Low temperature CO oxidation catalysed by flower-like Ni-Co-O: how physicochemical properties influence catalytic performance.

In this work, mesoporous Ni-Co composite oxides were synthesized by a facile liquid-precipitation method without the addition of surfactant, and their ability to catalyse a low temperature CO oxidation reaction was investigated. To explore the effect of the synergetic interaction between Ni and Co on the physicochemical properties and catalytic performance of these catalysts, the as-prepared samples were characterized using XRF, XRD, LRS, N 2 -physisorption (BET), SEM, TEM, XPS, H 2 -TPR, O 2 -TPD and in situ DRIFTS characterization techniques. The results are as follows: (1) the doping of cobalt can reduces the size of NiO, thus massive amorphous NiO have formed and highly dispersed on the catalyst surface, resulting in the formation of abundant surface Ni 2+ ions; (2) Ni 2+ ions partially substitute Co 3+ ions to form a Ni-Co spinel solid solution, generating an abundance of surface oxygen vacancies, which are vital for CO oxidation; (3) the Ni 0.8 Co 0.2 catalyst exhibits the highest catalytic activity and a satisfactory stability for CO oxidation, whereas a larger cobalt content results in a decrease in activity, suggesting that the amorphous NiO phase is the dominant active phase instead of Co 3 O 4 for CO oxidation; (4) the introduction of Co can alter the morphology of catalyst from plate-like to flower-like and then to dense granules. This morphological variation is related to the textural properties and catalytic performance of the catalysts. Lastly, a possible mechanism for CO oxidation reaction is tentatively proposed.