Mn-Modified MIL-100(Fe)-Derived FeOx to Boost Toluene Photothermal Catalytic Degradation

The development of highly efficient catalysts is important for the photothermal catalytic oxidation of volatile organic compounds (VOCs). Herein, MIL-100(Fe) was used as the sacrificial template to prepare MnFeOxcatalysts with different Mn contents through the impregnation–calcination method, and their performance in photothermal catalytic oxidation of toluene was investigated. The results show that the content of Mn significantly affects the crystal phase structure, pore properties, surface chemical state, and optical response of the catalyst. Among them, 30%MnFeOxexhibits the best photothermal catalytic activity, with T50and T90being 211 and 237 °C, respectively, which are significantly lower than those of FeOx(232 and 260 °C). Characterization results suggested that the introduction of Mn caused the bandgap of FeOxto decrease from 1.96 to 1.67 eV. Meanwhile, the surface Fe2+, adsorbed oxygen (Oads) species, and oxygen vacancies were increased, enhancing visible light absorption and gaseous oxygen species adsorption and activation, which promoted the photothermal catalytic oxidation of toluene. Additionally, the 30%MnFeOxcatalyst presented good thermal stability and water resistance. Furthermore, during the reaction process, the in situ activation of the catalyst’s surface induced the increase in surface Fe2+, Mn3+,and Oadsspecies, which enhances the photothermal catalytic activity of the catalyst. Importantly, the in situ DRIFTS results further indicate that toluene is mainly oxidized along the path of toluene → benzyl alcohol → benzoate → maleic anhydride → CO2and H2O. This work provides a theoretical basis for the construction of low-cost, non-precious-metal Mn–Fe-based photothermal catalysts.