Semi-interpenetrating network based on cross-linked poly(vinyl alcohol) and poly(styrene sulfonic acid-co-maleic anhydride) as proton exchange fuel cell membranes

被引:75
|
作者
Lin, C. W.
Huang, Y. F.
Kannan, A. M.
机构
[1] Arizona State Univ, Dept Elect Syst, Mesa, AZ 85212 USA
[2] Natl Yunlin Univ Sci & Technol, Dept Chem Engn, Yunlin, Taiwan
关键词
proton conducting membrane; semi-interpenetrating network; poly(vinyl alcohol); poly(styrene sulfonic acid-co-maleic acid); membrane electrode assembly; fuel cells;
D O I
10.1016/j.jpowsour.2006.10.081
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 series of promising proton conducting membranes have been synthesized by using poly(vinyl alcohol), with sulfosuccinic acid (SSA) as a cross-linking agent and poly(styrene sulfonic acid-co-maleic acid) (PSSA-MA) as proton source, which form a semi-interpenetrating network (semi-IPN) PVA/SSA/PSSA-MA membrane. A bridge of SSA between PVA molecules not only reinforces the network but also provides extra proton conducting paths. PSSA-MA chains trapped in the network were the major sources of protons in the membrane. FT-IR spectra confirmed the success of the cross-linking reaction and molecular interactions between PVA and PSSA-MA. Associated characteristics of a proton conducting membrane including ion-exchange capacity (IEC), proton conductivity and water uptake were investigated. The measured IECs of the membranes increased with increase of PSSA-MA content varying from 20 to 80% and correlated well with the measured uptake water and proton conductivity. The semi-IPN membranes with PSSA-MA over 60% exhibited a higher proton conductivity than Nafion-115 and also a reasonable level of water uptake. Fuel cell performance of membrane electrode assemblies (MEA) was evaluated at various temperatures with H-2/air as well as H-2/O gases under ambient pressure. A power density of 0.7 W cm(-2) was obtained for the MEA using PVA/SSA20/PSSA-MA80 membrane using H-2/O-2 at 50 degrees C. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:449 / 456
页数:8
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