کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
184010 | 459566 | 2015 | 14 صفحه PDF | دانلود رایگان |
• Large water-filled connected ionic areas recognized by their difference in adhesion force
• Direct observation of ionomer interface formation at different humidity
• Formation of connected ionically conductive network by forced current flow observed
• First direct imaging of ionomer film in electrode
• Analysis of ionomer content across the catalytic layer of a fuel cell
Using material-sensitive and conductive atomic force microscopy (AFM) on cross sections of perfluorinated and sulfonated membranes at low humidity, crystalline polymer lamellae were imaged and their thickness determined to approximately 6 nm. In the capacitive current, water-rich and water-poor areas with different phase structures were investigated. The formation of a local electrochemical double layer within the water-rich ionically conductive areas at the contact of the AFM tip with the electrolyte enabled their visibility. The large water-filled ionically conductive areas include numerous ionic domains. Under equilibrium conditions, these areas are spherical (appearing circular in the images) and with distinct size distribution. Forcing a current through the membranes (current-induced activation) led to merging of the water-filled ionically conductive areas in the voltage direction and resulted in an anisotropic ionically conducting network with flat channels. The distribution of the current in the membrane and catalytic layers of a pristine membrane electrode assembly (MEA) was analyzed. From the adhesion force mappings, an inhomogeneous distribution of ionomer in the catalytic layer was detected. Cross currents between Pt/C particles through large ionomer particles within the catalytic layer were detected and the ionomer content across an electrode was evaluated.
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Journal: Electrochimica Acta - Volume 162, 20 April 2015, Pages 86–99