Molecular simulation of polymer crystallization under chain and space confinement

Abstract

Polymer crystallization under chain and space confinements is studied by Monte Carlo simulation. The simulation results show that the crystallinity and melting temperature of confined systems increase with the increase of free chain content. Furthermore, the crystallinity and melting temperature of confined systems with larger lateral size are higher than those with smaller lateral size. These findings are in good agreement with the conclusions obtained in some experiments. An important phenomenon that cannot be observed in experiments has been confirmed, that is, the tethering point can be used as the nucleation site. For the confined polymer system with the lateral size of 8 lattice points, with the increase of free chain content, the surface free energy of the nuclei and the diffusion activation energy of the chains decrease due to the combined effects of chain conformation size and chain movement ability, which leads to the enhancement of the nucleation ability of polymers. However, for the confined polymer system with lateral size of 12 lattice points, with the increase of free chain content, the nucleation sites decrease and the critical free energy barrier increases, which are not conducive to nucleation. Moreover, the existence of interfacial interactions can also significantly change the crystallization of confined polymers. Our results indicate the crystallization kinetics of the confined polymer from a microscopic point of view.