Splitting of Hydrogen Atoms into Proton-Electron Pairs at BaO-Ru Interfaces for Promoting Ammonia Synthesis under Mild Conditions

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dc.contributor.authorBaik, Yaejunko
dc.contributor.authorKwen, Minjaeko
dc.contributor.authorLee, Kyunghoko
dc.contributor.authorChi, Seunghyuckko
dc.contributor.authorLee, Susungko
dc.contributor.authorCho, Kangheeko
dc.contributor.authorKim, Hyungjunko
dc.contributor.authorChoi, Minkeeko
dc.date.accessioned2023-07-13T03:00:12Z-
dc.date.available2023-07-13T03:00:12Z-
dc.date.created2023-07-13-
dc.date.created2023-07-13-
dc.date.issued2023-05-
dc.identifier.citationJOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.145, no.20, pp.11364 - 11374-
dc.identifier.issn0002-7863-
dc.identifier.urihttp://hdl.handle.net/10203/310484-
dc.description.abstractRu catalysts promoted with alkali and alkaline earthhave shownsuperior ammonia (NH3) synthesis activities under mildconditions. Although these promoters play a vital role in enhancingcatalytic activity, their function has not been clearly understood.Here, we synthesize a series of Ba-Ru/MgO catalysts with an optimalRu particle size (similar to 2.3 nm) and tailored BaO-Ru interfacialstructures. We discover that the promoting effect is created throughthe separate storage of H+/e(-) pairs atthe BaO-Ru interface. Chemisorbed H atoms on Ru dissociateinto H+/e(-) pairs at the BaO-Ruinterface, where strongly basic, nonreducible BaO selectively capturesH(+) while leaving e(-) on Ru. The resultingelectron accumulation in Ru facilitates N-2 activation viaenhanced pi-backdonation and inhibits hydrogen poisoning duringNH(3) synthesis. Consequently, the formation of intimateBaO-Ru interface without an excessive loss of accessible Rusites enables the synthesis of highly active catalysts for NH3 synthesis.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.titleSplitting of Hydrogen Atoms into Proton-Electron Pairs at BaO-Ru Interfaces for Promoting Ammonia Synthesis under Mild Conditions-
dc.typeArticle-
dc.identifier.wosid001009355900001-
dc.identifier.scopusid2-s2.0-85160003555-
dc.type.rimsART-
dc.citation.volume145-
dc.citation.issue20-
dc.citation.beginningpage11364-
dc.citation.endingpage11374-
dc.citation.publicationnameJOURNAL OF THE AMERICAN CHEMICAL SOCIETY-
dc.identifier.doi10.1021/jacs.3c02529-
dc.contributor.localauthorKim, Hyungjun-
dc.contributor.localauthorChoi, Minkee-
dc.contributor.nonIdAuthorKwen, Minjae-
dc.contributor.nonIdAuthorLee, Kyungho-
dc.contributor.nonIdAuthorChi, Seunghyuck-
dc.contributor.nonIdAuthorLee, Susung-
dc.contributor.nonIdAuthorCho, Kanghee-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordPlusTOTAL-ENERGY CALCULATIONS-
dc.subject.keywordPlusRUTHENIUM CATALYSTS-
dc.subject.keywordPlusLOW-CRYSTALLINE-
dc.subject.keywordPlusBARIUM-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusSUPPORT-
dc.subject.keywordPlusOXIDE-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusSENSITIVITY-
dc.subject.keywordPlusEFFICIENCY-
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CH-Journal Papers(저널논문)CBE-Journal Papers(저널논문)
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