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In situ identification of the metallic state of Ag nanoclusters in oxidative dispersion

Author

Listed:
  • Rongtan Li

    (Dalian Institute of Chemical Physics, The Chinese Academy of Sciences
    University of Chinese Academy of Sciences)

  • Xiaoyan Xu

    (Dalian Institute of Chemical Physics, The Chinese Academy of Sciences
    Dalian Institute of Chemical Physics, The Chinese Academy of Sciences)

  • Beien Zhu

    (Shanghai Advanced Research Institute, The Chinese Academy of Sciences
    Shanghai Institute of Applied Physics, The Chinese Academy of Sciences)

  • Xiao-Yan Li

    (University of Chinese Academy of Sciences
    Shanghai Institute of Applied Physics, The Chinese Academy of Sciences)

  • Yanxiao Ning

    (Dalian Institute of Chemical Physics, The Chinese Academy of Sciences)

  • Rentao Mu

    (Dalian Institute of Chemical Physics, The Chinese Academy of Sciences)

  • Pengfei Du

    (University of Chinese Academy of Sciences
    Dalian Institute of Chemical Physics, The Chinese Academy of Sciences)

  • Mengwei Li

    (Dalian Institute of Chemical Physics, The Chinese Academy of Sciences)

  • Huike Wang

    (Nankai University)

  • Jiajie Liang

    (Nankai University)

  • Yongsheng Chen

    (Nankai University)

  • Yi Gao

    (Shanghai Advanced Research Institute, The Chinese Academy of Sciences
    Shanghai Institute of Applied Physics, The Chinese Academy of Sciences)

  • Bing Yang

    (Dalian Institute of Chemical Physics, The Chinese Academy of Sciences
    Dalian Institute of Chemical Physics, The Chinese Academy of Sciences)

  • Qiang Fu

    (Dalian Institute of Chemical Physics, The Chinese Academy of Sciences
    Dalian Institute of Chemical Physics, The Chinese Academy of Sciences)

  • Xinhe Bao

    (Dalian Institute of Chemical Physics, The Chinese Academy of Sciences
    Dalian Institute of Chemical Physics, The Chinese Academy of Sciences)

Abstract

Oxidative dispersion has been widely used in regeneration of sintered metal catalysts and fabrication of single atom catalysts, which is attributed to an oxidation-induced dispersion mechanism. However, the interplay of gas-metal-support interaction in the dispersion processes, especially the gas-metal interaction has not been well illustrated. Here, we show dynamic dispersion of silver nanostructures on silicon nitride surface under reducing/oxidizing conditions and during carbon monoxide oxidation reaction. Utilizing environmental scanning (transmission) electron microscopy and near-ambient pressure photoelectron spectroscopy/photoemission electron microscopy, we unravel a new adsorption-induced dispersion mechanism in such a typical oxidative dispersion process. The strong gas-metal interaction achieved by chemisorption of oxygen on nearly-metallic silver nanoclusters is the internal driving force for dispersion. In situ observations show that the dispersed nearly-metallic silver nanoclusters are oxidized upon cooling in oxygen atmosphere, which could mislead to the understanding of oxidation-induced dispersion. We further understand the oxidative dispersion mechanism from the view of dynamic equilibrium taking temperature and gas pressure into account, which should be applied to many other metals such as gold, copper, palladium, etc. and other reaction conditions.

Suggested Citation

  • Rongtan Li & Xiaoyan Xu & Beien Zhu & Xiao-Yan Li & Yanxiao Ning & Rentao Mu & Pengfei Du & Mengwei Li & Huike Wang & Jiajie Liang & Yongsheng Chen & Yi Gao & Bing Yang & Qiang Fu & Xinhe Bao, 2021. "In situ identification of the metallic state of Ag nanoclusters in oxidative dispersion," Nature Communications, Nature, vol. 12(1), pages 1-9, December.
  • Handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-21552-2
    DOI: 10.1038/s41467-021-21552-2
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    Cited by:

    1. Yong Yin & Bingcheng Luo & Kezhi Li & Benjamin M. Moskowitz & Bar Mosevitzky Lis & Israel E. Wachs & Minghui Zhu & Ye Sun & Tianle Zhu & Xiang Li, 2024. "Plasma-assisted manipulation of vanadia nanoclusters for efficient selective catalytic reduction of NOx," Nature Communications, Nature, vol. 15(1), pages 1-12, December.

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