无机材料学报 ›› 2017, Vol. 32 ›› Issue (3): 235-240.DOI: 10.15541/jim20160340

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基于Pr0.6Sr0.4Co0.2Fe0.8O3-δ对称固体氧化物燃料电池的性能优化研究

杨 洋1,2, 田 冬2, 丁岩芝2, 卢肖永2, 林 彬2, 陈永红2   

  1. (1. 安徽理工大学 化学工程学院, 淮南232001; 2. 淮南师范学院 淮南低温共烧材料安徽省重点实验室, 淮南232038)
  • 收稿日期:2016-05-25 修回日期:2016-07-30 出版日期:2017-03-20 网络出版日期:2017-02-24
  • 作者简介:杨 洋(1992–), 男, 硕士研究生. E-mail: yangbegl@163.com
  • 基金资助:
    国家自然科学基金(51102107, 51202080);安徽省自然科学基金(1408085MKL43)

Improved Performance of Symmetrical Solid Oxide Fuel Cells with Redox-reversible Pr0.6Sr0.4Co0.2Fe0.8O3-δ Electrodes

YANG Yang1,2, TIAN Dong2, DING Yan-Zhi2, LU Xiao-Yong2, LIN Bin2, CHEN Yong-Hong2   

  1. (1. School of Chemical Engineering, Anhui University of Science and Technology, Huainan 232001, China; 2. Key Laboratory of Low Temperature Co-fired Materials; School of Chemical and Materials Engineering, Huainan Normal University, Huainan 232038, China)
  • Received:2016-05-25 Revised:2016-07-30 Published:2017-03-20 Online:2017-02-24
  • About author:YANG Yang. E-mail: yangbegl@163.com
  • Supported by:
    National Natural Science Foundation of China (51102107, 51202080);Anhui Provincial Natural Science Foundation (1408085MKL43)

摘要:

采用柠檬酸-硝酸盐自蔓延燃烧法分别合成了Pr0.6Sr0.4Co0.2Fe0.8O3-δ(PSCF)和Gd0.2Ce0.8O2-δ(GDC)粉体, 高温固相法合成La0.9Sr0.1Ga0.8Mg0.2O3-δ(LSGM)电解质粉体。以LSGM为电解质, PSCF同时作为阴极和阳极, GDC作为功能层材料, 构建了对称固体氧化物燃料电池PSCF│GDC│LSGM│GDC│PSCF。利用X射线衍射法研究材料的成相以及相互间的化学稳定性, 交流阻抗法记录界面极化行为, 用扫描电子显微镜观察电池的断面微结构, 用自组装的测试系统评价电池输出性能。结果表明, 合成的PSCF粉体呈立方钙钛矿结构, 具有良好的氧化-还原可逆性。使用GDC功能层明显改善了氢气环境下PSCF与LSGM材料间的化学相容性以及电池的输出性能, 800℃时, 电极│电解质界面极化电阻从6.892 Ω·cm2下降到0.314 Ω·cm2; 以加湿H2(含体积分数3%的水蒸气)为燃料气, 空气为氧化气时, 单电池输出功率密度由269 mW/cm2增大至463 mW/cm2。研究结果显示, PSCF是对称固体氧化物燃料电池良好的候选电极材料, GDC功能层对改善电池长期稳定性能具有潜在的应用价值。

关键词: 对称固体氧化物燃料电池, 氧化-还原可逆性, Pr0.6Sr0.4Co0.2Fe0.8O3-δ, GDC功能层

Abstract:

Pr0.6Sr0.4Co0.2Fe0.8O3-δ (PSCF) and Gd0.2Ce0.8O2-δ (GDC) powders were synthesized by a citric acid- nitrates self-propagating combustion method, and La0.9Sr0.1Ga0.8Mg0.2O3-δ (LSGM) electrolyte powder was prepared by conventional solid state reaction process. The LSGM-supported symmetrical solid oxide fuel cell of PSCF│GDC│LSGM│GDC│PSCF with GDC function layer was fabricated. The phase structure, chemical compatibility, polarization resistance, cross-section microstructure and the cell performance were investigated by X-ray diffraction (XRD), electrochemical impedance spectra, scanning electron microscope (SEM) and self-assembly SOFC test system, respectively. The results indicate that PSCF powder exhibits a single perovskite with cubic symmetry and a good redox reversibility. The GDC function layer dramatically improve the chemical compatibility among PSCF, LSGM in hydrogen and the cell performance. The area specific resistance (ASR) of PSCF│GDC decreased from 6.892 Ω·cm2 to 0.314 Ω·cm2 in hydrogen at 800℃ and the maximum power density increased from 269 mW/cm2 to 463 mW/cm2 using humidified hydrogen (3%H2O) as fuel and ambient air as oxidant. The results indicate that PSCF is a promising electrode material for symmetrical solid oxide fuel cells, and GDC function layer is a potential way to enhance the long-term stability.

Key words: symmetrical solid oxide fuel cell, redox reversibility, Pr0.6Sr0.4Co0.2Fe0.8O3-δ, GDC function layer

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