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Preparation of Biomass-Based Carbon Dots with Aggregation Luminescence Enhancement from Hydrogenated Rosin for Biological Imaging and Detection of Fe. | LitMetric

AI Article Synopsis

  • Fluorescent carbon dots (hr-CDs) were developed from sustainable hydrogenated rosin, using a hydrothermal method, showing enhanced fluorescence and overcoming quenching issues.
  • The hr-CDs exhibit strong blue fluorescence due to the formation of J aggregates and are resistant to photobleaching, maintaining their fluorescence even in solid form.
  • These carbon dots can selectively detect Fe, have good biocompatibility, and are effective for cell nuclear staining, comparable to traditional dyes like DAPI.

Article Abstract

Fluorescent carbon dots (CDs) have numerous important applications, but enhancing the fluorescence emission and overcoming fluorescence quenching are still big challenges. Here, fluorescence-enhanced carbon dots (named hr-CDs) were prepared from sustainable hydrogenated rosin, using a simple hydrothermal method in a water solvent. The hr-CDs were mainly composed of graphitized carbon cores with surface functional groups. With the increase in the concentration to hr-CDs aqueous solutions, the distance between the carbon cores decreased, which resulted in the formation of J aggregates and the enhanced blue fluorescence emission. Even in the solid state, the hr-CDs show fluorescence emission because the surface functional groups could prevent π-π stacking interactions between the carbon cores. The hr-CDs show excellent resistance to photobleaching under intense ultraviolet light (200 mW/cm). Vibrations and rotations of graphitized carbon core are restricted by low temperature and high viscosity, leading to increased radiative transition and thus increase in fluorescence intensity. The pH value in the range of 3.99-9.87 and anions have little effect on the fluorescence emission of hr-CDs. The fluorescence emission of the hr-CDs was selectively quenched by Fe and can thus be used to detect Fe. The hr-CDs also have good biocompatibility and show the same ability in cell nuclear staining as 4',6-diamidino-2-phenylindole (DAPI).

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7254789PMC
http://dx.doi.org/10.1021/acsomega.0c01527DOI Listing

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