September 12, 2000
We present a modified version of our "sliding model", where chain arcs, between two contacts at the surface, may move if all the barriers along the arc are weaker than a certain threshold.An important advance of the revised model is that the high limiting chain lengths N* observed in the experiments are naturally accoundted for. In this model, a film of thickness h, smaller than the coil size, can show either a "sandwich" structure with two mobile sublayers (at low temperatures T<T(h)), or a single mobile layer at T>T(h). But the accident occurring at T=T(h), does not necessarily coincide with the apparent glass transition, determined by the intersection of two tangents in a plot of thickness versus temperature.
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April 23, 2001
A simple and predictive model is put forward explaining the experimentally observed substantial shift of the glass transition temperature, Tg, of sufficiently thin polymer films. It focuses on the limit of small molecular weight, where geometrical `finite size' effects on the chain conformation can be ruled out. The model is based on the idea that the polymer freezes due to memory effects in the viscoelastic eigenmodes of the film, which are affected by the proximity of the b...
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This paper reviews recent Monte Carlo simulation studies of the glassy behavior in thin polymer films. The simulations employ a version of the bond-fluctuation lattice model, in which the glass transition is driven by the competition between a stiffening of the polymers and their dense packing in the melt. The melt is geometrically confined between two impenetrable walls separated by distances ranging from once to about fifteen times the bulk radius of gyration. The confineme...
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Thin polymer films have striking dynamical properties that differ from their bulk counterparts. With the simple geometry of a stepped polymer film on a substrate, we probe mobility above and below the glass transition temperature $T_{\textrm{g}}$. Above $T_{\textrm{g}}$ the entire film flows, while below $T_{\textrm{g}}$ only the near surface region responds to the excess interfacial energy. An analytical thin film model for flow limited to the free surface region shows excel...
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Freestanding thin polymer films with high molecular weights exhibit an anomalous decrease in the glass-transition temperature with film thickness. Specifically, in such materials, the measured glass-transition temperature evolves in an affine way with the film thickness, with a slope that weakly depends on the molecular weight. De Gennes proposed a sliding mechanism as the hypothetical dominant relaxation process in these systems, where stress kinks could propagate in a repta...
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The glass transition temperature and its connection to statistical properties of confined and free-standing polymer films of varying thickness containing unentangled to highly entangled bead-spring chains are studied by molecular dynamics simulations. For confined films, perfect scaling of the thickness-dependent end-to-end distance and radius of gyrations normalized to their bulk values in the directions parallel and perpendicular to the surfaces is obtained. Particularly, t...
August 24, 2004
Glass transition behavior of nanoscopically thin polymer films is investigated by means of molecular dynamics simulations. A thin polymer film that is composed of bead-spring model chains and supported on an idealized, fcc lattice substrate surface is studied in this work.
January 19, 2005
Glass transition process gets affected in ultrathin films having thickness comparable to the size of the molecules. We observe systematic broadening of glass transition temperature (Tg) as the thickness of the polymer film reduces below the radius of gyration but the change in the average Tg was found to be very small. Existence of reversible negative and positive thermal expansion below and above Tg increased the sensitivity of our thickness measurements performed using ener...
August 31, 2004
We present an analysis of heterogeneous dynamics in molecular dynamics simulations of a thin polymeric film, supported by an absorbing structured surface. Near the glass transition "immobile" domains occur throughout the film, yet the probability of their occurrence decreasing with larger distance from the surface. Still, enough immobile domains are located near the free surface to cause them to percolate in the direction perpendicular to surface, at a temperature near the gl...
January 8, 2003
Recent experiments have demonstrated that the glass transition temperature of thin polymer films can be shifted as compared to the same polymer in the bulk, the amplitude and the sign of this effect depending on the interaction between the polymer and the substrate. A model has been proposed recently for explaining these effects in two limiting cases: suspended films and strongly adsorbed films. We extend here this model for describing the cross-over between these two situati...
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To study the cooling behavior and the glass transition of polymer melts in bulk and with free surfaces a coarse-grained weakly semi-flexible polymer model is developed. Based on a standard bead spring model with purely repulsive interactions an attractive potential between non-bonded monomers is added, such that the pressure of polymer melts is tuned to zero. Additionally, the commonly used bond bending potential [Everaers et al., Science 303, 823 (2004)] controlling the chai...