Achieving atomic-scale precise control over material
layering is
critical for the development of future semiconductor technology. Area-selective
deposition (ASD) has emerged as an indispensable tool for crafting
semiconductor components and structures via bottom-up pattern transfer.
Ruthenium has attracted significant interest as a low-resistivity
conducting material for next-generation interconnect technology. However,
the oxidative counter-reactants such as O2 often used for
atomic layer deposition (ALD) of metallic Ru films result in a considerable
increase in contact resistance because of substrate oxidation, limiting
the applications of both ALD and ASD of Ru. In this study, Ru ASD
is demonstrated using two-step ALD with the sequential use of H2 and O2 as counter-reactants and dimethylamino-trimethylsilane
(DMATMS) as a precursor inhibitor. Both theoretical and experimental
results demonstrate that in the two-step Ru ALD, the oxide layer can
be eliminated via the reduction of the oxidized substrate metal surface
by the H2 counter-reactant. This mechanism simultaneously
facilitates the adsorption of the Ru precursor (tricarbonyl-(trimethylenemethane)-ruthenium)
and removal of the surface oxide layer. Consequently, Ru growth is
suppressed on the DMATMS-inhibited SiO2 surface during
ASD, enabling exclusive deposition of Ru on the Mo surface. The currently
proposed Ru ASD scheme using two-step ALD is highly promising for
driving advancements in interconnect technology for commercial applications.