烟气脱硫
硫黄
电化学
氩
材料科学
惰性
氢
基面
钼
化学
二硫化钼
化学工程
电极
结晶学
冶金
有机化学
物理化学
工程类
作者
Charlie Tsai,Hong Li,Sangwook Park,Joonsuk Park,Hyun Soo Han,Jens K. Nørskov,Xiaolin Zheng,Frank Abild‐Pedersen
摘要
Abstract Recently, sulfur (S)-vacancies created on the basal plane of 2 H -molybdenum disulfide (MoS 2 ) using argon plasma exposure exhibited higher intrinsic activity for the electrochemical hydrogen evolution reaction than the edge sites and metallic 1 T -phase of MoS 2 catalysts. However, a more industrially viable alternative to the argon plasma desulfurization process is needed. In this work, we introduce a scalable route towards generating S-vacancies on the MoS 2 basal plane using electrochemical desulfurization. Even though sulfur atoms on the basal plane are known to be stable and inert, we find that they can be electrochemically reduced under accessible applied potentials. This can be done on various 2 H -MoS 2 nanostructures. By changing the applied desulfurization potential, the extent of desulfurization and the resulting activity can be varied. The resulting active sites are stable under extended desulfurization durations and show consistent HER activity.
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