WSe2–VSe2 Alloyed Nanosheets to Enhance the Catalytic Performance of Hydrogen Evolution Reaction

催化作用 材料科学 合金 吉布斯自由能 密度泛函理论 过渡金属 相(物质) 化学工程 金属 化学物理 带隙 电解质 制氢 纳米技术 物理化学 计算化学 化学 热力学 冶金 有机化学 电极 光电子学 工程类 物理
作者
Ik Seon Kwon,In Hye Kwak,Getasew Mulualem Zewdie,Seung Jae Lee,Ju Yeon Kim,Seung Jo Yoo,Jin-Gyu Kim,Jeunghee Park,Hong Seok Kang
出处
期刊:ACS Nano [American Chemical Society]
卷期号:16 (8): 12569-12579 被引量:33
标识
DOI:10.1021/acsnano.2c04113
摘要

Tuning the electronic structures of transition metal dichalcogenides (TMD) is essential for their implementation in next-generation energy technologies. In this study, we synthesized composition-tuned WSe2-VSe2 (W1-xVxSe2, x = 0-1) alloyed nanosheets using a colloidal reaction. Alloying the semiconducting WSe2 with VSe2 converts the material into a metallic one, followed by a 2H-to-1T phase transition at x = 0.7. Over a wide composition range, WSe2 and VSe2 are atomically immiscible and form separate ordered domains. The miscible alloy at x = 0.1 displayed enhanced electrocatalytic activity toward the hydrogen evolution reaction (HER) in an acidic electrolyte. This trend was correlated with the d-band center via a volcano-type relationship. Spin-polarized density functional theory calculations consistently predicted the atomic immiscibility, which became more significant at the 2H-1T phase transition composition. The Gibbs free energy of H adsorption on the basal planes (Se or hole sites) and the activation barriers along the Volmer-Heyrovsky reaction pathway supported the enhanced HER performance of the alloy phase, suggesting that the dispersed V-doped structures were responsible for the best HER catalytic activity. Our study demonstrates how the atomic structure of TMD alloy nanosheets plays a crucial role in enhancing catalytic activity.
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