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Electron penetration triggering interface activity of Pt-graphene for CO oxidation at room temperature

Author

Listed:
  • Yong Wang

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

  • Pengju Ren

    (Institute of Coal Chemistry, Chinese Academy of Sciences
    Synfuels China Co. Ltd.)

  • Jingting Hu

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

  • Yunchuan Tu

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

  • Zhongmiao Gong

    (Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences)

  • Yi Cui

    (Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences)

  • Yanping Zheng

    (Xiamen University)

  • Mingshu Chen

    (Xiamen University)

  • Wujun Zhang

    (Hunan University)

  • Chao Ma

    (Hunan University)

  • Liang Yu

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

  • Fan Yang

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

  • Ye Wang

    (Xiamen University)

  • Xinhe Bao

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

  • Dehui Deng

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

Abstract

Achieving CO oxidation at room temperature is significant for gas purification but still challenging nowadays. Pt promoted by 3d transition metals (TMs) is a promising candidate for this reaction, but TMs are prone to be deeply oxidized in an oxygen-rich atmosphere, leading to low activity. Herein we report a unique structure design of graphene-isolated Pt from CoNi nanoparticles (PtǀCoNi) for efficiently catalytic CO oxidation in an oxygen-rich atmosphere. CoNi alloy is protected by ultrathin graphene shell from oxidation and therefore modulates the electronic property of Pt-graphene interface via electron penetration effect. This catalyst can achieve near 100% CO conversion at room temperature, while there are limited conversions over Pt/C and Pt/CoNiOx catalysts. Experiments and theoretical calculations indicate that CO will saturate Pt sites, but O2 can adsorb at the Pt-graphene interface without competing with CO, which facilitate the O2 activation and the subsequent surface reaction. This graphene-isolated system is distinct from the classical metal-metal oxide interface for catalysis, and it provides a new thought for the design of heterogeneous catalysts.

Suggested Citation

  • Yong Wang & Pengju Ren & Jingting Hu & Yunchuan Tu & Zhongmiao Gong & Yi Cui & Yanping Zheng & Mingshu Chen & Wujun Zhang & Chao Ma & Liang Yu & Fan Yang & Ye Wang & Xinhe Bao & Dehui Deng, 2021. "Electron penetration triggering interface activity of Pt-graphene for CO oxidation at room temperature," Nature Communications, Nature, vol. 12(1), pages 1-7, December.
  • Handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-26089-y
    DOI: 10.1038/s41467-021-26089-y
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    Cited by:

    1. Zheyuan Ding & Sai Chen & Tingting Yang & Zunrong Sheng & Xianhua Zhang & Chunlei Pei & Donglong Fu & Zhi-Jian Zhao & Jinlong Gong, 2024. "Atomically dispersed MoNi alloy catalyst for partial oxidation of methane," Nature Communications, Nature, vol. 15(1), pages 1-10, December.
    2. Tengfei Zhang & Peng Zheng & Jiajian Gao & Xiaolong Liu & Yongjun Ji & Junbo Tian & Yang Zou & Zhiyi Sun & Qiao Hu & Guokang Chen & Wenxing Chen & Xi Liu & Ziyi Zhong & Guangwen Xu & Tingyu Zhu & Fabi, 2024. "Simultaneously activating molecular oxygen and surface lattice oxygen on Pt/TiO2 for low-temperature CO oxidation," Nature Communications, Nature, vol. 15(1), pages 1-12, December.

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