JP5393154B2 - 太陽電池中での光増感剤としてのリレン誘導体の使用 - Google Patents
太陽電池中での光増感剤としてのリレン誘導体の使用 Download PDFInfo
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- JP5393154B2 JP5393154B2 JP2008539413A JP2008539413A JP5393154B2 JP 5393154 B2 JP5393154 B2 JP 5393154B2 JP 2008539413 A JP2008539413 A JP 2008539413A JP 2008539413 A JP2008539413 A JP 2008539413A JP 5393154 B2 JP5393154 B2 JP 5393154B2
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- 0 CC(N(*)C(C)=O)=O Chemical compound CC(N(*)C(C)=O)=O 0.000 description 4
- PRICFLFUMLTGEE-UHFFFAOYSA-N CC(C)c1cccc(C(C)C)c1N(C(c(cc1Oc2ccc(C(C)(C)CC(C)(C)C)cc2)c(c2cc(Oc3ccc(C(C)(C)CC(C)(C)C)cc3)c3-c(c(Oc4ccc(C(C)(C)CC(C)(C)C)cc4)c4)c5c(c(C(O6)=O)c7)c4C6=O)c3c1-c5c7Oc1ccc(C(C)(C)CC(C)(C)C)cc1)O)C2=O Chemical compound CC(C)c1cccc(C(C)C)c1N(C(c(cc1Oc2ccc(C(C)(C)CC(C)(C)C)cc2)c(c2cc(Oc3ccc(C(C)(C)CC(C)(C)C)cc3)c3-c(c(Oc4ccc(C(C)(C)CC(C)(C)C)cc4)c4)c5c(c(C(O6)=O)c7)c4C6=O)c3c1-c5c7Oc1ccc(C(C)(C)CC(C)(C)C)cc1)O)C2=O PRICFLFUMLTGEE-UHFFFAOYSA-N 0.000 description 2
- AAPOOPVCBRUVPH-UHFFFAOYSA-N CC(C)(C)CC(C)(C)c(cc1)ccc1Oc(cc1C(N(c(cc2)ccc2N(c2ccccc2)c2ccccc2)C2=O)=O)c(-c(c3c45)ccc4-c(c4c(c(C(OC6=O)=O)c7)c6c6)c7Oc7ccc(C(C)(C)CC(C)(C)C)cc7)c7c1c2cc(Oc1ccc(C(C)(C)CC(C)(C)C)cc1)c7-c3ccc5-c4c6Oc1ccc(C(C)(C)CC(C)(C)C)cc1 Chemical compound CC(C)(C)CC(C)(C)c(cc1)ccc1Oc(cc1C(N(c(cc2)ccc2N(c2ccccc2)c2ccccc2)C2=O)=O)c(-c(c3c45)ccc4-c(c4c(c(C(OC6=O)=O)c7)c6c6)c7Oc7ccc(C(C)(C)CC(C)(C)C)cc7)c7c1c2cc(Oc1ccc(C(C)(C)CC(C)(C)C)cc1)c7-c3ccc5-c4c6Oc1ccc(C(C)(C)CC(C)(C)C)cc1 AAPOOPVCBRUVPH-UHFFFAOYSA-N 0.000 description 1
- JMZUHPLNMYRFKD-UHFFFAOYSA-N CC(C)(C)CC(C)(C)c(cc1)ccc1Oc1c(-c(cccc23)c2c-2ccc3N3c4ccccc4Oc4c3cccc4)c3c-2c(Oc2ccc(C(C)(C)CC(C)(C)C)cc2)cc(C(OC2=O)=O)c3c2c1 Chemical compound CC(C)(C)CC(C)(C)c(cc1)ccc1Oc1c(-c(cccc23)c2c-2ccc3N3c4ccccc4Oc4c3cccc4)c3c-2c(Oc2ccc(C(C)(C)CC(C)(C)C)cc2)cc(C(OC2=O)=O)c3c2c1 JMZUHPLNMYRFKD-UHFFFAOYSA-N 0.000 description 1
- ZSAJRUAICXHQHI-UHFFFAOYSA-N CC(C)(C)CC(C)(C)c(cc1)ccc1Oc1cc(C(OC(c2cc(Oc3ccc(C(C)(C)CC(C)(C)C)cc3)c3-c(cc4)c56)=O)=O)c2c3c1-c5cccc6c4Oc(cc1)ccc1-[n]1cccc1 Chemical compound CC(C)(C)CC(C)(C)c(cc1)ccc1Oc1cc(C(OC(c2cc(Oc3ccc(C(C)(C)CC(C)(C)C)cc3)c3-c(cc4)c56)=O)=O)c2c3c1-c5cccc6c4Oc(cc1)ccc1-[n]1cccc1 ZSAJRUAICXHQHI-UHFFFAOYSA-N 0.000 description 1
- LBMJXDXXQAXQJN-UHFFFAOYSA-N CC(C)c1cccc(C(C)C)c1N(C(c(cc1OC2=CC=CCC2C)c(c2cc(Oc3ccccc3)c3-c(c(Oc4ccccc4)c4)c5c(c(C(O6)=O)c7)c4C6=O)c3c1-c5c7Oc1ccccc1)=O)C2=O Chemical compound CC(C)c1cccc(C(C)C)c1N(C(c(cc1OC2=CC=CCC2C)c(c2cc(Oc3ccccc3)c3-c(c(Oc4ccccc4)c4)c5c(c(C(O6)=O)c7)c4C6=O)c3c1-c5c7Oc1ccccc1)=O)C2=O LBMJXDXXQAXQJN-UHFFFAOYSA-N 0.000 description 1
- IBLCJBMYXIMKAB-UHFFFAOYSA-N CC(C)c1cccc(C(C)C)c1N(C(c1ccc-2c3c1c1ccc3-c3ccc(-c4ccc5C(N6CC(O)=O)=O)c7c3c-2ccc7-c(cc2)c4c5c2C6=O)=O)C1=O Chemical compound CC(C)c1cccc(C(C)C)c1N(C(c1ccc-2c3c1c1ccc3-c3ccc(-c4ccc5C(N6CC(O)=O)=O)c7c3c-2ccc7-c(cc2)c4c5c2C6=O)=O)C1=O IBLCJBMYXIMKAB-UHFFFAOYSA-N 0.000 description 1
- FWQSTFTUFUKPLR-UHFFFAOYSA-N CCCCCc1ccc(-c2ccc(-c(cc3)ccc3N(c(cc3)ccc3-c3ccc(-c4ccc(CCCCC)[s]4)[s]3)c(c3cccc-4c33)ccc3-c(c(Sc3ccc(C(C)(C)C)cc3)cc(C(OC3=O)=O)c5c3c3)c5c-4c3Sc3ccc(C(C)(C)C)cc3)[s]2)[s]1 Chemical compound CCCCCc1ccc(-c2ccc(-c(cc3)ccc3N(c(cc3)ccc3-c3ccc(-c4ccc(CCCCC)[s]4)[s]3)c(c3cccc-4c33)ccc3-c(c(Sc3ccc(C(C)(C)C)cc3)cc(C(OC3=O)=O)c5c3c3)c5c-4c3Sc3ccc(C(C)(C)C)cc3)[s]2)[s]1 FWQSTFTUFUKPLR-UHFFFAOYSA-N 0.000 description 1
- ZOHSVAILZOYNCB-UHFFFAOYSA-N CCCCCc1ccc(-c2ccc(-c(cc3)ccc3N(c(cc3)ccc3-c3ccc(-c4ccc(CCCCC)[s]4)[s]3)c3ccc(-c(c4c56)ccc5C(O5)=O)c7c3cccc7C4=CCC6C5=O)[s]2)[s]1 Chemical compound CCCCCc1ccc(-c2ccc(-c(cc3)ccc3N(c(cc3)ccc3-c3ccc(-c4ccc(CCCCC)[s]4)[s]3)c3ccc(-c(c4c56)ccc5C(O5)=O)c7c3cccc7C4=CCC6C5=O)[s]2)[s]1 ZOHSVAILZOYNCB-UHFFFAOYSA-N 0.000 description 1
- INNGFHSSAWHJRI-UHFFFAOYSA-N CCCCCc1ccc(-c2ccc(-c(cc3)ccc3N(c(cc3)ccc3-c3ccc(-c4ccc(CCCCC)[s]4)[s]3)c3ccc(-c4ccc5C(O6)=O)c7c3cccc7-c(cc3)c4c5c3C6=O)[s]2)[s]1 Chemical compound CCCCCc1ccc(-c2ccc(-c(cc3)ccc3N(c(cc3)ccc3-c3ccc(-c4ccc(CCCCC)[s]4)[s]3)c3ccc(-c4ccc5C(O6)=O)c7c3cccc7-c(cc3)c4c5c3C6=O)[s]2)[s]1 INNGFHSSAWHJRI-UHFFFAOYSA-N 0.000 description 1
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- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1088—Heterocyclic compounds characterised by ligands containing oxygen as the only heteroatom
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- 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
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- 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
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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
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/654—Aromatic compounds comprising a hetero atom comprising only nitrogen as heteroatom
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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
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/655—Aromatic compounds comprising a hetero atom comprising only sulfur as heteroatom
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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
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/656—Aromatic compounds comprising a hetero atom comprising two or more different heteroatoms per ring
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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
- Y02E10/542—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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- General Physics & Mathematics (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyrane Compounds (AREA)
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
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| DE102005053995A DE102005053995A1 (de) | 2005-11-10 | 2005-11-10 | Verwendung von Rylenderivaten als Photosensibilisatoren in Solarzellen |
| DE102005053995.5 | 2005-11-10 | ||
| PCT/EP2006/068102 WO2007054470A1 (de) | 2005-11-10 | 2006-11-06 | Verwendung von rylenderivaten als photosensibilisatoren in solarzellen |
Publications (3)
| Publication Number | Publication Date |
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| JP2009515846A JP2009515846A (ja) | 2009-04-16 |
| JP2009515846A5 JP2009515846A5 (enExample) | 2013-03-21 |
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| EP (1) | EP1951842B1 (enExample) |
| JP (1) | JP5393154B2 (enExample) |
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| WO (1) | WO2007054470A1 (enExample) |
| ZA (1) | ZA200804950B (enExample) |
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2005
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| KR101583382B1 (ko) | 2016-01-07 |
| US20080269482A1 (en) | 2008-10-30 |
| EP1951842B1 (de) | 2016-07-27 |
| AU2006311032A1 (en) | 2007-05-18 |
| KR20080075864A (ko) | 2008-08-19 |
| DE102005053995A1 (de) | 2007-05-24 |
| AU2006311032B8 (en) | 2013-07-25 |
| WO2007054470A1 (de) | 2007-05-18 |
| US8231809B2 (en) | 2012-07-31 |
| CN101351524A (zh) | 2009-01-21 |
| AU2006311032B2 (en) | 2013-03-21 |
| US8501046B2 (en) | 2013-08-06 |
| JP2009515846A (ja) | 2009-04-16 |
| EP1951842A1 (de) | 2008-08-06 |
| AU2006311032A8 (en) | 2013-07-25 |
| CN101351524B (zh) | 2015-01-21 |
| ZA200804950B (en) | 2010-02-24 |
| US20120283432A1 (en) | 2012-11-08 |
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