U and Co Dual Single‐Atom Doped MXene for Accelerating Electrocatalytic Hydrogen Evolution Activity

Abstract A large amount of radioactive waste is accumulated in the process of nuclear fuel preparation, causing serious pollution to the environment and abundant depleted uranium resources to be abandoned. One of the key issues affecting the development of nuclear energy is how to make full use of depleted uranium resources efficiently. Here, U element with unique coordination mode of 5f electron is spacer bonded to transition metal with 3d orbit through the adsorption and anchoring effect of MXene, thus U and Co dual doped MXene catalyst is constructed along with the comprehensive utilization of depleted uranium resources. The as‐prepared U‐Co/MXene catalyst demonstrates excellent overpotential of only 184 mV at −10 mA cm −2 and excellent stability up to 150 h, significantly surpassing the bare MXene substrate. Theoretical calculations indicate that the U and Co dual doping optimizes the electronic structure of MXene catalyst by forming the U‐O‐Co network, thereby improving the thermodynamics of H * adsorption during the catalytic transition state. This research opens up a new path for the recovery of depleted uranium resources and the development of functional actinide catalysts.