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Development of Operando Confocal Microprobe X-ray Fluorescence Techniques to Measure Cation Transport in PEM Fuel Cells

机译:开发Outmando共聚焦微竞和X射线荧光技术,以测量PEM燃料电池阳离子输送

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State of the art proton exchange membrane (PEM) fuel cells often use PtM (M= Co or Ni) as cathode catalysts and Ce-based additives in the membrane in order to enhance their performance and durability. During operation, however, these metals dissolve and cations transport from their initial positions, which decreases their efficacy and can cause fouling of ionomer regions, resulting in performance losses and local membrane failure. Here, we report the development of a confocal microprobe X-ray fluorescence technique to directly observe transient, μm-scale through-thickness migration of Ce~(3+) cations, in operando for the first time. At 80°C and 50% RH, Ce~(3+) migrates from the PEM into ionomer regions of the cathode catalyst layer (CL), saturating the CL ionomer and forming a gradient in the PEM after around 10 minutes at 100 mA cm~(-2). Upon removal of load, Ce~(3+) diffuses and equilibrates between ionomer regions of the CL and PEM. These results demonstrate the rapid effects of cation transport in the through-thickness direction over the range of current densities tested (50-100 mA cm~(-2)).
机译:现有技术的质子交换膜(PEM)燃料电池通常使用PTM(M = CO或Ni)作为阴极催化剂和膜中的CE基添加剂,以提高它们的性能和耐久性。然而,在运行过程中,这些金属溶解和阳离子从其初始位置运输,这降低了它们的功效,并可能导致离聚物区的污垢,导致性能损失和局部膜失效。在这里,我们首次报告了共聚焦微竞和X射线荧光技术的开发,直接观察Ce〜(3+)阳离子的瞬态,μm级通过厚度迁移,首次在Operando中。在80℃和50%RH下,Ce〜(3+)从PEM迁移到阴极催化剂层(Cl)的离聚物区域中,饱和Cl离聚物并在100 mA cm的约10分钟后在PEM中形成梯度〜(-2)。除去载荷后,Ce〜(3+)在CL和PEM的离聚物区域之间扩散和平衡。这些结果证明了在测试的电流密度范围内阳离子输送在通过厚度方向上的快速影响(50-100mA cm〜(-2))。

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