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Electron penetration triggering interface activity of Pt-graphene for CO oxidation at room temperature.
Wang, Yong; Ren, Pengju; Hu, Jingting; Tu, Yunchuan; Gong, Zhongmiao; Cui, Yi; Zheng, Yanping; Chen, Mingshu; Zhang, Wujun; Ma, Chao; Yu, Liang; Yang, Fan; Wang, Ye; Bao, Xinhe; Deng, Dehui.
Afiliação
  • Wang Y; State Key Laboratory of Physical Chemistry of Solid Surfaces, Collaborative Innovation Center of Chemistry for Energy Materials (iChEM), College of Chemistry and Chemical Engineering, Xiamen University, 361005, Xiamen, China.
  • Ren P; State Key Laboratory of Catalysis, iChEM, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 116023, Dalian, China.
  • Hu J; State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, 030001, Taiyuan, China.
  • Tu Y; National Energy Center for Coal to Liquids, Synfuels China Co. Ltd., 101407, Beijing, China.
  • Gong Z; State Key Laboratory of Physical Chemistry of Solid Surfaces, Collaborative Innovation Center of Chemistry for Energy Materials (iChEM), College of Chemistry and Chemical Engineering, Xiamen University, 361005, Xiamen, China.
  • Cui Y; State Key Laboratory of Catalysis, iChEM, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 116023, Dalian, China.
  • Zheng Y; State Key Laboratory of Physical Chemistry of Solid Surfaces, Collaborative Innovation Center of Chemistry for Energy Materials (iChEM), College of Chemistry and Chemical Engineering, Xiamen University, 361005, Xiamen, China.
  • Chen M; State Key Laboratory of Catalysis, iChEM, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 116023, Dalian, China.
  • Zhang W; Vacuum Interconnected Nanotech Workstation, Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences, 215123, Suzhou, China.
  • Ma C; Vacuum Interconnected Nanotech Workstation, Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences, 215123, Suzhou, China.
  • Yu L; State Key Laboratory of Physical Chemistry of Solid Surfaces, Collaborative Innovation Center of Chemistry for Energy Materials (iChEM), College of Chemistry and Chemical Engineering, Xiamen University, 361005, Xiamen, China.
  • Yang F; State Key Laboratory of Physical Chemistry of Solid Surfaces, Collaborative Innovation Center of Chemistry for Energy Materials (iChEM), College of Chemistry and Chemical Engineering, Xiamen University, 361005, Xiamen, China.
  • Wang Y; Center for High Resolution Electron Microscopy, College of Materials Science and Engineering, Hunan University, 410082, Changsha, China.
  • Bao X; Center for High Resolution Electron Microscopy, College of Materials Science and Engineering, Hunan University, 410082, Changsha, China.
  • Deng D; State Key Laboratory of Catalysis, iChEM, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 116023, Dalian, China.
Nat Commun ; 12(1): 5814, 2021 Oct 04.
Article em En | MEDLINE | ID: mdl-34608162
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.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Nat Commun Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Nat Commun Ano de publicação: 2021 Tipo de documento: Article