Balancing dimensional stability and performance of proton exchange membrane using hydrophilic nanofibers as the supports

被引:17
作者
Wang, Zhengbang [1 ,2 ]
Tang, Haolin [1 ]
Li, Junrui [1 ]
Jin, Aiping [3 ]
Wang, Zhao [1 ]
Zhang, Huijie [1 ]
Pan, Mu [1 ]
机构
[1] Wuhan Univ Technol, State Key Lab Adv Technol Mat Synth & Proc, Wuhan 430070, Peoples R China
[2] Karlsruhe Inst Technol, IFG, D-76344 Eggenstein Leopoldshafen, Germany
[3] Wuhan Text Univ, Sch Chem & Chem Engn, Wuhan 40073, Peoples R China
关键词
PEM fuel cell; Proton exchange membrane; Durability; Humidity-induced stress; Dynamic response; HIGH-TEMPERATURE; FUEL-CELL; DYNAMIC-BEHAVIOR; DEGRADATION; DURABILITY; FABRICATION;
D O I
10.1016/j.ijhydene.2013.01.176
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
In this work, we developed a novel composite membrane by anchoring perfluorosulfonic acid into the hydrophilic poly(lactic-co-glycolic acid) (PLGA) nanofibrous network which was synthesized by electrospinning method. It was clear that the PLGA/Nafion composite membranes possessed high Nafion loading, excellent dimensional stability and proton transport capacity. When the humidity of the membrane changed from soaking in water to 25 RH% at 90 degrees C, the PLGA fiber network effectively controlled the swelling of Nafion resin and reduced the humidity-generated shrinkage stress from 2.2 MPa (Nafion211 membranes) to 0.5 MPa (PLGA/Nafion composite membranes). The proportion of humidity-induced stress to the yield strength was also reduced to 4.4%, in comparison to 21.2% of that of Nafion211 membrane. The area proton conductivity of the PLGA/Nafion composite membrane achieved 48.2 S cm(-2), compared with 36.0 S cm(-2) of Nafion211 membranes in the same condition. The excellent proton transport capacity greatly improved the performance of fuel cell assembled with PLGA/Nafion composite membranes and effectively reduced the dynamic response time from 22 s (Nafion211 membranes) to 7 s (PLGA/Nafion composite membranes). Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:4725 / 4733
页数:9
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