过电位
分解水
电催化剂
催化作用
材料科学
电化学
热液循环
化学工程
电极
纳米技术
化学
生物化学
光催化
工程类
物理化学
作者
Xiaoshuang Zhang,Yangyang Ding,Guangping Wu,Xiaoqiang Du
标识
DOI:10.1016/j.ijhydene.2020.08.096
摘要
Electrocatalytic water splitting is identified as one of the most promising solutions to energy crisis. The CoSe2@NiSe2 materials were first prepared and in situ grown on nickel foam by typical hydrothermal and selenification process at 120 °C. The results show that the CoSe2@NiSe2 material used as the 3D substrates electrode can maximize the synergy between the CoSe2 and NiSe2, and also exhibits high efficiency of water splitting reaction. The lower overpotential of only 235 mV is presented to attain 20 mA cm−2 compared to the benchmark of RuO2 electrodes (270 mV @ 20 mA cm−2). Besides, the CoSe2@NiSe2 material also shows a remarkable improved hydrogen evolution reaction activity compared to NiSe2 (192 [email protected] mA cm−2) and Co precursor catalysts (208 [email protected] mA cm−2) individually, which a low overpotential of only 162 mV is achieved at 10 mA cm−2. The CoSe2@NiSe2 catalysts exhibit excellent water splitting performance (cell voltage of 1.50 [email protected] 10 mA cm−2) under alkaline conditions. It was proved that the high water splitting performance of the catalyst is attributed to high electrochemical activity area and synergistic effect. The work offers new ideas for the exploitation of synergistic catalysis of composite catalysts and adds new examples for the exploitation of efficient, better and relatively non-toxic electrocatalysts.
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