Authors

Jiaxun Wang

Type

Text

Type

Thesis

Advisor

Sokolov, Jonathon | Koga, Tadanori | Venkatesh, T. A..

Date

2015-08-01

Keywords

Materials Science

Department

Department of Materials Science and Engineering.

Language

en_US

Source

This work is sponsored by the Stony Brook University Graduate School in compliance with the requirements for completion of degree.

Identifier

http://hdl.handle.net/11401/76354

Publisher

The Graduate School, Stony Brook University: Stony Brook, NY.

Format

application/pdf

Abstract

Despite intensive studies over the last 20 years, the nature of wetting/dewetting of ultrathin polymer films (i.e. | thickness less than 100 nm) on impenetrable solid surfaces still remains unsolved. We report that stabilization of liquid polymer films on solids can be controlled by nanoscale architectures of polymer chains adsorbed on the solid surfaces. A series of monodisperse PS ultrathin films (20 nm in thickness) with different molecular weights (Mw) were prepared on silicon (Si) substrates with a natural amorphous Si dioxide layer. The PS thin films were annealed at high temperatures, and the film stability was studied by combining optical and atomic force microscopes. At the same time, the annealed PS films were further leached with a good solvent and the residue films (several nanometers thick) were characterized by ellipsometry and X-ray photoelectron spectroscopy. We found that the film stability is attributed to the wetting-dewetting transition at the interface between the free polymer chains and adsorbed polymer chains. The present findings provide a simple and effective alternative in place ofconventional end-grafting approach, by modifying the substrate surfaces with the chemically identical polymer chains bound to solids via physisorption. | 61 pages

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