Publication date: 22nd July 2026
Developing cobalt-free oxygen electrodes that combine fast oxygen-reduction kinetics with sufficient electronic transport remains a key challenge for intermediate-temperature solid oxide fuel cells (IT-SOFCs). Here, we investigate B-site Ce substitution in SrFe1-xCexO3-δ (x = 0, 0.05, 0.10, 0.15, and 0.20) as a strategy to control the coupled structure–defect–transport chemistry of SrFeO3-δ. The materials were synthesized by a solid-state route and characterized by X-ray diffraction with Rietveld refinement, electron microscopy, HRTEM/SAED, X-ray photoelectron spectroscopy, and temperature-dependent electrical conductivity.
Ce incorporation initially expands the perovskite lattice, whereas higher substitution levels lead to lattice-parameter saturation and weak CeO2/Sr3Fe2O7-δ segregation, indicating a composition-dependent limit of homogeneous incorporation. XPS reveals a Ce-induced redistribution of Fe3+/Fe4+ states and surface oxygen species, with SrFe0.85Ce0.15O3-δ showing the strongest defect-associated oxygen response. Electrical conductivity exhibits a non-monotonic dependence on Ce content and reaches its maximum at x = 0.15, demonstrating an optimum balance between defect activation and preservation of the electronically connected Fe–O–Fe network.
The optimized SrFe0.85Ce0.15O3-δ composition retains well-crystallized perovskite domains and was evaluated as the oxygen electrode in a NiO–YSZ | YSZ | SrFe0.85Ce0.15O3-δ single cell. The cell delivers a peak power density of 0.53 W cm-2 at 800 °C, while the polarization resistance decreases from 0.47 Ω at 600 °C to 0.36 Ω at 800 °C. These results demonstrate that controlled B-site Ce substitution provides an effective route to enhance oxygen-electrode performance through defect engineering without relying on cobalt or noble-metal co-catalysts, highlighting SrFe0.85Ce0.15O3-δ as a promising cathode for IT-SOFCs.
This research was supported by the Ministry of Science and Higher Education of the Republic of Kazakhstan under Project Number AP26103025.
