塔菲尔方程
钴
分解水
电催化剂
材料科学
无定形固体
电化学
介电谱
化学工程
析氧
电解水
无机化学
镍
电解
电极
双功能
催化作用
化学
冶金
电解质
物理化学
有机化学
光催化
工程类
作者
Feng Du,Yintong Zhang,Huichao He,Tao Li,Guihua Wen,Yong Zhou,Zhigang Zou
标识
DOI:10.1016/j.jpowsour.2019.05.063
摘要
The surface self-reconstruction during the water splitting is considered as one key factor for the high catalytic activity. Owing to the exposure of more dangling bonds, amorphous structure is the ideal precursor to convert into the actual active phase in the process of electrocatalysis. Herein, amorphous cobalt phosphosulfide electrocatalysts are fabricated by a facile electrodeposition method on nickel foams as efficient bifunctional electrodes for overall water splitting. And benefited from the introduction of phosphorus and sulfur, the quantities of precursor sites are increased and the electronic state around cobalt is reconstructed, which provides more active phases and facilitates the transport efficiency of electrons. Electrochemical test results reveal that, the as-prepared cobalt phosphosulfide electrodes require overpotentials as low as 58 and 283 mV to achieve 10 mA cm−2 for hydrogen and oxygen evolution reactions in 1.0 M KOH, respectively. Tafel slopes and electrochemical impedance spectroscopy further illustrate a favorable kinetic during electrolysis. Meanwhile, it only requires a low cell voltage of 1.6 V for cobalt phosphosulfide electrodes to reach 10 mA cm−2 for overall water splitting.
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