钙钛矿(结构)
氧化钇稳定氧化锆
电解质
氧化物
电化学
极化(电化学)
兴奋剂
电极
材料科学
氢
立方氧化锆
固体氧化物燃料电池
化学工程
无机化学
光电子学
化学
复合材料
冶金
陶瓷
物理化学
有机化学
工程类
作者
Chaohang Liu,Feng Wang,Yue Ni,Shun Wang,Bin Qian,Qing Ni,Yifeng Zheng,Han Chen,Ge Lin
标识
DOI:10.1016/j.ijhydene.2022.11.237
摘要
Symmetrical solid oxide fuel cells (S-SOFCs) have received considerable attention due to fewer preparation steps in recent years. The PrBaFe2O5+δ (PBF) is a candidate material due to good catalytic activity and electrochemical stability. In this work, Ta-substituted PBF materials (PrBaFe2-xTaxO5+δ, denoted as PBFTx, x = 0, 0.1, 0.2, 0.3) are prepared and evaluated as symmetrical electrodes on GDC(Gd0.1Ce0.9O2-δ)-YSZ(yttria-stabilized zirconia)-GDC three-layer electrolyte. The PrBaFe1.8Ta0.2O5+δ (PBFT0.2) symmetrical cell presents the lowest polarization resistance, and the value is 0.171 Ω cm2 and 0.503 Ω cm2 in air and hydrogen atmosphere at 800 °C, respectively. In addition, the PBFT0.2 cell shows a peak power density of 234 mW/cm2 using humidified hydrogen as fuel gas and air as oxidant at 800 °C, which is enhanced by 68% compared with that of PBF (138 mW/cm2). The results indicate that the strategy of Ta doping can improve the electrochemical performance of PBF and PBFT0.2 is a potential electrode for S-SOFCs.
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