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Band gap change in doped ZnO is an observed phenomenon that is very interesting from the fundamental point of view. This work is focused on the preparation of pure and single phase nanostructured ZnO and Cu as well as Mn-doped ZnO for the purpose of understanding the mechanisms of band gap narrowing in the materials. ZnO, Zn0.99Cu0.01O and Zn0.99Mn0.01O materials were prepared using a wet chemistry method, and X-ray diffraction (XRD) results showed that all samples were pure and single phase. UV-visible spectroscopy showed that materials in the nanostructured state exhibit band gap widening with respect to their micron state while for the doped compounds exhibited band gap narrowing both in the nano and micron states with respect to the pure ZnO materials. The degree of band gap change was dependent on the doped elements and crystallite size. X-ray photoelectron spectroscopy (XPS) revealed that there were shifts in the valence bands. From both UV-visible and XPS spectroscopy, it was found that the mechanism for band gap narrowing was due to the shifting of the valance band maximum and conduction band minimum of the materials. The mechanisms were different for different samples depending on the type of dopant and dimensional length scales of the crystallites.

We propose and numerically demonstrate an ultra-broadband graphene-based metamaterial absorber, which consists of multi-layer graphene/dielectric on the SiO 2 layer supported by a metal substrate. The simulated result shows that the proposed absorber can achieve a near-perfect absorption above 90% with a bandwidth of 4.8 Thz. Owing to the flexible tunability of graphene sheet, the state of the absorber can be switched from on (absorption > 90%) to off (reflection > 90%) in the frequencies range of 3–7.8 Thz by controlling the Fermi energy of graphene. Moreover, the absorber is insensitive to the incident angles. The broadband absorption can be maintained over 90% up to 50°. Importantly, the design is scalable to develop broader tunable terahertz absorbers by adding more graphene layers which may have wide applications in imaging, sensors, photodetectors, and modulators.

Energy transfer in mixed convection unsteady magnetohydrodynamic (MHD) flow of an incompressible nanofluid inside a channel filled with saturated porous medium is investigated. The channel with non-uniform walls temperature is taken in a vertical direction under the influence of a transverse magnetic field. Based on the physical boundary conditions, three different flow situations are discussed. The problem is modelled in terms of partial differential equations with physical boundary conditions. Four different shapes of nanoparticles of equal volume fraction are used in conventional base fluids, ethylene glycol (EG) (C2H6O2) and water (H2O). Solutions for velocity and temperature are obtained discussed graphically in various plots. It is found that viscosity and thermal conductivity are the most prominent parameters responsible for different results of velocity and temperature. Due to higher viscosity and thermal conductivity, C2H6O2 is regarded as better convectional base fluid compared to H2O.

A novel photocatalyst of Ta-doped ZnO nanoparticles was prepared by a modified Pechini-type method. The antimicrobial study of Ta-doped ZnO nanoparticles on several bacteria of Gram-positive Bacillus subtilis (B. subtilis) and Staphylococcus aureus (S. aureus) and Gram-negative Escherichia coli (E. coli) and Pseudomonas aeruginosa (P. aeruginosa) were performed using a standard microbial method. The Ta-doping concentration effect on the minimum inhibitory concentration (MIC) of various bacteria under dark ambient has been evaluated. The photocatalytical inactivation of Ta-doped ZnO nanoparticles under visible light irradiation was examined. The MIC results indicate that the incorporation of Ta5+ ions into ZnO significantly improve the bacteriostasis effect of ZnO nanoparticles on E. coli, S. aureus, and B. subtilis in the absence of light. Compared to MIC results without light irradiation, Ta-doped ZnO and pure ZnO nanoparticles show much stronger bactericidal efficacy on P. aeruginosa, E. coli, and S. aureus under visible light illumination. The possible antimicrobial mechanisms in Ta-doped ZnO systems under visible light and dark conditions were also proposed. Ta-doped ZnO nanoparticles exhibit more effective bactericidal efficacy than pure ZnO in dark ambient, which can be attributed to the synergistic effect of enhanced surface bioactivity and increased electrostatic force due to the incorporation of Ta5+ ions into ZnO. Based on the antibacterial tests, 5 % Ta-doped ZnO is a more effective antimicrobial agent than pure ZnO.

As one of the simple and efficient routes to access two-dimensional materials, liquid exfoliation has received considerable interest in recent years. Here, we reported on high-efficient liquid exfoliation of hexagonal boron nitride nanosheets (BNNSs) using monoethanolamine (MEA) aqueous solution. The resulting BNNSs were evaluated in terms of the yield and structure characterizations. The results show that the MEA solution can exfoliate BNNSs more efficiently than the currently known solvents and a high yield up to 42% is obtained by ultrasonic exfoliation in MEA-30 wt% H 2 O solution. Finally, the BNNS-filled epoxy resin with enhanced performance was demonstrated.

In the current study, we developed resveratrol (RES)-loaded solid lipid nanoparticle (SLN-RES) in order to improve insulin resistance through the upregulation of SNARE protein complex in rats with type 2 diabetes. The SLN-RES characteristics include the following: the average size of 248 nm, the zeta potential of − 16.5 mV, and 79.9% RES entrapment efficiency. The release profile of SLN-RES showed an initial burst followed by a sustained release in natural condition. Infrared spectroscopy results revealed good incorporation of RES into core SLN. Spherical nanoparticle with less aggregation was observed under electronic microscopic examination. Oral administration of SLN-RES prevented weight loss and showed better hypoglycemic effect than RES. Serum oxidative stress status was restored to the normal level by SLN-RES. Furthermore, expression of synaptosomal-associated protein 23 (Snap23), syntaxin-4 (Stx4), and vesicle-associated membrane protein 2 (Vamp2) as the major elements of SNARE protein complex were reduced by SLN-RES more significantly than RES treatment in muscle tissue. However, SLN-RES has a similar effect to RES treatment in adipose tissue. Taken together, our results revealed SLN-RES could be a modern and interestingly therapeutic approach for the improvement of insulin resistance through targeting the expression of Snap23, Stx4, and Vamp2 in adipose and muscle tissues.

A specific absorption rate of a dilute assembly of various random clusters of iron oxide nanoparticles in alternating magnetic field has been calculated using Landau–Lifshitz stochastic equation. This approach simultaneously takes into account both the presence of thermal fluctuations of the nanoparticle magnetic moments and magneto-dipole interaction between the nanoparticles of the clusters. It is shown that for usual 3D clusters, the intensity of the magneto-dipole interaction is determined mainly by the cluster packing density η  =  N p V / V cl , where N p is the average number of the particles in the cluster, V is the nanoparticle volume, and V cl is the cluster volume. The area of the low frequency hysteresis loop and the assembly-specific absorption rate have been found to be considerably reduced when the packing density of the clusters increases in the range of 0.005 ≤  η  < 0.4. The dependence of the specific absorption rate on the mean nanoparticle diameter is retained with an increase of η , but becomes less pronounced. For fractal clusters of nanoparticles, which arise in biological media, in addition to a considerable reduction of the absorption rate, the absorption maximum is shifted to smaller particle diameters. It is found also that the specific absorption rate of fractal clusters increases appreciably with an increase of the thickness of nonmagnetic shells at the nanoparticle surfaces.

An angle-insensitive broadband absorber of graphene covering the whole visible spectrum is numerically demonstrated, which is resulted from multiple couplings of the electric and magnetic dipole resonances in the narrow metallic grooves. This is achieved by integrating the graphene sheet with a multi-grooved metasurface separated by a polymethyl methacrylate (PMMA) spacer, and an average absorption efficiency of 71.1% can be realized in the spectral range from 450 to 800 nm. The location of the absorption peak of graphene can be tuned by the groove depth, and the bandwidth of absorption can be flexibly controlled by tailoring both the number and the depth of the groove. In addition, broadband light absorption enhancement of graphene is robust to the variations of the structure parameters, and good absorption properties can be maintained even the incident angle is increased to 60°.

In this work, Ag 3 PO 4 microparticles were decorated onto the surface of BiFeO 3 microcuboids through a precipitation method to obtain p-Ag 3 PO 4 /n-BiFeO 3 heterojunction composites. The composites were employed for the degradation of acid orange 7 (AO7) under visible-light irradiation. It is found that the composites exhibit much higher photocatalytic efficiency than bare BiFeO 3 . Meanwhile, the intrinsical visible-light-driven photocatalytic activity of Ag 3 PO 4 /BiFeO 3 composites was further confirmed by the degradation of phenol. In addition, the photo-Fenton-like catalysis property of the composite was also evaluated. The photocurrent analysis indicates that the combination of BiFeO 3 with Ag 3 PO 4 leads to the inhibition of recombination of photoinduced electrons and holes. The obvious enhancement in the photocatalytic activity of the composite is mainly ascribed to the efficient photogenerated charge separation and interfacial charge migration caused by the formation of Ag 3 PO 4 /BiFeO 3 p-n heterojunctions.

Efficient evolution of hydrogen through electrocatalysis holds tremendous promise for clean energy. The catalytic efficiency for hydrogen evolution reaction (HER) strongly depends on the number and activity of active sites. To this end, making vertically aligned, ultrathin, and along with rich metallic phase WS 2 nanosheets is effective to maximally unearth the catalytic performance of WS 2 nanosheets. Metallic 1T polymorph combined with vertically aligned ultrathin WS 2 nanosheets on flat substrate is successfully prepared via one-step simple hydrothermal reaction. The nearly vertical orientation of WS 2 nanosheets enables the active sites of surface edge and basal planes to be maximally exposed. Here, we report vertical 1T-WS 2 nanosheets as efficient catalysts for hydrogen evolution with low overpotential of 118 mV at 10 mA cm −2 and a Tafel slope of 43 mV dec −1 . In addition, the prepared WS 2 nanosheets exhibit extremely high stability in acidic solution as the HER catalytic activity and show no degradation after 5000 continuous potential cycles. Our results indicate that vertical 1T-WS 2 nanosheets are attractive alternative to the precious platinum benchmark catalyst and rival MoS 2 materials that have recently been heavily scrutinized for hydrogen evolution. Graphical Abstract Vertical 1T-WS2 for hydrogen evolution.