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      High-Performance Anode Material Sr2FeMo0.65Ni0.35O6−δ with In Situ Exsolved Nanoparticle Catalyst

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          Abstract

          A metallic nanoparticle-decorated ceramic anode was prepared by in situ reduction of the perovskite Sr2FeMo0.65Ni0.35O6-δ (SFMNi) in H2 at 850 °C. The reduction converts the pure perovksite phase into mixed phases containing the Ruddlesden-Popper structure Sr3FeMoO7-δ, perovskite Sr(FeMo)O3-δ, and the FeNi3 bimetallic alloy nanoparticle catalyst. The electrochemical performance of the SFMNi ceramic anode is greatly enhanced by the in situ exsolved Fe-Ni alloy nanoparticle catalysts that are homogeneously distributed on the ceramic backbone surface. The maximum power densities of the La0.8Sr0.2Ga0.8Mg0.2O3-δ electrolyte supported a single cell with SFMNi as the anode reached 590, 793, and 960 mW cm(-2) in wet H2 at 750, 800, and 850 °C, respectively. The Sr2FeMo0.65Ni0.35O6-δ anode also shows excellent structural stability and good coking resistance in wet CH4. The prepared SFMNi material is a promising high-performance anode for solid oxide fuel cells.

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          Author and article information

          Journal
          ACS Nano
          ACS Nano
          American Chemical Society (ACS)
          1936-0851
          1936-086X
          September 02 2016
          September 27 2016
          August 19 2016
          September 27 2016
          : 10
          : 9
          : 8660-8669
          Affiliations
          [1 ]School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083, China
          [2 ]The Beijing Municipal Key Laboratory of New Energy Materials and Technologies, Beijing 100083, China
          [3 ]Beijing National Laboratory for Condensed Matter Physics Institute of Physics, Chinese Academy of Sciences, Beijing 100190, China
          [4 ]Department of Materials Science and Engineering, Beijing Institute of Petrochemical Technology, Beijing 102617, China
          [5 ]Faculty of Energy and Fuels, Department of Hydrogen Energy, AGH University of Science and Technology, 30-059 Krakow, Poland
          Article
          10.1021/acsnano.6b03979
          27529355
          be38bd44-3520-45ee-8127-d891787d9d06
          © 2016
          History

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