Rhodium–platinum core–shell nanoparticles
on a carbon
support (Rh@Pt/C NPs) are promising candidates as anode catalysts
for polymer electrolyte membrane fuel cells. However, their electrochemical
stability needs to be further explored for successful application
in commercial fuel cells. Here we employ identical location scanning
transmission electron microscopy to track the morphological and compositional
changes of Rh@Pt/C NPs during potential cycling (10 000 cycles,
0.06–0.8 VRHE, 0.5 H2SO4)
down to the atomic level, which are then used for understanding the
current evolution occurring during the potential cycles. Our results
reveal a high stability of the Rh@Pt/C system and point toward particle
detachment from the carbon support as the main degradation mechanism.