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dc.contributor.author Heo, Hyojung -
dc.contributor.author Kim, Honggi -
dc.contributor.author Lee, Donghwa -
dc.contributor.author Jang, Seokhoon -
dc.contributor.author Ban, Lyeojin -
dc.contributor.author Lim, Bogyu -
dc.contributor.author Lee, Jaechol -
dc.contributor.author Lee, Youngu -
dc.date.available 2017-07-11T05:31:59Z -
dc.date.created 2017-04-10 -
dc.date.issued 2016-05-10 -
dc.identifier.issn 0024-9297 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/2685 -
dc.description.abstract A regioregular D1-A-D2-A terpolymer PDTSTTBDT incorporating dithieno[3,2-b:2′,3′-d]silole (DTS, D1) and benzo[1,2-b:4,5-b]dithiophene (BDT, D2) units with perfectly controlled thieno[3,4-b]thiophene (TT, A) orientation was synthesized for the first time. The thermal, optical, and electrochemical properties of the regioregular PDTSTTBDT were characterized and compared with the random PDTSTTBDT without structural regioregularity. The regioregular PDTSTTBDT showed ideal optical bandgap (1.45 eV), lower lying HOMO energy level, and higher degree of crystallinity compared to the random PDTSTTBDT. Moreover, it exhibited excellent solubility in nonhalogenated solvents as well as halogenated solvents. The inverted bulk-heterojunction polymer solar cells (PSCs) based on the regioregular PDTSTTBDT and o-xylene process solvent showed a power conversion efficiency as high as 6.14%, which is 500% higher than the random PDTSTTBDT-based PSCs. It was found that the remarkable enhancement of photovoltaic performance in regioregular PDTSTTBDT-based PSCs is mainly due to improved light absorption, effective polymer ordering, and high charge carrier mobility. © 2016 American Chemical Society. -
dc.publisher American Chemical Society -
dc.title Regioregular D-1-A-D-2-A Terpolymer with Controlled Thieno[3,4-b]thiophene Orientation for High-Efficiency Polymer Solar Cells Processed with Nonhalogenated Solvents -
dc.type Article -
dc.identifier.doi 10.1021/acs.macromol.6b00269 -
dc.identifier.scopusid 2-s2.0-84969509204 -
dc.identifier.bibliographicCitation Macromolecules, v.49, no.9, pp.3328 - 3335 -
dc.subject.keywordPlus Copolymers -
dc.subject.keywordPlus Degree of Crystallinity -
dc.subject.keywordPlus DITHIENOSILOLE -
dc.subject.keywordPlus Electromagnetic Wave Absorption -
dc.subject.keywordPlus Excellent Solubility -
dc.subject.keywordPlus Halogenated Solvents -
dc.subject.keywordPlus Halogenation -
dc.subject.keywordPlus Heterojunctions -
dc.subject.keywordPlus Light Absorption -
dc.subject.keywordPlus Morphology -
dc.subject.keywordPlus Nonhalogenated Solvent -
dc.subject.keywordPlus PHOTOVOLTAIC PERFORMANCE -
dc.subject.keywordPlus Polymer Solar Cell (PSCs) -
dc.subject.keywordPlus Polymer Solar Cells -
dc.subject.keywordPlus Polymers -
dc.subject.keywordPlus Power Conversion Efficiencies -
dc.subject.keywordPlus POWER CONVERSION EFFICIENCY -
dc.subject.keywordPlus Solar Cells -
dc.subject.keywordPlus Solvents -
dc.subject.keywordPlus Thieno[3,4-B]Thiophene -
dc.subject.keywordPlus Thiophene -
dc.citation.endPage 3335 -
dc.citation.number 9 -
dc.citation.startPage 3328 -
dc.citation.title Macromolecules -
dc.citation.volume 49 -
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Department of Energy Science and Engineering Organic & Printed Electronics Laboratory(OPEL) 1. Journal Articles

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