Synergistic Interfacial and Doping Engineering of Heterostructured NiCo(OH)x-CoyW as an Efficient Alkaline Hydrogen Evolution Electrocatalyst
Highlights A promising solar-powered environmentally friendly process for the synthesis and application of catalysts for hydrogen evolution reaction has been proposed. A delicate NiCo(OH) x -Co y W catalyst with a bush-like heterostructure was realized via gas-template-assisted electrodeposition, fo...
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Veröffentlicht in: | Nano-micro letters 2021-12, Vol.13 (1), p.120-120, Article 120 |
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Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Highlights
A promising solar-powered environmentally friendly process for the synthesis and application of catalysts for hydrogen evolution reaction has been proposed.
A delicate NiCo(OH)
x
-Co
y
W catalyst with a bush-like heterostructure was realized via gas-template-assisted electrodeposition, followed by electrochemical etching process.
The excellent catalytic effect of NiCo(OH)
x
-Co
y
W for the hydrogen evolution reaction was systematically investigated through various physical and electrochemical analyses.
To achieve high efficiency of water electrolysis to produce hydrogen (H
2
), developing non-noble metal-based catalysts with considerable performance have been considered as a crucial strategy, which is correlated with both the interphase properties and multi-metal synergistic effects. Herein, as a proof of concept, a delicate NiCo(OH)
x
-Co
y
W catalyst with a bush-like heterostructure was realized via gas-template-assisted electrodeposition, followed by an electrochemical etching-growth process, which ensured a high active area and fast gas release kinetics for a superior hydrogen evolution reaction, with an overpotential of 21 and 139 mV at 10 and 500 mA cm
−2
, respectively. Physical and electrochemical analyses demonstrated that the synergistic effect of the NiCo(OH)
x
/Co
y
W heterogeneous interface resulted in favorable electron redistribution and faster electron transfer efficiency. The amorphous NiCo(OH)
x
strengthened the water dissociation step, and metal phase of CoW provided sufficient sites for moderate H immediate adsorption/H
2
desorption. In addition, NiCo(OH)
x
-Co
y
W exhibited desirable urea oxidation reaction activity for matching H
2
generation with a low voltage of 1.51 V at 50 mA cm
−2
. More importantly, the synthesis and testing of the NiCo(OH)
x
-Co
y
W catalyst in this study were all solar-powered, suggesting a promising environmentally friendly process for practical applications. |
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ISSN: | 2311-6706 2150-5551 |
DOI: | 10.1007/s40820-021-00639-x |