Abstract
Lowering the thermal expansion coefficient (TEC) and promoting the catalytic activity of cobalt-based perovskite air electrodes is crucial for efficient solid oxide cells (SOCs) devices. However, the co-achievement of both merits has usually been largely compromised in most scenarios. Herein, a dual-doping strategy to manipulate the properties of perovskite cobaltate electrocatalyst is reported in which a high valence element of Ta5+ is incorporated into B-site to significantly suppress the dynamic reduction of Co4+ species and reduces the TEC value from PrBaCo2O5+δ (PBC, 17.8 × 10⁻6 K−1) to PrBaCo1.96Ta0.04O5+δ (PBCT, 12.5 × 10⁻6 K−1) and suppresses the oxygen loss in SOCs operation condition, revealing the improved structural stability. Meanwhile, the Ca2+ is doped into A-site of Ta-incorporated candidate, further decreasing the covalency of Co─O bonds and facilitating the formation of oxygen vacancies, benefiting the oxygen exchange kinetics and leading to a low polarization resistance of 0.026 Ω cm2 (800 °C) in as-prepared PrBa0.8Ca0.2Co1.96Ta0.04O5+δ (PBCCT) electrode. The cell with PBCTT demonstrates remarkable robustness during a 50 h thermal cycling test (25 cycles). Moreover, it delivers a high current density of 1.44 A cm⁻2 (1.6 V, 800 °C), as well as attractive durability over 100 h for pure CO2 electrolysis.
| Original language | English |
|---|---|
| Article number | 2410672 |
| Journal | Small |
| Volume | 21 |
| Issue number | 15 |
| DOIs | |
| Publication status | Published - 16 Apr 2025 |
| Externally published | Yes |
Keywords
- air electrodes
- dual-dopings
- oxygen vacancies
- perovskite cobaltates
- thermal expansion coefficients
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