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Efficient Diketopyrrolopyrrole-Based Small-Molecule Bulk-Heterojunction Solar Cells with Different Electron-Donating End-Groups

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dc.contributor.authorKim, Yu Jin-
dc.contributor.authorBack, Jang Yeol-
dc.contributor.authorKim, Seul-Ong-
dc.contributor.authorJeon, Chan-Woo-
dc.contributor.authorPark, Chan Eon-
dc.contributor.authorKim, Yun-Hi-
dc.date.accessioned2022-12-26T23:02:41Z-
dc.date.available2022-12-26T23:02:41Z-
dc.date.issued2014-09-
dc.identifier.issn1861-4728-
dc.identifier.issn1861-471X-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/18818-
dc.description.abstractA series of small molecules that contained identical pi-spacers (ethyne), a central diketopyrrolopyrrole (DPP) unit, and different aromatic electron-donating end-groups were synthesized and used in organic solar cells (OSCs) to study the effect of electron-donating groups on the device performance. The three compounds, DPP-A-Ph, DPP-A-Na, and DPP-A-An, possessed intense absorption bands that covered a wide range, from 350 to 750 nm, and relatively low HOMO energy levels, from -5.50 to -5.55 eV. DPP-A-An, which contained anthracene end-groups, demonstrated a stronger absorbance and a higher hole mobility than DPP-A-Ph, which contained phenyl groups, and DPP-A-Na, which contained naphthalene units. The power-conversion efficiencies (PCEs) of OSCs based on organic: PC71BM blends (1: 1, w/w) with a processed DIO additive were 3.93% for DPP-A-An, 3.02% for DPP-Na, and 2.26% for DPP-A-Ph. These findings suggest that a DPP core that is functionalized with electron-donating capping groups constitutes a promising new class of solution-processable small molecules for OSC applications.-
dc.format.extent9-
dc.language영어-
dc.language.isoENG-
dc.publisherWiley - V C H Verlag GmbbH & Co.-
dc.titleEfficient Diketopyrrolopyrrole-Based Small-Molecule Bulk-Heterojunction Solar Cells with Different Electron-Donating End-Groups-
dc.typeArticle-
dc.publisher.location독일-
dc.identifier.doi10.1002/asia.201402223-
dc.identifier.scopusid2-s2.0-84935835339-
dc.identifier.wosid000342677400024-
dc.identifier.bibliographicCitationChemistry - An Asian Journal, v.9, no.9, pp 2505 - 2513-
dc.citation.titleChemistry - An Asian Journal-
dc.citation.volume9-
dc.citation.number9-
dc.citation.startPage2505-
dc.citation.endPage2513-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusHIGH FILL FACTORS-
dc.subject.keywordPlusORGANIC SEMICONDUCTORS-
dc.subject.keywordPlusBENZODITHIOPHENE UNIT-
dc.subject.keywordPlusCONJUGATED POLYMERS-
dc.subject.keywordPlusSIDE-CHAIN-
dc.subject.keywordPlusPERFORMANCE-
dc.subject.keywordPlusDESIGN-
dc.subject.keywordPlusENERGY-
dc.subject.keywordPlusTRANSISTOR-
dc.subject.keywordPlusSEPARATION-
dc.subject.keywordAuthorabsorption-
dc.subject.keywordAuthoralkynes-
dc.subject.keywordAuthorconjugation-
dc.subject.keywordAuthorcross-coupling-
dc.subject.keywordAuthorsolar cells-
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