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In the aim to stabilize novel three-dimensional perovskite oxides based upon SrCoO 3- δ  , we have designed and prepared SrCo 1-x Re x O 3- δ  phases (x = 0.05 and 0.10), successfully avoiding the competitive hexagonal 2H polytypes. Their performance as cathode materials in intermediate-temperature solid oxide fuel cells (IT-SOFC) has been investigated. The characterization of these oxides included X-ray (XRD) and in situ temperature-dependent neutron powder diffraction (NPD) experiments for x = 0.10. At room temperature, SrCo 1-x Re x O 3- δ  perovskites are defined in the P4/mmm space group, which corresponds to a subtle tetragonal perovskite superstructure with unit-cell parameters a = b ≈ a o , c = 2a o (a o = 3.861 and 3.868 Å, for x = 0.05 and 0.10, respectively). The crystal structure evolves above 380 °C to a simple cubic perovskite unit cell, as observed from in-situ NPD data. The electrical conductivity gave maximum values of 43.5 S·cm -1 and 51.6 S·cm -1 for x = 0.05 and x = 0.10, respectively, at 850 °C. The area specific resistance (ASR) polarization resistance determined in symmetrical cells is as low as 0.087 Ω·cm² and 0.065 Ω·cm² for x = 0.05 and x = 0.10, respectively, at 850 °C. In single test cells these materials generated a maximum power of around 0.6 W/cm² at 850 °C with pure H₂ as a fuel, in an electrolyte-supported configuration with La 0.8 Sr 0.2 Ga 0.83 Mg 0.17 O 3-   δ  (LSGM) as the electrolyte. Therefore, we propose the SrCo 1-x Re x O 3- δ  (x = 0.10 and 0.05) perovskite oxides as promising candidates for cathodes in IT-SOFC.

New Rhenium-Doped SrCo1−xRexO3−δ Perovskites Performing as Cathodes in Solid Oxide Fuel Cells