Enhanced ionic conductivity of anion exchange membranes by grafting flexible ionic strings on multiblock copolymers

被引:13
|
作者
Lai, Ao Nan [1 ]
Zhuo, Yi Zhi [2 ]
Hu, Peng Cheng [1 ]
Zheng, Jing Wei [1 ]
Zhou, Shu Feng [1 ]
Zhang, Lei [3 ]
机构
[1] Huaqiao Univ, Coll Chem Engn, Xiamen 361021, Peoples R China
[2] Norwegian Univ Sci & Technol NTNU, Dept Struct Engn, NTNU Nanomech Lab, N-7491 Trondheim, Norway
[3] Fujian Univ Technol, Coll Mat Sci & Engn, Fuzhou 350118, Peoples R China
关键词
Anion exchange membrane; Ionic strings; Multiblock copolymers; Phenolphthalein group; Hydroxide conductivity; POLY(ARYLENE ETHER SULFONE)S; QUATERNARY AMMONIUM GROUPS; FUEL-CELLS; SIDE-CHAINS; CHEMICAL-STABILITY; IMIDAZOLIUM; WATER; PERFORMANCE; MORPHOLOGY; CATIONS;
D O I
10.1016/j.ijhydene.2019.11.090
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A new strategy to prepare high-conductivity anion exchange membranes (AEMs) is presented here. A series of phenolphthalein-based poly(arylene ether sulfone nitrile) multiblock AEMs has been synthesized by selectively grafting flexible ionic strings on hydrophilic segments to form ionic regions. Moreover, the phenolphthalein groups are introduced to force chains apart and create additional interchain spacing. In addition, the nitrile groups suspended on main chains are aimed at enhancing the anti-swelling behavior of as-prepared AEMs. Along these processes, well-defined phase separation has been attained, forming excellent ion-transport channels. The effective phase separation has been confirmed by atomic force microscopy. Finally, as-prepared AEMs exhibit a high hydroxide conductivity, ranging from 40.1 to 121.6 mS cm(-1) in the temperature range of 30 -80 degrees C, and superior ionic conductivity to IEC ratio at 80 degrees C. Furthermore, excellent thermal stability and desirable mechanical strength have been rendered by as-prepared AEMs. However, the alkaline stability of as-prepared AEMs requires further optimization. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1998 / 2008
页数:11
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