Quantify the contribution of chain length heterogeneity on block copolymer self-assembly

This work quantitatively explores the effect of chain length heterogeneity on self-assembly behaviors of block copolymer, focusing on the narrow distribution region. A library of discrete diblock copolymers consisting of oligo dimethylsiloxane (oDMS) and oligo lactic acid (oLA) blocks were modularly...

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Main Authors: Yanxiao Sun, Rui Tan, Zhuang Ma, Dongdong Zhou, Jinbin Li, Deyu Kong, Xue-Hui Dong
Format: Article
Language:English
Published: Elsevier 2020-12-01
Series:Giant
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2666542520300400
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spelling doaj-b1f1f08401354e7e958e23d7d1e51aab2020-12-13T04:19:50ZengElsevierGiant2666-54252020-12-014100037Quantify the contribution of chain length heterogeneity on block copolymer self-assemblyYanxiao Sun0Rui Tan1Zhuang Ma2Dongdong Zhou3Jinbin Li4Deyu Kong5Xue-Hui Dong6South China Advanced Institute for Soft Matter Science and Technology, School of Molecular Science and Engineering, South China University of Technology, Guangzhou 510640, ChinaSouth China Advanced Institute for Soft Matter Science and Technology, School of Molecular Science and Engineering, South China University of Technology, Guangzhou 510640, ChinaSouth China Advanced Institute for Soft Matter Science and Technology, School of Molecular Science and Engineering, South China University of Technology, Guangzhou 510640, ChinaSouth China Advanced Institute for Soft Matter Science and Technology, School of Molecular Science and Engineering, South China University of Technology, Guangzhou 510640, ChinaSouth China Advanced Institute for Soft Matter Science and Technology, School of Molecular Science and Engineering, South China University of Technology, Guangzhou 510640, ChinaSouth China Advanced Institute for Soft Matter Science and Technology, School of Molecular Science and Engineering, South China University of Technology, Guangzhou 510640, ChinaSouth China Advanced Institute for Soft Matter Science and Technology, School of Molecular Science and Engineering, South China University of Technology, Guangzhou 510640, China; State Key Laboratory of Luminescent Materials and Devices, South China University of Technology, Guangzhou 510640, China; Corresponding author at: South China Advanced Institute for Soft Matter Science and Technology, School of Molecular Science and Engineering, South China University of Technology, Guangzhou 510640, China.This work quantitatively explores the effect of chain length heterogeneity on self-assembly behaviors of block copolymer, focusing on the narrow distribution region. A library of discrete diblock copolymers consisting of oligo dimethylsiloxane (oDMS) and oligo lactic acid (oLA) blocks were modularly prepared with one monomer difference in composition, which form highly ordered nanostructures at room temperature. The molecular weight distribution of the oLA block was then precisely modulated through a reconstruction approach, achieving an absolute control on chain length heterogeneity. By meticulously tuning the breadth and symmetry of the distribution profile, the lattice dimension of the assembled nanostructure significantly expands, while no appreciable difference on the phase stability was observed. This work provides an explicit access to block copolymers with narrow dispersity that are not possible through conventional chemical approach, revealing the critical contribution of dispersity on self-assembly and bridging the existing gaps between experiments and theories.http://www.sciencedirect.com/science/article/pii/S2666542520300400DispersityPrecision macromoleculesBlock copolymerSelf-assembly
collection DOAJ
language English
format Article
sources DOAJ
author Yanxiao Sun
Rui Tan
Zhuang Ma
Dongdong Zhou
Jinbin Li
Deyu Kong
Xue-Hui Dong
spellingShingle Yanxiao Sun
Rui Tan
Zhuang Ma
Dongdong Zhou
Jinbin Li
Deyu Kong
Xue-Hui Dong
Quantify the contribution of chain length heterogeneity on block copolymer self-assembly
Giant
Dispersity
Precision macromolecules
Block copolymer
Self-assembly
author_facet Yanxiao Sun
Rui Tan
Zhuang Ma
Dongdong Zhou
Jinbin Li
Deyu Kong
Xue-Hui Dong
author_sort Yanxiao Sun
title Quantify the contribution of chain length heterogeneity on block copolymer self-assembly
title_short Quantify the contribution of chain length heterogeneity on block copolymer self-assembly
title_full Quantify the contribution of chain length heterogeneity on block copolymer self-assembly
title_fullStr Quantify the contribution of chain length heterogeneity on block copolymer self-assembly
title_full_unstemmed Quantify the contribution of chain length heterogeneity on block copolymer self-assembly
title_sort quantify the contribution of chain length heterogeneity on block copolymer self-assembly
publisher Elsevier
series Giant
issn 2666-5425
publishDate 2020-12-01
description This work quantitatively explores the effect of chain length heterogeneity on self-assembly behaviors of block copolymer, focusing on the narrow distribution region. A library of discrete diblock copolymers consisting of oligo dimethylsiloxane (oDMS) and oligo lactic acid (oLA) blocks were modularly prepared with one monomer difference in composition, which form highly ordered nanostructures at room temperature. The molecular weight distribution of the oLA block was then precisely modulated through a reconstruction approach, achieving an absolute control on chain length heterogeneity. By meticulously tuning the breadth and symmetry of the distribution profile, the lattice dimension of the assembled nanostructure significantly expands, while no appreciable difference on the phase stability was observed. This work provides an explicit access to block copolymers with narrow dispersity that are not possible through conventional chemical approach, revealing the critical contribution of dispersity on self-assembly and bridging the existing gaps between experiments and theories.
topic Dispersity
Precision macromolecules
Block copolymer
Self-assembly
url http://www.sciencedirect.com/science/article/pii/S2666542520300400
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