Multi-sites synergistic modulation in oxygen reduction electrocatalysis

Revealing the types of and interplays among multiple active-sites in iron-nitrogen-carbon (Fe N C) materials is of great significance for developing high-performance, Fe-based non-precious metal catalysts for oxygen reduction reaction (ORR). In this paper, a single-atom Fe N C catalyst is prepared through high-temperature pyrolyzing of melamine foam (MF), iron phthalocyanine (FePc), phthalocyanine (Pc), and zinc (Zn)-salts composite. The catalyst is found to contain a variety of active-sites, including carbon atom next to pyridinic-N (pyridinic N C), Fe-N 4 and pore defect. It is shown that MF with high N -content is responsible for the formation of the main pyridinic N C sites and in the meantime acts as the self-sacrificed template for framework of the catalyst. The presence of Pc can facilitate the formation of the predominant Fe-N 4 sites, since the interplay between Pc and FePc results in a confinement of Fe-N 4 . Zn-salts serve as the pore-forming additives to create sufficient pore defects which can also anchor pyridinic N C and Fe-N 4 structures. The results of density functional theory (DFT) calculations suggest that the multiple active-sites function synergistically to enable high-efficiency ORR electrocatalysis. The optimal Fe N C catalyst shows superior ORR activity with a half-wave potential of ∼0.88 V ( vs . RHE), as well as high methanol tolerance and electrochemical stability compared to the commercial carbon-supported platinum (Pt/C) catalyst.