硫化
单层
材料科学
二硫化钼
X射线光电子能谱
相(物质)
拉曼光谱
金属
催化作用
氢
Atom(片上系统)
氢原子
过渡金属
分析化学(期刊)
化学工程
硫黄
纳米技术
冶金
化学
有机化学
物理
光学
计算机科学
工程类
嵌入式系统
烷基
作者
Hien Duy,Sangmin Jeong,Gi‐Nam Bae,Tran Minh Ngoc,Jong‐Sang Youn,Cheol‐Min Park,Ki‐Joon Jeon
标识
DOI:10.1002/aenm.202300183
摘要
Abstract For single‐atom‐layer hydrogen evolution reaction catalysts, enrichment of the 1T‐phase in monolayer molybdenum disulfide is important to achieve ideal metal utilization efficiency and exposure of active surface atoms. Herein, it is discovered that the 1T‐phase degree in monolayer MoS 2 can be enhanced through sulfidation of the Pd species deposited on MoS 2 (Pd x S y /1T‐MoS 2 ). Raman and X‐ray photoelectron spectroscopy reveal that the sulfidation‐assisted phase transition results in considerably greater proportions of 1T‐phase fraction (up to 86%) without using alkali‐metal‐based approaches. Observations of S‐atom displacement/translation at the atomic level contribute to the understanding of the phase transformation of MoS 2 . The maximized surface atom activation and metal utilization efficiency in Pd x S y /1T‐MoS 2 lead to unprecedentedly high mass activity (−3444 A mg Pd −1 ) and turnover frequency (1892 s −1 ), three orders of magnitude higher than those of commercial Pt/C 10 wt% (3.6 A mg Pt −1 and 3.6 s −1 ). The sulfidation‐assisted 1T‐phase enrichment has major implications for the designs of efficient electrocatalysts through MoS 2 phase engineering.
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