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DC Field | Value | Language |
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dc.citation.endPage | 2862 | - |
dc.citation.number | 22 | - |
dc.citation.startPage | 2854 | - |
dc.citation.title | POLYMER CHEMISTRY | - |
dc.citation.volume | 10 | - |
dc.contributor.author | Lee, Sang Myeon | - |
dc.contributor.author | Lee, Hae Rang | - |
dc.contributor.author | Dutta, Gitish K. | - |
dc.contributor.author | Lee, Junghoon | - |
dc.contributor.author | Oh, Joon Hak | - |
dc.contributor.author | Yang, Changduk | - |
dc.date.accessioned | 2023-12-21T19:07:38Z | - |
dc.date.available | 2023-12-21T19:07:38Z | - |
dc.date.created | 2019-06-20 | - |
dc.date.issued | 2019-06 | - |
dc.description.abstract | Herein, we report the effects of chalcogen atoms on organic field-effect transistors (OFETs) by studying a series of furan-flanked diketopyrrolopyrrole copolymers (PFDPPF-Si, PFDPPT-Si, and PFDPPS-Si) with different chalcogenophene comonomers (furan, thiophene, and selenophene), where the siloxane-terminated chains are used as solubilizing groups. The optical/ electrochemical properties, microstructural analyses, and charge transport characteristics of the resulting copolymers are discussed as a function of the different chalcogenophenes. A larger heteroatom size led to a bathochromic shift in the absorption profiles and narrowing of the band gaps. Besides, as the heteroatomic size increased from O to S and Se, the degree of intramolecular steric hindrance observed in the density functional theory calculations followed the trend of deviating from the coplanar backbone conformations. Consequently, the morphological and crystalline features of PFDPPF-Si were shown to be pronounced with a highly crystalline structure and dense p-p stacking, which led to the best hole mobility of 2.48 cm2 V-1 s-1. In addition, we demonstrated a complementary-like inverter based on PFDPPS-Si with a high gain of 54. The systematic characterization of heteroaromatics enables the design of conjugated copolymers, which provides a clear understanding of their structure-property behaviors on OFET characteristics. | - |
dc.identifier.bibliographicCitation | POLYMER CHEMISTRY, v.10, no.22, pp.2854 - 2862 | - |
dc.identifier.doi | 10.1039/c9py00448c | - |
dc.identifier.issn | 1759-9954 | - |
dc.identifier.scopusid | 2-s2.0-85066949714 | - |
dc.identifier.uri | https://scholarworks.unist.ac.kr/handle/201301/27428 | - |
dc.identifier.url | https://pubs.rsc.org/en/content/articlelanding/2019/PY/C9PY00448C#!divAbstract | - |
dc.identifier.wosid | 000470708700009 | - |
dc.language | 영어 | - |
dc.publisher | ROYAL SOC CHEMISTRY | - |
dc.title | Furan-flanked diketopyrrolopyrrole-based chalcogenophene copolymers with siloxane hybrid side chains for organic field-effect transistors | - |
dc.type | Article | - |
dc.description.isOpenAccess | FALSE | - |
dc.relation.journalWebOfScienceCategory | Polymer Science | - |
dc.relation.journalResearchArea | Polymer Science | - |
dc.type.docType | Article | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.subject.keywordPlus | POLYMER SEMICONDUCTORS | - |
dc.subject.keywordPlus | CONJUGATED POLYMERS | - |
dc.subject.keywordPlus | MOLECULAR DESIGN | - |
dc.subject.keywordPlus | SOLAR-CELLS | - |
dc.subject.keywordPlus | HIGH HOLE | - |
dc.subject.keywordPlus | PERFORMANCE | - |
dc.subject.keywordPlus | MOBILITY | - |
dc.subject.keywordPlus | ACCEPTOR | - |
dc.subject.keywordPlus | THIOPHENE | - |
dc.subject.keywordPlus | DONOR | - |
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