Hydrogen evolution mediated by sulfur vacancies and substitutional Mn in few-layered molybdenum disulfide

Abstract

MoS2 is widely praised as a promising replacement for Pt as an electrocatalyst for the hydrogen evolution reaction (HER), but even today, it still suffers from low performance. This issue is tackled by using Mn3+ as a surface modifier to trigger sulfur vacancy formation and enhance electron transport in few-layered 2H MoS2. Only 10% of Mn is sufficient to transform the semiconductive MoS2 into an active HER electrocatalyst. The insertion of Mn reduces both HER onset potential and Tafel slope which allows reaching 100 mA/cm2 at an overpotential of 206 mV, ten times larger of what undoped MoS2 can achieve. The enhanced activity arises because Mn3+ introduces electronic states near the conduction band, promotes sulfur vacancies, and increases the hydrogen adsorption. In addition to its facile production and extended shelf-life, Mn–MoS2 exhibits an efficiency of 73% at 800 mA/cm2 and 2.0 V when used in proton exchange membrane water electrolyzers.