Enhancing catalytic toluene oxidation over MnO2@Co3O4 by constructing a coupled interface

作者:Ren, Quanming; Mo, Shengpeng; Fan, Jie; Feng, Zhentao; Zhang, Mingyuan; Chen, Peirong; Gao, Jiajian; Fu, Mingli; Chen, Limin; Wu, Junliang; Ye, Daiqi*
来源:CHINESE JOURNAL OF CATALYSIS, 2020, 41(12): 1873-1883.
DOI:10.1016/S1872-2067(20)63641-5

摘要

Herein, a bottom-down design is presented to successfully fabricate ZIF-derived Co3O4, grown in situ on a one-dimensional (1D) alpha-MnO2 material, denoted as alpha-MnO2@Co3O4. The synergistic effect derived from the coupled interface constructed between alpha-MnO2 and Co3O4 is responsible for the enhanced catalytic activity. The resultant alpha-MnO2@Co3O4 catalyst exhibits excellent catalytic activity at a T-90% (temperature required to achieve a toluene conversion of 90%) of approximately 229 degrees C, which is 47 and 28 degrees C lower than those of the pure alpha-MnO2 nanowire and Co3O4-beta obtained via pyrolysis of ZIF-67, respectively. This activity is attributed to the increase in the number of surface-adsorbed oxygen species, which accelerate the oxygen mobility and enhance the redox pairs of Mn4+/Mn3+ and Co2+/Co3+. Moreover, the result of in situ diffuse reflectance infrared Fourier transform spectroscopy suggests that the gaseous oxygen could be more easily activated to adsorbed oxygen species on the surface of alpha-MnO2@Co3O4 than on that of alpha-MnO2. The catalytic reaction route of toluene oxidation over the alpha-MnO2@Co3O4 catalyst is as follows: toluene. benzoate species. alkanes containing oxygen functional group. CO2 and H2O. In addition, the alpha-MnO2@Co3O4 catalyst shows excellent stability and good water resistance for toluene oxidation. Furthermore, the preparation method can be extended to other 1D MnO2 materials. A new strategy for the development of high-performance catalysts of practical significance is provided.

  • 单位
    南阳理工学院