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Aiming at dealing with organic and inorganic pollutants dissolved in aquatic environments, we introduce self-assembled fluorescent nanocomposite hydrogel based on a binary polysaccharide network (xanthan gum/chitosan) embedding nitrogen-doped carbon quantum dots not only as a hybrid solid optical sensor for detecting Cr(VI) ions but also to remove anionically charged contaminants Cr(VI) and methyl orange (MO) by acting as an adsorbent. This fluorescent nanocomposite achieved a detection limit of 0.29 µM when used to detect Cr(VI) and demonstrated a fluorescence quantum yield of 59.7 %. Several factors contributed to the effectiveness of the adsorption of Cr(VI) and MO in batch studies, including the solution pH, dosage of the adsorbent, temperature, initial contamination level, and contact time. Experimental results showed 456 mg/g maximum adsorption capacity at pH 4 for MO compared to 291 mg/g at pH 2 for Cr(VI) at 25 °C. In addition to conforming to Langmuir's model, Cr(VI) and MO's adsorption kinetics closely matched pseudo-second-order. Using thermodynamic parameters, the results indicate that Cr(VI) and MO adsorb spontaneously and exothermically. Recycling spent adsorbent for Cr(VI) and MO using NaOH at 0.1 M was possible; the respective adsorption efficiency remained at approximately 82.2 % and 83 % after the fifth regeneration cycle.

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Epinephrine (EP) is a catecholamine hormone with a variety of physiological activities. Monitoring the concentration of EP in drugs, food, biological samples and cosmetics is of great significance for their quality control. Herein, a novel fluorescence sensing method was designed for the high-specificity detection of EP based on N-doped carbon quantum dots (N-CDs). The EP could interact with the fluorescent senor of N-CDs which emits blue fluorescence to produce concentration- dependent fluorescence quenching through the photo-induced electron transfer (PET). The established sensing method has good linearity in the range of 0.5-10 µM with the LOD of 0.15 µM. More importantly, it is highly selective because similar components with phenolic hydroxyl groups or primary amino groups, even norepinephrine (NEP), could not interfere with the detection. This method can provide a low-cost, rapid and simple new way for the detection of EP, and has a good application prospect in point-of-care assay and in situ test.

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A synchronous fluorescence spectroscopy (SFS) sensor for pethidine detection is described based on UiO-66 metal-organic frameworks (MOFs) modified with N-doped carbon quantum dots (N-CQDs) embedded in hydrogel nanocomposites. Benefitting from the inovative  design of the doping method in the carbonaceous structure, N-CQDs were successfully deposited in the pores of the UiO-66 network. Then, N-CQDs were employed as a sensitive segment toward the target molecules. UiO-66 was used for sensitive and selective sensing of the bonding interactions between N-CQDs and pethidine so that the electron transfer process from UiO-66 to the pethidine-N-CQD complex results in quenching the SFS intensity of UiO-66. To embed the stable and suitable sensing interface for pethidine assessment, the designed nanomaterial was inserted into the hydrogel network. This nanocomposite hydrogel showed two well-resolved emission peaks at 300 nm and 350 nm under ∆λ = 70, which corresponded to N-CQDs and UiO-66, respectively. The SFS sensing platform was employed for ratiometric detection of pethidine with a low limit of detection of 0.002 µg mL-1 over a wide concentration range from 0.005 to 1.0 µg mL-1. The accurate monitoring of pethidine with a good recovery of 90.8-101.5% indicated their independency from matrix effects for pethidine detection in human plasma being a complicated biological matrix. Scheme 1. General procedure for synthesizing N-CQDs@UiO-66/PVA hydrogel-based nanoprobe and its application for pethidine determination.

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ortho-Nitroaniline (o-NA) compounds are deemed to be a strongly toxic pollutant in nature and potentially carcinogenic; however, they are frequently utilized to synthesize dyes, pesticides, medicines, fungicides, pigments, and other organic chemicals. Their detection in an aqueous medium is fundamentally required to avoid the potential hazardous being created by these compounds. In this study, a novel sensor based on an Iron oxide (Fe3O4) containing highly dispersed nitrogen-doped carbon quantum dots (N-CQDs@Fe3O4 NFs) was demonstrated for the electrochemical detection of o-NA using differential pulse voltammetry (DPV) and cyclic voltammetry (CV) techniques. N-CQDs@Fe3O4 NFs were synthesized by hydrothermal method and studied by various analytical and spectroscopy techniques, which collectively reveal that the as-prepared composite has superior physical and chemical properties. The DPV study indicated that the o-NA sensor had a good limit of detection, linear range, and sensitivity in the range of 1.2 nm, 0.03-386.84 µM, and 36.5575 µA µM-1 cm-2, respectively, along with the sensor showed superior sensitivity when compared to the previously reported modified electrodes. Further, N-CQD/Fe3O4 NFs worked as heterogeneous catalysts for the photocatalytic reduction of o-NA to o-phenylenediamine (o-PD) in an aqueous medium. The reaction was examined under UV-Visible spectroscopy, and the complete photocatalytic reduction was observed for the N-CQD/Fe3O4 NFs in about 6 min with 96% as compared to other control samples; thus, authenticating the superiority of the synthesized composite in rendering the real-time applications.

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In this work, different proportions of N-doped carbon quantum dots/porous Co3O4 (NCQDs/p-Co3O4) NCQDs/Co3O4 composite photocatalysts were prepared by a simple self-assembly method. It was demonstrated by a series of characterizations that 50% NCQDs/Co3O4 has a good visible light response and low electrochemical impedance. The photocatalytic degradation of TC was investigated by the 50% NCQDs/p-Co3O4 composite photocatalyst, and the results showed that the degradation effect of TC reached 81.2% within 120 min. The higher photocatalytic activity of 50% NCQDs/p-Co3O4 was analyzed probably because NCQDs can improve the separation efficiency of photogenerated electron-hole pairs and p-Co3O4 can provide a larger specific surface area and thus has more active sites. This study provides a new strategy for improving the photodegradation activity of Co3O4 photocatalysts.

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The rapid recombination of photogenerated carriers and weak light absorption capacity are two major challenges for bismuth-based photocatalysts. Here, N-CQDs/BiO1-xBr micro-flower photocatalysts with the visible-light activity were fabricated through the ethylene glycol solvothermal method for the first time, and oxygen vacancies (OVs) and N-doped carbon quantum dots (N-CQDs) were simultaneously introduced on the surface of BiOBr. OVs were introduced to form defective BiOBr (BiO1-xBr). N-CQDs and BiO1-xBr formed a strong binding effect. Then, the composition, morphology, crystal structure and photoelectric property of photocatalysts were studied, and the mechanism and pathway of ofloxacin (OFL) photodegradation were studied. N-CQDs/BiO1-xBr-4 was a micro-flower composed of nanosheets with a thickness of about 60 nm, this structure produced multiple light reflections. Photoelectrochemical analysis confirmed that the synergistic effect of OVs and N-CQDs significantly promoted the electron-hole separation (3 times vs BiOBr) and enhanced the light absorption range (Eg = 2.96 eV vs 3.24 eV). Meanwhile, the removal rate of OFL by N-CQDs/BiO1-xBr-4 was 6 times higher than that by BiOBr (Kobs of N-CQDs/BiO1-xBr-4 was 32 times higher than that of BiOBr). Electron spin resonances analysis and radical quenching experiments showed that ·O2- and h+ played dominant roles in the OFL photodegradation system, and their contribution rates were 89.84% and 70.31%, respectively. There were main degradation pathways for OFL, including oxidation, dealkylation, hydroxylation and decarboxylation. This study explored the synergistic and complementary effects between OVs and N-CQDs, and provided a promising strategy for the photodegradation of toxic antibiotics by visible-light-driven photocatalysts.

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To fabricate N-CQDs hybrid thermo-sensitive polymer (poly-N-CQDs), N-doped carbon quantum dots (N-CQDs) with strong blue fluorescence and poly(N-isopropylacrylamide-co-acrylic acid) (poly(NIPAAm-co-AAc)) copolymer with thermo-sensitivity were synthesized, respectively. Subsequently, the coupling reaction between. the -COOH groups of poly(NIPAAm-co-AAc) and the -NH2 groups on the surface of the N-CQDs was carried out. The fluorescence spectra show that the coil-globule transition of the poly-N-CQDs coincided with intensity changes in the scattering peak at excitation wavelength with the temperature variations. The phase transition temperature and the fluorescent intensity of poly-N-CQDs can be regulated by modulating the composition and concentration of poly-N-CQDs as well as the temperature and pH of the local medium. The thermo-sensitivity and fluorescent properties of the poly-N-CQDs displayed good stability and reversibility. The fluorescence intensity and emission wavelengths of the poly-N-CQDs significantly changed in different solvents for solvent recognition. The poly-N-CQDs was employed as a fluorescent probe for Fe3+ detection ranging from 0.025 to 1 mM with a limit of detection (LOD) of 9.49 µM. The hybrid polymer materials have the potential to develop an N-CQDs-based thermo-sensitive device or sensor.

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In recent years, antibiotic residues in food have been of great concern to regulators and consumers. In this study, a novel fluorescent sensor based on S, N-doped carbon quantum dots (S, N-CQDs) was established for rapid detection of tetracycline antibiotics (TCs). Through the internal filter effect (IFE), QDs fluorescence can be effectively quenched by TCs, endowing it an "off" condition. Under the optimal conditions, the TC concentration in the range of 1.88-60 µmol/L had a good linear relationship with the change of QDs fluorescence intensity, and the limit of detection (LOD) was calculated as 0.56 µmol/L (S/N = 3). Furthermore, the proposed "Turn-off" sensor could be employed to quickly and accurately quantify TCs residues even in milk, honey and tap water. The recovery rate was as high as between 93.61% and 102.31%. The established sensor has great application value in the fields of food safety and drug analysis, and provides broad prospects for the future food industry.

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In this work, fluorescent N-doped carbon quantum dots (N-CQDs) have been synthesized by simple hydrothermal heating of natural osmanthus fragrans, without any toxic ingredients or surface chemical modifications. The N-CQDs possess a high quantum yield of 21.9 %, outstanding blue fluorescence, good water dispersity, and excellent optical stability. Because the favorable inner filter effect (IFE) between N-CQDs and quercetin (QT) occurs, the addition of QT to N-CQDs can cause their fluorescence quenching. When Al3+ was added to the N-CQDs/QT system solution, it was found that the inhibition of IFE leads to the fluorescence intensity of N-CQDs/QT system enhancement by virtue of a specific binding of QT to aluminum ion (Al3+). Therefore, we used the N-CQDs as a novel off-on fluorescent nanosensor to detect QT and Al3+. Under optimal conditions, the fluorescent nanosensor can detect QT within the wide linear response in the range of 0.003-80 µmol/L with as low as 1 nmol/L detection limit. For the detection of Al3+, the N-CQDs/QT system showed linearity response toward Al3+ in a range of 0.1∼100 µmol/L and the limit of detection was found at 26 nmol/L. In addition, N-CQDs have been successfully used to efficient quantification QT in human plasma and monitor Al3+ in serum samples. Noteworthy, the N-CQDs demonstrated low toxicity toward T24 cells, which realized sensing QT and Al3+ in the living cells.

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A novel fluorescence "turn on" ratiometric fluorescent sensor was employed to determine carbendazim. The sensing process was achieved through the strong fluorescence resonance energy transfer (FRET) between nitrogen doped carbon quantum dots (N-CQDs) and gold nanocluster (AuNCs). The photoluminescence intensity of N-CQDs can be deactivated by AuNCs through FRET effect and recovered by the addition of carbendazim. The ratiometric detection of carbendazim is achieved by recording the photoluminescence and second-order Rayleigh scattering (SRS) signal of N-CQDs/AuNCs system. With the introduction of carbendazim to the sensing platform resulted in the photoluminescence and SRS signal of N-CQDS/AuNCs enhancing. UV-vis absorption, Zeta potential and fluorescence lifetime analyses indicate that the fluorescence turn on process can be attributed to the aggregation of AuNCs breaks the FRET process and increases SRS intensity. N-CQDs/AuNCs probe present a good sensitivity and selectivity for carbendazim detection, with two linear response ranges (1-100 µM, 150-1000 µM), low detection limit of 0.83 µM and 37.25 µM. Furthermore, real sample analyses indicate that the as-presented sensor has potentials in carbendazim determination in real sample analyses.

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The photoluminescence properties of carbon quantum dots depend on their size and the properties of surface functional groups. The N-doped carbon dots ( using small molecular ethylenediamine ) with high quantum yield and excellent dispersibility were synthesized by one-step hydrothermal method with biomass tar that was generated in the reductive smelting process as a precursor. Rapid and accurate Fe3+ detection based on the selective fluorescence quenching effect of N-doped carbon quantum dots was achieved. The results showed that the as-synthesized N-doped carbon quantum dots were regular spherical, uniform in size with an average particle size of 2. 64 nm with a quantum yield of 26. 1%, and the crystal lattice spacing was 0. 25 nm, corresponding to the ( 100 ) facet of graphitic carbon structure. The functional groups on the surface of N-doped carbon quantum dots could interact with Fe3+ to form complex compound by coordination, leading to the fluorescence quenching effect. Fluorescence emission ratios kept a linear relationship with the concentrations of Fe3+ in the range of 0. 23-600 μmol/L with the detection limit of 230 nmol/L.

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The photoluminescence properties of carbon quantum dots depend on their size and the properties of surface functional groups. The N-doped carbon dots ( using small molecular ethylenediamine ) with high quantum yield and excellent dispersibility were synthesized by one-step hydrothermal method with biomass tar that was generated in the reductive smelting process as a precursor. Rapid and accurate Fe3+ detection based on the selective fluorescence quenching effect of N-doped carbon quantum dots was achieved. The results showed that the as-synthesized N-doped carbon quantum dots were regular spherical, uniform in size with an average particle size of 2. 64 nm with a quantum yield of 26. 1%, and the crystal lattice spacing was 0. 25 nm, corresponding to the ( 100 ) facet of graphitic carbon structure. The functional groups on the surface of N-doped carbon quantum dots could interact with Fe3+ to form complex compound by coordination, leading to the fluorescence quenching effect. Fluorescence emission ratios kept a linear relationship with the concentrations of Fe3+ in the range of 0. 23-600 μmol/L with the detection limit of 230 nmol/L.