TY - JOUR
T1 - Dual-Doping Strategy for Lowering the Thermal Expansion Coefficient and Promoting the Catalytic Activity in Perovskite Cobaltate Air Electrodes for Solid Oxide Cells
AU - Wang, Shuxiong
AU - Zhang, Xiaoxin
AU - Chen, Yu
AU - Fan, Fan
AU - Jiang, Chang
AU - Xiang, Yongkang
AU - Xiao, Xiao
AU - Fang, Yuan
AU - Alodhayb, Abdullah N.
AU - Li, Jianhui
AU - Huang, Jijie
AU - Sun, Yifei
AU - Chen, Zhou
N1 - Publisher Copyright:
© 2024 Wiley-VCH GmbH.
PY - 2025/4/16
Y1 - 2025/4/16
N2 - 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.
AB - 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.
KW - air electrodes
KW - dual-dopings
KW - oxygen vacancies
KW - perovskite cobaltates
KW - thermal expansion coefficients
UR - http://www.scopus.com/inward/record.url?scp=105002570192&partnerID=8YFLogxK
U2 - 10.1002/smll.202410672
DO - 10.1002/smll.202410672
M3 - Article
C2 - 39688242
AN - SCOPUS:105002570192
SN - 1613-6810
VL - 21
JO - Small
JF - Small
IS - 15
M1 - 2410672
ER -