The Sr2.4Dy0.6Co2O7-δ Ruddlesden‒Popper Phase: Structural, thermoelectric, and magnetic properties

Abstract

―A new anion-deficient Sr2.4Dy0.6Co2O7‒δ (δ = 0.33–1.1) perovskite phase with a structure of the A3B2O7 Raddlesden‒Popper homologous series has been obtained by the solid-state synthesis in the reducing/oxidizing atmosphere and its structural characterization has been performed by the Rietveld refinement of the X-ray powder diffraction data. It has been stablished that the Sr2.4Dy0.6Co2O7‒δ compound (sp. gr. I4/mmm) has parameters of a = b = 3.8526(1) and c = 19.9431(7) Å in the reduced form (δ = 1.1) and a = b = 3.8086(1) and c = 19.9190(6) Å in the oxidized form (δ ≈ 0.33) and oxygen vacancies occupy mainly the sites linking CoO5 polyhedra inside two perovskite layers. It has been established using differential scanning calorimetry and thermogravimetry that, at T < 530 K, the synthesized phase is stable against the inert and oxidizing atmosphere; at higher temperatures, the Sr2.4Dy0.6Co2O7-δ compound can reversibly absorb/release oxygen. The magnetic properties of the Sr2.4Dy0.6Co2O6.09 compound have been investigated in the temperature range of 10–400 K and described in terms of the formation of dimers, in which the Co3+‒Co3+ and Co2+‒Co2+ ion pairs antiferromagnetically interact and are in the nonmagnetic ground state. The electrical conductivity and the Seebeck coefficient have been measured in air in the temperature range from 300 to 800 K. An observed sharp decrease in the Seebeck coefficient of the Sr2.4Dy0.6Co2O7-δ compound and the change in its sign near 700 K have been attributed to the transition of cobalt ions to the Co3+ state and the charge disproportionation of Co3+ ions to Co2+ and Co4+ ones.