Effect of the OH functionalization on the catalytic activity of single-atom catalyst

The existence of the hydroxyl ligand on a single- atom catalyst embedded in graphene, especially Fe(OH)−N4−C is suggested to improve the oxygen reduction reaction (ORR) from the pristine Fe−N4−C. However, the theoretical electrocatalytic activity of the ORR process is shown to be highly dependent on the electrolyte solution and the applied electrode potential. Herein, we performed the constant-potential simulation and microkinetic modeling to investigate the mechanism of ORR on well studied Fe(OH)−N4−C and Co(OH)−N4−C catalysts and compared to the pristine ones, using density functional theory (DFT) calculation combined with the effective screening medium method and the reference interaction site model (ESM-RISM).

It was found that the Fe(OH)−N4−C and Co(OH)−N4−C have comparable ORR activities to Fe−N4−C and Co−N4−C, and the calculated limiting potentials and half-wave potentials agree with the experimental values, in contrast to the results obtained using the constant-charge method (i.e., under the neutral condition) regardless of consideration of the solvation effect.