Abstract
Highly selective deposition of MoSix on Si in preference to SiO2 and SiNx was achieved via atomic layer deposition (ALD) using MoF6 and Si2H6 at 120 °C. The selectivity was enabled by the lack of chemical reactivity between the reactants and the SiO2 and SiNx substrates. In contrast, MoF6 nucleated in a self-limiting manner on H-terminated Si, and a following Si2H6 exposure reduced MoFx to Mo0 which is consistent with Mo-Si bond formation. X-Ray photoelectron spectroscopy (XPS) revealed that the 5 ALD cycles of MoF6 and Si2H6 selectively deposited a substoichiometric MoSi2 film on the Si substrate in contrast to previous results showing a nearly pure Mo deposition. Extra Si2H6 doses on the substoichiometric MoSi2 film incorporated more Si into the film without disturbing the inherent selectivity over SiO2 and SiNx. A depth-profiling study showed that the bulk of the film has Si/Mo = 1.7–1.9 with <10% F and O impurities. The data is consistent with higher pressure Si2H6 doses inducing silicide formation instead of metal deposition. To verify selectivity on the nanoscale, the selective deposition of MoSix was investigated on a patterned Si wafer containing three-dimensional (3D) nanoscale SiO2 and SiNx features. Cross-sectional transmission electron microscopy (TEM) showed that selective MoSix deposition was achieved on nanoscale 3D structures. AFM documented that there were less than 10 nuclei/µm2 on SiO2.; since SiO2 has ∼106/µm2 OH groups, this corresponds to an intrinsic selectivity of about 106:1 between the OH groups on SiO2 and Si-H groups on Si. This inherent substrate-dependent selectivity for silicide deposition allows the elimination of pre-positioning of passivants.
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