Abstract

Ni–Fe (oxy)hydroxides, Ni(1–z)FezOxHy, are among the fastest-known water oxidation catalysts in alkaline media on a per-cation basis. At current densities relevant for electrolysis (e.g., >0.5 A/cm–2), mass and electron transport through catalyst films with high mass loading are critical and depend substantially on the extended and intermediate catalyst architecture. Here we use X-ray pair distribution function (PDF) analysis to determine the intermediate nanostructures of electrodeposited Ni(1–z)FezOxHy films. We report the effects of electrodeposition technique (pulsed versus continuous), electrochemical cycling, and Fe content on the structure of the catalyst film. The PDF patterns for Ni(1–z)FezOxHy films are best simulated by model structures consisting of brucite-like β-Ni(OH)2 fragments 1 to 3 layers in thickness. Only the oxidation state of the film significantly affects the intralayer scattering behavior (i.e., metal–oxygen bond distance). The interlayer interactions, however, are affected by Fe ...

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