A core-shell structured CoMoO 4 •nH 2 O@Co 1-x Fe x OOH nanocatalyst for electrochemical evolution of oxygen

Nickel-iron oxyhydroxide (Ni Fe OOH) is well recognized as the best-performing oxygen evolution reaction (OER) catalyst in alkaline electrolytes, however its analogue cobalt-iron oxyhydroxide (Co Fe OOH) is surprisingly less explored despite their structural similarity. Inspired by our recent study...

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Veröffentlicht in:Electrochimica acta 2020, Vol.345
Hauptverfasser: Wang, Jiajun, Yin, Hui, Chen, Zhengjun, Cao, Guoxuan, Xu, Ning, Wu, Hui, Wang, Ping
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Sprache:eng
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Zusammenfassung:Nickel-iron oxyhydroxide (Ni Fe OOH) is well recognized as the best-performing oxygen evolution reaction (OER) catalyst in alkaline electrolytes, however its analogue cobalt-iron oxyhydroxide (Co Fe OOH) is surprisingly less explored despite their structural similarity. Inspired by our recent study on high-performance HER catalyst using the nanostructured CoMoO •nH O precursor, herein, we report a facile synthesis of Co Fe OOH 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 Co Fe OOH layer over the surface of crystalline CoMoO •nH O 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 CoMoO •nH O precursor as the cathode, we further developed and tested a simple water-splitting cell, which significantly surpasses the benchmarking IrO -Pt/C couple (1.63 V) and requires a voltage of only 1.517 V to afford 10 mA cm in 1.0 M KOH solution. Density functional theory calculations were conducted to gain insight into the Fe-doping induced improvement of OER activity.
ISSN:0013-4686
DOI:10.1016/j.electacta.2020.136125