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Redox-Sensitive Facet Dependency in Etching of Ceria Nanocrystals Directly Observed by Liquid Cell TEM

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dc.contributor.authorSung, Jongbaek-
dc.contributor.authorChoi, Back Kyu-
dc.contributor.authorKim, Byunghoon-
dc.contributor.authorKim, Byung Hyo-
dc.contributor.authorKim, Joodeok-
dc.contributor.authorLee, Donghoon-
dc.contributor.authorKim, Sungin-
dc.contributor.authorKang, Kisuk-
dc.contributor.authorHyeon, Taeghwan-
dc.contributor.authorPark, Jungwon-
dc.date.accessioned2020-04-25T07:41:10Z-
dc.date.available2020-04-25T07:41:10Z-
dc.date.created2020-02-13-
dc.date.created2020-02-13-
dc.date.issued2019-11-
dc.identifier.citationJournal of the American Chemical Society, Vol.141 No.46, pp.18395-18399-
dc.identifier.issn0002-7863-
dc.identifier.other90888-
dc.identifier.urihttps://hdl.handle.net/10371/164952-
dc.description.abstractDefining the redox activity of different surface facets of ceria nanocrystals is important for designing an efficient catalyst. Especially in liquid-phase reactions, where surface interactions are complicated, direct investigation in a native environment is required to understand the facet-dependent redox properties. Using liquid cell TEM, we herein observed the etching of ceria-based nanocrystals under the control of redox-governing factors. Direct nanoscale observation reveals facet-dependent etching kinetics, thus identifying the specific facet ({100} for reduction and {111} for oxidation) that governs the overall etching under different chemical conditions. Under each redox condition, the contribution of the predominant facet increases as the etching reactivity increases.-
dc.language영어-
dc.publisherAmerican Chemical Society-
dc.titleRedox-Sensitive Facet Dependency in Etching of Ceria Nanocrystals Directly Observed by Liquid Cell TEM-
dc.typeArticle-
dc.contributor.AlternativeAuthor박정원-
dc.contributor.AlternativeAuthor강기석-
dc.contributor.AlternativeAuthor현택환-
dc.identifier.doi10.1021/jacs.9b09508-
dc.citation.journaltitleJournal of the American Chemical Society-
dc.identifier.wosid000499738700007-
dc.identifier.scopusid2-s2.0-85074226069-
dc.citation.endpage18399-
dc.citation.number46-
dc.citation.startpage18395-
dc.citation.volume141-
dc.identifier.sci000499738700007-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorKang, Kisuk-
dc.contributor.affiliatedAuthorHyeon, Taeghwan-
dc.contributor.affiliatedAuthorPark, Jungwon-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusIN-SITU-
dc.subject.keywordPlusPALLADIUM NANOCRYSTALS-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusDISSOLUTION-
dc.subject.keywordPlusSURFACES-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordPlusREACTIVITY-
dc.subject.keywordPlusOXIDATION-
dc.subject.keywordPlusDEFECTS-
dc.subject.keywordPlusCEO2-
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  • College of Engineering
  • School of Chemical and Biological Engineering
Research Area Chemistry, Materials Science

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