Proton conductive inorganic-organic hybrid membranes functionalized with phosphonic acid for polymer electrolyte fuel cell

被引:31
|
作者
Umeda, Junji [1 ]
Suzuki, Masashi [2 ]
Kato, Masaki [2 ]
Moriya, Makoto [1 ]
Sakamoto, Wataru [1 ]
Yogo, Toshinobu [1 ]
机构
[1] Nagoya Univ, Div Nanomat Sci, EcoTopia Sci Inst, Chikusa Ku, Nagoya, Aichi 4648603, Japan
[2] Aichi Ind Technol Inst, Div Res & Dev, Aichi 4480003, Japan
关键词
Inorganic-organic hybrid; Proton-conducting membrane; Sol-gel process; Phosphonic acid; Fuel cell; DIFFERENTIAL SCANNING CALORIMETRY; INTERMEDIATE TEMPERATURE; SULFONATED POLYIMIDES; PROTOGENIC GROUP; PERFORMANCE; 3-GLYCIDOXYPROPYLTRIMETHOXYSILANE; DIFFUSION; GELS; NMR;
D O I
10.1016/j.jpowsour.2009.12.078
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
Proton conductive sol-gel derived hybrid membranes were synthesized from aromatic derivatives of methoxysilanes and ethyl 2-[3-(dihydroxyphosphoryl)-2-oxapropyl]acrylate (EPA). Two aromatic derivatives of methoxysilanes with different number of methoxy groups were used as the starting materials. Hybrid membranes from difunctional (methyldimethoxysilylmethyl)styrene (MDMSMS(D))/EPA revealed a higher chemical stability and mechanical properties than those from monofunctional (dimethylmethoxysilylmethyl)styrene (DMMSMS(M))/EPA. The membrane-electrode assembly (MEA) using the hybrid membranes as electrolytes worked as a fuel cell at 100 degrees C under saturated humidity. The DMMSMS(M)/EPA membrane-based MEA showed a larger current density than that from MDMSMS(D)/EPA. On the other hand, the MDMSMS(D)/EPA membrane-based MEA exhibited higher open circuit voltages than the DMMSMS(M)/EPA-based MEA, and was stable during fuel cell operation at 80 degrees C at least for 48 h. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:5882 / 5888
页数:7
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