4.6 Article

Facile Fabrication of Highly Fluorescent N-Doped Carbon Quantum Dots Using an Ultrasonic-Assisted Hydrothermal Method: Optical Properties and Cell Imaging

Journal

ACS OMEGA
Volume 6, Issue 48, Pages 32904-32916

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsomega.1c04903

Keywords

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Funding

  1. National Natural Science Foundation of China [41877499]

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In this study, two different N-doped carbon quantum dots (CQDs) were successfully synthesized using L-glutamic acid as a precursor. The two CQDs exhibited excellent optical properties and were found to be suitable for cell imaging applications. The photoluminescence mechanism of the CQDs was qualitatively explained, providing important insights for their future development in optoelectronic devices.
Fluorescent N-doped carbon nanodots (CNDs) are a type of environmentally friendly nanomaterial that is promising for application in cell imaging and optoelectronics. In this paper, a natural amino acid (L-glutamic acid) was used as a precursor, and two different morphological and structured N-doped carbon quantum dots (CQDs) were synthesized via a one-step ultrasonic-assisted hydrothermal method at 230 and 250 degrees C. Various microscopy and spectroscopy techniques were employed to characterize the morphology, structure, optical properties, and stability of the CQDs. The results showed that N-CQDs-1 are new CNDs composed of amorphous carbon with a large amount of pyroglutamic acid, and N-CQDs-2 are composed of pure amorphous carbon. The CQDs exhibit excellent optical properties, such as 40.5% quantum yield, strong photobleaching resistance, and superior photostability. Combining the fluorescence lifetimes and radiative and non-radiative decay constants, the photoluminescence mechanism of the CQDs was qualitatively explained. The two CQDs were used for BV2 cell imaging and showed good results, implying the ultrasonic-assisted hydrothermal approach as a facile method to obtain structure- and morphology-controllable N-doped CQDs with prospect for application in cell imaging.

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