Synthesis of Photoluminescent Carbon Dots Using IHibiscus/I Tea Waste and Heteroatom Doping for Multi-Metal Ion Sensing: Applications in Cell imaging and Environmental Samples

Novel photoluminescent carbon dots (CDs) were synthesized through a facile hydrothermal method using Hibiscus tea extract as a natural carbon source and boric acid as a boron source. The optical and physicochemical properties of the as-synthesized nitrogen- and boron-doped CDs (NB-CDs) were characte...

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Veröffentlicht in:Chemosensors 2023-08, Vol.11 (9)
Hauptverfasser: Mohandoss, Sonaimuthu, Ahmad, Naushad, Velu, Kuppu Sakthi, Khan, Mohammad Rizwan, Palanisamy, Subramanian, You, SangGuan, Lee, Yong Rok
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Sprache:eng
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Zusammenfassung:Novel photoluminescent carbon dots (CDs) were synthesized through a facile hydrothermal method using Hibiscus tea extract as a natural carbon source and boric acid as a boron source. The optical and physicochemical properties of the as-synthesized nitrogen- and boron-doped CDs (NB-CDs) were characterized using UV–Visible (UV–Vis), photoluminescence (PL) spectroscopy, Fourier-transform infrared (FTIR), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM). The as-synthesized NB-CDs showed spherical morphology of approximately 6.2 ± 0.5 nm with quantum yield (9.2%), high aqueous solubility, strong photo-stability, and excitation-dependent PL behavior. The obtained NB-CDs exhibited high stability over a wide pH range and high ionic strength. Additionally, NB-CDs exhibited PL enhancement response with excellent sensitivity toward multi-metal ions, including Ag[sup.+], Cd[sup.2+], and Cr[sup.3+] ions, with very low detection limits of 44.5, 164.4, and 54.6 nM, respectively, with a wide concentration range of 0–10 μM. Upon testing the cytotoxicity of the NB-CDs at a concentration of 20 μg/mL for 24 h, we found no obvious inhibition of cell viability. Therefore, the proposed sensor method can be successfully applied to detect Ag[sup.+], Cd[sup.2+], and Cr[sup.3+] ions in cell imaging as well as in real water environmental samples.
ISSN:2227-9040
DOI:10.3390/chemosensors11090474