Primarily isotropic nature of photorefractive screening solitons and the interactions between them

We present experimental evidence demonstrating that the photorefractive-index change responsible for the formation of photorefractive spatial screening solitons and coherent collisions between them is primarily isotropic in nature, even though the photorefractive medium is inherently anisotropic.     

Optically induced photovoltaic self-defocusing-to-self-focusing transition

We show theoretically and experimentally that the photovoltaic nonlinearity that gives rise to spatial solitons can be switched from self-defocusing to self-focusing (or vice versa) by use of background illumination. This raises the possibility of bright photovoltaic solitons in LiNbO(3) .     

Solitons in nonlinear media with an infinite range of nonlocality: first observation of coherent elliptic solitons and of vortex-ring solitons

We present an experimental study on wave propagation in highly nonlocal optically nonlinear media, for which far-away boundary conditions significantly affect the evolution of localized beams. As an example, we set the boundary conditions to be anisotropic and demonstrate the first experimental observation of coherent elliptic solitons. Furthermore, exploiting the natural ability of such nonlinearities to eliminate azimuthal instabilities, we perform the first observation of stable vortex-ring solitons. These features of highly nonlocal nonlinearities affected by far-away boundary conditions open new directions in nonlinear science by facilitating remote control over soliton propagation.     

Effect of interface traps on Debye thickness semiconductor films

The presence of the boundary interface trapping states and their role in determining the properties of Debye thickness thin semiconductor films, are demonstrated experimentally, using PbTe films deposited on mica. These charged states could not be observed earlier and be studied directly, because of the screening by the relatively high carrier density of the ordinary PbTe. Thin, Debye length thickness, PbTe films with a high concentration of interface trapping centers, possess an extraordinary high resistance. In this case the thermostimulated capacitor discharge method can be successfully applied to determine the energy of these levels, their carrier capture cross-sections and their donor- or acceptor-like character. The experimental results and theoretical calculations are discussed.     

Electrodeposition of Dye-Doped Titania Thin Films

We extend our novel low-voltage electrochemical method for oxide thin film formation from sol-gel monomers to include entrapment of organic molecules within the films. We also describe an extension of the method to titania thin films, which are obtained from titanium tetra-n-propoxide in alcoholic solutions by applying potentials in the range of +2.0 to ?1.4 V to indium tin oxide electrodes. The film thickness (ranging between 20–1000 nm) is controllable by changing either the potential or the duration of its application. We demonstrate that this electrochemical method provides a convenient way for entrapment of organic dopants within the film. Four dyes were used for that purpose: Basic Blue 41, methylene-blue, tris(2,2′-bipyridine)iron(II) and tris(2,2′-bipyridine)ruthenium(II).     

Electrochemically induced sol-gel deposition of zirconia thin films

A novel electrochemical method for deposition of ZrO(2) thin films is described. The films, 50-600 nm thick, were obtained by applying moderate positive or negative potentials (+2.5 V to -1.5 V versus SHE) on conducting surfaces immersed in a 2-propanol solution of zirconium tetra-n-propoxide [Zr(OPr)(4)] in the presence of minute quantities of water (water/monomer molar ratios in the range of 10(-5) to 10(-1)), which was the limiting reagent. Oxidative electrochemical formation of solvated H(+) and reductive formation of OH(-) catalyze the hydrolysis and condensation of the metal alkoxide precursor. The magnitude of the applied potential and its duration provide a convenient way of controlling the film thickness. The films consist of an amorphous phase, as revealed by XRD measurements. The effects of different parameters, such as the applied potential and its duration, the amount of added water and the current-time characteristics, were studied. A mechanism for the electrodeposition of the zirconia films which is in accordance with our findings is proposed.     

Effect of ions on the hydrophobic interaction between two plates

We use molecular dynamics simulations to investigate the solvent mediated attraction and drying between two nanoscale hydrophobic surfaces in aqueous salt solutions. We study these effects as a function of the ionic charge density, that is, the ionic charge per unit ionic volume, while keeping the ionic diameter fixed. The attraction is expressed by a negative change in the free energy as the plates are brought together, with enthalpy and entropy changes that both promote aggregation. We find a strong correlation between the strength of the hydrophobic interaction and the degree of preferential binding/exclusion of the ions relative to the surfaces. The results show that amplification of the hydrophobic interaction, a phenomenon analogous to salting-out, is a purely entropic effect and is induced by high-charge-density ions that exhibit preferential exclusion. In contrast, a reduction of the hydrophobic interaction, analogous to salting-in, is induced by low-charge-density ions that exhibit preferential binding, the effect being either entropic or enthalpic. Our findings are relevant to phenomena long studied in solution chemistry, as we demonstrate the significant, yet subtle, effects of electrolytes on hydrophobic aggregation and collapse.