Please use this identifier to cite or link to this item: https://doi.org/10.1038/s41467-018-05754-9
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dc.titleAtomic engineering of high-density isolated Co atoms on graphene with proximal-atom controlled reaction selectivity
dc.contributor.authorYan H.
dc.contributor.authorZhao X.
dc.contributor.authorGuo N.
dc.contributor.authorLyu Z.
dc.contributor.authorDu Y.
dc.contributor.authorXi S.
dc.contributor.authorGuo R.
dc.contributor.authorChen C.
dc.contributor.authorChen Z.
dc.contributor.authorLiu W.
dc.contributor.authorYao C.
dc.contributor.authorLi J.
dc.contributor.authorPennycook S.J.
dc.contributor.authorChen W.
dc.contributor.authorSu C.
dc.contributor.authorZhang C.
dc.contributor.authorLu J.
dc.date.accessioned2019-03-08T01:10:07Z
dc.date.available2019-03-08T01:10:07Z
dc.date.issued2018-12-01
dc.identifier.citationYan H., Zhao X., Guo N., Lyu Z., Du Y., Xi S., Guo R., Chen C., Chen Z., Liu W., Yao C., Li J., Pennycook S.J., Chen W., Su C., Zhang C., Lu J. (2018-12-01). Atomic engineering of high-density isolated Co atoms on graphene with proximal-atom controlled reaction selectivity. Nature Communications 9 (1) : 3197. ScholarBank@NUS Repository. https://doi.org/10.1038/s41467-018-05754-9
dc.identifier.issn2041-1723
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/152068
dc.description.abstractControllable synthesis of single atom catalysts (SACs) with high loading remains challenging due to the aggregation tendency of metal atoms as the surface coverage increases. Here we report the synthesis of graphene supported cobalt SACs (Co1/G) with a tuneable high loading by atomic layer deposition. Ozone treatment of the graphene support not only eliminates the undesirable ligands of the pre-deposited metal precursors, but also regenerates active sites for the precise tuning of the density of Co atoms. The Co1/G SACs also demonstrate exceptional activity and high selectivity for the hydrogenation of nitroarenes to produce azoxy aromatic compounds, attributable to the formation of a coordinatively unsaturated and positively charged catalytically active center (Co朞朇) arising from the proximal-atom induced partial depletion of the 3d Co orbitals. Our findings pave the way for the precise engineering of the metal loading in a variety of SACs for superior catalytic activities. � 2018, The Author(s).
dc.publisherNature Publishing Group
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.contributor.departmentMATERIALS SCIENCE AND ENGINEERING
dc.contributor.departmentDEPT OF PHYSICS
dc.description.doi10.1038/s41467-018-05754-9
dc.description.sourcetitleNature Communications
dc.description.volume9
dc.description.issue1
dc.description.page3197
dc.published.statepublished
dc.grant.idR-143-000-621-133
dc.grant.idR-143-000-637-112
dc.grant.idR-143-000-A06-112
dc.grant.id91645102
dc.grant.id51502174
dc.grant.id827-000113, KQTD2016053112042971
dc.grant.idNRF-CRP13-2014-03
dc.grant.idNRF-CRP16-2015-02
dc.grant.id2017M610541
dc.grant.fundingagencyNUS start-up
dc.grant.fundingagencyTier 1
dc.grant.fundingagencyMOE Tier 2
dc.grant.fundingagencyNSFC
dc.grant.fundingagencyNNSFC
dc.grant.fundingagencyShenzhen Peacock Plan
dc.grant.fundingagencySingapore National Research Foundation
dc.grant.fundingagencyChina Postdoctoral Science Foundation
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