Effects of additive elements on the phase formation and morphological stability of nickel monosilicide films

被引:127
作者
Lavoie, C. [1 ]
Detavernier, C.
Cabral, C., Jr.
d'Heurle, F. M.
Kellock, A. J.
Jordan-Sweet, J.
Harper, J. M. E.
机构
[1] IBM Corp, Thomas J Watson Res Ctr, Yorktown Hts, NY 10598 USA
[2] Ecole Polytech, Montreal, PQ H3C 3A7, Canada
[3] Univ Ghent, Dept Phys, B-9000 Ghent, Belgium
[4] IBM Corp, Almaden Res Ctr, San Jose, CA USA
[5] Univ New Hampshire, Dept Phys, Durham, NH 03824 USA
基金
美国国家科学基金会;
关键词
nickel silicides; NiSi; alloying; agglomeration; NiSi2;
D O I
10.1016/j.mee.2006.09.006
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
Alloying elements can substantially affect the formation and morphological stability of nickel monosilicide. A comprehensive study of phase formation was performed on 24 Ni alloys with varying concentrations of alloying elements. Silicide films have been used for more than 15 years to contact the source, drain and gate of state-of-the-art complementary-metal-oxide-semiconductor (CMOS) devices. In the past, the addition of alloying elements was shown to improve the transformation from the high resistivity C49 to the low resistivity C54-TiSi2 phase and to allow for the control of surface and interface roughness of CoSi2 films as well as produce significant improvements with respect to agglomeration of the films. Using simultaneous time-resolved X-ray diffraction (XRD), resistance and light scattering measurements, we follow the formation of the silicide phases in real time during rapid thermal annealing. Additions to the Ni-Si system lead to modifications in the phase formation sequence at low temperatures (metal-rich phases), to variations in the formation temperatures of NiSi and NiSi2, and to changes in the agglomeration behavior of the films formed. Of the 24 elements studied, additions of Mo, Re, Ta and W are amongst the most efficient to retard agglomeration while elements such as Pd, Pt and Rh are most efficient to retard the formation of NiSi,. (c) 2006 Published by Elsevier B.V.
引用
收藏
页码:2042 / 2054
页数:13
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