Bioinspired Single-Atom Sites Enable Efficient Oxygen Activation for Switching Anodic/Cathodic Electrochemiluminescence

Angew Chem Int Ed Engl. 2023 Jul 17;62(29):e202304625. doi: 10.1002/anie.202304625. Epub 2023 Jun 12.

Abstract

Exploring advanced co-reaction accelerators with superior oxygen reduction activity that generate rich reactive oxygen species (ROS) has attracted great attention in boosting luminol-O2 electrochemiluminescence (ECL). However, tuning accelerators for efficient and selective catalytic O2 activation to switch anodic/cathodic ECL is very challenging. Herein, we report that enzyme-inspired Fe-based single-atom catalysts with axial N/C coordination structures (FeN5 , FeN4 © SACs) can generate specific ROS for cathodic/anodic ECL conversion. Mechanistic studies reveal that FeN5 sites prefer to produce highly active hydroxyl radicals and afford direct cathodic luminescence by promoting the cleavage of O-O bonds through N-induced electron redistribution. In contrast, FeN4 © sites tend to produce superoxide radicals, resulting in inefficient anodic ECL. Benefiting from the enhanced cathodic ECL, FeN5 SAC-based immunosensor was constructed for the sensitive detection of cancer biomarkers.

Keywords: Electrochemiluminescence; Immunoassay; Oxygen Reduction Reactions; Reactive Oxygen Species; Single-Atom Catalysts.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biosensing Techniques* / methods
  • Electrochemical Techniques
  • Hydroxyl Radical
  • Immunoassay / methods
  • Luminescent Measurements / methods
  • Oxygen*
  • Reactive Oxygen Species

Substances

  • Oxygen
  • Reactive Oxygen Species
  • Hydroxyl Radical