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dc.contributor.authorKim, Se Hun-
dc.contributor.authorChoi, Jun-
dc.contributor.authorSakong, Chun-
dc.contributor.authorNamgoong, Jin Woong-
dc.contributor.authorLee, Woosung-
dc.contributor.authorKim, Dong Hoe-
dc.contributor.authorKim, Boeun-
dc.contributor.authorKo, Min Jae-
dc.contributor.authorKim, Jae Pil-
dc.date.accessioned2024-01-20T08:00:40Z-
dc.date.available2024-01-20T08:00:40Z-
dc.date.created2021-09-04-
dc.date.issued2015-02-
dc.identifier.issn0143-7208-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/125830-
dc.description.abstractFour new organic photosensitizers (SH-11 similar to 14) that introduced methoxy groups as an additional donor were synthesized, and used in dye-sensitized solar cells. The dyes were designed in order to investigate the effects on the dye photophysical properties and the cell photovoltaic performance, by the number, position, and shape of methoxy groups introduced at the para-/ortho- and para-/meta- and para-(open or closed ring shape) positions on the triphenylamine donor. The introduction of methoxy groups led to bathochromic shift of the absorption spectrum, and enhancement of the molar extinction coefficient of the dyes. Their introduction decreased the amount of dye adsorbed on TiO2 surface, due to the increased steric hindrance. As their number increased, an open-circuit voltage value decreased. All things considered, the dye (SH-14) with closed ring shape shows the best conversion efficiency of 6.01% under AM 1.5G conditions (N719 dye's 7.59% under the same conditions). (C) 2014 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER SCI LTD-
dc.subjectTRIARYLAMINE BASED DYES-
dc.subjectORGANIC-DYES-
dc.subjectPHENOXAZINE DYES-
dc.subjectCOUMARIN DYE-
dc.subjectIMPROVEMENT-
dc.subjectLINKERS-
dc.subjectBEARING-
dc.titleThe effect of the number, position, and shape of methoxy groups in triphenylamine donors on the performance of dye-sensitized solar cells-
dc.typeArticle-
dc.identifier.doi10.1016/j.dyepig.2014.09.014-
dc.description.journalClass1-
dc.identifier.bibliographicCitationDYES AND PIGMENTS, v.113, pp.390 - 401-
dc.citation.titleDYES AND PIGMENTS-
dc.citation.volume113-
dc.citation.startPage390-
dc.citation.endPage401-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000346543200050-
dc.identifier.scopusid2-s2.0-84907294940-
dc.relation.journalWebOfScienceCategoryChemistry, Applied-
dc.relation.journalWebOfScienceCategoryEngineering, Chemical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Textiles-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalResearchAreaMaterials Science-
dc.type.docTypeArticle-
dc.subject.keywordPlusTRIARYLAMINE BASED DYES-
dc.subject.keywordPlusORGANIC-DYES-
dc.subject.keywordPlusPHENOXAZINE DYES-
dc.subject.keywordPlusCOUMARIN DYE-
dc.subject.keywordPlusIMPROVEMENT-
dc.subject.keywordPlusLINKERS-
dc.subject.keywordPlusBEARING-
dc.subject.keywordAuthorDye-sensitized solar cell-
dc.subject.keywordAuthorTriphenylamine dye-
dc.subject.keywordAuthorElectron donor-
dc.subject.keywordAuthorMethoxy group-
dc.subject.keywordAuthorBathochromic shift-
dc.subject.keywordAuthorDihedral angle-
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