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Ultrastable In‐Plane 1T–2H MoS2 Heterostructures for Enhanced Hydrogen Evolution Reaction
Advanced Energy Materials ( IF 24.4 ) Pub Date : 2018-07-18 , DOI: 10.1002/aenm.201801345
Shuai Wang 1 , Di Zhang 1 , Bin Li 1 , Chao Zhang 1 , Zhiguo Du 1 , Haoming Yin 1 , Xiaofang Bi 1 , Shubin Yang 1
Affiliation  

Metallic 1T MoS2 is highly desirable for catalyzing electrochemical hydrogen production from water owing to its high electrical conductivity. However, stable 1T MoS2 is difficult to be produced in large‐scale by either common chemical or physical approaches. Here, ultrastable in‐plane 1T–2H MoS2 heterostructures are achieved via a simple one‐pot annealing treatment of 2H MoS2 bulk under a mixture gas of Ar and phosphorous vapor, where phosphorus cannot only occupy the interspace of MoS2 bulk, resulting in the expansion of MoS2, but also embed into the lattice of MoS2, inducing the partial phase transition from 2H to 1T phases of MoS2. Benefiting from its significantly improved electrical conductivity, highly exposed active sites, and hydrophily property, in‐plane 1T–2H MoS2 heterostructures exhibit largely improved electrocatalytic properties for hydrogen evolution reaction (HER) in alkaline electrolytes.

中文翻译:

超稳定平面内1T–2H MoS2异质结构,可增强氢释放反应

金属1T MoS 2由于其高电导率而非常需要用于催化从水中产生电化学氢。但是,很难通过常规化学或物理方法大规模生产稳定的1T MoS 2。在这里,通过在Ar和磷蒸气的混合气体下对2H MoS 2块进行简单的单锅退火处理,即可获得超稳定的面内1T–2H MoS 2异质结构,其中磷不能仅占据MoS 2块的空间,从而在硫化钼的膨胀2,而且还嵌入到硫化钼的晶格2,诱导从2H部分相转变为MO的1T相位2。平面内1T–2H MoS 2异质结构得益于其显着改善的电导率,高度暴露的活性位点和亲水性,在碱性电解质中对氢析出反应(HER)的电催化性能大大提高。
更新日期:2018-07-18
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