Block copolymers confined in a nanopore: Pathfinding in a curving and frustrating flatland

Details Block copolymers confined in a nanopore: Pathfinding in a curving and frustrating flatland Block copolymers confined in a nanopore: Pathfinding in a curving and frustrating flatland

2007-12-10

arxiv.org/abs/0712.1415v1

Physics

Condensed Matter

Soft Condensed Matter

The following article has been accepted by JCP. After it is published, it will be found at http://jcp.aip.org/

Scientific paper

10.1063/1.2829406

We have studied structure formation in a confined block copolymer melt by means of dynamic density functional theory (DDFT). The confinement is two-dimensional, and the confined geometry is that of a cylindrical nanopore. Although the results of this study are general, our coarse-grained molecular model is inspired by an experimental lamellae-forming PS-PBD diblock copolymer system (Shin et al, Science, 306, 76 (2004)), in which an exotic toroidal structure was observed upon confinement in alumina nanopores. Our computational study shows that a zoo of exotic structures can be formed, although the majority, including the catenoid, helix and double helix that were also found in Monte Carlo (MC) nanopore studies, are metastable states. We introduce a general classification scheme and consider the role of kinetics and elongational pressure on stability and formation pathway of both equilibrium and metastable structures in detail. We find that helicity and three-fold connections mediate structural transitions on a larger scale. Moreover, by matching the remaining parameter in our mesoscopic method, the Flory-Huggins parameter, to the experimental system, we obtain a structure that resembles the experimental toroidal structure in great detail. Here, the most important factor seems to be the roughness of the pore, i.e. small variations of the pore radius on a scale that is larger than the characteristic size in the system.

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