A phenylboric acid functionalized carbon dot (2-FPBA-CD) for rapid fluorescent sensing of glucose in blood was synthesized by simply mixing N, S-doped carbon dots (CDs) with phenylboric acid at room temperature. At pH 7.4, the response of 2-FPBA-CD to glucose could reach equilibrium in a very short time (10 min), with a wide responsive linear range of 19.70 μM to 2.54 mM, which can be applied to the detection of glucose in serum. The mechanism studies showed that the layered carbon film of 2-FPBA-CD aggregated after adding glucose, thereby leading to the fluorescence quenching of 2-FPBA-CD.

Heavy metal ions pollution has become of worldwide critical concern, thus, it is particularly important to monitor it in the environment and food for ensuring human health. In this study, p-phenylenediamine and 2-mercaptothiazoline were used to prepare nitrogen (N) and sulfur (S) co-doped carbon dots (N/SCDs) for fluorescent and colorimetric detection of Cu2+. The fabricated N/SCDs with bright green fluorescence showed excellent optical characteristics and favorable water solubility. In an aqueous system, a significant fluorescence quenching of N/SCDs at 512 nm is obtained in the presence of Cu2+. It also caused a significant colorimetric response with the color of prepared N/SCDs solution changed from colorless to yellow. Under optimal conditions, the analytical results showed that the linear range spanning from 5 to 400 μM, with a detection limit of 0.215 μM in fluorescence and 0.225 μM in colorimetric detection. In addition, N/SCDs displayed high selectivity toward Cu2+. No obvious interference was observed over other metal ions. Furthermore, we have also used N/SCDs to monitor Cu2+ in tap and lake water. The recovery of Cu2+ ranged between 89.6% and 113.1%. Exhibiting remarkable sensitivity and selectivity, the designed sensor offers a promising detection method for Cu2+ detection in the real sample.

Carbon dots (CDs) are versatile nanomaterials with tunable luminescent properties. We used a natural plant kaempferol as a carbon source to synthesize multicolor CDs by reacting it with various nitrogen sources. Blue, green, and red CDs (B-CDs, G-CDs, and R-CDs) with emission wavelengths of 445 nm, 510 nm, and 600 nm respectively were successfully synthesized. Their photoluminescence quantum yields of are up to 37.4%, 20.1%, and 30.8%, respectively. Surface analysis revealed abundant nitrogen groups influencing luminescence. B-CDs and G-CDs show excitation-dependent emissions, indicating a potential correlation between their luminescence and particle sizes, while R-CDs exhibit excitation-independent emission, suggesting they belong to molecular state CDs. All three CDs exhibit stable luminescent performance, as well as good salt resistance and photobleaching resistance. The practical application of multicolored CDs in anti-counterfeiting fluorescent inks was further explored. This work offers a straightforward, eco-friendly route to synthesize multicolor CDs.

4-Nitrophenol (4NP) is a vital intermediate in organic industries, and its exploitation creates serious environmental issues. We propose a fluorescence quenching-based strategy with nitrogen and sulfur co-doped carbon dots (NS-CDs) for highly sensitive 4NP detection with excellent selectivity. The NS-CDs are produced through the hydrothermal process, in which citric acid serves as a carbon source and cysteamine hydrochloride as a source of N and S. The effect of doping was also studied by synthesizing undoped CDs and examining their properties. As-developed NS-CDs exhibit a bright cyan blue color with maximum emission centered at 465 nm. The fluorescence of NS-CDs is significantly quenched in an approximately linear fashion with increasing 4NP concentration (7.5–97.5 μM). The inner filter effect (IFE) and static quenching (SQ) between NS-CDs and 4NP are responsible for such fluorescence reduction. The fluorimetry technique enables the quantification of 4NP with a limit of detection (LOD) of about 0.028 μM. Moreover, the fluorescence quenching is tested for several other chemical compounds but they generate false quenching signals; only 4NP leads to fluorescence quenching of NS-CDs, demonstrating excellent selectivity. The “turn-off” fluorescence properties and visually apparent color change of the fluorescent probe reveal the excellent performance for 4NP sensing. The NS-CDs’ capability of quantifying 4NP in real water samples (tap water and drinking water) produces an excellent recovery rate ranging between 96.24 and 98.36%.

Sulfur and nitrogen co-doped carbon dots (NSCDs) were quickly synthesized by the microwave-assisted method from triammonium citrate and thiourea. NSCDs showed a quantum yield of 11.5% with excitation and emission bands at 355 and 432 nm, respectively. Also, a fluorescence quenching was observed in the presence of Pb(II) ions, and the as-synthesized CDs were used as a sensitive probe for detecting Pb(II) in water and food samples. The results showed the optimal conditions for Pb(II) determination were CDs concentration of 0.02 mg mL− 1 at pH 6.0–7.0 and an incubation time of 20 min. The relative fluorescence intensity of NSCDs was proportional to Pb(II) concentrations in the range of 0.029–2.40 and 2.40–14.4 μmol L− 1 with a correlation coefficient (R2) of 0.998 and 0.955, respectively, and a detection limit of 9.2 × 10– 3 μmol L− 1. Responses were highly repeatable, with a standard deviation below 3.5%. The suggested method demonstrates the potential of a green, fast, and low-cost approach for Pb(II) determination in water, tea, and rice samples with satisfying results.

Stilbene-based fluorescent brighteners (FB) have been shown to enhance insecticidal activities of entomopathogenic viruses but little is known its effect on entomopathogenic bacteria. We investigated the effect of two FBs (FB 28 and FB 71) on the insecticidal activity of B. thuringiensis var. kurstaki (Btk) as well as the Lymantria dispar multiple nuclear polyhedrosis virus (LdMNPV) in Lymantria dispar asiatica. FB 28 increased the mortality at the combination with low concentration (1.6×102 IU/ml) of Btk, but FB 71 slightly reduced the mortality with middle and high concentrations (1.6×103 and 1.6×104 IU/ml) of Btk in comparison to Btk alone. Both FB 28 and FB 71 increased mortality in combination with LdMNPV at all concentrations (3×102, 3×104, and 3×106 POBs/ml) compared to LdMNPV alone. Our findings suggest that FBs enhanced pathogenic activities but depend on chemical nature of FBs.

The rapid synthesis techniques and interesting multidisciplinary applications make carbon nanodots (CNDs) stand out from semiconductor quantum dots. Moreover, CNDs derived from green precursors have gained more importance beyond chemically derived CNDs due to sustainable synthesis opportunities. However, the presence of molecular impurities or intermediates or fluorophores was neglected during the entire process. Herein, we illustrate the sustainable synthesis of CNDs from Hemigraphis alternata plant leaves with extended carbonization procedure (3 and 9 min) along with simultaneous ethylene glycol and diethyl ether solvent treatment method for the successful removal of interfering fluorophores. To unravel the distinction between purified CNDs (P-CNDs) and organic fluorescent carbon nanostructures (org-FCNs), we carried out photophysical, structural, and morphological studies. A quantum yield (QY) of 69 and 42% was observed for crude org-FCNs, and crude P-CNDs; however after purification, QY of 1% and absence of one component from the fluorescent decays curve suggest the removal of fluorophores. Further, HR-TEM and DLS studies showed the quasi-spherical amorphous particles having < 10 nm particle size for P-CNDs. Besides, in vitro biocompatibility investigation and cellular uptake assay (1–100 μg/mL) against the MDA-MB 468 cell lines proves the ≥ 95% cell viability and good internalization for both org-FCNs and P-CNDs. Hence, our study shows the presence of fluorophore impurities in plant-derived CNDs, the removal and resemblance in biocompatibility properties. Hence, this information can be considered during the synthesis and isolation of CNDs. Simple and effective removal of impurities to harvest pure carbon nanodots (CNDs) through solvent-based selective separation method, and revelation of the cocktail flourphores similar to biocompatible blue fluorescent CNDs were studied.

Organisms constituting a large proportion of marine ecosystems, ranging from bacteria to fish, exhibit fluorescence and bioluminescence. A variety of marine organisms utilize these biochemically generated light sources for feeding, reproduction, communication, and defense. Since the discovery of green fluorescent protein and the luciferin-luciferase system more than a century ago, numerous studies have been conducted to characterize their function and regulatory mechanism. The unique properties of fluorescent and bioluminescent proteins offer great potential for their use in a broad range of applications. This short review briefly describes the functions and characteristics of fluorescent and bioluminescent proteins, in addition to summarizing the recent status of their applications.

Food toxins are regarded as a major source of health risks, serious illnesses susceptible to even death. These dangerous pathogens may lead to significant economic impact worldwide. The food production chain undergoes different stages like harvesting, processing, storage, packaging, distribution, and lastly preparation, and consumption. Therefore, each step is susceptible to risks of environmental contamination. Nowadays, the carbon quantum dots (CDs) are regarded as one of the most widely used hybrid carbon nanomaterials due to their different magical physical and chemical properties. The CDs have a size below 10 nm and show the fluorescent property. The CDs find vast applications in different fields like sensing, food safety, drug delivery, bioimaging, catalyst, energy conversion, etc. Compared to other available methods, the fluorescence detection techniques have low cost, easy handling, and safe operating system. There is a need for a review to compile the fluorescence properties of carbon nanodots used to detect food pathogens. This brief review is addressed in that direction and mostly focused on the synthesis of carbon dots-based fluorescence sensors for detecting pathogens and toxins in foods and beverages. The detailed mechanisms and origin of fluorescence properties of carbon quantum dots are also highlighted herewith.

Fluorescent carbon nano-materials with quantum confinement and edge effects have recently piqued attention in a variety of applications, including biological imaging, drug delivery, optoelectronics and sensing. These nano-materials can be synthesized from a variety of carbon-based precursors using both top-down and bottom-up methods. Coal and its derivatives typically include a vast crystalline network and condensed aromatic ring cluster, which can be easily exfoliated by chemical, electrochemical, or physical processes to produce nano-materials. As a result, they are regarded as a low-cost, abundant and efficient carbon source for the fabrication of high-yield nano-materials. Nano-materials synthesized from coal-based precursors have outstanding fluorescence, photostability, biocompatibility and low toxicity, among other properties. Their properties in optical sensors, LED devices, bio-imaging, and photo and electro-catalyst applications have already been investigated. In this review, we have highlighted current developments in the synthesis, structural properties and fluorescence properties of nano-materials synthesized from coal-based precursors.

Herein, a facile bottom–up approach for producing nitrogen-doped carbon quantum dots (N-CQDs) was carried out by the hydrothermal treatment of microcrystalline cellulose, in the presence of different nitrogen sources (blank/urea/ammonia water/ethanediamine(EDA)/Hexamethylenetetramine). The result showed that the fluorescence intensity and quantum yields (QYs) of N-CQDs with different nitrogen sources are all higher than that without nitrogen source. Compared with the other three nitrogen sources, N-CQDs prepared by EDA not only have the highest fluorescence intensity but also the largest QYs of 51.39%. Therefore, EDA was chosen as the nitrogen source to prepare N-CQDs. The obtained N-CQDs are uniform spherical particles with a diameter of 2.76 nm. The N-CQDs also exhibit excitation-dependent and long-wave emission properties. The emission range of N-CQDs is 470–540 nm. Moreover, N-CQDs as fluorescent agents successfully acted on purple LEDs (λem = 365 nm) to achieve white LEDs light emission. At the same time, a fluorescent thin layer chromatography plate was successfully prepared using N-CQDs, silica gel G and Sodium carboxymethylcellulose as raw materials. The separation trajectory of mixed sample of Sudan red III and kerosene on the fluorescent TLC plate is obviously clearer than that of the TLC plate.

An extract of fresh guava leaves (Psidium guajava) was used as a green carbon precursor to fabricate blue fluorescent carbon quantum dots (GCQDs) by hydrothermal process. The GCQDs show bright blue fluorescence emission under UV light with an excitation wavelength of 350 nm and emission at 450 nm. The physical structure of GCQDs was characterized by Fourier-transform infrared spectroscopy (FT-IR), Raman spectroscopy, X-ray diffraction (XRD), High-resolution transmission electron microscope (HR-TEM) and atomic force microscopy (AFM). GCQDs 80 μg inhibited the growth of waterborne pathogens Escherichia coli and Salmonella typhi. We also investigated the catalytic activity of the GCQDs on the removal of two azo dyes, namely Congo red and bromophenol blue, with and without NaBH4. The GCQDs showed an excellent reduction of color intensity of both dyes without NaBH4 within 30 min of treatment.

Highly luminescent carbon quantum dots (CQDs) are developed as fluorescent probes for selective detection of the heavy-ion Fe3+, where the CQDs exhibit excellent nontoxicity, functionalizability, sensitivity, and selectivity. Biomass-based CQDs and nitrogen-doped CQDs (N-CQDs) are synthesized for the selective detection of Fe3+ by using H2O2 as an oxidant and polyetherimide (PEI) as a nitrogen precursor by a green hydrothermal synthesis method. The prepared CQDs and N-CQDs exhibit an elliptical morphology and with an average particle size of 7 and 4 nm, respectively, and emit blue photoluminescence at 445 and 468 nm under excitation at 367 and 343 nm, respectively. The CQDs and N-CQDs exhibit good water solubility because of the abundant hydroxyl and carboxyl/carbonyl groups and graphic/pyrrolic/pyridinic nitrogen on the surfaces, giving rise to a quantum yield of about 24.2% and 30.7%, respectively. Notably, the Matrimony vine-PEI-based CQDs exhibit excellent Fe3+ selectivity and sensitivity relative to the Matrimony vine-based CQDs due to complexation of the numerous phenolic hydroxyl groups and nitrogen-containing groups with Fe3+, leading to increased fluorescence quenching, which greatly improves the sensitivity of detection. The minimum detection limit was 2.22 μmol L− 1 with a complexation constant of 44.7.

In this study, we report a controlled one-pot green synthesis of multiwalled carbon nanotubes (MWCNTs) via pyrolysis of sustainable agriculture waste (chickpea peel) at 400 °C in aqueous medium. These MWCNTs demonstrated 7.0 nm diameter, 0.28 nm graphitic spacing with carbonyl, hydroxyl, and carboxylic acid functionality. The D band (presence of sp3 defects) and G band ( E2g mode of graphite) at 1350 cm−1 and 1580 cm−1 originated in Raman spectrum, respectively. The prepared MWCNTs showed blue fluorescence with 10% fluorescence quantum yield in aqueous medium. The MWCNTs showed triple exponential decay characteristics with an average fluorescence lifetime of 4.7 ns. The synthesized MWCNTs revealed a consistent fluorescence in the cytoplasm of 22RV1 human prostate carcinoma cell line without exerting any sign of cytotoxicity. The MWCNTs also exhibited remarkable cytocompatibility in human immortalized prostate epithelial RWPE1 cells.