NiFeP nanosheets for efficient and durable hydrazine-assisted electrolytic hydrogen production
Hydrazine-assisted electrochemical water splitting is an important avenue toward low cost and sustainable hydrogen production, which can significantly reduce the voltage of electrochemical water splitting. Herein, we took a simple approach to fabricate NiFeP nanosheet arrays on nickel foam (NiFeP/NF...
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Veröffentlicht in: | Dalton transactions : an international journal of inorganic chemistry 2024-03, Vol.53 (1), p.4574-4579 |
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Sprache: | eng |
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Zusammenfassung: | Hydrazine-assisted electrochemical water splitting is an important avenue toward low cost and sustainable hydrogen production, which can significantly reduce the voltage of electrochemical water splitting. Herein, we took a simple approach to fabricate NiFeP nanosheet arrays on nickel foam (NiFeP/NF), which exhibit superior electrocatalytic activity for the hydrogen evolution reaction (HER) and the hydrazine oxidation reaction (HzOR). Our investigations revealed that the excellent electrocatalytic activity of NiFeP/NF mainly arises from the bimetallic synergistic effect, abundant electrocatalytically active sites facilitated by the porous nanosheet morphology, high intrinsic conductivity of NiFeP/NF and strong NiFeP-NF adhesion. We assembled a hydrazine-boosted electrochemical water splitting cell using NiFeP/NF as a bifunctional catalyst for both electrodes, and the overall hydrazine splitting (OHzS) exhibits a considerably low overpotential (100 mV at 10 mA cm
−2
), and is stable for 40 h continuous electrolysis in a 1 M KOH + 0.5 M N
2
H
4
electrolyte. When it is applied to hydrogen production by seawater electrolysis, its catalytic activity shows strong tolerance. This work provides a promising approach for low cost, high-efficiency and stable hydrogen production based on hydrazine-assisted electrolytic seawater splitting for future applications.
NiFeP nanosheets have excellent OHzS properties, reducing voltages at 10 mA cm
−2
and 100 mA cm
−2
by 1.43 V and 1.42 V. |
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ISSN: | 1477-9226 1477-9234 |
DOI: | 10.1039/d3dt04373h |