Topology and shape control for assemblies of block copolymer blends in solution

We study binary blends of asymmetric diblock copolymers (AB/AC) in selective solvents with a mesoscale model. We investigate the morphological transitions induced by the concentration of the AC block copolymer and the difference in molecular weight between the AB and AC copolymers, when segments B a...

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Main Authors: Moreno, N., Nunes, S., Peinemann, K., Calo, Victor
Format: Journal Article
Published: American Chemical Society 2015
Online Access:http://hdl.handle.net/20.500.11937/51527
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author Moreno, N.
Nunes, S.
Peinemann, K.
Calo, Victor
author_facet Moreno, N.
Nunes, S.
Peinemann, K.
Calo, Victor
author_sort Moreno, N.
building Curtin Institutional Repository
collection Online Access
description We study binary blends of asymmetric diblock copolymers (AB/AC) in selective solvents with a mesoscale model. We investigate the morphological transitions induced by the concentration of the AC block copolymer and the difference in molecular weight between the AB and AC copolymers, when segments B and C exhibit hydrogen-bonding interactions. To the best of our knowledge, this is the first work modeling mixtures of block copolymers with large differences in molecular weight. The coassembly mechanism localizes the AC molecules at the interface of A and B domains and induces the swelling of the B-rich domains. The coil size of the large molecular weight block copolymer depends only on the concentration of the short block copolymer (AC or AB), regardless of the B-C interactions. However, the B-C interactions control the morphological transitions that occur in these blends.
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format Journal Article
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institution Curtin University Malaysia
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last_indexed 2025-11-14T09:48:29Z
publishDate 2015
publisher American Chemical Society
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spelling curtin-20.500.11937-515272018-03-29T09:08:37Z Topology and shape control for assemblies of block copolymer blends in solution Moreno, N. Nunes, S. Peinemann, K. Calo, Victor We study binary blends of asymmetric diblock copolymers (AB/AC) in selective solvents with a mesoscale model. We investigate the morphological transitions induced by the concentration of the AC block copolymer and the difference in molecular weight between the AB and AC copolymers, when segments B and C exhibit hydrogen-bonding interactions. To the best of our knowledge, this is the first work modeling mixtures of block copolymers with large differences in molecular weight. The coassembly mechanism localizes the AC molecules at the interface of A and B domains and induces the swelling of the B-rich domains. The coil size of the large molecular weight block copolymer depends only on the concentration of the short block copolymer (AC or AB), regardless of the B-C interactions. However, the B-C interactions control the morphological transitions that occur in these blends. 2015 Journal Article http://hdl.handle.net/20.500.11937/51527 10.1021/acs.macromol.5b01891 American Chemical Society restricted
spellingShingle Moreno, N.
Nunes, S.
Peinemann, K.
Calo, Victor
Topology and shape control for assemblies of block copolymer blends in solution
title Topology and shape control for assemblies of block copolymer blends in solution
title_full Topology and shape control for assemblies of block copolymer blends in solution
title_fullStr Topology and shape control for assemblies of block copolymer blends in solution
title_full_unstemmed Topology and shape control for assemblies of block copolymer blends in solution
title_short Topology and shape control for assemblies of block copolymer blends in solution
title_sort topology and shape control for assemblies of block copolymer blends in solution
url http://hdl.handle.net/20.500.11937/51527