纳米片
电催化剂
镍
催化作用
材料科学
计时安培法
分解水
电解质
电化学
无机化学
纳米技术
化学工程
化学
物理化学
循环伏安法
冶金
电极
生物化学
光催化
工程类
作者
Yangyang Ding,Xiaoqiang Du,Xiaoshuang Zhang
出处
期刊:Chemcatchem
[Wiley]
日期:2021-01-15
卷期号:13 (7): 1824-1833
被引量:25
标识
DOI:10.1002/cctc.202001838
摘要
Abstract Ni 3 S 2 has been widely reported as an effective electrochemical catalyst for hydrogen evolution reaction (HER). However, the electrochemical activity of the cathode reduction reaction needs to be further improved due to the drawback of strong S−H bond interaction on the surface of Ni 3 S 2 . Herein, a series of non‐precious metal Cu element doped Ni 3 S 2 materials were prepared on the Nickel foam support (Cu−Ni 3 S 2 /NF) though a two‐step hydrothermal method. Moreover, we optimized the performance of the catalyst by adjusting the molar amount of doped copper ion in the first hydrothermal process. When the molar ratio of copper ion and nickel ion is 1 : 4, the Cu−Ni 3 S 2 /NF‐1/4 material with independent and clustered rose‐shaped cross‐nanosheet arrays structure have been used as a highly efficient electrochemical hydrogen evolution reaction (HER) catalyst. In HER process, the Cu−Ni 3 S 2 /NF‐1/4 material drives the current densities of 10 mA cm −2 and 50 mA cm −2 under low overpotentials of 92 mV and 256 mV respectively, while Ni 3 S 2 /NF needs 210 mV and 397 mV to reach the same current densities. Density functional theory (DFT) calculation shows that the superior electrocatalytic activities are attributed to optimized water adsorption energy and enhanced electrical conductivity. The stability of catalyst was tested in 1 M KOH for 12 hours by chronoamperometry, indicating the current density has no an apparent attenuation.
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