KR20010110117A - 홀 전송제 및 이를 포함하는 광전기 전환 장치 - Google Patents
홀 전송제 및 이를 포함하는 광전기 전환 장치 Download PDFInfo
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- KR20010110117A KR20010110117A KR1020010029726A KR20010029726A KR20010110117A KR 20010110117 A KR20010110117 A KR 20010110117A KR 1020010029726 A KR1020010029726 A KR 1020010029726A KR 20010029726 A KR20010029726 A KR 20010029726A KR 20010110117 A KR20010110117 A KR 20010110117A
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- photoelectric conversion
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- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
- 238000007738 vacuum evaporation Methods 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/04—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
- C07C217/78—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton
- C07C217/80—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings
- C07C217/82—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings of the same non-condensed six-membered aromatic ring
- C07C217/92—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings of the same non-condensed six-membered aromatic ring the nitrogen atom of at least one of the amino groups being further bound to a carbon atom of a six-membered aromatic ring
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- H—ELECTRICITY
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- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K30/00—Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation
- H10K30/10—Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation comprising heterojunctions between organic semiconductors and inorganic semiconductors
- H10K30/15—Sensitised wide-bandgap semiconductor devices, e.g. dye-sensitised TiO2
- H10K30/151—Sensitised wide-bandgap semiconductor devices, e.g. dye-sensitised TiO2 the wide bandgap semiconductor comprising titanium oxide, e.g. TiO2
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- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/10—Organic polymers or oligomers
- H10K85/141—Organic polymers or oligomers comprising aliphatic or olefinic chains, e.g. poly N-vinylcarbazol, PVC or PTFE
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- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/611—Charge transfer complexes
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- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/631—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine
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- H—ELECTRICITY
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- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/631—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine
- H10K85/633—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine comprising polycyclic condensed aromatic hydrocarbons as substituents on the nitrogen atom
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- H10K85/649—Aromatic compounds comprising a hetero atom
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- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
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- H10K85/60—Organic compounds having low molecular weight
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
- H10K85/6572—Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ring system, e.g. phenanthroline or carbazole
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- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K2102/00—Constructional details relating to the organic devices covered by this subclass
- H10K2102/10—Transparent electrodes, e.g. using graphene
- H10K2102/101—Transparent electrodes, e.g. using graphene comprising transparent conductive oxides [TCO]
- H10K2102/102—Transparent electrodes, e.g. using graphene comprising transparent conductive oxides [TCO] comprising tin oxides, e.g. fluorine-doped SnO2
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- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/10—Organic polymers or oligomers
- H10K85/141—Organic polymers or oligomers comprising aliphatic or olefinic chains, e.g. poly N-vinylcarbazol, PVC or PTFE
- H10K85/146—Organic polymers or oligomers comprising aliphatic or olefinic chains, e.g. poly N-vinylcarbazol, PVC or PTFE poly N-vinylcarbazol; Derivatives thereof
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- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/30—Coordination compounds
- H10K85/341—Transition metal complexes, e.g. Ru(II)polypyridine complexes
- H10K85/344—Transition metal complexes, e.g. Ru(II)polypyridine complexes comprising ruthenium
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- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
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- H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
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- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/631—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine
- H10K85/636—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine comprising heteroaromatic hydrocarbons as substituents on the nitrogen atom
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- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/654—Aromatic compounds comprising a hetero atom comprising only nitrogen as heteroatom
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- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/656—Aromatic compounds comprising a hetero atom comprising two or more different heteroatoms per ring
-
- 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
- Y02E10/542—Dye sensitized solar cells
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- 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
- Y02E10/549—Organic PV cells
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
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- Computer Hardware Design (AREA)
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- General Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP00111493A EP1160888A1 (en) | 2000-05-29 | 2000-05-29 | Hole transporting agents and photoelectric conversion device comprising the same |
| EP00111493.3 | 2000-05-29 |
Publications (1)
| Publication Number | Publication Date |
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| KR20010110117A true KR20010110117A (ko) | 2001-12-12 |
Family
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| KR1020010029726A KR20010110117A (ko) | 2000-05-29 | 2001-05-29 | 홀 전송제 및 이를 포함하는 광전기 전환 장치 |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8753916B2 (en) | 2001-10-24 | 2014-06-17 | The Regents Of The University Of California | Semiconductor-nanocrystal/conjugated polymer thin films |
Families Citing this family (54)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AT410859B (de) * | 2000-04-27 | 2003-08-25 | Qsel Quantum Solar Energy Linz | Verfahren zum herstellen einer photovoltaischen zelle mit einer photoaktiven schicht aus zwei organischen komponenten |
| AT411306B (de) * | 2000-04-27 | 2003-11-25 | Qsel Quantum Solar Energy Linz | Photovoltaische zelle mit einer photoaktiven schicht aus zwei molekularen organischen komponenten |
| AT410729B (de) | 2000-04-27 | 2003-07-25 | Qsel Quantum Solar Energy Linz | Photovoltaische zelle mit einer photoaktiven schicht aus zwei molekularen organischen komponenten |
| EP1160888A1 (en) * | 2000-05-29 | 2001-12-05 | Sony International (Europe) GmbH | Hole transporting agents and photoelectric conversion device comprising the same |
| US6710366B1 (en) | 2001-08-02 | 2004-03-23 | Ultradots, Inc. | Nanocomposite materials with engineered properties |
| US6819845B2 (en) | 2001-08-02 | 2004-11-16 | Ultradots, Inc. | Optical devices with engineered nonlinear nanocomposite materials |
| DE60132450T2 (de) * | 2001-09-04 | 2008-04-17 | Sony Deutschland Gmbh | Solarzelle und Herstellungsmethode |
| EP1289030A1 (en) * | 2001-09-04 | 2003-03-05 | Sony International (Europe) GmbH | Doping of a hole transporting material |
| US7989695B2 (en) * | 2001-12-18 | 2011-08-02 | Steven Allen Carlson | Organic photovoltaic cells |
| CN101068041B (zh) * | 2002-07-19 | 2010-08-18 | 出光兴产株式会社 | 有机电致发光装置和有机发光介质 |
| JP4631386B2 (ja) * | 2004-02-25 | 2011-02-16 | 株式会社デンソー | 有機ｅｌ素子 |
| WO2005114748A2 (en) * | 2004-04-13 | 2005-12-01 | Solaris Nanosciences, Inc. | Plasmon enhanced sensitized photovoltaic cells |
| US7135405B2 (en) * | 2004-08-04 | 2006-11-14 | Hewlett-Packard Development Company, L.P. | Method to form an interconnect |
| US7540978B2 (en) * | 2004-08-05 | 2009-06-02 | Novaled Ag | Use of an organic matrix material for producing an organic semiconductor material, organic semiconductor material and electronic component |
| EP1648042B1 (en) | 2004-10-07 | 2007-05-02 | Novaled AG | A method for doping a semiconductor material with cesium |
| DE502005009415D1 (de) * | 2005-05-27 | 2010-05-27 | Novaled Ag | Transparente organische Leuchtdiode |
| EP2045843B1 (de) * | 2005-06-01 | 2012-08-01 | Novaled AG | Lichtemittierendes Bauteil mit einer Elektrodenanordnung |
| EP1739765A1 (de) * | 2005-07-01 | 2007-01-03 | Novaled AG | Organische Leuchtdiode und Anordnung mit mehreren organischen Leuchtdioden |
| DE502005009802D1 (de) * | 2005-11-10 | 2010-08-05 | Novaled Ag | Dotiertes organisches Halbleitermaterial |
| US7919010B2 (en) * | 2005-12-22 | 2011-04-05 | Novaled Ag | Doped organic semiconductor material |
| ES2310380T3 (es) | 2006-03-21 | 2009-01-01 | Novaled Ag | Radical o dirradical heterociclicos, sus dimeros, oligomeros, polimeros, compuestos diespiro y policiclos, su utilizacion, material semiconductor organico asi como componente electronico. |
| EP1837927A1 (de) * | 2006-03-22 | 2007-09-26 | Novaled AG | Verwendung von heterocyclischen Radikalen zur Dotierung von organischen Halbleitern |
| EP1837929A1 (en) * | 2006-03-23 | 2007-09-26 | Ecole Polytechnique Fédérale de Lausanne (EPFL) | Liquid Charge Transporting Material |
| US8257267B2 (en) * | 2007-01-09 | 2012-09-04 | Boston Scientific Scimed, Inc. | Self-aligning IVUS catheter rotational core connector |
| DE102007012794B3 (de) * | 2007-03-16 | 2008-06-19 | Novaled Ag | Pyrido[3,2-h]chinazoline und/oder deren 5,6-Dihydroderivate, deren Herstellungsverfahren und diese enthaltendes dotiertes organisches Halbleitermaterial |
| DE102007018456B4 (de) * | 2007-04-19 | 2022-02-24 | Novaled Gmbh | Verwendung von Hauptgruppenelementhalogeniden und/oder -pseudohalogeniden, organisches halbleitendes Matrixmaterial, elektronische und optoelektronische Bauelemente |
| EP1988587B1 (de) | 2007-04-30 | 2016-12-07 | Novaled GmbH | Oxokohlenstoff-, Pseudooxokohlenstoff- und Radialenverbindungen sowie deren Verwendung |
| EP1990847B1 (de) * | 2007-05-10 | 2018-06-20 | Novaled GmbH | Verwendung von chinoiden Bisimidazolen und deren Derivaten als Dotand zur Dotierung eines organischen halbleitenden Matrixmaterials |
| DE102007031220B4 (de) | 2007-07-04 | 2022-04-28 | Novaled Gmbh | Chinoide Verbindungen und deren Verwendung in halbleitenden Matrixmaterialien, elektronischen und optoelektronischen Bauelementen |
| US7915068B2 (en) * | 2008-03-14 | 2011-03-29 | Atomic Energy Council—Institute of Nuclear Energy Research | Method for making solar cells with sensitized quantum dots in the form of nanometer metal particles |
| US8057712B2 (en) * | 2008-04-29 | 2011-11-15 | Novaled Ag | Radialene compounds and their use |
| KR20100009323A (ko) * | 2008-07-18 | 2010-01-27 | 삼성전자주식회사 | 벌브 타입 집광형 태양전지 모듈 |
| US8158096B2 (en) * | 2008-09-19 | 2012-04-17 | The United States Of America, As Represented By The Secretary Of The Navy | Barium copper sulfur fluoride transparent conductive thin films and bulk material |
| TWI381537B (zh) * | 2009-05-13 | 2013-01-01 | Ind Tech Res Inst | 太陽能電池裝置及其製造方法 |
| KR101072089B1 (ko) * | 2009-09-30 | 2011-10-10 | 엘지이노텍 주식회사 | 태양전지 및 이의 제조방법 |
| JP5418172B2 (ja) * | 2009-11-24 | 2014-02-19 | コニカミノルタ株式会社 | 光電変換素子及び太陽電池 |
| TWI394309B (zh) * | 2009-12-30 | 2013-04-21 | Ind Tech Res Inst | 染料敏化太陽能電池 |
| JP2014508822A (ja) * | 2011-01-14 | 2014-04-10 | ソルヴェイ（ソシエテ アノニム） | フタロシアニン色素、その製造方法、および、色素増感型太陽電池におけるその使用 |
| EP2678346B9 (en) | 2011-02-25 | 2018-08-08 | Ecole Polytechnique Fédérale de Lausanne (EPFL) | Metal complexes for use as dopants and other uses |
| EP2551949A1 (en) | 2011-07-28 | 2013-01-30 | Ecole Polytechnique Fédérale de Lausanne (EPFL) | Metal complexes for use as dopants and other uses |
| US10038150B2 (en) | 2011-02-25 | 2018-07-31 | Ecole Polytechnique Federale De Lausanne (Epfl) | Metal complexes for use as dopants and other uses |
| US9181475B2 (en) | 2012-02-21 | 2015-11-10 | Northwestern University | Photoluminescent compounds |
| CN104781368B (zh) | 2012-10-12 | 2018-05-01 | 默克专利有限公司 | 具有芳族单元的发光体和主体 |
| KR20160004389A (ko) | 2013-05-06 | 2016-01-12 | 그레이트셀 솔라 에스.에이. | 유기-무기 페로브스카이트 기반 태양 전지 |
| MX2015015395A (es) | 2013-05-06 | 2016-08-04 | Abengoa Res Sl | Celulas solares mesoscopicas sensibilizadas con perovskita de alto rendimiento. |
| EP2804232A1 (en) | 2013-05-16 | 2014-11-19 | Abengoa Research S.L. | High performance perovskite-sensitized mesoscopic solar cells |
| EP2822009A1 (en) | 2013-07-01 | 2015-01-07 | Ecole Polytechnique Fédérale de Lausanne (EPFL) | Solar cell and process for producing the same |
| KR101551074B1 (ko) * | 2014-03-31 | 2015-09-07 | 현대자동차주식회사 | 피리딘계 첨가제가 함유된 장기안정성 고체상 염료감응 태양전지 |
| WO2015159192A1 (en) * | 2014-04-15 | 2015-10-22 | Basf Se | Process for the production of a solid dye-sensitized solar cell or a perovskite solar cell |
| WO2015164731A1 (en) | 2014-04-24 | 2015-10-29 | Northwestern University | Solar cells with perovskite-based light sensitization layers |
| BR112017028382B1 (pt) * | 2015-07-30 | 2022-08-16 | Sekisui Chemical Co., Ltd | Célula solar e material semicondutor orgânico |
| EP3223323A1 (en) | 2016-03-24 | 2017-09-27 | Ecole Polytechnique Fédérale de Lausanne (EPFL) | High efficiency large area perovskite solar cells and process for producing the same |
| KR102464556B1 (ko) | 2016-03-18 | 2022-11-07 | 에꼴 뽈리떼끄닉 뻬데랄 드 로잔느 (으뻬에프엘) | 고효율 대면적 페로브스카이트 태양광 전지 및 이를 제조하기 위한 공정 |
| CN106518691B (zh) * | 2016-10-28 | 2018-06-26 | 南京工业大学 | 钙钛矿太阳能电池中一类修饰材料-三苯胺衍生物的合成及其应用 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5554450A (en) * | 1995-03-08 | 1996-09-10 | Eastman Kodak Company | Organic electroluminescent devices with high thermal stability |
| WO2000005628A1 (en) * | 1998-07-21 | 2000-02-03 | Lexmark International, Inc. | Photoconductor with charge generation binder blend |
| KR20000011696A (ko) * | 1998-07-16 | 2000-02-25 | 구라우치 노리타카 | 트리페닐아민유도체와그것을이용한유기일렉트로루미네선스소자 |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4288379A (en) * | 1977-05-31 | 1981-09-08 | The Dow Chemical Company | Hydrocarbon polyl gem-bis(t-alkylperoxy)alkanoates derived from β-keto-acids |
| US4710520A (en) * | 1986-05-02 | 1987-12-01 | Max Klein | Mica-polymer micro-bits composition and process |
| JPH01219838A (ja) * | 1988-02-29 | 1989-09-01 | Fujitsu Ltd | 電子写真感光体 |
| JP3419534B2 (ja) * | 1993-02-10 | 2003-06-23 | 靖彦 城田 | トリスアリールアミノベンゼン誘導体、有機ｅｌ素子用化合物および有機ｅｌ素子 |
| EP0611148B1 (en) * | 1993-02-10 | 1998-06-03 | Yasuhiko Shirota | Trisarylaminobenzene derivatives, compounds for organic EL element, and organic EL element |
| ES2244958T3 (es) * | 1994-12-21 | 2005-12-16 | Hydro Quebec | Sales hidrofobicas liquidas, su prepracion y su aplicacion en electroquimica. |
| DE19533850A1 (de) * | 1995-09-13 | 1997-03-27 | Hoechst Ag | Photovoltaische Zelle |
| DE19711713A1 (de) * | 1997-03-20 | 1998-10-01 | Hoechst Ag | Photovoltaische Zelle |
| JPH11144773A (ja) * | 1997-09-05 | 1999-05-28 | Fuji Photo Film Co Ltd | 光電変換素子および光再生型光電気化学電池 |
| JP3817045B2 (ja) * | 1997-09-12 | 2006-08-30 | 四国化成工業株式会社 | 溶融塩型高分子電解質 |
| DE60029151T2 (de) * | 1999-03-01 | 2007-05-31 | Fuji Photo Film Co., Ltd., Minami-Ashigara | Photoelektrochemische Zelle mit einem Elektrolyten aus Flüssigkristallverbindungen |
| US6291763B1 (en) * | 1999-04-06 | 2001-09-18 | Fuji Photo Film Co., Ltd. | Photoelectric conversion device and photo cell |
| DE60027512T2 (de) * | 1999-08-04 | 2006-10-12 | Fuji Photo Film Co., Ltd., Minami-Ashigara | Elektrolytzusammensetzung und photolektrochemische Zelle |
| JP2001085076A (ja) * | 1999-09-10 | 2001-03-30 | Fuji Photo Film Co Ltd | 光電変換素子および光電池 |
| EP1160888A1 (en) * | 2000-05-29 | 2001-12-05 | Sony International (Europe) GmbH | Hole transporting agents and photoelectric conversion device comprising the same |
-
2000
- 2000-05-29 EP EP00111493A patent/EP1160888A1/en not_active Withdrawn
-
2001
- 2001-05-25 US US09/866,199 patent/US6700058B2/en not_active Expired - Fee Related
- 2001-05-29 CN CNB011219009A patent/CN1199296C/zh not_active Expired - Fee Related
- 2001-05-29 JP JP2001161515A patent/JP4804650B2/ja not_active Expired - Fee Related
- 2001-05-29 KR KR1020010029726A patent/KR20010110117A/ko not_active Application Discontinuation
-
2003
- 2003-12-03 US US10/726,476 patent/US7132598B2/en not_active Expired - Fee Related
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5554450A (en) * | 1995-03-08 | 1996-09-10 | Eastman Kodak Company | Organic electroluminescent devices with high thermal stability |
| KR20000011696A (ko) * | 1998-07-16 | 2000-02-25 | 구라우치 노리타카 | 트리페닐아민유도체와그것을이용한유기일렉트로루미네선스소자 |
| WO2000005628A1 (en) * | 1998-07-21 | 2000-02-03 | Lexmark International, Inc. | Photoconductor with charge generation binder blend |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8753916B2 (en) | 2001-10-24 | 2014-06-17 | The Regents Of The University Of California | Semiconductor-nanocrystal/conjugated polymer thin films |
Also Published As
| Publication number | Publication date |
|---|---|
| JP4804650B2 (ja) | 2011-11-02 |
| CN1326231A (zh) | 2001-12-12 |
| US20040177879A1 (en) | 2004-09-16 |
| US20020036298A1 (en) | 2002-03-28 |
| CN1199296C (zh) | 2005-04-27 |
| US7132598B2 (en) | 2006-11-07 |
| EP1160888A1 (en) | 2001-12-05 |
| JP2002037763A (ja) | 2002-02-06 |
| US6700058B2 (en) | 2004-03-02 |
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