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Silole-spaced triarylamine derivatives as highly efficient organic sensitizers in dye-sensitized solar cells (DSSCs)

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dc.contributor.authorKo, Sangwon-
dc.contributor.authorChoi, Hyunbong-
dc.contributor.authorKang, Moon-Sung-
dc.contributor.authorHwang, Hyonseok-
dc.contributor.authorJi, Heesun-
dc.contributor.authorKim, Jinho-
dc.contributor.authorKo, Jaejung-
dc.contributor.authorKang, Youngjin-
dc.date.accessioned2021-09-08T10:13:42Z-
dc.date.available2021-09-08T10:13:42Z-
dc.date.created2021-06-11-
dc.date.issued2010-
dc.identifier.issn0959-9428-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/118600-
dc.description.abstractThree new organic dyes that contain the dithienosilole (DTS) moiety as spacer have been synthesized and their photophysical/electrochemical properties, theoretical calculation and dye-sensitized solar cell (DSSC) performance have been investigated. The overall conversion efficiencies for DSSCs based on these dyes range from 6.73 to 7.50%, comparable to a (3-5'-[N,N-bis(9,9-dimethylfluorene-2-yl)-phenyl] 2,2'-bithiophene-5-yl}-2-cyanoacrylic acid (JK-2)-sensitized device (7.63%), fabricated and measured under the same experimental conditions. The DSSC constructed from one of the three compounds shows a higher open-circuit voltage (V-OC) compared to those of the other two dye sensitized solar cells due to an increased electron lifetime (tau(e)) in the conduction band of TiO2.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherROYAL SOC CHEMISTRY-
dc.subjectELECTRON-TRANSPORTING PROPERTIES-
dc.subjectENERGY-CONVERSION EFFICIENCY-
dc.subjectTIO2-
dc.subjectTHIOPHENE-
dc.subjectDITHIENOSILOLES-
dc.subjectSEMICONDUCTOR-
dc.subjectSOLVENT-
dc.subjectPOLYMER-
dc.titleSilole-spaced triarylamine derivatives as highly efficient organic sensitizers in dye-sensitized solar cells (DSSCs)-
dc.typeArticle-
dc.contributor.affiliatedAuthorKo, Jaejung-
dc.identifier.doi10.1039/b926163j-
dc.identifier.scopusid2-s2.0-77949385641-
dc.identifier.wosid000275380000017-
dc.identifier.bibliographicCitationJOURNAL OF MATERIALS CHEMISTRY, v.20, no.12, pp.2391 - 2399-
dc.relation.isPartOfJOURNAL OF MATERIALS CHEMISTRY-
dc.citation.titleJOURNAL OF MATERIALS CHEMISTRY-
dc.citation.volume20-
dc.citation.number12-
dc.citation.startPage2391-
dc.citation.endPage2399-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.subject.keywordPlusELECTRON-TRANSPORTING PROPERTIES-
dc.subject.keywordPlusENERGY-CONVERSION EFFICIENCY-
dc.subject.keywordPlusTIO2-
dc.subject.keywordPlusTHIOPHENE-
dc.subject.keywordPlusDITHIENOSILOLES-
dc.subject.keywordPlusSEMICONDUCTOR-
dc.subject.keywordPlusSOLVENT-
dc.subject.keywordPlusPOLYMER-
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