The present work aims at investigating the catalytic decomposition of N 2 O over CuO-CeO 2 single or mixed oxides prepared by different synthesis routes, i.e., impregnation, precipitation and exotemplating. To gain insight into the particular role of CeO 2 as well as of CuO-CeO 2 interactions, three different types of materials are prepared and tested for N 2 O decomposition both in the absence and presence of excess O 2 : (i) bare CeO 2 prepared by precipitation and exotemplating, (ii) CuO/CeO 2 oxides synthesized by impregnation of CeO 2 samples prepared in (i) with CuO and iii) single stage synthesized CuO-CeO 2 mixed oxides employing the coprecipitation and exotemplating methods. The corresponding commercial samples were also examined for comparison purposes. All materials were characterized by N 2 adsorption at -196 °C, X-ray diffraction (XRD), H 2 temperature-programmed reduction (H 2 -TPR), X-ray photoelectron spectroscopy (XPS), micro-Raman spectroscopy (micro-Raman) and scanning electron microscopy (SEM). The results demonstrated the key role of preparation procedure on the direct catalytic decomposition of N 2 O. Among the bare CeO 2 samples, the best performance was obtained with the samples prepared by the precipitation method, followed by exotemplating, while commercial CeO 2 showed the lowest performance. All bare oxides demonstrated low N 2 O conversion, never exceeding 40% at 600 °C. Amongst the CuO-CeO 2 oxides, the optimum performance was observed for those prepared by co-precipitation, which achieved complete N 2 O conversion at 550 ºC. In the presence of excess oxygen in the feed stream, a slight degradation is observed, with the sequence of deN 2 O performance to remain unchanged. The superiority of Cu-Ce mixed oxides prepared by precipitation compared to all other materials can be mainly ascribed to their excellent redox properties, linked to Ce 4+ /Ce 3+ and Cu 2+ /Cu + redox pairs. A redox mechanism for N 2 O catalytic decomposition is proposed involving N 2 O adsorption on Cu + sites and their regeneration through Cu-ceria interactions. and mobile emissions is nowadays a challenging environmental issue.Several after-treatment techniques have been developed for N 2 O abatement, including thermal decomposition 6 , non-selective catalytic reduction 4 , selective catalytic reduction 7,8 and direct catalytic decomposition 9-12 . Among these, direct catalytic decomposition of N 2 O (deN 2 O) is the most promising method, due to its high efficiency and low energy requirements. The decomposition of N 2 O has been studied on various catalytic systems, such as transition and noble metal catalysts, perovskites, hexaluminates, spinels, zeolites, etc 4,9,[13][14][15][16][17][18][19][20] . In spite of the excellent catalytic performance of noble metals (NMs)-based catalysts, their high cost and sensitivity to oxygen poisoning limit their practical applications 9 . Therefore, the development of NMs-free catalysts of low cost and adequate de-N 2 O performance is of crucial importance from both practical ...