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신태주

Shin, Tae Joo
Synchrotron Radiation Research Lab.
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dc.citation.endPage 12318 -
dc.citation.number 31 -
dc.citation.startPage 12308 -
dc.citation.title JOURNAL OF MATERIALS CHEMISTRY A -
dc.citation.volume 4 -
dc.contributor.author Hadmojo, Wisnu Tantyo -
dc.contributor.author Nam, So Youn -
dc.contributor.author Shin, Tae Joo -
dc.contributor.author Yoon, Sung Cheol -
dc.contributor.author Jang, Sung-Yeon -
dc.contributor.author Jung, Im Hwan -
dc.date.accessioned 2023-12-21T23:19:08Z -
dc.date.available 2023-12-21T23:19:08Z -
dc.date.created 2016-08-23 -
dc.date.issued 2016-08 -
dc.description.abstract Organic small molecule (SM) acceptors containing a perylene diimide (PDI) moiety, F2B-T2PDI and T2PDI are synthesized, and the effects of their molecular geometry on the performance of fullerene-free organic photovoltaic (OPV) devices are investigated. The SM acceptors possess a PDI-core-PDI structure in which the PDI wing is connected to conjugated core units. By incorporation of a 2,5-difluorobenzene (F2B) moiety within the core unit, the planarity of the conjugated core is enhanced and the energy levels of the SM acceptor are down-shifted. In terms of molecular geometry, the F2B-containing SM acceptor, F2B-T2PDI, has a rigid core, which can symmetrically align the two PDI wings and enhance molecular packing. As a result, improved electron transport and bulk heterojunction morphology of the active layers are achieved. Furthermore, the incorporation of the F2B moiety effectively down-shifts the HOMO energy level, preventing back-transfer of holes from the acceptor to the cathode and enhancing the absorption of complementary wavelengths of the donor polymer, PTB7-Th. Leveraged by the beneficial geometric and energetic effects from the incorporation of F2B units, the power conversion efficiency of fullerene-free OPV devices using F2B-T2PDI reached 5%, whereas that using T2PDI was 3.63%. -
dc.identifier.bibliographicCitation JOURNAL OF MATERIALS CHEMISTRY A, v.4, no.31, pp.12308 - 12318 -
dc.identifier.doi 10.1039/c6ta04344e -
dc.identifier.issn 2050-7488 -
dc.identifier.scopusid 2-s2.0-84982786867 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/20268 -
dc.identifier.url http://pubs.rsc.org/en/Content/ArticleLanding/2016/TA/C6TA04344E#!divAbstract -
dc.identifier.wosid 000382095100038 -
dc.language 영어 -
dc.publisher ROYAL SOC CHEMISTRYROYAL SOC CHEMISTRY -
dc.title Geometrically controlled organic small molecule acceptors for efficient fullerene-free organic photovoltaic devices -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Chemistry, Physical; Energy & Fuels; Materials Science, Multidisciplinary -
dc.relation.journalResearchArea Chemistry; Energy & Fuels; Materials Science -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordPlus ELECTRON-ACCEPTORS -
dc.subject.keywordPlus CONVERSION EFFICIENCY -
dc.subject.keywordPlus EXCEEDING 10-PERCENT -
dc.subject.keywordPlus ULTIMATE EFFICIENCY -
dc.subject.keywordPlus ENERGY-CONVERSION -
dc.subject.keywordPlus PHASE-SEPARATION -
dc.subject.keywordPlus BANDGAP POLYMER -
dc.subject.keywordPlus POLYMER SOLAR-CELLS -
dc.subject.keywordPlus OPEN-CIRCUIT VOLTAGE -
dc.subject.keywordPlus CONJUGATED POLYMERS -

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