纳米片
二硫化钼
过电位
电催化剂
材料科学
相(物质)
电极
化学工程
石墨烯
热液循环
可逆氢电极
纳米技术
电化学
化学
复合材料
有机化学
物理化学
工作电极
工程类
作者
Zhipeng Liu,Lei Zhao,Yuhua Liu,Zhichao Gao,Shisheng Yuan,Xiaotian Li,Nan Li,Shiding Miao
标识
DOI:10.1016/j.apcatb.2019.01.062
摘要
Metallic 1 T phase of molybdenum disulfide (1 T-phase MoS2) was proposed as an more ideal electrocatalyst for the hydrogen evolution reaction (HER) than 2H-phase owing to its proliferated density of active sites and superior electroconductivity. Nevertheless, the conventional synthetic route of 1 T-phase MoS2 through lithium intercalation suffers from tedious laboratory work and low yield, and the resulting powdery products are undesirable for practical applications. Herein, we developed a facile and scalable hydrothermal route to fabricate a self-supported electrode based on 1 T-phase MoS2, which enables the 1 T-phase MoS2 nanosheets to in-situ vertically grow on conductive carbon fiber cloth (1 T-MoS2/CC). The resultant 1 T-MoS2/CC combines advantages of the highly catalytically active phase of MoS2 and the unique self-supported structure. MoS2 nanosheets in 1 T-phase provide abundant active sites and high conductivity, while the self-supported structure endows the electrode with enhanced accessibility to active sites and efficient electron transfer throughout the structure. Owing to these merits, 1 T-MoS2/CC delivered remarkable activity towards the HER with a small overpotential of 151 mV to afford 10 mA·cm−2 current density as well as brilliant stability, which is far superior to 2H-MoS2/CC and its powdery counterpart (1 T-MoS2). Therefore, this strategy makes the 1 T-MoS2/CC a competitive electrocatalyst for hydrogen evolution.
科研通智能强力驱动
Strongly Powered by AbleSci AI