Catalytic SrMoO4 nanoparticles and conducting polymer composite sensor for monitoring of K+-induced dopamine release from neuronal cells

Octahedral SrMoO4 nanoparticles (NPs) with a high degree of crystallinity and controlled size (250-350 nm) were synthesized for the first time by employing a facile hydrothermal method. The prepared NPs...

A novel electrochemical sensor for the detection of enrofloxacin based on a 3D flower-like metal tungstate incorporated reduced graphene oxide nanocomposite.

In recent times metal tungstates have received a lot of attention in the various research field. Accordingly, the CaWO4/RGO (CW/RGO) nanocomposite was prepared by the facile hydrothermal method. The electrocatalytic...

Assembling Ultrafine SnO2 Nanoparticles on MIL-101(Cr) Octahedrons for Efficient Fuel Photocatalytic Denitrification

Effectively reducing the concentration of nitrogen-containing compounds (NCCs) remains a significant but challenging task in environmental restoration. In this work, a novel step-scheme (S-scheme) SnO2@MCr heterojunction was successfully fabricated via a facile hydrothermal method. At this heterojunction, MIL-101(Cr) octahedrons are decorated with highly dispersed SnO2 quantum dots (QDs, approximate size 3 nm). The QDs are evenly wrapped around the MIL-101(Cr), forming an intriguing zero-dimensional/three-dimensional (0D/3D) S-scheme heterostructure. Under simulated sunlight irradiation (280 nm < λ < 980 nm), SnO2@MCr demonstrated superior photoactivity toward the denitrification of pyridine, a typical NCC. The adsorption capacity and adsorption site of SnO2@MCr were also investigated. Tests using 20%SnO2@MCr exhibited much higher activity than that of pure SnO2 and MIL-101(Cr); the reduction ratio of Cr(VI) is rapidly increased to 95% after sunlight irradiation for 4 h. The improvement in the photocatalytic activity is attributed to (i) the high dispersion of SnO2 QDs, (ii) the binding of the rich adsorption sites with pyridine molecules, and (iii) the formation of the S-scheme heterojunction between SnO2 and MIL-101(Cr). Finally, the photocatalytic mechanism of pyridine was elucidated, and the possible intermediate products and degradation pathways were discussed.

Printed copper-nanoplate conductor for electro-magnetic interference

As one of the conductive ink materials with high electric conductivity, elemental copper (Cu) based nanocrystals promise for printable electronics. Here, single crystalline Cu nanoplates were synthesized using a facile hydrothermal method. Size engineering of Cu nanoplates can be rationalized by using the LaMer model and the versatile Cu conductive ink materials are suitable for different printing technologies. The printed Cu traces show high electric conductivity of 6 MS/m, exhibiting electro-magnetic interference shielding efficiency value of 75 dB at an average thicknesses of 11 μm. Together with flexible alumina ceramic aerogel substrates, it kept 87% conductivity at the environmental temperature of 400 ℃, demonstrating the potential of Cu conductive ink for high-temperature printable electronics applications.

In-situ hybridization of ZnO nanorod and graphene oxide with enhancing photocatalytic activity

In this work, nanohybridization of ZnO nanorod and graphene oxide (GO) were prepared by a facile hydrothermal method. The effects of GO on crystal structure and surface morphology of ZnO were revealed by Scanning electron microscopy (SEM), Raman, and X-ray diffraction (XRD). The presence of GO in the composite resulted the ZnO nanorod more uniform which its diameter size was decreased. Optical properties characterized by UV-vis diffuse reflectance spectra (DRS) showed that the ZnO/GO composite has the narrower bandgap value and the better visible-light absorption characterisitics in compare to the bare ZnO. As a result, the photocatalytic ability in degradation of methylene blue under solar irradiation was enhanced in the ZnO/GO composite.

Flexible Tellurium-Based Electrode for High-Performance Lithium-Tellurium Battery

Low-dimensional nanomaterials have attracted considerable attention for next-generation flexible energy devices owing to their excellent electrochemical properties and superior flexibility. Herein, uniform Tellurium nanotubes (Te NTs) were prepared through a facile hydrothermal method, and then a flexible and freestanding electrode was fabricated with Te NTs as active materials and a small amount of nanofibrillated celluloses (NFCs) as a flexible matrix through a vacuum filtration method without adding extra conductive carbon or a binder. The resulting Te-based electrode exhibits a high volumetric capacity of 1512 mAh cm−3 at 200 mA g−1, and delivers admirable cyclic stability (capacity retention of 104% over 300 cycles) and excellent rate performance (833 mAh cm−3 at 1000 mA g−1), which benefits from the unique structure and intrinsically superior conductivity of Te NTs. After bending 50 times, the Te-based electrode delivers a desirable volumetric capacity of 1117 mAh cm−3, and remains 93% of initial capacity after 100 cycles. The results imply that the Te-based electrode exhibits excellent electrochemical properties and superior flexibility simultaneously, which can serve as a potential candidate for the flexible lithium batteries.

Catalytic Performance of Phosphorus Incorporated HZSM-5 in Coupling Transformation of Methanol with 1-butene to Propylene

Directly incorporated phosphorus species into the framework of HZSM-5 zeolite (H[P, Al]-ZSM-5) was successfully synthesized by the facile hydrothermal method. It was characterized by employing XRD, ICP-OES, SEM, FT-IR, N2 adsorption-desorption, NH3-TPD, XPS and TG-DTA, respectively. The effects of the phosphorus species content, temperature, WHSV, and the molar ratio of methanol/1-butene in coupling transformation of methanol with 1-butene to propylene catalyzed by H[P, Al]-ZSM-5 in a fixed bed reactor were studied systematically. Tests have suggested the acid content and specific surface area of H[P, Al]-ZSM-5 are reduced. Under the condition of reaction temperature at 550�Z, molar ratio of methanol/1-butene to 1.0, reaction pressure at 0.1 MPa and WHSV= 3.53 h-1, the P-modified HZSM-5 zeolite (with the P2O5 molar composition of 0.4 )the selectivity and yield of propylene are 35.6% and 32.5%, respectively.

Bi2S3/rGO Composite Based Electrochemical Sensor for Ascorbic Acid Detection

The engineering of an efficient electrochemical sensor based on a bismuth sulfide/reduced graphene oxide (Bi2S3/rGO) composite to detect ascorbic acid (AA) is reported. The Bi2S3 nanorods/rGO composite was synthesized using a facile hydrothermal method. By varying the amount of graphene oxide (GO) added to the synthesis, the morphology and size of Bi2S3 nanorods anchored on the surface of rGO can be tuned. Compared to a bare glassy carbon electrode (GCE), the GCE modified with Bi2S3/rGO composite presented enhanced electrochemical performance, which was attributed to the optimal electron transport between the rGO support and the loaded Bi2S3 as well as to an increase in the number of active catalytic sites. Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) analysis of Bi2S3/rGO/GCE demonstrate that the active Bi2S3/rGO layer on GCE plays an important role in the electrochemical behavior of the sensor. In particular, the Bi2S3/rGO/GCE sensor shows a wide detecting range (5.0–1200 μM), low detection limit (2.9 µM), good sensitivity (268.8 μA mM−1 cm−2), and sufficient recovery values (97.1–101.6%) for the detection of ascorbic acid.