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[Display omitted] • Carbon nanodots (CNDs) were synthesized through a facile microwave method. • The fluorescence of CNDs was selectively quenched by gold nanoparticles (AuNPs). • Once introduced, thiourea triggered the reversion of quenched fluorescence. • Effective applications in environmental water and compound fruit-vegetable juice. Illegal abuse results in the presence of thiourea (TU) in soil, wastewater, and even fruits, which is harmful for the environment and human health. It has urgent practical significance to design an efficient and reliable probe for TU detection. Herein, a sensitive fluorescent probe with off–on response for harmful TU was reported. The probe was designed with fluorescent carbon nanodots (CNDs) and gold nanoparticles (AuNPs) based on fluorescence resonance energy transfer (FRET) effect. Firstly, the CNDs were pre-combined with AuNPs and the fluorescence of CNDs was quenched due to the FRET effect. Upon addition of TU, the fluorescence of CNDs recovered due to the unbinding of CNDs and AuNPs, since the coordination interaction between TU and AuNPs is stronger than the electrostatic interaction among CNDs and AuNPs. Under the optimum parameters, a linear relationship was found between the relative fluorescence intensity of the probe and the concentration of TU in the range of 5.00 × 10-8-1.00 × 10-6 M (R2 = 0.9958), with the limit of detection (LOD) calculated to be 3.62 × 10-8 M. This proposed method is easy to operate and has excellent selectivity and sensitivity for TU, which can be effectively applied in environmental water and compound fruit-vegetable juice. [ABSTRACT FROM AUTHOR]

[Display omitted] • This is the first time that carbon dots have been synthesized using ammonium citrate and glutamic acid as precursors. • The fluorescence stability of carbon dots is fully explored, facilitating their use in real-world environments. • This method achieves high selectivity and sensitivity in the trace detection range. • Monitoring Cd2+ ions in tap water and lake water. In this study, fluorescent carbon dots were synthesized for the first time using ammonium citrate and glutamic acid as precursors via a one-pot hydrothermal method. The synthesized carbon dots emit blue fluorescence at 436 nm (excited at 320 nm) and demonstrate excellent photobleaching resistance and fluorescence stability in high salt environments. Within the range of 1–25 μM, the fluorescence of CDs gradually increases with the increasing concentration of Cd2+, reaching a limit of detection as low as 13 nM. This phenomenon could be ascribed to the chelation-enhanced fluorescence, a result of Cd2+ forming complexes with the abundant surface functional groups such as CN–, –COOH, –OH, –NH 2 in CDs. Furthermore, this turn-on fluorescent probe has been successfully used for the detection of Cd2+ in tap water and lake water, providing an efficient and sensitive method for the analysis of environmental metals. [ABSTRACT FROM AUTHOR]

In this paper, fluorescent carbon dots were prepared by hydrothermal method using 3,5-dihydroxybenzoic acid and l -Arginine as precursors. The synthesized CDs have excitation-dependent emission with emission peaks at 354 nm and 460 nm, corresponding to the optimal excitation wavelengths of 295 nm and 330 nm, respectively. CDs have good dispersion and resistance to photobleaching in aqueous solution, and can maintain stable fluorescence in highly concentrated salt environment. Based on the inner filter effect, Cr(VI) with strong absorption can shield the excitation light of CDs at 295 nm and absorb the emission fluorescence at 354 nm simultaneously. Due to the intermolecular electrostatic interaction, Hg(II) can coordinate with CDs surface groups and cause static quenching, which significantly reduces the fluorescence intensity of CDs emitted at 460 nm. The linear ranges were 0.1–2 μM and 0.4–5 μM for Cr(VI) and Hg(II) detection, respectively, and limits of detection were 0.024 μM and 0.084 μM. Additionally, the probe was successfully applied to tap water and lake water samples. With high sensitivity and spectral selectivity, this sensing strategy realized the detection of two heavy metal ions by a single fluorescent probe, demonstrating its great potential in the field of environmental metal analysis. [Display omitted] • First synthesis of carbon dots with spectral selectivity using 3,5-dihydroxybenzoic acid and l -arginine as precursors. • Separate detection of Cr(VI) and Hg(II) ions using the same carbon dots under different excitations. • This method achieves high selectivity and sensitivity in the trace detection range. • Monitoring Cr(VI) and Hg(II) ions in tap water and lake water. [ABSTRACT FROM AUTHOR]

[Display omitted] • This is the first time that carbon dots were synthesized using cysteine and ethylenediamine as precursors. The synthesis method is green and simple, and the prepared N -CDs have good fluorescence stability. • The developed experimental conditions for the detection of Fe3+ using nitrogen-doped carbon dots as fluorescent probes have been fully optimized to significantly improve the sensitivity. • The method is simple, sensitive and highly feasible, with LOD as low as 0.069 μM in deionized water. And, linear models were also constructed in tap water and lake water with LOD of 0.21 μM and 0.59 μM, respectively. In this study, we synthesized stable nitrogen-doped carbon dots by a simple and economical one-step hydrothermal method using l -cysteine and anhydrous ethylenediamine as precursors. The prepared carbon dots have bright and stable blue light emission near 383 nm and can be used as fluorescent probes to detect the concentration of Fe3+ in environmental waters. It was demonstrated that due to intermolecular electrostatic interaction, a non-fluorescent complex N -CDs/Fe3+ is formed by coordination of Fe3+ with amino and carboxyl functional groups on the surface of carbon dots. Therefore, in combination with internal filtration effect, the fluorescence of carbon dots can be quenched in the presence of Fe3+, and the degree of quenching is linearly related to the concentration of Fe3+. The limit of detection in deionized water was as low as 0.069 μM with R2 of 0.998 and a linear range of 0.3 to 20 μM. In addition, satisfactory recoveries were achieved for the determination of Fe3+ in environmental water samples. The method is reliable, with highly sensitivity and selectivity, and has potential for practical applications in environmental metal analysis. [ABSTRACT FROM AUTHOR]