Excellent Water Dispersibility Research Articles

Fabrication of three-dimension hierarchical structure CuO nanoflowers and their antifungal mechanism against Bipolaris sorokiniana

Nanomaterials are widely investigated in sustainable agriculture owing to their unique physicochemical properties, especially Cu-based nanomaterial with eco-friendliness and essential for plant. However, the effect of CuO nanomaterial on Bipolaris sorokiniana (B. sorokiniana) is yet to be systematically understood. In this study, a three-dimension hierarchical structure CuO nanoflower (CuO NF) with ultrathin petals and excellent dispersibility in water was constructed and proved to have outstanding antifungal activity against B. sorokiniana with the inhibition rate of 86 % in mycelial growth, 74 % in mycelial dry weight and 75 % in conidial germination. Furthermore, the antifungal mechanism was assigned to the production of reactive oxygen species in intracellular caused by antioxidant mimicking activity of CuO NF to damage of cell membrane integrity and result cellular leakage. Additionally, the good control effect of CuO NF on wheat diseases caused by B. sorokiniana was demonstrated through pot experiment. This article firstly reveals the antifungal activity and mechanism of CuO NF on B. sorokiniana, and establishes the relationship between enzyme-like activity of CuO NF and its antifungal activity, which provides a promising application of Cu-based nanomaterial as nanofungicide in plant protection and a theoretical foundation for structure design of nanomaterials to improve their antifungal activities.

Highly water-dispersible methylpyridinium salt functionalized reduced graphene oxide and poly(vinyl alcohol) composites

The main issues with developing graphene as a reinforcement are its mono-dispersive properties and strong interfacial bonding between matrix and graphene. In this study, we synthesized reduced graphene oxide (rGO) that is mono-dispersive in polar solvents, by designing structural isomers (-para and -meta) for poly(vinyl alcohol) (PVA) nanocomposites. The hydrazine-methylpyridine synthesized with different structural isomers was used to reduce and functionalize graphene oxide (GO). The -meta structural isomers showed a higher reduction rate and functional groups on GO than -para due to the difference in electrophilic strain. In particular, the prepared rGO reduced by meta-hydrazine-methylpyridine (m-Py-rGO) exhibited excellent mono dispersive characteristics in water solvents as well as in PVA matrix. As a result, nanocomposites containing 1 wt % m-Py-rGO increased in tensile strength and modulus by 48 % (85.95 MPa) and 82 % (4.27 GPa), respectively, compared to pristine PVA. In this study, a method for manufacturing rGO with excellent dispersibility in water, an inexpensive solvent, and its application method are presented.

High dispersibility ratiometric fluorescence sensor designed by functionalized mesoporous silica nanopraticles for sensing and imaging of hydrogen peroxide

Herein, a mesoporous silica nanoparticle (MSN) based ratiometric fluorescence nanosensor (MSN-BA-SiCD) with improved performance was designed for monitoring hydrogen peroxide (H2O2). Specifically, H2O2 response molecule (BA) with AIE feature was synthesized and encapsulated into MSN channel as the fluoresent recognition site. Afterwards, silane-modified carbon dot (SiCD) was covalently connected to the MSN surface which can effectively prevent the leakage of BA and improve the water dispersibility of the nanosensor. The presence of H2O2 could result in a “turn-on” fluorescence of BA as well as concurrent variation in the fluorescence resonance energy transfer (FRET) signal between SiCD and BA. MSN-BA-SiCD displays a specific blue-to-green resolved emission change in response to H2O2 and the detection limit can be as low as 4.78 × 10−6 M. In addition, the nanosensor exhibited enhanced photostability due to the protection of the material framework. Moreover, the nanosensing system was successfully applied to detect H2O2 in beer, orange juice and living cells. The excellent water dispersibility and photostability of the nanosensor, together with high specificity and biocompatibility, constituted an advanced set of characteristics among existing MSNs, which was expected to further promote the development of H2O2 sensors in the environmental and biological fields.

Functionalized magnetic metal organic framework nanocomposites for high throughput automation extraction and sensitive detection of antipsychotic drugs in serum samples

Due to the complexity of biological sample matrix, the automated and high-throughput pretreatment technology is urgently needed for monitoring the antipsychotic drugs for mental patients. In this study, functionalized magnetic zirconium-based organic framework nanocomposites (Fe3O4@SiO2@Zr-MOFs) were successfully designed and synthesized by the layer-by-layer growth. Among them, Fe3O4@SiO2@UiO-67-COOH showed the best adsorption performance, and at the same time it exhibited excellent water dispersibility, high thermal stability, chemical stability and high hydrophobicity. Results of adsorption kinetics, isotherm and FT-IR showed that the adsorption process was dominated by chemical adsorption (hydrogen bond, electrostatic interaction, π-π interaction) and monolayer adsorption. Moreover, the smaller pore size improved the protein exclusion rate which reached 98.9–99.8%. Based on the above result, the synthesized magnetic nanoparticles were introduced to 96-well automatic extractor, antipsychotic drugs in 96 serum samples were automatically extracted within 9 min, which most greatly saved the time and labor costs and avoided artificial errors. By further integrating with ultra-high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS), antipsychotic drugs can be detected in the range of 0.2–3.0 ng mL−1 with a quantitative limit of 0.06–0.9 ng mL−1. The recoveries of antipsychotic drugs and their metabolites in serum ranged from 95.7% to 112.3% within 1.4–6.5% of RSD. These features indicate that the proposed method is promising for high throughput and sensitively monitoring of drugs and other hazardous substances.

Cross-linked polymer nanocomposite networks coated nano sand light-weight proppants for hydraulic fracturing applications

Three-dimensionally cross-linked polymer nanocomposite networks coated nano sand light-weight proppants (LWPs) were successfully prepared via ball-milling the macro sand and subsequently modifying the resultant nano sand with sequential polymer nanocomposite coating. The modified nano sand proppants had good sphericity and roundness. Thermal analyses showed that the samples can withstand up to 411 ℃. Moreover, the proppant samples’ specific gravity (S.G.) was 1.02–1.10 g/cm3 with excellent water dispersibility. Therefore, cross-linked polymer nanocomposite networks coated nano sand particles can act as potential candidates as water-carrying proppants for hydraulic fracturing operations.

Kilogram-Scale Synthesis of Extremely Small Gadolinium Oxide Nanoparticles as a T1-Weighted Contrast Agent for Magnetic Resonance Imaging.

Magnetic resonance imaging contrast agents are frequently used in clinics to enhance the contrast between diseased and normal tissues. The previously reported poly(acrylic acid) stabilized exceedingly small gadolinium oxide nanoparticles (ES-GdON-PAA) overcame the problems of commercial Gd chelates, but limitations still exist, i.e., high r2/r1 ratio, long blood circulation half-life, and no data for large scale synthesis and formulation optimization. In this study, polymaleic acid (PMA) is found to be an ideal stabilizer to synthesize ES-GdONs. Compared with ES-GdON-PAA, the PMA-stabilized ES-GdON (ES-GdON-PMA) has a lower r2/r1 ratio (2.05, 7.0 T) and a lower blood circulation half-life (37.51min). The optimized ES-GdON-PMA-9 has an exceedingly small particle size (2.1nm), excellent water dispersibility, and stability. A facile, efficient, and environmental friendly synthetic method is developed for large-scale synthesis of the ES-GdONs-PMA. The weight of the optimized freeze-dried ES-GdON-PMA-26 synthesized in a 20L of reactor reaches the kilogram level. The formulation optimization is also finished, and the concentrated ES-GdON-PMA-26 formulation (CGd=100mm) after high-pressure steam sterilization possesses eligible physicochemical properties (i.e., pH value, osmolality, viscosity, and density) for investigational new drug application.

A food-grade and senescent cell-targeted fisetin delivery system based on whey protein isolate-galactooligosaccharides Maillard conjugate

Cellular senescence is the results of aging and age-related diseases, and the development of anti-aging methods may improve health and extend longevity. The natural flavonol fisetin has been shown to antagonize senescence in vitro and increases longevity in vivo, but has poor water solubility and limited bioavailability. In this study, a food-grade and senescent cell-targeted delivery system for fisetin was developed based on whey protein isolate-galactooligosaccharides (WPI-GOS) Maillard conjugate, which could recognize senescence associated β-galactosidase in senescent cells. The fisetin nanoparticles possessed a high encapsulation efficiency, excellent dispersibility in water, good storage stability and well biocompatibility. Moreover, they could effectively accumulate and retain in senescent cells with excellent senescent cell-targeting efficacy, and inhibit the oxidative stress-induced cellular senescence in vitro. Thus, this novel nanoparticle system based on WPI-GOS Maillard conjugate showed promise to deliver hydrophobic bioactive ingredients like fisetin to senescent cells to improve their bioavailability and anti-senescence effect.

Highly efficient color-tunable organic co-crystals unveiling polymorphism, isomerism, delayed fluorescence for optical waveguides and cell-imaging

Photofunctional co-crystal engineering strategies based on donor-acceptor π-conjugated system facilitates expedient molecular packing, consistent morphology, and switchable optical properties, conferring synergic ‘structure-property relationship’ for optoelectronic and biological functions. In this work, a series of organic co-crystals were formulated using a twisted aromatic hydrocarbon (TAH) donor and three diverse planar acceptors, resulting in color-tunable solid and aggregated state emission via variable packing and through-space charge-transfer interactions. While, adjusting the strength of acceptors, a structural transformation into hybrid stacking modes ultimately results in color-specific polymorphs, a configurational cis-isomer with very high photoluminescence quantum yield. The cis-isomeric co-crystal exhibits triplet-harvesting thermally activated delayed fluorescence (TADF) characteristics, presenting a key discovery in hydrocarbon-based multicomponent systems. Further, 1D-microrod-shaped co-crystal acts as an efficient photon-transducing optical waveguides, and their excellent dispersibility in water endows efficient cellular internalization with bright cell imaging performances. These salient approaches may open more avenues for the design and applications of TAH based co-crystals.

Aggregation-Induced Enhanced Electrochemiluminescence from Tris(bipyridine)ruthenium(II) Derivative Nanosheets for the Ultrasensitive Detection of Human Telomerase RNA.

The traditional tris(bipyridine)ruthenium(II) complex suffers from the notorious aggregation-caused quenching effect, which greatly compromises its electrochemiluminescence (ECL) efficiency, thus hindering further applications in biosensing and clinical diagnosis. Here, the ultrathin tetraphenylethylene-active tris(bipyridine)ruthenium(II) derivative nanosheets (abbreviated as Ru-TPE NSs) are synthesized through a protein-assisted self-assembly strategy for ultrasensitive ECL detection of human telomerase RNA (hTR) for the first time. The synthesized Ru-TPE NSs exhibit the aggregation-induced enhanced ECL behavior and excellent water-dispersion. Surprisingly, up to a 106.5-fold increase in the ECL efficiency of Ru-TPE NSs is demonstrated compared with the dispersed molecules in an organic solution. The restriction of intramolecular motions is confirmed to be responsible for the significant ECL enhancement. Therefore, this proposed ECL biosensor shows high sensitivity and excellent selectivity for hTR based on Ru-TPE NSs as efficient ECL beacons and the catalytic hairpin assembly as signal amplification, whose detection limit is as low as 8.0fm, which is far superior to the previously reported works. Here, a promising analytical method is provided for early clinical diagnosis and a new type of efficient ECL emitters with great application prospects is represented.

Bendable transparent films from cellulose nanocrystals–Study of surface and microstructure-property relationship

The presented work focuses on preparing transparent bendable films from nanocellulose. In comparison to cellulose nanofibrils and bacterial cellulose, nanocrystalline cellulose are shorter and have higher crystallinity (CI<95 %). Sulfated CNC (CNCIH-OSO3H) were prepared, and by changing their counter ions from H+ to Na+ and Et4N+ (Tetraethyl ammonium) flexible films were prepared with a strength of 70.5 MPa and 2.6 % elongation at break. The CNC suspensions showed excellent dispersibility in DI water with Zeta-potential (ζ) values > -35 mV. In the preparation of films, pre-sonication was key in improving the tensile strength and improved elongation (>30 % increase compared to films prepared without sonication) and hydrophobicity. The change of counter ion, H+ to Na+ or Et4N+, improved the thermal and mechanical properties of CNC films. The films were investigated with UV–Vis spectroscopy and optical polarized spectroscopy to explain the arrangement of nanocellulose crystals in correlation with the mechanical properties. The wettability of CNC samples was also studied and explained in detail. CNC from CelluForce was also studied as commercial reference samples. The modified CNC films have adequate properties for application in flexible electronics, energy storage, and biodegradable smart packaging.

Anticorrosive coatings made from polydopamine modified graphitic C3N4 composites with synergistic anticorrosion effects

Since uniform dispersion and robust interfacial compatibility of nanofiller with epoxy resin are the most critical parameters to improve the corrosion protection property, a new effective anticorrosion nanofiller [polydopamine (PDA)@g-C3N4-CeO2] is designed by stacking PDA modified g-C3N4 and nano-CeO2 with the help of a silane coupling agent. The structure and morphology of PDA@g-C3N4-CeO2 are characterized by FTIR, XRD, XPS, SEM, and TEM. Furthermore, the PDA@g-C3N4-CeO2 nanofiller is loaded within waterborne epoxy coating (WEC) and the corrosion resistance of the prepared nanocomposite coating is studied. It can be inferred from the dispersion test that g-C3N4 modified by PDA and nano-CeO2 exhibits excellent dispersion and compatibility in de-ionized water. The Electrochemical impedance spectroscope (EIS) results indicate that nanocomposite coating with PDA@g-C3N4-CeO2 exhibits the best corrosion resistance, and its low-frequency impedance (Zf=0.01Hz) is 1.78 × 109 Ω cm2, which is two orders of magnitude higher than that of pure WEC (4.27 × 107 Ω cm2). In the salt spray test, PDA@g-C3N4-CeO2/WEC also showed excellent long-term corrosion resistance with few corrosion products even after 600 h, which was consistent with the results of the EIS test. In addition, PDA@g-C3N4-CeO2/WEC also reflects the most fantastic adhesion strength (14.22 MPa), which is improved by 45.40% than that of pure WEC (9.78 MPa). Generally, the excellent protection properties of PDA@g-C3N4-CeO2/WEC are attributed to the presence of PDA and KH-550 modified nano-CeO2 on the surface of g-C3N4, which increase the compatibility and surface interactions between nanofillers and epoxy resin.

One-pot synthesis of nano Zr-based metal-organic frameworks for fluorescence determination of quercetin and Hg2+

In this study, a nanoscale Zr-based metal–organic framework (nano-Zr-MOF) was prepared by one-pot method using meso-tetra(4-carboxyphenyl)porphyrin as organic ligand and Zr4+ as metal unit. The nanoscale structure endows it with excellent dispersion in water. The nano-Zr-MOF exhibited intense red fluorescence, which could be significantly quenched by the addition of quercetin, probably due to its electron-rich framework. The high selectivity for quercetin detection was verified with analogues and common ions as interfering agents. Moreover, the nano-Zr-MOF could be used as a highly selective and sensitive sensor for the detection of Hg2+. The detection limits for quercetin and Hg2+ were 0.026 μM and 0.039 μM, respectively. This fluorometric method was successfully applied to detect quercetin in red wine and food samples with satisfactory recoveries ranging from 83.7–112.3% and 81.8–115.9%, respectively. The recovery in detection of Hg2+ in lake water were ranging from 97.1–109.2%.

Multifunctional Carbon Nanodot‐Based Advanced Diagnostics and Therapeutics

AbstractCarbon nanodots (CNDs) are an emerging class of zero dimensional (0D) carbon nanomaterials that accumulated immense interest from researchers in the past two decades due to their facile synthesis and unique photo‐physical and ‐chemical properties. In particular, their long wavelength fluorescence emission, enhanced tissue penetration depth, excellent water dispersibility, tunable surface chemistry, charge transfer properties, and biocompatibility have unveiled newer avenues for advanced application in therapeutics, diagnostics, theranostics, and tissue regeneration. The review typically emphasizes CNDs, excluding the other members of the carbon dots (CDs) family, which has not been covered before. After introducing CNDs in the carbon nanomaterial hierarchy, their synthesis, general properties, functionalization, and characterization are subsequently discussed. The following section elaborates on mechanisms of CNDs fluorescence, quenching, and associated factors based on the latest theories and models. The diagnostic, theranostic, and therapeutic applications of red/NIR‐emitting CNDs are thoroughly reviewed to cover the latest developments, including in vitro/in vivo bioimaging, thermoelectric and piezoelectric biosensing, and various soft and hard tissue regeneration. Overall, this work will enlighten passionate readers about the present status and futuristic aspects of CNDs in healthcare management, besides reported toxicities and challenges associated with their bench‐to‐bedside translation.

Grafting α-aminoketone to SMA via highly efficient amide bond and their performances as macrophotoinitiators

Water-soluble macrophotoinitiators that can realize a high photoactivity together with low migration in waterborne photopolymerization systems are very necessary. However, the precise, highly efficient preparation of macrophotoinitiators remains a substantial challenge, such as grafting side chains according to stoichiometric ratios. Herein, based on styrene maleic anhydride copolymer (SMA) prepared by photopolymerization, water soluble macrophotoinitiators SMA5k-Ns and SMA13k-Ns series with controllable structure were successfully prepared through the amino bond of α-aminoketone small-molecule photoinitiator with maleic anhydride moieties. All of them exhibited excellent water dispersion properties, and solution photopolymerizations investigation showed they can be used as photoinitiators for radical polymerization with high conversion (up to 95%) in waterborne systems under LED@365–405 nm. Furthermore, the migration stabilities of these photoinitiators in photocured hydrogels were better than those of commercial photoinitiators. High efficiency and low migration make them have great potential applications in food packaging and biological materials.

Facile Synthesis of Ultrafine and Highly Dispersible MnO2 Nanoparticles for Energy Storage in Supercapacitors

AbstractManganese dioxide (MnO2) has been extensively investigated as an electrode material for supercapacitors because of its high theoretical capacitance, great abundance, and low toxicity. To obtain satisfactory capacitance performance, in recent years, many efforts have been dedicated to the fabrication of MnO2 nanoparticles that offer a larger specific surface area and an escalated chemical activity. Beyond them, the ideal dispersibility of nanoparticles in a liquid medium is also of vital importance when processing those powdery materials into slurry ones for some particular uses, such as editable and ink‐printing supercapacitor devices. In this study, the as‐synthesized ultrafine MnO2 nanoparticles having excellent dispersibility in water can be prepared via a facile one‐step hydrothermal route, with a uniform size in diameter of 200 nm exhibiting a large specific surface area of ~389.7 m2 g−1, and a high specific capacitance of 135.7 F g−1 at 5 mV s−1.

De Novo Design of Aggregation‐Induced Emission Luminogen for Three‐Photon Fluorescence Imaging of Subcortical Structures Excited at Both NIR‐III and NIR‐IV Windows

AbstractThree‐photon fluorescence (3PF) imaging excited at 1700 nm window is an enabling technology for visualizing deep brain structures and dynamics. Recently, the 2200 nm window has emerged as the longest excitation window suitable for deep‐brain 3PF imaging. Bright fluorescent probes lay the material basis for deep‐brain 3PF imaging. Among various fluorescent probes, aggregation‐induced emission luminogens (AIEgens) have great potential in 3PF imaging excited at the 1700 nm window in vivo. However, to the best of knowledge, there is no AIEgens applicable to 3PF imaging excited at both the 1700 and 2200 nm windows. To readily fill this gap, here this study designs and synthesizes a novel AIEgen, namely TPE‐DPTT‐ICP, which generates bright 3PF signals excited at both 1700 and 2200 nm. The accordingly fabricated TPE‐DPTT‐ICP nanoparticles (NPs) possess excellent water dispersibility, colloidal stability, biocompatibility, photostability and large 3P action cross section, key to in vivo imaging. In mouse brain in vivo, TPE‐DPTT‐ICP NPs enable deep‐brain 3PF imaging of subcortical structures excited at both the two windows, reaching depths of 1640 and 880 µm below the brain surface, respectively. TPE‐DPTT‐ICP NPs are thus a versatile material simultaneously catering to the need at two infrared optical windows with deep tissue penetration.

Facile production of cellulose nanofibers from raw elephant grass by an aluminum chloride-enhanced acidic deep eutectic solvent

To develop a greener and more efficient method for producing cellulose nanofibers (CNFs) from raw plants, an AlCl3-enhanced ternary deep eutectic solvent, DES2 (consisting of choline chloride, citric acid, and AlCl3·6H2O in a molar ratio of 1:0.4:0.08), was synthesized. Raw elephant grass (EG) was pretreated with DES2, followed by sodium chlorite (NaClO2) bleaching and ultrasonic disruption to extract high-performance CNFs. The DES2 and NaClO2 treatments effectively removed hemicellulose and lignin, achieving removal rates of 99.23 % and 99.62 %, respectively, while maintaining a cellulose content of 78.3 %. DES2 demonstrated easy recyclability and maintained excellent biomass pretreatment performance even after multiple cycles. Following a brief 30-min intermittent ultrasound treatment, the resulting CNFs demonstrated superior crystallinity, increased carboxyl content, and a narrower width distribution compared to CNFs obtained from AlCl3-free DES1. Optimized conditions at 110 °C yielded CNFs with 85.3 % crystallinity, 0.64 mmol/g carboxyl content, 5.15 nm width distribution, and excellent dispersion in water for at least six months. Additionally, CNFs enhanced the tensile strength of chia seed mucilage (CM) composite films, showing a significant improvement to 26.6 MPa, representing a 231.3 % increase over the control film. This study offers a promising approach for efficiently producing CNFs from raw plants.

An Ultra-stable Eu3+ Doped Yttrium Coordination Polymer with Dual-function Sensing for Cr(VI) and Fe(III) Ions in Aqueous Solution

The exploration of a dual-functional sensor is the key to effectively detect the Cr(VI) and Fe(III) cations in water, which is important to human health and environmental sustainability. Because of the phase stability and excellent luminescence, the rare-earth coordination polymers have great potential as dual-functional sensors. Here, we develop a Y0.91Eu0.09(H2O)2{C6H3(CO2)3}(MIL-92(Y):9%Eu3+)-based dual-function luminescent sensor on Cr(VI) and Fe(III), which exhibits excellent phase stability and dispersibility in water. The luminescence of MIL-92(Y):9%Eu3+ aqueous suspension quenches on Fe3+ with Stern-Volmer constant Ksv of 1.79 × 103 M-1 and limit of detection of 17 μM. The MIL-92(Y):9%Eu3+ aqueous suspension also has turn-off sensing ability towards Cr2O72- and CrO42- with Ksv values of 3.5 × 103 and 6.14 × 103 M-1, respectively. It has detection limitations of 10 and 5 μM on Cr2O72- and Cr2O72- ions, respectively.

Novel one-pot strategy for fabrication of a pH-Responsive bone-targeted drug self-frame delivery system for treatment of osteoporosis.

Osteoporosis (OP) is a systemic metabolic orthopedic disorder prevalent in elderly people, that is characterized by a decrease in bone mass. Although many therapeutics have been adopted for OP treatment, many of them are still not well satisfied clinical requirements and therefore development of novel therapeutics is of great significance. In this work, a novel bone-targeting drug self-frame delivery system (DSFDS) with high drug loading efficiency and pH responsive drug release was fabricated by condensation of curcumin (Cur), amino group terminated polyethylene glycol (NH2-PEG), and alendronate (ALN) using hexachlorocyclotriphosphonitrile (HCCP) as the linker. The final product named as HCCP-Cur-PEG-ALN (HCPA NPs) displayed excellent water dispersity with small size (181.9​±​25.9​nm). Furthermore, the drug loading capacity of Cur can reach 25.8%, and Cur can be released from HCPA NPs under acidic environment. Owing to the introduction of ALN, HCPA NPs exhibited strong binding to HAp in vitro and excellent bone-targeting effect in vivo. Results from cellular and biochemical analyses revealed that HCPA NPs could effectively inhibit the formation and differentiation function of osteoclasts. More importantly, we also demonstrated that HCPA NPs could effectively reduce bone loss in OVX mice with low toxicity to major organs. The above results clearly demonstrated that HCPA NPs are promising for OP treatment. Given the simplicity and well designability of fabrication strategy, explicit therapy efficacy and low toxicity of HCPA NPs, we believe that this work should be of great interest for fabrication of various DSFDS to deal with many diseases.

Vancomycin-modified nitrogen and chloride doped carbon dots and their application as a Staphylococcus aureus probe

In this research, N, Cl-doped carbon dots (N, Cl-CDs) were prepared in choline chloride-glycerol deep eutectic solvent (DES) by microwave method. N, Cl-CDs surface was modified with vancomycin for detection of Staphylococcus aureus (S. aureus) bacteria in the range of 102-107 colony-forming unit per milliliter (CFU/mL). The detection limit was 101 CFU/mL. Morphology and structure of N, Cl-CDs were characterized by transmission electron microscopy (TEM), X-ray photon spectroscopy (XPS), photoluminescence spectroscopy, FT-IR spectroscopy, energy dispersive X-ray spectroscopy (EDXS) and zeta potential. The prepared N, Cl-CDs had excellent dispersion in water, particle size range of 2–3 nm, and quantum yield of 38.75%. Speed, wide linear range and more convenient were advantages of new probe with respect to other methods.