Nanoscale graphenes were used as cathode catalyst supports in proton exchange membrane fuel cells (PEMFCs). Surface-initiated polymerization that covalently bonds polybenzimidazole (PBI) polymer on the surface of graphene supports enables the uniform distribution of the Pt nanoparticles, as well as allows the sealing of the unterminated carbon bonds usually present on the edge of graphene from the chemical reduction of graphene oxide. The nanographene effectively shortens the length of channels and pores for O 2 diffusion/water dissipation and significantly increases the primary pore volume. Further addition of p-phenyl sulfonic functional graphitic carbon particles as spacers, increases the specific volume of the secondary pores and greatly improves O 2 mass transport within the catalyst layers. The developed composite cathode catalyst of Pt/PBI-nanographene (50 wt%) + SO 3 H-graphitic carbon black demonstrates a higher beginning of life (BOL) PEMFC performance as compared to both Pt/PBI-nanographene (50 wt%) and Pt/PBI-graphene (50 wt%) + SO 3 H-graphitic carbon black (GCB). Accelerated stress tests show excellent support durability compared to that of traditional Pt/Vulcan XC72 catalysts, when subjected to 10,000 cycles from 1.0 V to 1.5 V. This study suggests the promise of using PBI-nanographene + SO 3 H-GCB hybrid supports in fuel cells to achieve the 2020 DOE targets for transportation applications. High stability is required for polymer electrolyte membrane fuel cells (PEMFCs) catalyst supports because they play a critical role in determining the overall durability of PEMFC systems.1 Carbon-based supports have been widely used to support Pt or Pt alloy catalysts in PEMFCs.2 High-surface-area carbon (HSAC) supports minimize the aggregation of the catalyst nanoparticles as HSAC provides more sites for catalyst to nucleate than low-surface-area-carbon (LSAC), thereby avoiding forming big aggregates. Thus, it increases the Pt utilization that leads to more active electro-catalysts with low platinum loadings (< 0.1 mg-Pt/cm 2 ), 2 yet HSAC is vulnerable for corrosion due to the increased surface area. Good electrical conductivity of the carbon materials provides good electron transport.3 In addition, the random aggregates of the primary carbon particles help the distribution of ionomer to access the active sites during the fabrication of membrane electrode assemblies (MEA), and also allow the construction of a highly porous catalyst layer that enables O 2 diffusion and the water dissipation in PEMFCs. The most commonly used carbon blacks in low temperature PEMFCs include Vulcan XC72 (Cabot Corp., USA), Black Pearls 2000 (Cabot Corp., USA) Ketjen Black EC300j (AkzoNobel Corp., the Netherlands), Ketjen Black EC600 (AkzoNobel Corp., the Netherlands), etc. These carbon blacks consist of inhomogeneous graphitic structures and amorphous carbons. 4 The small size of the graphitic domains cause a high density of edge sites, (particularly in the case of high BET (Brunauer-Emmett-Teller) surface area carbon supports), ...