Conductivity and electrochemical ORR mass transport properties of solid polymer electrolytes containing poly(styrene sulfonic acid) graft chains

被引:33
作者
Chuy, C
Ding, JF
Swanson, E
Holdcroft, S [1 ]
Horsfall, J
Lovell, KV
机构
[1] Simon Fraser Univ, Dept Chem, Burnaby, BC V5A 1S6, Canada
[2] Cranfield Univ, Dept Mat & Med Sci, Swindon SN6 8LA, Wilts, England
关键词
D O I
10.1149/1.1561632
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Graft copolymers (PAN-g-macPSSNa) were prepared by copolymerization of acrylonitrile with poly(sodium styrene sulfonate) macromonomers (macPSSNa). Macromonomers were prepared by stable free radical polymerization. Polymers containing different graft chain densities were solvent-cast to provide a series of membranes of varying ionic content. Membranes were protonated and characterized with respect to water content, ionic conductivity, and as a medium for the electrochemical reduction of oxygen. Membrane properties were compared to other solid polymer electrolytes containing poly(styrenesulfonic acid) graft chains. Compared to analogous membranes that contain the more hydrophobic polystyrene backbone, polyacrylonitrile-based membranes uptake more water for a given ion exchange capacity. This has the effect of lowering proton conductivity, due to dilution of ions; increasing the diffusion coefficient of oxygen; and decreasing the oxygen solubility in the membrane. Due to the offsetting effects of the increased diffusion coefficient and decreased solubility, the oxygen permeability through polystyrene- and polyacryonitrile-based membranes is similar for a given ion exchange capacity. (C) 2003 The Electrochemical Society.
引用
收藏
页码:E271 / E279
页数:9
相关论文
共 33 条
[11]   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
[12]   A self-organized network of nanochannels enhances ion conductivity through polymer films [J].
Ding, JF ;
Chuy, C ;
Holdcroft, S .
CHEMISTRY OF MATERIALS, 2001, 13 (07) :2231-+
[13]   Electrophysical properties of polymer electrolyte membranes: A random network model [J].
Eikerling, M ;
Kornyshev, AA ;
Stimming, U .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (50) :10807-10820
[14]   Proton transfer in a single pore of a polymer electrolyte membrane [J].
Eikerling, M ;
Kornyshev, AA .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2001, 502 (1-2) :1-14
[15]   Mechanisms of proton conductance in polymer electrolyte membranes [J].
Eikerling, M ;
Kornyshev, AA ;
Kuznetsov, AM ;
Ulstrup, J ;
Walbran, S .
JOURNAL OF PHYSICAL CHEMISTRY B, 2001, 105 (17) :3646-3662
[16]   MEASUREMENT OF MEMBRANE CONDUCTIVITIES USING AN OPEN-ENDED COAXIAL PROBE [J].
GARDNER, CL ;
ANANTARAMAN, AV .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1995, 395 (1-2) :67-73
[17]   Small-angle scattering study of short pendant chain perfuorosulfonated ionomer membranes [J].
Gebel, G ;
Moore, RB .
MACROMOLECULES, 2000, 33 (13) :4850-4855
[18]   Small-angle scattering study of water-swollen perfluorinated ionomer membranes [J].
Gebel, G ;
Lambard, J .
MACROMOLECULES, 1997, 30 (25) :7914-7920
[19]   Structural evolution of water swollen perfluorosulfonated ionomers from dry membrane to solution [J].
Gebel, G .
POLYMER, 2000, 41 (15) :5829-5838
[20]  
Gupta B, 1996, J POLYM SCI POL CHEM, V34, P1873