多孔性
塔菲尔方程
材料科学
电催化剂
过电位
电化学
双金属片
催化作用
化学工程
电解
电流密度
电阻率和电导率
电导率
复合材料
电极
化学
金属
冶金
物理化学
电解质
工程类
电气工程
生物化学
物理
量子力学
作者
Tiantian Ma,Zheng Dai,Xueran Shen,Qingze Jiao,Yun Zhao,Hansheng Li,Caihong Feng
标识
DOI:10.1002/celc.202200552
摘要
Abstract The design and development of oxygen evolution electrocatalyst with stable structure and outstanding performance is of great significance for hydrogen production by water electrolysis. Inspired by the high stability of the self‐supported catalyst and the synergistic effect of the bimetallic transition metal catalyst, MnCo 2 S 4 microrugby balls were successfully prepared on carbon cloth by a two‐step hydrothermal method in this work. The prepared MnCo 2 S 4 /CC exhibits remarkable electrochemical performance due to the stable self‐supporting design and lavish porous structure, as well as the high inherent electrical conductivity of sulphide. The overpotential of MnCo 2 S 4 /CC is only 180 mV at the current density of 10 mA cm −2 , which is 161 mV lower than that of MnCo 2 O 4 /CC (341 mV). The Tafel slope of MnCo 2 S 4 /CC is 145.7 mV dec −1 , which is less than that of MnCo 2 O 4 /CC (157.5 mV dec −1 ). The OER performance of MnCo 2 S 4 /CC is significantly improved due to its high electrochemically active surface area and conductivity. Density functional theory (DFT) calculations show that MnCo 2 S 4 /CC has a higher electron density than MnCo 2 O 4 /CC, which indicates that it has better conductivity. These results indicate that it is a feasible method to optimize the performance of the electrocatalysts by combining the large electrochemical surface area provided by the porous structure of the self‐supported catalyst and the large electrical conductivity of the sulphide.
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