In this work, a strategy of sulfur-rich doped nitrogen dots (S-Ndots) based on a single-source precursor (SSP) was developed and applied to sensing of Hg 2+ . Fluorescent S-Ndots were synthesized by microwave-assisted method using 2-azidothiazole as a single-source precursor, which served as carbon, nitrogen and sulfur source simultaneously. This SSP approach guarantee efficient core doping and improve the effect of doping in a molecular level, which is more efficient and simpler than the doping strategy with multiple precursors. The results showed that the as-synthesized S-Ndots have high sulfur component up to 24.6%, and their specific structure effectively promoted artificial peroxidase activity and coordination interaction. Interestingly, the fluorescence intensity could be quenched obviously and the peroxidase activity of the S-Ndots were selectively inhibited by Hg 2+ , then the S-Ndots were applied to the dual-mode sensing of Hg 2+ with both fluorometric and colorimetric readout. The S-Ndots-based sensing assay with simplicity and rapidity showed high selectivity to Hg 2+ with the detection limit of 0.1 μmol/L by fluorescence spectroscopy and a distinguishable change in the color was observed by the naked eye. In addition, the accuracy and precision were evaluated based on the quantitative detection of Hg 2+ in industrial waste water samples with satisfactory results. Moreover, the S-Ndots with good biocompatibility were further explored for imaging of Hg 2+ in A549 cells. As a novel member of nitrogen quantum dots family, the S-Ndots hold great promise to broaden its applications in environmental and biological sensing.
Li Lihua,Feng Dexiang,Fang Xian,Han Xiaowei,Zhang Yuzhong
In this work, we have developed a novel visual Hg 2+ sensor in aqueous solution using unmodified Au@Ag core–shell nanoparticles at room temperature, based on a redox reaction between Ag-shell and Hg 2+ . The prepared Au@Ag core–shell nanoparticles exhibited good monodispersity. In the presence of Hg 2+ , Hg 2+ was reduced into Hg (0) by Ag-shell, and deposited on the surface of Au-core to form Au–Hg alloys and caused nanoparticles aggregation, leading to the color changes of the solution from yellow to purplish red, and the surface plasmon resonance spectra of Au@Ag core–shell nanoparticles red shift. Under the optimal conditions, the visual sensor could selectively detect Hg 2+ as low as 0.4 µM with the naked eye and 5.0 nM by UV–vis spectra analysis methods. The designed sensor had several advantages: (1) the nanoparticles surface need not be functionalized. (2) The color change of the solution was in 2 s and could easily be observed with naked eyes. The visual sensor had been applied to detection of Hg 2+ in tap and lake water, which obtained satisfied result.