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High Throughput Mapping of Single Molecules’ Redox Potentials on Electrode
Author(s) -
Chenghong Lei,
Dehong Hu
Publication year - 2021
Publication title -
analytical chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.117
H-Index - 332
eISSN - 1520-6882
pISSN - 0003-2700
DOI - 10.1021/acs.analchem.1c00984
Subject(s) - chemistry , redox , synchronizing , fluorescence , molecule , electrode , electrochemistry , single molecule experiment , throughput , microscope , resolution (logic) , fluorescence microscope , ultramicroelectrode , microscopy , nanotechnology , analytical chemistry (journal) , cyclic voltammetry , inorganic chemistry , materials science , organic chemistry , optics , computer science , telecommunications , wireless , mathematics , artificial intelligence , topology (electrical circuits) , physics , combinatorics
By synchronizing electrochemical potential scanning with a single-molecule localization super-resolution fluorescence microscope, kinetic fluorescence changes of hundreds of single molecular redox events were tracked simultaneously with high throughput, and subsequent cross-correlation function analysis mapped single molecules' redox potentials (times) out on the imaging area from site to site in unprecedented detail by extracting electrochemically induced fluorescence change from apparently random fluorescence on/off blinking. This work paves the way toward mapping redox states at single-molecule levels in high throughput in chemical and biological systems.

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