材料科学
塔菲尔方程
异质结
过电位
析氧
分解水
电解
X射线光电子能谱
电解水
贵金属
纳米技术
电化学
化学工程
电极
金属
光电子学
催化作用
光催化
冶金
物理化学
工程类
电解质
生物化学
化学
作者
Jinman Bai,Tao Meng,Donglei Guo,Shuguang Wang,Baoguang Mao,Minhua Cao
标识
DOI:10.1021/acsami.7b14997
摘要
The development of efficient non-noble-metal electrocatalysts is of critical importance for clean energy conversion systems, such as fuel cells, metal-air batteries, and water electrolysis. Herein, uniform Co9S8@MoS2 core-shell heterostructures have been successfully prepared via a solvothermal approach, followed by an annealing treatment. Transmission electron microscopy, X-ray absorption near-edge structure, and X-ray photoelectron spectroscopy measurements reveal that the core-shell structure of Co9S8@MoS2 can introduce heterogeneous nanointerface between Co9S8 and MoS2, which can deeply influence its charge state to boost the electrocatalytic performances. Besides, due to the core-shell structure that can promote the synergistic effect of Co9S8 and MoS2 and provide abundant catalytically active sites, Co9S8@MoS2 exhibits a superior hydrogen evolution reaction performance with a small overpotential of 143 mV at 10 mA cm-2 and a small Tafel slope value of 117 mV dec-1 under alkaline solution. Meanwhile, the activity of Co9S8@MoS2 toward oxygen evolution reaction is also impressive with a low operating potential (∼1.57 V vs reversible hydrogen electrode) at 10 mA cm-2. By using Co9S8@MoS2 catalyst for full water splitting, an alkaline electrolyzer affords a cell voltage as low as 1.67 V at a current density of 10 mA cm-2. Also, Co9S8@MoS2 reveals robust oxygen reduction reaction performance, making it an excellent catalyst for Zn-air batteries with a long lifetime (20 h). This work provides a new means for the development of multifunctional electrocatalysts of non-noble metals for the highly demanded electrochemical energy technologies.
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