Area-selective
atomic layer deposition (AS-ALD) is a highly sought-after
strategy for the fabrication of next-generation electronics. This
work reveals how key precursor design parameters strongly influence
the efficacy of AS-ALD by comparing a series of precursors possessing
the same metal center but different ligands. When the number of methyl
and chloride groups in Al(CH3)
x
Cl3–x
(x = 0,
2, and 3) and the chain length of alkyl ligands in AlC
y
H2y+1 (y = 1 and 2) are changed, the effect of precursor chemistry (reactivity
and molecular size) on the selectivity is elucidated. The results
show that optimized parameters for the Al2O3 ALD processes on a self-assembled monolayer (SAM)-terminated substrate,
which serves as the nongrowth surface, differ significantly from those
on a Si substrate. Chlorine-containing precursors need a much longer
purging time on the SAMs because of a stronger Lewis acidity compared
to that of alkyl precursors. With reoptimized conditions, the ALD
of Al2O3 using the Al(C2H5)3 precursor is blocked most effectively by SAM inhibitors,
whereas the widely employed Al(CH3)3 precursor
is blocked least effectively among the precursors tested. Finally,
we show that a selectivity exceeding 0.98 is achieved for up to 75
ALD cycles with Al(C2H5)3, for which
6 nm of Al2O3 film grows selectively on SiO2-covered Si. Quantum chemical calculations show significant
differences in the energetics of dimer formation across the Al precursors,
with only ∼1% of AlCl3 and Al(CH3)2Cl precursors but 99% of the alkyl precursors, Al(CH3)3 and Al(C2H5)3, existing
as monomers at 200 °C. We propose that a combination of precursor
reactivity and effective molecular size affects the blocking of the
different precursors, explaining why Al(C2H5)3, with weaker Lewis acidity and relatively large size,
exhibits the best blocking results.