摘要
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 Ta 5+ is incorporated into B-site to significantly suppress the dynamic reduction of Co 4+ species and reduces the TEC value from PrBaCo 2 O 5+δ (PBC, 17.8 × 10 ⁻6 K −1 ) to PrBaCo 1.96 Ta 0.04 O 5+δ (PBCT, 12.5 × 10⁻ 6 K −1 ) and suppresses the oxygen loss in SOCs operation condition, revealing the improved structural stability. Meanwhile, the Ca 2+ 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 cm 2 (800 °C) in as-prepared PrBa 0.8 Ca 0.2 Co 1.96 Ta 0.04 O 5+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 CO 2 electrolysis.
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