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A New Benzodithiophene Based Donor-Acceptor pi-Conjugated Polymer for Organic Solar Cells

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dc.contributor.authorReddy, Saripally Sudhaker-
dc.contributor.authorAryal, Um Kanta-
dc.contributor.authorJin, Hyunjung-
dc.contributor.authorGokulnath, Thavamani-
dc.contributor.authorRajalapati, Durga Gayathri-
dc.contributor.authorKranthiraja, Kakaraparthi-
dc.contributor.authorShin, Sung Tae-
dc.contributor.authorJin, Sung-Ho-
dc.date.accessioned2021-08-31T11:43:49Z-
dc.date.available2021-08-31T11:43:49Z-
dc.date.created2021-06-18-
dc.date.issued2020-02-
dc.identifier.issn1598-5032-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/57927-
dc.description.abstractA new benzodithiophene based donor-acceptor pi-conjugated polymer (P1) is designed and explored as the photoactive donor for organic solar cells (OSCs). The synthesized donor polymer, P1 displays a wide absorption profile ranging from 300-750 nm with optical band gap of 1.61 eV and moderate ionization potential of -5.30 eV. It has good solubility in non-halogenated and halogenated organic solvents. Next, we fabricated OSCs with P1 by blending with PC71BM, the pristine polymer processed from chlorobenzene showed PCE of 2.79%. Upon addition of external additive diphenyl ether to the blend showed a dramatic improvement in PCE with maximum of 5.33%. DPE tailored the active layer morphology and showed two times higher PCE than pristine films. These results clearly indicate that the new polymer has a great potentiality for enhancing efficiency upon solvent additives, which will provide new routes for the development of new class of polymers for high-performance air-stable OSCs.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherPOLYMER SOC KOREA-
dc.subjectBAND-GAP POLYMERS-
dc.subjectSIDE-CHAIN-
dc.subjectEFFICIENCY-
dc.subjectNETWORK-
dc.titleA New Benzodithiophene Based Donor-Acceptor pi-Conjugated Polymer for Organic Solar Cells-
dc.typeArticle-
dc.contributor.affiliatedAuthorShin, Sung Tae-
dc.identifier.doi10.1007/s13233-020-8079-z-
dc.identifier.scopusid2-s2.0-85079674538-
dc.identifier.wosid000515005700013-
dc.identifier.bibliographicCitationMACROMOLECULAR RESEARCH, v.28, no.2, pp.179 - 183-
dc.relation.isPartOfMACROMOLECULAR RESEARCH-
dc.citation.titleMACROMOLECULAR RESEARCH-
dc.citation.volume28-
dc.citation.number2-
dc.citation.startPage179-
dc.citation.endPage183-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.identifier.kciidART002558092-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaPolymer Science-
dc.relation.journalWebOfScienceCategoryPolymer Science-
dc.subject.keywordPlusBAND-GAP POLYMERS-
dc.subject.keywordPlusSIDE-CHAIN-
dc.subject.keywordPlusEFFICIENCY-
dc.subject.keywordPlusNETWORK-
dc.subject.keywordAuthorbenzodithiophene based pi-conjugated polymer-
dc.subject.keywordAuthoroctyl side chain-
dc.subject.keywordAuthororganic solar cell-
dc.subject.keywordAuthormorphology-
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