Electromodified NiFe Alloys as Electrocatalysts for Water Oxidation: Mechanistic Implications of Time-Resolved UV/Vis Tracking of Oxidation State Changes

被引:38
作者
Loos, Stefan [1 ,3 ]
Zaharieva, Ivelina [1 ]
Chernev, Petko [1 ,4 ]
Lissner, Andreas [2 ]
Dau, Holger [1 ]
机构
[1] Free Univ Berlin, Inst Expt Phys, Arnimallee 14, D-014195 Berlin, Germany
[2] Tech Univ Bergakad Freiberg, Inst Phys Chem, Leipziger Str 29, D-09599 Freiberg, Germany
[3] Fraunhofer Inst Mfg Technol & Adv Mat IFAM, Winterbergstr 28, D-01277 Dresden, Germany
[4] Uppsala Univ, Dept Chem, Angstrom Lab, Lagerhyddsvagen 1, S-75237 Uppsala, Sweden
关键词
electrocatalysis; NiFe oxyhydroxides; spectroelectrochemistry; water oxidation; X-ray photoelectron spectroscopy; OXYGEN-EVOLUTION ELECTROCATALYSTS; STAINLESS-STEEL; PASSIVE FILM; SPLITTING CATALYST; OXIDE CATALYSTS; NICKEL; IRON; REDOX; SPECTROSCOPY; DYNAMICS;
D O I
10.1002/cssc.201802737
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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 Ni2+/Ni3+ oxidation step and b)increased reactivity of the most oxidized catalyst state detectable at catalytic potentials. This state may involve an equilibrium between Ni4+ ions and Ni2+ ions with neighboring ligand holes, possibly in the form of bound peroxides.
引用
收藏
页码:1966 / 1976
页数:11
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