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Solvent Effects on Fluorescence Properties of Carbon Dots: Implications for Multicolor Imaging. | LitMetric

Solvent Effects on Fluorescence Properties of Carbon Dots: Implications for Multicolor Imaging.

ACS Omega

Department of Material Physics, Faculty of Science, Bengbu University, Bengbu 233030, P. R. China.

Published: October 2021

AI Article Synopsis

  • Carbon dots (CDs) are created using a solvothermal method with various solvents, producing solutions that emit blue, green, yellow, and orange fluorescence.
  • Different techniques like TEM, DLS, and FTIR are used to analyze the CDs' structures and optical properties, showing that DMF significantly influences redshift in fluorescence emission.
  • The presence of functional groups in the CDs is affected by the solvents, which relates to their potential applications in multicolor imaging.

Article Abstract

Carbon dots (CDs) are synthesized by the solvothermal method with four kinds of solvents including water, dimethylformamide (DMF), ethanol, and acetic acid (AA). The aqueous solutions of the above CDs emit multiple colors of blue (470 nm), green (500 nm), yellow (539 nm), and orange (595 nm). The structures, sizes, and chemical composition of the CDs are characterized by transmission electron microscopy (TEM), dynamic light scattering (DLS), X-ray diffraction (XRD), Fourier transform infrared (FTIR), and X-ray photoelectron spectroscopy (XPS). The optical properties of multicolored CDs are analyzed by UV-vis absorption and photoluminescence (PL) spectra. It has been revealed that DMF is the key solvent to synthesized CDs for the red shift of fluorescence emission, which could be enhanced by adding an AA solvent. The structures of functional groups such as the contents of graphitic N in carbon cores and oxygen-containing functional groups on the surface of CDs are affected by these four solvents. According to the oxidation and selective reduction of NaBH, the implication for multicolor imaging has been discussed based on the COOH, C-O-C, and C=O functional groups.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8515583PMC
http://dx.doi.org/10.1021/acsomega.1c03731DOI Listing

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