过电位
材料科学
化学工程
多孔性
催化作用
电流密度
钴
氢
电极
吸附
镍
离解(化学)
复合材料
电化学
化学
冶金
有机化学
物理化学
工程类
物理
量子力学
作者
Yuantao Pei,Liang Huang,Lei Han,Haijun Zhang,Longhao Dong,Quanli Jia,Shaowei Zhang
标识
DOI:10.1016/j.gee.2020.10.019
摘要
Developing user-friendly electrodes for efficiently producing hydrogen from water to substitute non-renewable fossil fuels is one of the challenges in the hydrogen energy field. For the first time, we have prepared self-supporting ultrahigh porosity cobalt foam loaded with NiCoP/NiOOH nanoflowers (NiCoP/CF) via freeze-drying and phosphorization. The as-prepared hierarchical NiCoP/CF electrodes showed superior catalytic activity for hydrogen evolution reaction (HER) in alkaline media. The one resulted from phosphorization at 350 °C (NiCoP/CF-350) only required overpotential of −47, and −126 mV to deliver geometrical current density of −10 mA cm−2 and −100 mA cm−2, respectively, demonstrating improved catalytic activity than the electrodes prepared using a commercial nickel foam as a support. Moreover, it could retain its superior stability at a current density higher than −500 mA cm−2 for 16 h. Such an outstanding performance can be attributed to the ultrahigh porosity of Co foam support, optimal adsorption energies of HER intermediates (H∗), facile water dissociation on the NiCoP/NiOOH hetero-interfaces, and the assistance of NiOOH facilitating the electrons transfer from the Co foam inside to the NiCoP outside. The work would provide a new strategy for future design of advanced HER electrocatalysts.
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