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Fluorene-based conjugated polymers containing acetylene linkages for photovoltaics
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Ko, Yun-Hyuk | - |
| dc.contributor.author | Chandran, Deepak | - |
| dc.contributor.author | Park, Jea-Gun | - |
| dc.contributor.author | Lee, Kwang-Sup | - |
| dc.date.accessioned | 2021-08-02T14:30:03Z | - |
| dc.date.available | 2021-08-02T14:30:03Z | - |
| dc.date.issued | 2017-09 | - |
| dc.identifier.issn | 1542-1406 | - |
| dc.identifier.issn | 1543-5318 | - |
| dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/18804 | - |
| dc.description.abstract | Conjugated polymers have attracted considerable attention due to their versatile applications in the fields of organic optoelectronic devices. In this study, we describe the synthesis and photovoltaic applications of a series of donor-acceptor (D-A) type conjugated polymers having acetylene-linked fluorene-based donor monomers and benzothiadiazole-based acceptor monomers. The link pattern (carbon-carbon single, triple bond) has a significant influence on the solubility, thermal, optical, and structural properties of these polymers. Compared to C-C single-bond linked polymers PFu-1 and PFu-3, the UV absorption of triple-bond linked PFu-2 and PFu-4 polymers is red-shifted due to higher coplanarity and effective p-p stacking of polymer backbones. The range of the power conversion efficiency of bulk heterojunction solar cells fabricated by the resulting polymer series is 1.02-1.30%. | - |
| dc.format.extent | 9 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | Taylor & Francis | - |
| dc.title | Fluorene-based conjugated polymers containing acetylene linkages for photovoltaics | - |
| dc.type | Article | - |
| dc.publisher.location | 영국 | - |
| dc.identifier.doi | 10.1080/15421406.2017.1362935 | - |
| dc.identifier.scopusid | 2-s2.0-85038363434 | - |
| dc.identifier.wosid | 000423110900017 | - |
| dc.identifier.bibliographicCitation | Molecular Crystals and Liquid Crystals, v.655, no.1, pp 150 - 158 | - |
| dc.citation.title | Molecular Crystals and Liquid Crystals | - |
| dc.citation.volume | 655 | - |
| dc.citation.number | 1 | - |
| dc.citation.startPage | 150 | - |
| dc.citation.endPage | 158 | - |
| dc.type.docType | Article; Proceedings Paper | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | sci | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Chemistry | - |
| dc.relation.journalResearchArea | Crystallography | - |
| dc.relation.journalResearchArea | Materials Science | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Multidisciplinary | - |
| dc.relation.journalWebOfScienceCategory | Crystallography | - |
| dc.relation.journalWebOfScienceCategory | Materials Science, Multidisciplinary | - |
| dc.subject.keywordPlus | HETEROJUNCTION SOLAR-CELLS | - |
| dc.subject.keywordPlus | BAND-GAP | - |
| dc.subject.keywordPlus | EFFICIENCY | - |
| dc.subject.keywordPlus | COPOLYMER | - |
| dc.subject.keywordPlus | SENSORS | - |
| dc.subject.keywordAuthor | Benzothiadiazole | - |
| dc.subject.keywordAuthor | conjugated polymers | - |
| dc.subject.keywordAuthor | fluorene | - |
| dc.subject.keywordAuthor | organic photovoltaics | - |
| dc.identifier.url | https://www.tandfonline.com/doi/full/10.1080/15421406.2017.1362935 | - |
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