过电位
塔菲尔方程
催化作用
纳米棒
分解水
析氧
材料科学
氧化钴
电化学
化学工程
氧化物
无机化学
钴
制氢
碱性水电解
磷化物
化学
纳米技术
电极
电解
冶金
物理化学
工程类
生物化学
光催化
电解质
作者
Jinfa Chang,Yao Xiao,Meiling Xiao,Junjie Ge,Changpeng Liu,Wei Xing
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2015-10-16
卷期号:5 (11): 6874-6878
被引量:454
标识
DOI:10.1021/acscatal.5b02076
摘要
Electrochemical water splitting in alkaline solution plays a growing role in alternative energy devices due to the need for clean and sustainable energy. However, catalysts that are active for both hydrogen evolution and oxygen evolution reactions are rare. Herein, we demonstrate that cobalt phosphide (CoP), which was synthesized via the hydrothermal route and has been shown to have hydrogen evolution activity, is highly active for oxygen evolution. A current density of 10 mA cm–2 was generated at an overpotential of only 320 mV in 1 M KOH for a CoP nanorod-based electrode (CoP NR/C), which was competitive with commercial IrO2. The Tafel slope for CoP NR/C was only 71 mV dec–1, and the catalyst maintained high stability during a 12 h test. This high activity was attributed to the formation of a thin layer of ultrafine crystalline cobalt oxide on the CoP surface.
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