This work reveals the structural evolution and transport behavior of chromium-substituted Ba2In2O5 (BIO) as a mixed ionic electronic conductor for oxygen transport membranes. Controlled substitution of In3+ by Cr6+ induces a transition from an orthorhombic brownmillerite to an on average cubic defect-perovskite (ABO3−δ) phase while suppressing the high-temperature phase transformations typical of undoped BIO. A comprehensive set of structural and spectroscopic techniques confirms the stabilization of Cr6+ in the lattice and its function as a donor dopant. The aliovalent substitution introduces additional electrons while reducing the oxygen-vacancy concentration in the lattice, resulting in increased electronic and decreased ionic conductivities. The composition with x = 0.1 achieves a well-balanced contribution from ionic and electronic carriers, yielding the highest ambipolar conductivity and oxygen permeation flux among the studied samples. At higher substitution levels (e.g., x = 0.2), where In3+ and Cr6+ coexist on the B-site of the perovskite framework, a coupled donor/acceptor system (Cr6+/In3+) is formed, giving rise to complex charge compensation mechanisms and mixed electronic conduction. These findings provide fundamental insights into the crystal structure, defect chemistry, and charge transport mechanisms in Cr-substituted BIO, offering a rational design strategy for efficient oxygen transport membranes.
Xiao et al. (2026) studied this question.