Nickel Single-Atom Catalyst-Mediated Efficient Redox Cycle Enables Self-Checking Photoelectrochemical Biosensing with Dual Photocurrent Readouts

ACS Sens. 2023 Jan 27;8(1):263-269. doi: 10.1021/acssensors.2c02125. Epub 2023 Jan 9.

Abstract

Developing a self-checking photoelectrochemical biosensor with dual photocurrent signals could efficiently eliminate false-positive or false-negative signals. Herein, a novel biosensor with dual photocurrent responses was established for the detection of acetylcholinesterase activity. To achieve photocurrent polarity-switchable behavior, the iodide/tri-iodide redox couple was innovatively introduced to simultaneously consume the photoexcited electrons and holes, which circumvents the inconvenience caused by the addition of different hole- and electron-trapping agents in the electrolyte. Importantly, benefiting from the high catalytic activity, the enhanced photoelectric responsivity can be realized after decorating the counter electrode with nickel single-atom catalysts, which promotes a more efficient iodide/tri-iodide redox reaction under low applied voltages. It is envisioned that the proposed photocurrent polarity switching system offers new routes to sensitive and reliable biosensing.

Keywords: acetylcholinesterase activity assay; photocurrent polarity switching; photoelectrochemical biosensing; self-checking; single-atom catalysts.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholinesterase
  • Biosensing Techniques*
  • Catalysis
  • Electrochemical Techniques*
  • Iodides
  • Nickel
  • Oxidation-Reduction

Substances

  • Acetylcholinesterase
  • Iodides
  • Nickel