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Origin of strong red emission in Er3+-based upconversion materials: role of intermediate states and cross relaxation

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dc.contributor.authorLee, Chiho-
dc.contributor.authorPark, Heeyeon-
dc.contributor.authorKim, Woong-
dc.contributor.authorPark, Sungnam-
dc.date.accessioned2021-08-31T23:02:31Z-
dc.date.available2021-08-31T23:02:31Z-
dc.date.created2021-06-18-
dc.date.issued2019-11-21-
dc.identifier.issn1463-9076-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/61552-
dc.description.abstractAmong the various upconversion (UC) materials, sodium yttrium fluoride doped with ytterbium and erbium (NaYF4:Yb3+,Er3+) is the most widely studied owing to its high UC efficiency. Nonetheless, UC mechanisms are not yet fully understood and, in particular, near-infrared-to-red UC mechanisms are still under debate. Herein, we examine UC mechanisms in Er3+-based UC materials. Most importantly, the F-4(3/2) and F-4(5/2) states of Er3+ were found to be important intermediate states for strong red emission, for the first time. The cross relaxation between the Er3+ ions, back energy transfer from Er3+ to Yb3+, and relative doping concentrations of Er3+ and Yb3+ in NaYF4:Yb3+,Er3+ were found to play important roles in the relative intensity between red and green emissions. The proposed UC mechanism will provide design principles for various Er3+-based UC materials.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherROYAL SOC CHEMISTRY-
dc.subjectDOPANT-CONTROLLED SYNTHESIS-
dc.subjectLANTHANIDE-DOPED NAYF4-
dc.subjectCHARGE-TRANSFER-
dc.subjectNANOPARTICLES-
dc.subjectLUMINESCENCE-
dc.subjectNANOCRYSTALS-
dc.subjectCORE-
dc.subjectNANOPHOSPHORS-
dc.subjectFLUORESCENCE-
dc.subjectENHANCEMENT-
dc.titleOrigin of strong red emission in Er3+-based upconversion materials: role of intermediate states and cross relaxation-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Woong-
dc.contributor.affiliatedAuthorPark, Sungnam-
dc.identifier.doi10.1039/c9cp04692e-
dc.identifier.scopusid2-s2.0-85074676263-
dc.identifier.wosid000496151800019-
dc.identifier.bibliographicCitationPHYSICAL CHEMISTRY CHEMICAL PHYSICS, v.21, no.43, pp.24026 - 24033-
dc.relation.isPartOfPHYSICAL CHEMISTRY CHEMICAL PHYSICS-
dc.citation.titlePHYSICAL CHEMISTRY CHEMICAL PHYSICS-
dc.citation.volume21-
dc.citation.number43-
dc.citation.startPage24026-
dc.citation.endPage24033-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaPhysics-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryPhysics, Atomic, Molecular & Chemical-
dc.subject.keywordPlusDOPANT-CONTROLLED SYNTHESIS-
dc.subject.keywordPlusLANTHANIDE-DOPED NAYF4-
dc.subject.keywordPlusCHARGE-TRANSFER-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusLUMINESCENCE-
dc.subject.keywordPlusNANOCRYSTALS-
dc.subject.keywordPlusCORE-
dc.subject.keywordPlusNANOPHOSPHORS-
dc.subject.keywordPlusFLUORESCENCE-
dc.subject.keywordPlusENHANCEMENT-
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