pi-Conjugated Main Chain Polymers Containing Bis(bithiophenyl dithienothiophene)-based Repeating Group and their Application to Polymer Solar Cells
DC Field | Value | Language |
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dc.contributor.author | Kim, Kyung Hwan | - |
dc.contributor.author | Chung, Dae Sung | - |
dc.contributor.author | Park, Chan Eon | - |
dc.contributor.author | Choi, Dong Hoon | - |
dc.date.accessioned | 2021-09-07T21:59:28Z | - |
dc.date.available | 2021-09-07T21:59:28Z | - |
dc.date.issued | 2011 | - |
dc.identifier.issn | 1542-1406 | - |
dc.identifier.issn | 1543-5318 | - |
dc.identifier.uri | https://scholar.korea.ac.kr/handle/2021.sw.korea/115063 | - |
dc.description.abstract | New dithienothiophene (DTT)-containing conjugated polymers, such as poly(2,6-bis(2-thiophenyl-3-dodecylthiophene-2-yl) dithieno[3,2-b; 2',3'-d] thiophene, 1 and poly(2,6-bis(2-thiophenyl-4-dodecylthiophene-2-yl) dithieno[3,2-b; 2',3'-d] thiophene, 2 have been successfully synthesized via Stille coupling reactions using dodecylsubstituted thiophene-based monomer, bistributyltin dithienothiophene, and bistributyltin bithiophene. The main difference between two polymers is the substitution position of dodecyl side chains in a repeating group. The semiconducting properties of the two polymers have been evaluated in organic photovoltaics (OPVs). Two conjugated polymers are also well mixed with methanofullerene [6,6]-phenyl C61-butyric acid methyl ester (PCBM) for fabricating bulk heterojunction PV devices. As a result, the polymer solar cell devices made of polymers 1 and 2 had the best preliminary results with an open-circuit voltage of 0.43-0.44 V, a short-circuit current density of 5.95-5.96mA/cm(2), and a fill factor of 0.34, offering an overall power conversion efficiency (PCE) of 0.9%. | - |
dc.format.extent | 6 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | TAYLOR & FRANCIS LTD | - |
dc.title | pi-Conjugated Main Chain Polymers Containing Bis(bithiophenyl dithienothiophene)-based Repeating Group and their Application to Polymer Solar Cells | - |
dc.type | Article | - |
dc.publisher.location | 영국 | - |
dc.identifier.doi | 10.1080/15421406.2011.563720 | - |
dc.identifier.wosid | 000290677300029 | - |
dc.identifier.bibliographicCitation | MOLECULAR CRYSTALS AND LIQUID CRYSTALS, v.538, pp 187 - 192 | - |
dc.citation.title | MOLECULAR CRYSTALS AND LIQUID CRYSTALS | - |
dc.citation.volume | 538 | - |
dc.citation.startPage | 187 | - |
dc.citation.endPage | 192 | - |
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 | PHOTOVOLTAIC CELLS | - |
dc.subject.keywordPlus | EFFICIENT | - |
dc.subject.keywordPlus | PERFORMANCE | - |
dc.subject.keywordAuthor | Absorption | - |
dc.subject.keywordAuthor | conjugated polymers | - |
dc.subject.keywordAuthor | dithienothiophene | - |
dc.subject.keywordAuthor | mobility | - |
dc.subject.keywordAuthor | organic photovoltaics | - |
dc.subject.keywordAuthor | semiconductor | - |
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