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The Chemical Vapor Deposition of Al-Cu Films Utilizing Independent Aluminum and Copper Organometallic Sources in a Simultaneous Deposition

Published online by Cambridge University Press:  15 February 2011

Matthew D. Healy
Affiliation:
SCHUMACHER, Technology Department, 1969 Palomar Oaks Way, Carlsbad, CA 92009
John A. T. Norman
Affiliation:
SCHUMACHER, Technology Department, 1969 Palomar Oaks Way, Carlsbad, CA 92009
Arthur K. Hochberg
Affiliation:
SCHUMACHER, Technology Department, 1969 Palomar Oaks Way, Carlsbad, CA 92009
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Abstract

The chemical vapor deposition (CVD) of aluminum is now gaining accceptance as a viable metallization technology for the fabrication of sub-0.5 micron interconnects. The incorporation of 0.5% copper into these aluminum films to enhance their electromogration resistance has been achieved by a number of different approaches. These techniques include the sequential CVD of the individual metals and the consecutive growth of CVD Al / PVD Cu followed by an interdiffusing thermal anneal. The potentially more elegant and streamlined solution explored in this paper is the simultaneous deposition of Al and Cu by CVD. A key requirement of this approach is the selection of copper precursors which are stable, volatile and free from oxygen and fluorine. The absence of the latter two elements is essential due to the high probablity of their extraction from the copper precursor by aluminum to form involatile aluminum oxyfluoride species. In our investigation of simultaneous Al/Cu we have utilized two well known aluminum hydride based precursors (DMAH and DMEAA) with two different copper precursors and we herein report the successful deposition of Al-Cu alloys using this approach. A discussion is presented of the dependence of the resulting Al-Cu film quality upon the choice of Al and Cu precursors used in addition to the CVD process parameters utilized for film growth.

Type
Research Article
Copyright
Copyright © Materials Research Society 1996

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References

1 See for example: Kikkawa, T. in Advanced Metallization for ULSI Applications in 1993, edited by Favreau, D P, Shacham-Diamond, Y, and Horiike, Y Proc. (Mater. Res. Soc., Pittsburg, 1993), p. 3.Google Scholar
ii. Li, J., Siedel, T.E., and Mayer, J. W., MRS Bulletin 19 No. 8, 15 (1994).Google Scholar
iii. Laxman, R.K., Semiconductor International 18 No. 5, 71 (1995).Google Scholar
iv. Thomas, M. and Colgan, E. in Advanced Metallization for ULSI Applications in 1993, edited by Favreau, D P, Shacham-Diamond, Y, and Horiike, Y Proc. (Mater. Res. Soc., Pittsburg, 1993), p. 595.Google Scholar
v Xu, Z., Kieu, H., Yao, T.–Y., and Raaijmakers, I., Proc. 11 th Int. VLSI Multilevle Interconnects Conf., 158 (1994).Google Scholar
vi. Simmonds, M. G. and Gladfelter, W. L. in The Chemistry of Metal CVD, edited by Kodas, T and Hampden-Smith, M (VCH, NewYork, 1994) p. 45.Google Scholar
vii Kondoh, E., Kawano, Y., Takeyasu, N., and Ohta, T., J. Electrochem. Soc. 141, 3494 (1994).Google Scholar
viii Wilkinson, G. and Piper, T.S., J. Inorg. Nucl. Chem. 2, 32 (1956).Google Scholar
ix. See for example: Hampden-Smith, M. J. and Kodas, T. T. in The Chemistry of Metal CVD, edited by Kodas, T and Hampden-Smith, M (VCH, New York, 1994) p. 239.Google Scholar
x. Scouting experiments indicate that the interaction of (hfac)CuTMVS and DMAH is highly exothermic.Google Scholar
xi. Matsumiya, Y., Ohtsuka, N., Yamazaki, S., and Nakajima, K., presented at the 1995 Advanced Metallization and Interconnect Systems for ULSI Applications Conference, Portland, OR, 1995 (unpublished).Google Scholar
xii. a) Simmonds, M.G., Phillips, E.C., Hwang, J.–W., and Gladfelter, W.L., Chemtronics 5, 155 (1991). b) D.M.Frigo, G.J.M.van Eijden, P.J.Reuvers, and C.J.Smit, Chem. Mater. 6, 190 (1994).Google Scholar
xiii. Norman, J.A.T., Roberts, D.A., and Hochberg, A.K. in Chemical Perspectives of Microelectronic Materials III, edited by Abernathy, C.R, Bates, C.W. Jr., Bohling, D.A, and Hobson, W.S (Mater. Res. Soc. Proc. 282, Pittsburg, PA 1993) p. 347.Google Scholar
xiv. Boer, H.J., Solid State Technology 29 No. 3, 149, (1996).Google Scholar
xv. We do not recommend a quartz bubbler for this material. This was undertaken to observe decomposition of the material over a period of months.Google Scholar
xvi Blessman, D., Grafe, A., Heinen, R., Jansen, F., Kruck, T., and Terfloth, C., Mater. Sci. Eng. B 17, 104 (1993).Google Scholar
xvii. Pasynkiewicz, S. and Maciaszek, S., J. Organomet. Chem. 15, 301 (1968).Google Scholar