4.7 Article

Template-assisted interfacial self-assembly of amphiphilic poly(ethylene oxide)-poly(propylene oxide)-based triblock copolymers for automatic control of molecular alignment

Journal

JOURNAL OF MOLECULAR LIQUIDS
Volume 343, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.molliq.2021.117593

Keywords

Amphiphilic triblock copolymer; Interfacial self-assembly; Liquid crystal; Molecular alignment; Polymer nanolayer

Funding

  1. National Research Foundation of Korea (NRF) - Korea government (MSIT) [NRF-2018R1A5A1024127]
  2. Korea Institute for Advancement of Technology (KIAT) - Korea Government (MOTIE) [P0012770]

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A hierarchical self-assembled nanoarchitecture based on the unique self-assembly of block copolymers has been developed for the nanofabrication of functionally versatile materials with a wide range of potential applications. The ultrafast responsive and highly reliable self-constructed polymer nanolayer was fabricated using template-assisted interfacial self-assembly, enabling automatic molecular alignment control. This approach demonstrated improved electro-optical switching speed and alignment stability compared to commercial polyimide layers.
Hierarchical self-assembled nanoarchitectures based on peculiar self-assembly of block copolymers are advantageous for the nanofabrication of functionally versatile materials with a wide range of potential applications from bioelectronic devices to flexible displays. Herein, we developed a simple yet efficient, cost-effective, scalable strategy for the fabrication of an ultrafast responsive and highly reliable self-constructed polymer nanolayer for automatic control of molecular alignment by using the template-assisted interfacial self-assembly of amphiphilic poly(ethylene oxide)-poly(propylene oxide)-based triblock copolymers. A new type of ultrathin polymer nanolayer was facilely fabricated on polar electrode surface using simple doping in liquid crystal (LC) medium and in situ interfacial self-assembly of a small amount of amphiphilic triblock copolymers in the closed LC cell. A hydrophobic and ultrathin polymer nanolayer with dense nanoneedle arrays formed by interfacial hydrogen bonding between hydrophilic poly(ethylene oxide) block and hydrophilic indium tin oxide electrode induces a spontaneous homeotropic alignment of LCs during programmed self-assembly process. Moreover, this facile approach endows the polymer nanolayer with ultrafast electro-optical switching and high molecular alignment force characteristics, as well as an excellent alignment stability during long-term operation. Compared to commercial polyimide layer, our polymer nanolayer accomplishes the ultrafast falling response time with an improvement of 55.3% and fast rising response time with a reduction of 36.4%. (C) 2021 Elsevier B.V. All rights reserved.

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