Boosting Toluene Combustion by Tuning Electronic Metal-Support Interactions in In Situ Grown Pt@Co3O4 Catalysts

Electronic metal-support interaction (EMSI) has attracted great attention in volatile organic compound (VOC) abatement. Herein, Pt@Co3O4 catalysts were prepared via a metal-organic framework (MOF) in situ growth approach to boost toluene degradation. The partial electron transfer from Co3O4 to Pt species was induced by the EMSI effect to generate the electron- rich Pt and Co3+ species. The electrophilic O-2 molecules could be activated by picking up the electrons from electron-rich Pt species to form nucleophilic oxygen species, which is conducive to attack C-H bonds in toluene. The redox ability and surface oxygen species activity of catalysts were improved due to strong EMSI. As expected, the excellent toluene activity was achieved, meanwhile exhibiting satisfactory water resistance and long-term stability for toluene combustion. In situ diffuse reflectance infrared Fourier transform spectroscopy results elucidated that surface lattice oxygen species should deeply participate in toluene degradation, which could be efficiently replenished by gaseous oxygen. This work may provide a new idea for exploring the relationship between the electron transfer effect and efficient catalytic performance of VOCs.

Automated summary

The study focused on the electronic metal-support interaction to enhance the catalytic performance of Pt@Co3O4 catalysts in toluene degradation. The catalyst showed excellent activity, water resistance, and long-term stability. Surface oxygen species played a crucial role in toluene degradation and could efficiently be replenished by gaseous oxygen.