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A novel CO2-stable and reduction-tolerant Ce0.8Sm0.2O(2-δ)-La0.9Sr0.1FeO(3-δ) (SDC-LSF) dense dual-phase oxygen-permeable membrane was designed and evaluated in this work. Homogeneous SDC-LSF composite powders for membrane fabrication were synthesized via a one-pot combustion method. The chemical compatibility and ion interdiffusion behavior between the fluorite phase SDC and perovskite phase LSF during the synthesis process was studied. The oxygen permeation flux through the dense dual-phase composite membranes was evaluated and found to be highly dependent on the volume ratio of SDC and LSF. The SDC-LSF membrane with a volume ratio of 7:3 (SDC70-LSF30) possessed the highest permeation flux, achieving 6.42 × 10(-7) mol·cm(-2)·s(-1) under an air/CO gradient at 900 °C for a 1.1-mm-thick membrane. Especially, the membrane performance showed excellent durability and operated stably without any degradation at 900 °C for 450 h with helium, CO2, or CO as the sweep gas. The present results demonstrate that a SDC70-LSF30 dual-phase membrane is a promising chemically stable device for oxygen production and CO2 capture with sufficiently high oxygen permeation flux.

Acceptor-doped barium cerate is considered as one of the state-of-the-art high temperature proton conductors (HTPCs), and the proton conductivity of such HTPCs is heavily dependent on the dopant. In this work, a codoping strategy is employed to improve the electrical conductivity and sinterability of BaCeO3-based HTPC. BaCe0.8Sm(x)Y(0.2-x)O(3-δ) (0 ≤ x ≤ 0.2) powders are synthesized by a typical citrate-nitrate combustion method. The XRD and Raman spectra reveal all the compounds have an orthorhombic perovskite structure. The effects of Sm and/or Y doping on the sinterability and electrical conductivity under different atmospheres are carefully investigated. The SEM results of the sintered BaCe0.8Sm(x)Y(0.2-x)O(3-δ) pellets indicate a significant sintering enhancement with increasing Sm concentration. BaCe0.8Sm0.1Y0.1O(3-δ) exhibits the highest electrical conductivity in hydrogen among the BaCe0.8Sm(x)Y(0.2-x)O(3-δ) pellets. Anode-supported BaCe0.8Sm0.1Y0.1O(3-δ) electrolyte membranes are also fabricated via a drop-coating process, and the corresponding single cell exhibits desirable power performance and durability at low temperatures. The results demonstrate that BaCe0.8Sm0.1Y0.1O(3-δ) is a promising proton conductor with high conductivity and sufficient sinterability for proton-conducting solid oxide fuel cells operating at reduced temperatures.

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