Phase behavior of copolymers confined in multi-walled nanotubes: Insights from simulations

Abstract

In this paper, the self-assembly process of diblock copolymers confined in multi-walled cylindrical nanotubes is systematically investigated using a molecular dynamics (MD) method. The dependence of resultant morphologies on the degree of confinement and on the interaction strength between nanotubes and copolymers is studied comprehensively. When the wall surfaces are not preferential, results indicate that geometric confinement significantly influences copolymer conformations. In addition, the thickness of the helical lamellar structure increases with interaction strength and confinement size. In cases where the nanotubes are strongly attracted to one copolymer block, the confinement effect weakens as geometric space increases. Findings explain the dependence of chain conformation on the degree of confinement and the strength of surface preferences.