Hydrogen evolution reaction mechanism on Ti₃C₂ MXene revealed by <i>in situ</i>/operando Raman spectroelectrochemistry

Abstract

MXenes have shown great promise as electrocatalysts for the hydrogen evolution reaction (HER), but their mechanism is still poorly understood. Currently, the benchmark Ti₃C₂ MXene suffers from a large overpotential. In order to reduce this overpotential, modifications must be made to the structure to increase the reaction rate of the H⁺/e^- coupled transfer steps. These modifications heavily depend on understanding the HER mechanism. To remedy this, <i>in situ</i>/operando Raman spectroelectrochemistry combined with density functional theory (DFT) calculations are utilized to probe the HER mechanism of the Ti₃C₂ MXene catalyst in aqueous media. In acidic electrolytes, the -O- termination groups are protonated to form Ti-OH bonds, followed by protonation of the adjacent Ti site, leading to H₂ formation. DFT calculations show that the large overpotential is due to the lack of an optimum balance between O and Ti sites. In neutral electrolytes, H₂O reduction occurs on the surface and leads to surface protonation, followed by H₂ formation. This results in an overcharging of the structure that leads to the observed large HER overpotential. This study provides new insights into the HER mechanisms of MXene catalysts and a pathway forward to design efficient and cost-effective catalysts for HER and related electrochemical energy conversion systems.