Analysis of the components of parasitic series resistance in ULSI devi
ces shows that interfacial contact resistivities less than 10(-7) Ohm
cm(2) will be required for sub 100-nm ULSI devices in order to stay on
the historical performance trend. With dimensional scaling, the serie
s resistance-width product decreases because channel lengths are scale
d, while it increases in contacts because the contact length is decrea
sed. Unless the contact resistivity is also reduced, the contact resis
tance ultimately becomes higher than the channel resistance, and no pe
rformance advantage will be obtained by making the device smaller. The
challenge in meeting the contacting requirements in the 1997 National
Technology Roadmap for Semiconductors is especially difficult in ligh
t of the desire to simultaneously contact both n(+) and p(+) junctions
with a single material and given the trend towards lower processing t
emperatures, in which the equilibrium dopant electrical activity is lo
wer. Several techniques, such as dielectric capping during junction an
nealing, are effective in reducing contact resistivity by maximizing i
nterfacial dopant concentrations and minimizing contact barrier height
s. Higher saturated drive currents, due to lowered parasitic series re
sistance, are observed in deep submicron devices made using silicides
as diffusion sources (SADS); this technique eliminates the interfacial
dopant segregation that is associated with conventional silicidation.
The use of elevated source drains (ESD) also allows the use of thicke
r silicides while minimizing the consumption-induced increase in conta
ct resistivity that normally accompanies silicidation; as a result, ES
D devices give higher drive currents. The recrystallization of amorpho
us layers has been observed to result in non-equilibrium dopant activa
tion which can be many times the equilibrium value. Finally, the use o
f heterojunction contacts using Si-Ge in the context of elevated sourc
e/drain devices presents another way to achieve lower contact resistan
ce. (C) 1998 Elsevier Science S.A. All rights reserved.