The effect of free space on molecular motion inside the
polymer
“dead layer” or adsorbed nanolayers on solid surfaces
is investigated. Free space is introduced into the nanolayer by choosing
a polymer with a relatively big side group, poly n-butyl methacrylate (PnBMA), and polarization-resolved single-molecule
fluorescence microscopy is adopted as the method. The rotational motion
of the doped fluorescent probes is found to be considerably excited
at moderate temperatures, attributed to the free space brought by
the side group of the PnBMA. The development of the adsorbed nanolayer
by the prolonged annealing of the parent film is carefully monitored,
together with the evolution of the molecular motion and the glass
transition temperature (Tg). The Tg values of the exposed nanolayers are considerably
lower than that of the bulk system, while they become higher than
those in the bulk situation when the nanolayer is covered with a polymer
top layer. The experimental evidence has demonstrated that the free
space made available by the side group and the air–polymer
interface has considerably promoted the molecular motion inside the
adsorbed nanolayers, even under the situation of overwhelming surface
attraction