The development of stable, highly
active, and inexpensive catalysts
for the ozone catalytic oxidation of volatile organic compounds (VOCs)
is challenging but of great significance. Herein, the micro-coordination
environment of Al in commercial Y zeolite was regulated by a specific
dealumination method and then the dealuminated Y zeolite was used
as the support of Cu–Mn oxides. The optimized catalyst Cu–Mn/DY
exhibited excellent performance with around 95% of toluene removal
at 30 °C. Besides, the catalyst delivered satisfactory stability
in both high-humidity conditions and long-term reactions, which is
attributed to more active oxygen vacancies and acidic sites, especially
the strong Lewis acid sites newly formed in the catalyst. The decrease
in the electron cloud density around aluminum species enhanced electron
transfer at the interface between Cu–Mn oxides. Moreover, extra-framework
octahedrally coordinated Al in the support promoted the electronic
metal–support interaction (EMSI). Compared with single Mn
catalysts, the incorporation of the Cu component changed the degradation
pathway of toluene. Benzoic acid, as the intermediate of toluene oxidation,
can directly ring-open on Cu-doped catalysts rather than being further
oxidized to other byproducts, which increased the rate of the catalytic
reaction. This work provides a new insight and theoretical guidance
into the rational design of efficient catalysts for the catalytic
ozonation of VOCs.