TW201107381A - Fluorescence conversion solar cell-production in an injection moulding process - Google Patents
Fluorescence conversion solar cell-production in an injection moulding process Download PDFInfo
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- TW201107381A TW201107381A TW099111289A TW99111289A TW201107381A TW 201107381 A TW201107381 A TW 201107381A TW 099111289 A TW099111289 A TW 099111289A TW 99111289 A TW99111289 A TW 99111289A TW 201107381 A TW201107381 A TW 201107381A
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- shaped polymer
- polymer body
- acrylate
- methyl
- poly
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- 238000001746 injection moulding Methods 0.000 title claims abstract description 28
- 238000004519 manufacturing process Methods 0.000 title claims description 9
- 238000006243 chemical reaction Methods 0.000 title abstract description 10
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- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 229910052981 lead sulfide Inorganic materials 0.000 description 1
- 229940056932 lead sulfide Drugs 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 125000005641 methacryl group Chemical group 0.000 description 1
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 1
- 229940117841 methacrylic acid copolymer Drugs 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229910052754 neon Inorganic materials 0.000 description 1
- GKAOGPIIYCISHV-UHFFFAOYSA-N neon atom Chemical compound [Ne] GKAOGPIIYCISHV-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000011022 opal Substances 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 1
- 239000003504 photosensitizing agent Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- GGYFMLJDMAMTAB-UHFFFAOYSA-N selanylidenelead Chemical compound [Pb]=[Se] GGYFMLJDMAMTAB-UHFFFAOYSA-N 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 125000005504 styryl group Chemical group 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- WYKYCHHWIJXDAO-UHFFFAOYSA-N tert-butyl 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOC(C)(C)C WYKYCHHWIJXDAO-UHFFFAOYSA-N 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- 238000009757 thermoplastic moulding Methods 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 239000003451 thiazide diuretic agent Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 235000012431 wafers Nutrition 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F77/00—Constructional details of devices covered by this subclass
- H10F77/40—Optical elements or arrangements
- H10F77/42—Optical elements or arrangements directly associated or integrated with photovoltaic cells, e.g. light-reflecting means or light-concentrating means
- H10F77/45—Wavelength conversion means, e.g. by using luminescent material, fluorescent concentrators or up-conversion arrangements
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F120/00—Homopolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F120/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F120/10—Esters
- C08F120/12—Esters of monohydric alcohols or phenols
- C08F120/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F120/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
- C08L33/10—Homopolymers or copolymers of methacrylic acid esters
- C08L33/12—Homopolymers or copolymers of methyl methacrylate
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F19/00—Integrated devices, or assemblies of multiple devices, comprising at least one photovoltaic cell covered by group H10F10/00, e.g. photovoltaic modules
- H10F19/80—Encapsulations or containers for integrated devices, or assemblies of multiple devices, having photovoltaic cells
- H10F19/804—Materials of encapsulations
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F77/00—Constructional details of devices covered by this subclass
- H10F77/40—Optical elements or arrangements
- H10F77/42—Optical elements or arrangements directly associated or integrated with photovoltaic cells, e.g. light-reflecting means or light-concentrating means
- H10F77/488—Reflecting light-concentrating means, e.g. parabolic mirrors or concentrators using total internal reflection
-
- 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
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/52—PV systems with concentrators
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Injection Moulding Of Plastics Or The Like (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102009002386A DE102009002386A1 (de) | 2009-04-15 | 2009-04-15 | Fluoreszenzkonversionssolarzelle - Herstellung im Spritzgussverfahren |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TW201107381A true TW201107381A (en) | 2011-03-01 |
Family
ID=42110239
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW099111289A TW201107381A (en) | 2009-04-15 | 2010-04-12 | Fluorescence conversion solar cell-production in an injection moulding process |
Country Status (3)
| Country | Link |
|---|---|
| DE (1) | DE102009002386A1 (de) |
| TW (1) | TW201107381A (de) |
| WO (1) | WO2010118920A1 (de) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104540677A (zh) * | 2012-05-16 | 2015-04-22 | 诺沃聚合物公司 | 聚合物片材 |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102010028180A1 (de) * | 2010-04-26 | 2011-10-27 | Evonik Röhm Gmbh | Fluoreszenzkonversionssolarzelle - Herstellung im Extrusionslaminationsverfahren oder im Kleberlaminationsverfahren |
| JP5976675B2 (ja) * | 2011-01-05 | 2016-08-24 | 日東電工株式会社 | 波長変換ペリレンジエステル発色団および発光膜 |
| EP2671263A2 (de) * | 2011-03-31 | 2013-12-11 | Dow Global Technologies LLC | Lichtdurchlässige thermoplastische harze mit einem abwärtsumsetzungsmaterial und ihre verwendung für pv-module |
| CN105419379B (zh) | 2011-09-26 | 2018-11-20 | 日东电工株式会社 | 用于提高的日光采集效率的高荧光且光稳定性生色团 |
| WO2013052381A2 (en) | 2011-10-05 | 2013-04-11 | Nitto Denko Corporation | Wavelength conversion film having pressure sensitive adhesive layer to enhance solar harvesting efficiency |
| CN103195240A (zh) * | 2013-03-25 | 2013-07-10 | 江苏百新塑业有限公司 | 中空塑料建筑模板的挤塑封边工艺 |
| TWI641645B (zh) * | 2016-07-08 | 2018-11-21 | 羅門哈斯電子材料有限公司 | 用於囊封量子點之多層聚合物複合物 |
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| CH612541A5 (de) | 1976-05-06 | 1979-07-31 | Fraunhofer Ges Forschung | |
| DE2737847A1 (de) * | 1977-08-23 | 1979-03-08 | Fraunhofer Ges Forschung | Vorrichtung mit lumineszenz-lichtkonzentratoren zur umwandlung von solarenergie |
| US4175980A (en) * | 1978-12-18 | 1979-11-27 | Atlantic Richfield Company | Luminescent solar collector |
| DE2908770A1 (de) * | 1979-03-06 | 1980-10-02 | Siemens Ag | Verfahren zur sammlung von licht und vorrichtung zur durchfuehrung eines solchen verfahrens |
| US4488047A (en) * | 1981-11-25 | 1984-12-11 | Exxon Research & Engineering Co. | High efficiency multiple layer, all solid-state luminescent solar concentrator |
| DE3300526A1 (de) | 1983-01-10 | 1984-07-12 | Röhm GmbH, 6100 Darmstadt | Schlagzaehmodifizierungsmittel |
| US4845223A (en) * | 1985-12-19 | 1989-07-04 | Basf Aktiengesellschaft | Fluorescent aryloxy-substituted perylene-3,4,9,10-tetracarboxylic acid diimides |
| DE3545004A1 (de) * | 1985-12-19 | 1987-06-25 | Basf Ag | Fluoreszierende aroxysubstituierte perylen-3,4,9,10-tetracarbonsaeurediimide und ihre verwendung zur flaechenmaessigen konzentriertung von licht |
| JPH0347856A (ja) | 1989-04-18 | 1991-02-28 | Kuraray Co Ltd | 耐光性に優れたメタクリル樹脂 |
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| DE4121652A1 (de) | 1991-06-29 | 1993-01-07 | Roehm Gmbh | Schlagzaeh-modifizierungsmittel |
| US5489297A (en) | 1992-01-27 | 1996-02-06 | Duran; Carlos M. G. | Bioprosthetic heart valve with absorbable stent |
| DE4417559A1 (de) | 1994-05-19 | 1995-11-23 | Roehm Gmbh | Verfahren zum Entwässern einer wasserhaltigen Kunststoffschmelze in einem Doppelschneckenextruder |
| US5622821A (en) | 1994-06-29 | 1997-04-22 | The Regents Of The University Of California | Luminescent lanthanide chelates and methods of use |
| WO1997008756A1 (en) * | 1995-08-28 | 1997-03-06 | Minnesota Mining And Manufacturing Company | Durable fluorescent solar collectors |
| DE69627205T2 (de) * | 1996-05-17 | 2004-02-05 | Smith, Geoffrey Burton, Epping | Verbesserungen bei fluoreszierenden materialien |
| DE19705046A1 (de) * | 1996-08-20 | 1998-02-26 | Fraunhofer Ges Forschung | Vorrichtung und Verfahren zur Nutzung der Solarenergie |
| CA2283075A1 (en) | 1997-03-03 | 1998-09-11 | Akzo Nobel Nv | Polymeric optical waveguide doped with a lanthanide-sensitizer complex |
| FR2792461B3 (fr) * | 1999-04-19 | 2001-06-29 | Biocube | Generateurs photovoltaiques a cascade lumineuse et variation de flux elecromomagnetique |
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| AU2001278446A1 (en) | 2000-06-15 | 2001-12-24 | Merck Patent G.M.B.H | A method for producing sphere-based crystals |
| EP1337695B1 (de) | 2000-10-04 | 2010-12-08 | The Board Of Trustees Of The University Of Arkansas | Synthese von kolloidalen metall chalcogenide nanokristallen |
| AU2002229534A1 (en) | 2000-11-30 | 2002-06-11 | Merck Patent G.M.B.H | Particles with opalescent effect |
| DE10228228A1 (de) | 2001-09-14 | 2003-04-03 | Merck Patent Gmbh | Formkörper aus Kern-Mantel-Partikeln |
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| DE10233684A1 (de) | 2002-07-24 | 2004-02-12 | Röhm GmbH & Co. KG | Verfahren zum Verkleben von mindestens zwei Kunststoffplatten sowie Vorrichtung zur Durchführung des Verfahrens |
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| DE10245848A1 (de) | 2002-09-30 | 2004-04-01 | Merck Patent Gmbh | Verfahren zur Herstellung inverser opalartiger Strukturen |
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| DE10357681A1 (de) | 2003-12-10 | 2005-07-21 | Merck Patent Gmbh | Verwendung von Kern-Mantel-Partikeln |
| DE102004009569A1 (de) | 2004-02-25 | 2005-09-15 | Merck Patent Gmbh | Verwendung von Kern-Mantel-Partikeln |
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| DE102004032120A1 (de) | 2004-07-01 | 2006-02-09 | Merck Patent Gmbh | Beugungsfarbmittel für die Kosmetik |
| WO2006045567A2 (de) | 2004-10-25 | 2006-05-04 | Merck Patent Gmbh | Verwendung von Formkörpern aus Kern-Mantel-Partikeln |
| DE102004055303A1 (de) | 2004-11-16 | 2006-05-18 | Röhm GmbH & Co. KG | Kern-Mantel-Partikel |
| KR100657639B1 (ko) | 2004-12-13 | 2006-12-14 | 재단법인서울대학교산학협력재단 | 반도체 양자점의 대량 합성 방법 |
| DE102005040351B4 (de) * | 2005-08-25 | 2007-05-24 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Strahlungsmodule, diese enthaltende Anordnungen sowie Verfahren zur Detektion, Kontrolle und Überwachung |
| DE102005043572A1 (de) | 2005-09-12 | 2007-03-15 | Basf Ag | Fluoreszenzkonversionssolarzellen auf Basis von Terrylenfluoreszenzfarbstoffen |
| US7414294B2 (en) | 2005-12-16 | 2008-08-19 | The Trustees Of Princeton University | Intermediate-band photosensitive device with quantum dots having tunneling barrier embedded in organic matrix |
| US20070137696A1 (en) * | 2005-12-21 | 2007-06-21 | Hans-Joachim Krokoszinski | Solar panels, methods of manufacture thereof and articles comprising the same |
| DE102006017163A1 (de) | 2006-04-12 | 2007-10-18 | Merck Patent Gmbh | Verfahren zur Herstellung von inversen Opalen mit einstellbaren Kanaldurchmessern |
| US20080149165A1 (en) * | 2006-12-22 | 2008-06-26 | General Electric Company | Luminescent solar collector |
| US8676016B2 (en) * | 2007-02-16 | 2014-03-18 | The Governing Council Of The University Of Toronto | Compressible photonic crystal |
| EP2130233A1 (de) * | 2007-03-13 | 2009-12-09 | Basf Se | Fotovoltische module mit verbesserter quanteneffizienz |
| CN101828264B (zh) * | 2007-08-17 | 2014-04-30 | 巴斯夫欧洲公司 | 太阳能电池结构 |
-
2009
- 2009-04-15 DE DE102009002386A patent/DE102009002386A1/de not_active Withdrawn
-
2010
- 2010-03-11 WO PCT/EP2010/053065 patent/WO2010118920A1/de not_active Ceased
- 2010-04-12 TW TW099111289A patent/TW201107381A/zh unknown
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104540677A (zh) * | 2012-05-16 | 2015-04-22 | 诺沃聚合物公司 | 聚合物片材 |
| CN104540677B (zh) * | 2012-05-16 | 2018-05-22 | 北欧化工公司 | 聚合物片材 |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2010118920A1 (de) | 2010-10-21 |
| DE102009002386A1 (de) | 2010-10-21 |
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