析氧
过电位
磷化物
电催化剂
材料科学
催化作用
电解
化学工程
电化学
金属
纳米技术
化学
冶金
电极
物理化学
电解质
生物化学
工程类
作者
Peng Fei Liu,Li Xu,Shuang Yang,Meng Zu,Porun Liu,Bo Zhang,Lirong Zheng,Huijun Zhao,Hua Gui Yang
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2017-08-16
卷期号:2 (10): 2257-2263
被引量:185
标识
DOI:10.1021/acsenergylett.7b00638
摘要
Oxygen evolution reaction (OER) plays a paramount role in renewable energy technologies. However, the slow kinetics of OER seriously limits the overall performance and commercialization. Here, we rationally design a metallic Ni2P/Fe2P interface, which can be in situ oxidized to a Ni2P(O)/Fe2P(O) interface to enhance OER efficiency, with active doped oxyhydroxides and phosphates on the surface and conductive phosphide in the bulk. The resulting catalysts require a low overpotential of 179 mV to achieve a current density of 10 mA/cm2 (without iR compensation) and can continuously drive OER for 120 h without any obvious degradation, which rivals most reported OER catalysts. These results suggest that we are able to design multicomponent metallic precatalysts to construct most active surface layers and conductive bulks, further boosting OER performance for real-world electrolysis utilization.
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