Hostname: page-component-76fb5796d-5g6vh Total loading time: 0 Render date: 2024-04-25T17:27:26.952Z Has data issue: false hasContentIssue false

Particle-shape control and formation mechanisms of hydrothermally derived lead titanate

Published online by Cambridge University Press:  31 January 2011

Jooho Moon
Affiliation:
Department of Materials Science and Engineering, University of Florida, Gainesville, Florida 32611
Melanie L. Carasso
Affiliation:
Department of Materials Science and Engineering, University of Florida, Gainesville, Florida 32611
Henrik G. Krarup
Affiliation:
Department of Materials Science and Engineering, University of Florida, Gainesville, Florida 32611
Jeffrey A. Kerchner
Affiliation:
Department of Materials Science and Engineering, University of Florida, Gainesville, Florida 32611
James H. Adair
Affiliation:
Department of Materials Science and Engineering, University of Florida, Gainesville, Florida 32611
Get access

Abstract

Phase-pure perovskite lead titanate with various morphologies has been synthesized by a hydrothermal method at 150 °C. Particle shapes include cubic, tabular, and aggregated platelike shapes. The feedstock concentration greatly influences particle morphology of the hydrothermally derived PbTiO3. At a concentration of 0.05 M, the tabular particles form while cubic particles are produced at 0.1 M. Aggregated plateletlike particles are synthesized at 0.125 M. It was observed that both tabular and cubic particles directly precipitate from the coprecipitated precursor gel. In contrast, the plateletlike shaped intermediate phase appears during the initial stage of reaction at 0.125 M and in situ transforms into perovskite PbTiO3 during further hydrothermal treatment. The intermediate phase preserves its particle shape during transformation and, acting as a template, gives rise to the final tabular PbTiO3 particles. It is demonstrated that only base reagents such KOH and NaOH, which provide a highly basic condition (i.e., pH > 14), promote transformation of the coprecipitated gel into the perovskite PbTiO3. A Hancock and Sharp kinetic analysis in conjunction with microstructural evidence suggests that the formation mechanism is dissolution and recrystallization in which the degree of supersaturation plays an important role in dictating the crystallographic particle phase and morphology of the particles. An experimentally constructed solubility diagram indicates that an excess lead condition is necessary to compensate for loss of lead species and to increase supersaturation to expedite precipitation of PbTiO3 at highly alkaline conditions.

Type
Articles
Copyright
Copyright © Materials Research Society 1999

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

REFERENCES

1.Sugimoto, T., MRS Bull., December, 23 (1989).CrossRefGoogle Scholar
2.Givargizov, E.I., Oriented Crystallization on Amorphous Substrate (Plenum Press, New York, 1991).CrossRefGoogle Scholar
3.Sugimoto, T., Adv. Colloid Interface Sci. 28, 65 (1987).CrossRefGoogle Scholar
4.Matijevic, E., in Chemical Processing of Advanced Materials, edited by Hench, L.L. and West, J.K. (John Wiley & Sons, New York, 1992), p. 513.Google Scholar
5.Dawson, W.J., Am. Ceram. Soc. Bull. 67 (10), 1673 (1988).Google Scholar
6.Kim, M. J. and Matjevic, E., Chem. Mater. 1, 363 (1989).CrossRefGoogle Scholar
7.Moon, J., Li, T., Randall, C. A., and Adair, J.H., J. Mater. Res., 12, 189197 (1997).CrossRefGoogle Scholar
8.Sato, S., Murakata, T., Yanagi, H., Miyasaka, F., and Iwaya, S., J. Mater. Sci. 29, 5657 (1994).CrossRefGoogle Scholar
9.Cheng, H., Ma, J., Zhao, Z., Zhang, H., Qiang, D., Li, Y., and Yao, X., in Proceedings of C-MRS International ′90, Vol. II, edited by Han, Y. (Elsevier, Amsterdam, The Netherlands, 1990), p. 509.Google Scholar
10.Cheng, H., Ma, J., Zhao, Z., Zhang, H., Qiang, D., Li, Y., and Yao, X., J. Am. Ceram. Soc. 75 (5), 1125 (1992).Google Scholar
11.Ohara, Y., Koumoto, K., Shimizu, T., and Yanagida, H., J. Ceram. Soc. Jpn. 102 (1), 88 (1994).CrossRefGoogle Scholar
12.Dowty, E. and Richards, R.P., SHAPE: A Computer Program for Drawing Crystals (v4.0, Kingport, TN, 1993).Google Scholar
13.Beal, K. C., in Advances in Ceramics, Vol. 21, Ceramic Powder Science, edited by Messing, G. L., Mazdiyasni, K. S., Mc-Cauley, J. W., and Haber, R. A. (The American Ceramic Society Inc., Westerville, OH, 1987), p. 33.Google Scholar
14.Adair, J. H., Krarup, H., Venigalla, S., and Tsukada, T., Aqueous Chemistry and Geochemistry of Oxides, Oxyhydroxides, and Related Materials, edited by Voigt, J. A., Wood, T. E., Bunker, B. C., Casey, W. H., and Crossey, L. J. (Mater. Res. Soc. Symp. Proc. 432, Pittsburgh, PA, 1996), pp. 101112.Google Scholar
15.Utech, B. L., The Effect of Solution Chemistry on Barium Titanate Ceramics (The Pennsylvania State University, University Park, PA, 1990).Google Scholar
16.Lencka, M.M. and Riman, R.E., Chem. Mater. 5, 61 (1993).CrossRefGoogle Scholar
17.Lencka, M.M. and Riman, R. E., J. Am. Ceram. Soc. 76 (10), 2649 (1993).CrossRefGoogle Scholar
18.Lencka, M. M. and Riman, R. E., Ferroelectrics 151, 159 (1994).CrossRefGoogle Scholar
19.Lencka, M.M. and Riman, R.E., Chem. Mater. 7, 18 (1995).CrossRefGoogle Scholar
20.Baes, C. F. and Mesmer, R. E., Am. J. Sci. 281, 935 (1981).CrossRefGoogle Scholar
21.Miller, D. V., Adair, J. H., and Newnham, R. E., Ceram. Trans. [1] (The American Ceramic Society, Inc., Westerville, OH, 1988), pp. 493500.Google Scholar
22.Avrami, M. J., J. Chem. Phys. 7, 1103 (1939).CrossRefGoogle Scholar
23.Hulbert, S. F., J. Brit. Ceram. Soc. 6, 11 (1969).Google Scholar
24.Hancock, J. D. and Sharp, J. H., J. Am. Ceram. Soc. 55 (5), 74 (1972).CrossRefGoogle Scholar
25.Rossetti, G. A. Jr, Watson, D. J., Newnham, R. E., and Adair, J. H., J. Cryst. Growth 116, 251 (1992).CrossRefGoogle Scholar
26.Hartman, P. and Bennema, P., J. Cryst. Growth 49, 145 (1980).CrossRefGoogle Scholar
27.Tani, T., Xu, Z., and Payne, D., in Ferroelectric Thin Films III, edited by Myers, E. R., Tuttle, B. A., Desu, S. B., and Lauser, P. K. (Mater. Res. Soc. Symp. Proc. 310, Pittsburgh, PA, 1993), p. 269.Google Scholar
28.Bennema, P., in Handbook of Crystal Growth, Vol. 1 (Part A), edited by Hurle, D. T. J. (North-Holland, Amsterdam, The Netherlands, 1993), p. 456.Google Scholar
29.Cheng, H., Ma, J., and Zhao, Z., Chem. Mater. 6, 1033 (1994).CrossRefGoogle Scholar
30.Nyvlt, J., Sohnel, O., Matuchova, M., and Broul, M., The Kinetics of Industrial Crystallization (Chemical Engineering Monographs, Elsevier, New York, 1985), Vol. 19.Google Scholar
31.LaMer, V.K. and Dinegar, R. H., J. Am. Chem. Soc. 72, 4847 (1950).CrossRefGoogle Scholar