For better water management in polymer electrolyte fuel cells (PEFCs), microporous layers (MPLs) are generally used. In this paper, hydrophilic MPLs having various pore volumes and diameters were prepared using a range of carbon materials, and the effect of the MPL on the membrane electrode assembly (MEA) performance was investigated under dry and wet conditions. Under the dry condition (80 • C, 30%RH), the MEA employing an MPL with a larger median pore diameter showed higher cell voltage, suggesting that the MPL with a larger pore diameter has better gas diffusivity, leading to better MEA performance. Under the wet condition (80 • C, 100%RH), it was confirmed that pore volume of the MPL has a significant impact on the MEA performance and that the hydrophilic MPL with a large pore volume was effective in reducing water flooding in the cathode catalyst layer. When used in an MPL, VGCF-H (carbon fiber with a fiber diameter of 150 nm) gives the largest pore diameter and pore volume. This MEA with a hydrophilic MPL (made of VGCF-H and ionomer) showed the best MEA performance under both dry and wet operating conditions.
The qualitative evaluation of the dispersion of prefluorosulfonic ionomer (PFSI) with different ionomer/carbon mixing ratios (I/C) using electron microscopy was carried out without the use of a stain treatment. Both low acceleration voltage transmission electron microscopy (LAV-TEM) and ultralow acceleration voltage scanning electron microscopy with a retarding method (ULV-SEM) use a characteristically low acceleration voltage, which allows the selective examination of the sensitive ionomer morphology. The high-performance charge-coupled device enables one to obtain high contrast ionomer images without the use of lead or cesium staining, which could otherwise result in morphological changes during these pre-treatments. The electrochemically active surface area of the polymer electrolyte fuel cell using Pt/GCB increased with increasing PFSI content and saturated at an ionomer/carbon weight ratio (I/C) of 1.2, where full coverage of the ionomer was detected by LAV-TEM. The ULV-SEM images showed the obvious occlusion of the primary and secondary pores of the Pt/GCB catalyst layers above I/C = 1.2. The nitrogen gas adsorption measurement, carried out by use of quenched solid-density-functional theory analysis, also supported the occlusion of the primary and secondary pores of the Pt/GCB catalyst layers above I/C = 1.2.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.