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Solution-Processed Organic Photovoltaic Cells with Anthracene Derivatives

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dc.contributor.authorChung, Dae Sung-
dc.contributor.authorPark, Jong Won-
dc.contributor.authorYun, Won Min-
dc.contributor.authorCha, Hyojung-
dc.contributor.authorKim, Yun-Hi-
dc.contributor.authorKwon, Soon-Ki-
dc.contributor.authorPark, Chan Eon-
dc.date.accessioned2022-12-27T05:03:26Z-
dc.date.available2022-12-27T05:03:26Z-
dc.date.issued2010-06-
dc.identifier.issn1864-5631-
dc.identifier.issn1864-564X-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/26054-
dc.description.abstractSolution-processed small-molecule bulk heterojunction photovoltaic cells are fabricated by using [6,6]-phenyl-C-61-butyric acid methyl ester (PCBM) as electron acceptor and triisopropylsilylethynyl anthracene (TIPSAnt) derivatives substituted with naphthalene (TIPSAntNa) and bithiophene (TIPSAntBT) as electron donors. In contrast to TIPS-pentacene, the TIPSAnt derivatives are not susceptible to Die Is-Alder reactions with PCBM when processed in solution, as confirmed by UV/Vis measurements. Photoluminescence quenching measurements show exciton diffusion lengths of 5 and 3 nm for TIPSAntBT and TIP-SAntNa, respectively. Blending TIPSAntBT and TIPSAntNa with PCBM (1:1, 1:2, 1:3, and 1:4 weight ratios) produces films that possess adequate hole and electron mobilities. The morphological changes that result from varying the blending ratio range from obvious phase-segregated crystalline domains at a 1:1 ratio to homogeneous, nearly amorphous phases at a 1:4 ratio. Bulk heterojunction solar cells prepared by using a TIPSAntBT:PCBM blend reach power conversion efficiencies as high as 1.4%.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherWiley - V C H Verlag GmbbH & Co.-
dc.titleSolution-Processed Organic Photovoltaic Cells with Anthracene Derivatives-
dc.typeArticle-
dc.publisher.location독일-
dc.identifier.doi10.1002/cssc.201000037-
dc.identifier.scopusid2-s2.0-77953863506-
dc.identifier.wosid000279753300018-
dc.identifier.bibliographicCitationChemSusChem, v.3, no.6, pp 742 - 748-
dc.citation.titleChemSusChem-
dc.citation.volume3-
dc.citation.number6-
dc.citation.startPage742-
dc.citation.endPage748-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryGreen & Sustainable Science & Technology-
dc.subject.keywordPlusHETEROJUNCTION SOLAR-CELLS-
dc.subject.keywordPlusEXCITON DIFFUSION LENGTH-
dc.subject.keywordPlusFIELD-EFFECT TRANSISTORS-
dc.subject.keywordPlusFUNCTIONALIZED ACENES-
dc.subject.keywordPlusEFFICIENCY-
dc.subject.keywordPlusTRANSPORT-
dc.subject.keywordPlusSEMICONDUCTORS-
dc.subject.keywordPlusPHOTOCURRENT-
dc.subject.keywordPlusPERFORMANCE-
dc.subject.keywordPlusABSORPTION-
dc.subject.keywordAuthoranthracenes-
dc.subject.keywordAuthorphotophysics-
dc.subject.keywordAuthorsemiconductors-
dc.subject.keywordAuthorsolar cells-
dc.subject.keywordAuthorthin films-
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