EP2715823A1 - Composition d'une cellule photovoltaïque organique d'un module photovoltaïque - Google Patents
Composition d'une cellule photovoltaïque organique d'un module photovoltaïqueInfo
- Publication number
- EP2715823A1 EP2715823A1 EP12728705.0A EP12728705A EP2715823A1 EP 2715823 A1 EP2715823 A1 EP 2715823A1 EP 12728705 A EP12728705 A EP 12728705A EP 2715823 A1 EP2715823 A1 EP 2715823A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- poly
- blocks
- copolymer
- active layer
- composition according
- 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.)
- Withdrawn
Links
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Classifications
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- 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
- H10K85/10—Organic polymers or oligomers
- H10K85/151—Copolymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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Abstract
Description
Claims
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR1154654A FR2975831B1 (fr) | 2011-05-27 | 2011-05-27 | Composition d'une cellule photovoltaique organique d'un module photovoltaique |
FR1160510A FR2975832B1 (fr) | 2011-05-27 | 2011-11-18 | Composition d'une cellule photovoltaique organique d'un module photovoltaique |
PCT/FR2012/051102 WO2012164194A1 (fr) | 2011-05-27 | 2012-05-16 | Composition d'une cellule photovoltaïque organique d'un module photovoltaïque |
Publications (1)
Publication Number | Publication Date |
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EP2715823A1 true EP2715823A1 (fr) | 2014-04-09 |
Family
ID=45855909
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP12728705.0A Withdrawn EP2715823A1 (fr) | 2011-05-27 | 2012-05-16 | Composition d'une cellule photovoltaïque organique d'un module photovoltaïque |
Country Status (8)
Country | Link |
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US (1) | US20140130850A1 (fr) |
EP (1) | EP2715823A1 (fr) |
JP (1) | JP6082925B2 (fr) |
KR (1) | KR20140033461A (fr) |
CN (1) | CN103733367B (fr) |
FR (2) | FR2975831B1 (fr) |
SG (1) | SG195167A1 (fr) |
WO (1) | WO2012164194A1 (fr) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102006047045A1 (de) * | 2006-10-02 | 2008-04-03 | Universität Paderborn | Photovoltaische Einrichtung |
CN106129248B (zh) * | 2016-06-23 | 2018-06-05 | 南昌航空大学 | 一种水/醇溶性嵌段共轭聚合物作为阴极缓冲层的有机光伏电池制作方法 |
GB2577561A (en) * | 2018-09-28 | 2020-04-01 | Sumitomo Chemical Co | Method of manufacturing an organic photodetector |
CN117024874B (zh) * | 2023-08-04 | 2024-03-15 | 链行走新材料科技(广州)有限公司 | 一种p3ht复合官能材料及其应用 |
Family Cites Families (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7758890B2 (en) * | 2001-06-23 | 2010-07-20 | Lyotropic Therapeutics, Inc. | Treatment using dantrolene |
WO2003075364A1 (fr) * | 2002-03-07 | 2003-09-12 | Nippon Oil Corporation | Dispositif de conversion photoelectrique |
CN1711647A (zh) | 2002-11-14 | 2005-12-21 | 孙沙京 | 基于新型嵌段共聚物的光伏打装置 |
JP4133452B2 (ja) * | 2003-03-03 | 2008-08-13 | 出光ユニテック株式会社 | 多層構造体及び包装体 |
JP2006073900A (ja) * | 2004-09-03 | 2006-03-16 | Nippon Oil Corp | 光電変換素子 |
US20080319131A1 (en) * | 2005-08-26 | 2008-12-25 | Mccullough Richard D | Electrically Conductive Polymers and Raft Polymerization |
JP4673266B2 (ja) * | 2006-08-03 | 2011-04-20 | 日本電信電話株式会社 | パターン形成方法及びモールド |
US7985919B1 (en) * | 2006-08-18 | 2011-07-26 | Nanosolar, Inc. | Thermal management for photovoltaic devices |
US8715606B2 (en) * | 2007-12-21 | 2014-05-06 | Plextronics, Inc. | Organic photovoltaic devices comprising fullerenes and derivatives thereof and improved methods of making fullerene derivatives |
US20090229667A1 (en) | 2008-03-14 | 2009-09-17 | Solarmer Energy, Inc. | Translucent solar cell |
JP2009267092A (ja) * | 2008-04-25 | 2009-11-12 | Toray Ind Inc | 光起電力素子用材料および光起電力素子 |
US8211996B2 (en) * | 2008-12-01 | 2012-07-03 | The Regents Of The University Of California | Well-defined donor-acceptor rod-coil diblock copolymer based on P3HT containing C60 |
WO2010135701A1 (fr) * | 2009-05-21 | 2010-11-25 | Polyera Corporation | Polymères conjugués et leur utilisation dans des dispositifs opto-électroniques |
JP5601039B2 (ja) * | 2009-06-08 | 2014-10-08 | 三菱化学株式会社 | チアジアゾール含有高分子 |
GB0912041D0 (en) * | 2009-07-10 | 2009-08-19 | Cambridge Entpr Ltd | Optoelectronic devices |
US8059350B2 (en) * | 2009-10-22 | 2011-11-15 | Hitachi Global Storage Technologies Netherlands B.V. | Patterned magnetic recording disk with patterned servo sectors having chevron servo patterns |
KR101114955B1 (ko) * | 2009-10-28 | 2012-03-06 | 한국과학기술연구원 | 폴리(3-헥실티오펜) 기반 블록공중합체의 자기조립 구조 제어방법 |
CN101698572B (zh) * | 2009-10-29 | 2012-12-12 | 中国科学院长春应用化学研究所 | 一种高聚物梯度孔隙率宽波抗反射膜的制备方法 |
CN101831056B (zh) * | 2010-05-17 | 2012-05-23 | 中国科学院宁波材料技术与工程研究所 | 一种高光转化率的含氟聚噻吩光电材料及其制备方法 |
-
2011
- 2011-05-27 FR FR1154654A patent/FR2975831B1/fr not_active Expired - Fee Related
- 2011-11-18 FR FR1160510A patent/FR2975832B1/fr not_active Expired - Fee Related
-
2012
- 2012-05-16 KR KR1020137034628A patent/KR20140033461A/ko not_active Application Discontinuation
- 2012-05-16 EP EP12728705.0A patent/EP2715823A1/fr not_active Withdrawn
- 2012-05-16 WO PCT/FR2012/051102 patent/WO2012164194A1/fr active Application Filing
- 2012-05-16 SG SG2013087457A patent/SG195167A1/en unknown
- 2012-05-16 CN CN201280025540.4A patent/CN103733367B/zh not_active Expired - Fee Related
- 2012-05-16 JP JP2014511934A patent/JP6082925B2/ja not_active Expired - Fee Related
- 2012-05-16 US US14/122,566 patent/US20140130850A1/en not_active Abandoned
Non-Patent Citations (2)
Title |
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None * |
See also references of WO2012164194A1 * |
Also Published As
Publication number | Publication date |
---|---|
WO2012164194A1 (fr) | 2012-12-06 |
CN103733367A (zh) | 2014-04-16 |
JP2014519202A (ja) | 2014-08-07 |
KR20140033461A (ko) | 2014-03-18 |
JP6082925B2 (ja) | 2017-02-22 |
FR2975831B1 (fr) | 2013-11-22 |
CN103733367B (zh) | 2017-11-07 |
US20140130850A1 (en) | 2014-05-15 |
FR2975831A1 (fr) | 2012-11-30 |
FR2975832A1 (fr) | 2012-11-30 |
FR2975832B1 (fr) | 2015-09-25 |
SG195167A1 (en) | 2013-12-30 |
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