二硫化钼
材料科学
硫化
化学工程
化学气相沉积
成核
亚稳态
氢
电化学
薄脆饼
纳米技术
催化作用
制氢
电催化剂
化学
硫黄
电极
物理化学
冶金
有机化学
工程类
作者
Hyeong‐U Kim,Mansu Kim,Hyunho Seok,Kyu‐Young Park,Ji‐Yun Moon,Jonghwan Park,Byeong‐Seon An,Hee Joon Jung,Vinayak P. Dravid,Dongmok Whang,Jae‐Hyun Lee,Taesung Kim
出处
期刊:Chemsuschem
[Wiley]
日期:2021-01-06
卷期号:14 (5): 1344-1350
被引量:35
标识
DOI:10.1002/cssc.202002578
摘要
Abstract The octahedral structure of 2D molybdenum disulfide (1T‐MoS 2 ) has attracted attention as a high‐efficiency and low‐cost electrocatalyst for hydrogen production. However, the large‐scale synthesis of 1T‐MoS 2 films has not been realized because of higher formation energy compared to that of the trigonal prismatic phase (2H)‐MoS 2 . In this study, a uniform wafer‐scale synthesis of the metastable 1T‐MoS 2 film is performed by sulfidation of the Mo metal layer using a plasma‐enhanced chemical vapor deposition (PE‐CVD) system. Thus, plasma‐containing highly reactive ions and radicals of the sulfurization precursor enable the synthesis of 1T‐MoS 2 at 150 °C. Electrochemical analysis of 1T‐MoS 2 shows enhanced catalytic activity for the hydrogen evolution reaction (HER) compared to that of previously reported MoS 2 electrocatalysts 1T‐MoS 2 does not transform into stable 2H‐MoS 2 even after 1000 cycles of HER. The proposed low‐temperature synthesis approach may offer a promising solution for the facile production of various metastable‐phase 2D materials.
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