磷化物
催化作用
过电位
塔菲尔方程
析氧
镍
材料科学
无机化学
氧化物
化学工程
纳米颗粒
过渡金属
电解质
氢氧化物
电化学
化学
纳米技术
电极
冶金
物理化学
工程类
生物化学
作者
Junyuan Xu,Xian‐Kui Wei,J. D. Costa,José L. Lado,Bryan Owens‐Baird,Liliana P. L. Gonçalves,Soraia Fernandes,Marc Heggen,Dmitri Y. Petrovykh,Rafal E. Dunin-Borkowski,Kirill Kovnir,Yury V. Kolen’ko
标识
DOI:10.1021/acscatal.7b01954
摘要
An approach to significantly enhance the performance of the cost-effective nickel phosphide catalyst for electrochemical water oxidation has been developed via interfacing with Mg oxide-hydroxide. We have synthesized Ni2P nanoparticles anchored on Mg2O(OH)2-like phase supported on carbon paper. During the oxygen evolution reaction, the well-defined Ni2P nanoparticles serve as precursors for the immediate formation of active and stable nanostructured nickel hydroxide catalyst. As the anode for the oxygen evolution reaction in an alkaline electrolyte, the electrode shows a modest Tafel slope of 48 mV dec–1 and a large turnover frequency of 0.05 s–1 at an overpotential of 0.4 V. Microstructure and composition studies of the catalyst suggest that interfacial strain between Mg- and Ni-containing phases is responsible for high catalytic activity. A significant increase in catalytic activity upon the combination of magnesium compound and transition-metal phosphide suggests an interesting strategy for the controlled and reproducible preparation of active Earth-abundant oxygen-evolving catalysts.
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