过电位
材料科学
催化作用
密度泛函理论
X射线吸收精细结构
兴奋剂
硫化镍
分解水
镍
化学工程
硫化物
无机化学
纳米技术
电化学
物理化学
化学
光电子学
计算化学
冶金
有机化学
电极
工程类
光谱学
物理
光催化
量子力学
作者
Wen-Jun He,Hui Liu,Jianing Cheng,Ying Li,Caichi Liu,Cong Chen,Jianling Zhao,Huolin L. Xin
标识
DOI:10.1021/acsami.1c23251
摘要
The exploration of indurative and stable low-cost catalysts for hydrogen evolution reaction (HER) is of great importance for hydrogen energy economy, but it still faces challenges. Herein, we report a Cl-doped Ni3S2 (Cl-Ni3S2) nanoplate catalyst vertically grown on Ni foam with outstanding activity and durability for HER, which only requires an overpotential of 67 mV to reach a current density of 10 mA cm-2 in alkaline media and exhibits negligible degradation after 30 h of operation. Both the advanced X-ray absorption fine structure (XAFS) and density functional theory (DFT) calculation validate that Cl doping can optimize the electronic structure and the intrinsic activity of Ni3S2. This study devoted to the revelation of the impact of ionic doping on the activity of catalysts at the atomic scale can provide the direction for the rational design of novel and advanced HER electrocatalysts.
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