惰性
催化作用
材料科学
退火(玻璃)
钨
过渡金属
氢
电催化剂
烟气脱硫
纳米技术
二硫化钨
金属
化学工程
分解水
纳米颗粒
化学
电化学
电极
物理化学
冶金
工程类
光催化
生物化学
有机化学
作者
Longfei Wu,Arno J. F. van Hoof,Nelson Y. Dzade,Lu Gao,Marie‐Ingrid Richard,Heiner Friedrich,Nora H. de Leeuw,Emiel J. M. Hensen,Jan P. Hofmann
摘要
Transition metal dichalcogenides (TMDs), such as MoS2 and WS2, are promising alternative non-noble metal catalysts to drive the electrocatalytic H2 evolution reaction (HER). However, their catalytic performance is inherently limited by the small number of active sites as well as their poor electrical conductivity. Here, we grow vertically aligned 2H-WS2 on different substrates to expose their edge sites for the HER and introduce a scalable approach to tune these active sites via defect engineering. In a thermal hydrogen treatment procedure, sulfur vacancies and metallic tungsten nanoparticles are formed. The extent of desulfurization, and thus the HER activity, can be tuned via controlling the H2 annealing conditions. The obtained W/WS2-x electrocatalysts are evaluated experimentally and theoretically to arrive at a better understanding of how to modify the inherently inert 2H-WS2 for more efficient HER.
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