The bipolar plate is of critical importance to the efficient and long lasting operation of a polymer electrolyte fuel cell (PEMFC) stack. With advances in membrane electrode assembly design, greater attention has been focused on the bipolar plate and the important role it plays. Although carbon composite plates are a likely candidate for the mass introduction of fuel cells, it is metallic plates made from thin strip materials which could deliver significant advantages in terms of part cost, electrical performance and size. However, there are some disadvantages. Firstly, interfacial stability of the metal interconnect is difficult to achieve. Secondly, and the issue addressed here, is the difficultly and cost in developing new plate designs when there are very significant tooling costs associated with manufacture. The use of selective laser melting (SLM: an additive manufacturing technique) was explored to produce metallic bipolar plates for PEMFC as a route to inexpensively test several plate designs without committing to tooling. Crucial to this was proving that, electrically, bipolar plates fabricated by SLM behave similarly to those produced by conventional manufacturing techniques. This research presents the development of a small stack to compare the short term performance of metallic plates made by machining against those made by SLM. Experimental results demonstrate that the cell performance in this case was unaffected by the manufacturing method used and it is therefore concluded that additive manufacturing could be a very useful tool to aid the rapid development of metallic bipolar plate designs.
Changes that carbon-supported platinum electrocatalysts undergo in a proton exchange membrane fuel cell environment were simulated by ex situ heat treatment of catalyst powder samples at 150 C and 100% relative humidity. In order to study modifications that are introduced to chemistry, morphology, and performance of electrocatalysts, XPS, HREELS and three-electrode rotating disk electrode experiments were performed. Before heat treatment, graphitic content varied by 20% among samples with different types of carbon supports, with distinct differences between bulk and surface compositions within each sample. Following the aging protocol, the bulk and surface chemistry of the samples were similar, with graphite content increasing or remaining constant and Pt-carbide decreasing for all samples. From the correlation of changes in chemical composition and losses in performance of the electrocatalysts, we conclude that relative distribution of Pt particles on graphitic and amorphous carbon is as important for electrocatalytic activity as the absolute amount of graphitic carbon present.
The object of this work was to identify correlations between performance losses of Pt electrocatalysts on carbon support materials and the chemical and morphological parameters that describe them. Accelerated stress testing, with an upper potential of 1.2 V, was used to monitor changes to cathode properties, including kinetic performance and effective platinum surface area losses. The structure and chemical compositions were studied using X-ray Photoelectron Spectroscopy and Scanning Electron Microscopy coupled with Digital Image Processing. As this is an ongoing study, it is difficult to draw firm conclusions, though a trend between support surface area overall performance loss was found to exist.
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