Christopher L. Schreiber, Anna M. Kapulwa, Sonja Blaseio, Hui Jing Cham, Mehtap Oezaslan, Junji Inukai
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引用次数: 0
摘要
在聚合物电解质燃料电池的运行过程中,物理和化学参数(如温度、水/氢/氧分压)在电池内部的分布是不均匀的,对电池的性能和耐久性有很大的影响。在本研究中,在温度为80、100和110°C的发电过程中,使用20 mm × 20 mm具有10个直气流通道的单个电池,在气体扩散层(GDL)表面使用氧敏染料实时/空间地显示了氧气分压(p(O2))。在高于100°C的温度下,GDL表面的p(O2)首次被可视化,这尤其适用于重型车辆应用,因为它具有诸如对催化剂中毒的敏感性较小以及可选择使用更小更轻的散热器等优点。监测到gdl表面的氧分压高于简单模型的预期值,并且随着电流密度的增加,沿气体流道仅略有下降。研究表明,GDL表面的高p(O2)是由于气体流道短和在GDL内部积累的水蒸汽和催化剂层限制了气体的扩散。
Visualization of the Oxygen Partial Pressure on the Gas Diffusion Layer inside a Polymer Electrolyte Fuel Cell during Cell Operation at Temperatures Higher than 100 °C
Physical and chemical parameters, such as temperature, water/hydrogen/oxygen partial pressures, are distributed inhomogeneous inside a polymer electrolyte fuel cell during the operation and have a large influence on its performance and durability. In this study, the oxygen partial pressure (p(O2)) is visualized in real-time/space using an oxygen-sensitive dye on the surface of the gas diffusion layer (GDL) during power generation at temperatures of 80, 100, and 110 °C using a 20 mm × 20 mm single cell with ten straight gas flow channels. p(O2) on the surface of the GDL is visualized for the first time at temperatures higher than 100 °C, desired especially for heavy-duty vehicle application, due to advantages such as less susceptibility to catalyst poisoning and the option to use smaller and lighter radiators. The oxygen partial pressure on the surface of the GDLs is monitored to be higher than the values expected from a simple model and decreased only slightly along the gas flow channel with increasing current densities. The work shows that high p(O2) on the surface of the GDL is due to the short gas flow channels and accumulating water/vapor inside the GDL and the catalyst layer limiting the gas diffusion.
期刊介绍:
ChemElectroChem is aimed to become a top-ranking electrochemistry journal for primary research papers and critical secondary information from authors across the world. The journal covers the entire scope of pure and applied electrochemistry, the latter encompassing (among others) energy applications, electrochemistry at interfaces (including surfaces), photoelectrochemistry and bioelectrochemistry.