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Synthesis of dipyrrolopyrazine-based sensitizers with a new pi-bridge end-capped donor-acceptor framework for DSSCs: a combined experimental and theoretical investigation

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dc.contributor.authorMeti, Puttavva-
dc.contributor.authorNagaraju, Goli-
dc.contributor.authorYang, Jung-Won-
dc.contributor.authorJung, Sun Hwa-
dc.contributor.authorGong, Young-Dae-
dc.date.accessioned2023-04-28T05:40:37Z-
dc.date.available2023-04-28T05:40:37Z-
dc.date.issued2019-02-21-
dc.identifier.issn1144-0546-
dc.identifier.issn1369-9261-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/8386-
dc.description.abstractThe strategy of developing organic dyes with exceptional optical, thermal, and stable photovoltaic properties has attracted substantial attention in the replacement of high-cost traditional dyes in DSSCs. Herein, we synthesized four dyes with a D-pi-A configuration in order to study the variation produced in the optical, thermal, redox and photovoltaic properties by substitution of different donors and acceptors in the dipyrrolopyrazine (DPP) system. These push-pull systems are based on a pyrrolopyrazine spacer, end-capped with donors (N,N-dimethylamine, and thiophene) and acceptors (pyridine, -COOH, and -CN). The multidisciplinary study concerning the optical, thermal, redox, and photovoltaic characterization of the dyes reveals that compound 3a exhibits the best overall conversion efficiency as a sensitizer in TiO2 dye sensitized solar cells. The theoretical calculations together with experimental data allow us to quantify the charge transfer character of dyes.-
dc.format.extent9-
dc.language영어-
dc.language.isoENG-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleSynthesis of dipyrrolopyrazine-based sensitizers with a new pi-bridge end-capped donor-acceptor framework for DSSCs: a combined experimental and theoretical investigation-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1039/c8nj06083e-
dc.identifier.scopusid2-s2.0-85061372002-
dc.identifier.wosid000459944500020-
dc.identifier.bibliographicCitationNEW JOURNAL OF CHEMISTRY, v.43, no.7, pp 3017 - 3025-
dc.citation.titleNEW JOURNAL OF CHEMISTRY-
dc.citation.volume43-
dc.citation.number7-
dc.citation.startPage3017-
dc.citation.endPage3025-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusFREE ORGANIC-DYES-
dc.subject.keywordPlusSOLAR-CELLS-
dc.subject.keywordPlusPHOTOVOLTAIC PERFORMANCE-
dc.subject.keywordPlusFLUORESCENT DYES-
dc.subject.keywordPlusSMALL MOLECULES-
dc.subject.keywordPlusEFFICIENT-
dc.subject.keywordPlusTIO2-
dc.subject.keywordPlusCHROMOPHORE-
dc.subject.keywordPlusDESIGN-
dc.subject.keywordPlusPHOTOCURRENT-
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