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Catalyst Degradation Under Potential Cycling as an Accelerated Stress Test for PBI-Based High-Temperature PEM Fuel Cells-Effect of Humidification

机译:催化剂降解潜在循环作为PBI的高温PEM燃料电池的加速应力测试 - 加湿的效果

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In the present work, high-temperature polymer electrolyte membrane fuel cells were subjected to accelerated stress tests of 30,000 potential cycles between 0.6 and 1.0 V at 160 degrees C (133 h cycling time). The effect that humidity has on the catalyst durability was studied by testing either with or without humidification of the nitrogen that was used as cathode gas during cycling segments. Pronounced degradation was seen from the polarization curves in both cases, though permanent only in the humidified case. In the unhumidified case, the performance loss was more or less recoverable following 24 h of operation at 200 mA cm(-2). A difference in degradation behavior was verified with electron microscopy, X-ray diffraction, and electrochemical impedance spectroscopy. The strong effect of humidification is explained by drying of the phosphoric acid that is in the catalyst layer(s) versus maintaining humidification of this region. Catalyst degradation due to platinum dissolution, transport of its ions, and eventual recrystallization is reduced when this portion of the acid dries out. Consequently, catalyst particles are only mildly affected by the potential cycling in the unhumidified case.
机译:在本作工作中,在160℃(133 H循环时间)下,对高温聚合物电解质膜燃料电池进行加速30,000次电位循环的延长循环。通过在循环段期间的氮气的含量进行测试,研究了湿度对催化剂耐久性的影响。从两种情况下的极化曲线都观察到明显的劣化,但仅在加湿的情况下永久性。在未受吸收的情况下,在200mA cm(-2)的操作后24小时后,性能损失或多或少可恢复。用电子显微镜,X射线衍射和电化学阻抗光谱验证降解行为的差异。通过干燥在催化剂层中的磷酸与维持该区域的湿化的磷酸来解释加湿的强烈效果。当该部分酸干燥时,由于铂溶解而导致的催化剂降解,其离子输送和最终重结晶。因此,催化剂颗粒仅受到未受吸收的情况下的潜在循环的温和性影响。

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