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Mesoporous sulfur-decorated Pt–Al2O3 for dehydrogenation of perhydro benzyltoluenes: Activity-favorable adsorption of reaction species onto electron-deficient Pt atoms

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dc.contributor.authorJo, Yeongin-
dc.contributor.authorKim, Tae Won-
dc.contributor.authorOh, Jinho-
dc.contributor.authorKim, Donghyeon-
dc.contributor.authorSuh, Young Woong-
dc.date.accessioned2024-01-16T13:35:23Z-
dc.date.available2024-01-16T13:35:23Z-
dc.date.issued2022-09-
dc.identifier.issn0021-9517-
dc.identifier.issn1090-2694-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/194642-
dc.description.abstractThe addition of sulfur to supported Pt catalysts often regulates Pt defect sites causing side reactions, where the interaction between Pt and sulfur depends on catalyst preparation methods. Herein, we report the solvent-deficient precipitation (SDP) to afford mesoporous sulfur-decorated Pt–Al2O3 catalysts with different sulfur contents. In the dehydrogenation of perhydro benzyltoluenes, the degree of dehydrogenation shows the volcano-shaped dependence on the sulfur content at the maximum with 0.21 wt% sulfur. The best performance catalyst is robust in recycle runs owing to negligible Pt growth and sulfur loss. The sulfur added lowers the electron density of Pt atoms because of the favorable contact between Pt and sulfur species by the SDP method compared to the conventional impregnation. The electron-deficient Pt atoms weaken the adsorption of aromatic products and induce appropriate H2 adsorption. Thus, the titled catalyst is tolerant to the dehydrogenation products and less selective to the side product methylfluorene.-
dc.format.extent11-
dc.language영어-
dc.language.isoENG-
dc.publisherAcademic Press-
dc.titleMesoporous sulfur-decorated Pt–Al2O3 for dehydrogenation of perhydro benzyltoluenes: Activity-favorable adsorption of reaction species onto electron-deficient Pt atoms-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1016/j.jcat.2022.06.025-
dc.identifier.scopusid2-s2.0-85132736802-
dc.identifier.wosid000833527600002-
dc.identifier.bibliographicCitationJournal of Catalysis, v.413, pp 127 - 137-
dc.citation.titleJournal of Catalysis-
dc.citation.volume413-
dc.citation.startPage127-
dc.citation.endPage137-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryEngineering, Chemical-
dc.subject.keywordPlusORGANIC HYDROGEN CARRIER-
dc.subject.keywordPlusCATALYTIC DEHYDROGENATION-
dc.subject.keywordPlusHIGHLY EFFICIENT-
dc.subject.keywordPlusCHEMICAL-STATE-
dc.subject.keywordPlusPLATINUM-
dc.subject.keywordPlusRELEASE-
dc.subject.keywordPlusALUMINA-
dc.subject.keywordPlusSULFURIZATION-
dc.subject.keywordPlusDEPENDENCE-
dc.subject.keywordPlusISOBUTANE-
dc.subject.keywordAuthorLiquid organic hydrogen carrier-
dc.subject.keywordAuthorDehydrogenation-
dc.subject.keywordAuthorSupported Pt catalysts-
dc.subject.keywordAuthorSulfur decoration-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0021951722002603?via%3Dihub-
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