Related Experiment Video
Updated: Apr 20, 2026

From Fast Fluorescence Imaging to Molecular Diffusion Law on Live Cell Membranes in a Commercial Microscope
Published on: October 9, 2014
Imaging transient formation of diffusion layers with fluorescence-enabled electrochemical microscopy
1Department of Chemistry, University of Washington , Seattle, Washington 98195-1700, United States.
Fluorescence-enabled electrochemical microscopy (FEEM) visualizes redox species concentration near ultramicroelectrodes. This technique images dynamic diffusion layers in 2D and 3D, advancing electrochemical analysis.
Area of Science:
- Electrochemistry
- Analytical Chemistry
- Microscopy
Background:
- Ultramicroelectrodes (UMEs) are crucial in electrochemical studies.
- Imaging dynamic concentration profiles around UMEs is challenging.
- Existing methods lack the resolution and speed for transient phenomena.
Purpose of the Study:
- To introduce Fluorescence-enabled electrochemical microscopy (FEEM) as a novel imaging technique.
- To demonstrate FEEM's capability for visualizing diffusion layers around UMEs.
- To enable 2D and 3D imaging of transient concentration profiles.
Main Methods:
- FEEM couples redox reactions to fluorogenic reporters via bipolar electrodes.
- An array of thousands of bipolar electrodes is used for imaging.
- FEEM captures 2D lateral cross-sections and builds 3D images from multiple sections.
Main Results:
- FEEM successfully imaged the diffusion layer of a 10 μm carbon fiber electrode.
- FEEM-generated images were compared with numerical simulations.
- Diffusion layers of a two-electrode array were imaged during a potential step experiment.
Conclusions:
- FEEM is a powerful new technique for imaging transient electrochemical processes.
- The method allows for detailed visualization of diffusion layers in 2D and 3D.
- FEEM offers a significant advancement in understanding electrochemical reactions at the microscale.
More Related Videos
07:54Fluorescence Recovery after Merging a Droplet to Measure the Two-dimensional Diffusion of a Phospholipid Monolayer
Published on: October 15, 2015
05:56Spot Variation Fluorescence Correlation Spectroscopy for Analysis of Molecular Diffusion at the Plasma Membrane of Living Cells
Published on: November 12, 2020
Related Concept Videos
Super-resolution Fluorescence Microscopy
Total Internal Reflection Fluorescence Microscopy
Protein Dynamics in Living Cells
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...