Static and dynamics of entanglements in the lamellar phase of block copolymers

NICOLÁS A GARCÍA; BARRAT, JEAN-LOUIS

Bariloche

Encuentro; Yielding phenomena in disordered systems; 2019

A comprehensive understanding of the underlying physics in the viscoelastic behavior of polymers is of fundamental interest but also is relevant to consider their technological applications. It is well-known that the mechanical properties of polymers in melts and concentrated solutions depend fundamentally on the molecular weight of the chains. Indeed, the inherent inability of the chains to cross each other comes into play when the chain-length increases inducing mobility constraints for them; thus, the so-called entanglements appear. Nowadays, we know the entanglements are a universal aspect of the polymer physics which occur in any flexible polymer system if the chain is sufficiently long and the concentration is high enough.Polymer entanglements in homogenous systems under bulk conditions have been extensively studied through simulations and experiments, and some elegant theories provide the conceptual frameworks to interpret their behavior. Furthermore, similar studies were recently reported on inhomogeneous systems like confined environments: thin films, nanocylinders, etc. However little is known about those topological constraints on heterogeneous systems and multicomponent polymers such as the block copolymers (BCPs), a fascinating system which in the proper conditions of temperature and composition tends to self-assembly in periodic nanopatterns of high technological interest.In this work, we use a novel coarse-graining for simulating entangled polymers to investigate the viscoelastic properties of BCPs when they segregate in a lamellar morphology. We have performed a thorough analysis to characterize the statics and dynamics of such a system.We found the entanglements are not homogeneously distributed in space but instead adopt a distribution related to the underlying pattern as a direct consequence of the periodic location of the segregated domains. Moreover, the interface separating nearby domains induces a surface effect decreasing the density of entanglement locally, this effect seems to depend on the segregation regime, being more extended and notorious for sharp interfaces, i.e., in strong segregation.Regarding the dynamics, we found the process of self-assembly disentangle the system in the kinetic pathway to the equilibrium.