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dc.contributor.authorKumar, Rangaraju Satish-
dc.contributor.authorJeong, Hansol-
dc.contributor.authorJeong, Jaemyeng-
dc.contributor.authorChitumalla, Ramesh Kumar-
dc.contributor.authorKo, Min Jae-
dc.contributor.authorKumar, Kempahanumakkagaari Suresh-
dc.contributor.authorJang, Joonkyung-
dc.contributor.authorSon, Young-A.-
dc.date.accessioned2024-01-20T04:32:07Z-
dc.date.available2024-01-20T04:32:07Z-
dc.date.created2022-01-25-
dc.date.issued2016-04-
dc.identifier.issn2046-2069-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/124196-
dc.description.abstractHerein, we report porphyrin sensitizers for DSSCs, coded CNU-0C8 and CNU-TBU, which were synthesized using a donor-pi-bridge-acceptor approach. The porphyrin sensitizers were subjected to electrochemical experiments to study their electron distribution, intramolecular charge transfer and HOMO-LUMO levels. The optical and photovoltaic properties of these synthesized porphyrins were measured and compared with those of the YD2-OC8 benchmark dye. To further characterize, we simulated the electrochemical and optical properties of the dyes, which are perfectly in agreement with the experimental data. The new CNU-0C8 and CNU-TBU porphyrin sensitizers provided power conversion efficiencies of 6.49% and 3.19%, respectively, compared to a conversion efficiency of 6.10% for YD2-0C8 under similar conditions. These results indicate that CNU-0C8 exhibits better photovoltaic performance than the benchmark YD2-0C8 sensitizer in a liquid 1(-)/I-3(-) redox electrolyte.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleSynthesis of porphyrin sensitizers with a thiazole group as an efficient pi-spacer: potential application in dye-sensitized solar cells-
dc.typeArticle-
dc.identifier.doi10.1039/c6ra00353b-
dc.description.journalClass1-
dc.identifier.bibliographicCitationRSC ADVANCES, v.6, no.47, pp.41294 - 41303-
dc.citation.titleRSC ADVANCES-
dc.citation.volume6-
dc.citation.number47-
dc.citation.startPage41294-
dc.citation.endPage41303-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000375270600084-
dc.identifier.scopusid2-s2.0-84968901385-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusEFFECTIVE CORE POTENTIALS-
dc.subject.keywordPlusAB-INITIO-
dc.subject.keywordPlusMOLECULAR CALCULATIONS-
dc.subject.keywordPlusTRIPHENYLAMINE DONOR-
dc.subject.keywordPlusANCHORING GROUP-
dc.subject.keywordPlusDESIGN-
dc.subject.keywordPlusTIO2-
dc.subject.keywordPlusCONTINUUM-
dc.subject.keywordPlusELEMENTS-
dc.subject.keywordPlusACCEPTOR-
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KIST Article > 2016
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