Controlled Synthesis and Visible-Light-Driven Photocatalytic Activity of BiOBr Particles for Ultrafast Degradation of Pollutants.

For the purpose of regulating the visible-light-driven photocatalytic properties of photocatalysts, we selected BiOBr as the research target and various routes were used. Herein, via the use of a hydrothermal method with various solvents, BiOBr particles with controllable morphology and photocatalytic activities are obtained. In particular, through changing the volume ratio of ethylene glycol (EG) to ethanol (EtOH), BiOBr compounds possess microspheres, in which samples synthesized by using EG:EtOH = 1:2 have the highest photocatalytic activity, and can completely decompose RhB under visible light irradiation within 14 min. Furthermore, we also used different volume ratios of EG and H2O reaction solvents to prepare BiOBr particles so as to further improve its pollutant removal ability. When the volume ratio of EG to H2O is 1:1, the synthesized BiOBr particles have the best photocatalytic activity, and RhB can be degraded in only 10 min upon visible light irradiation. Aside from the reaction solvent, the impact of sintering temperature on the photocatalytic properties of BiOBr particles is also explored, where its pollutant removal capacities are restrained due to the reduced specific surface area. Additionally, the visible-light-triggered photocatalytic mechanism of BiOBr particles is determined by h+, ·OH and ·O2- active species.

Synthesis, Structure-Activity Relationship, and Mechanism of a Series of Diarylhydrazide Compounds as Potential Antifungal Agents.

A series of simple diarylhydrazide derivatives (45 examples) were well-designed, prepared, and screened for their antifungal activities both in vitro and in vivo. Bioassay results suggested that all designed compounds had significant activity against Alternaria brassicae (EC50 = 0.30-8.35 µg/mL). Among of them, 2c, as the highest activity compound, could effectively inhibit the growth of plant pathogens Pyricularia oryza, Fusarium solani, Alternaria solani, Alternaria brassicae, and Alternaria alternate and was more potent than carbendazim and thiabendazole. 2c showed almost 100% protection at 200 µg/mL in vivo activity against A. solani in tomato. Moreover, 2c did not affect the germination of cowpea seed and the growth of normal human hepatocytes. The preliminary mechanistic exploration documented that 2c could result in the abnormal morphology and irregular structure of the cell membrane, destroy the function of mitochondria, increase the reactive oxygen species, and inhibit the proliferation of hypha cell. The above results manifested that target compound 2c could be a potential fungicidal candidate against phytopathogenic diseases for its excellent fungicidal activities.

A highly selective and sensitive CdS fluorescent quantum dot for the simultaneous detection of multiple pesticides.

The abuse of pesticides has introduced a large number of residues in soil and drinking water, which can then enter the food chain and the human body. Monitoring pesticide residues and developing simple and fast detection systems for pesticide residues is urgently needed. In this study, we presented one-pot prepared CdS fluorescent quantum dots (QDs) and explored their sensing application for organic pesticides. The CdS QDs can sensitively and selectively detect three different pesticides, dichlorvos (DDVP), paraquat, and glufosinate-ammonium, through different fluorescence responses. Paraquat can effectively quench the fluorescence of the QDs and DDVP can cause remarkable fluorescent enhancement. Glufosinate-ammonium can induce both 150 nm fluorescent blueshifting and 30-fold fluorescent enhancement. The probe exhibited low detection limits for the three pesticides: 1.44 µM for paraquat, 0.23 mM for DDVP, and 49.8 µM for glufosinate-ammonium. Furthermore, based on the results, we utilized the powerful functions of smartphones to establish a concentration-gray value standard curve through RGB values and gray values to realize the qualitative detection and quantitative analysis of DDVP. It is believed that this work presents a new platform for the simultaneous detection of multiple pesticides using a single QDs probe. The present on-site method using a smartphone is of great potential for water monitoring in rural areas.

Preparation of chitosan crosslinked with metal-organic framework (MOF-199)@aminated graphene oxide aerogel for the adsorption of formaldehyde gas and methyl orange.

Chitosan crosslinked with metal-organic framework (MOF-199)@aminated graphene oxide aerogel (MOF-199@AFGO/CS) were prepared to adsorb formaldehyde and methyl orange. The prepared MOF-199@AFGO/CS aerogel was well characterized via SEM, EDX, FT-IR, XRD and XPS to reveal the microstructure and composition. Besides, the mechanical property and the stability of MOF-199@AFGO/CS aerogel were investigated. The results showed that MOF-199@AFGO/CS aerogel had good stability in water, compression resilience and thermostability. The study on the ability to adsorb formaldehyde gas and methyl orange showed that the adsorption capacity of MOF-199@AFGO/CS aerogel was related to the pore size and the surface functional groups of MOF-199@AFGO/CS aerogel. When the pore size is moderate, as the amino group and MOF-199 on the aerogel increased, the adsorption capacity of formaldehyde gas (197.89 mg/g) and methyl orange (412 mg/g) can reach the maximum. Furthermore, the adsorption process at equilibrium followed the Freundlich isotherm model. The kinetic behavior was well fitted by the pseudo-second-order model, indicating chemisorption as the rate-determining step. This work can provide a reliable basis for the adsorbent to remove pollutants in different forms at the same time, and has potential application in simultaneously adsorbing liquid pollutants and gas pollutants.

Modified Camellia oleifera Shell Carbon with Enhanced Performance for the Adsorption of Cooking Fumes.

Using Camellia oleifera shell (COS) as a raw material and phosphoric acid as the activator, activated Camellia oleifera shell carbon (COSC-0) was prepared and then modified by Fenton's reagent (named as COSC-1). SEM, GC-MS, FTIR, and specific surface area and pore analyzers were used to study the adsorption performance of COS, COSC-0, and COSC-1 on cooking fumes. Results showed that COSC-1 was the best adsorbent compared with COS and COSC-0. The adsorption quantity and penetrating time of COSC-1 were 44.04 mg/g and 4.1 h, respectively. Most aldehydes could be adsorbed by COSC-1, which was due to the large number of carbonyl and carboxyl groups generated on the surface of COSC-1 from the action of Fenton's reagent. The adsorption effect of COSC-1 on different types of pollutants in cooking fumes was analyzed based on the similar compatibility principle. COSC-1 showed a much higher adsorption effect on the strong polarity functional groups than on weak polar groups. The results provide a theoretical basis for the application of Camellia oleifera shell carbon adsorption technology in the treatment of cooking fumes.

Dual-channel fluorescent signal readout strategy for cysteine sensing.

Cysteine (Cys) is a biological thiol. Aberrant changes in thiol levels are associated with the development and pathogenesis of various diseases, including liver damage, Alzheimer's disease, weakness, and cardiovascular diseases. Therefore, thiol detection in biological samples has great importance in health monitoring and disease prediction. In this study, we developed a ratiometric fluorescence nanosensor combined with carbon dots (CDs)-doped mesoporous silica and fluorescein-based fluorescent probes loaded in pores for Cys detection. The nanosensor emitted fluorescence at 450 nm upon excitation at 370 nm. In the presence of Cys, the fluorescence emission from the probe could be selectively enhanced, whereas that from CDs could be changed. Thus, a ratiometric fluorescent sensor was developed. This sensor can eliminate the potential influence of background fluorescence and other analyte-independent external environmental factors. The nanosensor was utilized to monitor Cys levels in human serum, and satisfactory results were obtained. Results indicated that the nanosensor can be utilized as an excellent fluorescent nanocomposite material in practical biological applications.

Luminescence investigation of red-emitting Sr2MgMoO6:Eu3+ phosphor for visualization of latent fingerprint.

Fingerprints are widely studied due to their unique shape and lifelong properties. The latent fingerprint (LFP) visualization is critical in identifying crime scenes and personal information. At present, the powder dusting method for LFP detection is favored due to its environmental friendliness and nontoxicity. However, this method has low resolution, low sensitivity, and large background interference. To address these shortcomings, the red-emitting Sr2MgMoO6:xEu3+ (x = 0-0.50) phosphors were synthesized using the solid-state reaction process. The products were systematically studied through the structural phase, luminescent property, decay curve, and color purity. Sr2MgMoO6:xEu3+ phosphors were monitored at 596 nm and exhibited a commendable broad excitation band between 250 and 475 nm. This result indicated that the disadvantage of the poor absorption of commercial red phosphors (Y2O2S:Eu3+) in the near-ultraviolet region was overcome. Under excitation at 393 nm, the synthesized Sr2MgMoO6:Eu3+ phosphor exhibited intense red light at 596 and 616 nm, due to the 5D0 â†’ 7F1 and 5D0 â†’ 7F2 transitions of Eu3+ ions. The optimal concentration for the Sr2MgMoO6:xEu3+ phosphor was x = 20 mol%, and the concentration quenching effect was ascribed to the dipole-dipole interaction. The Commission International del'Eclairage (CIE) chromaticity coordinates of Sr2MgMoO6:Eu3+ were (0.643, 0.356), and the color purity was 99.8%. Furthermore, the fluorescent LFP images developed by Sr2MgMoO6:0.20Eu3+ phosphors were well visualized, and level 1-3 details were well identified with high resolution, contrast, sensitivity, and selectivity. The obtained results suggested that the Sr2MgMoO6:Eu3+ phosphor can be applied for LFP detection.

Facile synthesis of N,B-co-doped carbon dots with the gram-scale yield for detection of iron (III) and E. coli.

A simple method was developed to prepare fluorescent nitrogen/boron-doped carbon dots (N,B-CDs) in the gram scale. The results showed that the CDs exhibited blue photoluminescence (PL) under 365 nm ultraviolet radiation and excitation-dependent emission. Heteroatoms entered the CDs to enhance the photochemical properties, and their positive properties can be attributed to the presence of guanidino group and functionalized with boronic acid for realizing their utilization in certain applications. These materials could be applied to monitor Fe3+ via static PL quenching, yielding a limit of detection (LOD) of 0.74 µM. Furthermore, the charged and boronic acid groups on the prepared N,B-CDs enabled their use as recognition elements to bind with the bacteria through electrostatic interaction and allowed covalent interactions to form the corresponding boronate ester with E. coli (E. coli) bacterial membrane. This method could satisfy a linear range of 102-107 with LOD of 165 cfu ml-1 for E. coli. This method was applied for the determination of E. coli in tap water and orange juice samples, and satisfactory results were obtained.

Highly luminescent N-doped carbon dots as a fluorescence detecting platform for Fe3+ in solutions and living cells.

Iron (Fe3+) is one of the most essential elements in the human body; deficiency or overdose of Fe3+ may have adverse effects on human health and immunity. Hence, it is essential to establish a sensitive and selective method for ion detection. In this study, novel green fluorescent N-doped carbon dots (N-CDs) were prepared with caffeic acid as the carbon source via a simple hydrothermal method. The solution of the as-prepared N-CDs exhibits 21.5% quantum yield, good salt stability, excellent water solubility, low cytotoxicity and good photobleaching resistance. The N-CDs can be used as a fluorescent probe for the detection of Fe3+ ions in aqueous solutions and bioimaging in living cells.

Preparation, characterization, and luminescence properties of BiLaWO6:Eu3+ red-emitting phosphors for w-LEDs.

Eu3+-doped bismuth lanthanum tungstate BiLaWO6 phosphors were synthesized for the first time by a conventional solid-state reaction at 1273K. By powder X-ray diffraction (XRD), the crystal structure of the phosphor was verified, which revealed its single-phase structure. Under the 467nm wavelength excitation, the Eu3+-doped BiLaWO6 phosphor powders showed red emission (617nm) that was ascribed to the 5D0→7F2 transitions of Eu3+. The effects of concentration on luminescence properties indicated that the optimal doping concentration was x=0.50mol. The thermal stability by the emission intensities at various temperatures was verified, and the activation energy (Ea) was approximately 0.29eV. The luminescence lifetime was analyzed by the decay curve. The chromaticity coordinates of BiLaWO6:0.50Eu3+ were x=0.650, y=0.347, which had a high color purity at 99.2%. The phosphors had potential application for white light-emitting diodes.

Carboxyl hydrogel particle film as a local pH buffer for voltammetric determination of luteolin and baicalein.

Electrochemical determination of luteolin and baicalein always needs acidic supporting electrolyte to guarantee good sensitivity. Therefore, most of the reported electrochemical sensors of luteolin and baicalein are unsuitable for detection of neutral actual samples. It is necessary to design a highly sensitive sensor for direct determination of them in neutral conditions. In this study, poly(N-isopropylacrylamide-acrylic acid) hydrogel particles (NIPA/AA) and multiwall carbon nanotubes (MWCNTs) composite modified glassy carbon electrode (GCE) was fabricated by a simple casting method. The voltammetric results showed that the NIPA/AA particle film provided acidic environment for proton-electron coupled reaction in neutral mediums. The near-surface pH of the electrode was related on the loaded amount of the NIPA/AA particles in pH range from 4.2 to 5.9. The voltammetric behaviors of luteolin and baicalein at the NIPA/AA-MWCNTs-GCE were studied by cyclic voltammetry. The peak separations between cathodic and anodic peaks were decreased and peak currents were increased because of decrease in pH and increase in ion conductivity at the local electrode surface. The sensitivity of the electrode was investigated by differential pulse voltammetry. Even under neutral conditions, the plots of the oxidation currents of luteolin and baicalein were dependent linearly on their concentration with detection limit of 14.5 pM and 44.4 pM, respectively. Moreover, the proposed NIPA/AA-MWCNTs-GCE was also successfully applied for determination of luteolin and baicalein in peanut shell, Huang-qin and tomato samples.

Correlation between narrow-band imaging endoscopy results and hPTTG expression indicated by angiogenensis and its distribution in the initial phase of colorectal adenoma-carcinoma sequence.

The aim of the present study was to investigate the correlation between vascular characteristics under narrow band imaging endoscopy (NBI) and the expression of angiogenic factors of colorectal carcinoma and adenoma, and to evaluate the feasibility and validity of NBI in vivo visualizing angiogenesis. Patients with colorectal polyps, which were pathologically confirmed as early carcinoma, adenoma and hyperplastic polyp, were recruited and examined by NBI. The endoscopic vascular pattern was classified by Showa classification. Immunohistochemical staining was performed by cluster of differentiation (CD34), microvessel density (MVD) and Human Pituitary Tumor-Transforming Gene (hPTTG). The histologic results were compared with the vascular pattern under NBI. Overall, 83 colorectal lesions including 9 intramucosal colorectal carcinomas, 44 adenomas (18 tubular adenomas, 26 tubulovillous adenomas) and 30 hyperplastic polyps were recruited and examined by NBI. A higher proportion (88.6%, 47/53) of intramucosal carcinomas and adenomas were more likely to have the dense pattern (DP) or network pattern (NP), while that of hyperplastic polyps was only 30.0% (9/30). There was an obvious increase in the MVD-CD34 counting from hyperplastic polyps, to adenoma to carcinoma, and a significant difference among the three groups as well. Also, a clear difference can be seen in the expression of hPTTG, which was expressed more in carcinoma than in adenoma and HP group (P < 0.05). Conclusion: NBI might be a useful tool as in vivo visualizing angiogenesis. hPTTG expression in colorectal adenoma and carcinoma is related to angiogenesis.

Eu3+ -Activated Gd8 V2 O17 : Energy Transfer, Luminescence, and Temperature-Dependence Characteristics.

A new phosphor of the type Gd8(1-x) Eu8 x V2 O17 (x=0-1.0) was synthesized through the solid-state reaction ceramics method. A pure phase formation was verified by using X-ray powder diffraction measurements. The luminescence of Gd8 V2 O17 :Eu3+ was investigated through optical and laser excitation spectroscopy. The luminescence curves were investigated in the temperature region 10 to 300 K. Gd8 V2 O17 shows a self-activated luminescence under excitation with UV- and near-UV light. The spectra, the decay lifetimes, and the thermal stability of Gd8(1-x) Eu8 x V2 O17 (x=0.005-1.0) strongly depend on both the Eu3+ concentration and the temperature. The tunable luminescence is realized by controlling the Eu3+ -doping level to adjust the host energy-transfer efficiency from the VO43- groups to the Eu3+ activators. At low Eu3+ concentrations (<30 mol %), the intensity and lifetime show an unusual change with an increase of the temperature from 10-300 K, that is, the luminescence experiences a straightforward enhancement. The energy transfer from the VO43- group to the Eu3+ ions could be accelerated with an increase of the temperature resulting in an unusual enhancement of the Eu3+ luminescence and lifetime. However, the emission of the Eu3+ ions decreased for highly Eu-doped samples (>30 mol %) with an increase of the temperature. The luminescence mechanism was discussed on the basis of the charge-transfer band of the Eu3+ ions, the doping concentration, and the proposed microstructures in the lattices.

One-step synthesis of Nickle Iron-layered double hydroxide/reduced graphene oxide/carbon nanofibres composite as electrode materials for asymmetric supercapacitor.

A novel NiFe-LDH/RGO/CNFs composite was produced by using a facile one-step hydrothermal method as electrode for supercapacitor. Compared with NiFe-LDH/CNFs, NiFe-LDH/CNTs and NiFe-LDH/RGO, NiFe-LDH/RGO/CNFs demonstrated a high specific capacitance of 1330.2 F g-1 at 1 A g-1 and a super rate capability of 64.2% from 1 to 20 A g-1, indicating great potential for supercapacitor application. Additionally, an asymmetric supercapacitor using NiFe-LDH/RGO/CNFs composite as positive electrode material and activated carbon as negative electrode material was assembled. The asymmetric supercapacitor can work in the voltage range of 0-1.57 V. It displayed high energy density of 33.7 W h kg-1 at power density of 785.8 W kg-1 and excellent cycling stability with 97.1% of the initial capacitance after 2500 cycles at 8 A g-1. Two flexible AC//LDH-RGO-CNFs ASC devices connected in series were able to light up a red LED indicator after being fully charged. The results demonstrate that the AC//LDH-RGO-CNFs ASC has a promising potential in commercial application.

High performance asymmetric supercapacitor based on Cobalt Nickle Iron-layered double hydroxide/carbon nanofibres and activated carbon.

A novel Cobalt Nickle Iron-layered double hydroxide/carbon nanofibres (CoNiFe-LDH/CNFs-0.5) composite was successfully fabricated through an easy in situ growth approach. The morphology and composition of the obtained materials were systematically investigated. When the two derived materials were used for supercapacitor electrodes, the CoNiFe-LDH/CNFs-0.5 composite displayed high specific surface area (114.2 m2 g-1), specific capacitance (1203 F g-1 at 1 A g-1) and rate capability (77.1% from 1 A g-1 to 10 A g-1), which were considerably higher than those of pure CoNiFe-LDH. Moreover, the specific capacitance of CoNiFe-LDH/CNFs-0.5 composite remained at 94.4% after 1000 cycles at 20 A g-1, suggesting excellent long-time cycle life. The asymmetric supercapacitor based on CoNiFe-LDH/CNFs-0.5 as a positive electrode and activated carbon as a negative electrode was manufactured and it exhibited a specific capacitance of 84.9 F g-1 at 1 A g-1 and a high energy density of 30.2 W h kg-1. More importantly, this device showed long-term cycling stability, with 82.7% capacity retention after 2000 cycles at 10 A g-1. Thus, this composite with outstanding electrochemical performance could be a promising electrode material for supercapacitors.

Ultrasensitive direct competitive FLISA using highly luminescent quantum dot beads for tuning affinity of competing antigens to antibodies.

Herein, for the first time we report a novel direct competitive fluorescence-linked immunosorbent assay (dcFLISA) for the ultrasensitive detection of ochratoxin A (OTA) by introducing a large size polymer beads loaded with quantum dots (QBs) as carrier of competing antigen for decreasing binding affinity to antibody and enhancing the fluorescent signal intensity. When using 255 nm QBs as carrier of competing antigen, the equilibrium dissociation constant of QB based competing antigen to antibodies can be tuned to 100 times higher than that of the horseradish peroxidase (HRP) based competing antigen by controlling labeled amounts of antigen on the surface of QBs. Various parameters that influenced the sensitivity of dcFLISA were investigated and optimized. Under optimum detection parameters, the dynamic linear range of developed dcFLISA for detecting OTA was established at 0.05 pg/mL to 1.56 pg/mL with a half maximal inhibitory concentration at 0.14 ± 0.04 pg/mL (n = 5), which is three orders of magnitude lower than that of conventional HRP-based dcELISA (0.24 ng/mL). The developed FLISA is also highly accurate, reliable, and shows no cross reaction to other mycotoxins. In summary, the proposed method offers a straightforward approach to improve the sensitivity of direct competitive immunoassay for trace small chemical molecule detection in food quality control, environmental monitoring, and clinical diagnosis.

Intracellular delivery of proteins by nanocarriers.

Intracellular delivery of proteins is potentially a game-changing approach for therapeutics. However, for most applications, the protein needs to access the cytosol to be effective. A wide variety of strategies have been developed for protein delivery, however access of delivered protein to the cytosol without acute cytotoxicity remains a critical issue. In this review we discuss recent trends in protein delivery using nanocarriers, focusing on the ability of these strategies to deliver protein into the cytosol.

Observation of intrinsic emission in ß-BiNbO4 available for excitation of both UV light and high energy irradiation.

ß-BiNbO4 with a high temperature triclinic form was prepared via a high-temperature solid-state reaction ceramic method. Structural refinement and surface characteristic studies were performed. The optical absorption, and electronic calculation of the band structures and density of states were also studied. ß-BiNbO4 ceramic has an indirect transition with a band energy of 3.05 eV. The valence band is dominated by O-2p states whereas the conduction band has predominantly Nb 4d and Bi 6s character. The intrinsic luminescence properties of ß-BiNbO4 were reported, and present a blue emission band peak at 435 nm under the excitation of UV light. The ß-BiNbO4 ceramic presents scintillation properties under high energy irradiation. The luminescence was studied via the combinations of the color centers, band calculation and energy transfer from NbO6 to Bi(3+) in the lattices. The thermal quenching and activation energy for the luminescence were reported. ß-BiNbO4 has potential applications in photoluminescence and scintillation materials.

Fluorescence ELISA for sensitive detection of ochratoxin A based on glucose oxidase-mediated fluorescence quenching of CdTe QDs.

The present study described a novel fluorescence enzyme-linked immunosorbent assay (ELISA) used to detect ochratoxin A (OTA) by using the glucose oxidase (GOx)-mediated fluorescence quenching of mercaptopropionic acid-capped CdTe quantum dots (MPA-QDs), in which GOx was used as an alternative to horseradish peroxidase (HRP) for the oxidization of glucose into hydrogen peroxide (H2O2) and gluconic acid. The MPA-QDs were used as a fluorescent signal output, whose fluorescence variation was extremely sensitive to the presence of H2O2 or hydrogen ions in the solution. Under the optimized conditions, the proposed fluorescence ELISA demonstrated a good linear detection of OTA in corn extract from 2.4 pg mL(-1) to 625 pg mL(-1) with a limit of detection of 2.2 pg mL(-1), which was approximately 15-fold lower than that of conventional HRP-based ELISA. Our developed fluorescence immunoassay was also similar to HRP-based ELISA in terms of selectivity, accuracy, and reproducibility. In summary, this study was the first to use the GOx-mediated fluorescence quenching of QDs in immunoassay to detect OTA, offering a new possibility for the analysis of other mycotoxins and biomolecules.

Preparation and Luminescent Properties of Sm3+-Doped High Thermal Stable Sodium Yttrium Orthosilicate Phosphor.

Orange-red-emitting sodium yttrium orthosilicate NaYSiO4:xSm3+ (x = 0.005, 0.01, 0.02, 0.05, 0.10, 0.15, and 0.20) were synthesized. The phase structure and photoluminescence properties of these phosphors were investigated. The emission spectrum obtained by excitation into 406 nm contains exclusively the characteristic emissions of Sm3+ at 571 nm, 602 nm, 648 nm, and 710 nm, which correspond to the transitions from 4G5/2 to 6H5/2, 6H7/2, 6H9/2, and 6H11/2 of Sm3+, respectively. The strongest one is located at 602 nm due to the 4G5/2 --> 6H7/2 transition of Sm3+, generating bright orange-red light. The optimum dopant concentration of Sm3+ ions in NaYSiO4:xSm3+ is around 2 mol%, and the critical transfer distance of Sm3+ is calculated as 23 Å. The thermal quenching temperature is above 500 K. The fluorescence lifetime of Sm3+ in NaYSiO4:0.02Sm3+ is 1.83 ms. The NaYSiO4:Sm3+ phosphors may be potentially used as red phosphors for white light emitting diodes.