Area-Selective Atomic Layer Deposition of Ruthenium via Minimization of Interfacial Oxidation

Journal
Chemistry of Materials
Date
2024.09.13
Abstract

In the forefront of future semiconductor technology lies the criticality of precise material control and layering, where variations in properties play a pivotal role. In this endeavor, area-selective atomic layer deposition (ASD) methods emerge as indispensable tools for crafting semiconductor components and structures tailored to specific characteristics and requirements. Ruthenium (Ru) is attracting significant interest as a low-resistivity conducting material poised for next-generation interconnect technology. However, oxidants such as O2, O3, and H2O have been identified as counter reactants for depositing metallic Ru films. Consequently, the notable rise in contact resistance due to substrate oxidation by these oxidant counter reactants has posed a significant drawback in both ALD and ASD Ru processes. In this study, Ru ASD is studied using a two-step ALD process with sequential use of H2 and O2 as counter reactants and an aminosilane precursor inhibitor (PI), dimethylaminotrimethylsilane (DMATMS). Both theoretically and experimentally, it has been demonstrated that in the 2-step Ru ALD process, the oxide layer can be significantly eliminated through the reduction reaction mechanism involving the H2 counter reactant and the oxidized metal surface. This principle allows for the simultaneous adsorption of Ru precursor, tricarbonyl-(trimethylenemethane)-ruthenium (TRuST) while removing the oxide layer from the oxidized metal surface. As a result, it suppresses Ru growth on the DMATMS-inhibited SiO2 surface in the ASD process, enabling deposition exclusively on the metal (Mo) surface. The proposed Ru ASD for anti-oxidation using the two-step ALD process could hold significant promise for driving advancements in interconnect technology for commercial applications.

Reference
Chem. Mater. 2024, 36, 8663?8672
DOI
http://dx.doi.org/10.1021/acs.chemmater.4c01133