Abstract

Monolithic Co3O4 and Co3O4@MnOx catalysts have been successfully prepared by in-situ growth. The morphology control and formation mechanism of Co3O4 on Ni foam was investigated in detail. Among the different samples, bamboo leaf-like Co3O4-NF-10 presented good catalytic activity for acetone oxidation (T50 = 179 °C, T90 = 193 °C), which was attributed to its low temperature reducibility, abundant Co3+ and surface adsorbed oxygen species (Oads). Therefore, Co3O4@MnOx-NF was further prepared to obtain abundant Co3+ and Oads species due to the redox reaction between MnO4− and Co2+. As expected, the Co3O4@MnOx-NF catalyst presented significantly improved activity for not only acetone but ethyl acetate and toluene oxidation compared to the Co3O4-NF-10. The high catalytic performance of Co3O4@MnOx-NF was ascribed to its good low-temperature reducibility, abundant Co3+ and Oads species. In addition, Co3O4@MnOx-NF presented a satisfactory cycle and long-term stability. This work shed light on the design of monolithic catalysts in VOC oxidation.

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