ATE409948T1 - 2,2 -bipyridin ligand, sensibilisierungsfarbstoff und farbstoffsensibilisierte solarzelle - Google Patents

2,2 -bipyridin ligand, sensibilisierungsfarbstoff und farbstoffsensibilisierte solarzelle

Info

Publication number
ATE409948T1
ATE409948T1 AT05762935T AT05762935T ATE409948T1 AT E409948 T1 ATE409948 T1 AT E409948T1 AT 05762935 T AT05762935 T AT 05762935T AT 05762935 T AT05762935 T AT 05762935T AT E409948 T1 ATE409948 T1 AT E409948T1
Authority
AT
Austria
Prior art keywords
dye
solar cell
sensitized solar
ligand
anchoring
Prior art date
Application number
AT05762935T
Other languages
German (de)
English (en)
Inventor
Shaik Zakeeruddin
Cedric Klein
Peng Wang
Michael Graetzel
Original Assignee
Ecole Polytech
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 Ecole Polytech filed Critical Ecole Polytech
Application granted granted Critical
Publication of ATE409948T1 publication Critical patent/ATE409948T1/de

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/28—Radicals substituted by singly-bound oxygen or sulphur atoms
    • C07D213/30—Oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
    • C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
    • C07F15/0046—Ruthenium compounds
    • C07F15/0053—Ruthenium compounds without a metal-carbon linkage
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B82—NANOTECHNOLOGY
    • B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y10/00—Nanotechnology for information processing, storage or transmission, e.g. quantum computing or single electron logic
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B82—NANOTECHNOLOGY
    • B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B57/00—Other synthetic dyes of known constitution
    • C09B57/10—Metal complexes of organic compounds not being dyes in uncomplexed form
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K3/00—Materials not provided for elsewhere
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
    • H01G9/20—Light-sensitive devices
    • H01G9/2027—Light-sensitive devices comprising an oxide semiconductor electrode
    • H01G9/2031—Light-sensitive devices comprising an oxide semiconductor electrode comprising titanium oxide, e.g. TiO2
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
    • H01G9/20—Light-sensitive devices
    • H01G9/2059—Light-sensitive devices comprising an organic dye as the active light absorbing material, e.g. adsorbed on an electrode or dissolved in solution
    • 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
    • H10F10/00—Individual photovoltaic cells, e.g. solar cells
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • 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
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
    • H01G9/20—Light-sensitive devices
    • H01G9/2004—Light-sensitive devices characterised by the electrolyte, e.g. comprising an organic electrolyte
    • H01G9/2013—Light-sensitive devices characterised by the electrolyte, e.g. comprising an organic electrolyte the electrolyte comprising ionic liquids, e.g. alkyl imidazolium iodide
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • 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
    • 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
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Power Engineering (AREA)
  • Nanotechnology (AREA)
  • Materials Engineering (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Physics & Mathematics (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • General Physics & Mathematics (AREA)
  • Composite Materials (AREA)
  • Theoretical Computer Science (AREA)
  • Mathematical Physics (AREA)
  • Inorganic Chemistry (AREA)
  • Hybrid Cells (AREA)
  • Photovoltaic Devices (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyridine Compounds (AREA)
AT05762935T 2004-07-29 2005-07-29 2,2 -bipyridin ligand, sensibilisierungsfarbstoff und farbstoffsensibilisierte solarzelle ATE409948T1 (de)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP04405484A EP1622178A1 (en) 2004-07-29 2004-07-29 2,2 -Bipyridine ligand, sensitizing dye and dye sensitized solar cell

Publications (1)

Publication Number Publication Date
ATE409948T1 true ATE409948T1 (de) 2008-10-15

Family

ID=34932222

Family Applications (1)

Application Number Title Priority Date Filing Date
AT05762935T ATE409948T1 (de) 2004-07-29 2005-07-29 2,2 -bipyridin ligand, sensibilisierungsfarbstoff und farbstoffsensibilisierte solarzelle

Country Status (9)

Country Link
US (2) US7932404B2 (enExample)
EP (2) EP1622178A1 (enExample)
JP (1) JP5065021B2 (enExample)
KR (1) KR101125391B1 (enExample)
CN (1) CN101023502B (enExample)
AT (1) ATE409948T1 (enExample)
AU (1) AU2005266755B2 (enExample)
DE (1) DE602005010087D1 (enExample)
WO (1) WO2006010290A1 (enExample)

Families Citing this family (82)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1730757B1 (en) * 2004-03-31 2016-11-09 The Yokohama Rubber Co., Ltd. Electrolyte for photovoltaic device as well as photovoltaic device and dye-sensitized solar cell including that electrolyte
JP4507834B2 (ja) * 2004-11-04 2010-07-21 ソニー株式会社 色素増感光電変換素子およびその製造方法
US8124777B2 (en) 2005-09-22 2012-02-28 Sumitomo Chemical Company, Limited Compound, photoelectric converter and photoelectrochemical cell
TW200728409A (en) * 2005-10-19 2007-08-01 Jsr Corp A pigment and pigment-sensitized solar battery
WO2007091525A1 (ja) 2006-02-08 2007-08-16 Shimane Prefectural Government 光増感色素
JP5087857B2 (ja) * 2006-04-07 2012-12-05 宇部興産株式会社 ターピリジル配位子を含む金属錯体原料およびその製造方法
JP2008021496A (ja) * 2006-07-12 2008-01-31 Nippon Kayaku Co Ltd 色素増感光電変換素子
ATE437206T1 (de) * 2006-08-07 2009-08-15 Preentec Ag Nanopartikel eines authentifizierungssystems
JP2008053631A (ja) * 2006-08-28 2008-03-06 Toyota Motor Corp 電気化学活性を有する有機薄膜、その製造方法、およびそれを用いた素子
US20100101650A1 (en) * 2006-12-18 2010-04-29 Sumitomo Chemical Company ,Limited Compound, photoelectric conversion device and photoelectrochemical battery
KR101472308B1 (ko) * 2007-02-21 2014-12-15 주식회사 동진쎄미켐 신규한 루테늄계 염료 및 이의 제조방법
US20100101643A1 (en) * 2007-03-29 2010-04-29 Sumitomo Chemical Company, Limited Compound, photoelectric converter and photoelectrochemical cell
JP2008266634A (ja) * 2007-03-29 2008-11-06 Sumitomo Chemical Co Ltd 化合物、光電変換素子及び光電気化学電池
KR100932901B1 (ko) * 2007-08-21 2009-12-22 한국전자통신연구원 염료감응 태양전지 및 그 제조 방법
EP2036955B1 (en) 2007-09-17 2012-05-16 JSR Corporation Dyestuff, dye-sensitized solar cell, and method for manufacturing same
JP2009080988A (ja) * 2007-09-25 2009-04-16 Panasonic Electric Works Co Ltd 光電変換素子
GB0720553D0 (en) * 2007-10-19 2007-11-28 Isis Innovation Branched materials for photovoltaic devices
CN101215298B (zh) * 2007-12-29 2011-08-17 清华大学 钌多吡啶配合物及其衍生物的合成方法
US20090229652A1 (en) * 2008-01-14 2009-09-17 Mapel Jonathan K Hybrid solar concentrator
TWI370120B (en) * 2008-01-31 2012-08-11 Everlight Chem Ind Corp Ruthenium complex
EP2276103A4 (en) * 2008-05-02 2013-04-17 Peccell Technologies Inc Dye-sensitized photoelectric conversion element
CN101723983B (zh) * 2008-10-21 2012-08-08 明德国际仓储贸易(上海)有限公司 钌金属络合物及用此络合物制作的光电组件
EP2230702A1 (en) 2009-03-19 2010-09-22 Ecole Polytechnique Fédérale de Lausanne (EPFL) Modified surface
CN101538416B (zh) * 2009-04-03 2013-09-18 新奥科技发展有限公司 金属有机染料、染料敏化电极、太阳能电池和反应器
KR101054250B1 (ko) * 2009-04-20 2011-08-08 포항공과대학교 산학협력단 극소수성 화합물이 도입된 금속산화물 반도체 전극. 이를 포함하는 염료감응 태양전지 및 그 제조 방법
CN101570645B (zh) * 2009-06-05 2012-09-19 中国科学院长春应用化学研究所 含双氮芴配体的钌染料及用其制备的染料敏化太阳能电池
EP2301932A1 (en) 2009-09-29 2011-03-30 Ecole Polytechnique Fédérale de Lausanne (EPFL) Novel ligands for sensitizing dyes of dye-sensitized solar cells
KR101027714B1 (ko) * 2009-09-29 2011-04-12 한국에너지기술연구원 염료 및 리간드가 흡착된 나노 산화물층을 포함한 음극계 전극을 포함하는 염료감응/리간드금속전하전이 하이브리드 태양전지 및 이의 제조방법
AU2010309019A1 (en) * 2009-10-20 2012-05-31 Ube Industries, Ltd. Photoelectric conversion device wherein dye consisting of binuclear ruthenium complex having substituted bipyridyl groups is used, and photochemical cell
CN101735641B (zh) * 2009-11-12 2012-12-12 中国科学院长春应用化学研究所 有机染料及其应用
CN102115481B (zh) * 2009-12-31 2014-07-02 国立成功大学 氧化铁/载体催化剂的制备方法
JP2011204662A (ja) * 2010-03-05 2011-10-13 Sony Corp 光電変換素子およびその製造方法ならびに電子機器
WO2011125024A1 (en) 2010-04-05 2011-10-13 Ecole Polytechnique Federale De Lausanne (Epfl) Improved electrode
US8535574B2 (en) * 2010-04-15 2013-09-17 National Taipei University Of Technology Transition metal complexes, manufacturing method thereof, photovoltaic cells and manufacturing method thereof
AU2011273006B2 (en) * 2010-06-29 2016-05-26 Basf Se Photoelectric conversion device comprising hydroxamic acid derivative or salt thereof as additive and process for producing same
KR101297258B1 (ko) * 2010-07-09 2013-08-16 삼성에스디아이 주식회사 염료 감응 태양 전지용 염료, 그 제조 방법 및 이를 채용한 태양 전지
DE102010033026B4 (de) * 2010-07-29 2014-10-09 Mainrad Martus Verfahren zum Aufbau einer als Tandemzelle weitergebildeten organischen Kunststoffsolarzelle
WO2012037269A1 (en) 2010-09-16 2012-03-22 Nitto Denko Corporation Substituted bipyridines for use in organic light-emitting devices
DE102010046412B4 (de) 2010-09-23 2022-01-13 Merck Patent Gmbh Metall-Ligand Koordinationsverbindungen
JP5894372B2 (ja) * 2010-11-01 2016-03-30 パナソニック株式会社 光電気素子、及び光電気素子の製造方法
DE102010054525A1 (de) 2010-12-15 2012-04-26 Merck Patent Gmbh Organische Elektrolumineszenzvorrichtung
DE102010055902A1 (de) 2010-12-23 2012-06-28 Merck Patent Gmbh Organische Elektrolumineszenzvorrichtung
US10038150B2 (en) 2011-02-25 2018-07-31 Ecole Polytechnique Federale De Lausanne (Epfl) Metal complexes for use as dopants and other uses
EP2511924A1 (en) 2011-04-11 2012-10-17 Ecole Polytechnique Fédérale de Lausanne (EPFL) Transition metal complexes as redox couples for electrochemical and optoelectronic devices
WO2012114316A1 (en) 2011-02-25 2012-08-30 Ecole Polytechnique Federale De Lausanne (Epfl) Metal complexes for use as dopants and other uses
EP2492277A1 (en) 2011-02-25 2012-08-29 Ecole Polytechnique Fédérale de Lausanne (EPFL) Improved redox couple for electrochemical and optoelectronic devices
US9779879B2 (en) 2011-02-25 2017-10-03 Ecole Polytechnique Federale De Lausanne (Epfl) Redox couple for electrochemical and optoelectronic devices
EP2551949A1 (en) 2011-07-28 2013-01-30 Ecole Polytechnique Fédérale de Lausanne (EPFL) Metal complexes for use as dopants and other uses
US8585926B2 (en) * 2011-03-03 2013-11-19 Nitto Denko Corporation Substituted bipyridines for use in light-emitting devices
US9923152B2 (en) 2011-03-24 2018-03-20 Merck Patent Gmbh Organic ionic functional materials
US9496502B2 (en) 2011-05-12 2016-11-15 Merck Patent Gmbh Organic ionic compounds, compositions and electronic devices
JP2013026082A (ja) * 2011-07-22 2013-02-04 Sony Corp 光電変換装置、電子機器および建築物
DE102012016192A1 (de) 2011-08-19 2013-02-21 Merck Patent Gmbh Neue Materialien für organische Elektrolumineszenzvorrichtungen
US9328094B2 (en) 2011-09-19 2016-05-03 Nitto Denko Corporation Substituted biaryl compounds for light-emitting devices
WO2013049019A1 (en) 2011-09-26 2013-04-04 North Carolina State University Antenna ligands for dye-sensitized solar cells
JP6224600B2 (ja) 2011-10-18 2017-11-01 エコール ポリテクニーク フェデラル ドゥ ローザンヌ（エーペーエフエル） 電気化学および／または光電子デバイス用化合物
WO2013085285A1 (ko) * 2011-12-05 2013-06-13 고려대학교 산학협력단 정공전도특성을 갖는 염료감응 태양전지용 공흡착체 및 그를 포함하는 염료감응 태양전지
CN104106118B (zh) 2011-12-08 2018-06-22 洛桑联邦理工学院 包括阻挡层的半导体电极
JP5809954B2 (ja) * 2011-12-15 2015-11-11 富士フイルム株式会社 光電変換素子及び色素増感太陽電池
JP5840040B2 (ja) * 2012-03-15 2016-01-06 大阪瓦斯株式会社 光電変換素子用光電極及びその製造方法
WO2014026285A1 (en) * 2012-08-15 2014-02-20 Curtis Berlinguette System for sensitization of metal oxides by dyes stabilized by distinctive anchoring groups
CN102851036A (zh) * 2012-10-09 2013-01-02 深圳市华星光电技术有限公司 液晶介质组合物及使用其制作的液晶显示面板
US8801965B2 (en) 2012-10-09 2014-08-12 Shenzen China Star Optoelectronic Technology co., Ltd. Liquid crystal medium composition and liquid crystal display panel manufactured with same
KR102105810B1 (ko) 2012-11-20 2020-04-29 메르크 파텐트 게엠베하 전자 장치 제조용 고순도 용매 중의 제형
KR101320394B1 (ko) * 2013-01-18 2013-10-23 삼성에스디아이 주식회사 염료 감응 태양 전지용 염료, 그 제조 방법 및 이를 채용한 태양 전지
CN103205135B (zh) * 2013-04-25 2015-10-28 大连理工大学 光敏染料锇配合物及其制备方法、癌变早期dna氧化损伤快速检测试剂盒及检测方法
EP2822009A1 (en) 2013-07-01 2015-01-07 Ecole Polytechnique Fédérale de Lausanne (EPFL) Solar cell and process for producing the same
EP2846371A1 (en) 2013-09-10 2015-03-11 Ecole Polytechnique Fédérale de Lausanne (EPFL) Inverted solar cell and process for producing the same
EP2896660A1 (en) 2014-01-16 2015-07-22 Ecole Polytechnique Federale De Lausanne (Epfl) Hole transporting and light absorbing material for solid state solar cells
EP2903047A1 (en) 2014-01-31 2015-08-05 Ecole Polytechnique Fédérale de Lausanne (EPFL) Hole transporting and light absorbing material for solid state solar cells
US10141118B2 (en) 2014-02-06 2018-11-27 Adeka Corporation Carrier system and photoelectric conversion device
EP2966703A1 (en) 2014-07-11 2016-01-13 Ecole Polytechnique Fédérale de Lausanne (EPFL) Template enhanced organic inorganic perovskite heterojunction photovoltaic device
US20170301479A1 (en) 2014-09-10 2017-10-19 Ecole Polytechnique Federale De Lausanne (Epfl) Photodetector
EP3065190A1 (en) 2015-03-02 2016-09-07 Ecole Polytechnique Fédérale de Lausanne (EPFL) Small molecule hole transporting material for optoelectronic and photoelectrochemical devices
LT6540B (lt) 2016-09-19 2018-06-25 Kauno technologijos universitetas Skyles transportuojančios organinės molekulės, turinčios enamino grupių, skirtos optoelektroniniams bei fotoelektroniniams prietaisams
WO2018081120A1 (en) * 2016-10-24 2018-05-03 University Of Massachusetts All-day solar cell system integrating high capacity photochromic storage and discharge
EP3407361A1 (en) 2017-05-24 2018-11-28 Ecole Polytechnique Fédérale de Lausanne (EPFL) Redox melts formed by copper (i)/(ii) complexes as charge transfer and charge storage materials
EP3489240A1 (en) 2017-11-28 2019-05-29 Ecole Polytechnique Fédérale de Lausanne (EPFL) In-situ cross-linkable hole transporting triazatruxene monomers for optoelectronic devicestr
CN109628042A (zh) * 2018-12-26 2019-04-16 深圳日高胶带新材料有限公司 一种光交联胶黏剂
EP3828948A1 (en) * 2019-11-26 2021-06-02 Exeger Operations AB A working electrode for a photovoltaic device, and a photovoltaic device including the working electrode
CN113512068B (zh) * 2021-04-13 2022-05-31 山西大学 一种双配体的亚硝酰钌配合物及其制备方法和应用
WO2023158782A1 (en) * 2022-02-18 2023-08-24 The Board Of Regents Of The Nevada System Of Higher Education On Behalf Of The University Of Nevada, Las Vegas Dicationic ionic liquid electrolytes with high ionic conductivity

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4545028A (en) * 1982-10-13 1985-10-01 Hewlett-Packard Company Partial product accumulation in high performance multipliers
DE3677527D1 (de) * 1985-11-20 1991-03-21 Mead Corp Ionische farbstoffe als initiatoren enthaltende fotosensitive materialien.
CH674596A5 (enExample) 1988-02-12 1990-06-15 Sulzer Ag
US5216134A (en) * 1989-10-23 1993-06-01 Wallac Oy Spectrofluorometric method and compounds that are of value for the method
ATE131953T1 (de) * 1990-04-17 1996-01-15 Ecole Polytech Photovoltaische zellen
JPH0733410B2 (ja) * 1990-08-03 1995-04-12 東洋シール工業株式会社 架橋可能なアクリルゴムの製造方法
GB9217811D0 (en) 1992-08-21 1992-10-07 Graetzel Michael Organic compounds
US5728487A (en) 1993-12-29 1998-03-17 Ecole Polytechnique Federale De Lausanne Photoelectrochemical cell and electrolyte for this cell
DE69415350T2 (de) 1994-05-02 1999-07-01 Ecole Polytechnique Federale De Lausanne (Epfl), Lausanne Phosphonierte polypyridyl-verbindungen und ihre metall-komplexe
DE69810421T2 (de) * 1997-10-23 2003-10-02 Fuji Photo Film Co., Ltd. Photoelektrische Umwandlungsanordnung und photoelektrochemische Zelle
DE60040372D1 (de) 1999-09-24 2008-11-13 Toshiba Kawasaki Kk Elektrolyt-Zusammensetzung, Sonnenzelle, die solche Elektrolyt-Zusammensetzung anwendet, und Herstellungsverfahren der Sonnenzelle
JP4874454B2 (ja) * 2000-01-31 2012-02-15 富士フイルム株式会社 光電変換素子および光電池
ATE556845T1 (de) * 2001-07-20 2012-05-15 Life Technologies Corp Lumineszierende nanopartikel und ihre herstellung
MXPA04000695A (es) * 2001-07-23 2005-08-26 Galileo Pharmaceuticals Inc Compuestos citoprotectores, formulaciones farmaceuticas y cosmeticas y metodos.
FR2838241B1 (fr) * 2002-04-09 2004-06-25 Commissariat Energie Atomique Materiaux luminescents constitues de nanocristaux a structure coeur/coquille et leur procede de preparation
CA2497451A1 (en) * 2002-09-05 2004-03-18 Nanosys, Inc. Organic species that facilitate charge transfer to or from nanostructures
JP4377148B2 (ja) * 2003-03-26 2009-12-02 三井化学株式会社 光電変換素子用材料および光電変換素子
JP4409261B2 (ja) * 2003-11-26 2010-02-03 株式会社豊田中央研究所 金属錯体色素、光電極及び色素増感型太陽電池

Also Published As

Publication number Publication date
US8440843B2 (en) 2013-05-14
WO2006010290A1 (en) 2006-02-02
EP1774550A1 (en) 2007-04-18
KR101125391B1 (ko) 2012-04-02
KR20070085221A (ko) 2007-08-27
US20090000658A1 (en) 2009-01-01
EP1622178A1 (en) 2006-02-01
CN101023502B (zh) 2010-07-28
JP5065021B2 (ja) 2012-10-31
EP1774550B1 (en) 2008-10-01
US20110190501A1 (en) 2011-08-04
DE602005010087D1 (de) 2008-11-13
CN101023502A (zh) 2007-08-22
EP1774550B9 (en) 2009-04-01
AU2005266755B2 (en) 2011-12-08
WO2006010290A8 (en) 2007-03-08
AU2005266755A1 (en) 2006-02-02
US7932404B2 (en) 2011-04-26
JP2008507570A (ja) 2008-03-13

Similar Documents

Publication Publication Date Title
ATE409948T1 (de) 2,2 -bipyridin ligand, sensibilisierungsfarbstoff und farbstoffsensibilisierte solarzelle
ATE438192T1 (de) Farbstoffsensibilisierte solarzelle
Cao et al. Dye-sensitized solar cells with a high absorptivity ruthenium sensitizer featuring a 2-(hexylthio) thiophene conjugated bipyridine
Chen Emerging organic and organic/inorganic hybrid photovoltaic devices for specialty applications: low‐level‐lighting energy conversion and biomedical treatment
Jahandar et al. Indoor organic photovoltaics for self‐sustaining IoT devices: progress, challenges and practicalization
Ehrler et al. Singlet exciton fission-sensitized infrared quantum dot solar cells
Shan et al. Near‐infrared sunlight harvesting in dye‐sensitized solar cells via the insertion of an upconverter‐TiO2 nanocomposite layer
Kim et al. Organic dye design tools for efficient photocurrent generation in dye‐sensitized solar cells: exciton binding energy and electron Acceptors
ES2967341T3 (es) Arquitectura de dispositivo
Jradi et al. Near-infrared asymmetrical squaraine sensitizers for highly efficient dye sensitized solar cells: the effect of π-bridges and anchoring groups on solar cell performance
Kim et al. Molecular design principle of all‐organic dyes for dye‐sensitized solar cells
Pashaei et al. Influence of ancillary ligands in dye-sensitized solar cells
Chen et al. Nanochemistry and nanomaterials for photovoltaics
Ning et al. All‐inorganic colloidal quantum dot photovoltaics employing solution‐phase halide passivation
ES2549604T3 (es) Dispositivo de heterounión p-n de estado sólido
Yella et al. Porphyrin-sensitized solar cells with cobalt (II/III)–based redox electrolyte exceed 12 percent efficiency
Nguyen et al. Molecular engineering of organic dyes for improved recombination lifetime in solid-state dye-sensitized solar cells
Gao et al. Conjugation of selenophene with bipyridine for a high molar extinction coefficient sensitizer in dye-sensitized solar cells
Jiang et al. Molecular engineering of quinoxaline-based D–A− π–A organic sensitizers: taking the merits of a large and rigid auxiliary acceptor
Batmunkh et al. Plasmonic Gold Nanostars Incorporated into High‐Efficiency Perovskite Solar Cells
Shen et al. Synthesis and photovoltaic properties of powerful electron-donating indeno [1, 2-b] thiophene-based green D–A− π–A sensitizers for dye-sensitized solar cells
Dos Santos et al. Designing new quinoline-based organic photosensitizers for dye-sensitized solar cells (DSSC): a theoretical investigation
Li et al. Near-IR photoresponse of ruthenium dipyrrinate terpyridine sensitizers in the dye-sensitized solar cells
Wang et al. A Perylene‐Based Polycyclic Aromatic Hydrocarbon Electron Donor for a Highly Efficient Solar Cell Dye
Buhbut et al. Quantum dot antennas for photoelectrochemical solar cells

Legal Events

Date Code Title Description
RER Ceased as to paragraph 5 lit. 3 law introducing patent treaties