We report the effect of various alcohols on the transport mechanism an
d reaction kinetics of Cu(hfac)(2) reduction for copper CVD. A variety
of transport experiments are performed, all of which indicate that th
e presence of alcohol does nothing to increase the vapor phase transpo
rt rate of Cu(hfac)(2). In contrast, steady-state kinetic measurements
reveal a significant increase in CVD growth rates upon addition of an
alcohol co-reactant, which we therefore attribute to an alcohol-assis
ted enhancement of the intrinsic kinetics of Cu(hfac)(2) reduction. Fo
r the series of alcohols studied, the enhancement factor increases in
the order: MeOH < EtOH < i-PrOH; this correlates with the pK(a) values
of the alcohols. The dependence of the growth rate on alcohol partial
pressure is first-order, which can be described using a simple modifi
cation of our earlier Langmuir-Hinshelwood rate expression for H-2 red
uction of Cu(hfac)(2). The revised expression is consistent with a mec
hanism in which the rate limiting step involves H+ transfer between an
adsorbed alcohol molecule and the first dissociated (hfac) ligand fro
m an adsorbed Cu(hfac)(2) molecule. (C) 1998 Elsevier Science S.A. All
rights reserved.