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handle: 10261/341081
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.
Animated movie with segmented high-resolution tomographic reconstruction and orthoslice cut of as-synthesized Rh@Pt/C NPs.
Peer reviewed
Current evolution occurring, Carbon support, 2, Potential cycles, Main degradation mechanism, Electrochemical stability, High stability, Successful application, 06 – 0, Commercial fuel cells, Potential cycling, Electrochemical stability needs, 10.000 cycles, c nps, Results reveal, Promising candidates, c system, Compositional changes
Current evolution occurring, Carbon support, 2, Potential cycles, Main degradation mechanism, Electrochemical stability, High stability, Successful application, 06 – 0, Commercial fuel cells, Potential cycling, Electrochemical stability needs, 10.000 cycles, c nps, Results reveal, Promising candidates, c system, Compositional changes
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