Ceria Nanoparticles' Morphological Effects on the N2O Decomposition Performance of Co3O4/CeO2 Mixed Oxides

Ceria-based oxides have been widely explored recently in the direct decomposition of N2O (deN(2)O) due to their unique redox/surface properties and lower cost as compared to noble metal-based catalysts. Cobalt oxide dispersed on ceria is among the most active mixed oxides with its efficiency strongly affected by counterpart features, such as particle size and morphology. In this work, the morphological effect of ceria nanostructures (nanorods (R), nanocubes (NC), nanopolyhedra (NP)) on the solid-state properties and the deN(2)O performance of the Co3O4/CeO2 binary system is investigated. Several characterization methods involving N-2 adsorption at -196 degrees C, X-ray diffraction (XRD), temperature programmed reduction (TPR), X-ray photoelectron spectroscopy (XPS) and transmission electron microscopy (tau Epsilon M) were carried out to disclose structure-property relationships. The results revealed the importance of support morphology on the physicochemical properties and the N2O conversion performance of bare ceria samples, following the order nanorods (NR) > nanopolyhedra (NP) > nanocubes (NC). More importantly, Co3O4 impregnation to different carriers towards the formation of Co3O4/CeO2 mixed oxides greatly enhanced the deN(2)O performance as compared to bare ceria samples, without, however, affecting the conversion sequence, implying the pivotal role of ceria support. The Co3O4/CeO2 sample with the rod-like morphology exhibited the best deN(2)O performance (100% N2O conversion at 500 degrees C) due to its abundance in Co2+ active sites and Ce3+ species in conjunction to its improved reducibility, oxygen kinetics and surface area.