Search

Abstract: This work presents a study of multi-phase flow through the cathode side of a polymer electrolyte membrane fuel cell employing an interdigitated flow field plate. A previously published model has been extended in order to account for phase change kinetics, and a comparison between the interdigitated flow field design and a conventional straight channel design has been conducted. It is found that the parasitic pressure drop in the interdigitated design is in the range of a few thousand Pa and could be reduced to a few hundred Pa by choosing diffusion media with high in-plane permeability. The additional compressor work due to the increased pressure loss will only slightly increase, and this may be offset by operating at lower stoichiometries as the interdigitated design is less mass transfer controlled, which means that the overall efficiency of the interdigitated arrangement will be higher. In the interdigitated design more product water is carried out of the cell in the vapor phase compared to the straight channel design which indicates that liquid water management might be less problematic. This effect also leads to the finding that in the interdigitated design more waste heat is carried out of the cell in the form of latent heat which reduces the load on the coolant. Finally we see that the micro-porous layer might help keep the gas diffusion layer substrate dry due to a potentially higher evaporation rate caused by a combination of the Kelvin effect and a larger specific surface area compared to the diffusion layer substrate. [Copyright &y& Elsevier]

A new platinum group metal (PGM)-free proton exchange membrane fuel cell (PEMFC) cathode catalyst materials, synthesized using the VariPore™ method by Pajarito Powder, LLC, are characterized for their structure and activity. The physico-chemical analysis of the iron-nitrogen-carbon (Fe-N-C) electrocatalysts show mesoporous carbon material effectively doped with iron and nitrogen. The materials have an average pore size of 7–8 nm and high specific surface area. The Fe-N-C catalysts exhibit good oxygen reduction reaction (ORR) activity in 0.5 M H 2 SO 4 electrolyte with high half-wave potential and sustainable electrochemical stability over 10,000 repeated potential cycles with insignificant losses in their activities. As cathode catalysts in a PEMFC, the Fe-N-C materials deliver remarkably good fuel cell performance at low overpotential approaching that of the commercial Pt catalyst. The high ORR electrocatalytic activity of these Fe-N-C catalysts is credited to the synergy between nitrogen-moieties, specifically pyrrolic-N, pyridinic-N, and graphitic-N, and iron in addition to the high mesoporosity that facilitate an effective reaction path in boosting the electrocatalytic activity and stability. [Display omitted] • State-of-the-art commercial PGM-free catalysts for ORR were characterized and evaluated. • Was shown that active centres are atomically dispersed. • Performance of electrocatalysts was evaluated in industrially manufactured MEA form-factor. • The fuel cell performance is close to the state-of-the-art R&D PGM-free catalysts. [ABSTRACT FROM AUTHOR]