Block copolymer self-assembly in ionic liquids
Author(s) -
Ryota Tamate,
Kei Hashimoto,
Takeshi Ueki,
Masayoshi Watanabe
Publication year - 2018
Publication title -
physical chemistry chemical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.053
H-Index - 239
eISSN - 1463-9084
pISSN - 1463-9076
DOI - 10.1039/c8cp04173c
Subject(s) - copolymer , ionic liquid , block (permutation group theory) , materials science , self assembly , ionic bonding , polymer chemistry , chemical engineering , polymer science , chemistry , nanotechnology , organic chemistry , ion , polymer , engineering , composite material , catalysis , mathematics , combinatorics
Ionic liquids (ILs), solely composed of cations and anions, are regarded as a novel class of promising liquids, potentially applicable to energy devices, reaction media, separation materials, etc. ILs have also attracted great attention as new media for molecular self-assembly, capable of producing novel soft materials with unique features never observed for conventional soft materials containing organic and aqueous solvents. In this review, we focus on recent developments in block copolymer (BCP) self-assembly in ILs. Self-assembled structures formed by dilute and concentrated BCP solutions in ILs are discussed in detail. Ion gels formed by BCP self-assembly have received special interest because they exhibit excellent physical properties of tunable viscoelasticity and solution processability without impairing the intrinsic properties of ILs, such as nonvolatility, nonflammability, and high ionic conductivity. Applications of ion gels based on BCP self-assembly for electric double layer capacitors, lithium-ion batteries, and electroactive soft actuators are also addressed.
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