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The most active Cu facet for low-temperature water gas shift reaction

Author

Listed:
  • Zhenhua Zhang

    (University of Science and Technology of China)

  • Sha-Sha Wang

    (University of Chinese Academy of Sciences)

  • Rui Song

    (University of Science and Technology of China)

  • Tian Cao

    (University of Science and Technology of China)

  • Liangfeng Luo

    (University of Science and Technology of China)

  • Xuanye Chen

    (Zhejiang Normal University)

  • Yuxian Gao

    (University of Science and Technology of China)

  • Jiqing Lu

    (Zhejiang Normal University)

  • Wei-Xue Li

    (University of Science and Technology of China
    University of Chinese Academy of Sciences)

  • Weixin Huang

    (University of Science and Technology of China)

Abstract

Identification of the active site is important in developing rational design strategies for solid catalysts but is seriously blocked by their structural complexity. Here, we use uniform Cu nanocrystals synthesized by a morphology-preserved reduction of corresponding uniform Cu2O nanocrystals in order to identify the most active Cu facet for low-temperature water gas shift (WGS) reaction. Cu cubes enclosed with {100} facets are very active in catalyzing the WGS reaction up to 548 K while Cu octahedra enclosed with {111} facets are inactive. The Cu–Cu suboxide (CuxO, x ≥ 10) interface of Cu(100) surface is the active site on which all elementary surface reactions within the catalytic cycle proceed smoothly. However, the formate intermediate was found stable at the Cu–CuxO interface of Cu(111) surface with consequent accumulation and poisoning of the surface at low temperatures. Thereafter, Cu cubes-supported ZnO catalysts are successfully developed with extremely high activity in low-temperature WGS reaction.

Suggested Citation

  • Zhenhua Zhang & Sha-Sha Wang & Rui Song & Tian Cao & Liangfeng Luo & Xuanye Chen & Yuxian Gao & Jiqing Lu & Wei-Xue Li & Weixin Huang, 2017. "The most active Cu facet for low-temperature water gas shift reaction," Nature Communications, Nature, vol. 8(1), pages 1-10, December.
  • Handle: RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_s41467-017-00620-6
    DOI: 10.1038/s41467-017-00620-6
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    Cited by:

    1. Hao Meng & Yusen Yang & Tianyao Shen & Wei Liu & Lei Wang & Pan Yin & Zhen Ren & Yiming Niu & Bingsen Zhang & Lirong Zheng & Hong Yan & Jian Zhang & Feng-Shou Xiao & Min Wei & Xue Duan, 2023. "A strong bimetal-support interaction in ethanol steam reforming," Nature Communications, Nature, vol. 14(1), pages 1-13, December.

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