The structure and catalytic properties of Rh-doped CeO2 catalystsElectronic supplementary information (ESI) available. See DOI: 10.1039/c7cp06573f

• Main Authors: Derevyannikova, E. A, Kardash, T. Yu, Kibis, L. S, Slavinskaya, E. M, Svetlichnyi, V. A, Stonkus, O. A, Ivanova, A. S, Boronin, A. I
• Format: Article
• Language: English
• ISSN: 1463-9076; 1463-9084
• DOI: 10.1039/c7cp06573f

The average structure and the local structure of nanocrystalline Rh-doped CeO 2 catalysts, prepared using a co-precipitation method, were studied using a set of structural (PDF, HRTEM, XRD) and spectral (XPS, Raman spectroscopy) methods. The samples with Rh content less than 10 wt%, calcined at 450 °C, were homogeneous solid solutions. A comparison of the experimental results and Pair distribution function (PDF) modeling data showed that Rh 3+ substitutes Ce 4+ ions in the fluorite phase. Charge equilibrium is obtained by the oxygen vacancy for each Rh 3+ cation introduced into the ceria cell. The solid solution demonstrated high catalytic activity in low-temperature CO oxidation (LTO CO). The solid solutions were stable only in a nanocrystalline state and decomposed upon thermal treatment. The calcination of the solid solution at T > 450 °C results in a decrease in the catalytic activity that is accompanied by Rh association in the subsurface area and strong distortion of the anionic subcell. At T = 800 °C α-Rh 2 O 3 nanoparticles are formed on the surface of the fluorite phase. The XRD-detectable Rh oxide phases are formed after calcination at 1000 °C. However, some parts of Rh within the subsurface Rh x Ce 1− x O 2− δ solid solution remain and they preserve catalytic properties for low-temperature oxidation. The PDF analysis with TEM, XPS and Raman spectroscopy indicates the formation of homogenous Rh x Ce 1− x O 2− δ nanocrystalline solid solutions.