High-Surface-Area Synthesis of Iron-Doped CaTiO 3 at Low Temperatures: New Insights into Oxygen Activation, Iron States, and the Impact on Methane Oxidation.

In the present work, a series of CaTiFeO (0 < < 0.5) materials are prepared using a modified Pechini method based on citric acid and a polyol as chelating agents. The synthesis conditions are optimized with respect to the specific surface area and phase purity by varying polyols (ethylene glycol, glycerol, and 1.6-hexanediol) and the ratio between citric acid, polyols, and cations. The impact of the polyols and the iron content (up to 40 mol % on the B site) is studied with respect to the oxygen exchange rate, reducibility using H-TPR, and catalytic performance for methane total oxidation. A correlation between the oxygen exchange rate studied using O exchange in powdered samples of CaTiFeO (0 < < 0.5) and ferric sites determined using Mössbauer spectroscopy and H-TPR is established. The oxygen activation and diffusion in CaTiFeO (0 < < 0.5) continuously increase in the studied range of Ti substitution. The methane oxidation performance does not increase above = 0.3, showing that methane oxidation is not limited by surface oxygen activation and CH is activated by specific iron sites in Fe-doped perovskites.