Paper
14 June 1996 Factors affecting the dissolution rate of novolac resins II: developer composition effects
Clifford L. Henderson, Pavlos C. Tsiartas, Logan L. Simpson, Kelly D. Clayton, Sanju Pancholi, Adam R. Pawlowski, C. Grant Willson
Author Affiliations +
Abstract
Resist function depends upon photoinduced changes in the dissolution rate of phenolic polymer films in aqueous base. The events that occur as the molecules in these films move from the glassy state into solution are not well understood. This paper presents an extensive study of the influence of developer composition and concentration on the dissolution rate of novolac films in aqueous base. The dissolution rate is shown to be a function of both the cation and anion composition and concentration in the developer at a constant pH. When salts are added to the base, the rate first increases, reaches a maximum, and then decreases with increasing salt concentration. In the concentration regime below the maximum, the rate increases linearly with cation concentration and is independent of anion composition. The dissolution of novolac is dependent on cation concentration and not ionic strength in this regime. In the concentration regime above the maximum, the composition of the anion has a marked influence on the rate.
© (1996) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Clifford L. Henderson, Pavlos C. Tsiartas, Logan L. Simpson, Kelly D. Clayton, Sanju Pancholi, Adam R. Pawlowski, and C. Grant Willson "Factors affecting the dissolution rate of novolac resins II: developer composition effects", Proc. SPIE 2724, Advances in Resist Technology and Processing XIII, (14 June 1996); https://doi.org/10.1117/12.241846
Lens.org Logo
CITATIONS
Cited by 1 scholarly publication.
Advertisement
Advertisement
RIGHTS & PERMISSIONS
Get copyright permission  Get copyright permission on Copyright Marketplace
KEYWORDS
Ions

Polymers

Alkali metals

Macromolecules

Potassium

Interfaces

Molecules

Back to Top