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Effects of n-type perylene derivative as an additive on the power conversion efficiencies of polymer solar cells
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dc.contributor.author Jeong, Seonju -
dc.contributor.author Han, Yoon Soo -
dc.contributor.author Kwon, Younghwan -
dc.contributor.author Choi, Myung-Seok -
dc.contributor.author Cho, Gwijeong -
dc.contributor.author Kim, Ki-Soo -
dc.contributor.author Kim, Youngkyoo -
dc.date.available 2017-07-11T07:09:22Z -
dc.date.created 2017-04-10 -
dc.date.issued 2010-10 -
dc.identifier.issn 0379-6779 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/3498 -
dc.description.abstract The synthesized n-type perylene derivative, N,N′-bis-(5- bromopyridine-2-yl)-1,6,7,12-tetrakis(4-n-butoxyphenoxy)-3,4,9,10-perylene tetracarboxydiimide (PPyB), was applied to polymer solar cells as an additive in P3HT [poly(3-hexylthiophene)]:PCBM [[6,6]-phenyl C61-butyric acid methyl ester] blend films. The addition of 1 wt% PPyB into a P3HT:PCBM layer led to a considerable improvement of over 70% in power conversion efficiency due to the enhanced short circuit current when compared with that of reference cell without an additive. Photoluminescence, X-ray measurements and carrier mobility studies revealed that the perylene additives increased electron mobility and contributed to more effective exciton dissociation due to the presence of the additive, PPyB, in the interfaces between the P3HT and PCBM domains. © 2010 Elsevier B.V. All rights reserved. -
dc.publisher Elsevier -
dc.title Effects of n-type perylene derivative as an additive on the power conversion efficiencies of polymer solar cells -
dc.type Article -
dc.identifier.doi 10.1016/j.synthmet.2010.07.040 -
dc.identifier.wosid 000283681900011 -
dc.identifier.scopusid 2-s2.0-77957678124 -
dc.identifier.bibliographicCitation Jeong, Seonju. (2010-10). Effects of n-type perylene derivative as an additive on the power conversion efficiencies of polymer solar cells. Synthetic Metals, 160(19–20), 2109–2115. doi: 10.1016/j.synthmet.2010.07.040 -
dc.subject.keywordAuthor Perylene derivative -
dc.subject.keywordAuthor Polymer solar cell -
dc.subject.keywordAuthor Additive -
dc.subject.keywordAuthor P3HT -
dc.subject.keywordAuthor PCBM -
dc.subject.keywordPlus ACIDs -
dc.subject.keywordPlus Additive -
dc.subject.keywordPlus Additives -
dc.subject.keywordPlus ANNEALING-FREE APPROACH -
dc.subject.keywordPlus Blend Films -
dc.subject.keywordPlus Butyric ACIDs -
dc.subject.keywordPlus Conversion Efficiency -
dc.subject.keywordPlus DIIMIDES -
dc.subject.keywordPlus Electron Mobility -
dc.subject.keywordPlus Esters -
dc.subject.keywordPlus Exciton Dissociation -
dc.subject.keywordPlus Fatty ACIDs -
dc.subject.keywordPlus IMPROVemENT -
dc.subject.keywordPlus METHANofULLERENES -
dc.subject.keywordPlus Methyl Esters -
dc.subject.keywordPlus NETWORK -
dc.subject.keywordPlus OPTICAL-PROPERTIES -
dc.subject.keywordPlus P3HT -
dc.subject.keywordPlus PCBM -
dc.subject.keywordPlus PERFORMANCE -
dc.subject.keywordPlus Perylene Derivative -
dc.subject.keywordPlus Perylene Derivatives -
dc.subject.keywordPlus Perylenes -
dc.subject.keywordPlus PHOTOVOLTAIC CELLS -
dc.subject.keywordPlus Poly (3-Hexylthiophene) -
dc.subject.keywordPlus POLY(3-HEXYLTHIOPHENE) -
dc.subject.keywordPlus Polymer Solar Cell -
dc.subject.keywordPlus Polymer Solar Cells -
dc.subject.keywordPlus Polymers -
dc.subject.keywordPlus Power Conversion Efficiencies -
dc.subject.keywordPlus SELF-ORGANIZATION -
dc.subject.keywordPlus Solar Cells -
dc.subject.keywordPlus Tetrakis -
dc.subject.keywordPlus X Ray Measurements -
dc.citation.endPage 2115 -
dc.citation.number 19-20 -
dc.citation.startPage 2109 -
dc.citation.title Synthetic Metals -
dc.citation.volume 160 -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.relation.journalResearchArea Materials Science; Physics; Polymer Science -
dc.relation.journalWebOfScienceCategory Materials Science, Multidisciplinary; Physics, Condensed Matter; Polymer Science -
dc.type.docType Article -
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