4.7 Article

Self-Supported FeNiP Nanosheet Arrays as a Robust Bifunctional Electrocatalyst for Water Splitting

Journal

ACS APPLIED ENERGY MATERIALS
Volume 5, Issue 5, Pages 5855-5866

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsaem.2c00190

Keywords

FeNiP; oxidative etching; overall water splitting; pH-universal hydrogen evolution reaction; oxygen evolution reaction

Funding

  1. National Key R&D Program of China [2019YFB1504502]

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Bimetallic FeNiP nanosheet arrays on a nickel foam (FeNiP@NFO) were fabricated using in situ oxidative etching and phosphorization, exhibiting remarkable catalytic activity for hydrogen and oxygen evolution reactions. The overall water-splitting electrolyzer assembled with FeNiP@NFO achieved a low cell voltage and high current density.
Bimetallic FeNiP nanosheet arrays on a nickel foam (FeNiP@NFO) are fabricated by an in situ oxidative etching process coupled with phosphorization. The self-supported FeNiP@NFO catalyst exhibits prominent catalytic activity for a hydrogen evolution reaction with overpotentials as low as 64, 82, and 54 mV at 10 mA.cm(-2) in 1.0 M PBS, 1.0 M KOH, and 0.5 M H2SO4, respectively, surpassing most reported non-noble catalysts. Moreover, FeNiP@NFO requires an overpotential of 193 mV in 1.0 M KOH to drive 10 mA.cm(-2) for an oxygen evolution reaction. The overall water-splitting electrolyzer assembled with FeNiP@NFO as both the anodic and cathodic electrodes exhibits an extremely low cell voltage of 1.49 V to achieve a current density of 10 mA.cm(-2), which is much lower than that of most alkaline electrolysis systems. The extraordinary electrocatalytic activity of FeNiP@NFO is ascribed to the synergistic effect between elements and the special network compiled by nanosheet arrays, which offers high conductivity, abundant accessible active sites, easy hydrogen release channels, and fast electron transportation.

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