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The active sites of Cu–ZnO catalysts for water gas shift and CO hydrogenation reactions

  • Zhenhua Zhang
  • , Xuanye Chen
  • , Jincan Kang
  • , Zongyou Yu
  • , Jie Tian
  • , Zhongmiao Gong
  • , Aiping Jia
  • , Rui You
  • , Kun Qian
  • , Shun He
  • , Botao Teng
  • , Yi Cui
  • , Ye Wang*
  • , Wenhua Zhang*
  • , Weixin Huang*
  • *Corresponding author for this work
  • University of Science and Technology of China
  • Zhejiang Normal University
  • Xiamen University
  • CAS - Suzhou Institute of Nano-Tech and Nano-Bionics
  • CAS - Dalian Institute of Chemical Physics

Research output: Contribution to journalArticlepeer-review

Abstract

Cu–ZnO–Al2O3 catalysts are used as the industrial catalysts for water gas shift (WGS) and CO hydrogenation to methanol reactions. Herein, via a comprehensive experimental and theoretical calculation study of a series of ZnO/Cu nanocrystals inverse catalysts with well-defined Cu structures, we report that the ZnO–Cu catalysts undergo Cu structure-dependent and reaction-sensitive in situ restructuring during WGS and CO hydrogenation reactions under typical reaction conditions, forming the active sites of CuCu(100)-hydroxylated ZnO ensemble and CuCu(611)Zn alloy, respectively. These results provide insights into the active sites of Cu–ZnO catalysts for the WGS and CO hydrogenation reactions and reveal the Cu structural effects, and offer the feasible guideline for optimizing the structures of Cu–ZnO–Al2O3 catalysts.

Original languageEnglish
Article number4331
JournalNature Communications
Volume12
Issue number1
DOIs
StatePublished - 1 Dec 2021
Externally publishedYes

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