A double carbon dot system composed of N, Cl-doped carbon dots and N, Cu-doped carbon dots as peroxidase mimics and as fluorescent probes for the determination of hydroquinone by fluorescence

A fluorescence method is described for the determination of hydroquinone based on the double carbon dot system as peroxide mimic enzymes and fluorescent probes. Deep eutectic solvent (DES)–based fluorescent carbon dots (N/Cl-CDs) and copper-doped carbon dots (N/Cu-CDs) were prepared by the hydrothermal method. Both carbon dots were characterized with transmission electron microscopy (TEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), ultraviolet-visible (UV-Vis) spectroscopy, X-ray photoelectron spectrometry (XPS), Fourier transform infrared (FT-IR) spectroscopy, and fluorescence spectroscopy. N/Cl-CDs displayed intrinsic peroxidase-like activity and were able to catalyze the oxidation of hydroquinone (H 2 Q) to p-benzoquinone (BQ) along with an intermediate. The intermediate (BQ) did quench the N/Cu-CD photoluminescence (PL) at 450 nm using an excitation wavelength of 347 nm. Based on the results, a fluorescent platform is proposed for the determination of hydroquinone with a promising determination limit of 0.04 μM (linear range, 1.0–75 μM). The recoveries of spiked water samples were in the range 89.5–105.1%, with relative standard deviations (RSDs) of 1.5–2.9%. This method was applied to determination of H 2 Q in environmental water samples. A fluorescence method was established for the determination of hydroquinone based on the double carbon dot system as peroxide-mimic enzymes and fluorescent probes. Chlorine-doped carbon dots (N/Cl-CDs) derived from deep eutectic solvent (DES) displayed intrinsic peroxidase-like activity, and were able to catalyze the oxidation of hydroquinone (H2Q) to p-benzoquinone (BQ) along with an intermediate. The intermediate (BQ) did quench the N/Cu-CD photoluminescence (PL). This method was applied to H2Q in environmental water samples.