期刊
JOURNAL OF ALLOYS AND COMPOUNDS
卷 753, 期 -, 页码 292-299出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2018.04.215
关键词
Solid oxide fuel cells; Cathodes; Electrochemical performance; Binary composite
资金
- Natural Science Foundation of China [51632001, 51764048]
- Shanghai Key Laboratory of Rare Earth Functional Materials
Oxygen-ion transport property greatly affects the electro-catalytic activity of a cathode material in the solid oxide fuel cells. In this work, to enhance the electrochemical activity of hexagonal Ca(3)Co(2)0(6) cathode, fast ion-conductor Ce0.8Sm0.2O1.9 is introduced as the second phase, and thus a binary composite is developed, expressed as (l-x)Ca3Co2O6/xCe(0.8)Sm(0.2)O(1.9) in nominal form. The composites are prepared by one-pot method and X-ray diffraction results reveal that these compositional phases are highly compatible. Analysis of X-ray photoelectron spectroscopy indicates the existence of Co3+ and Co2+ mixed valences in the composites. Compared with single-phase Ca3Co2O6, thermal expansion coefficient of the composite is favorably low and matches better with the electrolyte of solid oxide fuel cells. Test of electrical conductivity shows that the composites are comparable to the pure Ca3Co2O6 in charge transport capacity. Electrochemical measurements indicate that the x=0.5 composite cathode exhibit the lowest area specific resistance and produces the maximum power density. In the electrolyte-supported single cell along with Ni-SDC cermet as anode and pure H-2 gas as fuel, power density peak of 680 mWcm(-2) is achieved from the x = 0.5 composite cathode at 800 degrees C. (c) 2018 Elsevier B.V. All rights reserved.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据