Okra peel-derived nitrogen-doped carbon dots: Eco-friendly synthesis and multi-functional applications in heavy metal ion sensing, nitro compound detection and environmental remediation.

The present study explores the kitchen waste okra peels derived synthesis of nitrogen doped carbon dots (N-CDs) via simple carbonization followed by reflux method. The synthesized N-CDs was characterized using, TEM, XPS, FTIR, XRD, Raman, UV-Visible and Fluorescence Spectroscopy. The N-CDs emits bright blue emission at 420 nm with 12 % of quantum yield as well as it follows excitation dependent emission. Further, the N-CDs were employed as a fluorescence sensor for detection of hazardous metal ions and nitro compounds. Among various metal ions and nitro compounds, the N-CDs shows fluorescence quenching response towards Cr6+, and Mn7+ metal ions as well as 4-nitroaniline (4-NA) and picric acid (PA) with significant hypsochromic and bathochromic shift for Mn7+, 4-NA and PA respectively. The developed fluorescent probe shows relatively low limit of detection (LOD) of 1.46 µg/mL, 1.05 µg/mL, 2.1 µg/mL and 2.2 µg/mL for the above analytes respectively. The N-CDs did not show any significant interference with coexisting ions and successfully applied for real water sample analysis. In addition, circular economy approach was employed for adsorption of dyes by reactivating leftover waste carbon residue which was obtained after reflux. Thus, the kitchen waste valorization and circular economy approach based N-CDs have potential applications in the field of detection of emerging pollutants, and environmental remediation.

Facile synthesis of sulphur-doped carbon dots (S-CDs) using a hydrothermal method for the selective sensing of Cr6+ and Fe3+ ions: application to environmental water sample analysis.

In this work, we used a one-step hydrothermal method to synthesize blue-emission sulfur-doped carbon dots (S-CDs) using jaggery as a carbon precursor. The synthesized carbon quantum dots showed low toxicity, good water solubility, anti-interference properties, and stable fluorescence. When excited at 310 nm, the S-CDs produced bright emission with a quantum yield of 7.15% at 397 nm. The S-CDs exhibited selective and sensitive quenching responses with limits of detection (LODs) of 4.25 µg mL-1 and 3.15 µg mL-1 for variable concentrations of Cr6+ and Fe3+, respectively, accompanied by a consistent linear relationship between fluorescence intensity and these concentrations. Fluorescence lifetime measurements were used to investigate the fluorescence quenching mechanism, which supports the static type of quenching. Outstanding benefits of the developed S-CD based fluorescence probe include its low cost, excellent sensitivity and selectivity, and ease of use for the detection of Cr6+ and Fe3+ ions. The developed carbon dot based fluorescent probe was successfully used to detect Cr6+ and Fe3+ ions in real water samples with an excellent recovery ratio.

Sawmill waste derived carbon dots as a fluorescent probe for synthetic dyes in soft drinks.

Herein, for the first time the carbon dots (CDs) were synthesized by reflux method from sawmill waste material. We also represent a novel strategy based on fluorescent CDs for determination of ponceau 4R and allura red dyes in soft drinks. Interestingly, both the dyes were sensitive and showed effective fluorescence quenching of the CDs owing to the interaction between them. The analytical applicability of CDs were evaluated for detection of both the dyes with a good linear relationship between the concentration range of 0.0 to 3.0 µg mL-1 and having detection limit 0.45 and 0.47 µg mL-1 for allura red and ponceau 4R dyes respectively. Meanwhile, the potential application of this novel fluorescent probe for dyes determination in real samples was validated in different soft drink samples with good accuracy and precision. Thus, these findings provides new insights for the potential risk assessment of both the dyes. Moreover, CDs acted as an excellent fluorescent material in cellular imaging owing to their cellular uptake and localization.

Fluorescence-based sensor for selective and sensitive detection of amoxicillin (Amox) in aqueous medium: Application to pharmaceutical and biomedical analysis.

We here for the first time demonstrate an analytical approach for the highly selective and sensitive detection of amoxicillin (Amox) in aqueous medium based on the fluorescence quenching of quantum dots (QDs). The change in fluorescence intensity of mercaptopropionic acid-capped cadmium sulphide (MPA-CdS) QDs is attributed to the increasing concentration of Amox. The results show that the fluorescence quenching of QDs by Amox takes place through both static and dynamic types of quenching mechanism. The fluorescence quenching of QDs with increase in concentration of Amox shows the linear range between 5 µg ml-1 and 30 µg ml-1 and the limit of detection (LOD) is 5.19 µg ml-1 . There is no interference of excipients, which are commonly present in pharmaceutical formulation and urine samples. For the practical application approach, the developed method has been successfully applied for the determination of Amox in pharmaceutical formulations and urine samples with acceptable results.

CdS nanocrystals as fluorescent probe for detection of dolasetron mesylate in aqueous solution: Application to biomedical analysis.

A simple and straightforward method for the determination of dolasetron mesylate (DM) in aqueous solution was developed based on the fluorescence quenching of 3-Mercaptopropionic acid (MPA) capped CdS quantum dots (QDs). The structure, morphology, and optical properties of synthesized QDs were characterized by using UV-Vis absorption spectroscopy, fluorescence spectroscopy, transmission electron microscopy (TEM) and dynamic light scattering (DLS) measurements. Under the optimum conditions, the MPA-CdS QDs fluorescence probe offered good sensitivity and selectivity for detecting DM. The probe provided a highly specific selectivity and a linear detection of DM in the range of 2-40 µg/mL with detection limit (LOD) 1.512 µg/mL. The common excipients did not interfere in the proposed method. The fluorescence quenching mechanism of CdS QDs is also discussed. The developed sensor was applied to the quantification of DM in urine and human serum sample with satisfactory results.

Spectroscopic Investigation of Interaction Between Carbon Quantum Dots and D-Penicillamine Capped Gold Nanoparticles.

This study reports the interaction and energy transfer between fluorescent carbon quantum dots (CQDs) and D-Penicillamine capped gold nanoparticles (DPA-AuNPs). The CQDs was synthesized by a simple chemical oxidation method at room temperature. The prepared CQDs shows a strong fluorescence at λ em = 430 nm when excited at λ ex = 320 nm. The interaction of CQDs with DPA-AuNPs was characterized by fluorescence spectroscopy, Transmission Electron Microscopy (TEM) study and Dynamic Light Scattering (DLS) techniques. The fluorescence study shows the continuous quenching in the fluorescence intensity of CQDs in presence of increasing concentrations of DPA-AuNPs. The change in fluorescence spectra of CQDs in presence of increasing concentration of DPA-AuNPs and quenching are suggestive of a rapid adsorption of CQDs on the surface of DPA-AuNPs. The K sv , K, K q and n values were calculated and results indicated that the dynamic type of quenching takes place. The distance between donor and acceptor (r) is 6.07 nm which supports the energy transfer by Fluorescence Resonance Energy Transfer (FRET) phenomenon. The plausible mechanism for FRET is also discussed.