Non-isothermal cold start of polymer electrolyte fuel cells
被引:128
作者:
Jiang, Fangming
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Penn State Univ, Dept Mech & Nucl Engn & Electrochem Engine Ctr, University Pk, PA 16802 USAPenn State Univ, Dept Mech & Nucl Engn & Electrochem Engine Ctr, University Pk, PA 16802 USA
Jiang, Fangming
[1
]
Fang, Weifeng
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Penn State Univ, Dept Mech & Nucl Engn & Electrochem Engine Ctr, University Pk, PA 16802 USAPenn State Univ, Dept Mech & Nucl Engn & Electrochem Engine Ctr, University Pk, PA 16802 USA
Fang, Weifeng
[1
]
Wang, Chao-Yang
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Penn State Univ, Dept Mech & Nucl Engn & Electrochem Engine Ctr, University Pk, PA 16802 USAPenn State Univ, Dept Mech & Nucl Engn & Electrochem Engine Ctr, University Pk, PA 16802 USA
Wang, Chao-Yang
[1
]
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[1] Penn State Univ, Dept Mech & Nucl Engn & Electrochem Engine Ctr, University Pk, PA 16802 USA
A multiphase, three-dimensional model has been developed to describe non-isothermal cold start of a polymer electrolyte fuel cell (PEFC) and to delineate intricate interactions between ice formation and heat generation during cold start. The effect of rising cell temperature is numerically explored by comparing a non-isothermal cold start with an isothermal one. It is found that more water is transported into the membrane and less ice formation occurs in the cathode catalyst layer (CL) in the presence of rising cell temperature. In addition, the more hydrated membrane and the rising cell temperature greatly lower the membrane resistance, thus giving rise to higher cell voltage. A lumped thermal analysis significantly over-estimates the overall thermal requirement of self-startup as a cell requires only a portion of its active area to reach the freezing point and be ice-free and operable. It is also found that pre-startup conditions have significant influence on cold start. Procedures to minimize residual water inside the cell prior to cold start, such as gas purge, are critically important. Finally, non-isothermal cold start becomes much easier from higher ambient temperatures. (c) 2007 Elsevier Ltd. All rights reserved.
机构:
Chinese Acad Sci, Dalian Inst Chem Phys, Fuel Cell Res & Dev Ctr, Dalian 116203, Peoples R ChinaChinese Acad Sci, Dalian Inst Chem Phys, Fuel Cell Res & Dev Ctr, Dalian 116203, Peoples R China
Hou, Junbo
Yu, Hongmei
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机构:Chinese Acad Sci, Dalian Inst Chem Phys, Fuel Cell Res & Dev Ctr, Dalian 116203, Peoples R China
Yu, Hongmei
Yi, Baolian
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机构:Chinese Acad Sci, Dalian Inst Chem Phys, Fuel Cell Res & Dev Ctr, Dalian 116203, Peoples R China
Yi, Baolian
Xiao, Yu
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机构:Chinese Acad Sci, Dalian Inst Chem Phys, Fuel Cell Res & Dev Ctr, Dalian 116203, Peoples R China
Xiao, Yu
Wang, Hongwei
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机构:Chinese Acad Sci, Dalian Inst Chem Phys, Fuel Cell Res & Dev Ctr, Dalian 116203, Peoples R China
机构:
Chinese Acad Sci, Dalian Inst Chem Phys, Fuel Cell Res & Dev Ctr, Dalian 116203, Peoples R ChinaChinese Acad Sci, Dalian Inst Chem Phys, Fuel Cell Res & Dev Ctr, Dalian 116203, Peoples R China
Hou, Junbo
Yu, Hongmei
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h-index: 0
机构:Chinese Acad Sci, Dalian Inst Chem Phys, Fuel Cell Res & Dev Ctr, Dalian 116203, Peoples R China
Yu, Hongmei
Yi, Baolian
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机构:Chinese Acad Sci, Dalian Inst Chem Phys, Fuel Cell Res & Dev Ctr, Dalian 116203, Peoples R China
Yi, Baolian
Xiao, Yu
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h-index: 0
机构:Chinese Acad Sci, Dalian Inst Chem Phys, Fuel Cell Res & Dev Ctr, Dalian 116203, Peoples R China
Xiao, Yu
Wang, Hongwei
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机构:Chinese Acad Sci, Dalian Inst Chem Phys, Fuel Cell Res & Dev Ctr, Dalian 116203, Peoples R China