Oxygen transport in Ce 0.8Gd 0.2O 2− δ-based composite membranes

Abstract

Gadolinia-doped ceria electrolyte Ce 0.8Gd 0.2O 2− δ (CGO) and perovskite-type mixed conductor La 0.8Sr 0.2Fe 0.8Co 0.2O 3− δ (LSFC), having compatible thermal expansion coefficients (TECs), were combined in dual-phase ceramic membranes for oxygen separation. Oxygen permeability of both LSFC and composite LSFC/CGO membranes at 970–1220 K was found to be limited by the bulk ambipolar conductivity. LSFC exhibits a relatively low ionic conductivity and high activation energy for ionic transport (∼200 kJ/mol) in comparison with doped ceria. As a result, oxygen permeation through LSFC/CGO composite membranes, containing similar volume fractions of the phases, is determined by the ionic transport in CGO. The permeation fluxes through LSFC/CGO and La 0.7Sr 0.3MnO 3− δ /Ce 0.8Gd 0.2O 2− δ (LSM/CGO) composites have comparable values. An increase in the p-type electronic conductivity of ceria in oxidizing conditions, which can be achieved by co-doping with variable-valence metal cations, such as Pr, leads to a greater permeability. The oxygen ionic conductivity of the composites consisting of CGO and perovskite oxides depends strongly of processing conditions, decreasing with interdiffusion of the phase components, particularly lanthanum and strontium cations from the perovskite into the CGO phase.