Abstract
Iron and nitrogen co-doped carbon (Fe–N/C) nanomaterials are promising non-Pt catalysts toward the oxygen reduction reaction (ORR). Both spectroscopy and density functional theory studies reveal that Fe–Nx accounts for the ORR activity. However, Fe–N/C catalysts prepared by traditional high-temperature pyrolysis always contain less active Fe or Fe3C nanoparticles, and it remains a great challenge to obtain Fe–N/C catalysts with high-content Fe–Nx active sites. Herein, a 3D space-confined strategy for the pyrolysis of double-network aerogels is reported, to obtain Fe–N/C network catalysts with exclusive Fe–Nx active sites without the generation of Fe or Fe3C nanoparticles. The as-prepared Fe–N/C network exhibits more positive half-wave potential, higher diffusion-limited current density, and better selectivity for the ORR than catalysts derived from single aerogels and commercial Pt/C. Additionally, the ORR activity measured in potassium thiocyanate (KSCN) poisoned electrolyte corroborates that Fe–Nx is the active site. This work opens a new guideline for designing the M–N/C catalysts with exclusive active sites in porous carbon matrices for boosting energy electrocatalysis.
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