PEM fuel cells operated at 0% relative humidity in the temperature range of 23-120°C

被引:116
作者
Zhang, Jianlu [1 ]
Tang, Yanghua [1 ]
Song, Chaojie [1 ]
Cheng, Xuan [1 ]
Zhang, Jiujun [1 ]
Wang, Haijiang [1 ]
机构
[1] Xiamen Univ, Dept Mat Sci & Engn, State Key Lab Phys Chem Solid Surfaces, Xiamen 361005, Peoples R China
基金
中国国家自然科学基金;
关键词
PEM fuel cells; high temperature; dry reactant gas (or 0% relative humidity); external humidification;
D O I
10.1016/j.electacta.2007.02.002
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Operation of a proton exchange membrane (PEM) fuel cell without external humidification (or 0% relative humidity, abbreviated as 0% RH) of the reactant gases is highly desirable, because it can eliminate the gas humidification system and thus decrease the complexity of the PEM fuel cell system and increase the system volume power density (W/l) and weight power density (W/kg). In this investigation, a PEM fuel cell was operated in the temperature range of 23-120 degrees C, in particular in a high temperature PEM fuel cell operation range of 80-120 degrees C, with dry reactant gases, and the cell performance was examined according to varying operation parameters. An ac impedance method was used to compare the performance at 0% RH with that at 100% RH; the results suggested that the limited proton transfer process to the Pt catalysts, mainly in the inonomer within the membrane electrode assembly (MEA) could be responsible for the performance drop. It was demonstrated that operating a fuel cell using a commercially available membrane (Nafion (R) 112) is feasible under certain conditions without external humidification. However, the cell performance at 0% RH decreased with increasing operation temperature and reactant gas flow rate and decreasing operation pressure. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5095 / 5101
页数:7
相关论文
共 57 条
[21]   Nafion/ZrSPP composite membrane for high temperature operation of PEMFCs [J].
Kim, YT ;
Song, MK ;
Kim, KH ;
Park, SB ;
Min, SK ;
Rhee, HW .
ELECTROCHIMICA ACTA, 2004, 50 (2-3) :645-648
[22]   The effect of platinum loading in the self-humidifying polymer electrolyte membrane on water uptake [J].
Kwak, SH ;
Yang, TH ;
Kim, CS ;
Yoon, KH .
JOURNAL OF POWER SOURCES, 2003, 118 (1-2) :200-204
[23]  
Larminie James., 2000, FUEL CELL SYSTEMS EX, DOI DOI 10.1002/9781118878330
[24]   Development of novel self-humidifying composite membranes for fuel cells [J].
Liu, FQ ;
Yi, BL ;
Xing, DM ;
Yu, JR ;
Hou, ZJ ;
Fu, YZ .
JOURNAL OF POWER SOURCES, 2003, 124 (01) :81-89
[25]   Membrane-supported nonvolatile acidic electrolytes allow higher temperature operation of proton-exchange membrane fuel cells [J].
Malhotra, S ;
Datta, R .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1997, 144 (02) :L23-L26
[26]   A WATER AND HEAT MANAGEMENT MODEL FOR PROTON-EXCHANGE-MEMBRANE FUEL-CELLS [J].
NGUYEN, TV ;
WHITE, RE .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1993, 140 (08) :2178-2186
[27]   Measurement of current distribution in a free-breathing PEMFC [J].
Noponen, M ;
Mennola, T ;
Mikkola, M ;
Hottinen, T ;
Lund, P .
JOURNAL OF POWER SOURCES, 2002, 106 (1-2) :304-312
[28]   Theory for water management in membranes for polymer electrolyte fuel cells - Part 2. The effect of impurity ions at the cathode side on the membrane performances [J].
Okada, T .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1999, 465 (01) :18-29
[29]   Modelistic interpretation of the impedance response of a polymer electrolyte fuel cell [J].
Paganin, VA ;
Oliveira, CLF ;
Ticianelli, EA ;
Springer, TE ;
Gonzalez, ER .
ELECTROCHIMICA ACTA, 1998, 43 (24) :3761-3766
[30]   TEMPERATURE-DEPENDENCE OF THE ELECTRODE-KINETICS OF OXYGEN REDUCTION AT THE PLATINUM NAFION(R) INTERFACE - A MICROELECTRODE INVESTIGATION [J].
PARTHASARATHY, A ;
SRINIVASAN, S ;
APPLEBY, AJ ;
MARTIN, CR .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1992, 139 (09) :2530-2537