Oxygen reduction reaction mechanism and kinetics on M-NxCyand M@N-C active sites present in model M-N-C catalysts under alkaline and acidic conditions

M-N-C electrocatalysts (where M is Fe or Co) have been investigated for mitigating the dependence on noble metals when catalyzing the oxygen reduction reaction (ORR) for fuel cell technologies in acidic or alkaline conditions. Rotating disk and rotating ring-disk electrode measurements for Fe-N-C and Co-N-C catalysts demonstrate promising performances and stability for the ORR, while the activity of main suspected active sites (M-N(x)C(y)and M@N-C) has been discussed on the basis of the known physical-chemical properties of the catalysts in acid and alkaline media. Thereupon, it is observed that atomically dispersed Fe-N(x)C(y)sites reach the highest ORR activity in acid media when amplified by an adequate energy binding between the metallic center and the oxygenated reaction intermediates. In contrast, Fe@N-C core-shell sites reach a maximum ORR mass activity in alkaline media through a synergistic effect involving catalyst particles with metallic iron in the core and nitrogen-doped carbon in the shell.

Automated summary

This study investigates the performance and stability of Fe-N-C and Co-N-C catalysts in the oxygen reduction reaction (ORR), with atomically dispersed Fe-N(x)C(y) sites showing the highest activity in acidic media and Fe@N-C core-shell sites exhibiting maximum mass activity in alkaline media. The activity of main suspected active sites (M-N(x)C(y)and M@N-C) was discussed based on the known physical-chemical properties of the catalysts, highlighting the role of adequate energy binding and synergistic effects for enhancing catalytic performance.