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Microstructural development of BaTiO3 powders synthesized by aqueous methods

Published online by Cambridge University Press:  31 January 2011

L. Zhao ,
A. T. Chien ,
F. F. Lange  and
J. S. Speck
L. Zhao
Affiliation:
Materials Research Laboratory and Materials Department, University of California, Santa Barbara, Santa Barbara, California 93106
A. T. Chien
Affiliation:
Materials Research Laboratory and Materials Department, University of California, Santa Barbara, Santa Barbara, California 93106
F. F. Lange
Affiliation:
Materials Research Laboratory and Materials Department, University of California, Santa Barbara, Santa Barbara, California 93106
J. S. Speck
Affiliation:
Materials Research Laboratory and Materials Department, University of California, Santa Barbara, Santa Barbara, California 93106
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Abstract

The hydrothermal growth of perovskite BaTiO3 powders has been studied by transmission electron microscopy. The growth is carried out under high alkaline conditions (pH — 14) achieved with Ba(OH)2. Anatase (TiO2) is used as a titanium source. The perovskite BaTiO3 nucleates heterogeneously on anatase TiO2 particles with an epitaxial relationship of (001)TiO2 ‖ (001)BaTiO3 and [010]TiO2 ‖ [010]BaTiO3. This epitaxial relationship preserves the parallel alignment of the oxygen octahedra between the structures. A mosaic misorientation between (001)TiO2 and (001)BaTiO3 along 〈110〉 is seen in this relationship due to the lattice mismatch between TiO2 and BaTiO3. After complete conversion of the anatase to BaTiO3, the BaTiO3 particles develop into {111} octahedrons with ∼10 nm {001} and {110} microfacets on the {111} faces. This evolution suggests that {111} becomes the stable crystallographic facet for BaTiO3 under highly alkaline conditions.

Type
Articles
Information
Journal of Materials Research , Volume 11 , Issue 6 , June 1996 , pp. 1325 - 1328
Copyright
Copyright © Materials Research Society 1996

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References

REFERENCES

1.Hennings, D., Int. J. High Tech. Ceram. 3, 91 (1987).CrossRefGoogle Scholar
2.Dawson, W., Ceram. Bull. 67, 1673 (1988).Google Scholar
3.Roy, R. and Tuttle, O.F., Phys. Chem. Earth. 1, 138 (1956).CrossRefGoogle Scholar
4.Lilley, E. and Wusirika, R.R., U.S. Patent No. 4 764 493 (August 1988).Google Scholar
5.Chien, A.T., Speck, J.S., Lange, F.F., Daykin, A.C., and Levi, C. G., J. Mater. Res. 10, 1784 (1995).CrossRefGoogle Scholar
6.Kastrissios, T., Stephenson, M., Turner, P. S., and White, T.J., J. Am. Ceram. Soc. 70, C–144 (1987).CrossRefGoogle Scholar
7.Banfield, J.F. and Veblen, D. R., Am. Mineral. 77, 545 (1992).Google Scholar
8.Doukhan, N. and Doukhan, J.C., Phys. Chem. Minerals 13, 403 (1986).CrossRefGoogle Scholar
9.Clark, G. M., The Structures of Non-Molecular Solids (Halsted Press, New York, 1972), p. 151 and p. 240.Google Scholar