Oxygen non-stoichiometry and defect structure of LaMn1-zCuzO3+δ

The quantitative model analysis of the defect structure of copper doped lanthanum manganites LaMn1-zCuzO3+δ (z = 0.05 and 0.1) was performed. In the framework of the model, the independent course of the three reactions of defect formation, including the electronic exchange between manganese and copper, completion of a lattice by the absorption of oxygen and the disproportionation of manganese was considered. It is shown that the increase in the dopant content leads to a change in the dominant electronic process. This is reflected in the lock and disproportionation and leads to the increase in the concentration of holes and decrease the concentration of electrons localized on the manganese atoms

Study and optimization of the synthesis routine of the single phase YBaCo2O6–δ double perovskite

Received: 07.09.2017; accepted: 25.09.2017; published: 20.10.2017.The chemical interaction of YCoO3–δ and BaCoO3-δ with formation of double perovskite was studied depending on temperature and oxygen partial pressure. The stability of YCoO3 was shown to have а crucial influence on the kinetics and mechanism of YBaCo2O6-δ formation. It was found that at 1000 °C in air, i.e. under conditions when YCoO3 is unstable, the double perovskite YBaCo2O6-δ is formed much slower compared to the pure oxygen atmosphere where YCoO3 is stable at the same temperature. Thus controlling YCoO3 stability was shown to be the factor of key importance for optimal preparation of the YBaCo2O6-δ single phase

Investigation of GdBaCo2-xFexO6-δ (x = 0, 0.2) - Ce0.8Sm0.2O2 composite cathodes for intermediate temperature solid oxide fuel cells

The double perovskites GdBaCo2-xFexO 6-δ (x = 0, 0.2) and composites (100 - y) GdBaCo 2-xFexO6-δ (x = 0, 0.2) - y Ce 0.8Sm0.2O2 (y = 10-50 wt.%) were investigated as cathode materials for intermediate temperature solid oxide fuel cells (IT-SOFCs). Chemical compatibility of GdBaCo2-xFexO 6-δ (x = 0, 0.2) with solid electrolyte Ce0.8Sm 0.2O2, thermal expansion, DC conductivity and electrochemical performance of (100 - y) GdBaCo2-xFe xO6-δ (x = 0, 0.2) - y Ce0.8Sm 0.2O2 (y = 10-50 wt.%) were studied. Partial substitution of Fe for Co was shown to lead to decrease of double perovskite GdBaCo 2-xFexO6-δ reactivity with the solid electrolyte Ce0.8Sm0.2O2. Polarization resistance of cathodes studied was found to depend significantly on firing temperature. Variation of solid electrolyte content in (100 - y) GdBaCo 2-xFexO6-δ (x = 0, 0.2) - y Ce 0.8Sm0.2O2 (y = 10-50 wt.%) composites was shown to allow to optimize their electrochemical performance. Cathode materials of 80 wt.% GdBaCo2O6-δ - 20 wt.% Ce 0.8Sm0.2O2 and 65 wt.% GdBaCo 1.8Fe0.2O6-δ - 35 wt.% Ce 0.8Sm0.2O2 were found to have the lowest polarization resistances and reasonable values of thermal expansion coefficient (TEC) and, therefore, can be considered as promising cathode materials for IT-SOFCs. © 2013 Elsevier B.V. All rights reserved

Crystal structure and oxygen content of the double perovskites GdBaCo 2-xFexO6-δ

The iron solubility limit, x, in GdBaCo2-xFexO 6-δ determined by means of X-ray diffraction was found to be close to 0.65 in air. The crystal structure changes of the double perovskites GdBaCo2-xFexO6-δ (x=0-0.6) were studied by means of in situ X-ray diffraction in temperature range from 25 to 900 °C in air. The oxygen content, 6-δ, was determined for these double perovskites in air as a function of temperature by means of thermogravimetric technique in range 25≤T, °C≤ 1100. The Pmmm-P4/mmm structure transition was found to occur in GdBaCo2-xFexO 6-δ (0≤x≤0.4) with increasing temperature. This transition is observed at the same temperature for the compositions with 0≤x≤0.1 while the transition temperature reaches maximum for x=0.2 and that decreases linearly with further iron increase. The double perovskite GdBaCo1.4Fe0.6O6-δ was shown to have the tetragonal P4/mmm structure at room temperature. The P4/mmm-Pmmm structure transition occurs at temperature as low as 170 °C for this double perovskite while reverse one is already observed at 290 °C in air. The Pmmm-P4/mmm structure transition was found to be strongly related to the oxygen content for the undoped and slightly doped (x≤0.2) double perovskites while there is no such relation for the double perovskites enriched by iron (x≥0.2). © 2012 Elsevier Inc. All rights reserved