Rare-Earth-Element-FreeFerrite Cathode for ProtonicSolid Oxide Fuel Cells

Cu doping in ferrite perovskites was reported to enhance the low-temperature performance for the oxygen reduction reaction (ORR) of a protonic solid oxide fuel cell (H-SOFC). Zr<sup>4+</sup> as a donor for doping in rare-earth-element-free BaFe<sub>0.9–<i>x</i></sub>Cu<sub>0.1</sub>Zr<sub><i>x</i></sub>O<sub>3−δ</sub> (<i>x</i> = 0, 0.05, and 0.1) was studied to achieve a trade-off between the high-performance electrocatalysis and stability of the Cu-containing perovskite. Zr<sup>4+</sup> stabilized the cubic structure of the perovskite and inhibited the formation of hexagonal BaFeO<sub>3</sub> by decreasing the Goldschmidt tolerance factor of the perovskite. Compared with BaFe<sub>0.9</sub>Cu<sub>0.1</sub>O<sub>3−δ</sub> (Zr0), BaFe<sub>0.85</sub>Cu<sub>0.1</sub>Zr<sub>0.05</sub>O<sub>3−δ</sub> (Zr5) and BaFe<sub>0.8</sub>Cu<sub>0.1</sub>Zr<sub>0.1</sub>O<sub>3−δ</sub> (Zr10) exhibit higher electric conductivity and surface exchange kinetics but a lower thermal expansion coefficient. At 600 °C, the cell with Zr10 exhibits a peak power of 547.73 mW cm<sup>–2</sup>, a polarization resistance of 0.03 Ω cm<sup>2</sup>, and a chronoamperometry of 673.13 mA cm<sup>–2</sup> at 0.6 V after 140 h. Therefore, Zr<sup>4+</sup> doping in the ferrite cathode can improve the ORR kinetics and durability of low-temperature H-SOFCs.

Publication Details

Journal
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Published
2025-02-19
DOI
https://doi.org/10.1021/acsaem.4c03318.s001
Primary Topic
Advancements in Solid Oxide Fuel Cells
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article

Rare-Earth-Element-FreeFerrite Cathode for ProtonicSolid Oxide Fuel Cells

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Advancements in Solid Oxide Fuel Cells
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Rare-Earth-Element-FreeFerrite Cathode for ProtonicSolid Oxide Fuel Cells

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Abstract

Cu doping in ferrite perovskites was reported to enhance the low-temperature performance for the oxygen reduction reaction (ORR) of a protonic solid oxide fuel cell (H-SOFC). Zr<sup>4+</sup> as a donor for doping in rare-earth-element-free BaFe<sub>0.9–<i>x</i></sub>Cu<sub>0.1</sub>Zr<sub><i>x</i></sub>O<sub>3−δ</sub> (<i>x</i> = 0, 0.05, and 0.1) was studied to achieve a trade-off between the high-performance electrocatalysis and stability of the Cu-containing perovskite. Zr<sup>4+</sup> stabilized the cubic structure of the perovskite and inhibited the formation of hexagonal BaFeO<sub>3</sub> by decreasing the Goldschmidt tolerance factor of the perovskite. Compared with BaFe<sub>0.9</sub>Cu<sub>0.1</sub>O<sub>3−δ</sub> (Zr0), BaFe<sub>0.85</sub>Cu<sub>0.1</sub>Zr<sub>0.05</sub>O<sub>3−δ</sub> (Zr5) and BaFe<sub>0.8</sub>Cu<sub>0.1</sub>Zr<sub>0.1</sub>O<sub>3−δ</sub> (Zr10) exhibit higher electric conductivity and surface exchange kinetics but a lower thermal expansion coefficient. At 600 °C, the cell with Zr10 exhibits a peak power of 547.73 mW cm<sup>–2</sup>, a polarization resistance of 0.03 Ω cm<sup>2</sup>, and a chronoamperometry of 673.13 mA cm<sup>–2</sup> at 0.6 V after 140 h. Therefore, Zr<sup>4+</sup> doping in the ferrite cathode can improve the ORR kinetics and durability of low-temperature H-SOFCs.

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Advancements in Solid Oxide Fuel Cells
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