Crystal structure, microstructure and reducibility of LaNixCo1−xO3 and LaFexCo1−xO3 Perovskites (0<x≤0.5)

Nickel and iron substituted LaCoO3 with rhombohedrally distorted perovskite structure were obtained in the temperature range of 600–900 °C by thermal decomposition of freeze-dried citrates and by the Pechini method. The crystal structure, morphology and defective structure of LaCo1−xNixO3 and LaCo1−xFexO3 were characterized by X-ray diffraction and neutron powder diffraction, TEM and SEM analyses and electron paramagnetic resonance spectroscopy. The reducibility was tested by temperature programmed reduction with hydrogen. The products of the partial and complete reduction were determined by ex-situ XRD experiments. The replacement of Co by Ni and Fe led to lattice expansion of the perovskite structure. For perovskites annealed at 900 °C, there was a random Ni, Fe and Co distribution. The morphology of the perovskites does not depend on the Ni and Fe content, nor does it depend on the type of the precursor used. LaCo1−xNixO3 perovskites (x>0.1) annealed at 900 °C are reduced to Co/Ni transition metal and La2O3 via the formation of oxygen deficient Brownmillerite-type compositions. For LaCo1−xNixO3 annealed at 600 °C, Co/Ni metal, in addition to oxygen-deficient perovskites, was formed as an intermediate product at the initial stage of the reduction. The interaction of LaCo1−xFexO3 with H2 occurs by reduction of Co3+ to Co2+ prior to the Fe3+ ions. The reducibility of Fe-substituted perovskites is less sensitive towards the synthesis procedure in comparison with that of Ni substituted perovskites.

LaCo1−xNixO3 and LaCo1−xFexO3 with rhombohedrally distorted perovskite structure were obtained in the temperature range of 600–900 °C by thermal decomposition of freeze-dried La–Co/Ni(Fe)-citrates and by the Pechini method. The complete reduction of LaCo1−xNixO3 with H2 proceeds to Co/Ni-metal and La2O3, while the interaction of LaCo1−xFexO3 with H2 is not complete up to 700 °C. For LaCo1−xFexO3, the reaction proceeds by preferential oxidation of Co3+ to Co2+ without affecting Fe3+ ions.Figure optionsDownload as PowerPoint slide