Unveiling the Potential of an Fe Bis(terpyridine) Complex for Precise Development of an Fe-N-C Electrocatalyst to Promote the Oxygen Reduction Reaction.

ABSTRACT

Improvements in highly efficient precious-metal-free electrocatalysts for the oxygen reduction reaction (ORR) are extremely important but still a significant challenge. Herein, we report a novel catalyst design strategy integrating a bis(terpyridine) (hexadentate chelating ligand) with Fe which acts as nitrogen, a self-supporting carbon source, and a potent metal-ligand active site binding structure (Fe-btpy) and promotes the formation of Fe-Nx/C active sites, bypassing the complications induced during Fe-N-C catalyst synthesis. The resulting Fe-N/C(H,P) electrocatalyst shows a very high ORR onset (Eonset) and half-wave potential (E1/2) of 1.05 and 0.89 V (vs reversible hydrogen electrode), respectively, outperforming the commercial Pt/C catalyst in alkaline medium. Most importantly, the Fe-N/C(H,P) catalyst displays decent stability and remarkable methanol tolerance in comparison to the Pt/C catalyst. A fabricated rechargeable zinc-air battery with an Fe-N/C(H,P) cathode catalyst demonstrated an excellent peak power density of 225 mW cm-2 at a current density of 240 mA cm-2, in comparison to the Pt/C cathode catalyst. This work illuminates blueprints utilizing a new long-chain one-dimensional macromolecule that could be viable to produce Fe-N/C-based carbon electrocatalysts toward energy conversion applications.