过电位
塔菲尔方程
溶解
材料科学
氢氧化物
析氧
层状双氢氧化物
催化作用
水镁石
化学工程
无机化学
镍
分解水
物理化学
冶金
有机化学
化学
电极
工程类
镁
光催化
电化学
作者
Haixia Liu,Yanrong Wang,Xinyao Lu,Yi Hu,Guoyin Zhu,Renpeng Chen,Lianbo Ma,Hongfei Zhu,Zuoxiu Tie,Jie Liu,Zhong Jin
出处
期刊:Nano Energy
[Elsevier]
日期:2017-04-06
卷期号:35: 350-357
被引量:258
标识
DOI:10.1016/j.nanoen.2017.04.011
摘要
Recently, Ni–based layered double hydroxide (LDH) materials have attracted growing interest owing to the remarkable performance for oxygen evolution reaction (OER). Here we demonstrate the preparation of ultrathin Ni3FeAlx trinary LDH nanosheets with higher activity and stability than NiFe–LDH nanosheets for OER. The enhancement was derived from Al substitution, which increased the concentration of Ni3+ active sites on the catalyst surface. Besides, low-coordinated Ni and Fe atoms and defects were formed by partial etching/dissolution of Al3+ in alkaline solution, which further increased the activity towards OER. To improve the conductivity, Ni3FeAlx–LDH (x=0, 0.91, 1.27 or 2.73) nanosheets were also in-situ grown on three-dimensional-networked nickel foam. The binder-free Ni3FeAlx–LDH/Ni foam electrodes exhibited further improved catalytic performance compared to the electrodes made of powdery Ni3FeAlx–LDHs and nafion binder. The best OER performance was presented by Ni3FeAl0.91–LDH/Ni foam, showing a Tafel slope of 57 mV/dec, a low overpotential (304 mV) at the current density of 20 mA/cm2, and a current density of 235 mA/cm2 at 1.60 V (vs. RHE). Furthermore, the Ni3FeAl0.91–LDHs/Ni foam electrode showed excellent long-term stability, maintaining a stable overpotential of 320 mV at 20 mA/cm2 after testing for 18 h.
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