1779
Porous Hollow Ptni/C Electrocatalysts: Carbon Support Considerations to Meet Stability Requirements

Wednesday, 16 May 2018: 10:20
Room 611 (Washington State Convention Center)
T. Asset (Univ. Grenoble Alpes, LEPMI, F-38000 Grenoble, France, University of New Mexico, Albuquerque, NM 87131, USA), N. Job (Université de Liège), Y. Busby (University of Namur ASBL, 5000 Namur, Belgium), A. Crisci (SIMaP), V. Martin (CNRS, LEPMI, F-38000 Grenoble, France), V. Stergiopoulos (University of Liège, 4000 Liège, Belgium), C. Bonnaud (CNRS, LEPMI, F-38000 Grenoble, France), A. Serov, P. Atanassov (University of New Mexico), R. Chattot (CNRS, LEPMI, F-3800 Grenoble, France), L. Dubau, and F. Maillard (CNRS, LEPMI, F-38000 Grenoble, France)
Porous hollow PtNi/C nanoparticles (NPs), an highly active electrocatalyst for the oxygen reduction reaction (ORR)1, were successfully synthesized on different carbon supports. The latter plays an essential role in the NPs synthesis, providing a way to control their morphology and Ni content. The physico-chemical properties of the different carbon supports were crucial during accelerated stress tests simulating start-stop events at a PEMFC cathode (i.e. step potentials between 1.0 and 1.5 V vs. RHE) and were discussed by the means of identical-location transmission electron microscopy (IL-TEM) and electrochemistry (see. Figure 1). It was observed that electrocatalysts supported on graphene nanosheets and carbon xerogel suffer from NPs detachment and carbon complete corrosion while COsurf forms on carbon blacks supports (i.e. incomplete oxidation of the surface). The degradation of the carbon support resulted in mass activity and specific activity losses, as the result of the increase of the resistance of the catalytic layers (ΔRk).