过电位
阳极
析氧
分解水
材料科学
电解水
电化学
阴极
电解
化学工程
电流密度
电极
制氢
纳米技术
氢
催化作用
化学
电解质
物理化学
工程类
有机化学
物理
光催化
量子力学
生物化学
作者
Feng Yan,Dong Guo,Jianyu Kang,Lina Liu,Chunling Zhu,Peng Gao,Xitian Zhang,Yujin Chen
标识
DOI:10.1016/j.electacta.2018.06.202
摘要
Electrochemical water splitting is an efficient way for large-scale production of clean hydrogen fuel. However, high overpotential is required to catalyzing oxygen evolution reaction (OER). Here we fabricate self-supported CoMn-LDH nanosheets with a thickness of approximately 1.9 nm on carbon fiber cloth through electrodeposition method within 50 s. The self-supported, binder-free anodes exhibit excellent OER performance with an overpotential of 258 mV at 10 mA cm−2 in 0.1 M KOH solution, remarkably lower than those of Co and Mn single counterparts, and the-state-of-the-art IrO2 catalyst. Furthermore, self-supported, binder-free anodes exhibit robust stability for OER with a negligible current loss even at a high current density (>370 mA cm−2) over 15 h. Flexible and bendable measurements indicate no obvious degradation in the OER performance of the anode even as being bended to 180°. Moreover, the water electrolysis with the CoMn-LDH/CFC as anode and Pt/C/CFC as cathode only needs a cell voltage of 1.54 V to deliver the current density of 10 mA cm−2 in 0.1 M KOH solution. Our experimental results demonstrate that the electron interaction between Mn and Co, increased electrochemical active area and decreased charge-transfer resistance contribute to the enhancement of the optimized anode in OER performance.
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