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La2Zr2O7 Formation Between Yttria-Stabilized Zirconia and La0.85Sr0.15MnO3 at 1373 K

Published online by Cambridge University Press:  15 February 2011

A. Mitterdorfer
Affiliation:
ETH Zurich, Department of Materials, Chair of Nonmetallic Materials, Swiss Federal Institute of Technology, CH-8092, Zurich, Switzerlandgauckler@nonmet.mat.ethz.ch
L. J. Gauckler
Affiliation:
ETH Zurich, Department of Materials, Chair of Nonmetallic Materials, Swiss Federal Institute of Technology, CH-8092, Zurich, Switzerlandgauckler@nonmet.mat.ethz.ch
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Abstract

Oxygen ion conducting yttria-stabilized zirconia and perovskite-type Sr-doped LaMnO3 have been widely used as solid electrolyte and cathode materials in solid oxide fuel cells. The electrochemical properties of the cathode depend largely on the nanostructure and the phase composition of the interface between cathode and electrolyte. Interfaces between single crystals of 9.5mol% Y2O3-stabilized ZrO2 and porous La0.85Sr0.15MnyO3 (y = 0.95…1.10) were investigated. Atomic force microscopy was used for interface studies of YSZ single crystals after removal of sintered perovskite cathodes. High resolution transmission electron microscopy, electron diffraction and electrochemical impedance spectroscopy were employed for interface characterization. Pyrochlore-type lanthanum zirconate formed at the interface during sintering at 1100°C. Nucleation, growth kinetics, and morphology were largely depending on cathode stoichiometry. Lanthanum zirconate formation was retarded in case of A-site deficient perovskite.

Type
Research Article
Copyright
Copyright © Materials Research Society 1997

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References

REFERENCES

[1] Lau, S. K. and Singhal, S. C. in Proc. Corrosion 85, Boston. (1985), p. 7980.Google Scholar
[2] van Roosmalen, J. A. M. and Cordfunke, E. H. P.. Solid State Ionics 52, p. 303, (1992).Google Scholar
[3] Yamamoto, O., Takeda, Y., Kanno, R., and Kojima, T. in Proceedings of the First International Symposium on Solid Oxide Fuel Cells, edited by Singhal, S. C. (The Electrochemical Society, Inc., Pennington, NJ, 1989), p. 240246 Google Scholar
[4] Taimatsu, H., Wada, K., Kaneko, H., and Yamamura, H.. J. Am. Ceram. Soc. 75, p. 401 (1992).Google Scholar
[5] Mitterdorfer, A. and Gauckler, L. J., J. Am. Ceram. Soc, to be submitted.Google Scholar
[6] Mitterdorfer, A. and Gauckler, L. F. in Proc. on the 17th Risø Int. Symp. on Mat. Sci., edited by Poulsen, F. W., Bonanos, N., Lindenroth, S., Mogensen, M., and Zachau-Christiansen, B. (Risø National Laboratory, Roskilde, Denmark, 1996), p. 357362.Google Scholar