Scinovex
articleTop 1% cited

Efficient and Stable Bifunctional Electrocatalysts Ni/Ni<i><sub>x</sub></i>M<i><sub>y</sub></i> (M = P, S) for Overall Water Splitting

Advanced Functional Materials · 2016 · Vol. 26(19) · pp. 3314–3323
Gao‐Feng ChenTianyi MaZhao‐Qing LiuNan LiYu‐Zhi SuKenneth DaveyShi‐Zhang Qiao

Abstract

Development of easy‐to‐make, highly active, and stable bifunctional electrocatalysts for water splitting is important for future renewable energy systems. Three‐dimension (3D) porous Ni/Ni 8 P 3 and Ni/Ni 9 S 8 electrodes are prepared by sequential treatment of commercial Ni‐foam with acid activation, followed by phosphorization or sulfurization. The resultant materials can act as self‐supported bifunctional electrocatalytic electrodes for direct water splitting with excellent activity toward oxygen evolution reaction and hydrogen evolution reaction in alkaline media. Stable performance can be maintained for at least 24 h, illustrating their versatile and practical nature for clean energy generation. Furthermore, an advanced water electrolyzer through exploiting Ni/Ni 8 P 3 as both anode and cathode is fabricated, which requires a cell voltage of 1.61 V to deliver a 10 mA cm −2 water splitting current density in 1.0 m KOH solution. This performance is significantly better than that of the noble metal benchmark—integrated Ni/IrO 2 and Ni/Pt–C electrodes. Therefore, these bifunctional electrodes have significant potential for realistic large‐scale production of hydrogen as a replacement clean fuel to polluting and limited fossil‐fuels.

Electrocatalysts for Energy ConversionAdvanced Photocatalysis TechniquesAdvanced battery technologies researchBifunctionalWater splittingMaterials scienceOxygen evolutionAnodeCathodeElectrolysisChemical engineeringElectrodeElectrocatalyst

Funding

  • Australian Research Council
Citations
906
FWCI
47.25
field-weighted impact
References
57
Percentile
100%
vs. same field & year
Citations per year
Citation Network

How this paper connects to the literature. Drag to explore, click any node to open that paper.