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Spin Glass Magnetic Behavior of Iron/Silica Gel Nanocomposites

Published online by Cambridge University Press:  28 February 2011

Robert D. Shull
Affiliation:
Materials Science and Engineering Laboratory, National Institute of Standards and Technology, Gaithersburg, MD 20899
Joseph J. Ritter
Affiliation:
Materials Science and Engineering Laboratory, National Institute of Standards and Technology, Gaithersburg, MD 20899
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Abstract

Homogeneous gelled composites of iron and silica containing 5-40 wt.%Fe prepared by low temperature polymerization of aqueous solutions of ferric nitrate, tetraethoxysilane, and ethanol (with an HF catalyst) were heated to 380°C in the presence of hydrogen gas. X-ray diffraction and M6ssbauer effect measurements, and transmission electron microscope (TEM) observations show these materials are comprised of nanometer-sized regions of iron compounds embedded in a silica gel matrix. Magnetic susceptibility data indicate the materials became either superparamagnetic or ferromagnetic at room temperature. On cooling, the magnetization data furthermore show that the hydrogenated materials containing ll-30% Fe become magnetic spin glasses at temperatures less than 30 K. Magnetic history effects are observed in addition to displaced hysteresis loops below their spin freezing temperatures (Tf). For field-cooled materials at 10 K, the displacement of the hysteresis loops along the field axis indicates the presence of a unidirectional anisotropy which decreases with the cooling field. Both superparamagnetic-to-spin glass and ferromagnetic-to-spin glass transitions are observed in these nanocomposites. Tf varies with the Fe content from ∼30 K for the 11%Fe nanocomposite to ∼10 K for a content near 33%Fe.

Type
Research Article
Copyright
Copyright © Materials Research Society 1990

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References

REFERENCES

1. Shull, R. D., Ritter, J. J., Shapiro, A. J., Swartzendruber, L. J., and Bennett, L. H., Mat. Res. Soc. Symp. Proc. 132, 179 (1989).Google Scholar
2. Shull, R. D., Ritter, J. J., Shapiro, A. J., Swartzendruber, L. J., and Bennett, L. H., J. Appl. Physics 67, 4490 (1990).Google Scholar
3. Yamato, D. P., Landis, A. L., and Kuan, T. S., Mat. Res. Soc. Symp. Proc. 132, 73 (1989).Google Scholar
4. Kouvel, J. S., J. Phys. Chem. Solids 21, 57 (1961).Google Scholar
5. Mukhopadhyay, A. K., Shull, R. D., and Beck, P. A., J. Less Common Metals 43, 69 (1975).Google Scholar
6. Holtzberg, F., Tholence, J. L., Godrin, H., and Tournier, R., J. Appl. Phys. 50, 1717 (1979).Google Scholar
7. Xiao, Gang, Liou, S. H., Levy, A., Taylor, J. N., and Chien, C. L., Phys. Rev. B34, 7573 (1986).Google Scholar
8. Cochrane, R. W. and Mydosh, J. A., Magnetism and Magnetic Materials-1974, AIP Conf. Proc. 18, 651 (1973).Google Scholar
9. Kouvel, J. S., J. Phys. Chem. Solids 24, 795 (1963).Google Scholar
10. Shull, R. D. and Beck, P. A., Magnetism and Magnetic Materials-1974, AIP Conf. Proc. 24, 95 (1975).Google Scholar
11. Shull, R. D., Okamoto, H., and Beck, P. A., Solid State Commun. 20, 863 (1976).Google Scholar
12. Böni, P., Shapiro, S. M., and Motoya, K., Solid State Commun. 60, 881 (1986).Google Scholar