Issue 19, 2014

Formation of interconnected morphologies via nanorod inclusion in the confined assembly of symmetric block copolymers

Abstract

We have investigated the effect of nanorods on the symmetry breaking of a model diblock copolymer under cylindrical confinement using coarse-grained molecular dynamics. Unlike nanoparticles, nanorods can readily be interconnected with each other and also induce connection across self-assembly domains at much lower loading than nanoparticles. Such interconnecting nanorods, when incorporated within the nanofiber confined assembled block copolymer, have great potential for providing highly conductive pathways for energy applications, such as battery electrodes and separators. Symmetric block copolymers (BCP) under cylindrical confinement with a nanorod aspect ratio (N) of 1, 5, and 10 are examined with three different types of nanorod–BCP attractions: (a) neutral nanorods, (b) A (wall-attractive phase)-attractive nanorods, and (c) B (wall-repulsive phase)-attractive nanorods. The system was studied with both selective and neutral walls, which affect the orientation of the interconnected nanorod network. Upon close examination of the BCP–nanorod self-assembly, we discovered that the ratio of the interphase distance to the nanorod aspect ratio (I/N) can be correlated to the onset of nanorod interconnectivity and formation of asymmetrical interconnected BCP morphology. By developing a phase diagram with respect to I/N, one can predict the formation of desired BCP morphology and the critical loading of nanorods for connected morphologies in cylindrical confinement.

Graphical abstract: Formation of interconnected morphologies via nanorod inclusion in the confined assembly of symmetric block copolymers

Article information

Article type
Paper
Submitted
23 Jan 2014
Accepted
11 Mar 2014
First published
17 Mar 2014

Phys. Chem. Chem. Phys., 2014,16, 8865-8871

Author version available

Formation of interconnected morphologies via nanorod inclusion in the confined assembly of symmetric block copolymers

J. H. Park and Y. L. Joo, Phys. Chem. Chem. Phys., 2014, 16, 8865 DOI: 10.1039/C4CP00352G

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