AVS 64th International Symposium & Exhibition | |
Thin Films Division | Tuesday Sessions |
Session TF-TuA |
Session: | ALD Precursors and Surface Reactions |
Presenter: | Nicholas Strandwitz, Lehigh University |
Authors: | N.C. Strandwitz, Lehigh University L. Ju, Lehigh University |
Correspondent: | Click to Email |
Cyclic azasilanes are a promising class of reactants for atomic and molecular layer deposition due to their volatility, reactivity, and diverse set of peripheral chemical functionalities. The reactivity of this class of molecules stems from ring strain and unstable Si-N bonding. Reaction with water or OH groups results in ring opening and Si-O bond formation and is a useful chemical step for controlled film growth. This work focuses on using and understanding this class of molecules for use in atomic and molecular layer deposition ( ALD, MLD). The efficacy of the ring opening reaction and the diversity of functional groups on the cyclic azasilanes deem this precursor group highly promising for MLD. We report the growth of various MLD films based on reaction with anhydrides, metal-organics, and water. The film growth was found to be optimal near 100 °C. The two chemistries reported here are the sequential reaction of (1) a cyclic azasilane, maleic anhydride, and water and (2) a cyclic azasilane, maleic anhydride, trimethylaluminum (TMA), and water. Reaction 1 showed clear evidence of diffusion and reaction within the film as evidenced by large growth rates (~10 nm per cycle) after ~15 growth cycles, regardless of purge time. However, use of TMA in reaction 2 arrested this diffusion, presumably due to consumption of reactive groups or through densification of the film. Film properties were measured as a function of annealing temperature using ellipsometry, x-ray reflectivity, and infrared absorption measurements. These measurements indicate a densification of the films while maintaining low surface roughness. Porosity is evident after removal of organic components by a low dielectric constant for the films derived from reaction 1.These MLD chemistries offer a route to tunable hybrid thin films on high aspect ratio substrates and have potential applications in diffusion barriers, low dielectric constant layers, and passivation layers.