双功能
电催化剂
阳极
电化学
制氢
交换电流密度
电解
材料科学
催化作用
异质结
无机化学
电流密度
析氧
化学工程
电极
化学
物理化学
电解质
光电子学
塔菲尔方程
工程类
生物化学
物理
量子力学
作者
Kaixun Li,Binbin Xie,Dongmei Feng,Yun Tong
出处
期刊:Chemsuschem
[Wiley]
日期:2022-09-16
卷期号:15 (21)
被引量:9
标识
DOI:10.1002/cssc.202201656
摘要
Coupling urea oxidation reaction (UOR) with hydrogen evolution reaction (HER) is an attractive alternative anode reaction for electrochemical hydrogen generation with low energy consumption. However, the development of highly efficient bifunctional electrocatalysts is still a challenge. In this work, Ni2 Se3 -CuSex heterostructure was synthesized on copper foam (Ni3 Se2 @CuSex /CF) by electrodeposition accompanied by a selenization process. Benefiting from the abundant active sites, faster reaction kinetics, and modulated electronic structure, the self-supporting Ni3 Se2 @CuSex /CF electrode exhibited superior catalytic performance. Extremely low overpotentials of 120 and 140 mV were achieved at the current density of 100 mA cm-2 for HER/UOR, respectively. Respectively, in HER||UOR coupled electrolyzer for H2 generation, the Ni3 Se2 @CuSex /CF||Ni3 Se2 @CuSex /CF delivered a low cell voltage of 1.49 V to reach a high current density of 100 mA cm-2 along with good stability, outperforming most of the other well-developed materials to date. The rational design of coupled heterostructure as bifunctional electrodes is a promising approach for energy-saving H2 production.
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