硫化钴
催化作用
塔菲尔方程
X射线光电子能谱
电催化剂
硫化物
拉曼光谱
钴
无机化学
化学
过渡金属
钼
异质结
材料科学
化学工程
电化学
电极
物理化学
生物化学
物理
光电子学
有机化学
光学
工程类
作者
Lee Kendall,Qiyuan Lin,Giovanni Zangari,Stephen McDonnell
标识
DOI:10.1149/1945-7111/acc9e0
摘要
MoS 2 has attracted significant attention as a non-platinum group electrocatalyst for the hydrogen evolution reaction (HER). There have been extensive efforts demonstrating that by doping MoS 2 with various transition metals, such as Co, the HER activity of the catalyst is enhanced. In particular, this work has shown that various cobalt sulfide phases can act as a co-catalyst with MoS 2 . Here, we report on the electrodeposition of a c-CoS x /MoS 2 heterostructure catalyst for the HER reaction in both acidic and alkaline conditions. Using Raman spectroscopy, X-ray photoelectron spectroscopy, X-ray diffraction, and scanning electron microscopy, it is demonstrated that depending on the precursor concentrations, various morphologies, grain size, and c-CoS x phases can be achieved, all of which have an impact on the activity and stability of the c-CoS x /MoS 2 catalysts. The most promising catalyst composition demonstrated excellent stability in both acidic and alkaline conditions with low overpotentials to reach 10 mA cm −2 of 112 mV and 60 mV and with Tafel slopes of 113 mV dec −1 and 81 mV dec −1 , respectively. This report demonstrates that the c-CoS x /MoS 2 heterostructure is one of the most catalytically active materials for HER, especially in alkaline conditions.
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