Defect-Engineered Cobalt-Free SrFeO3-δ-Based Electrodes for Advanced Solid Oxide Fuel Cells
Asset Kabyshev a, Packiaraj Rajagopal a, Ainur Aimakhanova a, Aliya Baratova a, Marzhan Kubenova a, Mahitha Rajasekaran b
a Institute of Physical and Technical Sciences, L.N. Gumilyov Eurasian National University, Astana 010008, Kazakhstan
b Department of Physics, School of Advanced Sciences, Kalasalingam Academy of Research and Education, Krishnankoil, Tamil Nadu 626 126, India
Proceedings of MATSUS Fall 2026 Conference (MATSUSFall26)
D7 High Throughput Electrode Synthesis and Manufacturing
Palma, Spain, 2026 October 26th - 30th
Organizers: Dries De Sloovere, Nadia Farag and Chengyin Fu
Poster, Asset Kabyshev, 491
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.

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