单层
材料科学
基面
等离子体
氢
催化作用
过渡金属
纳米技术
Crystal(编程语言)
化学物理
化学工程
光电子学
结晶学
化学
有机化学
计算机科学
工程类
物理
量子力学
程序设计语言
作者
Chia-Chin Cheng,Ang‐Yu Lu,Chien‐Chih Tseng,Xiulin Yang,Mohamed Nejib Hedhili,Min-Cheng Chen,Kung‐Hwa Wei,Lain‐Jong Li
出处
期刊:Nano Energy
[Elsevier BV]
日期:2016-09-09
卷期号:30: 846-852
被引量:161
标识
DOI:10.1016/j.nanoen.2016.09.010
摘要
Abstract Two-dimensional layered transition metal dichalcogenide (TMD) materials such as Molybdenum disufide (MoS2) have been recognized as one of the low-cost and efficient electrocatalysts for hydrogen evolution reaction (HER). The crystal edges that account for a small percentage of the surface area, rather than the basal planes, of MoS2 monolayer have been confirmed as their active catalytic sites. As a result, extensive efforts have been developing in activating the basal planes of MoS2 for enhancing their HER activity. Here, we report a simple and efficient approach—using a remote hydrogen-plasma process—to creating S-vacancies on the basal plane of monolayer crystalline MoS2; this process can generate high density of S-vacancies while mainly maintaining the morphology and structure of MoS2 monolayer. The density of S-vacancies (defects) on MoS2 monolayers resulted from the remote hydrogen-plasma process can be tuned and play a critical role in HER, as evidenced in the results of our spectroscopic and electrical measurements. The H2-plasma treated MoS2 also provides an excellent platform for systematic and fundamental study of defect-property relationships in TMDs, which provides insights for future applications including electrical, optical and magnetic devices.
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