Influence of anode pore forming additives on the densification of supported BaCe0.7Ta0.1Y0.2O3-δ electrolyte membranes based on a solid state reaction

被引:33
作者
Bi, Lei [1 ]
Fang, Shumin [1 ,2 ,3 ]
Tao, Zetian [1 ]
Zhang, Shangquan [1 ]
Peng, Ranran [1 ]
Liu, Wei [1 ]
机构
[1] Univ Sci & Technol China, Lab Adv Funct Mat & Devices, Dept Mat Sci & Engn, Hefei 230026, Anhui, Peoples R China
[2] Univ Twente, Fac Sci & Technol, NL-7500 AE Enschede, Netherlands
[3] Univ Twente, MESA Inst, NL-7500 AE Enschede, Netherlands
基金
中国国家自然科学基金;
关键词
Sintering; Solid state reaction; Fuel cell; Membranes; Pore forming additive; OXIDE FUEL-CELLS; THIN-FILM; IN-SITU; BACEO3; FABRICATION; SOFC;
D O I
10.1016/j.jeurceramsoc.2009.02.017
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
We describe a solid state reaction for the preparation of both NiO-BaCe0.7Ta0.1Y0.2O3-delta anode substrates and BaCe0.7Ta0.1Y0.2O3-delta (BCTY10) electrolyte membranes on porous NiO-BCTY10 anode substrates. The amounts of the pore forming additive in the substrates showed a significant influence on the densification of the BCTY10 membranes. After sintering at 1450 degrees C for 5 h, the BCTY10 membrane on a NiO-BCTY10 anode containing 30 wt.% starch achieved a high density and showed adequate chemical stability against H2O and CO2. The chemical stability of BCTY10 was even better than that of BaCe0.7Zr0.1Y0.2O3-delta. With a mixture of BaCe0.7Zr0.1Y0.2O3-delta (BZCY7) and La0.7Sr0.3FeO3-delta (LSF) as a cathode, a single fuel cell with 12 mu m thick BCTY10 electrolyte generated maximum power densities of 142, 93, 29 mW/cm(2) at 700, 600 and 500 degrees C, respectively. The electrolyte resistance and interfacial polarization resistance of the cell under open circuit conditions were also investigated. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2567 / 2573
页数:7
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