Molecular motion activated by residual stress in a glassy polymer thin film

The activation, by residual stress, of the fast portion of rotational motion of single fluorescent probe molecules inside a polymer thin film near its glass transition temperature is studied at a single molecular level. Spin-casted poly n-butyl methacrylate thin films without thermal annealing are chosen as the model system and single molecule fluorescence defocused microscopy is adopted as the method. The rotational motion of the probes under residual stress is found to be more activated than that under mere thermal activation, and the kinetic energy exhibits a monotonic increase with the stress strength. A rough linear dependence of rotational kinetic energy at low stress is found, yielding the value of characteristic volume for the residual stress to activate the motion of the probes. The values of the volume are close to the van der Waals volume of the probes, indicating that the activation of the fast dynamics by residual stress is localized. The activation effect is weakened and vanishes at or above the glass transition temperature due to stress relaxation. The effect is also absent at temperatures far below T-g due to the frozen molecular motion with a much higher activation energy.

Automated summary

The study focuses on the activation of fast rotational motion of single fluorescent probe molecules inside a polymer thin film near its glass transition temperature by residual stress. The kinetic energy of the probes shows a monotonic increase with stress strength and exhibits a rough linear dependence at low stress levels. The activation effect is localized and diminishes above the glass transition temperature.