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양창덕

Yang, Changduk
Advanced Tech-Optoelectronic Materials Synthesis Lab.
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dc.citation.endPage 19840 -
dc.citation.number 45 -
dc.citation.startPage 19835 -
dc.citation.title ANGEWANDTE CHEMIE-INTERNATIONAL EDITION -
dc.citation.volume 59 -
dc.contributor.author Fan, Qunping -
dc.contributor.author Su, Wenyan -
dc.contributor.author Chen, Shanshan -
dc.contributor.author Liu, Tao -
dc.contributor.author Zhuang, Wenliu -
dc.contributor.author Ma, Ruijie -
dc.contributor.author Wen, Xin -
dc.contributor.author Yin, Zhihong -
dc.contributor.author Luo, Zhenghui -
dc.contributor.author Guo, Xia -
dc.contributor.author Hou, Lintao -
dc.contributor.author Moth-Poulsen, Kasper -
dc.contributor.author Li, Yu -
dc.contributor.author Zhang, Zhiguo -
dc.contributor.author Yang, Changduk -
dc.contributor.author Yu, Donghong -
dc.contributor.author Yan, He -
dc.contributor.author Zhang, Maojie -
dc.contributor.author Wang, Ergang -
dc.date.accessioned 2023-12-21T16:45:32Z -
dc.date.available 2023-12-21T16:45:32Z -
dc.date.created 2020-09-18 -
dc.date.issued 2020-11 -
dc.description.abstract A non-conjugated polymer acceptor PF1-TS4 was firstly synthesized by embedding a thioalkyl segment in the mainchain, which shows excellent photophysical properties on par with a fully conjugated polymer, with a low optical band gap of 1.58 eV and a high absorption coefficient >10(5) cm(-1), a high LUMO level of -3.89 eV, and suitable crystallinity. Matched with the polymer donor PM6, the PF1-TS4-based all-PSC achieved a power conversion efficiency (PCE) of 8.63 %, which is approximate to 45 % higher than that of a device based on the small molecule acceptor counterpart IDIC16. Moreover, the PF1-TS4-based all-PSC has good thermal stability with approximate to 70 % of its initial PCE retained after being stored at 85 degrees C for 180 h, while the IDIC16-based device only retained approximate to 50 % of its initial PCE when stored at 85 degrees C for only 18 h. Our work provides a new strategy to develop efficient polymer acceptor materials by linkage of conjugated units with non-conjugated thioalkyl segments. -
dc.identifier.bibliographicCitation ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.59, no.45, pp.19835 - 19840 -
dc.identifier.doi 10.1002/anie.202005662 -
dc.identifier.issn 1433-7851 -
dc.identifier.scopusid 2-s2.0-85089996257 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/48229 -
dc.identifier.url https://onlinelibrary.wiley.com/doi/full/10.1002/anie.202005662 -
dc.identifier.wosid 000564582300001 -
dc.language 영어 -
dc.publisher WILEY-V C H VERLAG GMBH -
dc.title A Non-Conjugated Polymer Acceptor for Efficient and Thermally Stable All-Polymer Solar Cells -
dc.type Article -
dc.description.isOpenAccess TRUE -
dc.relation.journalWebOfScienceCategory Chemistry, Multidisciplinary -
dc.relation.journalResearchArea Chemistry -
dc.type.docType Article; Early Access -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordAuthor all-polymer solar cells -
dc.subject.keywordAuthor non-conjugated polymer acceptors -
dc.subject.keywordAuthor power conversion efficiency -
dc.subject.keywordAuthor thermal stability -
dc.subject.keywordAuthor thioalkyl chain linkages -
dc.subject.keywordPlus POWER CONVERSION EFFICIENCY -
dc.subject.keywordPlus FULLERENE ACCEPTORS -
dc.subject.keywordPlus PERFORMANCE -
dc.subject.keywordPlus STABILITY -
dc.subject.keywordPlus DONOR -

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