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Grain Boundary Conductivities of 0.58% Y203 Doped CeO2 Thin Films

Published online by Cambridge University Press:  15 February 2011

Chunyan Tian
Affiliation:
Materials Science & Engineering Program, School of Engineering and Applied Science, Columbia University, New York, NY 10027
Siu-Wai Chan
Affiliation:
Materials Science & Engineering Program, School of Engineering and Applied Science, Columbia University, New York, NY 10027
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Abstract

We have prepared Y2O3 doped CeO2 thin films on various substrates using electron beam evaporation. Both polycrystalline and single crystal-like textured films were shown by x-ray diffraction and transmission electron microscopy analyses. AC impedance spectroscopy was used to study the electrical properties of the films. The ionic conductivities of the films are dominated by grain boundaries, and higher as compared to that of a bulk material having the same dopant concentration sintered at 1500°C. The grain boundary conductivities of the films were investigated with regard to grain size, grain boundary impurity segregation, space charge on grain boundaries, and grain boundary misorientations. The contribution of grai boundary misorientation to the resistance of the grain boundary is considered to be negligible with respect to those of the impurity layer and space-charge layers. The grain boundary resistance may originate from the oxygen vacancy depletion in the space-charge layers.

Type
Research Article
Copyright
Copyright © Materials Research Society 1999

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References

REFERENCES

1. Souza, S. de, Visco, S. J.. Jonghe, L. C. De, Solid State Ionics, 98, 5761 (1997).Google Scholar
2. Tsai, T.. Barnett, S. A., Solid State Ionics, 98, 191196 (1997).Google Scholar
3. Tian, C., Chan, S. W., Mat. Res. Soc. Symp. Proc. 575, 533 (1997).Google Scholar
4. Steele, B. C. H., Solid State Ionics, 12, 391406 (1984).Google Scholar
5. Wang, D. Y., Nowick, A. S., J. Solid State Chem., 35, 325333 (1980).Google Scholar
6. Gerhardt, R., Nowick, A. S., J. Ame. Ceram. Soc., 69 [9], 641646 (1986).Google Scholar
7. Tian, C. and Chan, S. W., Mat. Res. Soc. Symp. Proc., 411, (1996).Google Scholar
8. Tian, C., Du, Y., Chan, S. W., J. Vac. Sci.Technol. A, 15 [1], 8592 (1997).Google Scholar
9. Tian, C. and Chan, S. W., Mat. Res. Soc. Symp. Proc., 500, (1997).Google Scholar
10. Tian, C., Doctoral Disertation, Columbia University, 1998.Google Scholar
11. Tian, C. and Chan, S. W., to be published.Google Scholar
12. Kosacki, I., Anderson, H. U., Appl. Phys. Lett., 69 [27], 41714173 (1996).Google Scholar
13. Tiku, S. K. and Kroger, F. A., J. Am. Ceram. Soc., 63 [3–4], 183 (1980).Google Scholar