Hostname: page-component-78c5997874-g7gxr Total loading time: 0 Render date: 2024-11-08T02:03:02.516Z Has data issue: false hasContentIssue false

Reactions of Bare Silicon Cluster Ions: Prototypical Deposition and Etching Versus Cluster Size

Published online by Cambridge University Press:  28 February 2011

M. L. Mandich
Affiliation:
AT&T Bell Laboratories, 600 Mountain Ave., Murray Hill, NJ 07974
W. D. Reents Jr
Affiliation:
AT&T Bell Laboratories, 600 Mountain Ave., Murray Hill, NJ 07974
V. E. Bondybey
Affiliation:
AT&T Bell Laboratories, 600 Mountain Ave., Murray Hill, NJ 07974
Get access

Abstract

Prototypical silicon deposition and etching reactions have been observed in gas phase reactions of size selected bare silicon cluster ions at room temperature. Laser evaporation of bulk silicon just outside the ion cell of a Fourier transform mass spectrometer produces abundant positive and negative silicon cluster ions. These cluster ions are trapped inside the cell for subsequent study of their bimolecular reactivity with various neutral reagents. Deposition type reactions occur with silanes, e.g. CH3SiH3, and increase the number of silicon atoms in the cluster. Etching reactions occur in reactions with certain halogen or oxygen containing reagents. For example, NO2 and XeF2 react to destroy the silicon clusters by sequential loss of a silicon atom. Overall the reactivity of small silicon cluster ions correlates with chemistry which occurs at two distinct types of dangling bonds in the clusters: either a lone pair of electrons or a single unpaired electron.

Type
Articles
Copyright
Copyright © Materials Research Society 1987

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

1. Mandich, M. L., Reents, W. D. Jr and Bondybey, V. E., J. Phys. Chem. 90, 2315 (1986).Google Scholar
2. Reents, W. D. Jr, Mandich, M. L., and Bondybey, V. E., Chem. Phys. Lett. 131, 1 (1986).Google Scholar
3. Mandich, M. L., Bondybey, V. E., and Reents, W. D. Jr, Reactive etching of positive and negative silicon cluster ions by nitrogen dioxide, to be published in J. Chem. Phys.Google Scholar
4. Reents, W. D. Jr Mujsce, A. M., Bondybey, V. E. and Mandich, M. L., Reactions of cationic silicon clusters with xenon difluoride, to be published in J. Chem. Phys.Google Scholar
5. Another study of silicon cluster cation reactions has recently been reported by Creasy, W. R., McElvany, S. W., and O'Keefe, A., Proc. of the 34Th Ann. Conf. on Mass Spectrom. and Allied Topics, June 9–13, 1986.Google Scholar
6. An excellent review of ion cyclotron resonance mass spectrometry (with application to the study of ion-molecule reactions) is given in Beauchamp, J. L., Annu. Rev. Phys. Chem. 22, 527 (1971).Google Scholar
7. Su, T. and Bowers, M. T., in Gas Phase Ion Chemistry, Vol.1, edited by Bowers, M. T. (Academic, New York, 1979).Google Scholar
8. Raghavachari, K. and Logovinsky, V., Phys. Rev. Lett. 55, 2853 (1985).Google Scholar
9. Wilt, J., in Reactive Intermediates, Vol.3, edited by Abramovitch, R. A. (Plenum Press, New York, 1983).Google Scholar
10. Terminal silicon-oxygen double bonds are so unstable that, in spite of a number of synthetic attempts, not one stable species has been prepared except in cryogenic rare gas matrices. See, for example, Barton, T. J. and Groh, B. L., J. Am. Chem. Soc. 107, 7221 (1985); R. Withnall and L. Andrews, J. Am. Chem. Soc. 107 2567 (1985).Google Scholar
11. Bell, T. N., Perkins, K. A., and Perkins, P. G., J. Chem. Soc., Faraday Trans. 1. 77, 1779 (1981).CrossRefGoogle Scholar
12. McMillen, D. F., and Golden, D. M., Annu. Rev. Phys. Chem. 33, 493 (1982).Google Scholar
13. Levin, R. D. and Lias, S. B., National Stand. Ref. Data Ser., (Nat. Bur. Stand., Washington D. C., 1982).Google Scholar
14. Tang, Y., in Reactive Intermediates, Vol.2, edited by Abramovitch, R. A. (Plenum Press, New York, 1982).Google Scholar
15. Tomanek, D. and Schluter, M. A., Phys. Rev. Lett. 56, 1055 (1985).Google Scholar
16. Pacchioni, G. and Koutecky, J., J. Chem. Phys. 84, 3301 (1986).Google Scholar
17. Flamm, D. L., Donnelly, V. M., and Mucha, J. A., J. Appl. Phys. 52,3633 (1981).CrossRefGoogle Scholar
18. Ibbotson, D. E., Flamm, D. L., Mucha, J. A., and Donnelly, V. M., Appl. Phys. Lett. 44, 1129 (1984).CrossRefGoogle Scholar
19. Winters, H. F., Coburn, J. W., Chuang, T. J., J. Vac. Sci. Technol. B1, 469 (1983).Google Scholar
20. Houle, F. A., J. Appl. Phys., submitted.Google Scholar