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Cation vacancy stabilization of single-atomic-site Pt1/Ni(OH)x catalyst for diboration of alkynes and alkenes.


ABSTRACT: Development of single-atomic-site catalysts with high metal loading is highly desirable but proved to be very challenging. Although utilizing defects on supports to stabilize independent metal atoms has become a powerful method to fabricate single-atomic-site catalysts, little attention has been devoted to cation vacancy defects. Here we report a nickel hydroxide nanoboard with abundant Ni2+ vacancy defects serving as the practical support to achieve a single-atomic-site Pt catalyst (Pt1/Ni(OH)x) containing Pt up to 2.3?wt% just by a simple wet impregnation method. The Ni2+ vacancies are found to have strong stabilizing effect of single-atomic Pt species, which is determined by X-ray absorption spectrometry analyses and density functional theory calculations. This Pt1/Ni(OH)x catalyst shows a high catalytic efficiency in diboration of a variety of alkynes and alkenes, yielding an overall turnover frequency value upon reaction completion for phenylacetylene of ~3000?h-1, which is much higher than other reported heterogeneous catalysts.

SUBMITTER: Zhang J 

PROVIDER: S-EPMC5843605 | biostudies-literature | 2018 Mar

REPOSITORIES: biostudies-literature

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Cation vacancy stabilization of single-atomic-site Pt<sub>1</sub>/Ni(OH)<sub>x</sub> catalyst for diboration of alkynes and alkenes.

Zhang Jian J   Wu Xi X   Cheong Weng-Chon WC   Chen Wenxing W   Lin Rui R   Li Jia J   Zheng Lirong L   Yan Wensheng W   Gu Lin L   Chen Chen C   Peng Qing Q   Wang Dingsheng D   Li Yadong Y  

Nature communications 20180308 1


Development of single-atomic-site catalysts with high metal loading is highly desirable but proved to be very challenging. Although utilizing defects on supports to stabilize independent metal atoms has become a powerful method to fabricate single-atomic-site catalysts, little attention has been devoted to cation vacancy defects. Here we report a nickel hydroxide nanoboard with abundant Ni<sup>2+</sup> vacancy defects serving as the practical support to achieve a single-atomic-site Pt catalyst (  ...[more]

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