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dc.contributor.authorSun, Y.
dc.contributor.authorCao, Y.
dc.contributor.authorWang, , L.
dc.contributor.authorMu, , X.
dc.contributor.authorZhao, Q.
dc.contributor.authorSi, , R.
dc.contributor.authorZhu, , X.
dc.contributor.authorChen, , S.
dc.contributor.authorZhang, , B.
dc.contributor.authorChen, De
dc.contributor.authorWan, Ying
dc.date.accessioned2022-09-01T09:05:44Z
dc.date.available2022-09-01T09:05:44Z
dc.date.created2021-01-28T20:43:45Z
dc.date.issued2020
dc.identifier.citationNature Communications. 2020, 11 1-9.en_US
dc.identifier.issn2041-1723
dc.identifier.urihttps://hdl.handle.net/11250/3015052
dc.description.abstractSupported gold nanoparticles are emerging catalysts for heterogeneous catalytic reactions, including selective hydrogenation. The traditionally used supports such as silica do not favor the heterolytic dissociation of hydrogen on the surface of gold, thus limiting its hydrogenation activity. Here we use gold catalyst particles partially embedded in the pore walls of mesoporous carbon with carbon atoms occupying interstitial sites in the gold lattice. This catalyst allows improved electron transfer from carbon to gold and, when used for the chemoselective hydrogenation of 3-nitrostyrene, gives a three times higher turn-over frequency (TOF) than that for the well-established Au/TiO2 system. The d electron gain of Au is linearly related to the activation entropy and TOF. The catalyst is stable, and can be recycled ten times with negligible loss of both reaction rate and overall conversion. This strategy paves the way for optimizing noble metal catalysts to give an enhanced hydrogenation catalytic performance.en_US
dc.language.isoengen_US
dc.publisherNature Researchen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleGold Catalysts Containing Interstitial Carbon Atoms Boost Hydrogenation Activityen_US
dc.title.alternativeGold Catalysts Containing Interstitial Carbon Atoms Boost Hydrogenation Activityen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber1-9en_US
dc.source.volume11en_US
dc.source.journalNature Communicationsen_US
dc.identifier.doi10.1038/s41467-020-18322-x
dc.identifier.cristin1881708
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2


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