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Structural Properties of Strontium Vanadate Glasses

Published online by Cambridge University Press:  31 January 2011

S. Sen
Affiliation:
Solid State Physics Department, Indian Association for the Cultivation of Science, Jadavpur, Calcutta-700032, India
A. Ghosh*
Affiliation:
Solid State Physics Department, Indian Association for the Cultivation of Science, Jadavpur, Calcutta-700032, India
*
a)Address all correspondence to this author. e-mail: [email protected]
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Abstract

Structural studies of the strontium vanadate glasses of compositions xV2O5–(100 − x)SrO are reported. X-ray diffractograms, density, and oxygen molar volume, etc., of the glasses show that single-phase and homogeneous glasses were obtained in the composition domain x = 50 to 90 mol%. The network structure for the glass compositions with 90 and 80 mol% V2O5 is built up of the VO5 polyhedra, while the other glass compositions consist of the VO4 polyhedra. Density and glass transition temperature are observed to decrease with an increase in the V2O5 content. The magnetic susceptibility of the glasses shows an increase of concentration of the reduced V4+ ion with the increase of vanadium oxide content in the compositions. The well-resolved electron spin resonance structure observed for the glass composition with 50 mol% V2O5 gradually becomes poor and reduces to a single component line, which has been attributed to the increase of the hopping rate of charge carriers with the increase of the V2O5 content in the compositions.

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Articles
Copyright
Copyright © Materials Research Society 2000

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References

REFERENCES

1.Sayer, M. and Mansingh, A., Phys. Rev. B 6, 4629 (1972).CrossRefGoogle Scholar
2.Greaves, G.N., J. Non-Cryst. Solids 11, 427 (1973).CrossRefGoogle Scholar
3.Cheng, C.H., Meckenzie, J.D., and Murawski, L., Rev. Chem. Miner. 16, 308 (1979).Google Scholar
4.Cheng, C.H. and Meckenzie, J.D., J. Non-Cryst. Solids 42, 151 (1980).Google Scholar
5.Ghosh, A., Phys. Rev. B 42, 5665 (1990).CrossRefGoogle Scholar
6.Ghosh, A., J. Appl. Phys. 64, 2652 (1988).CrossRefGoogle Scholar
7.Livage, J., Jollivet, J.P., and Tronc, E., J. Non-Cryst. Solids 121, 35 (1990).CrossRefGoogle Scholar
8.Sakuri, Y. and Yamaki, J., J. Electrochem. Soc. 132, 512 (1985).CrossRefGoogle Scholar
9.Mott, N.F., J. Non-Cryst. Solids 1, 1 (1968).CrossRefGoogle Scholar
10.Austin, G. and Mott, N.F., Adv. Phys. 18, 41 (1969).CrossRefGoogle Scholar
11.Dimitrov, V., Dimitiev, Y., Arnaudov, M., and Topalov, D., J. Non-Cryst. Solids 57, 147 (1983).CrossRefGoogle Scholar
12.Mandal, S. and Ghosh, A., Phys. Rev. B 48, 9388 (1993).CrossRefGoogle Scholar
13.Chen, H.S. and Miller, C.E., Rev. Sci. Instrum. 41, 1237 (1970).CrossRefGoogle Scholar
14.Quan, J.T. and Adams, C.F., J. Phys. Chem. 70, 331 (1966).CrossRefGoogle Scholar
15.Borelli, N.F., McSwain, B.D., and Su, G., Phys. Chem. Glasses 4, 11 (1963).Google Scholar
16.Dachille, E. and Roy, R., J. Am. Ceram. Soc. 42, 78 (1965).CrossRefGoogle Scholar
17.Botto, I.L., Baran, E.J., and Aymonino, P.J., Z. Chem. 16, 163 (1976).CrossRefGoogle Scholar
18.Drake, C.F., Stephens, J.A., and Yates, B., J. Non-Cryst. Solids 28, 61 (1978).CrossRefGoogle Scholar
19.Shelby, J.E., J. Am. Ceram. Soc. 57, 473 (1975).Google Scholar
20.Nishida, T., Ogata, M., and Takashina, Y., Bull. Chem. Soc. Jpn. 59, 2401 (1986).CrossRefGoogle Scholar
21.Sen, S. and Ghosh, A., J. Non-Cryst. Solids 258, 29 (1999).CrossRefGoogle Scholar
22.Nagiev, V.M., Fiz. Tverd. Tela 7, 2204 (1966).Google Scholar
23.Landsberger, F.R. and Bray, P.T., J. Chem. Phys. 53, 2757 (1970).CrossRefGoogle Scholar
24.Sen, S. and Ghosh, A., J. Phys.: Condens. Matter 11, 1529 (1999).Google Scholar