Dynamics of polymer film formation during spin coating
Author(s) -
Youmna Mouhamad,
Parvaneh MokarianTabari,
Nigel Clarke,
Richard Jones,
Mark Geoghegan
Publication year - 2014
Publication title -
journal of applied physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.699
H-Index - 319
eISSN - 1089-7550
pISSN - 0021-8979
DOI - 10.1063/1.4896674
Subject(s) - viscosity , polystyrene , polymer , volume fraction , materials science , spin coating , evaporation , toluene , methyl methacrylate , coating , deposition (geology) , thermodynamics , polymer chemistry , chemistry , composite material , organic chemistry , physics , copolymer , paleontology , sediment , biology
Standard models explaining the spin coating of polymer solutions generally fail to describe the early stages of film formation, when hydrodynamic forces control the solution behavior. Using in situ light scattering alongside theoretical and semi-empirical models, it is shown that inertial forces (which initially cause a vertical gradient in the radial solvent velocity within the film) play a significant role in the rate of thinning of the solution. The development of thickness as a function of time of a solute-free liquid (toluene) and a blend of polystyrene and poly(methyl methacrylate) cast from toluene were fitted to different models as a function of toluene partial pressure. In the case of the formation of the polymer blend film, a concentration-dependent (Huggins) viscosity formula was used to account for changes in viscosity during spin coating. A semi-empirical model is introduced, which permits calculation of the solvent evaporation rate and the temporal evolution of the solute volume fraction and solution viscosity. (C) 2014 Author(s)
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