三元运算
材料科学
吉布斯自由能
合金
电催化剂
催化作用
化学工程
吸附
金属
摩尔分数
过渡金属
电化学
纳米技术
物理化学
冶金
化学
热力学
电极
有机化学
工程类
物理
程序设计语言
计算机科学
作者
Ik Seon Kwon,Seung Jae Lee,Ju Yeon Kim,In Hye Kwak,Getasew Mulualem Zewdie,Seung Jo Yoo,Jin-Gyu Kim,Kug‐Seung Lee,Jeunghee Park,Hong Seok Kang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2023-01-19
卷期号:17 (3): 2968-2979
被引量:30
标识
DOI:10.1021/acsnano.2c11528
摘要
Ternary alloying of transition metal dichalcogenides (TMDs) has the potential for altering the electronic structure of materials to suit electrochemical applications. Herein, we synthesized (MoWV)Se2 nanosheets at various compositions via a colloidal reaction. The mole fraction of V atoms (xV) was successfully increased up to 0.8, producing a metallic phase that is highly durable against hydration. Furthermore, we synthesized (MoW)Se2 nanosheets over the entire composition range. The atomic mixing of the ternary alloys is more random than that of the constitutional binary alloys, as supported by first-principles calculations. Compared to binary alloying, ternary alloying more effectively enhanced the electrocatalytic activity for acidic hydrogen evolution reaction (HER). The HER performance increased upon increasing xV to 0.44, and thereafter, it declined at higher xV primarily owing to surface oxidation. The analysis of Gibbs free energy for H adsorption revealed that ternary alloying strongly activates the basal plane for the HER. VSe2 contains numerous sites favorable for H adsorption, facilitating the composition-dependent HER. These results provide a pioneering strategy for designing multicomponent TMD catalysts that maximize the advantages of each component.
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