Abstract

In this work, we investigate and contrast the perovskite structure of and (both for , 0.7, 0.9, and 1.0) as well as their oxygen nonstoichiometry, oxygen bulk-diffusion, and surface exchange coefficients to describe their distinct performance as ceramic oxygen ionic transport membranes. Le Bail refinements of x-ray diffraction data demonstrate that except for , the structure for all title compounds at room temperature can be fitted adequately using rhombohedrally distorted perovskite structure. The presence of lanthanum is found to reduce the solubility of niobium in perovskite lattice. Aside from , structure deterioration or transformation occurs for all title compounds upon subjected to modest reducing atmosphere of nitrogen. Oxygen permeation testing reveals that membrane exhibits the largest fluxes among all the title compounds, followed by and and . The oxygen permeation values exhibit exact the same trend as a function of composition with the bulk-diffusion and surface exchange coefficients values indicating both bulk-diffusion and surface exchange limits the oxygen transport through title compounds. In addition, permeation testing on the best doped compounds, and demonstrates that has better performance stability, e.g. lower degradation percentage with time relative to its non niobium doped counterpart.

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