Long Term Testing in Continuous Mode of HT-PEMFC Based H3PO4/PBI Celtec-P MEAs for μ-CHP Applications

被引:57
作者
Mocoteguy, Ph. [1 ]
Ludwig, B. [1 ]
Scholta, J. [2 ]
Barrera, R. [3 ]
Ginocchio, S. [3 ]
机构
[1] EIFER, European Inst Energy Res, D-76131 Karlsruhe, Germany
[2] Zentrum Sonnenenergie & Wasserstoff Forsch, D-89081 Ulm, Germany
[3] Ctr Ric & Sviluppo Trofarello, I-10028 Trofarello, TO, Italy
关键词
Cell Voltage Distribution; Continuous Mode; CO Effect; CO2; Effect; High Temperature PEMFC; Impedance Spectroscopy (EIS); Long Term Testing; Mass Transfer; Micro-CHP; Oxygen Effect; PBI/H3PO4; Performance Degradation; HIGH-TEMPERATURE PEMFC; POLYMER ELECTROLYTE MEMBRANES; ACID DOPED POLYBENZIMIDAZOLE; MICRO-COMBINED HEAT; FUEL-CELLS; PHOSPHORIC-ACID; PERFORMANCE DEGRADATION; OXYGEN REDUCTION; WATER; CONDUCTIVITY;
D O I
10.1002/fuce.200800134
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Fuel cells have a promising market in micro-combined heat and power (mu-CHP) applications by reducing primary energy demand and CO2 emissions. But current proton exchange membrane fuel cells (PEMFC) operate at too low temperatures to cope with return temperatures of typical heating systems and needs complex regulations at system level to prevent degradations. Operating beyond 150 degrees C, high temperature PEMFC (HT-PEMFC), based on H3PO4/PBI technology, would avoid these issues and allow system simplification. Single cell and 500 We stack integrating Celtec P1000 MEAs were operated in continuous made at 0.4 A cm(-2) and 160 degrees C, under simulated reformate and air. Single cell's ohmic resistivity was almost unaffected by 1,100 h of ageing but the cell progressively switched from a cathodic to an anodic mass transfer limited operation. The stack was operated for 658 h, exhibiting the same behaviour and an additional increase in cell voltage distribution heterogeneity. CO2 proved to have negligible effect on performances but performance losses induced by ageing are doubled in the presence of CO. Post-testing experiments revealed that anode electrochemical active area was dramatically decreased and that platinum content was also decreased. Finally, results showed that a convenient shut-down procedure could prevent or limit degradations associated with storage.
引用
收藏
页码:325 / 348
页数:24
相关论文
共 45 条
[1]  
BAURMEISTER J, 2004, Patent No. 2004034498
[2]   THE ANALYSIS OF ELECTRODE IMPEDANCES COMPLICATED BY THE PRESENCE OF A CONSTANT PHASE ELEMENT [J].
BRUG, GJ ;
VANDENEEDEN, ALG ;
SLUYTERSREHBACH, M ;
SLUYTERS, JH .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1984, 176 (1-2) :275-295
[3]  
CALUNDANN G, 2003, Patent No. 10144815
[4]  
CALUNDANN G, 2004, Patent No. 10239701
[5]   TEMPERATURE-DEPENDENCE OF THE TAFEL SLOPE FOR OXYGEN REDUCTION ON PLATINUM IN CONCENTRATED PHOSPHORIC-ACID [J].
CLOUSER, SJ ;
HUANG, JC ;
YEAGER, E .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 1993, 23 (06) :597-605
[6]  
COLELLA W, 2002, J POWER SOURCES, P106
[7]   PROTON CONDUCTIVITY IN FUSED PHOSPHORIC-ACID - A H-1 P-31 PFG-NMR AND QNS STUDY [J].
DIPPEL, T ;
KREUER, KD ;
LASSEGUES, JC ;
RODRIGUEZ, D .
SOLID STATE IONICS, 1993, 61 (1-3) :41-46
[8]  
GAUTIER L, 2007, Z ENERGIEWIRTSCHAFT, V31, P4
[9]  
Hamann C.H., 2007, Electrochemistry
[10]  
He C., 2005, ELECTROCHEM SOC INTE, V14, P41