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Synthesis and characterization of push-pull organic semiconductors with various acceptors for solution-processed small molecule organic solar cells

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dc.contributor.authorCho, Nara-
dc.contributor.authorKim, Jooyoung-
dc.contributor.authorSong, Kihyung-
dc.contributor.authorLee, Jae Kwan-
dc.contributor.authorKo, Jaejung-
dc.date.accessioned2021-09-06T19:39:14Z-
dc.date.available2021-09-06T19:39:14Z-
dc.date.created2021-06-18-
dc.date.issued2012-05-27-
dc.identifier.issn0040-4020-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/108393-
dc.description.abstractNew efficient push-pull organic semiconductors comprising of the bis(9,9-dimethyl-9H-fluoren-2-yl) aniline (bisDMFA) donor and the various acceptors such as NO2, DCBP, and TCF, which were linked with bithiophene or vinyl bithiophene pi-conjugation bridges, were synthesized, and their photovoltaic characteristics were investigated in solution-processed small molecule organic solar cells (SMOSCs). The intramolecular charge transfers of these materials were effectively appeared in between bisDMFA donor and acceptors, depending on the electron-withdrawing strength of acceptors. The organic semiconductors having NO2 and DCBP acceptors exhibited the most efficient photovoltaic performance, showing power conversion efficiency (PCE) of 1.98% (+/- 0.17) and 2.01% (+/- 0.21), respectively. When the TiOx thin layer was treated on photoactive layer, the organic semiconductor having NO2 showed the best PCE of 2.70% with short circuit current of 8.19 mA/cm(2), fill factor of 0.40, and open circuit voltage of 0.83 V in SMOSC devices. (C) 2012 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectINTERNAL CHARGE-TRANSFER-
dc.subjectTRIPHENYLAMINE-
dc.subjectEFFICIENCY-
dc.subjectBENZOTHIADIAZOLE-
dc.subjectCHROMOPHORES-
dc.subjectSYSTEMS-
dc.subjectDESIGN-
dc.subjectDONORS-
dc.titleSynthesis and characterization of push-pull organic semiconductors with various acceptors for solution-processed small molecule organic solar cells-
dc.typeArticle-
dc.contributor.affiliatedAuthorKo, Jaejung-
dc.identifier.doi10.1016/j.tet.2012.03.061-
dc.identifier.scopusid2-s2.0-84860171985-
dc.identifier.wosid000303846900016-
dc.identifier.bibliographicCitationTETRAHEDRON, v.68, no.21, pp.4029 - 4036-
dc.relation.isPartOfTETRAHEDRON-
dc.citation.titleTETRAHEDRON-
dc.citation.volume68-
dc.citation.number21-
dc.citation.startPage4029-
dc.citation.endPage4036-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.subject.keywordPlusINTERNAL CHARGE-TRANSFER-
dc.subject.keywordPlusTRIPHENYLAMINE-
dc.subject.keywordPlusEFFICIENCY-
dc.subject.keywordPlusBENZOTHIADIAZOLE-
dc.subject.keywordPlusCHROMOPHORES-
dc.subject.keywordPlusSYSTEMS-
dc.subject.keywordPlusDESIGN-
dc.subject.keywordPlusDONORS-
dc.subject.keywordAuthorBulk heterojunction-
dc.subject.keywordAuthorIntramolecular charge transfer-
dc.subject.keywordAuthorElectron-withdrawing acceptor-
dc.subject.keywordAuthorOrganic solar cell-
dc.subject.keywordAuthorOrganic semiconductor-
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