[go: up one dir, main page]

WO2019188541A1 - Sous-couche pour dispositif de stockage d'énergie - Google Patents

Sous-couche pour dispositif de stockage d'énergie Download PDF

Info

Publication number
WO2019188541A1
WO2019188541A1 PCT/JP2019/011333 JP2019011333W WO2019188541A1 WO 2019188541 A1 WO2019188541 A1 WO 2019188541A1 JP 2019011333 W JP2019011333 W JP 2019011333W WO 2019188541 A1 WO2019188541 A1 WO 2019188541A1
Authority
WO
WIPO (PCT)
Prior art keywords
undercoat layer
energy storage
storage device
group
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.)
Ceased
Application number
PCT/JP2019/011333
Other languages
English (en)
Japanese (ja)
Inventor
辰也 畑中
康志 境田
真令 飯塚
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nissan Chemical Corp
Original Assignee
Nissan Chemical Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Nissan Chemical Corp filed Critical Nissan Chemical Corp
Priority to JP2020510720A priority Critical patent/JPWO2019188541A1/ja
Publication of WO2019188541A1 publication Critical patent/WO2019188541A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D201/00—Coating compositions based on unspecified macromolecular compounds
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/24—Electrically-conducting paints
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/20—Diluents or solvents
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40—Additives
    • C09D7/60—Additives non-macromolecular
    • C09D7/61—Additives non-macromolecular inorganic
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40—Additives
    • C09D7/65—Additives macromolecular
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
    • H01B1/20—Conductive material dispersed in non-conductive organic material
    • H01B1/24—Conductive material dispersed in non-conductive organic material the conductive material comprising carbon-silicon compounds, carbon or silicon
    • 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
    • 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
    • H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
    • 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
    • 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

Definitions

  • the present invention relates to an undercoat layer of an energy storage device.
  • a lithium ion secondary battery is a secondary battery that has been developed most vigorously at present because it has a high energy density and a high voltage and has no memory effect during charging and discharging.
  • the development of electric vehicles has been actively promoted due to recent efforts to deal with environmental problems, and higher performance has been demanded for secondary batteries as a power source.
  • a lithium ion secondary battery contains a positive electrode and a negative electrode capable of occluding and releasing lithium, and a separator interposed therebetween in a container, and an electrolyte solution (liquid in the case of a lithium ion polymer secondary battery) therein. It has a structure filled with a gel-like or all solid electrolyte instead of the electrolyte.
  • an active material capable of occluding and releasing lithium, a conductive material mainly composed of a carbon material, and a composition containing a polymer binder are generally applied on a current collector such as a copper foil or an aluminum foil. It is manufactured by doing.
  • This binder is used to bond an active material and a conductive material, and further to the metal foil, and is a fluorine-based resin soluble in N-methylpyrrolidone (NMP) such as polyvinylidene fluoride (PVdF) or an olefin-based heavy polymer.
  • NMP N-methylpyrrolidone
  • PVdF polyvinylidene fluoride
  • olefin-based heavy polymer Combined aqueous dispersions are commercially available.
  • the adhesive strength of the binder to the current collector is not sufficient, and a part of the active material or conductive material is peeled off from the current collector during the manufacturing process such as the electrode cutting process or the winding process. , Causing a short circuit and variation in battery capacity.
  • the contact resistance between the electrode mixture and the current collector increases due to the volume change of the electrode mixture due to the swelling of the binder due to the electrolytic solution and the volume change due to the lithium occlusion and release of the active material after long-term use.
  • battery capacity is deteriorated due to part of the active material or conductive material peeling off from the current collector or dropping off, and further, there is a problem in terms of safety.
  • Patent Document 1 discloses a technique in which a conductive layer containing carbon as a conductive filler is used as an undercoat layer and disposed between a current collector and an electrode mixture layer, and the undercoat layer is provided.
  • a conductive layer containing carbon as a conductive filler is used as an undercoat layer and disposed between a current collector and an electrode mixture layer, and the undercoat layer is provided.
  • Patent Document 2 and Patent Document 3 disclose similar techniques.
  • Patent Document 4 and Patent Document 5 disclose an undercoat layer using carbon nanotubes (hereinafter also abbreviated as CNT) as a conductive filler.
  • CNT carbon nanotubes
  • the undercoat is expected not only to lower the resistance of the battery but also to suppress the increase in resistance, but depending on the conductive carbon material used, the resistance of the battery is increased and the resistance increase is accelerated. There is a case to let you. In this regard, it is not clear what conductive carbon material is used to reduce the resistance of the battery and suppress the increase in resistance.
  • This invention is made
  • the present inventors have found that the film thickness converted from the basis weight of the undercoat layer formed on the current collector and the average surface roughness Ra thereof The inventors have found that an undercoat layer that exhibits a low resistance effect and a resistance increase suppressing effect can be obtained by optimizing the relationship, and the present invention has been completed.
  • the present invention 1.
  • the average surface roughness Ra of the undercoat layer is 1 g / cm 3 when the average surface roughness Ra of the undercoat layer is obtained from a composition comprising a carbon nanotube, a carbon nanotube dispersant, and a solvent
  • An undercoat layer of an energy storage device characterized by being 45% or more with respect to a film thickness obtained from the basis weight; 2.
  • 1 undercoat layer for energy storage devices whose said average surface roughness Ra is 47% or more with respect to the film thickness calculated
  • 6 an undercoat layer for an energy storage device, wherein the basis weight is 300 mg / m 2 or less, 8).
  • An electrode for an energy storage device comprising a composite current collector for an electrode of 16 energy storage devices; 18.
  • An energy storage device comprising 17 energy storage device electrodes; 19. 18 energy storage devices that are lithium ion batteries, 20.
  • the average surface roughness Ra of the conductive coating film is 1 g / cm 3 of the density of the conductive coating film.
  • a conductive coating film is provided that is 45% or more with respect to the film thickness obtained from the basis weight.
  • the undercoat layer of the energy storage device of the present invention is suitable for bonding the current collector constituting the electrode of the energy storage device and the active material layer, and the undercoat layer is formed on the current collector. By forming, it is possible to reduce the resistance of the energy storage device and to suppress an increase in resistance.
  • the undercoat layer of the energy storage device according to the present invention is obtained from a composition containing carbon nanotubes, a carbon nanotube dispersant, and a solvent, and the average surface roughness Ra of the undercoat layer is that of the undercoat layer.
  • the density is 1 g / cm 3 , it is 45% or more with respect to the film thickness obtained from the basis weight (hereinafter referred to as equivalent film thickness).
  • the ratio of the average surface roughness Ra of the undercoat layer to the converted film thickness is 45% or more, but considering that the effect of lowering the resistance and increasing the resistance of the obtained device is further increased, it is 47% or more. Is preferable, 50% or more is more preferable, and 55% or more is even more preferable. Although the upper limit of the said ratio is not specifically limited, 1,000% or less is preferable and 500% or less is more preferable.
  • the average surface roughness Ra of the undercoat layer is not particularly limited as long as the above ratio is satisfied, but is preferably 10 nm or more, more preferably 15 nm or more, and further preferably 20 nm or more. Further, the upper limit is not particularly limited as long as it is within the range of the film thickness, but is preferably 1,000 nm or less, and more preferably 500 nm or less. In the present invention, the average surface roughness Ra is obtained from each of the prepared undercoat layers by measuring three locations within a predetermined region, for example, an arbitrary 30 ⁇ m ⁇ 30 ⁇ m region using an atomic force microscope. It is the average value of the surface roughness (arithmetic average roughness).
  • the equivalent film thickness of the undercoat layer is a value calculated from the basis weight of the undercoat layer when the density of the undercoat layer is 1 g / cm 3 .
  • the weight per unit area of the undercoat layer is a ratio of the mass (mg) of the undercoat layer to the area (m 2 ) of the undercoat layer, and when the undercoat layer is formed in a pattern, the area is the undercoat layer.
  • the area of the current collector exposed between the undercoat layers formed in a pattern is not included.
  • the mass of the undercoat layer is obtained by, for example, cutting a test piece of an appropriate size from the undercoat foil, measuring its mass W0, and then removing the undercoat layer from the undercoat foil and removing the undercoat layer.
  • the mass W1 is measured and calculated from the difference (W0-W1), or the mass W2 of the current collector is measured in advance, and then the mass W3 of the undercoat foil on which the undercoat layer is formed is measured.
  • the difference (W3 ⁇ W2) can be calculated.
  • the weight per unit area is a predetermined size, for example, the mass of the undercoat foil cut out to a size of 8 cm ⁇ 16 cm, and the undercoat foil is immersed in a 0.1N hydrochloric acid aqueous solution to form only the undercoat layer. It is a value calculated from the difference with the mass of the metal foil after removing.
  • Basis weight of the undercoat layer per one surface of the current collector is preferably 1,000 mg / m 2 or less, more preferably 500 mg / m 2 or less, more preferably more that 300 mg / m 2 or less, 200 mg / m 2 or less Further preferred.
  • the basis weight of the undercoat layer per side of the current collector is preferably 1 mg / m 2 or more, more preferably 5 mg / m 2. m 2 or more, more preferably 10 mg / m 2 or more, and further preferably 15 mg / m 2 or more.
  • the basis weight of the undercoat layer is 1,000 mg / m 2
  • the converted film thickness is 1,000 nm.
  • the basis weight can be adjusted by a known method.
  • the solid content concentration of the coating liquid for forming the undercoat layer (undercoat layer forming composition), the number of times of coating, the coating liquid inlet of the coating machine It can be adjusted by changing the clearance.
  • increase the weight per unit area increase the solid content concentration, increase the number of coatings, or increase the clearance.
  • the solid content concentration is decreased, the number of coatings is decreased, or the clearance is decreased.
  • the above-described undercoat layer can be formed using an undercoat layer forming composition containing the following CNT, CNT dispersant, and solvent.
  • CNTs are generally produced by arc discharge, chemical vapor deposition (CVD), laser ablation, etc., but the CNTs used in the present invention may be obtained by any method. .
  • a single-walled CNT in which a single carbon film (graphene sheet) is wound in a cylindrical shape
  • DWCNT double-walled CNT
  • MWCNT multi-layer CNTs in which a plurality of graphene sheets are concentrically wound.
  • SWCNT, DWCNT, and MWCNT can be used alone or in combination.
  • a multilayer CNT having a diameter of 2 nm or more is particularly preferable, and from the viewpoint that a thin film can be formed, a multilayer CNT having a diameter of 500 nm or less is particularly preferable, a multilayer CNT having a diameter of 100 nm or less is more preferable, and a multilayer having a diameter of 50 nm or less is preferable. CNT is even more preferable, and multilayer CNT having a diameter of 30 nm or less is most preferable.
  • the diameter of CNT can be measured by observing the thin film obtained by drying what disperse
  • the CNT it is preferable to use a CNT that is easy to disperse in the dispersion liquid in order to exert an effect of lowering the battery resistance when the dispersion liquid is used as an undercoat layer.
  • Such CNTs preferably have many crystal discontinuities that can be easily cut with small energy.
  • the CNT used in the present invention preferably has a constricted portion.
  • the CNT having a constricted portion is a CNT wall having a constricted portion having a tube outer diameter of 90% or less of the parallel portion and the tube outer diameter of the parallel portion. Since this constricted part is a part created by changing the growth direction of CNTs, it has a discontinuous crystal part and becomes an easily breakable part that can be easily cut with a small mechanical energy.
  • FIG. 1 shows a schematic cross-sectional view of a CNT having a parallel portion 1 and a constricted portion 3.
  • the parallel part 1 is a part where the wall can be recognized as two parallel straight lines or two parallel curves.
  • the distance between the outer walls of the parallel line in the normal direction is the tube outer diameter 2 of the parallel part 1.
  • the constricted portion 3 is a portion where both ends thereof are connected to the parallel portion 1 and the distance between the walls is closer than that of the parallel portion 1, more specifically, the tube outer diameter 2 of the parallel portion 1 is increased.
  • it is a portion having a tube outer diameter 4 of 90% or less.
  • the tube outer diameter 4 of the constricted portion 3 is the distance between the outer walls of the constricted portion 3 where the wall constituting the outer wall is closest. As shown in FIG. 1, many of the constricted portions 3 have portions where crystals are discontinuous.
  • the shape of the CNT wall and the outer diameter of the tube can be observed with a transmission electron microscope or the like. Specifically, it is possible to prepare a 0.5% dispersion of CNT, dry the dispersion on a sample stage, and confirm the constricted portion by an image taken at 50,000 times with a transmission electron microscope. it can.
  • the CNT For the CNT, a 0.1% dispersion of CNT was prepared, the dispersion was placed on a sample stage and dried, and an image taken at 20,000 times with a transmission electron microscope was divided into 100 nm square sections, and 100 nm When 300 sections with CNT occupying 10% to 80% in all four sections are selected, the total number of easily breakable portions depends on the ratio of the section with at least one constricted portion in one section to 300 sections. The ratio (the ratio of the presence of easily breakable parts) is determined. When the area occupied by CNTs in the compartment is less than 10%, measurement is difficult because the amount of CNTs is too small.
  • the existence ratio of easily breakable portions is 60% or more.
  • the proportion of easily breakable portions is less than 60%, CNT is difficult to disperse, and when excessive mechanical energy is applied to disperse, it leads to the destruction of the crystal structure of the graphite surface, which is a characteristic of CNT. Characteristics such as electrical conductivity are reduced.
  • the presence ratio of easily breakable portions is preferably 70% or more.
  • CNTs usable in the present invention include TC-2010, TC-2020, TC-, which are CNTs having a constricted structure disclosed in International Publication Nos. 2016/076393 and JP-A-2017-206413.
  • TC series such as 3210L and TC-1210LN (manufactured by Toda Kogyo Co., Ltd.), spar-growth CNT (manufactured by National Research and Development Corporation, Shinshin Energy and Industrial Technology Development Organization), eDIPS-CNT (national research and development corporation, Shinshin Energy and Industry) SWNT series (made by Meijo Nanocarbon Co., Ltd .: trade name), VGCF series (made by Showa Denko KK: trade name), FloTube series (made by CNano Technology Co., Ltd .: trade name), AMC ( Ube Industries, Ltd.
  • the dispersant can be appropriately selected from those conventionally used as a dispersant for conductive carbon materials such as CNTs.
  • CMC carboxymethylcellulose
  • PVP polyvinylpyrrolidone
  • acrylic resin emulsion water-soluble Acrylic polymer
  • styrene emulsion silicone emulsion
  • acrylic silicone emulsion fluororesin emulsion
  • EVA emulsion vinyl acetate emulsion
  • vinyl chloride emulsion urethane resin emulsion
  • triarylamine hyperbranched polymer described in International Publication No. 2014/04280
  • polymers having an oxazoline group in the side chain described in International Publication No. 2015/029949 polymers having an oxazoline group in the side chain described in International Publication No. 2015/029949.
  • the side chain described in International Publication No. 2015/029949 is included in the side chain.
  • Dispersing agents and comprising a polymer having a Kisazorin group it is preferable to use a dispersant comprising a triarylamine hyperbranched polymer of WO 2014/04280 Patent forth.
  • a polymer having an oxazoline group in the side chain (hereinafter referred to as oxazoline polymer) is obtained by radical polymerization of an oxazoline monomer having a polymerizable carbon-carbon double bond-containing group at the 2-position as shown in Formula (1).
  • oxazoline polymer is obtained by radical polymerization of an oxazoline monomer having a polymerizable carbon-carbon double bond-containing group at the 2-position as shown in Formula (1).
  • Preferred is a vinyl polymer having a repeating unit bonded to the polymer main chain or spacer group at the 2-position of the oxazoline ring and having an oxazoline group in the side chain.
  • X represents a polymerizable carbon-carbon double bond-containing group
  • R 1 to R 4 are independently of each other a hydrogen atom, a halogen atom, an alkyl group having 1 to 5 carbon atoms, or a 6 to 20 carbon atoms.
  • An aryl group or an aralkyl group having 7 to 20 carbon atoms is represented.
  • the polymerizable carbon-carbon double bond-containing group of the oxazoline monomer is not particularly limited as long as it contains a polymerizable carbon-carbon double bond, but a chain containing a polymerizable carbon-carbon double bond.
  • a hydrocarbon group having 2 to 8 carbon atoms such as vinyl group, allyl group and isopropenyl group is preferable.
  • examples of the halogen atom include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom.
  • the alkyl group having 1 to 5 carbon atoms may be linear, branched or cyclic, for example, methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, sec-butyl group. Tert-butyl group, n-pentyl group, cyclohexyl group and the like.
  • Specific examples of the aryl group having 6 to 20 carbon atoms include phenyl group, xylyl group, tolyl group, biphenylyl group, naphthyl group and the like.
  • Specific examples of the aralkyl group having 7 to 20 carbon atoms include benzyl group, phenylethyl group, phenylcyclohexyl group and the like.
  • oxazoline monomer having a polymerizable carbon-carbon double bond-containing group at the 2-position represented by the formula (1) include 2-vinyl-2-oxazoline, 2-vinyl-4-methyl-2-oxazoline, 2-vinyl-4-ethyl-2-oxazoline, 2-vinyl-4-propyl-2-oxazoline, 2-vinyl-4-butyl-2-oxazoline, 2-vinyl-5-methyl-2-oxazoline, 2- Vinyl-5-ethyl-2-oxazoline, 2-vinyl-5-propyl-2-oxazoline, 2-vinyl-5-butyl-2-oxazoline, 2-isopropenyl-2-oxazoline, 2-isopropenyl-4- Methyl-2-oxazoline, 2-isopropenyl-4-ethyl-2-oxazoline, 2-isopropenyl-4-propyl-2-oxazoline, 2- Sopropenyl-4-butyl
  • the oxazoline polymer is also preferably water-soluble.
  • a water-soluble oxazoline polymer may be a homopolymer of the oxazoline monomer represented by the above formula (1), but has a oxazoline monomer and a hydrophilic functional group in order to further enhance the solubility in water (meta ) It is preferable to be obtained by radical polymerization of at least two monomers with an acrylate monomer.
  • (meth) acrylic monomer having a hydrophilic functional group examples include (meth) acrylic acid, 2-hydroxyethyl acrylate, methoxypolyethylene glycol acrylate, monoesterified product of acrylic acid and polyethylene glycol, acrylic acid 2-aminoethyl and its salt, 2-hydroxyethyl methacrylate, methoxypolyethylene glycol methacrylate, monoesterified product of methacrylic acid and polyethylene glycol, 2-aminoethyl methacrylate and its salt, sodium (meth) acrylate, ( Ammonium methacrylate, (meth) acrylonitrile, (meth) acrylamide, N-methylol (meth) acrylamide, N- (2-hydroxyethyl) (meth) acrylamide, sodium styrenesulfonate, etc. The like, which may be used singly or may be used in combination of two or more. Among these, (meth) acrylic acid methoxypolyethylene glycol and mono
  • (Meth) acrylic acid ester monomers such as perfluoroethyl acid and phenyl (meth) acrylate; ⁇ -olefin monomers such as ethylene, propylene, butene and pentene; haloolefins such as vinyl chloride, vinylidene chloride and vinyl fluoride Monomers: Styrene monomers such as styrene and ⁇ -methylstyrene; Vinyl ester monomers such as vinyl acetate and vinyl propionate; Vinyl ether monomers such as methyl vinyl ether and ethyl vinyl ether, and the like. Even two or more You may use it in combination.
  • the content of the oxazoline monomer is preferably 10% by mass or more, more preferably 20% by mass from the viewpoint of further improving the conductive carbon material dispersibility of the obtained oxazoline polymer.
  • the above is more preferable, and 30% by mass or more is even more preferable.
  • the upper limit of the content rate of the oxazoline monomer in a monomer component is 100 mass%, and the homopolymer of an oxazoline monomer is obtained in this case.
  • the content of the (meth) acrylic monomer having a hydrophilic functional group in the monomer component is preferably 10% by mass or more, more preferably 20% by mass or more from the viewpoint of further increasing the water solubility of the obtained oxazoline polymer. 30% by mass or more is even more preferable.
  • the content of other monomers in the monomer component is in a range that does not affect the dispersibility of the obtained oxazoline polymer in the conductive carbon material as described above. However, it may be set appropriately in the range of 5 to 95% by mass, preferably 10 to 90% by mass.
  • the average molecular weight of the oxazoline polymer is not particularly limited, but the weight average molecular weight is preferably 1,000 to 2,000,000, and more preferably 2,000 to 1,000,000.
  • the weight average molecular weight is a polystyrene conversion value determined by gel permeation chromatography.
  • the oxazoline polymer that can be used in the present invention can be synthesized by a conventional radical polymerization of the above-mentioned monomers, but can also be obtained as a commercial product, and as such a commercial product, for example, Epocross WS-300 (Manufactured by Nippon Shokubai Co., Ltd., solid content concentration 10% by mass, aqueous solution), Epocross WS-700 (manufactured by Nippon Shokubai Co., Ltd., solid content concentration 25% by mass, aqueous solution), Epocross WS-500 (manufactured by Nippon Shokubai Co., Ltd.) Manufactured, solid content concentration 39% by mass, water / 1-methoxy-2-propanol solution), Poly (2-ethyl-2-oxazoline) (Aldrich), Poly (2-ethyl-2-oxazoline) (AlfaAesar), Poly (2-ethyl-2-oxazole) (
  • hyperbranched polymers obtained by condensation polymerization of triarylamines and aldehydes and / or ketones represented by the following formulas (2) and (3) under acidic conditions are also preferably used.
  • Ar 1 to Ar 3 each independently represents any divalent organic group represented by formulas (4) to (8).
  • the substituted or unsubstituted phenylene group represented by (4) is preferred.
  • Z 1 and Z 2 are each independently a hydrogen atom, an alkyl group which may have a branched structure having 1 to 5 carbon atoms, or the formula (9) (1) represents any monovalent organic group represented by (12) (provided that Z 1 and Z 2 do not simultaneously become the above alkyl group), but Z 1 and Z 2 are each independently A hydrogen atom, a 2- or 3-thienyl group, or a group represented by the formula (9) is preferable, and in particular, one of Z 1 and Z 2 is a hydrogen atom, and the other is a hydrogen atom, 2- or More preferred is a 3-thienyl group, a group represented by the formula (9), particularly those in which R 141 is a phenyl group, or R 141 is a methoxy group.
  • R 141 is a phenyl group
  • an acidic group may be introduced onto the phenyl group when a method for introducing an acidic group after polymer production is used in the acidic group introduction method described later.
  • alkyl group which may have a branched structure having 1 to 5 carbon atoms include those similar to those exemplified above.
  • R 101 to R 138 are each independently a hydrogen atom, a halogen atom, an alkyl group which may have a branched structure having 1 to 5 carbon atoms, or a carbon number of 1 Represents an alkoxy group which may have a branched structure of 1 to 5, a carboxyl group, a sulfo group, a phosphoric acid group, a phosphonic acid group or a salt thereof;
  • examples of the halogen atom include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom.
  • examples of the alkyl group which may have a branched structure having 1 to 5 carbon atoms include methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, sec-butyl group, tert-butyl group, n -Pentyl group and the like.
  • alkoxy group which may have a branched structure having 1 to 5 carbon atoms include methoxy group, ethoxy group, n-propoxy group, isopropoxy group, n-butoxy group, sec-butoxy group, tert-butoxy group, Examples thereof include an n-pentoxy group.
  • salts of carboxyl group, sulfo group, phosphoric acid group and phosphonic acid group include alkali metal salts such as sodium and potassium; group 2 metal salts such as magnesium and calcium; ammonium salts; propylamine, dimethylamine, triethylamine, ethylenediamine, etc. Aliphatic amine salts; alicyclic amine salts such as imidazoline, piperazine and morpholine; aromatic amine salts such as aniline and diphenylamine; and pyridinium salts.
  • R 139 to R 162 are each independently a hydrogen atom, a halogen atom, an alkyl group which may have a branched structure having 1 to 5 carbon atoms, or a carbon number of 1 Haloalkyl group, phenyl group, OR 163 , COR 163 , NR 163 R 164 , COOR 165 , which may have a branched structure of ⁇ 5 (in these formulas, R 163 and R 164 are each independently hydrogen Represents an atom, an alkyl group which may have a branched structure having 1 to 5 carbon atoms, a haloalkyl group which may have a branched structure having 1 to 5 carbon atoms, or a phenyl group, and R 165 represents the number of carbon atoms Represents an alkyl group which may have a branched structure of 1 to 5, a haloalkyl group which may have a branched structure of 1 to 5 carbon
  • the haloalkyl group which may have a branched structure having 1 to 5 carbon atoms includes difluoromethyl group, trifluoromethyl group, bromodifluoromethyl group, 2-chloroethyl group, 2-bromoethyl group, 1,1 -Difluoroethyl group, 2,2,2-trifluoroethyl group, 1,1,2,2-tetrafluoroethyl group, 2-chloro-1,1,2-trifluoroethyl group, pentafluoroethyl group, 3 -Bromopropyl group, 2,2,3,3-tetrafluoropropyl group, 1,1,2,3,3,3-hexafluoropropyl group, 1,1,1,3,3,3-hexafluoropropane Examples include -2-yl group, 3-bromo-2-methylpropyl group, 4-bromobutyl group, perfluoropentyl group and the like. Examples of the halogen
  • the hyperbranched polymer has a carboxyl group, in at least one aromatic ring of the repeating unit represented by the formula (2) or (3), Those having at least one acidic group selected from a sulfo group, a phosphoric acid group, a phosphonic acid group, and salts thereof are preferable, and those having a sulfo group or a salt thereof are more preferable.
  • aldehyde compound used for the production of the hyperbranched polymer examples include formaldehyde, paraformaldehyde, acetaldehyde, propylaldehyde, butyraldehyde, isobutyraldehyde, valeraldehyde, capronaldehyde, 2-methylbutyraldehyde, hexylaldehyde, undecylaldehyde, 7 -Saturated aliphatic aldehydes such as methoxy-3,7-dimethyloctylaldehyde, cyclohexanecarboxaldehyde, 3-methyl-2-butyraldehyde, glyoxal, malonaldehyde, succinaldehyde, glutaraldehyde, adipine aldehyde; acrolein, methacrolein Unsaturated aldehydes such as: furfural, pyridine aldehy
  • Examples of the ketone compound used in the production of the hyperbranched polymer include alkyl aryl ketones and diaryl ketones, such as acetophenone, propiophenone, diphenyl ketone, phenyl naphthyl ketone, dinaphthyl ketone, phenyl tolyl ketone, and ditolyl ketone. Etc.
  • the hyperbranched polymer used in the present invention includes, for example, a triarylamine compound that can give the above-described triarylamine skeleton as represented by the following formula (A), and the following formula, for example: It can be obtained by condensation polymerization of an aldehyde compound and / or a ketone compound as shown in (B) in the presence of an acid catalyst.
  • a bifunctional compound (C) such as phthalaldehyde such as terephthalaldehyde is used as the aldehyde compound, not only the reaction shown in Scheme 1 but also the reaction shown in Scheme 2 below occurs.
  • a hyperbranched polymer having a crosslinked structure in which two functional groups contribute to the condensation reaction may be obtained.
  • an aldehyde compound and / or a ketone compound can be used at a ratio of 0.1 to 10 equivalents with respect to 1 equivalent of the aryl group of the triarylamine compound.
  • the acid catalyst include mineral acids such as sulfuric acid, phosphoric acid and perchloric acid; organic sulfonic acids such as p-toluenesulfonic acid and p-toluenesulfonic acid monohydrate; carboxylic acids such as formic acid and oxalic acid. Etc. can be used.
  • the amount of the acid catalyst to be used is variously selected depending on the kind thereof, but is usually 0.001 to 10,000 parts by mass, preferably 0.01 to 1,000 parts by mass with respect to 100 parts by mass of the triarylamines. Part, more preferably 0.1 to 100 parts by weight.
  • the above condensation reaction can be carried out without a solvent, it is usually carried out using a solvent.
  • Any solvent that does not inhibit the reaction can be used.
  • cyclic ethers such as tetrahydrofuran and 1,4-dioxane; N, N-dimethylformamide (DMF), N, N-dimethylacetamide ( DMAc), amides such as N-methyl-2-pyrrolidone (NMP); ketones such as methyl isobutyl ketone and cyclohexanone; halogenated hydrocarbons such as methylene chloride, chloroform, 1,2-dichloroethane and chlorobenzene; benzene, Examples thereof include aromatic hydrocarbons such as toluene and xylene, and cyclic ethers are particularly preferable.
  • These solvents can be used alone or in combination of two or more.
  • the acid catalyst used is a liquid such as formic acid, the acid catalyst can also serve as a solvent.
  • the reaction temperature during the condensation is usually 40 to 200 ° C.
  • the reaction time is variously selected depending on the reaction temperature, but is usually about 30 minutes to 50 hours.
  • the obtained hyperbranched polymer may be introduced by a method of treating with a reagent capable of introducing an acidic group on the aromatic ring, but the latter method may be used in consideration of the ease of production. preferable.
  • the method for introducing the acidic group onto the aromatic ring is not particularly limited, and may be appropriately selected from conventionally known various methods according to the type of the acidic group. For example, when a sulfo group is introduced, a technique of sulfonation using an excessive amount of sulfuric acid can be used.
  • the average molecular weight of the hyperbranched polymer is not particularly limited, but the weight average molecular weight is preferably 1,000 to 2,000,000, and more preferably 2,000 to 1,000,000.
  • Specific examples of the hyperbranched polymer include, but are not limited to, those represented by the following formula.
  • the mixing ratio of the CNT and the dispersant can be about 1,000: 1 to 1: 100 by mass ratio.
  • the concentration of the dispersant in the composition is not particularly limited as long as it is a concentration capable of dispersing CNTs in a solvent, but is preferably about 0.001 to 30% by mass in the composition, More preferably, it is about 0.002 to 20% by mass.
  • the concentration of CNT in the composition varies in the amount of the target undercoat layer and the required mechanical, electrical, and thermal characteristics, and at least a part of the CNT is present.
  • the composition is preferably about 0.0001 to 30% by mass in the composition, and about 0.001 to 20% by mass. More preferably, it is more preferably about 0.001 to 10% by mass.
  • the solvent is not particularly limited as long as it is conventionally used for the preparation of a conductive composition.
  • ethers such as tetrahydrofuran (THF), diethyl ether, 1,2-dimethoxyethane (DME); Halogenated hydrocarbons such as methylene chloride, chloroform, 1,2-dichloroethane; N, N-dimethylformamide (DMF), N, N-dimethylacetamide (DMAc), N-methyl-2-pyrrolidone (NMP), etc.
  • Ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone, cyclohexanone
  • Alcohols such as methanol, ethanol, n-propanol, isopropanol, n-butanol, t-butanol; n-heptane, n-hexane, cyclohexane, etc.
  • Aliphatic hydrocarbons such as ethylene, xylene and ethylbenzene
  • Aromatic hydrocarbons such as ethylene, xylene and ethylbenzene
  • glycol ethers such as ethylene glycol monoethyl ether, ethylene glycol monobutyl ether and propylene glycol monomethyl ether
  • organic solvents such as glycols such as ethylene glycol and propylene glycol .
  • These solvent can be used individually by 1 type or in mixture of 2 or more types.
  • water, NMP, DMF, THF, methanol, ethanol, n-propanol, isopropanol, n-butanol, and t-butanol are preferable because the ratio of isolated dispersion of CNT can be improved.
  • methanol, ethanol, n-propanol, isopropanol, n-butanol, and t-butanol are preferable from the point that cost can be reduced.
  • these solvents can be used singly or in combination of two or more for the purpose of increasing the ratio of isolated dispersion, increasing the coatability, and reducing the cost.
  • a polymer serving as a matrix may be added.
  • the matrix polymer include polyvinylidene fluoride (PVdF), polytetrafluoroethylene, tetrafluoroethylene-hexafluoropropylene copolymer, vinylidene fluoride-hexafluoropropylene copolymer [P (VDF-HFP)], Fluorine resins such as vinylidene fluoride-trichloroethylene copolymer [P (VDF-CTFE)]; polyvinylpyrrolidone, ethylene-propylene-diene terpolymer, PE (polyethylene), PP (polypropylene), Polyolefin resins such as EVA (ethylene-vinyl acetate copolymer), EEA (ethylene-ethyl acrylate copolymer); PS (polystyrene), HIPS (high impact polystyrene), AS (acrylonitrile-st
  • PVdF polyvin
  • Examples thereof include sodium boxymethylcellulose, water-soluble cellulose ether, sodium alginate, polyvinyl alcohol, polystyrene sulfonic acid, polyethylene glycol and the like, and particularly, sodium polyacrylate and sodium carboxymethylcellulose are preferable.
  • the matrix polymer can also be obtained as a commercial product.
  • a commercial product examples include sodium polyacrylate (manufactured by Wako Pure Chemical Industries, Ltd., degree of polymerization 2,700 to 7,500), carboxy Sodium methylcellulose (manufactured by Wako Pure Chemical Industries, Ltd.), sodium alginate (manufactured by Kanto Chemical Co., Ltd., deer grade 1), Metrol's SH series (hydroxypropylmethylcellulose, Shin-Etsu Chemical Co., Ltd.), Metrolose SE series (hydroxyl) Ethyl methyl cellulose, manufactured by Shin-Etsu Chemical Co., Ltd.), JC-25 (completely saponified polyvinyl alcohol, manufactured by Nippon Vineyard Poval Co., Ltd.), JM-17 (intermediate saponified polyvinyl alcohol, Nippon Vinegared / Poval) Manufactured by Co., Ltd.), JP-03 (partially saponified polyvinyl alcohol, Nippon Vinegar Po
  • the composition of the present invention may contain a crosslinking agent that causes a crosslinking reaction with the dispersant to be used or a crosslinking agent that self-crosslinks. These crosslinking agents are preferably dissolved in the solvent used.
  • the crosslinking agent for the oxazoline polymer is particularly limited as long as it is a compound having two or more functional groups having reactivity with an oxazoline group such as a carboxyl group, a hydroxyl group, a thiol group, an amino group, a sulfinic acid group, and an epoxy group. Although not intended, compounds having two or more carboxyl groups are preferred.
  • a compound having a functional group that causes a crosslinking reaction by heating during thin film formation or in the presence of an acid catalyst such as a sodium salt, potassium salt, lithium salt, or ammonium salt of a carboxylic acid is also crosslinked. It can be used as an agent.
  • an acid catalyst such as a sodium salt, potassium salt, lithium salt, or ammonium salt of a carboxylic acid
  • Specific examples of compounds that undergo a crosslinking reaction with an oxazoline group include metal salts of synthetic polymers such as polyacrylic acid and copolymers thereof and natural polymers such as carboxymethylcellulose and alginic acid that exhibit crosslinking reactivity in the presence of an acid catalyst.
  • ammonium salts of the above synthetic polymers and natural polymers that exhibit crosslinking reactivity by heating especially sodium polyacrylate that exhibits crosslinking reactivity in the presence of an acid catalyst or under heating conditions, Preference is given to lithium polyacrylate, ammonium polyacrylate, sodium carboxymethylcellulose, lithium carboxymethylcellulose, carboxymethylcellulose ammonium and the like.
  • Such a compound that causes a crosslinking reaction with an oxazoline group can also be obtained as a commercial product.
  • a commercial product examples include sodium polyacrylate (manufactured by Wako Pure Chemical Industries, Ltd., degree of polymerization of 2, 700-7,500), sodium carboxymethylcellulose (manufactured by Wako Pure Chemical Industries, Ltd.), sodium alginate (manufactured by Kanto Chemical Co., Ltd., deer grade 1), Aron A-30 (ammonium polyacrylate, Toagosei Co., Ltd.) ), Solid concentration 32% by mass, aqueous solution), DN-800H (carboxymethylcellulose ammonium, manufactured by Daicel Finechem Co., Ltd.), ammonium alginate (produced by Kimika Co., Ltd.), and the like.
  • crosslinking agent for the triarylamine-based hyperbranched polymer examples include melamine-based, substituted urea-based, or their polymer-based crosslinking agents. These crosslinking agents may be used alone or in combination of two or more. Can be used.
  • the cross-linking agent has at least two cross-linking substituents, such as CYMEL (registered trademark), methoxymethylated glycoluril, butoxymethylated glycoluril, methylolated glycoluril, methoxymethylated melamine, butoxymethyl.
  • Melamine methylolated melamine, methoxymethylated benzoguanamine, butoxymethylated benzoguanamine, methylolated benzoguanamine, methoxymethylated urea, butoxymethylated urea, methylolated urea, methoxymethylated thiourea, methoxymethylated thiourea, methylolated thio
  • Examples include compounds such as urea, and condensates of these compounds.
  • crosslinking agent examples include, for example, an aldehyde group, an epoxy group, a vinyl group, an isocyanate group, an alkoxy group, a carboxyl group, an aldehyde group, an amino group, an isocyanate group, an epoxy group, and an amino group.
  • crosslinkable functional groups that react with each other in the same molecule, such as isocyanate groups and aldehyde groups, hydroxyl groups that react with the same crosslinkable functional groups (dehydration condensation), mercapto groups (disulfide bonds), Examples thereof include compounds having an ester group (Claisen condensation), a silanol group (dehydration condensation), a vinyl group, an acrylic group, and the like.
  • Specific examples of the crosslinking agent that self-crosslinks include polyfunctional acrylate, tetraalkoxysilane, a monomer having a blocked isocyanate group, a hydroxyl group, a carboxylic acid, and an amino group that exhibit crosslinking reactivity in the presence of an acid catalyst.
  • the block copolymer of the monomer which has is mentioned.
  • Such a self-crosslinking crosslinking agent can also be obtained as a commercial product.
  • a commercial product examples include A-9300 (ethoxylated isocyanuric acid triacrylate, Shin-Nakamura Chemical ( ), A-GLY-9E (Ethoxylatedinglycerine triacrylate (EO9 mol), Shin-Nakamura Chemical Co., Ltd.), A-TMMT (pentaerythritol tetraacrylate, Shin-Nakamura Chemical Co., Ltd.), tetraalkoxysilane In the case of tetramethoxysilane (manufactured by Tokyo Chemical Industry Co., Ltd.), tetraethoxysilane (manufactured by Toyoko Chemical Co., Ltd.), and polymers having a blocked isocyanate group, Elastron series E-37, H-3, H38, BAP, NEW BAP-15, C-52, F-2 9, W-11P, MF-9, MF-25K (D
  • the amount of these crosslinking agents to be added varies depending on the solvent used, the substrate used, the required viscosity, the required film shape, etc., but is 0.001 to 80% by mass, preferably 0.8%, based on the dispersant. The amount is from 01 to 50% by mass, more preferably from 0.05 to 40% by mass.
  • These cross-linking agents may cause a cross-linking reaction by self-condensation, but they cause a cross-linking reaction with the dispersant. If a cross-linkable substituent is present in the dispersant, the cross-linking reaction is caused by those cross-linkable substituents. Promoted.
  • a catalyst for accelerating the crosslinking reaction p-toluenesulfonic acid, trifluoromethanesulfonic acid, pyridinium p-toluenesulfonic acid, salicylic acid, sulfosalicylic acid, citric acid, benzoic acid, hydroxybenzoic acid, naphthalenecarboxylic acid And / or a thermal acid generator such as 2,4,4,6-tetrabromocyclohexadienone, benzoin tosylate, 2-nitrobenzyl tosylate, and organic sulfonic acid alkyl ester can be added.
  • the addition amount of the catalyst is preferably 0.0001 to 20% by mass, more preferably 0.0005 to 10% by mass, and still more preferably 0.001 to 3% by mass with respect to the dispersant.
  • the method for preparing the composition of the present invention is not particularly limited, and a conductive carbon material, a dispersant and a solvent, and a matrix polymer and a crosslinking agent used as necessary are mixed and dispersed in an arbitrary order. What is necessary is just to prepare a liquid. At this time, it is preferable to disperse the mixture, and this treatment can further improve the CNT dispersion ratio.
  • the dispersion treatment include mechanical treatment, wet treatment using a ball mill, bead mill, jet mill, and the like, and ultrasonic treatment using a bath-type or probe-type sonicator. In particular, wet treatment using a jet mill. Or sonication is preferred.
  • the time for the dispersion treatment is arbitrary, but is preferably about 1 minute to 10 hours, and more preferably about 5 minutes to 5 hours. At this time, heat treatment may be performed as necessary.
  • heat treatment may be performed as necessary.
  • the solid content concentration of the composition is not particularly limited, but considering the formation of the undercoat layer with a desired basis weight and film thickness, it is preferably 20% by mass or less, and 15% by mass. The following is more preferable, and 10 mass% or less is still more preferable. Moreover, the minimum is arbitrary, but 0.1 mass% or more is preferable from a practical viewpoint, 0.5 mass% or more is more preferable, and 1 mass% or more is still more preferable.
  • solid content is the total amount of components other than the solvent which comprises a composition.
  • An undercoat foil (composite current collector) can be produced by applying the composition described above to at least one surface of a current collector and naturally or heat drying it to form an undercoat layer.
  • the current collector those conventionally used as current collectors for electrodes for energy storage devices can be used.
  • copper, aluminum, titanium, stainless steel, nickel, gold, silver and alloys thereof, carbon materials, metal oxides, conductive polymers, etc. can be used, but welding such as ultrasonic welding is applied.
  • a metal foil made of copper, aluminum, titanium, stainless steel, or an alloy thereof it is preferable to use a metal foil made of copper, aluminum, titanium, stainless steel, or an alloy thereof.
  • the thickness of the current collector is not particularly limited, but is preferably 1 to 100 ⁇ m in the present invention.
  • Examples of the method for applying the composition include spin coating, dip coating, flow coating, ink jet, casting, spray coating, bar coating, gravure coating, slit coating, roll coating, and flexographic printing.
  • Method, transfer printing method, brush coating, blade coating method, air knife coating method, die coating method, etc., but from the point of work efficiency etc., inkjet method, casting method, dip coating method, bar coating method, blade coating method A roll coating method, a gravure coating method, a flexographic printing method, a spray coating method, and a die coating method are suitable.
  • the temperature for drying by heating is also arbitrary, but is preferably about 50 to 200 ° C, more preferably about 80 to 150 ° C.
  • the electrode for energy storage devices of the present invention can be produced by forming an electrode mixture layer on the undercoat layer.
  • the energy storage device in the present invention include various energy storage devices such as an electric double layer capacitor, a lithium secondary battery, a lithium ion secondary battery, a proton polymer battery, a nickel hydrogen battery, an aluminum solid capacitor, an electrolytic capacitor, and a lead storage battery.
  • the undercoat foil of the present invention can be suitably used for electric double layer capacitors and lithium ion secondary batteries.
  • an active material the various active materials conventionally used for the electrode for energy storage devices can be used.
  • a chalcogen compound capable of adsorbing / leaving lithium ions or a lithium ion-containing chalcogen compound, a polyanion compound, a simple substance of sulfur and a compound thereof may be used as a positive electrode active material. It can.
  • the chalcogen compound that can adsorb and desorb lithium ions include FeS 2 , TiS 2 , MoS 2 , V 2 O 6 , V 6 O 13 , and MnO 2 .
  • lithium ion-containing chalcogen compound examples include LiCoO 2 , LiMnO 2 , LiMn 2 O 4 , LiMo 2 O 4 , LiV 3 O 8 , LiNiO 2 , Li x Ni y M 1-y O 2 (where M is It represents at least one metal element selected from Co, Mn, Ti, Cr, V, Al, Sn, Pb, and Zn, and 0.05 ⁇ x ⁇ 1.10, 0.5 ⁇ y ⁇ 1.0 ) And the like.
  • the polyanionic compound examples include LiFePO 4 .
  • sulfur compound examples include Li 2 S and rubeanic acid.
  • the negative electrode active material constituting the negative electrode at least one element selected from alkali metals, alkali metal alloys, elements of Groups 4 to 15 of the periodic table that occlude / release lithium ions, oxides, sulfides, A nitride or a carbon material capable of reversibly occluding and releasing lithium ions can be used.
  • alkali metal include Li, Na, and K.
  • alkali metal alloy include Li—Al, Li—Mg, Li—Al—Ni, Na—Hg, and Na—Zn.
  • Examples of the simple substance of at least one element selected from Group 4 to 15 elements of the periodic table that store and release lithium ions include silicon, tin, aluminum, zinc, and arsenic.
  • examples of the oxide include tin silicon oxide (SnSiO 3 ), lithium bismuth oxide (Li 3 BiO 4 ), lithium zinc oxide (Li 2 ZnO 2 ), lithium titanium oxide (Li 4 Ti 5 O 12 ), and oxidation.
  • examples include titanium.
  • examples of the sulfide include lithium iron sulfide (Li x FeS 2 (0 ⁇ x ⁇ 3)) and lithium copper sulfide (Li x CuS (0 ⁇ x ⁇ 3)).
  • the carbon material capable of reversibly occluding and releasing lithium ions include graphite, carbon black, coke, glassy carbon, carbon fiber, carbon nanotube, and a sintered body thereof.
  • a carbonaceous material can be used as an active material.
  • the carbonaceous material include activated carbon and the like, for example, activated carbon obtained by carbonizing a phenol resin and then activating treatment.
  • the electrode mixture layer is formed by applying an active material described above, an electrode slurry prepared by combining the binder polymer described below and a solvent as necessary, onto the undercoat layer, and then naturally or by heating and drying. can do.
  • the binder polymer can be appropriately selected from known materials and used, for example, polyvinylidene fluoride (PVdF), polyvinylpyrrolidone, polytetrafluoroethylene, tetrafluoroethylene-hexafluoropropylene copolymer, vinylidene fluoride- Hexafluoropropylene copolymer [P (VDF-HFP)], vinylidene fluoride-trichloroethylene copolymer [P (VDF-CTFE)], polyvinyl alcohol, polyimide, ethylene-propylene-diene ternary copolymer Examples thereof include conductive polymers such as coalescence, styrene-butadiene rubber, carboxymethyl cellulose (CMC), polyacrylic acid (PAA), and polyaniline.
  • PVdF polyvinylidene fluoride
  • PVdF polyvinylidene fluoride
  • PVDF-HFP vinylidene fluoride- Hexafluor
  • the added amount of the binder polymer is preferably 0.1 to 20 parts by mass, particularly 1 to 10 parts by mass with respect to 100 parts by mass of the active material.
  • the solvent include the solvents exemplified in the above solvent for the composition, and may be appropriately selected according to the type of the binder, but NMP is preferable in the case of a water-insoluble binder such as PVdF. In the case of a water-soluble binder such as PAA, water is preferable.
  • the electrode slurry may contain a conductive material.
  • the conductive material include carbon black, ketjen black, acetylene black, carbon whisker, carbon fiber, natural graphite, artificial graphite, titanium oxide, ruthenium oxide, aluminum, nickel and the like.
  • Examples of the method for applying the electrode slurry include the same method as the method for applying the composition described above.
  • the temperature for drying by heating is arbitrary, but is preferably about 50 to 400 ° C, more preferably about 80 to 150 ° C.
  • the electrode may be pressed as necessary.
  • the press pressure is preferably 1 kN / cm or more.
  • the pressing method a generally adopted method can be used, but a die pressing method and a roll pressing method are particularly preferable.
  • the pressing pressure is not particularly limited, but is preferably 2 kN / cm or more, and more preferably 3 kN / cm or more.
  • the upper limit of the pressing pressure is preferably about 40 kN / cm, more preferably about 30 kN / cm.
  • An energy storage device includes the above-described electrode for an energy storage device, and more specifically includes at least a pair of positive and negative electrodes, a separator interposed between these electrodes, and an electrolyte. And at least one of the positive and negative electrodes is composed of the energy storage device electrode described above. Since this energy storage device is characterized by the use of the above-described electrode for energy storage device as an electrode, other device constituent members such as separators and electrolytes may be appropriately selected from known materials and used. it can. Examples of the separator include a cellulose separator and a polyolefin separator.
  • the electrolyte may be either liquid or solid, and may be either aqueous or non-aqueous.
  • the electrode for an energy storage device of the present invention is practically sufficient even when applied to a device using a non-aqueous electrolyte. Performance can be demonstrated.
  • non-aqueous electrolyte examples include a non-aqueous electrolyte obtained by dissolving an electrolyte salt in a non-aqueous organic solvent.
  • electrolyte salts include lithium salts such as lithium tetrafluoroborate, lithium hexafluorophosphate, lithium perchlorate, and lithium trifluoromethanesulfonate; tetramethylammonium hexafluorophosphate, tetraethylammonium hexafluorophosphate, tetrapropylammonium hexa Quaternary ammonium salts such as fluorophosphate, methyltriethylammonium hexafluorophosphate, tetraethylammonium tetrafluoroborate, tetraethylammonium perchlorate, lithium imides such as lithium bis (trifluoromethanesulfonyl) imide, lithium bis (fluo
  • non-aqueous organic solvent examples include alkylene carbonates such as propylene carbonate, ethylene carbonate, and butylene carbonate; dialkyl carbonates such as dimethyl carbonate, methyl ethyl carbonate, and diethyl carbonate; nitriles such as acetonitrile; and amides such as dimethylformamide. .
  • the form of the energy storage device is not particularly limited, and conventionally known various types of cells such as a cylindrical type, a flat wound square type, a laminated square type, a coin type, a flat wound laminated type, and a laminated laminate type are adopted. can do.
  • the above-described electrode for an energy storage device of the present invention may be used by punching it into a predetermined disk shape.
  • a lithium ion secondary battery one electrode is placed on a lid to which a washer and a spacer of a coin cell are welded, and a separator of the same shape impregnated with an electrolytic solution is stacked thereon.
  • the energy storage device electrode of the present invention can be overlaid with the composite material layer facing down, a case and a gasket can be placed thereon, and sealed with a coin cell caulking machine.
  • the electrode mixture layer is welded to the metal tab at the portion where the electrode mixture layer is not formed (welded part) in the electrode formed on part or the entire surface of the undercoat layer.
  • the obtained electrode structure may be used.
  • the basis weight of the undercoat layer per surface of the current collector is preferably 0.1 g / m 2 or less, more preferably 0.09 g / m 2 or less, even more preferably less than 0.05 g / m 2.
  • one or a plurality of electrodes constituting the electrode structure may be used, but generally a plurality of positive and negative electrodes are used.
  • the plurality of electrodes for forming the positive electrode are preferably alternately stacked one by one with the plurality of electrodes for forming the negative electrode, and the separator described above is interposed between the positive electrode and the negative electrode. It is preferable. Even if the metal tab is welded at the welded portion of the outermost electrode of the plurality of electrodes, the metal tab is welded with the metal tab sandwiched between the welded portions of any two adjacent electrodes among the plurality of electrodes. Also good.
  • the material of the metal tab is not particularly limited as long as it is generally used for energy storage devices.
  • metal such as nickel, aluminum, titanium, copper; stainless steel, nickel alloy, aluminum alloy
  • An alloy such as a titanium alloy or a copper alloy can be used, but in view of welding efficiency, an alloy including at least one metal selected from aluminum, copper and nickel is preferable.
  • the shape of the metal tab is preferably a foil shape, and the thickness is preferably about 0.05 to 1 mm.
  • a known method used for metal-to-metal welding can be used. Specific examples thereof include TIG welding, spot welding, laser welding, ultrasonic welding, and the like. It is preferable to join the metal tab.
  • a technique of ultrasonic welding for example, a plurality of electrodes are arranged between an anvil and a horn, a metal tab is arranged in a welded portion, and ultrasonic welding is applied to collect a plurality of electrodes. The technique of welding first and then welding a metal tab is mentioned.
  • the metal tab and the electrode are not only welded at the welded portion, but a plurality of electrodes are also ultrasonically welded to each other.
  • the pressure, frequency, output, processing time, and the like during welding are not particularly limited, and may be set as appropriate in consideration of the material used, the presence or absence of the undercoat layer, the basis weight, and the like.
  • the electrode structure produced as described above is housed in a laminate pack, and after injecting the above-described electrolyte, heat sealing is performed to obtain a laminate cell.
  • the undercoat layer of the present invention is suitable as an undercoat layer for joining the current collector constituting the electrode of the energy storage device and the active material layer. It can also be used as a coating film.
  • the obtained mixture was subjected to ultrasonic treatment for 30 minutes using a probe-type ultrasonic irradiation device to prepare a dispersion liquid in which the conductive carbon material was uniformly dispersed.
  • Aron A-30 Toagosei Co., Ltd., solid content concentration 31.6% by mass
  • PAA-NH 4 ammonium polyacrylate
  • PAA-NH 4 ammonium polyacrylate
  • 2-propanol manufactured by Junsei Chemical Co., Ltd., reagent special grade
  • Preparation Example 1-2 An undercoat solution was prepared in the same manner as in Preparation Example 1-1 except that CNT was changed to VGCF-X (manufactured by Showa Denko KK, multilayer CNT).
  • Preparation Example 1-3 An undercoat liquid was prepared in the same manner as in Preparation Example 1-1 except that CNT was changed to NC-7000 (multilayer CNT manufactured by Nanocyl SA).
  • Preparation Example 1-4 An undercoat solution was prepared in the same manner as in Preparation Example 1-1 except that CNT was changed to AMC (manufactured by Ube Industries, Ltd., multilayer CNT).
  • Example 1-1 The undercoat liquid of Preparation Example 1-1 was uniformly spread on a current collector aluminum foil (thickness 15 ⁇ m) with a wire bar coater (OSP-13, wet film thickness 13 ⁇ m), and then dried at 150 ° C. for 30 minutes. An undercoat layer was formed to prepare an undercoat foil.
  • OSP-13 wire bar coater
  • Example 1 except that the undercoat liquids obtained in Preparation Examples 1-2 to 1-5 and Comparative Preparation Examples 1-1 to 1-2 were used in place of the undercoat liquid of Preparation Example 1-1, respectively.
  • Undercoat foil was prepared in the same manner as in Example-1.
  • the prepared undercoat foil was cut out to 8 ⁇ 16 cm and measured for mass, then immersed in a 0.1N hydrochloric acid aqueous solution to remove only the undercoat layer, and the mass of the metal foil was measured.
  • the basis weight per unit area was determined from the difference in mass before and after removal of the undercoat layer.
  • Average surface roughness Ra Measure the area of 30 ⁇ m ⁇ 30 ⁇ m using an atomic force microscope at three locations of the prepared undercoat foil, and calculate the average value of the surface roughness Ra (arithmetic average roughness) obtained from the measurement of each area as the average surface It calculated
  • the obtained electrode slurry was spread evenly (wet film thickness 100 ⁇ m) on the undercoat foil prepared in Example 1-1, and then dried at 80 ° C. for 30 minutes and then at 120 ° C. for 30 minutes to form on the undercoat layer. An electrode mixture layer was formed, and further crimped with a roll press to produce an electrode.
  • Example 2-2 to 2-5 Comparative Examples 2-1 to 2-2
  • the electrode of Example 1-1 it was the same as Example 2-1 except that the electrodes obtained in Examples 1-2 to 1-5 and Comparative Examples 1-1 to 1-2 were used, respectively. Thus, a secondary battery was produced.
  • Example 2-3 A test secondary battery was produced in the same manner as in Example 2-1, except that solid aluminum foil was used as the electrode.
  • the average surface roughness Ra of the undercoat layer was optimized, so that the battery of the battery was compared with the battery manufactured in the comparative example. It can be seen that the direct current resistance is low and the increase in resistance after the cycle test is also suppressed.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Power Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Physics & Mathematics (AREA)
  • Dispersion Chemistry (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Cell Electrode Carriers And Collectors (AREA)
  • Battery Electrode And Active Subsutance (AREA)
  • Electric Double-Layer Capacitors Or The Like (AREA)
  • Conductive Materials (AREA)

Abstract

L'invention concerne une sous-couche qui est destinée à un dispositif de stockage d'énergie et qui peut être obtenue à partir d'une composition comprenant des nanotubes de carbone, un dispersant de nanotubes de carbone et un solvant, lorsque la densité de la sous-couche est de 1 g/cm3, la rugosité de surface moyenne Ra de la sous-couche est de 45 % ou plus par rapport à l'épaisseur de couche qui peut être calculée à partir du poids de base.
PCT/JP2019/011333 2018-03-29 2019-03-19 Sous-couche pour dispositif de stockage d'énergie Ceased WO2019188541A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2020510720A JPWO2019188541A1 (ja) 2018-03-29 2019-03-19 エネルギー貯蔵デバイスのアンダーコート層

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2018-063718 2018-03-29
JP2018063718 2018-03-29

Publications (1)

Publication Number Publication Date
WO2019188541A1 true WO2019188541A1 (fr) 2019-10-03

Family

ID=68061628

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2019/011333 Ceased WO2019188541A1 (fr) 2018-03-29 2019-03-19 Sous-couche pour dispositif de stockage d'énergie

Country Status (2)

Country Link
JP (1) JPWO2019188541A1 (fr)
WO (1) WO2019188541A1 (fr)

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011146365A (ja) * 2009-12-14 2011-07-28 Hitachi Maxell Energy Ltd 電気化学素子
JP2012084612A (ja) * 2010-10-07 2012-04-26 Nippon Chemicon Corp 電気二重層キャパシタ用集電体及び電気二重層キャパシタ
WO2014030208A1 (fr) * 2012-08-21 2014-02-27 大日精化工業株式会社 Composition liquide aqueuse, liquide de revêtement aqueux, film de revêtement fonctionnel et matériau composite
JP2016207493A (ja) * 2015-04-23 2016-12-08 株式会社半導体エネルギー研究所 電極、蓄電池、及び電子機器
WO2017119288A1 (fr) * 2016-01-07 2017-07-13 日産化学工業株式会社 Électrode pour dispositifs de stockage d'énergie

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011146365A (ja) * 2009-12-14 2011-07-28 Hitachi Maxell Energy Ltd 電気化学素子
JP2012084612A (ja) * 2010-10-07 2012-04-26 Nippon Chemicon Corp 電気二重層キャパシタ用集電体及び電気二重層キャパシタ
WO2014030208A1 (fr) * 2012-08-21 2014-02-27 大日精化工業株式会社 Composition liquide aqueuse, liquide de revêtement aqueux, film de revêtement fonctionnel et matériau composite
JP2016207493A (ja) * 2015-04-23 2016-12-08 株式会社半導体エネルギー研究所 電極、蓄電池、及び電子機器
WO2017119288A1 (fr) * 2016-01-07 2017-07-13 日産化学工業株式会社 Électrode pour dispositifs de stockage d'énergie

Also Published As

Publication number Publication date
JPWO2019188541A1 (ja) 2021-04-01

Similar Documents

Publication Publication Date Title
JP6260740B2 (ja) エネルギー貯蔵デバイス電極用アンダーコート箔
WO2018101301A1 (fr) Film mince comprenant des nanotubes de carbone
JP2019140119A (ja) エネルギー貯蔵デバイス電極用アンダーコート箔
CN110062972B (zh) 薄膜和储能器件电极用底涂箔
WO2018101308A1 (fr) Électrode pour dispositif de stockage d'énergie, et dispositif de stockage d'énergie
EP3780191A1 (fr) Feuille de sous-couche pour électrode de dispositif de stockage d'énergie
JP2019140110A (ja) エネルギー貯蔵デバイス電極用アンダーコート箔
WO2019188545A1 (fr) Composition pour former un film mince conducteur
WO2019188550A1 (fr) Composition pour former une sous-couche de dispositif de stockage d'énergie
JP2019175730A (ja) エネルギー貯蔵デバイスのアンダーコート層
JP2019175744A (ja) エネルギー貯蔵デバイス用電極及びエネルギー貯蔵デバイス
JP7318637B2 (ja) エネルギー貯蔵デバイスのアンダーコート層形成用組成物
WO2019188540A1 (fr) Composition pour former une sous-couche de dispositif de stockage d'énergie
WO2019188547A1 (fr) Liquide de dispersion pour former un film mince conducteur
EP3780158A1 (fr) Électrode de dispositif de stockage d'énergie et dispositif de stockage d'énergie
JP2019175729A (ja) エネルギー貯蔵デバイスのアンダーコート層形成用組成物
JP7318638B2 (ja) エネルギー貯蔵デバイスのアンダーコート層形成用組成物
JP2019175749A (ja) エネルギー貯蔵デバイス用電極及びエネルギー貯蔵デバイス
WO2019188541A1 (fr) Sous-couche pour dispositif de stockage d'énergie
WO2019188539A1 (fr) Composition de formation de sous-couche de dispositif de stockage d'énergie
WO2022176789A1 (fr) Composition pour former un film mince pour électrodes de dispositif de stockage d'énergie

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 19774479

Country of ref document: EP

Kind code of ref document: A1

ENP Entry into the national phase

Ref document number: 2020510720

Country of ref document: JP

Kind code of ref document: A

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 19774479

Country of ref document: EP

Kind code of ref document: A1