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    A highly active and stable La0.5Sr0.5Ni0.4Fe0.6O3-δ perovskite electrocatalyst for oxygen evolution reaction in alkaline media

    Access Status
    Fulltext not available
    Authors
    Wang, C.
    Cheng, Y.
    Ianni, E.
    Jiang, San Ping
    Lin, B.
    Date
    2017
    Type
    Journal Article
    
    Metadata
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    Citation
    Wang, C. and Cheng, Y. and Ianni, E. and Jiang, S.P. and Lin, B. 2017. A highly active and stable La0.5Sr0.5Ni0.4Fe0.6O3-δ perovskite electrocatalyst for oxygen evolution reaction in alkaline media. Electrochimica Acta. 246: pp. 997-1003.
    Source Title
    Electrochimica Acta
    DOI
    10.1016/j.electacta.2017.06.161
    ISSN
    0013-4686
    School
    Fuels and Energy Technology Institute
    URI
    http://hdl.handle.net/20.500.11937/56999
    Collection
    • Curtin Research Publications
    Abstract

    Owing to the slow kinetics of oxygen evolution reaction (OER), developing highly active and stable OER catalysts is of great importance to realize the industrial operation for water electrolysis, reversible fuel cells and so on. Here, we report a highly active and stable La 0.5 Sr 0.5 Ni 0.4 Fe 0.6 O 3-d perovskite electrocatalyst for OER in alkaline media. La 0.5 Sr 0.5 Ni x Fe 1-x O 3-d (LSNF) perovskites with different Ni/Fe ratio were synthesized by a typical sol-gel route and investigated as potential cobalt-free OER perovskite electrocatalysts. Synchrotron XRD quantification analysis was applied to quantify the crystal structural details and changes. La 0.5 Sr 0.5 Ni 0.4 Fe 0.6 O 3-d (LSNF-5546) materials show significantly higher intrinsic activities and better stability in 0.1 M KOH for the OER including onset potential (1.56 V) and Tafel slope (76 mV/dec), higher than that of other LSNF and state-of-the-art perovskite electrocatalyst Ba 0.5 Sr 0.5 Co 0.8 Fe 0.2 O 3-d (BSCF-5582). This work demonstrates that La 0.5 Sr 0.5 Ni 0.4 Fe 0.6 O 3-d (LSNF-5546) can be a new kind of cost-effective and high-performance perovskite electrocatalyst for OER in alkaline solution, and the simple doping strategy would be a practical way to enhance oxygen evolution on perovskite electrocatalysts.

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