A Direct Quantitative Measure of Surface Mobility in a Glassy Polymer

Author:

Chai Y.1,Salez T.2,McGraw J. D.3,Benzaquen M.2,Dalnoki-Veress K.23,Raphaël E.2,Forrest J. A.14

Affiliation:

1. Department of Physics and Astronomy and Guelph-Waterloo Physics Institute, University of Waterloo, Waterloo, Ontario N2L 3G1, Canada.

2. Laboratoire de Physico-Chimie Théorique, UMR CNRS Gulliver 7083, École Supérieure de Physique et de Chimie Industrielles (ESPCI), Paris, France.

3. Department of Physics and Astronomy, McMaster University, Hamilton, Ontario L8S 4M1, Canada.

4. Perimeter Institute for Theoretical Physics, 31 Caroline Street North, Waterloo, Ontario N2L 2Y5, Canada.

Abstract

Polymer Film Behavior An ongoing debate in the understanding of the behavior of thin-film glassy polymers is whether there is nanoconfinement of large molecules or enhanced mobility near a free surface. Chai et al. (p. 994 ; see the Perspective by Chen et al. ) prepared polymer films with a sharp step in the profile by depositing broken film fragments onto a uniform underlay. Atomic force microscopy revealed changes to the overall film profile with time at various temperatures. A transition was observed from localized motions to relaxation of the entire film at a temperature close to that of the bulk glass transition temperature.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference35 articles.

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