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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.
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页码:5882 / 5888
页数:7
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