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pi-Conjugated Main Chain Polymers Containing Bis(bithiophenyl dithienothiophene)-based Repeating Group and their Application to Polymer Solar Cells

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dc.contributor.authorKim, Kyung Hwan-
dc.contributor.authorChung, Dae Sung-
dc.contributor.authorPark, Chan Eon-
dc.contributor.authorChoi, Dong Hoon-
dc.date.accessioned2021-09-07T21:59:28Z-
dc.date.available2021-09-07T21:59:28Z-
dc.date.created2021-06-14-
dc.date.issued2011-
dc.identifier.issn1542-1406-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/115063-
dc.description.abstractNew 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.languageEnglish-
dc.language.isoen-
dc.publisherTAYLOR & FRANCIS LTD-
dc.subjectPHOTOVOLTAIC CELLS-
dc.subjectEFFICIENT-
dc.subjectPERFORMANCE-
dc.titlepi-Conjugated Main Chain Polymers Containing Bis(bithiophenyl dithienothiophene)-based Repeating Group and their Application to Polymer Solar Cells-
dc.typeArticle-
dc.contributor.affiliatedAuthorChoi, Dong Hoon-
dc.identifier.doi10.1080/15421406.2011.563720-
dc.identifier.wosid000290677300029-
dc.identifier.bibliographicCitationMOLECULAR CRYSTALS AND LIQUID CRYSTALS, v.538, pp.187 - 192-
dc.relation.isPartOfMOLECULAR CRYSTALS AND LIQUID CRYSTALS-
dc.citation.titleMOLECULAR CRYSTALS AND LIQUID CRYSTALS-
dc.citation.volume538-
dc.citation.startPage187-
dc.citation.endPage192-
dc.type.rimsART-
dc.type.docTypeArticle; Proceedings Paper-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaCrystallography-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryCrystallography-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.subject.keywordPlusPHOTOVOLTAIC CELLS-
dc.subject.keywordPlusEFFICIENT-
dc.subject.keywordPlusPERFORMANCE-
dc.subject.keywordAuthorAbsorption-
dc.subject.keywordAuthorconjugated polymers-
dc.subject.keywordAuthordithienothiophene-
dc.subject.keywordAuthormobility-
dc.subject.keywordAuthororganic photovoltaics-
dc.subject.keywordAuthorsemiconductor-
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