Development of novel low-temperature SOFCs with co-ionic conducting SDC-carbonate composite electrolytes

被引:164
|
作者
Huang, Hanbing [1 ]
Mao, Zongqiang [1 ]
Liu, Zhixiang [1 ]
Wang, Cheng [1 ]
机构
[1] Tsinghua Univ, Inst Nucl & New Energy Technol, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
samaria doped ceria (SDC); carbonate; composite electrolyte; co-ionic; solid oxide fuel cells (SOFCs);
D O I
10.1016/j.elecom.2007.07.036
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
A series of ceria-based composite materials consisting of samaria doped ceria (SDC) and binary carbonates(Li2CO3-Na2CO3) were examined as functional electrolytes for low-temperature solid oxide fuel cells (SOFCs). DTA and SEM techniques were applied to characterize the phase- and micro-structural properties of the composite materials. Conductivity measurements were carried on the composite electrolytes with a.c. impedance in air. A transition of ionic conductivity with temperature was occurred among all samples with different carbonate content, which related to the interface phase. Single cells based on the composite electrolytes, NiO as anode and lithiated NiO as cathode, were fabricated by a simple dry-pressing process and tested at 400-600 degrees C. The maximum output power at 600 degrees C increased with the carbonate content in the composite electrolytes, and reached the maximum at 25 wt.%, then decreased. Similar trend has also shown at 500 degrees C, but the maximum was obtained at 20wt.%. The best performances of 1085 mW cm(-2) at 600 degrees C and 690 mW cm(-2) at 500 degrees C were achieved for the composite electrolytes containing 25 and 20 wt.% carbonates, respectively. During fuel cell operation, it found that the SDC-carbonate composites are co-ionic (O2-/H+) conductors. At lower carbonate contents, both oxide-ion and proton conductions were significant, when the content increased to 20-35 wt.%, proton conduction dominated. The detailed conduction mechanism in these composites needs further investigation. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:2601 / 2605
页数:5
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