Volume 14, Issue 1 1702439
Full Paper

Asymmetric Fullerene Nanosurfactant: Interface Engineering for Automatic Molecular Alignments

Dae-Yoon Kim

Dae-Yoon Kim

BK21 Plus Haptic Polymer Composite Research Team & Department of Polymer-Nano Science and Technology, Chonbuk National University, Jeonju, 54896 South Korea

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Sang-A Lee

Sang-A Lee

BK21 Plus Haptic Polymer Composite Research Team & Department of Polymer-Nano Science and Technology, Chonbuk National University, Jeonju, 54896 South Korea

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Soeun Kim

Soeun Kim

BK21 Plus Haptic Polymer Composite Research Team & Department of Polymer-Nano Science and Technology, Chonbuk National University, Jeonju, 54896 South Korea

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Changwoon Nah

Changwoon Nah

BK21 Plus Haptic Polymer Composite Research Team & Department of Polymer-Nano Science and Technology, Chonbuk National University, Jeonju, 54896 South Korea

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Seung Hee Lee

Seung Hee Lee

Department of BIN Convergence Technology, Chonbuk National University, Jeonju, 54896 South Korea

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Kwang-Un Jeong

Corresponding Author

Kwang-Un Jeong

BK21 Plus Haptic Polymer Composite Research Team & Department of Polymer-Nano Science and Technology, Chonbuk National University, Jeonju, 54896 South Korea

E-mail: [email protected]Search for more papers by this author
First published: 14 November 2017
Citations: 14

Abstract

Since the molecular self-assembly of nanomaterials is sensitive to their surface properties, the molecular packing structure on the surface is essential to build the desired chemical and physical properties of nanomaterials. Here, a new nanosurfactant is proposed for the automatic construction of macroscopic surface alignment layer for liquid crystal (LC) molecules. An asymmetric nanosurfactant (C60NS) consisted of mesogenic cyanobiphenyl moieties with flexible alkyl chains and a [60]fullerene nanoatom is newly designed and precisely synthesized. The C60NS directly introduced in the anisotropic LC medium is self-assembled into the monolayered protrusions on the surface because of its amphiphilic nature originated by asymmetrically programmed structural motif of LC-favoring moieties and LC-repelling groups. The monolayered protrusions constructed by the phase-separation and self-assembly of asymmetric C60NS nanosurfactant in the anisotropic LC media amplify and transfer the molecular orientational order from surface to bulk, and finally create the automatic vertical molecular alignment on the macroscopic length scale. The asymmetric C60NS nanosurfactant and its self-assembly described herein can offer the direct guideline of interface engineering for the automatic molecular alignments.

Conflict of Interest

The authors declare no conflict of interest.

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