RESUMEN
Nanocomposites with different ratios of titanium dioxide and bismuth vanadate [TiO2]/[BiVO4] give rise to compatible electronic band structure alignment at their interfaces to ensure enhanced photoactivated charge transfer under visible light. The sol-gel method and suitable post-synthesis thermal treatments were used to synthesize different compositions with stabilized anatase phase of TiO2 and monoclinic scheelite polymorph BiVO4. Structural, electronic and optical characterizations were performed and the results were analysed as a function of the stoichiometry, in which both crystalline structures show a clear junction formation among their characteristic stacking planes. Photocatalytic and (photo) electrochemical responses of the nanocomposites were investigated and tested for the degradation of azo dyes (Acid Blue-113, AB-113) (~ 99%) under visible light radiation. The nanocomposite with a mass ratio of (1:10) shows the highest photocatalytic efficiency compared to the other compositions. HRTEM images showed marked regions in which both crystalline structures form a clear junction and their characteristic planes. However, the increase of BiVO4 content in the network overcomes the photocatalytic activity due to the decrease in the reduction potential of the photo-generated electrons with high recombination rates.
RESUMEN
Photocatalytic hybrid systems were realized by associating bismuth vanadate (BiVO4) nanostructured thin films with anchored organic and metal-organic complex molecules. The chosen dyes are based on indoline and azo-based moieties. Optical and photoinduced charge transfer features were investigated experimentally and analysed theoretically through the electron band alignment on the organic/inorganic interface. Quantum calculations were carried out for the studied hybrid systems by using DFT and semi-empirical approaches. The calculations were performed by implementing a cluster model applied for the nanostructures and hybrid systems. The electronic density peculiarities point out efficient charge transfer for D149 based hybrids compared to azo-based systems. The electron distribution in hybrid systems inferred from the computational analysis and their experimental probing using Kelvin Force Microscopy (KFM) maps the way to understanding the photoinduced charge transfer occurring at the interfaces between organic dyes and an inorganic photocatalyst. The presented approach helps to predict suitable photoactive hybrid materials leading to efficient photocatalytic devices.
RESUMEN
Structural and morphological modulation of rf-sputtered BiVO4 thin films deposited using mechanochemical synthesis prepared BiVO4 nano-powders as sintered target are included in this data article. The crystalline nature of as-prepared films, namely amorphous and crystalline was acquired with time and temperature dependent in-situ high temperature X-ray diffraction (HT-XRD), at a time interval of 1â¯h. Typical Fourier transform infrared (FT-IR) spectra of annealed thin film of monoclinic BiVO4 structure is given. Furthermore, correlation between morphologies of various substrate temperature fabricated BiVO4 thin films are presented.
RESUMEN
Electron paramagnetic resonance (EPR) investigations are carried out on mesoporous silica (SBA15) functionalized by Ni-cyclam complexes (1,4,8,11-tetraazacyclotetradecane groups chelating nickel ions). The magnetic behaviour of nickel-cyclam groups, their mutual interactions and dispersions in the mesoporous silica are compared with respect to the doping rates and the synthesis procedures. The spin-spin interactions and the relaxation processes were clarified from the thermal evolution in the temperature range (4 K, 300 K) of the paramagnetic spin susceptibilities and EPR line widths. Thus, the relaxation mechanisms seem marked by the Jahn-Teller effect on the nickel ions mediated by exchange interactions between nearest spins. Isolated Ni-cyclam molecules are involved in some samples while others show the formation of clusters where phonon-assisted one-dimensional (1D) ferromagnetic ordering occurs below 45 K. The performed experiments point out the efficiency of the EPR technique to probe the degree of functionalization of mesoporous silica by Ni-cyclam molecules and to give valuable feedback to improve the synthesis routes.
RESUMEN
Results of the simultaneous in-situ UV-vis and open-circuit potential (OCP) monitoring of the low-concentrated aniline (An) polymerization in the presence of camphorsulfonic acid (CSA) suggested that during the induction period (IP) step a transition state formed, which probably included anilinium cation and the oxidant anion, antecedent to a propagation step. No aniline oligomers were registered at this stage but they appeared at the beginning of the propagation step under the investigation conditions. The moments of formation of insoluble pernigraniline phase and appearance of emeraldine units in the growing pernigraniline chains were ascertained by the comparison of kinetic and OCP profiles of the polymerization process both in the solution and in SiC dispersion water mediums. It is deduced that pernigraniline reduction by aniline molecules begins earlier than it is generally accepted (i.e., earlier than OCP maximum is reached) and probably in parallel to a continuing appearance of pernigraniline units even in the same chains that undergo the reduction. It was found that an addition of the SiC dispersion phase into the polymerization mixture accelerates differently all stages of the aniline polymerization. Finally, this polymerization process leads to the formation of polyaniline (PANI)-CSA shell with thickness in the range from 0.5 nm to a few nm at the SiC nanocrystals surface.
