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摘要
采用溶胶-凝胶法、固相法制备La0.7Sr0.3Fe0.7Co0.2Ni0.1O3-δ(LSFCN)中低温固体氧化物燃料电池阴极材料,通过热重-差热分析、X射线衍射、扫描电镜、直流四探针法、热膨胀系数、交流阻抗对材料的结构与性能进行研究。结果表明,2种方法制备的LSFCN均为单一的钙钛矿结构,并且与电解质SDC在950℃以下没发生化学反应,稳定性较好。溶胶-凝胶法制备的阴极粉体颗粒最小、形状规整、结晶度高。在测试温度400~800℃条件下,2种方法合成的阴极材料LSFCN是小极化子导电机制,电导率随着测试温度的升高而增大。溶胶-凝胶法制得的LSFCN的电导率均大于固相法,在800℃时最大达到619.4 S/cm。2种方法制备的LSFCN阴极样品与电解质SDC匹配性好。2种方法制备的LSFCN有利于氧在三相界面的传输,提高了材料的电化学性能。
Abstract
La0.7Sr0.3Fe0.7Co0.2Ni0.1O3-δ(LSFCN),a cathode material for medium and low temperature solid oxides fuel cell,is prepared by sol-gel method and solid state reaction method,respectively.The structure and properties of the material are measured by thermogravimetry-differential thermal analysis (TG-DTA),X-ray diffractometry (XRD),scanning electron microscopy (SEM),four-probe DC method,thermal expansion coefficient (TEC) and alternating-current impedance.It is shown that LSFCN prepared by two methods both have a single perovskite structure and do not react with the electrolyte SDC during 950℃ calcination,meaning a good stability.LSFCN prepared by sol-gel method has a smaller particle size,a more regular shape and a higher crystallinity.Both LSFCN by two methods exhibit a conductivity mechanism of small polaron at the test temperature of 400-800℃,their conductivities increase with the increase of the test temperature.The conductivity of LSFCN prepared by sol-gel method is higher than that of LSFCN prepared by the solid state reaction method.The maximum conductivity of LSFCN reaches 619.4 S·cm-1 at 800℃.LSFCN cathode samples prepared by the two methods have a good match with SDC electrolyte,and both are favorable for oxygen transfer through three-phase interface,which can improve the electro chemical properties of the materials.
关键词
溶胶-凝胶法
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交流阻抗
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热膨胀
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电导率
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钙钛矿
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固相法
Key words
sol-gel method
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alternating-current impedance
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thermal expansion
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conductivity
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perovskite
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solid state reaction method
Author summay
李向国(1984-),男,硕士研究生,研究方向为固体氧化物燃料电池阴极材料,2512866704@qq.com
SOFC阴极材料La0.7Sr0.3Fe0.7Co0.2Ni0.1O3-δ的制备与性能[J].
, 2019, 39(10): 92-96 DOI:10.16606/j.cnki.issn0253-4320.2019.10.020