Hostname: page-component-78c5997874-t5tsf Total loading time: 0 Render date: 2024-11-13T02:53:35.419Z Has data issue: false hasContentIssue false

Alternative Organometallic Precursors for CVD of Tungsten

Published online by Cambridge University Press:  22 February 2011

Rein U. Kirss
Affiliation:
Northeastern University, Department of Chemistry, Boston, MA 02115
Douglas Gordon
Affiliation:
ATM, Inc., 7 Commerce Drive, Danbury, CT, 06810
Peter S. Kirlin
Affiliation:
ATM, Inc., 7 Commerce Drive, Danbury, CT, 06810
Get access

Abstract

Two solid, air stable, volatile tungsten complexes, tris(methylvinylketone) tungsten, I, and tris(butadiene)tungsten, II, have been investigated as precursors for chemical vapor deposition (CVD) of tungsten containing films. Thermal gravimetic analysis, (TGA), of I and II under argon showed the onset of decomposition at 140°C and 150°C, respectively. A rapid weight decrease corresponding to loss of all three ligands, methylvinyl ketone or butadiene, was observed.

Tungsten film growth under hydrogen using I was investigated on Si, SiO2, Cu, TiN, Si, and Pt substrates. Selective tungsten film growth on platinum using a hydrogen carrier was observed at temperatures above 200°C. No appreciable tungsten deposition was observed on clean Si, SiO2. Cu or TiN surfaces below 400°C. No oxygen or carbon was detected in these films to the level of EDX analysis (∼1%) for depositions at 200°C. Increased growth temperatures resulted in increasing amounts of oxygen incorporation. The films grown at 200°C were smooth whereas cracking was observed in films grown at 300°C. The volatile products from the deposition were identified by a combination of gas chromatography and mass spectrometry. Small amounts of methylvinylketone. and methylethylketone were observed. Higher molecular weight species are as yet unidentified, but constituted the majority of the products.

Type
Research Article
Copyright
Copyright © Materials Research Society 1993

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. a. Sherman, A., Chemical Vapor Deposition for Microelectronics. (Noyes Publications, Park Ridge, N. J., 1987);Google Scholar
b. Wong, S. S. and Furukawa, S., eds., Tungsten and Other Refractory Metals for VLSI Applications V (Materials Research Society, Pittsburgh, PA, 1990);Google Scholar
c. Blewer, R. S. and McConica, C. M., eds., Tungsten and Other Refractory Metals for VLSI Applications IV (Materials Research Society, Pittsburgh, PA, 1989).Google Scholar
2. For a recent review of organometallic precursors for CVD see Girolami, G. S., and Gozum, J. E., in, J. E. Chemical Vapor Deposition of Refractory Metals and Ceramics, edited by Besmann, T. M. and Gallois, B. M. (Mater. Res. Soc. Proc., 168, Pittsburgh, PA, 1990) p. 319.Google Scholar
3. Watson, I.M., Connor, J. A., and Whyman, R.. Polyhedron, 8, 1794 (1989);Google Scholar
b. Diem, M., Fisk, M., and Goldman, J., Thin Solid Films, 107, 39 (1983);Google Scholar
c. Vogt, G. J., G. J. Vac. Sci. Technol., 20, 1336 (1982);Google Scholar
d. Gluck, N. S., Wolga, G. J., Bartosch, C. E., Ho, W., and Ying, Z., J. Appl. Phys., 61, 998 (1987);Google Scholar
e. Flynn, D. K., Steinfeld, J. I., and Sethi, D. S., J. Appl Phys., 59, 3914 (1984);Google Scholar
f. Kado, T. and Noda, Y., J. Electrochem. Soc., 136, 2184 (1989);Google Scholar
g. Christianz, G. I., Elms, T. J., Pain, G. N., and Pierson, R. R., J. Cryst. Growth, 93, 589 (1988).Google Scholar
4. a. Kirss, R. U., Appl. Organometal. Chem., in press, (1992);Google Scholar
b. Kirss, R. U., Chen, J., and, J., Hallock, R. B., Chemical Vapor Deposition of Refractory Metals and Ceramics-ll, edited by Besmann, T. M. and Gallois, B. M. (Mater. Res. Soc. Proc. 250, Pittsburgh, PA, 1992) p. 303.Google Scholar
5. Baxter, D. V., Chisholm, M. H., DiStasi, V., and Klang, J. A., Chem. Mater., 3, 221 (1991).Google Scholar
6. Niemer, B., Zinn, A. A., Stovall, W. K., Gee, P. E., Hicks, R. F., and Kaesz, H. D. J. Appl. Phys, 61, 1793 (1992)Google Scholar
7. a. King, R. B. and Fronzaglia, A., Inorg. Chem., 5, 1837, (1966);Google Scholar
b. Wreford, S. S. and Whitney, J. F., Inorg. Chem., 20, 3918, (1981).Google Scholar
8. Rosier, R. S., Mendonca, J., and Rice, M. J., J. Vac. Sci. Technol., B, 6, 1721, (1988)Google Scholar
9. Xue, Z., Strouse, M. J., Shuh, D. K., Knobler, C. B., Kaesz, H. D., Hicks, R. F., and Williams, R. S., J. Am. Chem. Soc., 111, 8779 (1989).Google Scholar