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dc.contributor.authorPark, Kwangho-
dc.contributor.authorLee, Kyung Rok-
dc.contributor.authorAhn, Sunghee-
dc.contributor.authorVan Nguyen, Canh-
dc.contributor.authorJung, Kwang- Deog-
dc.date.accessioned2024-03-13T07:30:04Z-
dc.date.available2024-03-13T07:30:04Z-
dc.date.created2024-03-13-
dc.date.issued2024-06-
dc.identifier.issn0926-3373-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/149459-
dc.description.abstractThis study explores the fabrication and characterization of mesoporous nitrogen -doped carbon replicas (MNCs) as Ru catalyst supports for CO2 hydrogenation to formate. MNC supports with a cubic Ia3d-like structure were successfully synthesized from a KIT -6 template. The mesoporosity, N content, and N states in the MNCs differed according to the precursor type, which substantially influenced the stability of single -atom Ru catalysts during CO2 conversion. In hydrogenation tests, the Ru/MNC prepared using acrylonitrile precursor (Ru/MNC-A) demonstrated the best stability, whereas the Ru/MNCs prepared using pyrrole and melamine exhibited low activity owing to Ru agglomeration and limited reactant diffusion, respectively. The excellent stability of Ru/ MNC-A resulted from Ru migration and rearrangement, as evidenced by near edge X-ray absorption fine structure analyses. Ru/MNC-A and Ru/MNC-A-400 achieved an outstanding turnover number of 69,000 in CO2 hydrogenation over 72 h. Remarkably, the Ru/MNC-A catalyst demonstrated exceptional stability, attaining a TON of 315,840 over 360 h.-
dc.languageEnglish-
dc.publisherElsevier BV-
dc.titleEffects of the chemical states of N sites and mesoporosity of N-doped carbon supports on single-atom Ru catalysts during CO2-to-formate conversion-
dc.typeArticle-
dc.identifier.doi10.1016/j.apcatb.2024.123751-
dc.description.journalClass1-
dc.identifier.bibliographicCitationApplied Catalysis B: Environment and Energy, v.346-
dc.citation.titleApplied Catalysis B: Environment and Energy-
dc.citation.volume346-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid001171809500001-
dc.identifier.scopusid2-s2.0-85182887727-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryEngineering, Environmental-
dc.relation.journalWebOfScienceCategoryEngineering, Chemical-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaEngineering-
dc.type.docTypeArticle-
dc.subject.keywordPlusCO2 HYDROGENATION-
dc.subject.keywordPlusFORMIC-ACID-
dc.subject.keywordPlusDIOXIDE-
dc.subject.keywordPlusFORMATE-
dc.subject.keywordPlusFRAMEWORKS-
dc.subject.keywordPlusMETHANOL-
dc.subject.keywordAuthorCO 2 hydrogenation-
dc.subject.keywordAuthorHydrogen storage-
dc.subject.keywordAuthorFormic acid-
dc.subject.keywordAuthorFormate-
dc.subject.keywordAuthorHeterogeneous catalysis-
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