Poly(ionic liquid)s: an emerging platform for green chemistry

被引:6
|
作者
Zhu, Maiyong [1 ]
Yang, Yu [1 ]
机构
[1] Jiangsu Univ, Res Sch Polymer Mat, Sch Mat Sci & Engn, Zhenjiang 212013, Peoples R China
关键词
POLYMERIZED IONIC LIQUID; DOPED POROUS CARBON; ELECTROCHEMICAL SENSOR; CO2; CAPTURE; POLYIONIC LIQUID; OXIDE NANOSHEETS; AQUEOUS-SOLUTION; ELECTROLYTES; EFFICIENT; COMPOSITE;
D O I
10.1039/d4gc00202d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Recently, poly(ionic liquid)s (PILs) have emerged as a family of polymeric materials which are being increasingly investigated for interdisciplinary applications. Their high electrical conductivity, excellent thermal/mechanical stability, low vapor pressure, and easy processibility render PILs exceptionally attractive as versatile platforms for green chemistry. Recent decades have witnessed fruitful efforts devoted to the development of PIL-based green chemistry platforms, achieving significant discoveries that will unfold their uniqueness in catalysis, separation, sensors, electrolyte, and functional materials. However, few review papers offer comprehensive discussion on PILs' application in the green chemistry field. In this review, we initially introduce the structure and types of PILs, which is followed by a systematical summary of the synthesis of PILs in terms of direct polymerization of monomer, polymerization after monomer modification, and modification of polymers. Furthermore, several aspects of the application of PILs related to green chemistry are highlighted, such as sensors, separation, catalysis, electrolytes for energy storage devices, and as versatile precursors yielding functional materials. Current challenges and corresponding research directions in PILs for green chemistry are clarified, to make PILs truly green platforms for existing technologies. This tutorial review provides a comprehensive and authoritative summary on the exciting research activities in the fields of poly(ionic liquid)s (PILs), covering their synthesis and their applications in a number of areas.
引用
收藏
页码:5022 / 5102
页数:81
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