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Synthesis and Characterization of a New Phenanthrenequinoxaline-Based Polymer for Organic Solar Cells

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dc.contributor.authorJo, Eunsol-
dc.contributor.authorPark, Jong Baek-
dc.contributor.authorLee, Woo-Hyung-
dc.contributor.authorKim, Ji-Hoon-
dc.contributor.authorJung, In Hwan-
dc.contributor.authorHwang, Do-Hoon-
dc.contributor.authorKang, In-Nam-
dc.date.accessioned2021-08-02T16:27:44Z-
dc.date.available2021-08-02T16:27:44Z-
dc.date.created2021-05-14-
dc.date.issued2016-09-
dc.identifier.issn0887-624X-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/22185-
dc.description.abstractTwo donor-acceptor (D-A) conjugated polymers, PQx and PphQx, composed of alkylthienyl-substituted benzo[1,2-b:4,5-b'] dithiophene (BDTT) as the electron donor and the new electron acceptors quinoxaline (Qx) or phenanthrenequinoxaline (phQx), were synthesized with Stille cross-coupling reactions. The number-averaged molecular weights (M-n) of PQx and PphQx were found to be 25.1 and 23.2 kDa, respectively, with a dispersity of 2.6. The band-gap energies of PQx and PphQx are 1.82 and 1.75 eV, respectively. These results indicate that, because phQx units have highly planar structures, their inclusion in D-A polymers will be a very effective method for increasing the polymers' effective conjugation lengths. The hole mobilities of PQx and PphQx were determined to be 5.0 x 10(-5) and 2.2 x 10(-4) cm(2) V-1 s(-1), respectively. A polymer solar cell device prepared with PphQx as the active layer was found to exhibit a power conversion efficiency (PCE) of 5.03%; thus, the introduction of phQx units enhanced both the short circuit current density and PCE of the device.-
dc.language영어-
dc.language.isoen-
dc.publisherWILEY-
dc.titleSynthesis and Characterization of a New Phenanthrenequinoxaline-Based Polymer for Organic Solar Cells-
dc.typeArticle-
dc.contributor.affiliatedAuthorJung, In Hwan-
dc.identifier.doi10.1002/pola.28166-
dc.identifier.scopusid2-s2.0-84971290078-
dc.identifier.wosid000383675800018-
dc.identifier.bibliographicCitationJOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, v.54, no.17, pp.2804 - 2810-
dc.relation.isPartOfJOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY-
dc.citation.titleJOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY-
dc.citation.volume54-
dc.citation.number17-
dc.citation.startPage2804-
dc.citation.endPage2810-
dc.type.rimsART-
dc.type.docType정기학술지(Article(Perspective Article포함))-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPolymer Science-
dc.relation.journalWebOfScienceCategoryPolymer Science-
dc.subject.keywordPlusCONJUGATED POLYMERS-
dc.subject.keywordPlusPHOTOVOLTAIC PROPERTIES-
dc.subject.keywordPlusAGGREGATION-
dc.subject.keywordPlusCOPOLYMERS-
dc.subject.keywordPlusOLIGOMERS-
dc.subject.keywordAuthorcharge transport-
dc.subject.keywordAuthorconjugated polymers-
dc.subject.keywordAuthorfunctionalization of polymers-
dc.subject.keywordAuthorheteroatom-containing polymers-
dc.subject.keywordAuthororganic solar cell-
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/10.1002/pola.28166-
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