等离子体子
催化作用
拉曼光谱
化学物理
材料科学
过渡金属
相变
密度泛函理论
氢
透射电子显微镜
金属
相(物质)
纳米技术
光电子学
化学工程
化学
凝聚态物理
计算化学
光学
工程类
物理
生物化学
有机化学
冶金
作者
Bo Shang,Xiaoqiang Cui,Lin Jiao,Kun Qi,Yingwei Wang,Jinchang Fan,Yuanyuan Yue,Haiyu Wang,Qiaoliang Bao,Xiaofeng Fan,Shuting Wei,Wei Song,Zhiliang Cheng,Shaojun Guo,Weitao Zheng
出处
期刊:Nano Letters
[American Chemical Society]
日期:2019-04-08
卷期号:19 (5): 2758-2764
被引量:126
标识
DOI:10.1021/acs.nanolett.8b04104
摘要
Abstract Metallic 1T-phase transition metal dichalcogenides (TMDs) are of considerable interest in enhancing catalytic applications due to their abundant active sites and good conductivity. However, the unstable nature of 1T-phase TMDs greatly impedes their practical applications. Herein, we developed a new approach for the synthesis of highly stable 1T-phase Au/Pd-MoS2 nanosheets (NSs) through a metal assembly induced ultrastable phase transition for achieving a very high electrocatalytic activity in the hydrogen evolution reaction. The phase transition was evoked by a novel mechanism of lattice-mismatch-induced strain based on density functional theory (DFT) calculations. Raman spectroscopy and transmission electron microscopy (TEM) were used to confirm the phase transition on experimental grounds. A novel heterostructured 1T MoS2–Au/Pd catalyst was designed and synthesized using this mechanism, and the catalyst exhibited a 0 mV onset potential in the hydrogen evolution reaction under light illumination. Therefore, this method can potentially be used to fabricate 1T-phase TMDs with remarkably enhanced activities for different applications.
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