双功能
硫族元素
密度泛函理论
纳米材料
过渡金属
兴奋剂
材料科学
纳米技术
电催化剂
单层
反应性(心理学)
化学
化学物理
催化作用
物理化学
计算化学
结晶学
电化学
光电子学
有机化学
病理
医学
替代医学
电极
作者
Shrish Nath Upadhyay,Srimanta Pakhira
摘要
Two-dimensional transition metal dichalcogenides (TMDs) are a new family of 2D materials with features that make them appealing for potential applications in nanomaterials science and engineering. Recently, these 2D TMDs have attracted significant research interest because of the abundant choice of materials with diverse and tunable electronic, optical, chemical, and electrocatalytic properties. Although, the edges of the 2D TMDs show excellent electrocatalytic performance, their basal plane (001) is inert, which hinders their industrial applications for electrocatalysis. Transition metal/chalcogen atom vacancies or doping with some other foreign atoms may be a remedy to activate the inert basal plane. Here, we have computationally designed 2D monolayer MoSe2 and studied its electronic properties with electrocatalytic activities. A Pt-atom has been doped in the pristine 2D MoSe2 (i.e., Pt-MoSe2) to activate the inert basal plane resulting in a zero band gap. This study reveals that the Pt-MoSe2 is an excellent bifunctional electrocatalyst for both the hydrogen evolution reaction (HER) and oxygen reduction reaction (ORR) with the aid of first priciples-based hybrid density functional theory (DFT). The periodic hybrid DFT method has been applied to compute the electronic properties of both the pristine MoSe2 and Pt-MoSe2. To determine both the HER and ORR mechanisms on the surface of the Pt-MoSe2 material, non-periodic DFT calculation has been performed by considering a molecular Pt1-Mo9Se21 cluster model. The present study shows that the 2D Pt-MoSe2 follows the Volmer-Heyrovsky mechanism for the HER with energy barriers of about 9.29 kcal mol-1 and 10.55 kcal mol-1 during the H˙-migration and Heyrovsky reactions. The ORR is achieved by a four-electron transfer mechanism with the formation of two transition energy barriers of about 14.94 kcal mol-1 and 11.10 kcal mol-1, respectively. The lower energy barriers and high turnover frequency during the reactions expose that the Pt-MoSe2 can be adopted as an efficient bifunctional electrocatalyst for both the HER and ORR. The present studies demonstrate that the exceptional HER and ORR activity and stability performance shown by the MoSe2 electrocatalyst can be enhanced by Pt-doping, opening a promising concept for the sensible design of high-performance catalysts for H2 production and O2 reduction.
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