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Charge-Dependent Fluorescence Lifetime Modulation in a Plasmonic Nanocavity.

Alexey I Chizhik1, Damir I Sakhapov1, Ingo Gregor1

  • 1Third Institute of Physics (Biophysics), Georg August University, 37077 Göttingen, Germany.

The Journal of Physical Chemistry Letters
|September 12, 2025
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Summary
This summary is machine-generated.

Researchers developed a new method using plasmonic nanocavities to precisely measure single-molecule electric charges in solution. This technique offers a simple, rapid, and calibration-free alternative for charge quantification.

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Area of Science:

  • Physical Chemistry
  • Biophysics
  • Nanotechnology

Background:

  • Molecular electric charges are crucial for biomolecular structure and function.
  • Accurate single-molecule charge measurement is technically challenging.
  • Existing methods lack sensitivity and simplicity.

Purpose of the Study:

  • To introduce a novel experimental methodology for quantifying molecular electric charges.
  • To achieve high sensitivity in charge measurements at the single-molecule level.
  • To provide a calibration-free and rapid alternative to current techniques.

Main Methods:

  • Utilizing plasmonic nanocavities to confine charged molecules.
  • Applying an external electric field to induce molecular redistribution.
  • Measuring fluorescence lifetime modulation for sensitive readout.
  • Validating experimental data with theoretical frameworks (statistical thermodynamics, electrodynamics).

Main Results:

  • Demonstrated proof-of-concept for measuring fluorescence lifetimes of charged dye molecules.
  • Quantified molecular charges as a function of applied electric field.
  • Experimental results were rigorously validated by theoretical modeling.
  • Achieved high sensitivity in charge detection within nanocavities.

Conclusions:

  • The developed method enables precise quantification of molecular electric charges in solution.
  • Plasmonic nanocavity-induced fluorescence lifetime modulation is a viable readout.
  • This technique offers a simple, rapid, and calibration-free approach for single-molecule charge analysis.
  • Opens new avenues for studying molecular charge dynamics.