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