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Published on: December 6, 2021
A core-shell structured CoMoO4•nH2O@Co1-xFexOOH nanocatalyst for electrochemical evolution of oxygen
Jiajun Wang1, Hui Yin1, Zhengjun Chen1
1School of Materials Science and Engineering, Key Laboratory of Advanced Energy Storage Materials of Guangdong Province, South China University of Technology, Guangzhou, 510641, PR China.
None:
Nickel-iron oxyhydroxide (Ni1-xFexOOH) is well recognized as the best-performing oxygen evolution reaction (OER) catalyst in alkaline electrolytes, however its analogue cobalt-iron oxyhydroxide (Co1-xFexOOH) is surprisingly less explored despite their structural similarity. Inspired by our recent study on high-performance HER catalyst using the nanostructured CoMoO4•nH2O precursor, herein, we report a facile synthesis of Co1-xFexOOH catalyst derived from the same precursor and its excellent electrocatalytic properties towards the OER in alkaline electrolytes. A core-shell structured nanocatalyst consisting of disordered Co1-xFexOOH layer over the surface of crystalline CoMoO4•nH2O nanosheets was synthesized using a simple hydrothermal method followed by anodic electrooxidation. Thus-prepared catalyst exhibited extraordinarily high and stable activity towards the OER in alkaline electrolyte, which outperformed most Co-based OER catalysts. Combined with the HER catalyst derived from the same CoMoO4•nH2O precursor as the cathode, we further developed and tested a simple water-splitting cell, which significantly surpasses the benchmarking IrO2-Pt/C couple (1.63 V) and requires a voltage of only 1.517 V to afford 10 mA cm-2 in 1.0 M KOH solution. Density functional theory calculations were conducted to gain insight into the Fe-doping induced improvement of OER activity.
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