The atomic layer
deposition process of SrTiO3 (STO) films at 230 °C
was studied with Sr(iPr3Cp)2 and
Ti(CpMe5)(OMe)3 (Pr, Cp, and Me are propyl,
cyclopentadienyl, and methyl groups, respectively) on Ru substrates.
The growth behavior and properties of STO films grown at 230 °C
were compared with those deposited at 370 °C. With the limited
over-reaction of the Sr precursor during the initial growth stage
at a lower temperature, the cation composition was more controllable,
and the surface morphology after crystallization annealing at 650
°C had more uniform grains with fewer defects. Here, the excess
reaction of the Sr precursor means the chemical-vapor-deposition-like
growth of the SrO component mediated through the thermal decomposition
of the adsorbed Sr precursor molecules. It was by the reaction of
the Sr precursor with the oxygen supplied from the partly oxidized
Ru substrate. The second STO was grown at 370 °C (main layer)
on the annealed first STO layer (crystallized seed layer) to lead
to the in situ crystallization of the main layer. Due to the improved
microstructure of STO films induced by the seed layer deposited at
230 °C, the bulk dielectric constant of 167 was obtained for
the main layer, which was higher than the value of 101 where the seed
layer was deposited at 370 °C, even though the crystallization
annealing condition of the seed layer and the deposition condition
of the main layer were consistent. The seed layer grown at 230 °C,
however, had a lower dielectric constant of only ∼49, whereas
the high-temperature seed layer had a dielectric constant of ∼106.
Therefore, the low-temperature seed layer posed a severe limitation
in acquiring an advanced capacitor property with the involvement of
a low-dielectric interfacial layer.