Fluorescent probes based on N-CQDs: For direct detection of food additives STPP and Al3.

Sodium tripolyphosphate (STPP), as one of the many food additives, can cause gastrointestinal discomfort and a variety of adverse reactions when ingested by the human body, which is a great potential threat to human health. Therefore, it is necessary to develop a fast, sensitive and simple method to detect STPP in food. In this study, we synthesized a kind of nitrogen-doped carbon quantum dots (N-CQDs), and were surprised to find that the addition of STPP led to the gradual enhancement of the emission peaks of the N-CQDs, with a good linearity in the range of 0.067-1.96 µM and a low detection limit as low as 0.024 µM. Up to now, there is no report on the use of carbon quantum dots for the direct detection of STPP. Meanwhile, we found that the addition of Al3+ effectively bursts the fluorescence intensity of N-CQDs@STPP solution and has a good linear relationship in the range of 0.33-6.25 µM with a lower detection limit of 0.24 µM. To this end, we developed a fluorescent probe to detect STPP and Al3+. In addition, the probe was successfully applied to the detection of bread samples, which has great potential for practical application.

Highly fluorescent CdTe/ZnSe quantum dot-based "turn-off" sensor for the on-site rapid detection of Lead ions in aqueous medium.

Lead (Pb) is a heavy metal known for its adverse effects on both human health and the environment. In recent years, the industrial utilization of Pb2+ has surged, underscoring the imperative need for efficient measurement methods. In this study, a rapid and simple photochemical method was used to synthesize thioglycolic acid (TGA)-stabilized CdTe/ZnSe core-shell quantum dots (QDs). These CdTe/ZnSe QDs emit vibrant green fluorescence and exhibit remarkable quenching in the presence of Pb2+ ions. This property enables the development of an on-site on/off sensor without the necessity of additional modifications. The proposed sensor possesses an outstanding sensitivity to Pb2+, with a detection limit and linear range of 31.8 nM and 50 nM-10 µM, respectively. Importantly, the selectivity of this fluorescence-based sensor was validated by analyzing various positively and negatively charged ions. Furthermore, the developed sensor showed reliable performance against real river, agricultural, and tap water, as confirmed by Inductively Coupled Plasma (ICP) analysis. Additionally, CdTe/ZnSe QDs immobilized on glass slides were successfully employed for on-site water sample analysis, providing a versatile solution for environmental monitoring.

Rational construction of CQDs-based targeted multifunctional nanoplatform for synergistic chemo-photothermal tumor therapy.

Photothermal therapy combined with chemotherapy has shown great promise in the treatment of cancer. In this synergistic system, a safe, stable, and efficient photothermal agent is desired. Herein, an effective photothermal agent, carbon quantum dots (CQDs), was initially synthesized and then rationally constructed a folic acid (FA)-targeted photothermal multifunctional nanoplatform by encapsulating CQDs and the anticancer drug doxorubicin (DOX) in the liposomes. Indocyanine green (ICG), a near infrared (NIR) photothermal agent, approved by the U.S. Food and Drug Administration, was embedded in the bilayer membrane to further enhance the photothermal effects and facilitate the rapid cleavage of liposomes for drug release. Triggered by the NIR laser, this engineered photothermal multifunctional nanoplatform, not only exhibited an excellent performance with the photothermal conversion efficiency of up to 47.14%, but also achieved controlled release of the payloads. In vitro, and in vivo experiments demonstrated that the photothermal multifunctional nanoplatform had excellent biocompatibility, enhanced tumor-specific targeting, stimuli-responsive drug release, effective cancer cell killing and tumor suppression through multi-modal synergistic therapy. The successful construction of this NIR light-triggered targeted photothermal multifunctional nanoplatform will provide a promising strategy for the design and development of synergistic chemo-photothermal combination therapy and improve the therapeutic efficacy of cancer treatment.

Resolving the interactions between hydrophilic CdTe quantum dots and positively charged membranes at the nanoscale.

The use of quantum dot nanoparticles (QDs) in bio-applications has gained quite some interest and requires a deep understanding of their interactions with model cell membranes. This involves assessing the extent of nanoparticle disruption of the membrane and how it depends on both nanoparticle and membrane physicochemical properties. Surface charge plays an important role in nanoparticle adsorption, which is primarily driven by electrostatic interactions; yet, once adsorbed, most reported works overlook the subsequent spatial nanoparticle insertion and location within the membrane. There is therefore a need for studies to assess the mutual role of membrane and nanoparticle charge into membrane structure and stability at the nanoscale, with a view to better design and control the functionality of these nanomaterials. In this work, we have resolved the extent of the interactions between hydrophilic, negatively charged CdTe QDs and positively charged lipid bilayers. A multiscale combination of surface-sensitive techniques enabled probing how surface charge mediates QD adsorption and membrane reorganization. Increasing membrane surface charge results into a larger adsorption of oppositely charged QDs, concomitantly inducing structural changes. Hydration of the membrane hydrophobic parts by QDs goes deeper into the inner leaflet with increasing membrane charge, resulting in supported lipid bilayers with decreased nanomechanical stability.

Robust construction of CeNi quantum dots/Ni-MOL nanosheets for superior photocatalytic CO2 reduction.

Since the intensification of global environmental pollution and energy shortages, photocatalytic CO2 reduction reaction (CO2RR) has emerged as a promising strategy to convert solar energy into clean chemical energy. Herein, we construct a robust and efficient heterojunction construction photocatalyst for CO2RR, composed of the highly reactive CeNi quantum dots (CeNi QDs) and nickel metal-organic layer (Ni-MOL) ultrathin nanosheets. This design facilitates the rapid separation of photogenerated charge carriers, as confirmed by X-ray photoelectron spectroscopy (XPS), photoluminescence spectroscopy (PL) and other characterizations. Mechanistic studies with in situ diffuse reflectance Fourier transform infrared spectroscopy (in situ DRIFTS) and the d-band center calculation indicate that the propensity of photocatalyst for CO2 absorption and CO desorption, leading to high performance and selectivity. The optimized loading amount of CeNi quantum dots and modified structure result in a CO yield of 30.53 mmol·g-1 within 6 h under irradiation. This work not only paves a new and convenient way for developing high-activity quantum dot materials for CO2RR but also exploits novel avenues to fabricate more heterojunction composites for solar energy conversion.

Graphene Oxide Quantum Dots-Preactivated Dental Pulp Stem Cells/GelMA Facilitates Mitophagy-Regulated Bone Regeneration.

Background: In bone tissue engineering (BTE), cell-laden scaffolds offer a promising strategy for repairing bone defects, particularly when host cell regeneration is insufficient due to age or disease. Exogenous stem cell-based BTE requires bioactive factors to activate these cells. Graphene oxide quantum dots (GOQDs), zero-dimensional derivatives of graphene oxide, have emerged as potential osteogenic nanomedicines. However, constructing biological scaffolds with GOQDs and elucidating their biological mechanisms remain critical challenges. Methods: We utilized GOQDs with a particle size of 10 nm, characterized by a surface rich in C-O-H and C-O-C functional groups. We developed a gelatin methacryloyl (GelMA) hydrogel incorporated with GOQDs-treated dental pulp stem cells (DPSCs). These constructs were transplanted into rat calvarial bone defects to estimate the effectiveness of GOQDs-induced DPSCs in repairing bone defects while also investigating the molecular mechanism underlying GOQDs-induced osteogenesis in DPSCs. Results: GOQDs at 5 µg/mL significantly enhanced the osteogenic differentiation of DPSCs without toxicity. The GOQDs-induced DPSCs showed active osteogenic potential in three-dimensional cell culture system. In vivo, transplantation of GOQDs-preactivated DPSCs/GelMA composite effectively facilitated calvarial bone regeneration. Mechanistically, GOQDs stimulated mitophagy flux through the phosphatase-and-tensin homolog-induced putative kinase 1 (PINK1)/Parkin E3 ubiquitin ligase (PRKN) pathway. Notably, inhibiting mitophagy with cyclosporin A prevented the osteogenic activity of GOQDs. Conclusion: This research presents a well-designed bionic GOQDs/DPSCs/GelMA composite scaffold and demonstrated its ability to promote bone regeneration by enhancing mitophagy. These findings highlight the significant potential of this composite for application in BTE and underscore the crucial role of mitophagy in promoting the osteogenic differentiation of GOQDs-induced stem cells.

Application of electrospun N-doped carbon dots loaded cellulose acetate membranes as cationic dyes adsorbent.

This work aims to apply carbon quantum dots (CQDs) from agriculture cellulosic waste (agro wastes), produced via an economically and eco-friendly single-step method, to be used into cellulose acetate composite microfibrous membranes as an innovative solution specifically designed to adsorb methylene blue (MB) and other cationic dyes that are present in various water effluents. Batch adsorption tests were conducted, with variations in contact time (1-24 h), initial MB concentration (25-300 ppm), and adsorbent doses (1-20 g/L). The maximum adsorption capacity of the membrane was 198 mg/g with an initial concentration of 300 ppm at 298 K. Thermodynamic parameters showed that the process is endothermic. Equilibrium experimental data for MB adsorption onto electrospun adsorbent were fitted using different isothermal models, with the Freundlich model showing the best fit. The pseudo-second-order model accurately described the kinetic data with high reliability (R2 > 0.99), and the calculated adsorption capacity was very close to the experimental data. N-CQDs loaded membranes were also tested for removing methyl violet and rhodamine B, demonstrating remarkably high dye removal efficiency. The underlying adsorption mechanism was also reported. Finally, it is worth mentioning that composite adsorbents can be efficiently applied to actual industrial cases because of the possibility of reusing them, opening the route to the fabrication of novel and highly performant adsorbents. These findings underscore N-CQDs' effectiveness in enhancing pollutant removal efficiency from wastewater, highlighting their environmental benefits and promoting a more sustainable approach to water treatment. Therefore, the prepared adsorbent, showing excellent adsorption performance, places them among adsorbents for practical applications in wastewater purification.

Highly Stable Biotemplated InP/ZnSe/ZnS Quantum Dots for In Situ Bacterial Monitoring.

Despite their unique optical and electrical characteristics, traditional semiconductor quantum dots (QDs) made of heavy metals or carbon are not ideally suited for biomedical applications. Cytotoxicity and environmental concerns are key limiting factors affecting the adoption of QDs from laboratory research to real-world medical applications. Recently, advanced InP/ZnSe/ZnS QDs have emerged as alternatives to traditional QDs due to their low toxicity and optical properties; however, bioconjugation has remained a challenge due to surface chemistry limitations that can lead to instability in aqueous environments. Here, we report water-soluble, biotemplated InP/ZnSe/ZnS-aptamer quantum dots (QDAPTs) with long-term stability and high selectivity for targeting bacterial membrane proteins. QDAPTs show fast binding reaction kinetics (less than 5 min), high brightness, and high levels of stability (3 months) after biotemplating in aqueous solvents. We use these materials to demonstrate the detection of bacterial membrane proteins on common surfaces using a hand-held imaging device, which attests to the potential of this system for biomedical applications.

Doping of Mn2+ ion into boron quantum dots with enhanced fluorescence properties for sensing of L-thyroxine biomarker and bioimaging applications.

L-thyroxine serves as a primary biomarker for diagnosing hypothyroidism and it is also utilized in hormone replacement therapy. Regular assessment of thyroxine levels is crucial for preventing health issues in hypothyroid patients, suggesting the requirement of a facile analytical tool for the detection of L-thyroxine. In this work, a straightforward and efficient synthetic method is introduced for in-situ preparation of Mn2+-doped boron quantum dots (Mn2+@B-QDs) derived from boron powder through a solvothermal reaction. The introduction of Mn2+ ion into B-QDs not only enhances fluorescence efficiency but also provides favorable sites within the QDs, expanding their potential applications in analytical chemistry. The blue fluorescent Mn2+ @B-QDs exhibited excellent performance for the selective recognition of L-thyroxine via a dynamic quenching mechanism. Under ideal conditions, a good linear relation was observed between the fluorescence emission intensity ratio of Mn2+@B-QDs and the concentration of L-thyroxine in the range of 0.125-5 µM, with a lower detection limit of 59.86 nM. The Mn2+@B-QDs exhibited the negligible cytotoxicity against A549 lung cancer cell lines and demonstrated good biocompatibility toward Saccharomyces cerevisiae cells.

Multifunctional nitrogen-sulfur codoped carbon quantum dots: Determining reduced glutathione, broad-spectrum antibacterial activity, and cell imaging.

In this study, nitrogen-sulfur codoped carbon quantum dots (N-S/CQDs) with various functions and properties were synthesized through a one-step method utilizing citric acid and cysteine as reaction substrates. The fluorescence of N-S/CQDs can be specifically quenched by permanganate ion (MnO4 -), and the quenched fluorescence can be recovered by the presence of reduced glutathione (GSH). A fluorescence sensing system based on N-S/CQDs@MnO4 - was developed and successfully applied for the determination of GSH in pharmaceutical preparations. Additionally, N-S/CQDs demonstrated broad-spectrum antibacterial activity, with minimum inhibitory concentrations of 32 µg/ml against Staphylococcus aureus (gram-positive bacterium) and 64 µg/ml against Escherichia coli (gram-negative bacterium). N-S/CQDs also proved effective for cell imaging, exhibiting excellent biocompatibility. These findings underscore the multifunctional characteristics and promising application potential of N-S/CQDs. Furthermore, this study provides a solid foundation for the development of multifunctional carbon quantum dots and the expansion of their applications in various fields.

A fluorescent nanocomposite probe of quantum dots and zinc oxide embedded in polymer for smartphone-assisted on-site determination of diflunisal.

A fluorescent sensor based on nitrogen-doped graphene quantum dots (N-GQDs) was developed for the smartphone-assisted colorimetric determination of diflunisal. The fluorescence source was embedded with zinc oxide (ZnO) in a molecularly imprinted polymer (ZnO@N-GQDs@MIP). The quantitative analysis was based on the fluorescence quenching caused by electron transfer from the nanoprobe to diflunisal. The sensor demonstrated linearity in the range of 0.10-50.0 µg L-1 with a limit of detection of 0.03 µg L-1. Smartphone-assisted on-site determination produced linearity in the range of 1.0-50.0 µg/L with a limit of detection of 0.30 µg L-1. The developed sensor was applied to determine diflunisal in milk, egg and yogurt samples. Recoveries ranging from 94.8 to 103.7 % were achieved with a RSD below 2.0 % measured by fluorescence spectroscopy, and from 94.9 to 106.9 % with a RSD of <6 % smatphone-assisted measurement. Comparison of the detection outcomes of both methods with those of high-performance liquid chromatography revealed consistent results, demonstrating the accuracy of the developed method, which was also sensitive, selective, and fast. Notably, the portable and easy-to-read smartphone-assisted method is suitable for on-site application.

Nitrogen-Doped Carbon Quantum Dots Activated Dandelion-Like Hierarchical WO3 for Highly Sensitive and Selective MEMS Sensors in Diabetes Detection.

High sensitivity, low concentration, and excellent selectivity are pronounced primary challenges for semiconductor gas sensors to monitor acetone from exhaled breath. In this study, nitrogen-doped carbon quantum dots (N-CQDs) with high reactivity were used to activate dandelion-like hierarchical tungsten oxide (WO3) microspheres to construct an efficient and stable acetone gas sensor. Benefiting from the synergistic effect of both the abundant active sites provided by the unique dandelion-like hierarchical structure and the high reaction potential generated by the sensitization of the N-CQDs, the resulting 16 wt % N-CQDs/WO3 sensor shows an ultrahigh response value (Ra/Rg = 74@1 ppm acetone), low detection limit (0.05 ppm), outstanding selectivity, and reliable stability to acetone at the optimum working temperature of 210 °C. Noteworthy that the N-CQDs facilitate the carrier migration and intensify the reaction between acetone and WO3 during the sensing process. Considering the above advantages, N-CQDs as a sensitizer to achieve excellent gas-sensitive properties of WO3 are a promising new strategy for achieving accurate acetone detection in real time and facilitating the development of portable human-exhaled gas sensors.

Investigation of the Application of Reduced Graphene Oxide-SPION Quantum Dots for Magnetic Hyperthermia.

Integrating hyperthermia with conventional cancer therapies shows promise in improving treatment efficacy while mitigating their side effects. Nanotechnology-based hyperthermia, particularly using superparamagnetic iron oxide nanoparticles (SPIONs), offers a simplified solution for cancer treatment. In this study, we developed composites of SPION quantum dots (Fe3O4) with reduced graphene oxide (Fe3O4/RGO) using the coprecipitation method and investigated their potential application in magnetic hyperthermia. The size of Fe3O4 nanoparticles was controlled within the quantum dot range (≤10 nm) by varying the synthesis parameters, including reaction time as well as the concentration of ammonia and graphene oxide, where their biocompatibility was further improved with the inclusion of polyethylene glycol (PEG). These nanocomposites exhibited low cytotoxic effects on healthy cells (CHO-K1) over an incubation period of 24 h, though the inclusion of PEG enhanced their biocompatibility for longer incubation periods over 48 h. The Fe3O4/RGO composites dispersed in acidic pH buffer (pH 4.66) exhibited considerable heating effects, with the solution temperature increasing by ~10 °C within 5 min of exposure to pulsed magnetic fields, as compared to their dispersions in phosphate buffer and aqueous dimethylsulfoxide solutions. These results demonstrated the feasibility of using quantum dot Fe3O4/RGO composites for magnetic hyperthermia-based therapy to treat cancer, with further studies required to systematically optimize their magnetic properties and evaluate their efficacy for in vitro and in vivo applications.

A Review on Pulsed Laser Preparation of Quantum Dots in Colloids for the Optimization of Perovskite Solar Cells: Advantages, Challenges, and Prospects.

In recent years, academic research on perovskite solar cells (PSCs) has attracted remarkable attention, and one of the most crucial issues is promoting the power conversion efficiency (PCE) and operational stability of PSCs. Generally, modification of the electron or hole transport layers between the perovskite layers and electrodes via surface engineering is considered an effective strategy because the inherent structural defects between charge carrier transport layers and perovskite layers can be reshaped and modified by adopting the functional nanomaterials, and thus the charge recombination rate can be naturally decreased. At present, large amounts of available nanomaterials for surface modification of the perovskite films are extensively investigated, mainly including nanocrystals, nanorods, nanoarrays, and even colloidal quantum dots (QDs). In particular, as unique size-dependent nanomaterials, the diverse quantum properties of colloidal QDs are different from other nanomaterials, such as their quantum confinement effects, quantum-tunable effects, and quantum surface effects, which display great potential in promoting the PCE and operational stability of PSCs as the charge carriers in perovskite layers can be effectively tuned by these quantum effects. However, preparing QDs with a neat and desirable size remains a technical difficulty, even though the present chemical engineering is highly advanced. Fortunately, the rapid advances in laser technology have provided new insight into the precise preparation of QDs. In this review, we introduce a new approach for preparing the QDs, namely pulsed laser irradiation in colloids (PLIC), and briefly highlight the innovative works on PLIC-prepared QDs for the optimization of PSCs. This review not only highlights the advantages of PLIC for QD preparation but also critically points out the challenges and prospects of QD-based PSCs.

Mixed Systems of Quaternary Ammonium Foam Drainage Agent with Carbon Quantum Dots and Silica Nanoparticles for Improved Gas Field Performance.

Foam drainage agents enhance gas production by removing wellbore liquids. However, due to the ultra-high salinity environments of the Hechuan gas field (salinity up to 32.5 × 104 mg/L), no foam drainage agent is suitable for this gas field. To address this challenge, we developed a novel nanocomposite foam drainage system composed of quaternary ammonium and two types of nanoparticles. This work describes the design and synthesis of a quaternary ammonium foam drainage agent and nano-engineered stabilizers. Nonylphenol polyoxyethylene ether sulfosuccinate quaternary ammonium foam drainage agent was synthesized using maleic anhydride, sodium chloroacetate, N,N-dimethylpropylenediamine, etc., as precursors. We employed the Stöber method to create hydrophobic silica nanoparticles. Carbon quantum dots were then prepared and functionalized with dodecylamine. Finally, carbon quantum dots were incorporated into the mesopores of silica nanoparticles to enhance stability. Through optimization, the best performance was achieved with a (quaternary ammonium foam drainage agents)-(carbon quantum dots/silica nanoparticles) ratio of 5:1 and a total dosage of 1.1%. Under harsh conditions (salinity 35 × 104 mg/L, condensate oil 250 cm3/m3, temperature 80 °C), the system exhibited excellent stability with an initial foam height of 160 mm, remaining at 110 mm after 5 min. Additionally, it displayed good liquid-carrying capacity (160 mL), low surface tension (27.91 mN/m), and a long half-life (659 s). These results suggest the effectiveness of nanoparticle-enhanced foam drainage systems in overcoming high-salinity challenges. Previous foam drainage agents typically exhibited a salinity resistance of no more than 25 × 104 mg/L. In contrast, this innovative system demonstrates a superior salinity tolerance of up to 35 × 104 mg/L, addressing a significant gap in available agents for high-salinity gas fields. This paves the way for future development of advanced foam systems for gas well applications with high salinity.

Simulating graphene-based single-electron transistor: incoherent current effects due to the presence of electron-electron interaction.

Carbon-based nanostructures have unparalleled electronic properties. At the same time, using an allotrope of carbon as the contacts can yield better device control and reproducibility. In this work, we simulate a single-electron transistor composed of a segment of a graphene nanoribbon coupled to carbon nanotubes electrodes. Using the non-equilibrium Green's function formalism we atomistically describe the electronic transport properties of the system including electron-electron interactions. Using this methodology we are able to recover experimentally observed phenomena, such as the Coulomb blockade, as well as the corresponding Coulomb diamonds. Furthermore, we separate the different contributions to transport and show that incoherent effects due to the interaction play a crucial role in the transport properties depending on the region of the stability diagram being considered.

Mercaptopropionic acid-capped CdZnTe Quantum dots as Fluorescence Probe for Sensitive Detection of Cr(III) ions.

Although Cr(III) ions are essential for the human body, excessive amounts can lead to skin inflammation, allergic reactions, and genotoxicity. A highly sensitive fluorescence probe was developed using mercaptopropionic acid (MPA) capped CdZnTe quantum dots (QDs) synthesized via an aqueous solution heating method for precise detection of Cr(III) ions. The synthesized MPA-CdZnTe QDs had a size of 2.38 ± 0.13 nm and exhibited a zinc-blende structure, with MPA molecules effectively capping the surface through Cd-S bonds. Investigation into the effects of reflux times and solution pH on the absorption and fluorescence spectra of MPA-CdZnTe QDs revealed the occurrence of Ostwald ripening during prolonged reflux processes. The quantum yield (QY) of the synthesized CdZnTe QDs could reach 89%, and the QY was higher under acidic conditions than alkaline. Leveraging the quenching effect of Cr(III) ions on MPA-CdZnTe QDs, a robust method for the quantitative detection of trace amounts of Cr(III) ions was established. Linear quenching behavior was observed within the concentration range of 3.33 × 10- 6 to 5.00 × 10- 4 mol L- 1 for Cr(III) ions, with the fluorescence quenching rate described by a linear regression equation: 1-F/F0 = 0.218 + 829.5268CCr(III). The limit of detection was determined to be 2.63 × 10- 6 mol L- 1. The mechanism of the fluorescence behavior of MPA capped CdZnTe QDs towards Cr(III) ions was photo-induced electron transfer.

Synthesis of CuInS2 Quantum Dots Modified with Alanine for Sensitive and Selective Detection of Pb2+ and Cysteine.

In this study, a novel fluorescent probe based on CuInS2 quantum dots modified with alanine (Ala-CuInS2 QDs) was developed for the detection of lead ions and cysteine (Pb2+ and Cys). Ala-CuInS2 QDs were synthesized through a one-step hydrothermal method exhibiting uniform size, good stability and water solubility. The QDs were then utilized as an "on-off-on" fluorescence sensor to detect Pb2+ and Cys in the ranges of 0-20 µM and 0-55 µM respectively, with detection limits of 0.29 µM and 0.66 µM. The mechanism of fluorescence quenching and recovery processes was also explored. Furthermore, Ala-CuInS2 QDs have been successfully applied to detect Pb2+ in tap and river water and detect cysteine in serum.

Development and challenge of coal-based nanocarbon materials and their application in water treatment: a review.

Under the dual pressures of environmental protection and energy security, the development and application of coal-based nanocarbon materials, supported by the technical concepts of molecular chemical engineering and nanomaterial science, is of significant importance for achieving the high-value clean utilization of coal. Furthermore, it serves as an effective means to assist in the realization of dual carbon goals. Coal, with its abundant reserves, high carbon content, and aromatic and hydrogenated aromatic groups, exhibits great advantages and potential in the synthesis of nanocarbon materials. In addition to its applications in traditional power and chemical industries, coal-based nanocarbon materials also demonstrate significant value in the field of environmental pollution control. This article succinctly summarizes the preparation methods and properties of coal-based carbon nanotubes, coal-based carbon quantum dots, and coal-based graphene, elucidates their current applications in water pollution control and governance, and anticipates their development trends in water pollution control, aiming to provide support for the clean and efficient utilization of coal and water pollution control.

Fluorescent cellulose hydrogels based on corn stalk of double sulfhydryl functional group modification for Hg(II) removal and detection.

Ions of mercury, one of the most hazardous heavy metals in nature, pose serious risks to the environment and human health. Blue sulfur-doped carbon dots (SCDs) from corn stalks were utilized as material. The SCDs were incorporated into a carboxylated hydrogel modified with sulfur, and a compound gel (SCDs-KTOCS gel) was successfully fabricated for simultaneous fluorescence detection and Hg(II) adsorption. This enabled the effective identification and removal of Hg(II) from contaminated water. The chemical content, fluorescence properties, and adsorption behaviors of the SCDs-KTOCS-gels were analyzed. The results demonstrate that the SCDs-KTOCS-gels exhibited effective Hg(II) adsorption (193 mg/g) and an extensive linear spectrum for Hg(II) fluorescence emission (150-500 mg/L; detection limit = 1.5668 mg/L). The adsorption values fit well with the Temkin models and pseudo-second-order kinetics. Additionally, Hg(II) detection and adsorption in the SCDs-KTOCS-gels were examined. By exchanging the existing probe for a suitable one that fits various relevant applications, this study suggests an environmentally friendly and sustainable method of producing materials for removing and detecting Hg(II) and constructing a fluorescence hydrogel for the detection and adsorption of different metals.