Please use this identifier to cite or link to this item: https://doi.org/10.1039/D1CY00273B
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dc.titleOxidation of methane to methanol over Pd@Pt nanoparticles under mild conditions in water
dc.contributor.authorChen Jianjun
dc.contributor.authorWang Sikai
dc.contributor.authorLaurent Peres
dc.contributor.authorVincent Colliere
dc.contributor.authorKarine Philippot
dc.contributor.authorPierre Lecante
dc.contributor.authorChen Yaoqiang
dc.contributor.authorYan Ning
dc.date.accessioned2021-08-16T07:10:00Z
dc.date.available2021-08-16T07:10:00Z
dc.date.issued2021-03-19
dc.identifier.citationChen Jianjun, Wang Sikai, Laurent Peres, Vincent Colliere, Karine Philippot, Pierre Lecante, Chen Yaoqiang, Yan Ning (2021-03-19). Oxidation of methane to methanol over Pd@Pt nanoparticles under mild conditions in water. ScholarBank@NUS Repository. https://doi.org/10.1039/D1CY00273B
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/197109
dc.description.abstractDirect methane oxidation into oxygen-containing chemicals under mild conditions has sparked increasing interest. Here, we report Pd@Pt core–shell nanoparticles that efficiently catalyse the direct oxidation of CH4 to CH3OH in water using H2O2 as an oxidant under mild conditions. The catalyst presents a methanol productivity of up to 89.3 mol kgcatalyst−1 h−1 with a high selectivity of 92.4% after 30 min at 50 °C, thus outperforming most of the previously reported catalysts. Electron-enriched Pt species in the Pd@Pt nanoparticles were identified by structural and electronic analysis. Pd in the core donates electrons to Pt, leading to higher rates of methane activation. Based on the results of control experiments and kinetic analysis, a consecutive oxidation pathway via a radical mechanism is proposed, which includes initial formation of CH3OOH and CH3OH followed by further oxidation of CH3OH to HCHO, HCOOH, and CO2.
dc.description.urihttps://pubs-rsc-org.libproxy1.nus.edu.sg/en/content/articlelanding/2021/cy/d1cy00273b/unauth#!divAbstract
dc.language.isoen
dc.publisherRoyal Society of Chemistry
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1039/D1CY00273B
dc.published.statePublished
dc.grant.fundingagencyThe French National Agency for Research and the Singapore National Research Foundation
dc.relation.dataset10.1039/D1CY00273B
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