Interfacial coupling of Ce-CoSe2 nanoneedle arrays with MXene for efficient overall water splitting

Designing highly effective, low-cost bifunctional electrocatalysts without noble metals for overall water splitting remains a significant challenge. In this work, interfacial coupling of Ce-doped CoSe 2 nanoneedle arrays with MXene (Ce-CoSe 2 /MXene) is developed via the facile hydrothermal and selenization methods. The extensive specific surface area and favorable hydrophilicity of Ti 3 AlC 2 , combined with the optimized electronic structure and abundant active sites from Ce-doping and selenization, contribute to the exceptional bifunctional electrocatalytic performance of the Ce-CoSe 2 /MXene electrode. Specifically, this heterostructure achieves a low hydrogen evolution reaction (HER) overpotential of 34 mV at 10 mA cm −2 , an oxygen evolution reaction (OER) overpotential of 279 mV at 100 mA cm −2 , and an overall water splitting (OWS) potential as low as 1.45 V at 10 mA cm −2 . In-situ Raman spectroscopy reveals that surface reconstruction would improve catalytic activity and stability. Theoretical calculations indicate that the Ce-CoSe 2 /MXene can improve the adsorption of intermediates and facilitate HER/OER process by lowering the kinetic barrier, thereby enhancing electrocatalytic activity. This research marks a substantial advancement in the development of low-cost, efficient electrocatalysts for overall water splitting.