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Published on: January 26, 2016
Shear modulation force microscopy study of near surface glass transition temperatures
1Department of Materials Science and Engineering, State University of New York, Stony Brook, New York 11794-2275, USA.
Physical Review Letters
|September 8, 2000
Summary
We measured the glass transition temperature (T(g)) of polymer thin films using atomic force microscopy. The T(g) was found to be independent of film thickness, substrate interactions, or the presence of a substrate.
Area of Science:
- Materials Science
- Polymer Science
- Surface Science
Background:
- Understanding the glass transition temperature (T(g)) of polymer thin films is crucial for their application in various technologies.
- Previous studies have indicated potential thickness-dependent T(g) behavior in polymer films, but experimental evidence remains debated.
- Atomic Force Microscopy (AFM) offers high-resolution surface analysis capabilities.
Purpose of the Study:
- To accurately measure the surface glass transition temperature (T(g)) of polymer thin films.
- To investigate the influence of film thickness, substrate interactions, and substrate presence on the measured T(g).
- To validate the utility of shear modulation force microscopy (SMFM) for T(g) determination.
Main Methods:
- Utilized Atomic Force Microscopy (AFM) in shear modulation force microscopy (SMFM) mode.
- Measured the temperature-dependent shear force exerted on an AFM tip modulated parallel to the polymer film surface.
- Analyzed thin polymer films with thicknesses ranging from 17 to 500 nm.
Main Results:
- The surface glass transition temperature (T(g)) was successfully measured for polymer thin films.
- T(g) was found to be independent of film thickness for films thicker than 17 nm.
- No significant influence of substrate interaction strength or the presence of a substrate was observed on the T(g).
Conclusions:
- The surface T(g) of polymer thin films is robust and not affected by film thickness above 17 nm.
- Shear modulation force microscopy (SMFM) is a reliable technique for determining the surface T(g) of polymer films.
- The findings suggest that surface T(g) is an intrinsic property of the polymer film material itself under these experimental conditions.

