Hostname: page-component-cd9895bd7-gxg78 Total loading time: 0 Render date: 2024-12-23T12:44:16.407Z Has data issue: false hasContentIssue false

Alternating current conductivity of the interfacial phase in copper oxide–silica gel nanocomposites

Published online by Cambridge University Press:  31 January 2011

D. Das
Affiliation:
Indian Association for the Cultivation of Science, Calcutta, 700 032, India
D. Chakravorty
Affiliation:
Indian Association for the Cultivation of Science, Calcutta, 700 032, India
Get access

Abstract

A nanocomposite structure was induced in gel of composition 60CuO · 40SiO2 (mol%) by first of all precipitating nano-sized copper particles by a reduction treatment and subsequently subjecting these to a controlled oxidation treatment. The particle size was of the order of 6.8 nm. Alternating current (ac) conductivity measurements were carried out on different specimens in the temperature range 300 to 630 K covering a frequency spectrum 0.1 kHz to 2 MHz. The ac conductivity was found to have a variation with frequency given by ωs, ω being the angular frequency and s the frequency exponent. The analysis of the variation of s as a function of temperature led to the conclusion that an overlapping large polaron tunneling mechanism was operative in this system. The effective barrier height for polaron transfer for infinite intersite separation was found to be almost twice in the case of the precursor gel as compared to that for the composite with the interfacial amorphous phase.

Type
Articles
Copyright
Copyright © Materials Research Society 2001

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.Alivisatos, A.P., Science 271, 933 (1996).CrossRefGoogle Scholar
2.Shi, J., Gider, S., Babcock, D., and Awschalom, D.D., Science 271, 937 (1996).Google Scholar
3.Micic, O.I., Cheong, H.M., Fu, H., Zunger, A., Sprague, J.R., Mascarenhas, A., and Nozik, A.J., J. Phys. Chem. B 101, 4904 (1997).CrossRefGoogle Scholar
4.Billas, I.M.L., Chatelain, A., and de Heer, W.A., J. Magn. Magn. Mater. 168, 64 (1997).Google Scholar
5.Weller, H., Angew. Chem. Int. Ed. Engl. 35, 1079 (1996).Google Scholar
6.Heath, J.R., Science 270, 1315 (1995).Google Scholar
7.Bethell, D. and Schiffrin, B.J., Nature 382, 581 (1996).CrossRefGoogle Scholar
8.Braun, P.V., Osenar, P., and Stupp, S.I., Nature 380, 325 (1996).Google Scholar
9.Vossmeyer, T., Rock, G., Katsikas, L., Haupt, E.T.K., Schulz, B., and Teller, H., Science 267, 1476 (1995).CrossRefGoogle Scholar
10.Alivisatos, A.P., Johnsson, K.P., Peng, X., Wilson, T.E., Loweth, C.J., Bruchez, M.P. Jr., and Schultz, P.G., Nature 382, 609 (1996).Google Scholar
11.Konrad, H., Karmonik, C., Weissmuller, J., Gleiter, H., Birringer, R., and Hempelmann, R., Physica B 234–236, 173 (1997).Google Scholar
12.Keblinski, P., Wolf, D., Phillpot, S.R., and Gleiter, H., Phil. Mag. Lett. 76, 143 (1997).Google Scholar
13.Das, D. and Chakravorty, D., Appl. Phys. Lett. 76, 1273 (2000).Google Scholar
14.Roy, S., Chatterjee, A., and Chakravorty, D., J. Mater. Res. 8, 689 (1993).Google Scholar
15.Elliott, S.R., Adv. Phys. 36, 135 (1987).CrossRefGoogle Scholar