Design of N‑Coordinated Dual-Metal Sites: A Stable and Active Pt-Free Catalyst for Acidic Oxygen Reduction Reaction.

We develop a host-guest strategy to construct an electrocatalyst with Fe-Co dual sites embedded on N-doped porous carbon and demonstrate its activity for oxygen reduction reaction in acidic electrolyte. Our catalyst exhibits superior oxygen reduction reaction performance, with comparable onset poten...

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Publicado en:Journal of the American Chemical Society Vol. 139; no. 48; pp. 17281 - 17285
Autores principales: Jing Wang, Zhengqing Huang, Wei Liu, Chunran Chang, Haolin Tang, Zhijun Li, Wenxing Chen, Chunjiang Jia, Tao Yao, Shiqiang Wei, Yuen Wu, Yadong Li
Formato: Artículo
Publicado: American Chemical Society 12/6/2017
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Acceso en línea:Ver este registro en EBSCOhost
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        00027863
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      dt: 12/6/2017
      vid: 139
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      pub: American Chemical Society
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        126761833
        10.1021/jacs.7b10385
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        atl: Design of N‑Coordinated Dual-Metal Sites: A Stable and Active Pt-Free Catalyst for Acidic Oxygen Reduction Reaction.
      aug:
        au:
          Jing Wang
          Zhengqing Huang
          Wei Liu
          Chunran Chang
          Haolin Tang
          Zhijun Li
          Wenxing Chen
          Chunjiang Jia
          Tao Yao
          Shiqiang Wei
          Yuen Wu
          Yadong Li
        affil:
          Department of Chemistry, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials), University of Science and Technology of China, Hefei 230026, China
          Institute of Industrial Catalysis, School of Chemical Engineering and Technology, Xi'an Jiaotong University, Xi'an 710049, China
          Hefei National Laboratory for Physical Sciences at the Microscale, University of Science and Technology of China, Hefei 230026, China
          State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070, China
          Department of Chemistry, Queen's University, Kingston, Ontario K7L 3N6, Canada
          Department of Chemistry, Tsinghua University, Beijing 100084, China
          Key Laboratory for Colloid and Interface Chemistry, Key Laboratory of Special Aggregated Materials, School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, China
      su:
        Oxygen reduction
        Platinum catalysts
        Iron compounds
        Cobalt compounds
        Density functional theory
      sug:
        subj:
          Oxygen reduction
          Platinum catalysts
          Iron compounds
          Cobalt compounds
          Density functional theory
      ab: We develop a host-guest strategy to construct an electrocatalyst with Fe-Co dual sites embedded on N-doped porous carbon and demonstrate its activity for oxygen reduction reaction in acidic electrolyte. Our catalyst exhibits superior oxygen reduction reaction performance, with comparable onset potential (E, 1.06 vs 1.03 V) and half-wave potential (E, 0.863 vs 0.858 V) than commercial Pt/C. The fuel cell test reveals (Fe,Co)/N-C outperforms most reported Pt-free catalysts in H/O and H2/air. In addition, this cathode catalyst with dual metal sites is stable in a long-term operation with 50 000 cycles for electrode measurement and 100 h for H/air single cell operation. Density functional theory calculations reveal the dual sites is favored for activation of O-O, crucial for four-electron oxygen reduction.
      pubtype: Academic Journal
      doctype: Article
      src: R
    language: English
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          year: 2017
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