过电位
塔菲尔方程
材料科学
催化作用
碳纤维
化学工程
基质(水族馆)
热液循环
可逆氢电极
无机化学
化学
电极
复合材料
电化学
物理化学
复合数
工作电极
有机化学
地质学
工程类
海洋学
作者
Jianhui Feng,Hu Zhou,Jinpei Wang,Ting Bian,Jinxiao Shao,Aihua Yuan
标识
DOI:10.1016/j.ijhydene.2018.09.057
摘要
In this work, the porous carbon polyhedra were firstly obtained by carbonizing the zeolite imidazole framework (ZIF-8). Then the carbon polyhedra and precursors of MoS2 were successfully combined by a hydrothermal reaction, forming the C-MoS2 composites with different carbon contents. The well-tuned C-MoS2 sample possesses a core-shell morphology, in which the carbon substrate is well decorated by vertically aligned MoS2 ultrathin nanosheets. The resulting composites can be used as electrocatalysts of hydrogen evolution reaction (HER), displaying significantly superior activities to pure MoS2 and carbon. It's found that the carbon content largely affects the architectures and HER behaviors of catalysts. In particular, the optimized catalyst yields the best catalytic activity with the lowest onset potential (35 mV), smallest Tafel slope (53 mv dec−1), lowest overpotential (200 mV at 10 mA cm−2), as well as extraordinary long-term stability in H2SO4. The enhanced HER activity can be attributed to the unique core-shell structure, where abundant active edge sites of MoS2 are exposed and the underlying carbon substrate effectively improves the conductivity of the electrode.
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