Precursor solution additives improve desiccated La0.6Sr0.4Co0.8Fe0.2O3-x infiltrated solid oxide fuel cell cathode performance

被引:25
作者
Burye, Theodore E. [1 ]
Nicholas, Jason D. [1 ]
机构
[1] Michigan State Univ, Dept Chem Engn & Mat Sci, E Lansing, MI 48824 USA
基金
美国国家科学基金会;
关键词
Electrode; Infiltration; Desiccation; Degradation; Stability; COMPOSITE CATHODES; TEMPERATURE; STABILITY; ELECTRODES; MODEL; PREDICTION; ANODE;
D O I
10.1016/j.jpowsour.2015.10.012
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Here, the addition of the surfactant Triton X-100 or the chelating agent citric acid to Solid Oxide Fuel Cell (SOFC) La0.6Sr0.4Co0.8Fe0.2O3-x (LSCF) precursor nitrate solutions is shown via scanning electron microscopy (SEM) and X-ray diffraction (XRD) to reduce average infiltrate nano-particle size and improve infiltrate phase purity. In addition, the desiccation of LSCF precursor solutions containing the aforementioned organic solution additives further reduces the average LSCF infiltrate nano-particle size and improves the low-temperature infiltrate phase purity. In particular, CaCl2-desiccation reduces the average size of Triton X-100 derived (TXD) LSCF particles fired at 700 degrees C from 48 to 22 nm, and reduces the average size of citric acid derived LSCF particles fired at 700 degrees C from 50 to 41 nm. Modeling and electrochemical impedance spectroscopy (EIS) tests indicate that particle size reductions alone are responsible for desiccation-induced cathode performance improvements such as CaCl2-desiccated TXD La0.6Sr0.4Co0.8Fe0.2O3-x - Ce0.9Gd0.1O1.95 (LSCF-GDC) cathodes reaching a polarization resistance of 0.17 Omega cm(2) at 540 degrees C, compared to 600 degrees C for undesiccated TXD LSCF-GDC cathodes. This excellent low-temperature performance, combined with a low open-circuit 540 degrees C degradation rate, suggests that the desiccation of organic-additive-containing infiltrate precursor solutions may be useful for the development of durable, high-power, low-temperature SOFCs. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:287 / 298
页数:12
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