过电位
杂原子
碲
基面
氢
替代(逻辑)
结晶学
密度泛函理论
材料科学
硫族元素
化学
杂质
非金属
催化作用
格子(音乐)
兴奋剂
硫系化合物
再结晶(地质)
吸附
化学物理
Boosting(机器学习)
纳米技术
无机化学
钝化
作者
Guomin Li,Meihan Xia,Ye Zhang,Qiao Zhao,Wangwang Zhang,Yanting Liu,Wei Liu,Liang Yu,Xiaoju Cui,Dehui Deng
摘要
ABSTRACT Heteroatom substitution is a promising strategy to enhance hydrogen evolution reaction (HER) activity of MoS 2 , yet synergistically activating both its basal plane and edge sites remains challenging. Herein, we report a dual‐site substitution of both Mo and S with tellurium in the MoS 2 lattice (Te‐MoS 2 ), which achieves a superior large‐current‐density HER performance in acidic electrolyte, surpassing all previously reported single‐element‐doped MoS 2 with nonmetal or non‐precious metal. The Te‐MoS 2 catalyst requires an overpotential of only 364 mV to achieve an industrial‐level current density of 1000 mA·cm −2 , significantly lower than 506 mV required by commercial 20 wt% Pt/C, and maintains this performance stably for 200 h without decay. Comprehensive analyses reveal that the simultaneous substitution of Mo and S with Te atoms activates neighboring S atoms and also promotes the formation of smaller, edge‐rich MoS 2 nanosheets, thereby generating abundant basal plane and edge S active sites with optimized hydrogen adsorption energy.
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