Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/97570
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dc.contributorDepartment of Building and Real Estateen_US
dc.creatorDai, Yen_US
dc.creatorYu, Jen_US
dc.creatorZhang, Zen_US
dc.creatorCheng, Cen_US
dc.creatorTan, Pen_US
dc.creatorShao, Zen_US
dc.creatorNi, Men_US
dc.date.accessioned2023-03-06T01:20:12Z-
dc.date.available2023-03-06T01:20:12Z-
dc.identifier.issn1944-8244en_US
dc.identifier.urihttp://hdl.handle.net/10397/97570-
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.rights© 2021 American Chemical Societyen_US
dc.rightsThis document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Applied Materials and Interfaces, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acsami.0c21859.en_US
dc.subjectElemental redistributionen_US
dc.subjectInterface engineeringen_US
dc.subjectOxygen evolutionen_US
dc.subjectPerovskite oxideen_US
dc.titleInterfacial la diffusion in the CeO2/LaFeO3hybrid for enhanced oxygen evolution activityen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage2799en_US
dc.identifier.epage2806en_US
dc.identifier.volume13en_US
dc.identifier.issue2en_US
dc.identifier.doi10.1021/acsami.0c21859en_US
dcterms.abstractThe electrochemical oxygen evolution reaction (OER) is of great significance for energy conversion and storage. The hybrid strategy is attracting increasing interest for the development of highly active OER electrocatalysts. Regarding the activity enhancement mechanism, electron coupling between two phases in hybrids has been widely reported, but the interfacial elemental redistribution is rarely investigated. Herein, we developed a CeO2/LaFeO3 hybrid electrocatalyst for enhanced OER activity. Interestingly, a selective interfacial La diffusion from LaFeO3 to CeO2 was demonstrated by the electron energy loss spectra and elemental mapping. This redistribution of cations triggers the change of the chemical environment of interface elements for charge compensation because of the electroneutrality principle, which results in increased oxygen vacancies and high-valent Fe species that promote the OER electrocatalysis. This mechanism might be extended to other hybrid systems and inspire the design of more efficient electrocatalysts.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationACS applied materials and interfaces, 20 Jan. 2021, v. 13, no. 2, p. 2799-2806en_US
dcterms.isPartOfACS applied materials and interfacesen_US
dcterms.issued2021-01-20-
dc.identifier.scopus2-s2.0-85099641928-
dc.identifier.pmid33412845-
dc.identifier.eissn1944-8252en_US
dc.description.validate202303 bcww-
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumberBRE-0136-
dc.description.fundingSourceRGCen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS45839356-
dc.description.oaCategoryGreen (AAM)en_US
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