Research on fuel cell technology is constantly gaining importance, while global emission requirements are becoming more and more restrictive. For environmentally neutral proton exchange membrane fuel cells (PEMFCs) to become a competitive technology, sustainable infrastructures need to be established. One of the main showstoppers is the utilization of the rare and therefore costly precious metal Pt as the key element in the electrocatalysis of hydrogen and oxygen. A huge amount of research is done on immensely reducing or even replacing Pt for future PEMFC technology. In this research update, the progress on oxygen reduction reaction catalysts in acidic media over the past two years is reviewed, with special attention to their durability.
The main objective of the present work is to study the effect of rapid solidification on the electrochemical performance of Zr based Laves type alloy with a nominal composition Ti 12 Zr 21.5 V 10 Cr 7.5 Mn 8.1 Co 8 Ni 32.2 Al 0.4 Sn 0.3. The samples were prepared from the as cast arc melted buttons by melt spinning at different copper wheel rotation speeds of 5, 16.5, 33, and 100 Hz, which are equivalent to linear speeds of 6.3, 21, 41, and 62.8 m s 1 respectively using a cooling wheel with a diameter of 20 cm. The phase composition and morphology of the ribbons were analyzed by X Ray diffraction (XRD) and scanning electron microscopy (SEM). The microstructural changes of the ribbons induced by the variations in the wheel rotation speed were found to be closely related to the electrochemical performances. High discharge capac ities exceeding 400 mAh•g 1 were achieved for the melt spun samples during the measure ments at low current densities. Furthermore, melt spun casting performed at the highest wheel rotation speed of 100 Hz resulted in the best rate performance of the alloy. As this alloy has the smallest crystallite size, this resulted in the shortest H atoms diffusion distances, and thus increased the efficient H diffusion rate and improved the electrochemical performance.
A comparative study of the effect of melt spinning on the electrochemical properties of the C14 and C15 AB2 alloys has been performed. The wheel speeds of 630, 2100, and 4100 cm/s were applied during the rapid solidification of both alloys. The structural analysis of the formed phases was performed by X-ray powder diffraction (XRD), while their microstructural morphology was studied by scanning electron microscopy (SEM). In both alloys a tremendous grain refinement due to the melt spinning process was observed: In addition, melt spinning also significantly contributed to the morphological variation of the microstructural changes in C14 alloys which showed changes from the equiaxed grain at lower speed to the small dendrites at higher speed. In contrast to the C14 alloys, the morphological variation was not observed for the C15 alloys. Furthermore, for both C14 and C15 alloys melt-spun at 2100 cm/s the maximum capacities of 435 and 414 mAh/g were achieved, respectively. As both alloys revealed the significant grain refinement due to the melt spinning, an increase in electrochemical capacity was achieved. However, the melt spinning parameters need to be further optimized to improve poor activation behavior of the rapidly solidified alloys.
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