“…Degradation of carbon under harsh PEMFC conditions is yet to be fully addressed. Electrochemical oxidative corrosion of carbon support due to the high electric fields developed in fuel cells during startup and shutdown cycles and/or insufficient fuel supply results in structural deterioration and metal catalyst (Pt) dissolution, which can severely impede the long-term durability of PEMFCs. − More specifically, at the cathode side, due to the cumulative effect of high potential, moisture, and in some cases, generation of hydrogen peroxide (H 2 O 2 ), the carbon supports suffer from the formation of surface oxides, which eventually leads to the evolution of CO and CO 2 . , The potential range between 0.6 and 1.0 V versus the reversible hydrogen electrode (RHE) thermodynamically favors the carbon oxidation reaction (COR). Further, it has been proposed that the COR can be catalyzed by Pt nanoparticles, most likely via the back-spillover of oxygen-containing surface groups (CO surf ) to the metal surface followed by their oxidation into CO 2 . , Especially, under the harsh working conditions of PEMFCs (e.g., frequent load cycles, high potential, and strong acidic and oxidizing conditions), Pt nanoparticles tend to suffer from dissolution, migration, and Ostwald ripening/coalescence induced by relatively weak interactions/binding between Pt and the carbon support, leading to significant degradation in the overall cell performance. , Therefore, a good catalyst support should possess excellent chemical stability to withstand the oxidative PEMFC environment, high electrical conductivity for rapid electron transfer, unique porous structure for the effective mass transport of reactants/byproducts, large surface area to maximize the catalyst utilization, and strong catalyst–support interactions .…”