Abstract

(Ba_0.5Sr_0.5)(Co_0.8Fe_0.2)_yO_3−δ ((BS)(CF)_y, 1.00 ≥ y ≥ 0.77) oxides were investigated for oxygen separation application with emphasis on long-term operational stability. Pure phase cubic perovskite was formed at y ≥ 0.83. The oxygen nonstoichiometry increased while electrical conductivity and permeability decreased with the decrease of y. However, the (BS)(CF)_0.97 membrane still displayed an attractive oxygen flux as high as 2.4 × 10⁻⁶ mol cm⁻² s⁻¹ at 900 °C, as compared to 2.5 × 10⁻⁶ mol cm⁻² s⁻¹ for a cation stoichiometric BSCF membrane. The B-site deficiency greatly restrained the A-site cation diffusion and stabilized the perovskite structure and permeation properties of the membranes. During the long-term operation of the (BS)(CF)_0.97 membrane at 850 °C for more than 300 h, a stable permeation flux of (1.8 ± 0.3) × 10⁻⁶ mol cm⁻² s⁻¹ was achieved. Further investigation demonstrated that the improved importance of oxygen bulk-diffusion regime in the rate-determination of oxygen permeation through the membranes.

Keywords: Oxygen permeation; Perovskite; Ceramic membrane; Ba_0.5Sr_0.5Co_0.8Fe_0.2O_3−δ