Regulating the mobility of lattice oxygen on hollow cobalt-manganese sub-nanospheres for enhanced catalytic oxidation of toluene and o-xylene.

Promoting lattice oxygen mobility of Co-based catalysts is crucial to making progress in catalytic oxidation technology. The addition of manganese, a transition metal with similar ionic radius to cobalt and variable valence, was supposed to enhance the mobility of lattice oxygen species of Co-based oxide. A range of hollow CoMnaOx sub-nanosphere catalysts with different Mn/Co ratios was synthesized via a template-sacrificed method, and the effects of different Mn/Co ratios on the structural properties of the catalysts and their catalytic performance for benzene series volatile organic compounds (VOCs) oxidation were investigated. Hollow CoMn2Ox sub-nanosphere exhibited good catalytic activity for oxidation of toluene (T90 = 265 °C) and o-xylene (T90 = 297 °C), as well as excellent recycling ability and water resistance. By adjusting the Mn/Co ratio, metal ions enter into the different tetrahedral or octahedral active sites. Compared with Co3O4, the desorption temperature of surface lattice oxygen on CoMn2Ox decreased by 110 °C. These results demonstrate that the addition of manganese can encourage the electron transfer on CoMnaOx, indicating that the introduction of the appropriate amount of manganese accelerates the activation of gas O2 and mobility of surface lattice oxygen species, thereby expediting the oxidation of benzene series VOCs.