Ultrasmall aqueous starch-capped CuS quantum dots with tunable localized surface plasmon resonance and composition for the selective and sensitive detection of mercury(ii) ions.

Abstract

Ultrasmall starch-capped CuS quantum dots (QDs) with controllable size were chemically fabricated in an aqueous medium. The phase of the CuS QDs was confirmed via X-ray diffraction (XRD), whereas the characteristic localized surface plasmon resonance (LSPR) peak in the near-infrared (NIR) region was measured using UV-Vis spectroscopy. Transmission electron microscopy and high bandgap analysis confirmed the formation of ultrasmall CuS QDs in the size range of 4–8 nm. CuS QDs have been used for the selective and sensitive detection of Hg2+ ions through colorimetric and spectroscopic techniques. The selective sensing of Hg2+ ions from various metal ions was detected via a remarkable change in color, damping in LSPR intensity, significant change in the Fourier-transform infrared spectra and X-ray photoelectron spectroscopic measurements. The mechanism of interaction between the CuS QDs and Hg2+ ions has been deeply explored in terms of the role played by the starch and the reorganization of sulfide and disulfide bonds to facilitate the access of Hg2+ ions into the CuS lattice. Finally, an intermediate Cu2−xHgxS nanostructure resulted in the leaching of Cu+ ions into the solution, which were further recovered and reused for the formation of fluorescent Cu2S nanoparticles. Thus, the entire process of synthesis, sensing and reuse paves the way for sustainable nanotechnology.