Integrated MXene and metal oxide electrocatalysts for the oxygen evolution reaction: synthesis, mechanisms, and advances.

Electrochemical water splitting is a promising approach to produce H through renewable electricity, but its energy efficiency is severely constrained by the kinetically slow anodic oxygen evolution reaction (OER), which uses about 90% of the electricity in the water-splitting process due to its multistep proton (H)-coupled electron (e) transfer process, high overpotential (), and low energy efficiency. Therefore, the quest for efficient, sustainable, and cost-effective electrocatalysts for hydrogen production through water electrolysis has intensified, highlighting the potential of two-dimensional (2D) MXenes. MXenes have emerged as a promising class of materials characterized by excellent stability, hydrophilicity, and conductivity. However, challenges such as low oxidation resistance, facile stacking, and the absence of intrinsic catalytically active sites limit their performance. This review thoroughly explores various synthesis methods for MXenes and their integration with transition metal oxides (TMOs) to tackle the challenges and enhance catalytic activity. The review also delves into advanced strategies for structural tuning of MXenes and TMOs, such as termination engineering, heteroatom doping, defect engineering, and the formation of heterojunctions. The integration of MXenes with TMOs has addressed the current limitations of MXenes and significantly boosted OER activity. By considering these structural tuning parameters and limitation factors, researchers can gain insights into the design principles and optimization strategies for MXene- and TMO-integrated electrocatalysts. The review concludes with a summary of the key findings and an outlook on future research directions, emphasizing the unexplored potential and innovative approaches that could further advance the field of electrocatalytic water splitting.