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Acid-Stable Ru Atom Array for Converting Methanol to Methyl Formate at Commercially Viable Current Densities

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dc.contributor.authorLin, Chao-
dc.contributor.authorLi, Ji-Li-
dc.contributor.authorYang, Shuai-
dc.contributor.authorZhao, Tiejun-
dc.contributor.authorKang, Qiang-
dc.contributor.authorWu, Xiaotong-
dc.contributor.authorLi, Xiaopeng-
dc.contributor.authorJiang, Zheng-
dc.contributor.authorLi, Ye-Fei-
dc.contributor.authorLiu, Zhi-Pan-
dc.contributor.authorLuo, Wei-
dc.contributor.authorLee, Jung-Ho-
dc.date.accessioned2023-09-18T05:31:06Z-
dc.date.available2023-09-18T05:31:06Z-
dc.date.issued2023-08-
dc.identifier.issn2155-5435-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/115320-
dc.description.abstractReplacingthe oxidation of water with the electrocatalytic oxidationof methanol is an attractive route to level the cost of H-2 production with value-added chemicals; however, this reaction hasbeen notoriously known for quickly poisoning electrocatalysts and/orsliding into complete oxidation, thereby producing CO2.Here, we report an acid-stable Ru metal atom array that is supportedby MnO2 nanofibers (Ru-MAC/MnO2) for the electrocatalyticvalorization of methanol to methyl formate (MF). The productivityof MF is 10 to 100 times higher than those reported in thermal- andphotocatalytic processes at commercially viable current densities.Our experimental and simulation results demonstrate that the atomarray possesses long-term electrochemical stability and prefers theMF pathway without generating *CO intermediates. The synergistic intersitemetal-metal and metal-support electronic interactionsendow Ru-MAC/MnO2 with outstanding structural stabilitytoward large-current-density methanol electrolysis.-
dc.format.extent12-
dc.language영어-
dc.language.isoENG-
dc.publisherAmerican Chemical Society-
dc.titleAcid-Stable Ru Atom Array for Converting Methanol to Methyl Formate at Commercially Viable Current Densities-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1021/acscatal.3c02644-
dc.identifier.scopusid2-s2.0-85170051356-
dc.identifier.wosid001052045100001-
dc.identifier.bibliographicCitationACS Catalysis, v.13, no.17, pp 11675 - 11686-
dc.citation.titleACS Catalysis-
dc.citation.volume13-
dc.citation.number17-
dc.citation.startPage11675-
dc.citation.endPage11686-
dc.type.docTypeArticle; Early Access-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.subject.keywordPlusIN-SITU-
dc.subject.keywordPlusOXYGEN EVOLUTION-
dc.subject.keywordPlusPERFORMANCE-
dc.subject.keywordPlusADSORPTION-
dc.subject.keywordPlusOXIDATION-
dc.subject.keywordPlusCATALYSTS-
dc.subject.keywordPlusHYDROGEN-
dc.subject.keywordPlusOXIDES-
dc.subject.keywordPlusFTIR-
dc.subject.keywordAuthorelectrocatalysis-
dc.subject.keywordAuthorselective methanol oxidation-
dc.subject.keywordAuthorstability mechanism-
dc.subject.keywordAuthormethyl formate-
dc.subject.keywordAuthorRu metal atomarray-
dc.identifier.urlhttps://pubs.acs.org/doi/10.1021/acscatal.3c02644-
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ERICA 첨단융합대학 (ERICA 신소재·반도체공학전공)
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