BROWSE

Related Scientist

jinhoon,jeong's photo.

jinhoon,jeong
분자활성촉매반응연구단
more info

ITEM VIEW & DOWNLOAD

Purely organic phosphorescent organic light emitting diodes using alkyl modified phenoselenazine

DC Field Value Language
dc.contributor.authorKim, Cho Long-
dc.contributor.authorJinhoon Jeong-
dc.contributor.authorJang, Ho Jin-
dc.contributor.authorLee, Kyung Hyung-
dc.contributor.authorSeoung-Tae Kim-
dc.contributor.authorMu-Hyun Baik-
dc.contributor.authorLee, Jun Yeob-
dc.date.accessioned2021-08-17T01:50:02Z-
dc.date.accessioned2021-08-17T01:50:02Z-
dc.date.available2021-08-17T01:50:02Z-
dc.date.available2021-08-17T01:50:02Z-
dc.date.created2021-08-09-
dc.date.issued2021-07-14-
dc.identifier.issn2050-7526-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/10113-
dc.description.abstract© The Royal Society of Chemistry 2021.Purely organic phosphorescent emitters have been developed with the incorporation of alkyl substituents into theN-phenylphenoselenazine core. The new emitter displayed efficient phosphorescence in amorphous film and featured pure phosphorescence in electroluminescence devices due to strong spin-orbit coupling for triplet to singlet transition. The steric bulk of the alkyl substituent, which could hamper triplet-exciton-quenching, is found to be essential for high efficiency of the device, and thetert-butyl group induces the highest external quantum efficiency (EQE) of 9.0%.-
dc.language영어-
dc.publisherRoyal Society of Chemistry-
dc.titlePurely organic phosphorescent organic light emitting diodes using alkyl modified phenoselenazine-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000661587800001-
dc.identifier.scopusid2-s2.0-85109370886-
dc.identifier.rimsid76178-
dc.contributor.affiliatedAuthorJinhoon Jeong-
dc.contributor.affiliatedAuthorSeoung-Tae Kim-
dc.contributor.affiliatedAuthorMu-Hyun Baik-
dc.identifier.doi10.1039/d1tc01741a-
dc.identifier.bibliographicCitationJournal of Materials Chemistry C, v.9, no.26, pp.8233 - 8238-
dc.relation.isPartOfJournal of Materials Chemistry C-
dc.citation.titleJournal of Materials Chemistry C-
dc.citation.volume9-
dc.citation.number26-
dc.citation.startPage8233-
dc.citation.endPage8238-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalResearchAreaPhysics-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryPhysics, Applied-
dc.subject.keywordPlusROOM-TEMPERATURE PHOSPHORESCENCE-
dc.subject.keywordPlusDENSITY-FUNCTIONAL THEORY-
dc.subject.keywordPlusCOMPLEXES-
dc.subject.keywordPlusDERIVATIVES-
dc.subject.keywordPlusEFFICIENCY-
Appears in Collections:
Center for Catalytic Hydrocarbon Functionalizations(분자활성 촉매반응 연구단) > 1. Journal Papers (저널논문)
Files in This Item:
There are no files associated with this item.

qrcode

  • facebook

    twitter

  • Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.
해당 아이템을 이메일로 공유하기 원하시면 인증을 거치시기 바랍니다.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse