In-Situ characterizations to investigate the nature of Co3+ coordination environment to activate surface adsorbed oxygen for methane oxidation

Identifying the activity origin of spinel Co3O4 catalysts is extremely important for fundamental research and practical application. It is reported that octahedrally coordinated Co3+ (Co-oh(3+)) is considered as active sites in spinel Co3O4, but there is still a lack of sufficient evidence to prove the effect of Co species. In this work, we synthesized accurately the three spinel Co3O4 samples with different exposed crystal planes to investigate the reaction mechanism between methane molecule and Co species. The activity results show that methane oxidation activities follow an order of Co3O4-(2 2 0) > Co3O4-(3 1 1) > Co3O4-(1 1 1). A series of in-situ characterization analyses are performed to explore the evolution process of Co species and the transform of lattice oxygen species for methane combustion. The results indicate that the high catalytic activity is assigned to the exposed state of surface lattice oxygen atoms and the mutual transformation of Co3+ oh and Co2+ 0h . Therefore, it explained that the high activity of the (2 2 0) crystal plane is mainly involved with the high exposure of Co3+ and surface lattice oxygen. Adsorption oxygen species were induced to reactive oxygen species during the transformation of Co3+ oh stable structure and Co2+ oh unstable structure.

Automated summary

The study found that the methane oxidation activity of spinel Co3O4 catalysts depends on the different exposed crystal planes, with the high catalytic activity mainly associated with the high exposure of Co3+ and surface lattice oxygen. Adsorption oxygen species play a role in generating reactive oxygen species during the transformation of Co3+ and Co2+ structures.