Abstract

Metallic bipolar plates are of increasing interest to automotive polymer electrolyte membrane fuel cell (PEMFC) manufacturers due to their low cost, high power density, ease of manufacture, high conductivity and good mechanical properties but minimising the undesirable effects of corrosion remains a key challenge. Unfortunately, reliable assessment of the applicability of stainless steels with a range of coatings and surface treatments has been hampered by a lack of representative ex situ test methods. Here we characterise the local environment experienced by a bipolar plate during fuel cell operation via in situ measurement of pH and corrosion potential for an uncoated 316L stainless steel bipolar plate in a single cell PEMFC. We demonstrate that the degradation mode is more akin to corrosion in relatively dilute thin liquid layers, rather than the fully immersed conditions employed in conventional ex situ screening tests. A key observation is that the corrosion potential of the bipolar plate is only weakly coupled to the potential of the nearest Pt electrode due to the low ionic conductivity of the discontinuous aqueous phase in the gas diffusion layer (GDL). However, localised polarisation of the steel can occur in the presence of oxygen as a result of galvanic coupling with the carbon GDL at wetted interfaces, a process which may be enhanced by the creviced geometry. The implications for development of more representative ex situ test protocols are discussed.

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