Abstract
Oxygen vacancies can regulate the coordination structure and electronic states of atoms, thus promoting the formation of surface-active sites and increasing the conductivity of the electrode material. This work presents a design for MXene@Ce-MOF composites with abundant oxygen vacancies. The hydroxyl groups on the surface of monolayer MXene attract cerium ions, which create surface defects in Ce-MOF and further promote the formation of oxygen vacancies. This results in a significant improvement in energy storage capacity, as well as performance in oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). The MXene@Ce-MOF composite exhibits a specific capacity of 496 F g−1, which is 1.8 times higher than that of pure Ce-MOF and 3.5 times higher than MXene alone. At a current density of 10 mA cm−2, the overpotential for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) is as low as 270 and 220 mV, respectively, and the composite exhibits excellent cycling stability. Oxygen vacancy-based MOF composites play a crucial role in electrocatalysis and energy conversion.
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