钒
材料科学
剥脱关节
二硫化钼
二硒醚
电化学
过渡金属
插层(化学)
无机化学
锂(药物)
氧化钒
磷酸钒锂电池
电催化剂
石墨烯
纳米技术
催化作用
物理化学
化学
电极
冶金
硒
内分泌学
医学
生物化学
作者
Yong Wang,Zdeněk Sofer,Jan Luxa,Martin Pumera
标识
DOI:10.1002/admi.201600433
摘要
Ultrathin 2D transition metal dichalcogenides (TMDs) have attracted widespread attention due to their excellent electrical, optical, and electrochemical properties. Ultrathin vanadium disulfide is a metallic member of two dimensional materials aside graphene which does not possess a bandgap in the electronic structure. Research on vanadium disulfide reveals its versatile application, such as supercapacitor, battery material, electrocatalyst, and moisture sensor. Considering the superior performance of vanadium disulfide, it is necessary and essential to study vanadium diselenide and vanadium ditelluride. In this study, an effort has been devoted to study the inherent electrochemistry of three vanadium dichalcogenides (VX 2 : VS 2 , VSe 2 , and VTe 2 ) and explore their potential as electrocatalysts for hydrogen evolution reaction. Following the exfoliation routes established for MoS 2 and WS 2 , Li intercalation route, using n ‐buthyllithium is utilized. Interestingly, upon exfoliation to single/few layer VX 2 become partly converted to nonstoichiometric vanadium oxide and lithium vanadates, which is strikingly different when compared to group 6 TMDs, such as MoX 2 and WX 2 .
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