Investigations of the charge transfer phenomenon at the hybrid dye/BiVO4 interface under visible radiation.

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.

Structural and morphological data of RF-Sputtered BiVO4 thin films.

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 1 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.

Structural, electronic, vibration and elastic properties of the layered AgInP2S6 semiconducting crystal - DFT approach.

Detailed first principles calculations of the structural, electronic and vibrational properties of the AgInP2S6 crystal are reported. The energy band spectra of the mentioned material using DFT/GGA-D methodology with the PBE functional was calculated for the first time. Stability of the AgInP2S6 crystals in contrast to Cu-containing representatives of M1M2P2X6 materials family (M1, M2 - metal, X - chalcogen) has been explained in the framework of the second-order Jahn-Teller effect. The high covalence of the Ag-[P2S6] bonds and strong hybridization of the 4d- and 5s-orbitals of the Ag atoms are responsible for the stability of the considered crystal. The calculated vibrational properties were compared with the available experimental data derived from Raman scattering spectroscopy and their good agreement was demonstrated. The electronic and vibration properties within the framework of a group theory approach were studied. Also elastic properties of the AgInP2S6 crystal were modeled and analyzed for the first time.

Corrosion inhibition of mild steel in 1M HCl by D-glucose derivatives of dihydropyrido [2,3-d:6,5-d'] dipyrimidine-2, 4, 6, 8(1H,3H, 5H,7H)-tetraone.

D-glucose derivatives of dihydropyrido-[2,3-d:6,5-d']-dipyrimidine-2, 4, 6, 8(1H,3H, 5H,7H)-tetraone (GPHs) have been synthesized and investigated as corrosion inhibitors for mild steel in 1M HCl solution using gravimetric, electrochemical, surface, quantum chemical calculations and Monte Carlo simulations methods. The order of inhibition efficiencies is GPH-3 > GPH-2 > GPH-1. The results further showed that the inhibitor molecules with electron releasing (-OH, -OCH3) substituents exhibit higher efficiency than the parent molecule without any substituents. Polarization study suggests that the studied compounds are mixed-type but exhibited predominantly cathodic inhibitive effect. The adsorption of these compounds on mild steel surface obeyed the Langmuir adsorption isotherm. SEM, EDX and AFM analyses were used to confirm the inhibitive actions of the molecules on mild steel surface. Quantum chemical (QC) calculations and Monte Carlo (MC) simulations studies were undertaken to further corroborate the experimental results.

Peculiarities of the environmental influence on the optical properties of push-pull nonlinear optical molecules: a theoretical study.

Gas-phase geometry optimization of NLO-active molecules is one of the standard approaches in the first principle computational methodology, whereas the important role of the environment is usually not considered during the evaluation of structural parameters. With a wide variety of environmentally influenced models in most cases only the high quality single point calculations are prepared. Among different approaches, the most used polarizable continuum model (PCM) seems to be promising. In this study, we have compared the electronic properties of gas-phase optimized geometries of imidazole-derived push-pull compounds with those optimized using PCM solvation approach including CH(2)Cl(2) and PMMA as media. We have focused particularly on the linear optical properties of investigated molecules, namely on the UV-vis absorption spectra. The analysis of presented results shows the applicability of the different quantum chemical (QC) methods for the UV-vis spectra calculations of linear NLO molecules. Herein we also present the need of molecule geometry optimization affected by the environment. Following the performed calculations, the electronic properties of gas-phase optimized molecules give conformable results with respect to those obtained by more time-consuming continuum optimizations. All computational data are supported by experimental investigations.

Optical operation by chromophores featuring 4,5-dicyanoimidazole embedded within poly(methyl methacrylate) matrices.

We have studied photoinduced absorption, birefringence, and optical second-harmonic generation in poly(methyl methacrylate) (PMMA) films doped by organic chromophores featuring 4,5-dicyanoimidazole in the weight content equal to 5%. The chromophores indicated as IM1-IM6 were synthesized from 2-bromo-1-methylimidazole-4,5-dicarbonitrile by either nucleophilic substitution or Suzuki-Miyaura cross-coupling reaction. The samples were obtained as films of several micrometers thickness by the spin-coating method on a quartz substrate. Measurements of the optically induced birefringence were done by the Senarmont method at wavelength 1150 nm, and photoinduced absorption was studied in the spectral range 250-700 nm under optical treatment by 300 mW cw 532 nm laser. Photoinduced optical effects were studied by bicolor 1064 and 532 nm coherent laser pulses. The maximal changes were observed for the ratio between fundamental and writing beam intensities equal to about 7:1. To interpret the observed experimental measurements, theoretical simulations of photoinduced optical properties were performed by quantum chemical computational methods.

Magnetic behaviour of nickel-cyclam complexes in mesoporous silica: EPR investigations.

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.

New aspects of the low-concentrated aniline polymerization in the solution and in SiC nanocrystals dispersion.

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.

Modelling of UV-molecular spectra of several bis-pyrazolopyridines derivatives.

Quantum chemical simulations of UV-absorption spectra in substituted bis-pyrazolopyridines were done. As a theoretical tool time dependent density functional theory (TDDFT) method with Vosko-Wilk-Nusair parameterisation was applied. Comparison of the theoretically simulated UV-absorption spectra with experimental data was performed. Crucial role of pi-conjugated bonds within the backside phenyl rings is demonstrated. Physical insight of the several observed discrepancies between the calculations and experimental data is discussed. A comparison of the TDDFT and several semi-empirical approaches is given.

Origin of the photoinduced optical second harmonic generation arising in N-phenyl microcrystalline films.

Photoinduced second-order nonlinear optical effects, particularly optical second harmonic generation (SHG) of N-phenyls with different numbers of aromatic rings deposited on glass substrates were studied. As a fundamental beam, a 5-ps pulsed Nd:YAG laser was used. Quantum chemical time-dependent density functional theory (TDDFT) simulations of the nonlinear optical properties were performed. The first-order hyperpolarizabilities of isolated molecules were calculated, under the influence of a polarized pumping beam, to evaluate the role played by the nanointerfaces separating the microcrystallites and the amorphous environment. Consideration was performed within a framework of steady-state Langevin order parameters for amorphous-like films. A strong dependence of the photoinduced SHG versus the number of aromatic rings determining the degree of film crystallinity was shown. A comparison of experimental data and theoretically evaluated results shows that for the photoinduced first-order nonlinear optical effect the dominant contribution is an amorphous-like structural component, unlike the transport properties, where the crucial role is played by the nanointerface region. This may reflect a specific feature of the multiphoton processes in such types of nanointerfaces because of nanoconfined effects.