Paper
30 January 1989 Silicon Oxidation During Bilayer Resist Etching
Mark A. Hartney, Justin N. Chiang, David S. Soane, Dennis W. Hess, Robert D. Allen
Author Affiliations +
Abstract
Steady-state etching rates and initial film losses were measured for two types of silicon-containing polymers (polysiloxanes and polysilyistyrenes) under a variety of oxygen plasma conditions. While steady state behavior was observed for most conditions, the silylstyrene resists showed higher etch rates than predicted from recent models. The deviations were explained by the fact that the oxidized layer formed from silylstyrene polymers has a large residual carbon content, and thus sputters at a rate higher than predicted for a stoichiometric SiO2 layer. The siloxane material showed good agreement with the model under all conditions and was determined to form a more SiO2-like oxidized layer. XPS analysis was used to monitor the conversion of carbon-bound silicon to oxidized species for the polysilylstyrenes. Conversion was more rapid and more complete when etching with higher ion energies. Polysilylmethylstyrene reached a steady-state oxide thickness between 3.4 and 5.8 nm, depending on etching conditions. A copolymer of this material with chloromethylstyrene showed a comparable thickness when etched at high ion energies, but did not reach a steady state when etched at conditions where the average ion energy was below 110 eV.
© (1989) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Mark A. Hartney, Justin N. Chiang, David S. Soane, Dennis W. Hess, and Robert D. Allen "Silicon Oxidation During Bilayer Resist Etching", Proc. SPIE 1086, Advances in Resist Technology and Processing VI, (30 January 1989); https://doi.org/10.1117/12.953027
Advertisement
Advertisement
RIGHTS & PERMISSIONS
Get copyright permission  Get copyright permission on Copyright Marketplace
KEYWORDS
Etching

Silicon

Oxides

Ions

Polymers

Silicon carbide

Signal to noise ratio

Back to Top