Journal of Materials Science

, Volume 21, Issue 11, pp 4035–4042 | Cite as

Characterization of the interface between (U, M)O2±x and yttria-zirconia

  • S. P. S. Badwal
  • F. T. Ciacchi
  • D. K. Sood


Solid-state electrochemical cells have been prepared by co-sintering pre-reacted electrode and electrolyte materials together. The electrodes investigated were the non-stoichiometric oxides of the general formula (U, M)Ox (M = Sc, Y) and the electrolyte used was yttria-stabilized zirconia. The specimens were characterized by X-ray diffraction, Rutherford back-scattering spectrometry, scanning electron microscopy with energy-dispersive analysis by X-rays, and optical microscopy. For M = Sc, an intermediate phase is formed at the interface and is responsible for the strong bonding of the electrode layer to the electrolyte. The thickness of the intermediate layer was about 2 to 3Μm. Considerable loss of uranium, which in some cases led to destabilization of the fluorite phase, was observed from the surface of the uraniascandia electrode layers. The intermediate phase is thought to be formed as a result of reaction between the electrolyte and volatile uranium-containing species produced by decomposition of the urania-scandia electrode material. For M = Y, no evidence for the formation of such a phase was found and the adhesion of the electrode to electrolyte was poor.


Scanning Electron Microscopy Zirconia Uranium Optical Microscopy Fluorite 
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  1. 1.
    H. Obayashi andT. Kudo, “Solid State Chemistry of Energy Conversion and Storage”, edited by J. B. Goodenough and M. S. Whittingham (American Chemical Society, Washington, DC, 1977) p. 316.Google Scholar
  2. 2.
    Proceedings of Workshop on High Temperature Solid Oxide Fuel Cells, edited by H. S. Isaacs, S. Srinivasan and I. L. Harry (US Department of Energy, BNL 50756/TID-4500, 1977).Google Scholar
  3. 3.
    S. P. S. Badwal,J. Electroanal. Chem. 146 (1983) 425.Google Scholar
  4. 4.
    Idem, ibid. 161 (1984) 75.Google Scholar
  5. 5.
    S. P. S. Badwal, M. J. Bannister andM. J. Murray,ibid. 168 (1984) 363.Google Scholar
  6. 6.
    S. P. S. Badwal andF. T. Ciacchi,J. Appl. Electrochem. 16 (1986) 28.Google Scholar
  7. 7.
    W. K. Chu, J. W. Mayer andM.-A. Nicolet, “Backscattering Spectrometry” (Academic Press, New York, 1978).Google Scholar
  8. 8.
    C. Keller, U. Berndt, M. Debbabi andH. Engerer,J. Nucl. Mater. 42 (1972) 23.Google Scholar
  9. 9.
    S. P. S. Badwal, PhD thesis, Flinders University of South Australia (1977).Google Scholar
  10. 10.
    J. H. Handwork, G. D. White andD. C. Hill,J. Amer. Ceram. Soc. 46 (1963) 29.Google Scholar
  11. 11.
    A. N. Belov, S. I. Lopatin, G. A. Semenov andI. V. Vinokurov,Russ. J. Inorg. Chem. 20 (1984) 384.Google Scholar
  12. 12.
    E. A. Aitken andR. A. Joseph,J. Phys. Chem. 70 (1966) 1090.Google Scholar
  13. 13.
    W. B. Wilson, C. A. Alexander andA. F. Gerds,J. Inorg. Nucl. Chem. 20 (1961) 242.Google Scholar
  14. 14.
    S. P. S. Badwal, F. T. Ciacchi andD. K. Sood,Solid State Ionics 18/19 (1986) 1033.Google Scholar

Copyright information

© Chapman and Hall Ltd. 1986

Authors and Affiliations

  • S. P. S. Badwal
    • 1
  • F. T. Ciacchi
    • 1
  • D. K. Sood
    • 2
  1. 1.Division of Materials ScienceCSIROClaytonAustralia
  2. 2.Microelectronics Technology CentreRoyal Melbourne Institute of TechnologyMelbourneAustralia

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