Hostname: page-component-848d4c4894-pjpqr Total loading time: 0 Render date: 2024-07-05T18:31:16.639Z Has data issue: false hasContentIssue false

Ferroelectric properties of tetragonal lead barium niobate (Pb1−xBaxNb2O6) crystals near the morphotropic phase boundary

Published online by Cambridge University Press:  31 January 2011

Myeongkyu Lee
Affiliation:
Department of Materials Science & Engineering, Stanford University, Stanford, California 94305
Robert S. Feigelson
Affiliation:
Department of Materials Science & Engineering, Stanford University, Stanford, California 94305
Get access

Abstract

Tungsten bronze ferroelectrics with a morphotropic phase boundary (MPB) have become increasingly important for a variety of applications because of their enhanced and unique properties near the MPB. Lead barium niobate (Pb1−xBaxNb2O6) crystals, which have a morphotropic phase boundary between the orthorhombic (1 − x > ∼0.63) and tetragonal (1 − x, <, 0.63) phases, were grown in sealed Pt crucibles by the vertical Bridgman method for tetragonal compositions near the MPB, and their ferroelectric properties were investigated. The ferroelectric domain structures in as-grown crystals were revealed either by etching in hydrofluoric acid or by polishing with colloidal silica, the latter providing clearer features. Domain size on the surface perpendicular to the polar axis was 10–50 μm. Crystals could be poled by slowly cooling from above the Curie temperatures (300–400 °C) under a dc field of 5 V/mm. The spontaneous polarization Ps of tetragonal Pb1−xBaxNb2O6 was found to be in the range of 0.40–0.70 μC/mm2 at room temperature depending on composition and increased as the composition approached morphotropic phase boundary (1 − x = ∼0.63), as expected.

Type
Articles
Copyright
Copyright © Materials Research Society 1998

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1.Jaffe, B., Cook, W. R., and Jaffe, H., Piezoelectric Ceramics (Academic Press, New York, 1971).Google Scholar
2.Smolensky, G. A., Isupov, V. A., and Agranovskaya, A. I., Sov. Phys. Solid State 1, 400 (1959).Google Scholar
3.Francombe, M. H., Acta Crystallog. 13, 131 (1960).CrossRefGoogle Scholar
4.Subbarao, E. C., Shirane, G., and Jona, F., Acta Crystallogr. 13, 226 (1960).CrossRefGoogle Scholar
5.Guo, R., Bhalla, A. S., Randall, C. A., Chang, Z. P., and Cross, L. E., Ferroelectrics 93, 193 (1989).CrossRefGoogle Scholar
6.Neurgaonkar, R. R., Cory, W. K., Oliver, J. R., Ewbank, M. D., and Hall, W. F., Opt. Eng. 26, 392 (1987).CrossRefGoogle Scholar
7.DiDomenico, M. and Wemple, S. H., J. Appl. Phys. 40, 720 (1969).CrossRefGoogle Scholar
8.Oliver, J. R., Neurgaonkar, R. R., and Cross, L. E., J. Am. Ceram. Soc. 72, 202 (1989).CrossRefGoogle Scholar
9.Shrout, T. R., Chen, H., and Cross, L. E., Ferroelectrics 74, 317 (1987).CrossRefGoogle Scholar
10.Lane, R., Mack, D. L., and Brown, K. R., Trans. J. Brit. Ceram. Soc. 71, 11 (1972).Google Scholar
11.Liu, A. Y., Bashaw, M. C., Hesselink, L., Lee, M., and Feigelson, R. S., Opt. Lett. 22, 187 (1997).CrossRefGoogle Scholar
12.Shrout, T. R. and Cross, L. E., Ferroelectrics Lett. 44, 325 (1983).CrossRefGoogle Scholar
13.Glass, A. M., J. Appl. Phys. 40, 4699 (1969).CrossRefGoogle Scholar
14.Myers, L. E., Miller, G. D., Eckardt, R. C., Fejer, M. M., Byer, R. L., and Bosenberg, W. R., Opt. Lett. 20, 52 (1995).CrossRefGoogle Scholar
15.Myers, L. E., Eckardt, R. C., Fejer, M. M., Byer, R. L., Bosenberg, W. R., and Pierce, J. W., J. Opt. Soc. Am. B 12, 2102 (1995).CrossRefGoogle Scholar