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用于增强析氢反应催化性能的WSe-VSe合金纳米片

WSe-VSe Alloyed Nanosheets to Enhance the Catalytic Performance of Hydrogen Evolution Reaction.

作者信息

Kwon Ik Seon, Kwak In Hye, Zewdie Getasew Mulualem, Lee Seung Jae, Kim Ju Yeon, Yoo Seung Jo, Kim Jin-Gyu, Park Jeunghee, Kang Hong Seok

机构信息

Department of Advanced Materials Chemistry, Korea University, Sejong 339-700, Republic of Korea.

Institute for Application of Advanced Materials, Jeonju University, Chonju, Chonbuk 55069, Republic of Korea.

出版信息

ACS Nano. 2022 Aug 23;16(8):12569-12579. doi: 10.1021/acsnano.2c04113. Epub 2022 Aug 8.

Abstract

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 WSe-VSe (WVSe, = 0-1) alloyed nanosheets using a colloidal reaction. Alloying the semiconducting WSe with VSe converts the material into a metallic one, followed by a 2H-to-1T phase transition at = 0.7. Over a wide composition range, WSe and VSe are atomically immiscible and form separate ordered domains. The miscible alloy at = 0.1 displayed enhanced electrocatalytic activity toward the hydrogen evolution reaction (HER) in an acidic electrolyte. This trend was correlated with the -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.

摘要

调节过渡金属二硫属化物(TMD)的电子结构对于其在下一代能源技术中的应用至关重要。在本研究中,我们通过胶体反应合成了成分可调的WSe-VSe(WVSe,x = 0-1)合金纳米片。将半导体WSe与VSe合金化可将材料转变为金属材料,随后在x = 0.7时发生2H到1T的相变。在很宽的成分范围内,WSe和VSe在原子尺度上互不相溶,形成单独的有序畴。x = 0.1时的互溶合金在酸性电解质中对析氢反应(HER)表现出增强的电催化活性。这种趋势通过火山型关系与费米能级中心相关联。自旋极化密度泛函理论计算一致预测了原子的互不相溶性,这在2H-1T相变成分处变得更加显著。H在基面(Se或空穴位点)上的吸附吉布斯自由能以及沿Volmer-Heyrovsky反应途径的活化能垒支持了合金相增强的HER性能,表明分散的V掺杂结构是最佳HER催化活性的原因。我们的研究证明了TMD合金纳米片的原子结构如何在增强催化活性中发挥关键作用。

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