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Effects of cationic dopants on the phase transition temperature of titania prepared by the sol-gel method

Published online by Cambridge University Press:  31 January 2011

S. Vargas
Affiliation:
Departamento de Física, UAM-Iztapalapa, Apdo. Postal 55–534, México, D.F. 09340
R. Arroyo
Affiliation:
Departamento de Química, UAM-Iztapalapa, Apdo. Postal 55–534, México, D.F. 09340
E. Haro
Affiliation:
Departamento de Física, UAM-Iztapalapa, Apdo. Postal 55–534, México, D.F. 09340
R. Rodríguez
Affiliation:
Departamento de Física, UAM-Iztapalapa, Apdo. Postal 55–534, México, D.F. 09340
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Abstract

The effect of different cations in the anatase–rutile phase transition temperatures for titania prepared by the sol-gel method was studied. The metal dopants were chosen from different periods and groups of the periodic table to see the role played by the electronic configuration, the oxidizing state, the atomic size, etc. on these temperature modifications. Linear relationships between the anatase–rutile phase transition temperatures and the ionic radii for alkali metal, alkaline earth metal, and group 3 and 13 elements were obtained. For elements of the period 4, there was not such a defined tendency; for most of them the modification of the phase transition temperature was too small. The cations used were Li+, Na+, K+, Mg2+, Ca2+, Sr2+, Ba2+, Al3+, Y3+, La3+, Er3+, Ti4+, Co2+, Ni2+, Cu2+, and Zn2+. In all cases the dopant's concentration was 2 mol% with respect to titanium, and the same anion (nitrate) was used for all salts. A variation of more than 330 °C in the anatase–rutile phase transition temperatures was obtained by using these dopants. The transition temperatures from amorphous to anatase and from anatase to rutile phases were obtained from the x-ray diffractograms.

Type
Articles
Copyright
Copyright © Materials Research Society 1999

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References

REFERENCES

1.Huheey, J.E., Keiter, E.A., and Keiter, R.L., Inorganic Chemistry, Principles of Structure and Reactivity (Harper Collins College, New York, 1993).Google Scholar
2.Cotton, F.A. and Wilkinson, G., Advanced Inorganic Chemistry (Interscience, John Wiley & Sons, New York, 1993).Google Scholar
3.Butler, I.S. and Harrod, J.F., Inorganic Chemistry, Principles and Applications (Benjamin/Cummings, Redwood City, CA, 1989).Google Scholar
4.Cruz, D., Chamizo, J.A., and Garritz, A., Estructura Química, Un Enfoque Químico (Addison Wesley Iberoamericana, 1986).Google Scholar
5.Parker, J.C. and Siegel, R.W., J. Mater. Res. 5, 1246 (1990).CrossRefGoogle Scholar
6.MacKenczie, K.J.D, Trans. J. Br. Ceram. Soc. 74, 2934 (1975); 74, 77–84 (1975).Google Scholar
7.Kamal Akhtar, M. and Pratsinis, S.E., J. Mater. Res. 9, 1241 (1994).CrossRefGoogle Scholar
8.Chen, C.J. and Wu, J.M., Mater. Sci. Eng. B5, 377383 (1990).CrossRefGoogle Scholar
9.Mezey, E.J., in Vapor Deposition, edited by Powell, C.F., Oxley, J.H., and Blocher, J.M. (John Wiley and Sons, New York, 1966).Google Scholar
10.Strawbridge, I., in Chemistry of Glasses, edited by Paul, A. (Chapman and Hall, New York, 1990).Google Scholar
11.Brinker, C.J. and Scherer, G.W., Sol-Gel Science, The Physics and Chemistry of Sol-Gel Processing (Academic Press, Boston, MA, 1990).Google Scholar
12.Better Ceramics Through Chemistry IV, edited by Zelinski, B.J.V, Brinker, C.F., Clark, D.E., and Ulrich, D.R. (Mater. Res. Soc. Symp. Proc. 180, Pittsburgh, PA, 1990).Google Scholar
13.Better Ceramics Through Chemistry V, edited by Hampden-Smith, M.J., Klemperer, W.G., and Brinker, C.J. (Mater. Res. Soc. Symp. Proc. 271, Pittsburgh, PA, 1992).Google Scholar
14.Synthesis and Processing of Ceramics: Scientific Issues, edited by Rhine, W., Shaw, T.M., Gottshalll, R.J., and Chen, Y., (Mater. Res. Soc. Symp. Proc. 249, Pittsburgh, PA, 1992).Google Scholar
15.Rodríguez-Talavera, R., Vargas, S., Arroyo-Murillo, R., Montiel-Campos, R., and Haro-Poniatowski, E., J. Mater. Res. 12, 439 (1997).CrossRefGoogle Scholar
16.Haro-Poniatowski, E., Rodríguez-Talavera, R., de la Cruz Heredia, M., and Cano-Corona, O., J. Mater. Res. 9, 2102 (1994).CrossRefGoogle Scholar
17.Kumar, K-N.P, Kaiser, K., Burggraaf, A.J., Okubo, T., and Nagamoto, H., J. Mater. Chem. 3, 923 (1993).CrossRefGoogle Scholar
18.Kumar, K-N.P, Kaiser, K., and Burggraaf, A.J., J. Mater. Chem. 3, 1141 (1993).CrossRefGoogle Scholar
19.Avrami, M., J. Chem. Phys. 7, 1103 (1939).CrossRefGoogle Scholar
20.Avrami, M., J. Chem. Phys. 8, 212 (1940).CrossRefGoogle Scholar
21.Avrami, M., J. Chem. Phys. 9, 177 (1941).CrossRefGoogle Scholar
22.Marseglia, E., J. Non-Cryst. Solids 41, 31 (1980).CrossRefGoogle Scholar
23.Christian, J., The Theory of Transformation in Metals and Alloys (Pergamon Press, Oxford, United Kingdom, 1975).Google Scholar
24.Erukhimovitch, V. and Baram, J., J. Non-Cryst. Solids 208, 288 (1996).CrossRefGoogle Scholar