Enhanced photocatalytic–electrolytic degradation of Reactive Brilliant Red X-3B in the presence of water jet cavitation

Photocatalysis, electrolysis, water jet cavitation (WJC), alone and in combinations were applied to degrade an azo dye, Reactive Brilliant Red X-3B (X-3B). Experiments were conducted in a 4.0 L aqueous solution with different initial dye concentrations, TiO₂ dose, and solution pH. WJC substantially increased the photocatalytic, electrolytic and photocatalytic–electrolytic rates of the dye removal. The observed first-order rate of X-3B decolorization in the process of combined photocatalysis and electrolysis coupled with WJC was 1.6–2.9 times of that in the process of combined photocatalysis and electrolysis coupled with mechanical stirring. The rate enhancements may be attributed primarily to the reduced diffusion layer thickness on the electrodes and the deagglomeration of photocatalyst particles due to the chemical and physical effects of WJC. Under the conditions of 80 mg/L X-3B solution, 100 mg/L TiO₂ dose and solution pH 6.3, 97% and 71% of color and chemical oxygen demand (COD_Cr) were removed, respectively, within 90-min photocatalytic–electrolytic treatment coupled with WJC. During this process, azo groups and naphthalene, benzene and triazine structures of the dye can be destroyed. Industrial textile effluent was also investigated, and a positive synergistic effect between photocatalytic–electrolytic system and WJC was observed considering color removal.     

Synthesis of Ag–ZnO powders by means of a mechanochemical process

Nowadays, Ag–CdO alloys are widely used in electrical contact applications, because of their good electrical and thermal conductivity is as well as high resistance to arc erosion and contact welding. Considering the restricted use of Cd due to its toxicity, it is necessary to find a material that can replace those alloys. The objective of this work was to study the possibility of obtaining an Ag–ZnO alloy from an Ag–Zn solid solution powders by means of a mechanochemical method. The mechanochemical process was carried out in a SPEX 8000D mill, under air and with ethanol as a reaction agent. Based on the results obtained, it can be concluded that an Ag–ZnO alloy with a fine and uniform ZnO distribution in the Ag matrix can be obtained by applying the mechanochemical process for 25 h.     

Ag–N dual-accept doping for the fabrication of p-type ZnO

P-type ZnO was realized by dual-doping with nitrogen and silver via electrostatic-enhanced ultrasonic spray pyrolysis. The structural, electrical, and optical properties were explored by XRD, Hall-effect, and optical transmission spectra. The resistivity of ZnO:(N,Ag) film was found to be 56 Ω cm⁻¹ with the high mobility of 76.1 cm²/V s. Compared with ZnO:Ag film, ZnO:(N,Ag) film exhibited a higher and more stable optical transmittance.     

Investigation on a novel ZnO/TiO2–B photocatalyst with enhanced visible photocatalytic activity

A new type of composite photocatalysts (ZnO/TiO₂–B) with Zinc oxide nanoparticles dispersed on boron doped titanium dioxide was prepared via a sol–gel method. The as-prepared powders were characterized by HRTEM, XRD, XPS, UV–vis DRS, and PL techniques. The results reveal that B³⁺ ions are doped into the TiO₂ lattice in interstitial mode, while ZnO nanoparticles are dispersed on the surface of TiO₂. The absorption of photocatalysts was extended into visible light region and the photogenerated electrons and holes were separated efficiently. Hence, ZnO/TiO₂–B composite photocatalyst exhibits much better photocatalytic activity than those of pure TiO₂ and TiO₂–B on photodegradation of 4-chlorophenol under visible light irradiation.     

Microstructural investigation of Fe–Zr–B–Ag soft magnetic thin films

A microstructural study of DC-sputtered Fe_93−xZr₃B₄Ag_x films on Si(0 0 1) substrates has been carried out using X-ray diffraction (XRD) and transmission electron microscopy (TEM). All samples were deposited as a function of additive Ag content (x=0–6 at%), and annealed in the range of temperature, 300–600°C, for 1 h in order to obtain enhanced soft magnetic properties. Through XRD and TEM investigation, Ag-free Fe₉₃Zr₃B₄ films on Si(0 0 1) substrates consisted of nano-crystalline Fe-based phases. In the presence of Ag additive element, the microstructure of as-deposited Fe_93−xZr₃B₄Ag_x films consisted of a mixture of majority of Fe-based amorphous and Ag crystalline phases. In this case, additive element, Ag played a role in retarding the formation of Fe-based crystalline phases during deposition, and insoluble nano-crystalline Ag particles were dispersed in the Fe-based amorphous matrix. As the content of Ag increased, the intensity of Ag crystalline XRD peak increased. Crystallization of Fe-based amorphous phase in the matrix of Fe₈₈Zr₃B₄Ag₅ thin films occurred at an annealing temperature of 400°C. In the case of Fe₈₈Zr₃B₄Ag₅ films annealed at 500°C, a much enhanced permeability of the Fe-based alloy thin films associated with nano-crystalline phases was achieved.     

Enhanced ethanol sensing properties of TiO2/ZnO core–shell nanorod sensors

TiO₂-core/ZnO-shell nanorods were synthesized using a two-step process: the synthesis of TiO₂ nanorods using a hydrothermal method followed by atomic layer deposition of ZnO. The mean diameter and length of the nanorods were ～300 nm and ～2.3 μm, respectively. The cores and shells of the nanorods were monoclinic-structured single-crystal TiO₂ and wurtzite-structured single-crystal ZnO, respectively. The multiple networked TiO₂-core/ZnO-shell nanorod sensors showed responses of 132–1054 % at ethanol (C₂H₅OH) concentrations ranging from 5 to 25 ppm at 150 ^°C. These responses were 1–5 times higher than those of the pristine TiO₂ nanorod sensors at the same C₂H₅OH concentration range. The substantial improvement in the response of the pristine TiO₂ nanorods to C₂H₅OH gas by their encapsulation with ZnO may be attributed to the enhanced absorption and dehydrogenation of ethanol. In addition, the enhanced sensor response of the core–shell nanorods can be attributed partly to changes in resistance due to both the surface depletion layer of each core–shell nanorod and the potential barriers built in the junctions caused by a combination of homointerfaces and heterointerfaces.     

Microleakage and antibacterial properties of ZnO and ZnO:Ag nanopowders prepared via a sol–gel method for endodontic sealer application

A novel method, recently proved useful for the synthesis of nanoparticles, has been now used for the preparation of very stable silver iodide–trihexyl(tetradecyl)phosphonium chloride ionanofluids. Only the ionic liquid and the AgI bulk powder were needed. Synthesized nanofluids are much more stable than those obtained by simple dispersion of the nanoparticles in the base fluid. The ionanofluids were synthesized at different concentrations (up to 50 % w/w) and characterized in terms of physical, electrical, and thermal properties (density, viscosity, refractive index, electric conductivity, and specific heat capacity). A very high increase in the electric conductivity of the base ionic liquid was expected due to the high concentration of nanoparticles achieved. Nonetheless, it was not found, probably due to the reduction of ions mobility caused by the increase of the viscosity in ionanofluids with concentrations over 20 % w/w. An appropriate characterization of nanoparticles composing the nanofluids was carried out (UV–Vis absorbance, shape and size distribution). The diameter of the particles was measured and calculated by different techniques and approximations, obtaining a value of 2–4 nm. They were spherical, well-defined, and not agglomerated, with a narrow size distribution. The X-ray powder diffraction confirmed that no structural change took place in the transformation of the bulk solid to nanoparticles.     

Ultrasonically induced ZnO–biosilica nanocomposite for degradation of a textile dye in aqueous phase

In the present study, a porous clay-like support with unique characteristics was used for the synthesis and immobilization of ZnO nanostructures to be used as sonocatalyst for the sonocatalytic decolorization of methylene blue (MB) dye in the aqueous phase. As a result, the sonocatalytic activity of ZnO–biosilica nanocomposite (77.8%) was higher than that of pure ZnO nanostructures (53.6%). Increasing the initial pH from 3 to 10 led to increasing the color removal from 41.8% to 88.2%, respectively. Increasing the sonocatalyst dosage from 0.5 to 2.5 g/L resulted in increasing the color removal, while further increase up to 3 g/L caused an obvious drop in the color removal. The sonocatalysis of MB dye over ZnO–biosilica nanocomposite was temperature-dependent. The presence of methanol produced the most adverse effect on the sonocatalysis of MB dye. The addition of chloride and carbonate ions had a negligible effect on the sonocatalysis, while the addition of persulfate ion led to increasing the color removal from 77.8% to 99.4% during 90 min. The reusability test exhibited a 15% drop in the color removal (%) within three consecutive experimental runs. A mineralization efficiency of 63.2% was obtained within 4 h.     

Direct Numerical Simulation of Acoustic Turbulence: Zakharov–Sagdeev Spectrum

JETP Letters - We present the results of direct numerical simulation of three-dimensional acoustic turbulence in medium with weak positive dispersion. It is shown that at the beginning of the...     

Optical and current transport properties of CuO/ZnO nanocoral p–n heterostructure hydrothermally synthesized at low temperature

We demonstrate the synthesis and investigate the electrical and optical characteristics of ‘nanocorals’ (NCs) composed of CuO/ZnO grown at low temperature through the hydrothermal approach. High-density CuO nanostructures (NSs) were selectively grown on ZnO nanorods (NRs). The synthesized NCs were used to fabricate p–n heterojunctions that were investigated by the current density–voltage (J–V) and the capacitance–voltage (C–V) techniques. It was found that the NC heterojunctions exhibit a well-defined diode behavior with a threshold voltage of about 1.52 V and relatively high rectification factor of ～760. The detailed forward J–V characteristics revealed that the current transport is controlled by an ohmic behavior for V≤0.15 V, whereas at moderate voltages 1.46≤V<1.5 the current follows a J? α?exp(βV) relationship. At higher voltages (≥1.5 V) the current follows the relation J? α? V ², indicating that the space-charge-limited current mechanism is the dominant current transport. The C–V measurement indicated that the NC diode has an abrupt junction. The grown CuO/ZnO NCs exhibited a broad light absorption range that is covering the UV and the entire visible parts of the spectrum.     

Enhanced photoluminescence of MoS2–Au nanostructures: Nanotriangle and nanohole arrays

We investigated the photoluminescence (PL) characteristics of MoS₂–Au hybrid nanostructures, fabricated by nanosphere lithography and wet-transfer techniques. Two kinds of Au nanostructures - such as nanotriangles (NTs) and nanoholes (NHs) - were fabricated for comparison. MoS₂ monolayers on both NT and NH arrays exhibited enhanced PL intensity, compared with those on SiO₂/Si substrates and flat Au thin films. Numerical simulations revealed clear distinction in the electric field intensity distributions in the NT and NH arrays at the PL excitation wavelength. Such difference could be attributed to the excitation of localized and propagating surface plasmon in the NT and NH arrays. This work helps us to understand how the plasmonic NT and NH arrays affect the physical properties of the MoS₂ monolayers on them.     

Electrical transport characteristics of ZnO–Bi2O3–B2O3 glasses

Optically clear glasses in the ZnO–Bi₂O₃–B₂O₃ (ZBBO) system were fabricated via the conventional melt-quenching technique. Dielectric constant and loss measurements carried out on ZBBO glasses unraveled nearly frequency (1 kHz–10 MHz)-independent dielectric characteristics associated with significantly low loss (D?=?0.004). However, weak temperature response was found with temperature coefficient of dielectric constant 18?±?4 ppm °C^?1 in the 35–250 °C temperature range. The conduction and relaxation phenomena were rationalized using universal AC conductivity power law and modulus formalism respectively. The activation energy for relaxation determined using imaginary parts of modulus peaks was 2.54 eV which was close to that of the DC conduction implying the involvement of similar energy barriers in both the processes. Stretched and power exponents were temperature dependent. The relaxation and conduction in these glasses were attributed to the hoping and migration of Bi³⁺ cations in their own and different local environment.     

Direct Detection of Al–O–Al Structure in Aluminosilicate Specimens: A Use of Homo-Nuclear DQMAS NMR

A general strategy of Al–O–Al structure in various aluminosilicate was evaluated by combining triple-quantum magic angle spinning (3QMAS) and double-quantum homo-nuclear correlation under magic angle spinning (DQMAS) solid-state nuclear magnetic resonance (NMR) measurements with the aid of high magnetic field NMR (800 MHz for ¹H Larmor frequency). The results show that in many cases the direct detection of Al–O–Al sites in aluminosilicate crystals and glasses is possible; hence the extent of aluminum avoidance can be directly elucidated. Specifically, experimental evidence of Al–O–Al linkages in several aluminosilicate materials with Si/Al >1 was straightforwardly confirmed; and the existence of Al–O–Al is considered to have little correlation with the Si/Al ratio, but it may be strongly related to the cation and local structural arrangement. In addition, the presence of tri-clusters of (Si, Al)O₄-tetrahedra in aluminosilicate framework was proposed, which was thought to act as nuclei for formation and incorporation of cations to achieve charge neutrality.     

Influence of Ag doping on structural and optical properties of ZnO thin films synthesized by the sol–gel technique

Thin films of Ag–ZnO samples deposited on glass substrates with a different percentage of Ag content (1, 2, and 3 at%) were synthesized, at room temperature, by a dip-coating sol-gel method. The obtained samples are hexagonal wurtzite structure. The average grain size of deposits is about 5 nm. Up to 3 at%, c-axis lattice parameter shifts toward a higher value, which indicates that silver atoms replace Zn atoms in the crystal lattice. As shown by the DRX spectra, growth rate in the (101) direction is favored by the presence of silver ions in the ZnO. The layers present a homogeneous crystallites distribution, as we can remark it on SEM micrographs and exhibit a very low roughness according to AFM images. The entire samples exhibit a transmission value greater than 80 %, in the visible region, while the maximum is obtained for those doped at 2 at%. Energy band varies between 3.15 eV and 3.25 eV. The wider gap obtained is that of the ZnO layer doped with 2 at%. It is worth noting a strong UV emission observed on PL spectrum, performed at very low temperature (liquid nitrogen temperature), for silver doped ZnO compared to that of pure ZnO.     

Synthesis of Photoactive ZnO–SnO2–Ag(AgCl) Nanomaterials for Medical and Ecological Applications and Study of Their Structure and Properties

Optics and Spectroscopy - Photoactive ZnO–SnO2–Ag(AgCl) nanomaterials capable of generating chemically active single oxygen under action of UV and blue light are synthesized using a...     

Properties of ZnO:Al,ZnO:Al–SiO2 Films Obtained in Sol Gel Process from Coating Solutions

Russian Physics Journal - The paper deals with ZnO, ZnO:Al 5 wt.% and ZnO:Al 5 wt.% – SiO2 5 wt.% thin films obtained on glass substrates by the sol gel process from film-forming solutions...     

Preparation,heat treatment and photoluminescence properties of V-doped ZnO–SiO2–B2O3 glasses

Four glasses in ZnO–SiO₂–B₂O₃ ternary system were prepared by the melt quenching method with the objective of optimizing sub-nanosecond emission over the UV region of zinc borosilicate glasses used in superfast scintillators. The effect of vanadium addition and heat treatment on phase formation, microstructure and photoluminescence properties of the glasses was characterized by means of DTA, XRD, SEM and fluorescence spectrophotometer. Vanadium contributed to the near-band-edge emission in two ways, by introducing donor levels in the energy band of ZnO particles and by facilitating the precipitation of ZnO and willemite crystals. Furthermore, nucleation of willemite and zinc oxide phases, which are both the origins of the intense emission bands in the UV region, was facilitated with increasing either the time or temperature of heat treatments. Photoluminescence spectra showed the elimination of the visible emission band which is favorable in scintillating glasses.     

Planar-to-wavy transition of Cu–Ag nanolayered metals: a precursor mechanism to twinning

The interface-mediated plastic deformation mechanisms of a semi-coherent Cu–Ag bimetal nanolayered structure subjected to out-of-plane tension are characterized by molecular dynamics simulations. Results show that the initially planar Cu–Ag nanolayers abruptly become wavy at a critical tensile strain. This planar-to-wavy interlayer transition is facilitated by the low shear resistance of the Cu–Ag interlayer interface, which slides to accommodate the out-of-plane deformation. The process redistributes misfit dislocations along the interface to reduce the bending energy of the wavy structure. High stress concentrations subsequently develop at the summits and valleys of the wavy Cu–Ag interlayer interfaces, from which micro-twinning partials are emitted. These results demonstrate that the wavelength of the wavy Cu–Ag nanolayer structure forms a critical length scale for the localization of spatially periodic defect sources for twin nucleation. This planar-to-wavy interlayer transition mechanism is only activated in nanolayered metals with interfaces that are amenable to sliding prior to twin or dislocation emissions.     

Effect of chain length and donor–acceptor substitution on the electrical responsive properties of conjugated biphenyls: a DFT-based computational study

The effect of donor–acceptor (D-A) substituent and chain length on the electrical polarisabilities and first hyper polarisability of cis and trans biphenyl oligomeric compounds have been investigated using density functional theory-based hybrid functional CAM-B3LYP with 6-311G (2d,2p) basis set. Our extensive computational study reveals that both average polarisability and first hyper polarisability of the studied compounds increase with the increasing ethylene spacer chain length. Again the substitution of donor (NMe₂) and acceptor (C≡N) at the para position of the phenyl rings to each oligomer shows order of magnitude increase of both α_av and β_av value compared to the unsubstituted one. This increased α_av and β_av values have been explained due to increasing charge transfer contribution resulting from decreasing optical energy gap (ΔE?=?S₁???S₀) upon D-A substitution. It is also observed that the charge transfer contribution to first hyperpolarisability (β_CT) is more than the polarisability (α_CT) for the studied molecules. The electronic spatial extent (<R²>) which is a measure of electron density volume around the molecule is found to play a major role along with the intramolecular charge transfer character to explain the non-linear variation of first hyperpolarisability (β_av) as a function of ethylene spacer chain length (n) and D-A substitution.