Nitrogen, sulfur, and phosphorus Co-doped carbon dots-based ratiometric chemosensor for highly selective sequential detection of Al(3+) and Fe(3+) ions in logic gate, cell imaging, and real sample analysis.

Heteroatom-doped photoluminescent (PL) carbon dots (CDs) have recently gained attention as optical sensors due to their excellent tunable properties. In this work, we propose a one-pot hydrothermal synthesis of PL nitrogen (N), sulfur (S), and phosphorus (P) co-doped carbon dots (NSP-CDs) using glutathione and phosphoric acid (H3PO4) as precursors. The synthesized NSP-CDs were characterized using different spectroscopic and microscopic techniques, including ultraviolet-visible (UV-Vis) spectroscopy, fluorescence spectroscopy, Fourier-transform infrared (FTIR), X-ray powder diffraction (XRD), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS) analysis. The NSP-CDs exhibited excellent PL properties with green emission at 492 nm upon excitation at 417 nm, a high quantum yield of 26.7%, and dependent emission behavior. The as-prepared NSP-CDs were spherical with a well-monodispersed average particle size of 5.2 nm. Moreover, NSP-CDs demonstrate high PL stability toward a wider pH, high salt ionic strength, and various solvents. Furthermore, the NSP-CDs showed a three-state "off-on-off" PL response upon the sequential addition of Al3+ and Fe3+ ions, with a low limit of detection (LOD) of 10.8 nM for Al3+ and 50.7 nM for Fe3+. The NSP-CD sensor can construct an INHIBIT logic gate with Al3+ and Fe3+ ions as the chemical inputs and emissions as the output mode. Owing to an excellent tunable PL property and biocompatibility, the NSP-CDs were applied for sensing Al3+ and Fe3+ ions as well as live cell imaging. Furthermore, NSP-CDs were designed as PL sensors for detecting Al3+ and Fe3+ ions in real water show their potential application.

Mohandoss S ，Ganesan S ，Palanisamy S ，You S ，Velsankar K ，Sudhahar S ，Lo HM ，Lee YR ... -  《-》

Nitrogen and sulfur co-doped photoluminescent carbon dots for highly selective and sensitive detection of Ag(+) and Hg(2+) ions in aqueous media: Applications in bioimaging and real sample analysis.

In this study, we report the synthesis of photoluminescent (PL) nitrogen (N) and sulfur (S) co-doped carbon dots (NS-CDs) from nitazoxanide and 3-mercaptopropionic acid as a precursors via a one-pot hydrothermal methods. N and S co-doped materials allows more active sites in the CDs surface resulting in an enhancement of their PL properties. NS-CDs show bright blue PL, excellent optical properties, good water solubility, and a high quantum yield (QY) of 32.1%. The as-prepared NS-CDs were confirmed by UV-Visible, photoluminescence, FTIR, XRD and TEM analysis. An optimized excitation at 345 nm, the NS-CDs exhibited strong PL emission at 423 nm with an average size of 3.53 ± 0.25 nm. Under optimized conditions, the NS-CDs PL probe shows high selectivity with Ag+/Hg2+ ions detected, while other cations no significant changes the PL signal. The PL intensity of NS-CDs linearly quenching and enhancement with Ag+ and Hg2+ ions from 0 to 50 × 10-6 M, with the detection limit of 2.15 × 10-6 M and 6.77 × 10-7 M (S/N = 3). More interestingly, as-synthesized NS-CDs shows a strong binding to Ag+/Hg2+ ions with the PL quenching and enhancement to precise and quantitative detection of Ag+/Hg2+ ions in living cells. The proposed system was effectively utilized for the sensing of Ag+/Hg2+ ions in real samples resulting in high sensitivity and good recoveries (98.4-109.7%).

Mohandoss S ，Ahmad N ，Khan MR ，Velu KS ，Palanisamy S ，You S ，Kumar AJ ，Lee YR ... -  《-》

Multicolor emission-based nitrogen, sulfur and boron co-doped photoluminescent carbon dots for sequential sensing of Fe(3+) and cysteine: RGB color sensor and live cell imaging.

Herein, a simple hydrothermal synthesis is used to prepare multiple heteroatom-doped photoluminescent carbon dots (CDs) from thiourea (N and S source) and boric acid (B source) as precursors. The optical and physicochemical properties of the as-synthesized NSB-CDs were studied using UV-Vis, photoluminescence, TEM, FT-IR, XRD, Raman, and XPS analyses. The NSB-CDs exhibited excellent stability, high photostability, pH, and ionic strength tolerance; they retained their excellent stability independent of excitation. The NSB-CDs featured small sizes of approximately 3.2 ± 0.4 nm (range: 2.0-5.0 nm) as evidenced using TEM measurements. The NSB-CDs were used as a photoluminescent sensing platform to detect Fe3+ as well as cysteine (Cys) molecules. The competitive binding of Cys to Fe3+ resulted in NSB-CDs that retained their photoluminescence. For the rapid identification and quantification of Fe3+ and Cys, NSB-CDs were developed as a "switch-on" dual-function sensing platform. The linear detection range of Fe3+ was 0-20 μM (limit of detection [LOD]: 54.4 nM) and that of Cys was 0-50 μM (LOD: 4.9 nM). We also introduced a smartphone RGB analysis method for detecting low-concentration solutions based on digital images. The NSB-CDs showed no toxicity at 100 μg/mL. Photoluminescent probes for multicolor live-cell imaging can be used with NSB-CDs at this concentration, suggesting that NSB-CDs may be promising photoluminescent probes.

Mohandoss S ，Ahmad N ，Rizwan Khan M ，Sakthi Velu K ，Kalaiselvi K ，Palanisamy S ，You S ，Rok Lee Y ... -  《-》

Nitrogen and sulfur co-doped highly luminescent carbon dots for sensitive detection of Cd (II) ions and living cell imaging applications.

In this work, we have developed a green, simple and fast one-pot microwave-assisted strategy for synthesis of nitrogen and sulfur co-doped fluorescent carbon dots (CDs) using scallion (SL) as the carbon source. Optical properties of the SL-CDs have been measured by UV-visible and fluorescent spectroscopy. The morphology of the prepared SL-CDs has been performed by transmission electron microscopy (TEM). Surface functionality and elemental composition of SL-CDs was analyzed by Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS) spectra. The photoluminescent (PL) quantum yield of the obtained scallion carbon dots (SL-CDs) can reach as high as 18.6%. We further demonstrated that the SL-CDs can be used as fluorescent probes for detection of Cd2+ ions with a high sensitivity and an excellent selectivity. Linear relationships between the variation of the luminescent intensity of the SL-CDs before and after exposing the Cd2+ ions versus the concentration of Cd2+ ions in the range of 0.1-3.0 μM and 5.0-30.0 μM. The detection limit of Cd2+ ions can reach 15.0 nM. Moreover, the as-prepared SL-CDs exhibit negligible or extremely low cytotoxicity, which makes them be able to be used as fluorescent probes for living cell imaging. Overall, the prepared SL-CDs have promising applications in sensing of Cd2+ ions and in vivo or in vitro bioimaging.

Gu D ，Hong L ，Zhang L ，Liu H ，Shang S ... -  《-》

Emission enhanced fluorometric biosensor by functionalized carbon polymer dots for glutathione detection in human real samples and molecular logic gate operation.

Glutathione (GSH), an active peptide, plays pivotal roles in many physiological processes and detection of GSH inside of human body is of great importance for the playing of its biological effects. Here silver-phosphorus co-doped carbonized polymer dots (Ag@PCPDs) were prepared via solvothermal treatment of citric acid and phytic acid in the presence of Ag+ for GSH determination. The physicochemical and optical performance of the Ag@PCPDs were characterized by X-ray photoelectron spectroscopy (XPS), Fourier-transform infrared (FT-IR), X-ray powder diffraction (XRD), Raman spectroscopy, transmission electron microscopy (TEM), fluorescence spectroscopy and ultraviolet-visible (UV-Vis) spectroscopy analyses. The prepared Ag@PCPDs have outstanding water solubility with high monodispersity (7.81 ± 0.31 nm) and exhibited excellent optical properties with excitation-dependent emission, high photostability, pH, and ionic strength tolerance. An optimized excitation at 358 nm, the Ag@PCPDs showed strong photoluminescent (PL) emission at 456 nm with a PL quantum yield (QYs) of 15.6%. Furthermore, the Ag@PCPDs were used as a PL sensing platform for detection GSH in a linear range of 0-200 μM with a low limit of detection at 0.68 μM. In addition, the proposed system can construct molecular logic gates with GSH and Fe3+ ions as the chemical inputs and PL emissions as the output. And the Ag@PCPDs were successfully used for GSH determination in real samples resulting in high sensitivity and satisfactory recoveries (92.81--107.45%). More importantly, the Ag@PCPDs showed low cytotoxicity at 500 μg/mL and superior cell imaging capability in HeLa cells, which offer a new path for detection and categorization of GSH in biomedical applications.

Zhou X ，Hu Y ，Xu L ，Li Y ，Zhang L ，Cao Y ，Zhou J ，Qian T ... -  《-》