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 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
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. |
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ISSN: | 0013-4686 |
DOI: | 10.1016/j.electacta.2020.136125 |