Pyridinic‐Nitrogen‐Dominated Graphene Aerogels with Fe–N–C Coordination for Highly Efficient Oxygen Reduction Reaction

Abstract

Here, pyridinic nitrogen dominated graphene aerogels with/without iron incorporation (Fe‐NG and NG) are prepared via a facile and effective process including freeze‐drying of chemically reduced graphene oxide with/without iron precursor and thermal treatment in NH 3. A high doping level of nitrogen has been achieved (up to 12.2 at% for NG and 11.3 at% for Fe‐NG) with striking enrichment of pyridinic nitrogen (up to 90.4% of the total nitrogen content for NG, and 82.4% for Fe‐NG). It is found that the Fe‐NG catalysts display a more positive onset potential, higher current density, and better four‐electron selectivity for ORR than their counterpart without iron incorporation. The most active Fe‐NG exhibits outstanding ORR catalytic activity, high durability, and methanol tolerance ability that are comparable to or even superior to those of the commercial Pt/C catalyst at the same catalyst loading in alkaline environment. The excellent ORR performance can be ascribed to the synergistic effect of pyridinic N and Fe‐N x sites (where iron probably coordinates with pyridinic N) that serve as active centers for ORR. Our Fe‐NG can be developed into cost‐effective and durable catalysts as viable replacements of the expensive Pt‐based catalysts in practical fuel cell applications.