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Azasiline-based thermally activated delayed fluorescence emitters for blue organic light emitting diodes

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dc.contributor.authorSun, Jin Won-
dc.contributor.authorBaek, Jang Yeol-
dc.contributor.authorKim, Kwon-Hyeon-
dc.contributor.authorHuh, Jin-Suk-
dc.contributor.authorKwon, Soon-Ki-
dc.contributor.authorKim, Yun-Hi-
dc.contributor.authorKim, Jang-Joo-
dc.date.accessioned2022-12-26T18:49:52Z-
dc.date.available2022-12-26T18:49:52Z-
dc.date.issued2017-02-
dc.identifier.issn2050-7526-
dc.identifier.issn2050-7534-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/13887-
dc.description.abstractRecently, the azasiline unit was introduced as a donor in thermally activated delayed fluorescence (TADF) emitters to realize efficient blue fluorescence from organic light emitting diodes (OLEDs). Utilizing the azasiline unit DTPPDDA in the formation of donor-connector-acceptor (D-C-A) materials resulted in deep blue emission with a Commission Internationale de l'Eclairage (CIE) coordinate of (0.151, 0.087), close to the blue standard of the National Television System Committee (NTSC) of (0.140, 0.080) with 4.7% External Quantum Efficiency (EQE). In the donor-acceptor-donor (D-A-D) type materials of BDAPM and SPDDA, carbonyl and sulfone units were used as the acceptors, respectively. The sulfonyl unit contributed to a large twist of the molecular structure while the carbonyl unit led to a small twist of the molecular structure. As a result, the blue fluorescent OLEDs containing BDAPM and SPDDA demonstrated 11.4% and 2.3% EQEs with CIE Y-values of 0.310 and 0.107, respectively.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherRoyal Society of Chemistry-
dc.titleAzasiline-based thermally activated delayed fluorescence emitters for blue organic light emitting diodes-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1039/c6tc04653c-
dc.identifier.scopusid2-s2.0-85011256387-
dc.identifier.wosid000395887300003-
dc.identifier.bibliographicCitationJournal of Materials Chemistry C, v.5, no.5, pp 1027 - 1032-
dc.citation.titleJournal of Materials Chemistry C-
dc.citation.volume5-
dc.citation.number5-
dc.citation.startPage1027-
dc.citation.endPage1032-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalResearchAreaPhysics-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryPhysics, Applied-
dc.subject.keywordPlusEXTERNAL QUANTUM EFFICIENCY-
dc.subject.keywordPlusCHARGE-TRANSFER COMPOUNDS-
dc.subject.keywordPlusCROSS-COUPLING REACTIONS-
dc.subject.keywordPlusDEVICES-
dc.subject.keywordPlusELECTROLUMINESCENCE-
dc.subject.keywordPlusDESIGN-
dc.subject.keywordPlusGREEN-
dc.subject.keywordPlusORIENTATION-
dc.subject.keywordPlusPREDICTION-
dc.subject.keywordPlusMOLECULES-
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