Hostname: page-component-848d4c4894-8bljj Total loading time: 0 Render date: 2024-06-19T15:25:04.276Z Has data issue: false hasContentIssue false

Auger valence electron spectra in Ca-silicides

Published online by Cambridge University Press:  31 January 2011

S. Abe
Affiliation:
Graduate School of Science and Technology, and Faculty of Engineering, Kobe University, 1–1 Rokkoudai, Nada-ku, Kobe 657, Japan
H. Nakayama
Affiliation:
Graduate School of Science and Technology, and Faculty of Engineering, Kobe University, 1–1 Rokkoudai, Nada-ku, Kobe 657, Japan
T. Nishino
Affiliation:
Graduate School of Science and Technology, and Faculty of Engineering, Kobe University, 1–1 Rokkoudai, Nada-ku, Kobe 657, Japan
S. Iida
Affiliation:
Department of Electrical Engineering and Electronics, Osaka Sangyo University, 3-1-1 Nakagaito, Daito, Osaka 574, Japan
Get access

Abstract

CaSi2 and CaSi have been investigated by Auger Valence Electron Spectroscopy (AVES). Some drastic differences of the Auger peak due to 3s states in the Si atoms were observed in the Si[2s, 2p, V] Auger spectra. The peak that arised from valence electron states in the Ca atoms was observed in the Ca[2p, 3p, V] Auger spectra for both Ca-silicides. This result suggests that the Ca–Si bonds are partially ionic. However, the number of the valence electrons in Ca atoms for CaSi was larger than that for CaSi2. This result implies that the part of homopolar bonds between the Si and Ca atoms in CaSi is stronger than that in CaSi2. Based on these results, it has been concluded that the change of the Si [2s, 2p,V] Auger spectra is associated with the difference of the part of homopolar bonds between the Si and Ca atoms.

Type
Articles
Copyright
Copyright © Materials Research Society 1997

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.Fahy, S. and Hamann, R., Phys. Rev. B 41, 7587 (1990).Google Scholar
2.Van de Walle, C. G., Phys. Rev. B 43, 11 913 (1991).CrossRefGoogle Scholar
3.Well, A. F., Structural Inorganic Chemistry (Oxford University, Oxford, 1962), p. 773.Google Scholar
4.Matunaga, Y., Bunsi To Kessho (Molecular and Crystal) (Shokabo, Tokyo, 1965), p. 146 (in Japanese).Google Scholar
5.Hirabayashi, I., Kotaibuturi (Solid State Physics) 17, 681 (1982) (in Japanese).Google Scholar
6.Fujita, H., Fuchida, Y., and Nakayama, H., Philos. Mag. A 59, 873 (1989).Google Scholar
7.Yasuda, H., Nakayama, H., and Fujita, H., Jpn. J. Appl. Phys. 28, 2234 (1989).CrossRefGoogle Scholar
8.Ueda, K., Nakayama, H., Sekine, M., and Fujita, H., Vacuum 42, 547 (1991).Google Scholar
9.Nakayama, H., Nishino, T., Ueda, K., Takeno, S., and Fujita, H., Ultramicroscopy 39, 329 (1991).CrossRefGoogle Scholar
10.Fujiwara, Y., Hirata, S., Nishikubo, M., Kobayashi, T., Nakayama, H., and Fujita, H., IEEE Trans. Magn. 27, 1166 (1991).Google Scholar
11.Bisi, O., in Auger Spectroscopy and Electronic Structure, edited by Cubiotti, G., Mondio, G., and Wandelt, K. (Springer, Berlin, 1989), p. 30.CrossRefGoogle Scholar
12.Sancrotti, M., Vescovo, E., Calliari, L., and Marchetti, F., in Auger Spectroscopy and Electronic Structure, edited by Cubiotti, G., Mondio, G., and Wandelt, K. (Springer, Berlin, 1989), p. 116.CrossRefGoogle Scholar
13.Sancrotti, M. and Rizzi, A., Phys. Rev. B 37, 3120 (1988).Google Scholar
14.Sancrotti, M., Abbati, I., Rizzi, A., Calliari, L., Marchetti, F., and Bisi, O., Surf. Sci. 189/190, 300 (1987).CrossRefGoogle Scholar
15.Calliari, L., Marchetti, F., Sancrotti, M., Bisi, O., Iandelli, A., Olcese, G. L., and Palenzona, A., Phys. Rev. B 41, 7569 (1990).Google Scholar
16.Bisi, O., Braicovich, L., Carbone, C., Lindau, I., Iandelli, A., Olcese, G. L., and Palenzona, A., Phys. Rev. B 40, 10 194 (1989).CrossRefGoogle Scholar