Role of Nitrogen Moieties in N-Doped 3D-Graphene Nanosheets for Oxygen Electroreduction in Acidic and Alkaline Media

This study elucidates the synthesis-structure-property correlations of nitrogen moieties present in nitrogen-functionalized graphene nanomaterials toward oxygen reduction reactions (ORRs) and their electrochemical pathways in acidic and alkaline electrolytes. Porous three-dimensional nitrogen-doped graphene nanosheets (N/3D-GNSs) were fabricated using the sacrificial support method and doped with nitrogen using 10 atom % NH₃ under thermal pyrolysis at T = 650, 850, and 1050 °C for evaluating the nitrogen species formed under different temperatures. The abundances of the various nitrogen species formed under pyrolytic conditions were evaluated with X-ray photoelectron spectroscopy. Using rotating ring-disk electrode, we analyzed the role played by the nitrogen moieties influencing the electrochemical activity of the N/3D-GNS supports for oxygen reduction reactions (ORRs) in both acidic and alkaline media. It was demonstrated that the concentrations of the nitrogen moieties: graphitic-N, quaternary, hydrogenated-N (hydrogenated nitrogen combined pyrrolic nitrogen and hydrogenated pyridine) and pyridinic-N varied considerably with pyrolysis temperatures. A decrease in graphitic-N content and an increase in the ratio of hydrogenated-N/pyridinic-N significantly improved the activity of the material. The half-wave and onset potentials as well as the current densities and hydrogen peroxide (H₂O₂)/(HO₂^-) yields of the N/3D-GNS materials also varied between acidic and alkaline electrolytes but followed the general trend in terms of pyrolysis temperatures and abundance of the nitrogen moieties. Among the synthesized materials, the 3D-graphene nanosheets that were doped with nitrogen at 850 °C, optimized to have the highest hydrogenated-N and lowest pyridinic-N as well as better catalyst-ionomer integration, showed the highest ORR performance. This strategy for the tunable synthesis of nitrogen-doped graphene materials with controlled nitrogen functionalization offers a platform for developing active supports or catalytic nanomaterials for fuel cell applications.