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Dual-site N-oxidation engineering enables modulated polarization in covalent organic frameworks for efficient photocatalytic N2 reduction

  • Hao Luo
  • , Hao Wang
  • , Shiyuan Wei
  • , Meng Li
  • , Ruoyan Li
  • , Jiawei Li*
  • , Jianhan Huang*
  • *Corresponding author for this work
  • College of Chemistry and Chemical Engineering

Research output: Contribution to journalArticlepeer-review

Abstract

N-Oxidation of imine linkages and pyridine moieties in pyridine-based covalent organic frameworks induces dual-site polarization. Due to the optimized polarization density and plentiful N+–O polar units, TFPyB-O-COF exhibits an exceptional NH3 production rate of 519.8 µmol g−1 h−1 for photocatalytic N2 reduction, which is proposed to proceed via an alternating association mechanism.

Original languageEnglish
Pages (from-to)14282-14285
Number of pages4
JournalChemical Communications
Volume62
Issue number57
DOIs
StatePublished - 23 Jul 2026
Externally publishedYes

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