Loos Stefan, Zaharieva Ivelina, Chernev Petko, Lißner Andreas, Dau Holger
Free University Berlin, Institute for Experimental Physics, Arnimallee 14, 014195, Berlin, Germany.
Current address: Fraunhofer Institute for Manufacturing Technology and Advanced Materials IFAM, Winterbergstraße 28, 01277, Dresden, Germany.
ChemSusChem. 2019 May 8;12(9):1966-1976. doi: 10.1002/cssc.201802737. Epub 2019 Jan 29.
Facile electromodification of metallic NiFe alloys leads to a series of NiFe oxyhydroxide surface films with excellent electrocatalytic performance in alkaline water oxidation. During cyclic voltammetry and after sudden potential jumps between noncatalytic and catalytic potentials, Ni oxidation/reduction was tracked with millisecond time resolution by a UV/Vis reflectance signal. Optimal catalysis at intermediate Ni/Fe ratios is explained by two opposing trends for increasing Fe content: a) pronounced slowdown of the Ni /Ni oxidation step and b) increased reactivity of the most oxidized catalyst state detectable at catalytic potentials. This state may involve an equilibrium between Ni ions and Ni ions with neighboring ligand holes, possibly in the form of bound peroxides.
金属镍铁合金的简易电改性可生成一系列在碱性水氧化中具有优异电催化性能的氢氧化氧镍表面膜。在循环伏安法期间以及在非催化电位和催化电位之间突然发生电位跃变之后,通过紫外/可见反射信号以毫秒级时间分辨率跟踪镍的氧化/还原过程。中间镍/铁比例下的最佳催化作用可由铁含量增加的两种相反趋势来解释:a)镍/镍氧化步骤明显减慢;b)在催化电位下可检测到的最氧化催化剂状态的反应活性增加。这种状态可能涉及镍离子与具有相邻配体空穴的镍离子之间的平衡,可能是以结合过氧化物的形式存在。