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Plasma production of metallic nanoparticles

Published online by Cambridge University Press:  31 January 2011

ChinHao Chou
Affiliation:
Department of Chemical Engineering, 133 Fenske Laboratory, The Pennsylvania State University, University Park, Pennsylvania 16802
Jonathan Phillips*
Affiliation:
Department of Chemical Engineering, 133 Fenske Laboratory, The Pennsylvania State University, University Park, Pennsylvania 16802
*
a)Author to whom correspondence should be addressed.
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Abstract

Metallic iron and iron oxide particles were produced by injecting ferrocene into the afterglow region of a low pressure, low power, plasma generated using a microwave power source. This was done as part of an effort to explore the feasibility of using flow type microwave plasmas for the production of metal nanoparticles. It was found that two parameters had the largest impact on the particles: injection point and plasma composition. Analysis done using Mössbauer effect spectroscopy, transmission electron microscopy, and x-ray diffraction indicated that low yields of small particles (ca. 10 nm) resulted from injection into the afterglow region. Much higher yields of large particles (ca. 50 nm) formed if the ferrocene was injected through the coupler. In hydrogen plasmas the particles that were produced were metallic iron, whereas in oxygen and argon plasmas the particles were iron oxide. In all cases significant amounts of graphitic carbon formed around the metal particles.

Type
Articles
Copyright
Copyright © Materials Research Society 1992

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References

1.Segal, D. L., Br. Ceram. Trans. J. 85, 184 (1986).Google Scholar
2.Rhodes, W. H. and Natansohn, S., Ceram. Bull. 68, 1804 (1989).Google Scholar
3.Bergstrom, L. and Pugh, R. J., J. Am. Ceram. Soc. 72, 103 (1989).CrossRefGoogle Scholar
4.Anderson, H., Kodas, T. T., and Smith, D. M., Ceram. Bull. 68, 996 (1989).Google Scholar
5.Danforth, S. C., Symons, W., Nilsen, K. J., and Riman, R. E., Adv. Ceram. Proc. Technol. 39 (1990).Google Scholar
6.Hayashi, C., Phys. Today 12, 44 (1987).CrossRefGoogle Scholar
7.Hayashi, C., J. Vac. Sci. Technol. A 5, 1375 (1987).CrossRefGoogle Scholar
8.Iijima, S., Surf. Sci. 156, 1003 (1985).CrossRefGoogle Scholar
9.Spear, K. E., J. Am. Ceram. Soc. 72, 171 (1989).CrossRefGoogle Scholar
10.Angus, J. C. and Hayman, C. C., Science 241, 931 (1988).CrossRefGoogle Scholar
11.Mitsui, A. and Kato, A., Yogyo-Kyokai-Shi 94, 517 (1986).CrossRefGoogle Scholar
12.Vogt, G. J., Hollabaugh, C. M., Hull, D. E., Newkirk, L. R., and Petrovic, J. J., in Plasma Processing and Synthesis of Materials, edited by Szekely, J. and Apelian, D. (Mater. Res. Soc. Symp. Proc. 30, 283 (1984).Google Scholar
13.Ho, P., Buss, R. J., and Loehman, R. E., J. Mater. Res. 4, 873 (1989).CrossRefGoogle Scholar
14.Chou, C. H. and Phillips, J., J. Appl. Phys. 68, 2415 (1990).CrossRefGoogle Scholar
15.Lin, S-C. and Phillips, J., J. Appl. Phys. 58, 1943 (1985).CrossRefGoogle Scholar
16.Sorensen, K., Internal Report No. 1, Laboratory of Applied Physics II (Technical University of Denmark, 1972).Google Scholar
17.Klug, H. P. and Alexander, L. E., X-ray Diffraction Procedures (Wiley, New York, 1967).Google Scholar
18.Lin, S. C. and Phillips, J., J. Appl. Phys. 58, 1943 (1985).CrossRefGoogle Scholar
19.Gatte, R. R. and Phillips, J., J. Catal. 104, 365 (1987).CrossRefGoogle Scholar
20.Treacy, M. M. J. and Howie, A., J. Catal. 63, 265 (1980).CrossRefGoogle Scholar