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Published on: July 24, 2015
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Tunable fluorescence quenching near the graphene-aqueous interface
Aaron W Chen1, Alejandro L Briseno1, Maria M Santore1
1Department of Polymer Science and Engineering, University of Massachusetts, Amherst, MA 01003, United States.
Journal of Colloid and Interface Science
|July 21, 2017
Summary
Ionic strength significantly impacts fluorescein emissions from proteins on graphene sensors, revealing an acidic interface due to graphene's negative charge. This effect can be used to measure distances near graphene surfaces.
Area of Science:
- Materials Science
- Biophysics
- Nanotechnology
Background:
- Graphene-based sensors are increasingly used for biomolecule detection.
- Understanding environmental factors affecting sensor performance is crucial.
- Fluorescein is a common labeling agent for biomolecules.
Purpose of the Study:
- To investigate the effect of ionic strength on fluorescein-labeled proteins adsorbed on graphene.
- To explore the implications of the aqueous environment near graphene surfaces.
Main Methods:
- Utilized fluorescein-tagged fibrinogen as a model system.
- Studied steady-state fluorescence emissions from adsorbed proteins on chemical vapor deposited (CVD)-graphene/silica.
- Varied salt concentration and employed Guoy Chapman modeling.
Main Results:
- Fluorescein emission intensity on adsorbed fibrinogen was highly sensitive to salt concentration, unlike in solution.
- Fluorescence quenching was linked to fluorescein's pH sensitivity and an acidic near-surface environment.
- The acidic environment is attributed to negative charge on the graphene or underlying silica support.
Conclusions:
- The aqueous interface near silica-supported graphene is acidic due to negative surface charge.
- Ionic strength can be used as a 'molecular ruler' to assess fluorescence emissions near graphene.
- Findings are relevant for any fluorescein-tagged species near graphene, impacting sensor design and interpretation.

