Construction of an electrode with hierarchical three-dimensional NiFe-oxyhydroxides by two-step electrodeposition for large-current oxygen evolution reaction

过电位 析氧 分解水 催化作用 电极 制氢 电解 碱性水电解 电解水 法拉第效率 电解质 材料科学 化学工程 化学 无机化学 电化学 冶金 物理化学 工程类 生物化学 光催化
作者
Menghua Liu,Jinyu Wang,Honglu Wu,Shuang Li,Yixiang Shi,Ningsheng Cai
出处
期刊:International Journal of Hydrogen Energy [Elsevier]
卷期号:51: 626-637 被引量:13
标识
DOI:10.1016/j.ijhydene.2023.07.005
摘要

Oxygen evolution reaction (OER) electrocatalysts are promised to be extremely important in hydrogen generation of water electrolysis as one of the renewable energy technologies. However, low efficiency and high cost are two crucial barriers that hinder its development and application. Herein, we developed highly efficient NiFe-based self-supported electrocatalysts by a facile two-step electrodeposition method focusing on the porosification of a nickel foam (NF) substrate. The porous nickel layer (PN/NF) formed in the first step by dynamic hydrogen bubble template electrodeposition proved to be effective in facilitating the mass transfer process, and the following second step of nickel-iron deposition (NiFe/PN/NF) continued to increase the intrinsic catalytic activity, with the two synergistically contributing to the excellent OER performance. As an oxygen evolution electrode, it exhibits high catalytic activity in alkaline water electrolysis, which requires only an overpotential of 211 mV to promote the oxidation reaction of water. The overpotentials for the OER at 100, 500 and 750 mA cm−2 are as low as 244, 297 and 326 mV in 1 M KOH, respectively. In 6 M KOH, the overpotentials for driving electrolytic oxygen production at 100, 500, 750 and 1000 mA cm−2 are even lowered spectacularly to 133 mV, 178 mV, 193 mV and 208 mV, respectively. In particular, the catalyst showed a catalytic stability of more than 40 h at a current density of 500 mA cm−2, which presents it as a highly promising candidate for future large-scale industrial applications.
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