Asymmetric Coordination of Bimetallic Fe-Co Single-Atom Pairs toward Enhanced Bifunctional Activity for Rechargeable Zinc-Air Batteries.
basic_science · Level V
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- Record sourced from PubMed, PMID 38736197.
- Also identified by DOI 10.1021/acsnano.4c01342.
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Abstract
The advancement of rechargeable zinc-air batteries (RZABs) faces challenges from the pronounced polarization and sluggish kinetics of oxygen reduction and evolution reactions (ORR and OER). Single-atom catalysts offer an effective solution, yet their insufficient or singular catalytic activity hinders their development. In this work, a dual single-atom catalyst, FeCo-SAs, was fabricated, featuring atomically dispersed N<sub>3</sub>-Fe-Co-N<sub>4</sub> sites on N-doped graphene nanosheets for bifunctional activity. Introducing Co into Fe single-atoms and secondary pyrolysis altered Fe coordination with N, creating an asymmetric environment that promoted charge transfer and increased the density of states near the Fermi level. This catalyst achieved a narrow potential gap of 0.616 V, with a half-wave potential of 0.884 V for ORR (vs the reversible hydrogen electrode) and a low OER overpotential of 270 mV at 10 mA cm<sup>-2</sup>. Owing to the superior activity of FeCo-SAs, RZABs exhibited a peak power density of 203.36 mW cm<sup>-2</sup> and an extended cycle life of over 550 h, exceeding the commercial Pt/C + IrO<sub>2</sub> catalyst. Furthermore, flexible RZABs with FeCo-SAs demonstrated the promising future of bimetallic pairs in wearable energy storage devices.