Investigation of the stability of ceria-gadolinia electrolytes in solid oxide fuel cell environments

被引:80
|
作者
Badwal, SPS
Ciacchi, FT
Drennan, J
机构
[1] CSIRO, Clayton, Vic 3169, Australia
[2] Ceram Fuel Cells Ltd, Noble Pk, Vic 3174, Australia
[3] Univ Queensland, Ctr Microscopy & Microanal, St Lucia, Qld 4072, Australia
关键词
D O I
10.1016/S0167-2738(99)00044-2
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
Doped ceria-based materials are potential electrolytes for use in lower operating temperature (500-700 degrees C) solid oxide fuel cells because of their high ionic conductivity. In this study, impedance behaviour and microstructure of the (Ce0.8Gd0.2)O-1.9 exposed to mild fuel environments (H-2-N-2 mixtures) have been investigated. The exposure of specimens to H-2-N-2 mixtures at 1000 degrees C resulted in a substantial expansion of the lattice as a consequence of the reduction of Ce4+ to Ce3+, which in turn led to the development of microcracks and loss of continuity at the grain boundary region and increase in both the grain boundary (major effect) and the lattice (minor effect) resistivity. The behaviour for the grain boundary resistivity after the 800 degrees C exposure was somewhat similar although expansion of the lattice at 800 degrees C (or lower temperatures) was considerably less conspicuous. After exposure to H-2-N-2 atmosphere at lower temperatures (650 and 500 degrees C), although no significant increase in the grain boundary resistivity for exposures up to 1000 h was observed, the shape of the grain boundary are was clearly affected. The large increase in the grain boundary resistivity in reduced specimens has been attributed to the observed microcracking, loss of continuity between grains and possibly the formation of new phase regions with extremely poor oxygen-ion conductivity along grain boundaries during the reduction. The disruption to the microstructure is not recovered on subsequent oxidation in air. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:253 / 262
页数:10
相关论文
共 50 条
  • [1] Microstructure - Ionic conductivity relationships in ceria-gadolinia electrolytes
    Christie, GM
    vanBerkel, FPF
    [J]. SOLID STATE IONICS, 1996, 83 (1-2) : 17 - 27
  • [2] Preparation of ceria-gadolinia electrolytes by the tape rolling technique
    Necati Özkan
    Brian J. Briscoe
    [J]. Journal of Materials Research, 1998, 13 : 665 - 674
  • [3] Gadolinia doped ceria/yttria stabilised zirconia electrolytes for solid oxide fuel cell applications
    J. Luo
    R. J. Ball
    R. Stevens
    [J]. Journal of Materials Science, 2004, 39 : 235 - 240
  • [4] Gadolinia doped ceria/yttria stabilised zirconia electrolytes for solid oxide fuel cell applications
    Luo, J
    Ball, RJ
    Stevens, R
    [J]. JOURNAL OF MATERIALS SCIENCE, 2004, 39 (01) : 235 - 240
  • [5] Preparation of ceria-gadolinia electrolytes by the tape rolling technique
    Ozkan, N
    Briscoe, BJ
    [J]. JOURNAL OF MATERIALS RESEARCH, 1998, 13 (03) : 665 - 674
  • [6] Ceria-gadolinia supported NiCu catalyst: A suitable system for dry reforming of biogas to feed a solid oxide fuel cell (SOFC)
    Bonura, G.
    Cannilla, C.
    Frusteri, F.
    [J]. APPLIED CATALYSIS B-ENVIRONMENTAL, 2012, 121 : 135 - 147
  • [7] Thermodynamic stability of gadolinia-doped ceria thin film electrolytes for micro-solid oxide fuel cells
    Rupp, Jennifer L. M.
    Infortuna, Anna
    Gauckler, Ludwig J.
    [J]. JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 2007, 90 (06) : 1792 - 1797
  • [8] Grain boundary conductivity enhancement in ceria-gadolinia solid solutions
    Ralph, JM
    Kilner, JA
    [J]. PROCEEDINGS OF THE FIFTH INTERNATIONAL SYMPOSIUM ON SOLID OXIDE FUEL CELLS (SOFC-V), 1997, 97 (40): : 1021 - 1030
  • [9] A solid oxide fuel cell with a gadolinia-doped ceria anode: preparation and performance
    Marina, OA
    Bagger, C
    Primdahl, S
    Mogensen, M
    [J]. SOLID STATE IONICS, 1999, 123 (1-4) : 199 - 208
  • [10] Reduction of CO2 to CO at Cu–ceria-gadolinia (CGO) cathode in solid oxide electrolyser
    C-Y. Cheng
    G. H. Kelsall
    L. Kleiminger
    [J]. Journal of Applied Electrochemistry, 2013, 43 : 1131 - 1144