Unveiling the role of 2D monolayer Mn-doped MoS2 material: toward an efficient electrocatalyst for H2 evolution reaction. Issue 1 (9th December 2021)

• Record Type: Journal Article
• Authors: Ekka, Joy; Upadhyay, Shrish Nath; Keil, Frerich J.; Pakhira, Srimanta
• Is Part Of: Physical chemistry chemical physics. Volume 24:Issue 1(2021)
• Page Start: 265
• Page End: 280
• Publication Date: 2021-12-09
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/d1cp04344g
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : Two-dimensional (2D) monolayer Mn-doped MoS2 transition metal dichalcogenide has shown excellent electrocatalytic activities for effective hydrogen evolution reaction due to the Mn-doping in the pristine MoS2 . Abstract : Two-dimensional (2D) monolayer pristine MoS2 transition metal dichalcogenide (TMD) is the most studied material because of its potential applications as nonprecious electrocatalyst for the hydrogen evolution reaction (HER). Previous studies have shown that the basal planes of 2D MoS2 are catalytically inert, and hence it cannot be used directly in desired applications such as electrochemical HER in industry. Here, we thoroughly studied a defect-engineered Mn-doped 2D monolayer MoS2 (Mn–MoS2 ) material, where Mn was doped in pristine MoS2 to activate its inert basal planes. Using the density functional theory (DFT) method, we performed rigorous inspection of the electronic structures and properties of the 2D monolayer Mn–MoS2 as a promising alternative to noble metal-free catalyst for effective HER. A periodic 2D slab of monolayer Mn–MoS2 was created to study the electronic properties (such as band gap, band structures and total density of states (DOS)) and the reaction pathways occurring on the surface of this material. The detailed HER mechanism was explored by creating an Mn1 Mo9 S21 non-periodic finite molecular cluster model system using the M06-L DFT method including solvation effects to determine the reaction barriers and kinetics. Our study revealed that the 2D Mn–MoS2 follows the most favorable Volmer–Heyrovsky reaction mechanism with a very low energy barrier during H2 evolution. It was found that the change in the free energy barrier (Δ G ) during the H˙-migration ( i.e., Volmer) and Heyrovsky reactions is about 10.34–10.79 kcal mol −1 (computed in the solvent phase), indicating that this material is an exceptional electrocatalyst for the HER. The Tafel slope ( y ) was lower in the case of the 2D monolayer Mn–MoS2 material due to the overlap of the s-orbital of hydrogen and d-orbitals of the Mn atoms in the HOMO and LUMO transition states (TS1 and TS2) of both the Volmer and Heyrovsky reaction steps, respectively. The better stabilization of the atomic orbitals in the HER rate-limiting step Heyrovsky TS2 is the key for reducing the reaction barrier, and thus the overall catalysis, indicating a better electrocatalytic performance for H2 evolution. This study focused on designing low-cost and efficient electrocatalysts for the HER using earth abundant transition metal dichalcogenides (TMDs) and decreasing the activation energy barriers by scrutinizing the kinetics of the reaction to achieve high reactivity.