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A Gibeon meteorite yields a high-performance water oxidation electrocatalyst

机译:Gibeon陨石产生高性能的水氧化电催化剂

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Examining the electrocatalytic performance of naturally-occurring metallic minerals is of interest for energy conversion applications given their unique atomic composition and formation history. Herein, we report the electrocatalytic function of an iron-based Gibeon meteorite for the oxygen evolution reaction (OER). After ageing under operational conditions in an alkaline electrolyte, an activity matching or possibly slightly superior to the best performing OER catalysts emerges, with stable overpotentials as low as 270 mV (for 10 mA cm(-2)) and Tafel slopes of 37 mV decade(-1). The Faradaic efficiency for the OER was unity and no deterioration in performance was detected during 1000 hours of OER operation at 500 mA cm(-2). Mechanistic studies suggest an operando surface modification involving the formation of a 3D oxy(hydroxide) layer with a metal atom composition of Co0.11Fe0.33Ni0.55, as indicated by Raman and XPS studies and trace Ir as indicated via elemental analysis. The growth of the catalyst layer was self-limiting to <200 nm after ca. 300 hours of operation as indicated through XPS depth profiling and cyclic voltammetry. The unique composition and structure of the Gibeon meteorite suggest that further investigation of Ir-Co-Ni-Fe systems or other alloys inspired by natural materials for water oxidation are of interest.
机译:考虑到天然金属矿物的独特的原子组成和形成历史,研究天然存在的金属矿物的电催化性能对于能量转换应用很重要。在此,我们报道了铁基基遍陨石对氧释放反应(OER)的电催化功能。在碱性电解液中在操作条件下老化后,出现了与最佳OER催化剂相匹配或可能略胜于其的活性,其稳定的低电势低至270 mV(对于10 mA cm(-2)),Tafel斜率为37 mV十倍(-1)。 OER的法拉第效率是统一的,并且在500 mA cm(-2)的OER操作1000小时期间未发现性能下降。机理研究表明,如Raman和XPS研究表明,操作表面改性涉及形成3D含金属原子成分为Co0.11Fe0.33Ni0.55的羟基氧化物(氢氧化物)层,而痕量Ir则通过元素分析表明。约200nm后,催化剂层的生长自限制为<200nm。通过XPS深度分析和循环伏安法显示,可运行300小时。 Gibeon陨石的独特组成和结构表明,对Ir-Co-Ni-Fe系统或受天然材料启发进行水氧化的其他合金的进一步研究非常有趣。

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  • 来源
    《Energy & environmental science》 |2016年第11期|3448-3455|共8页
  • 作者单位

    Ecole Polytech Fed Lausanne, Inst Chem Sci & Engn ISIC, CH-1015 Lausanne, Switzerland;

    Ecole Polytech Fed Lausanne, Inst Chem Sci & Engn ISIC, CH-1015 Lausanne, Switzerland;

    Ecole Polytech Fed Lausanne, Inst Chem Sci & Engn ISIC, CH-1015 Lausanne, Switzerland;

    Ecole Polytech Fed Lausanne, Inst Chem Sci & Engn ISIC, CH-1015 Lausanne, Switzerland;

    Ecole Polytech Fed Lausanne, Inst Chem Sci & Engn ISIC, CH-1015 Lausanne, Switzerland;

    Ecole Polytech Fed Lausanne, Inst Chem Sci & Engn ISIC, CH-1015 Lausanne, Switzerland;

    Ecole Polytech Fed Lausanne, Inst Chem Sci & Engn ISIC, CH-1015 Lausanne, Switzerland;

    Ecole Polytech Fed Lausanne, Inst Chem Sci & Engn ISIC, CH-1015 Lausanne, Switzerland;

    Ecole Polytech Fed Lausanne, Inst Chem Sci & Engn ISIC, CH-1015 Lausanne, Switzerland;

    Ecole Polytech Fed Lausanne, Inst Phys IPHYS, CH-1015 Lausanne, Switzerland;

    Ecole Polytech Fed Lausanne, Inst Chem Sci & Engn ISIC, CH-1015 Lausanne, Switzerland;

    Ecole Polytech Fed Lausanne, Inst Chem Sci & Engn ISIC, CH-1015 Lausanne, Switzerland;

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