Axial chlorine coordination reconstructs Fe–N4electronic structure for efficient pH-universal oxygen reduction reaction

  • Yanle Yuan
  • , Xia Zhang
  • , Feilong Qin
  • , Chunwu Lei
  • , Yang Wang
  • , Yaoyu Yang
  • , Guang Feng*
  • , Kaiyu Liu*
  • , Tao Chen*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Current Fe single-atom catalysts suffer from active-site blockage and aggregation. This study creates 2D nanosheet catalysts with axial chlorine-coordinated Fe–N4 sites (Fe–N4Cl) via molten salt-assisted pyrolysis. This configuration tunes the electronic structure, enhancing oxygen reduction. The catalyst outperforms Pt/C in alkaline, neutral, and acidic electrolytes, with half-wave potentials of 0.921 V, 0.742 V, and 0.771 V, respectively. In Zn–air batteries, it achieves a high power density of 176.5 mW cm−2 and stability over 720 hours, showing great potential for efficient energy conversion.

Original languageEnglish
JournalChemical Communications
DOIs
Publication statusAccepted/In press - 2026
Externally publishedYes

Fingerprint

Dive into the research topics of 'Axial chlorine coordination reconstructs Fe–N4electronic structure for efficient pH-universal oxygen reduction reaction'. Together they form a unique fingerprint.

Cite this