Electrical conductivity studies of anatase TiO2 with dominant highly reactive {0 0 1} facets

Nanostructured powders of titanium dioxide anatase nanoplates with dominant highly reactive {0 0 1} facets were fabricated using a solvothermal method. Two kinds of samples, as prepared and calcinated at 600 °C, were studied using X-ray diffraction (XRD), transmission electron microscopy (TEM), and electrical conductivity in vacuum and in air. The dependence of the conductivity versus the inverse of temperature in the temperature range 150-440 K indicated the contribution of at least two conduction mechanisms in vacuum. The electron transport was controlled by partially depleted of charge carriers grains and adiabatic small polaron conduction in the high temperature regime and by Mott variable-range hopping (VRH) at lower temperatures. The environment was found from the experimental results to influence significantly the electrical conductivity values and its temperature dependence. A decrease with temperature in air is observed in the ranges 290-370 and 285-330 K for the as prepared and the calcinated sample respectively. Potential barriers caused by partial depletion of carriers at grain boundaries control the electrical conductivity behavior in air at high temperatures and VRH in the lower temperature regime

Solvothermal synthesis and photocatalytic performance of Mn4+-doped anatase nanoplates with exposed {001} facets

The photocatalytic activity of TiO2 and manganese doped TiO2 nanoplates with various manganese atomic percentages, in the range of 2-7%, was studied. The undoped and doped nanoplates with exposed {001} facets were produced by a solvothermal method. The crystal structure as well as the shape of the TiO2 and Mn4+/TiO2 anatase nanoparticles was determined with X-ray powder diffraction (XRD) and transmission electron microscopy (TEM). Both techniques revealed that the nanocrystals are in the form of plates. Moreover, the anisotropic peak broadening of the X-ray diffraction patterns was studied using the Rietveld refining method. Chemical analysis of the photocatalyst that was carried out with X-ray photoelectron spectroscopy (XPS) showed the presence of manganese ions in the TiO2 anatase matrix. The Density Functional Theory (DFT) calculations exhibited a decrease in the energy gap and an increase in the density of the electronic stated inside the gap for the doped TiO2. These observations were in agreement with the results of the UV-visible diffuse reflectance spectroscopy (DRS) that demonstrated an adsorption shift towards the visible region for the same samples. The photocatalytic activity of the synthesized catalysts was investigated by the photocatalytic oxidation of the gaseous nitric oxide (NO) and decomposition of the gaseous acetaldehyde (CH3CHO) under visible light irradiation. The optimal concentration of dopant that improves the photocatalytic activity of the nanoplates was determined. © 2014 Elsevier B.V

Surface morphology of low temperature grown GaAs on singular and vicinal substrates

Abstract The evolution of the surface morphology of epitaxial GaAs layers grown at low substrate temperatures (LT-GaAs) on singular and vicinal (001) GaAs substrates is studied by means of kinetic Monte-Carlo simulations. The simulation model includes the effects of Ehrlich-Schwoebel barriers at step-edges as well as anisotropic surface diffusion. We find that the surface morphology is dominated by a pattern of elongated growth mounds, which are organized into columns parallel to [1( 10]. The formation of this pattern is gradually suppressed on vicinal substrates as the misorientation angle increases. Simulated surface morphologies are compared to atomic force microscopy measurements on LT-GaAs epilayers grown on singular GaAs(001) substrates at different temperatures and good quantitative agreement is found. We propose to use vicinal substrates for LT-GaAs growth in order to overcome the known problem of epitaxial breakdown above a certain epitaxial thickness

Synthesis of biocompatible silver nanoparticles by a modified polyol method for theranostic applications: Studies on red blood cells, internalization ability and antibacterial activity

Recently, there has been ongoing research in the field of nanotechnology and nanomedicine aiming at developing multifunctional biomaterials using noble metals. The unique properties of silver (Ag) are known from ancient times and thus are being explored for their behavior on the nano scale. Silver shows high antimicrobial activity against different microorganisms, while modification of the surface of its nanostructures can be useful in active targeting regarding cancer treatment. During the synthetic procedure, in order to obtain a more uniform sample of silver nanoparticles (Ag NPs) with spherical morphology, a stabilizer is essential. The stabilizers used not only control the progression of the reaction, but also increases the biocompatibility of the NPs. Thus, we managed to synthesize spherical and rod-like Ag NPs via a polyol method and stabilize them with polyvinylpyrrolidone (PVP). The resulted Ag NPs were characterized morphologically with Transmission Electron Microscopy (TEM) and further confirmed by their structural characterization (FT-IR, UV-Vis, Dynamic Light Scattering (DLS) and Zeta Potential). For their biocompatibility profile, we studied their interaction with red blood cells (RBCs) through hemolysis assay and we monitored their structural alterations through SEM. The antimicrobial activity was tested with the agar diffusion disc assay for Gram negative and Gram positive microorganisms E. coli and S. aureus respectively. Nanoparticles' (NPs) internalization and localization studies in cancer cells were monitored with fluorescence microscopy in MCF-7 and U87-MG. According to our results it is worth it to investigate the potential of these nanomaterials since they can have a significant role in applications of theranostics in nanomedicine. Copyright © 2020 Elsevier Inc. All rights reserved

Decoration of TiO2 anatase nanoplates with silver nanoparticles on the {101} crystal facets and their photocatalytic behaviour

Ag nanoparticles were photodeposited on the {101} crystal facets of the TiO2 anatase nanoplates. This was achieved with the photoreduction of AgNO3 in methanol solution in which TiO2 anatase nanoplates were suspended while UVA irradiation was performed. The size range of the photodeposited silver nanoparticles was between 5 and 20nm. The manipulation of their size was achieved by controlling the UVA light irradiation period of time whereas the formation on the specific facet of the TiO2 anatase nanocrystal was managed by using methanol as a hole scavenger. The silver ions (Ag+) were photoreduced by the electrons that were photogenerated due to the TiO2 anatase nanoplates irradiation with UVA light. The photocatalytic activity of the nanocomposites was examined in NO oxidation, showing a higher photocatalytic activity and photonic efficiency in comparison to the pure TiO2 anatase nanoplates. © 2014 Elsevier B.V

Efficient removal of hexavalent chromium from aqueous solutions using autohydrolyzed Scots Pine ( Pinus Sylvestris ) sawdust as adsorbent

In this work, a low-cost lignocellulosic adsorbent with high biosorption capacity is proposed, suitable for the efficient removal of hexavalent chromium from water and wastewater media. The adsorbent was produced by autohydrolyzing Scots Pine ( Pinus Sylvestris ) sawdust. The effect of the autohydrolysis conditions, i.e., pretreatment time and temperature, on hexavalent chromium biosorption was investigated using energy-dispersive X-ray spectroscopy (EDS) and UV-visible spectrophotometry. The Freundlich, Langmuir, Sips, Radke-Prausnitz, Modified Radke-Prausnitz, Tóth, UNILAN, Temkin and Dubinin- Radushkevich adsorption capacities and the rate constant values for pseudo-first- and pseudo-second-order kinetics indicated that the autohydrolyzed material exhibits significantly enhanced hexavalent chromium adsorption properties comparing with the untreated sawdust. The Freundlich's adsorption capacity KF increased from 2.276 to 8.928 (mg g-1)(L mg-1)1/n, and the amount of hexavalent chromium adsorbed at saturation (Langmuir constant qm ) increased from 87.4 to 345.9 mg g-1 , indicating that autohydrolysis treatment at 240°C for 50 min optimizes the adsorption behavior of the lignocellulosic material