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

  • Jian Zhang
  • , Xi Wu
  • , Weng Chon Cheong
  • , Wenxing Chen
  • , Rui Lin
  • , Jia Li
  • , Lirong Zheng
  • , Wensheng Yan
  • , Lin Gu
  • , Chen Chen
  • , Qing Peng
  • , Dingsheng Wang*
  • , Yadong Li
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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.

Original languageEnglish
Article number1002
JournalNature Communications
Volume9
Issue number1
DOIs
Publication statusPublished - 1 Dec 2018
Externally publishedYes

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