Acceleration of Molecular Oxygen Activation in <i>m</i>-Xylene Oxidation at Low-Temperature through Building the Cu–O–Mn Electron Bridge
Xueyun Zhong, Xinyang He, Juntai Tian, Chuan Yu, Wenjing Kong, Chuying Qiu, Sijia Weng, Yanjun Li, Yushu Chen, Chen Yang, Mingli Fu, Daiqi Ye
Abstract
The limitations of pure Mn 3 O 4 catalysts in oxygen activation and electron transfer impeded their efficiency for low-temperature catalytic oxidation of m -xylene. Herein, a Cu-substitution strategy was employed to construct the Cu–O–Mn electron bridge in Mn 3 O 4, enabling tailored electronic redistribution and enhanced molecular oxygen activation. A series of characterizations and DFT calculations revealed that the substitution of Cu decreased the electron density around the Mn atoms, generated abundant oxygen vacancies, and elevated the Mn 4+ concentration, improving oxidative capacity. The optimized CuMn 2 O 4 catalyst achieved 90% conversion of m -xylene at 246 °C, which was 12 °C lower than that of Mn 3 O 4 . The investigation of the mechanism demonstrated that the synergistic effect of Cu + species and oxygen vacancies accelerated molecular oxygen activation and dynamically replenished the consumed lattice oxygen. Furthermore, the Cu–O–Mn bridge facilitated interfacial electron transfer, weakening Mn–O bonds and lowering oxygen vacancy formation energy, which promoted surface lattice oxygen mobility. Additionally, the CuMn 2 O 4 catalyst exhibited excellent stability and water tolerance. This work provided new insights into electron regulation to accelerate molecular oxygen activation, which was beneficial for the targeted design of highly efficient catalysts for refractory m -xylene.