Jp. Endle et al., Iridium precursor pyrolysis and oxidation reactions and direct liquid injection chemical vapor deposition of iridium films, THIN SOL FI, 388(1-2), 2001, pp. 126-133
Pyrolysis and oxidation reactions of the iridium precursor, (methylcyclopen
tadienyl)(1,5 -cyclooctadiene)iridium (I), were studied to identify the rol
e of O-2 in chemical vapor deposition film growth. A toluene solution of (m
ethylcyclopentadienyl)(1,5-cyclooctadiene)iridium (1) was used in a direct
liquid injection chemical vapor deposition process with O-2 to deposit irid
ium films on SiO2 and TiN(111) substrates. The precursor decomposition stud
ies revealed O-2 decreases the reaction temperature of (methylcyclopentadie
nyl)(l,5 -cyclooctadiene)iridium (1) from near 760 K to temperatures below
465 K. Oxidation of the precursor ligands acts to prevent greater than 99%
of the carbon from incorporating into the deposited him, making the growth
surface more reactive. The precursor and oxygen react to form CO, CO2 and H
2O. Pure iridium films were deposited on SiO2 and TiN(III) substrates at te
mperatures between 550 and 625 K. Under identical conditions, the film nucl
eation and coalescence rates are nearly 2 times higher on the TiN(111) subs
trate with 0.22 torr O-2. The ratio of (111) to (200) X-ray diffraction int
ensities resembled Ir powder for films deposited on SiO2, the same ratio wa
s more than 9 times larger than that of Ir powder for Ir films produced on
TiN(111). Decreasing the oxygen partial pressure from 0.66 to 0.22 torr res
ulted in a 75% reduction in the film growth rate and a 40% reduction in fil
m roughness. Conformal (step coverage approaching unity) iridium films were
produced at 550 K in aspect ratio 1-0.25 mum vias in SiO2 and in aspect ra
tio 2.5-0.35 mum vias in TIN(111). (C) 2001 Elsevier Science B,V. All right
s reserved.