Highly fluorinated comb-shaped copolymers as proton exchange membranes (PEMs): Improving PEM properties through rational design

被引:167
作者
Norsten, Tyler B.
Guiver, Michael D.
Murphy, Jeffrey
Astill, Toby
Navessin, Titichai
Holdcroft, Steven
Frankamp, Benjamin L.
Rotello, Vincent M.
Ding, Jianfu
机构
[1] Natl Res Council Canada, Inst Chem Proc & Environm Technol, Ottawa, ON K1A 0R6, Canada
[2] CNR, Inst Fuel Cell Innovat, Vancouver, BC VT6 1W5, Canada
[3] Simon Fraser Univ, Dept Chem, Burnaby, BC V5A 1S6, Canada
[4] Univ Massachusetts, Dept Chem, Amherst, MA 01003 USA
关键词
D O I
10.1002/adfm.200500763
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new class of comb-shaped polymers for use as a proton conducting membrane is presented. The polymer is designed to combine the beneficial physical, chemical, and structural attributes of fluorinated Nafion-like materials with higher-temperature, polyaromatic-based polymer backbones. The comb-shaped polymer unites a rigid, polyaromatic, hydrophobic backbone with lengthy hydrophilic polymer side chains; this combination affords direct control over the polymer nanostructure within the membrane and results in distinct microphase separation between the opposing domains. The microphase separation serves to compartmentalize water into the hydrophilic polymer side chain domains, resulting in effective membrane water management and excellent proton conductivities.
引用
收藏
页码:1814 / 1822
页数:9
相关论文
共 29 条
[1]   PREPARATION OF OXIDATIVELY STABLE CATION-EXCHANGE MEMBRANES BY THE ELIMINATION OF TERTIARY HYDROGENS [J].
ASSINK, RA ;
ARNOLD, C ;
HOLLANDSWORTH, RP .
JOURNAL OF MEMBRANE SCIENCE, 1991, 56 (02) :143-151
[2]   Enhanced conductivity in morphologically controlled proton exchange membranes: Synthesis of macromonomers by SFRP and their incorporation into graft polymers [J].
Ding, JF ;
Chuy, C ;
Holdcroft, S .
MACROMOLECULES, 2002, 35 (04) :1348-1355
[3]  
ELADB YA, 2004, J MEMBRANE SCI, V231, P181
[4]   SMALL-ANGLE X-RAY-SCATTERING STUDY OF PERFLUORINATED IONOMER MEMBRANES .2. MODELS FOR IONIC SCATTERING MAXIMUM [J].
FUJIMURA, M ;
HASHIMOTO, T ;
KAWAI, H .
MACROMOLECULES, 1982, 15 (01) :136-144
[5]   New multiblock copolymers of sulfonated poly(4′-phenyl-2,5-benzophenone) and poly(arylene ether sulfone) for proton exchange membranes.: II [J].
Ghassemi, H ;
Ndip, G ;
McGrath, JE .
POLYMER, 2004, 45 (17) :5855-5862
[6]  
GHASSEMI H, 2004, POLYM PREPR, V45, P68
[7]   Alternative polymer systems for proton exchange membranes (PEMs) [J].
Hickner, MA ;
Ghassemi, H ;
Kim, YS ;
Einsla, BR ;
McGrath, JE .
CHEMICAL REVIEWS, 2004, 104 (10) :4587-4611
[8]   EPR investigation of HO. radical initiated degradation reactions of sulfonated aromatics as model compounds for fuel cell proton conducting membranes [J].
Hübner, G ;
Roduner, E .
JOURNAL OF MATERIALS CHEMISTRY, 1999, 9 (02) :409-418
[9]   Fuel cell membrane materials by chemical grafting of aromatic main-chain polymers [J].
Jannasch, P .
FUEL CELLS, 2005, 5 (02) :248-260
[10]   Polysulfone ionomers for proton-conducting fuel cell membranes: sulfoalkylated polysulfones [J].
Karlsson, LE ;
Jannasch, P .
JOURNAL OF MEMBRANE SCIENCE, 2004, 230 (1-2) :61-70