Interpenetrating anion exchange membranes using poly(1-vinylimidazole) as bifunctional crosslinker for fuel cells

被引:76
作者
Guo, Dong [1 ]
Zhuo, Yi Zhi [1 ]
Lai, Ao Nan [1 ]
Zhang, Qiu Gen [1 ]
Zhu, Ai Mei [1 ]
Liu, Qing Lin [1 ]
机构
[1] Xiamen Univ, Fujian Prov Key Lab Theoret & Computat Chem, Dept Chem & Biochem Engn, Coll Chem & Chem Engn, Xiamen 361005, Peoples R China
基金
中国国家自然科学基金;
关键词
Anion exchange membranes; Fuel cells; Poly(1-vinylimidazole); Bifunctional crosslinker; Interpenetrating polymer networks; POLYMER ELECTROLYTE MEMBRANES; POLY(ARYLENE ETHER SULFONE)S; HYBRID MEMBRANES; PVA; PERFORMANCE;
D O I
10.1016/j.memsci.2016.07.006
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
There is a balance between ionic conductivity and dimensional stability in anion exchange membranes (AEMs). High conductivity resulting from densely charged groups is normally accompanied with high water uptake and excessive swelling. Herein, a series of novel AEMs with interpenetrating network was prepared by the incorporation of poly(vinylbenzyl chloride) (PVBC) and poly(1-vinylimidazole)(PVIm) into the PVA matrix. PVBC and PVIm act as bifunctional macromolecular crosslinking agents to provide both imidazolium cations and to form crosslinked network in the membranes. The resulting AEMs were characterized by Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM). The effect of crosslinking density on conductivity, water uptake, swelling ratio and stability was investigated. The results reveal that the addition of PVBC-c-PVIm could be simultaneously conducive to higher conductivity and lower swelling ratio. Notably, the membrane containing 50 wt% PVBC-c-PVIm had IEC of 1.86 meq g(-1), water uptake of 39.4%, and hydroxide conductivity of 21.9 mS cm(-1) at 30 degrees C. A maximum power density of 37.1 mW cm(-2) is achieved at a current density of 64 mA cm(-2). The crosslinked AEMs also exhibit excellent alkaline stability in a 4 M KOH solution at 60 degrees C for 1320 h. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:295 / 304
页数:10
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