The concept of free volume underpins
the variations in polymer
dynamics. Annihilation of free-volume holes through diffusion to surfaces
has been proposed to determine the vitrification of the confined polymers.
In this work, we assessed the hole diffusion dynamics in glassy thin
poly (ethylene terephthalate) films with various thicknesses using
a strategy based on covering the film surface with crystals of different
sizes, which allows for changing the hole diffusion efficiency, thus
tuning the glass transition temperature of the thin film (T
g
film). The apparent activation energy
for hole diffusion (E
a,hole) in the thin
films was elucidated by modeling the correlation between T
g
film and surface coverage of crystals using
the free-volume hole diffusion model. Our results demonstrated a trend
of linear decrease in E
a,hole with the
increasing inverse film thickness (h
–1), suggesting that the presence of a free surface with faster dynamics
promotes hole diffusion in thin films. This finding demonstrates that
the free volume release in thin films and thus the confined polymer
dynamics can be modulated by changing the free surface properties
of the films.