Anion exchange membranes with clusters of alkyl ammonium group for mitigating water swelling but not ionic conductivity

被引:60
|
作者
Hossain, Md. Masem [1 ]
Hou, Jianqiu [1 ]
Wu, Liang [1 ]
Ge, Qianqian [1 ]
Liang, Xian [1 ]
Mondal, Abhishek N. [1 ]
Xu, Tongwen [1 ]
机构
[1] Univ Sci & Technol China, Sch Chem & Mat Sci, Collaborat Innovat Ctr Chem Energy Mat, CAS Key Lab Soft Matter Chem, Hefei 230026, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
Clustering; Bromination; Crosslinked membrane; Mitigating; Fuel cell; ALKALINE FUEL-CELLS; MULTIBLOCK POLY(ARYLENE ETHER)S; TRIBLOCK COPOLYMERS; CROSS-LINKING; SIDE-CHAINS; ACID GROUPS; STABILITY; HYDROXIDE; SULFONE); MORPHOLOGY;
D O I
10.1016/j.memsci.2017.12.062
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Crosslinked ionomers containing clusters of alkyl ammonium group at side chain was synthesized by attaching an unique amine (tris[2-(dimethylamino)ethyl]amine) on poly(2,6-dimethyl-1,4-phenylene oxide) (PPO) polymer backbone. These molecular structures show a dramatic enhancement in water resistance (low water uptake (9-13%) and dimensional swelling (4-6%) in water at room temperature) compared with non-cluster-shaped PPOs. Moreover, the temperature had less of an influence on the water uptake and swelling ratio of the membranes. The resulting anion exchange membranes exhibit good ionic (OH-) conductivities in water (up to 25.4 mS cm(-1) at 25 degrees C) and represent a new class of anion exchange membranes. A test of the alkaline stability of membranes (in 1 M KOH at 60 degrees C for 480 h) showed hydroxide conductivity about 51% of the original conductivity and indicated that these membranes are good candidates for application in alkaline fuel cells (AFCs). Membrane electrode assembly made from the as-fabricated membrane showed moderate fuel cell performance reaching peak power density 77 mW cm(-2) at 60 degrees C in a H-2/O-2 alkaline fuel cell. This simplistic synthetic tactic enables the preparation of densely functionalized materials with the potential to meet the demands of AFCs.
引用
收藏
页码:101 / 109
页数:9
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