Abstract
The degradation of volatile organic compounds (VOCs) at low temperature remains a big challenge. Photothermal catalysis coupling the advantages of photocatalysis and thermocatalysis is promising to address this issue. However, there is still a long way to construct highly active catalysts and deeply understand the mechanism of photothermal catalysis. Herein, maganese oxide (MnO2)catalysts embedded with Pt single-atoms (0.11 wt% Pt) have achieved greatly enhanced toluene conversion of 95%, far surpassing most supported Pt photothermal catalysts. The excellent catalytic activity has been disclosed to derive from the synergetic effect oflight-driven thermocatalysis and photocatalysis. The light-driven thermocatalysis predominates and the strong electron transfer from Pt single-atoms to MnO2 improves the activity of surface lattice oxygen to boost the generation of benzoic acid and the mineralization of toluene. Meanwhile, in photocatalytic process, Pt single-atoms accelerate the generation of superoxide radicals (O2−), which facilitate the ring-opening and deep oxidation of toluene. This understanding on the photothermal synergetic mechanism will inspire the design of highly efficient catalysts for VOCs oxidation.
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