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Phase behavior of triblock copolymer and homopolymer blends: Effect of copolymer topology

Jiayu Xie and An-Chang Shi
Phys. Rev. Materials 8, 015601 – Published 11 January 2024
An article within the collection: Self-Assembly of Complex Phases in Block Copolymer Materials

Abstract

Two distinct linear triblock copolymers with different block sequences, ABA or BAB, are obtained when two identical AB diblock copolymers are jointed at their B or A ends, respectively, resulting in three homologous, AB diblock, ABA, and BAB triblock copolymers with the same chemical composition but different topologies. We demonstrate that the topological effect on the phase behaviors of these copolymers is amplified when A homopolymers are added to the system. Specifically, the phase behaviors of binary blends composed of ABA or BAB linear triblock copolymers and A homopolymers are studied by using the random-phase approximation (RPA) and self-consistent field theory (SCFT). The RPA analysis predicts that the Lifshitz point for the ABA/A blends behaves like a second-order transition but that for the BAB/A blends behaves like a first-order transition. The Lifshitz point of the BAB/A mixtures is found to occur at a much lower homopolymer concentration than that of the ABA/A mixtures, indicating a poorer miscibility of the A homopolymers into the BAB than ABA triblocks, which is also confirmed by SCFT. For sphere-forming triblock copolymers mixed with homopolymers, the poorer miscibility and the more diffused distribution of the A homopolymers in the BAB/A blends result in a phase behavior drastically different from that of the ABA/A and AB/A blends. The ABA/A blends stabilize the Frank-Kasper (FK) phases similar to the AB/A blends, but the stability window of FK phases becomes negligibly small in the corresponding BAB/A blends. Our results demonstrate that the topological effect of block copolymers on the equilibrium phase behaviors can be more prominent in multicomponent systems and thus more attention should be paid to copolymer topologies in the design of polymeric blends.

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  • Received 20 August 2023
  • Accepted 18 December 2023

DOI:https://doi.org/10.1103/PhysRevMaterials.8.015601

Published by the American Physical Society under the terms of the Creative Commons Attribution 4.0 International license. Further distribution of this work must maintain attribution to the author(s) and the published article's title, journal citation, and DOI.

Published by the American Physical Society

Physics Subject Headings (PhySH)

  1. Research Areas
  1. Physical Systems
Condensed Matter, Materials & Applied Physics

Collections

This article appears in the following collection:

Self-Assembly of Complex Phases in Block Copolymer Materials

The Editors of Physical Review Materials are pleased to present the Collection on Self-Assembly of Complex Phases in Block Copolymer Materials, highlighting one of the most exciting fields in polymer science. Block copolymers offer an excellent model system for comprehending symmetry breaking in soft matter, as well as a unique platform for designing nanostructured materials. This Collection is being guest-edited by Kevin Dorfman from the University of Minnesota and Chris Bates from the University of California - Santa Barbara.

Authors & Affiliations

Jiayu Xie* and An-Chang Shi

  • Department of Physics and Astronomy, McMaster University, Hamilton, Ontario, Canada L8S 4M1

  • *xiej33@mcmaster.ca
  • shi@mcmaster.ca

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Issue

Vol. 8, Iss. 1 — January 2024

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