189B (en) * | 2005-04-19 | 2011-05-04 | 松下电器产业株式会社 | Nonaqueous electrolyte solution, electrochemical energy storage device using same, and nonaqueous electrolyte secondary battery |
| JP4213688B2 (en) * | 2005-07-07 | 2009-01-21 | 株式会社東芝 | Nonaqueous electrolyte battery and battery pack |
| CN101517817B (en) * | 2006-07-31 | 2013-03-20 | 株式会社Lg化学 | Hybrid Electrode Assembly of Capacitor-Battery Structure |
| US20090033286A1 (en) | 2007-07-31 | 2009-02-05 | Dean La Rosa | Cell and Supercapacitor Battery Pack |
| US20110164347A1 (en) * | 2008-09-09 | 2011-07-07 | Phillip Brett Aitchison | Package for an Electrical Device |
| US20110027664A1 (en) * | 2009-07-31 | 2011-02-03 | Revolt Technology Ltd. | Metal-air battery with improved environmental stability |
| US8481203B2 (en) | 2010-02-03 | 2013-07-09 | Bren-Tronies Batteries International, L.L.C. | Integrated energy storage unit |
| KR20110130909A (en) * | 2010-05-28 | 2011-12-06 | 현대자동차주식회사 | Electric storage systems |
| CN201927685U (en) | 2010-12-28 | 2011-08-10 | 杭州圣速电池科技有限公司 | Lightweight battery for automobile |
| JP2013016265A (en) * | 2011-06-30 | 2013-01-24 | Sanyo Electric Co Ltd | Nonaqueous secondary battery |
| CN102306755B (en) * | 2011-08-15 | 2013-09-04 | 淄博齐盛新能源科技有限公司 | Capacitor-battery bipolar inline combined nickel-hydrogen power capacitor battery |
| EP2826095A2 (en) | 2012-03-13 | 2015-01-21 | Maxwell Technologies, Inc. | Capacitor and battery combination |
| CN103280334B (en) * | 2013-04-03 | 2016-08-24 | 王子齐 | General power high energy storage multi-medium capacitor-battery container |
| CN103337602B (en) * | 2013-06-26 | 2015-05-13 | 宁德新能源科技有限公司 | Isolating film and electrochemical device |
| KR102490666B1 (en) * | 2013-11-28 | 2023-01-26 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | Power storage unit and electronic device including the same |
-
2015
- 2015-03-25 US US15/560,206 patent/US20180048040A1/en not_active Abandoned
- 2015-03-25 WO PCT/CN2015/075046 patent/WO2016149919A1/en not_active Ceased
-
2016
- 2016-02-04 US US15/015,227 patent/US10297885B2/en active Active
-
2017
- 2017-01-31 DE DE102017201561.6A patent/DE102017201561A1/en not_active Withdrawn
- 2017-02-04 CN CN201710065141.5A patent/CN107039711A/en active Pending
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20170256779A1 (en) * | 2016-03-02 | 2017-09-07 | Asustek Computer Inc. | Method for manufacturing electrode |
| US10461309B2 (en) * | 2016-03-02 | 2019-10-29 | Asustek Computer Inc. | Method for manufacturing electrode |
| CN110828189A (en) * | 2018-08-08 | 2020-02-21 | 丰田自动车株式会社 | Positive electrode for lithium ion capacitor, lithium ion capacitor using same, and method for producing same |
| US11462365B2 (en) * | 2018-08-08 | 2022-10-04 | Toyota Jidosha Kabushikt Kaisha | Positive electrode for lithium ion capacitor and lithium ion capacitor using the positive electrode, and production methods thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| US10297885B2 (en) | 2019-05-21 |
| CN107039711A (en) | 2017-08-11 |
| US20160285137A1 (en) | 2016-09-29 |
| DE102017201561A1 (en) | 2017-08-10 |
| WO2016149919A1 (en) | 2016-09-29 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US20180048040A1 (en) | Capacitor-battery hybrid formed by plasma powder electrode coating | |
| US10763550B2 (en) | Stacked all-solid-state battery and method of manufacturing the same | |
| US20170058389A1 (en) | Lithium battery fabrication process using multiple atmospheric plasma nozzles | |
| CN104106158B (en) | Bipolar electrode and use its bipolar lithium ion secondary battery | |
| JP6149106B2 (en) | Secondary battery electrode, manufacturing method thereof, secondary battery including the same, and cable-type secondary battery | |
| EP2503628B1 (en) | Current collector for bipolar secondary battery | |
| CN105074967B (en) | For manufacturing the multi-layer cell electrode design compared with thick electrode | |
| CN104995763B (en) | For manufacturing the method and electroplated components of electroplated components | |
| CN104145364B (en) | Stepped construction battery | |
| EP2327119B1 (en) | Bipolar secondary battery, method for manufacturing the bipolar secondary battery, bipolar electrode, method for manufacturing the bipolar electrode and assembled battery | |
| KR100671186B1 (en) | Manufacturing method of electrochemical device | |
| JP5286972B2 (en) | Negative electrode for lithium ion secondary battery | |
| WO2016082120A1 (en) | Combination of plasma coating and spray coating for lithium battery electrode fabrication | |
| CN112864546A (en) | Nonaqueous electrolyte secondary battery | |
| CN106797046A (en) | Laminated battery and manufacturing method thereof | |
| CN112714971B (en) | Negative electrode active material for lithium secondary battery, negative electrode comprising same, and lithium secondary battery | |
| US20160254533A1 (en) | Making lithium secondary battery electrodes using an atmospheric plasma | |
| US20160126509A1 (en) | Plasma coating for corrosion protection of light-metal components in battery fabrication | |
| WO2016086388A1 (en) | Plasma battery electrode coating on current collector pretreated with conducive material | |
| JP2010160985A (en) | Lithium ion secondary cell negative electrode and lithium ion secondary cell using the same | |
| KR102388122B1 (en) | Film for packaging secondary batteries and Secondary batteries comprising the same | |
| JP2009110767A (en) | Positive electrode for high-power lithium-ion battery | |
| KR102521578B1 (en) | Packaging for flexible secondary batteries and Flexible secondary batteries comprising the same | |
| US20200303741A1 (en) | Isotropic self-assembly of graphite particles for li-ion anode | |
| KR102917199B1 (en) | Cathode for lithium secondary battery based organic-inorganic active complex and preparing method for manufacturing of the same and lithium secondary battery comprising the same |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: GM GLOBAL TECHNOLOGY OPERATIONS LLC, MICHIGAN Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:LIU, HAIJING;GAYDEN, XIAOHONG Q.;YU, ZHIQIANG;REEL/FRAME:043931/0613 Effective date: 20150320 |
|
| STPP | Information on status: patent application and granting procedure in general |
Free format text: NON FINAL ACTION MAILED |
|
| STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |