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A Self‐Healing Dielectric Supramolecular Elastomer Functionalized with Aniline Tetramer
Author(s) -
Liu Ling,
Yan Shu,
Zhang Liqun
Publication year - 2018
Publication title -
macromolecular rapid communications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.348
H-Index - 154
eISSN - 1521-3927
pISSN - 1022-1336
DOI - 10.1002/marc.201800349
Subject(s) - supramolecular chemistry , materials science , dielectric , elastomer , amorphous solid , tetramer , hydrogen bond , self healing , supramolecular polymers , glass transition , stacking , composite material , crystallization , modulus , dynamic mechanical analysis , polymer chemistry , chemical engineering , polymer , molecule , crystallography , chemistry , organic chemistry , optoelectronics , medicine , enzyme , alternative medicine , pathology , engineering
A new design strategy to produce a supramolecular elastomer with self‐healing and dielectric properties by synthesizing an aniline tetramer (AT)‐functionalized supramolecular elastomer (SE‐AT) is demonstrated. The termination of AT in the supramolecular system not only shortens linear amide molecular chain to decrease glass transition temperature but also destroys the crystallization to achieve amorphous structure. The SE‐AT provides two kinds of noncovalent bonding including π–π stacking and the hydrogen bond, which makes the material more easily healed. The SE‐AT20% can heal mechanical properties within 24 h at room temperature without any external stimulus. The dielectric constant shows a continuous increase overall with increasing AT content. The material exhibits good electro‐mechanical properties, which is attributed to a simultaneous increase in dielectric constant and decrease in modulus. The maximum actuated strain significantly increases with the increasing AT content and the SE‐AT20% reaches 10% at 1 V µm −1 . Moreover, SE‐AT exhibits the ability to regain actuated strain on the location of the mechanical damage after self‐healing.