Influence of cathode functional layer composition on electrochemical performance of solid oxide fuel cells
详细信息    查看全文
  • 作者:Antônio de Pádua Lima Fernandes…
  • 刊名:Journal of Solid State Electrochemistry
  • 出版年:2016
  • 出版时间:September 2016
  • 年:2016
  • 卷:20
  • 期:9
  • 页码:2575-2580
  • 全文大小:4,084 KB
  • 刊物类别:Chemistry and Materials Science
  • 刊物主题:Chemistry
    Physical Chemistry
    Analytical Chemistry
    Industrial Chemistry and Chemical Engineering
    Characterization and Evaluation Materials
    Condensed Matter
    Electronic and Computer Engineering
  • 出版者:Springer Berlin / Heidelberg
  • ISSN:1433-0768
  • 卷排序:20
文摘
In this work, anode-supported solid oxide fuel cells (SOFC) were tested with a yttria-stabilized zirconia (YSZ) (8 mol% Y2O3-ZrO2)/gadolinium-doped ceria (GDC) (Ce0.9Gd 0.1O1.95) bilayer electrolyte and two lanthanum strontium cobalt ferrite (LSCF) composition as functional cathode layer: La0.6Sr0.4Co0.8Fe0.2O3-δ (LSCF 1) and La0.60Sr0.40Co0.2Fe0.8O3-δ (LSCF 2). The functional cathode layers were made of 50 % (w/w) LSCF and 50 % (w/w) GDC. Microstructural characterization was performed by scanning electron microscopy and X-ray diffraction. Electrochemical impedance spectroscopy (EIS) and power measurements were performed under oxygen and hydrogen atmospheres. The microscopy studies showed that the LSCF 2 functional layer is more uniform and adherent to the electrolyte and the cathode collector than the LSCF 1 functional layer, which has cracks, chips, and lower adhesion. The use of the LSCF 2 layer allowed an approximately 25-fold reduction in ohmic resistance (0.06 Ω cm−2) compared with the LSCF 1 layer (1.5 Ω cm−2). The power measurements showed a considerable increase in the power cell using LSCF 2 (approximately 420 mW cm−2) compared with the power cell using LSCF 1 (approximately 180 mW cm−2).KeywordsSOFCLSCFInterfaceElectrochemical performanceCathodeFunctional layer

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700