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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:催化剂降解在潜在循环下作为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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摘要

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 textdegreeC (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. 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篇文本(133 H循环时间)下,在0.6和1.0V之间进行30,000次电位循环的高温聚合物电解质膜燃料电池加速胁迫试验。通过在循环段期间使用或不加湿在循环段期间使用作为阴极气体的氮气进行湿润来研究湿度对催化剂耐久性的影响。两种情况下的极化曲线看到明显的劣化,但仅在加湿案例中永久性。在未经保育情况下,在200 mA cm的操作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效果。当该部分酸干燥时,催化剂降解,其离子的转运和最终重结晶。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的温和性。

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