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Research Article | Open Access

A-site doping enabled synergistic regulation of phase transition and electron spin state for improved performance of La0.6Ca0.4FeO3−δ cathodes in solid oxide fuel cells

Na Lv§Yumei Ma§Lina Su( )Ling Huang ( )
State Key Laboratory of Chemistry and Utilization of Carbon-Based Energy Resources, College of Chemistry, Xinjiang University, Urumqi 830046, China

§ Na Lv and Yumei Ma contributed equally to this work.

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Abstract

Although intermediate temperature solid oxide fuel cells (IT-SOFCs) show great potential to address energy conversion challenges, the sluggish oxygen reduction reaction (ORR) kinetics of cathode materials has severely hindered extended applications. Herein, we have demonstrated that Bi3+ doping on the A-site synergistically regulates the phase transition and electron spin state in La0.3Bi0.3Ca0.4FeO3−δ (LBCF3) for improved performance. An orthorhombic to cubic phase transition occurred with Bi3+ doping increases oxygen vacancy concentration and thus increases oxygen ion migration capacity. Simultaneously, the change of Fe from low to medium electron spin state strengths O2 adsorption and improves catalytic performances. Consequently, a peak power density improvement up to 48% (from 1.21 to 1.79 W·cm−2) at 800 °C is realized in the anode-supported single cell using LBCF3 as cathode, which remains stable for over 270 h at 750 °C.

Graphical Abstract

Doping of Bi3+ to replace the A-site La3+ enables synergistic regulation of phase transition and electron spin state of Fe and finally results in up to 48% (from 1.21 to 1.79 W·cm−2) peak power density improvement.

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Nano Research
Article number: 94908200

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Cite this article:
Lv N, Ma Y, Su L, et al. A-site doping enabled synergistic regulation of phase transition and electron spin state for improved performance of La0.6Ca0.4FeO3−δ cathodes in solid oxide fuel cells. Nano Research, 2026, 19(1): 94908200. https://doi.org/10.26599/NR.2025.94908200
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Received: 17 July 2025
Revised: 20 October 2025
Accepted: 27 October 2025
Published: 22 December 2025
© The Author(s) 2026. Published by Tsinghua University Press.

This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0, https://creativecommons.org/licenses/by/4.0/).