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Electrocatalytic activity mapping of model fuel cell catalyst films using scanning electrochemical microscopy

机译:使用扫描电化学显微镜对模型燃料电池催化剂薄膜的电催化活性作图

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Scanning electrochemical microscopy has been employed to spatially map the electrocatalytic activity of model proton exchange membrane fuel cell (PEMFC) catalyst films towards the hydrogen oxidation reaction (the PEMFC anode reaction). The catalyst films were composed of platinum-loaded carbon nanoparticles, similar to those typically used in PEMFCs. The electrochemical characterisation was correlated with a detailed physical characterisation using dynamic light scattering, transmission electron microscopy and field-emission scanning electron microscopy. The nanoparticles were found to be reasonably mono-dispersed, with a tendency to agglomerate into porous bead-type structures when spun-cast. The number of carbon nanoparticles with little or no platinum was surprisingly higher than would be expected based on the platinum-carbon mass ratio. Furthermore, the platinum-rich carbon particles tended to agglomerate and the clusters formed were non-uniformly distributed. This morphology was reflected in a high degree of heterogeneity in the film activity towards the hydrogen oxidation reaction.
机译:扫描电化学显微镜已被用于空间映射质子交换膜燃料电池(PEMFC)催化剂膜对氢氧化反应(PEMFC阳极反应)的电催化活性。催化剂膜由负载铂的碳纳米颗粒组成,类似于PEMFC中通常使用的那些。使用动态光散射,透射电子显微镜和场发射扫描电子显微镜,将电化学表征与详细的物理表征相关联。发现该纳米粒子合理地单分散,当纺丝时有聚集成多孔珠型结构的趋势。具有很少或没有铂的碳纳米颗粒的数量出乎意料地高于基于铂-碳质量比所预期的数量。此外,富铂碳颗粒趋于附聚并且形成的簇不均匀地分布。这种形态反映在膜对氢氧化反应的活性高度不均一性中。

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