AI Article Synopsis

  • Inexpensive carbon-based nitrogen-coordinated iron single-atom catalysts (CN-FeSACs) are emerging as effective alternatives to platinum for enhancing oxygen electrode performance in fuel cells and batteries.
  • A new ionothermal-transformation method is introduced to create hierarchically tubular porous CN-FeSACs with a high surface area of 2500 m²/g, improving oxygen reduction reaction kinetics and mass transport.
  • The resulting material achieves a superior ORR half-wave potential of 0.885 V and a peak power density of 208 mW/cm² in zinc-air batteries, surpassing the performance of Pt/C catalysts.

Article Abstract

Inexpensive carbon-based nitrogen-coordinated iron single-atom catalysts (CN-FeSACs) have been recently demonstrated as the most promising platinum substitutions for boosting the sluggish oxygen electrode performance in fuel cells and metal-air batteries. However, it is still a great challenge to develop economical and effective CN-FeSACs satisfying the needs of high output power. Herein, an ionothermal-transformation strategy is proposed to synthesize hierarchically tubular porous CN-FeSACs with an ultrahigh special surface area of 2500 m g to host abundant single-atom iron sites with an attempt to simultaneously boost sluggish oxygen reduction reaction (ORR) kinetics and mass transport. Benefiting from the unique feature, the final obtained material shows an ORR half-wave potential of 0.885 V, higher than that of benchmark Pt/C (0.850 V). When assembled into zinc-air battery, a large peak power density of 208 mW cm is achieved, which is far superior to that of Pt/C (119 mW cm). This work provides an economical and feasible strategy to prepare hierarchically porous CN-FeSACs for energy conversion.

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Source
http://dx.doi.org/10.1021/acsami.1c16915DOI Listing

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