In this paper, graphene was obtained on a copper substrate using the CVD method, and then it was transferred to various substrates such as glass and SiO2/Si patterned with metallic interdigitated electrodes. The graphene thus obtained was characterized using Raman spectroscopy, scanning electron microscopy (SEM), current-voltage measurements, and electrochemical methods, in order to be used for sensing applications.

In this work, a ZnO nanowires/graphene nanohybrid was synthesized by a three steps approach. Copper substrates were covered with graphene by chemical vapor deposition, further ZnO nanowires were electrochemically deposited on the as grown graphene on copper and finally a transfer process was employed for moving the heterostructure onto a different substrate. A comprehensive structural analysis which included scanning electron microscopy, X-ray diffraction and Raman measurements revealed that the ZnO nanowires crystallize in wurtzite structure perpendicular to graphene, the process leading to the formation of a nanohybrid heterostructure. The band gap energy of the ZnO nanowires deposited on graphene was estimated to be 3.11 eV, as calculated from the reflectance spectrum analysis. The GGA-PBE+U within Grimme (DFT-D) approach was used to provide an accurate description of the interface structure in terms of electronic and optical properties, confirming that the decrease in the band gap energy of ZnO nanowires is caused by the interaction with the graphene surface. The findings of this study could serve as an experimental and theoretical reference for upcoming studies on ZnO NWs/Graphene nanohybrid-based optoelectronic applications.

In this paper we report conformational changes recorded on a protein molecule (alpha-amylase) under green light irradiation. In order to explain the experimental results we advanced the hypothesis that green light induces electric dipoles in the protein, which interact with each other, generating conformational modifications toward a more compact design, with different physical properties. The experiments were carried out with un-polarized light (lambda = 520 nm) from a light-emitting-diode (1000 lm, 20 W, 105 mW on the target). In view of the character of our hypothesis, and corroborated with all our experimental results, we suggest that this phenomenon may be more extended and general, specific for a larger class of proteins, occurring on the protein macromolecules under the green light. The effects of a-amylase protein irradiation were revealed by circular dichroism, fluorescence, Raman and FTIR-spectroscopies, zeta potential, cyclic voltammetry, electric impedance spectroscopy and atomic force microscopy. Tentatively, we term the novel conformations as P* (polarized) proteins.

The recent revolution in modern optical techniques revealed that light interaction with matter generates a force, known as optical force, which produces material properties known in physics as optical matter. The basic technique of the domain uses forces exerted by a strongly focused beam of light to trap small objects and subsequently to manipulate their local structures. The purpose of this paper is to develop an alternative approach, using irradiations with high-density-green-photons, which induce electric dipoles by polarization effects. The materials used for the experiments were long carbon chains which represent the framework of biological macromolecules. The physical techniques used to reveal the locally induced molecular arrangements were: dynamic viscosity, zeta potential, chemiluminescence, liquid chromatography; mass spectrometry, and Raman and infrared spectroscopy. The principal result of our experiments was the detection of different molecular arrangements within the mixture of alkane chains, generated by our optical manipulations. This induced "optical matter" displayed two material properties: antioxidant effects and large molecular aggregation effects. In order to bring the experimental results in relation with theory, we developed a physical model and the interacting force between polarizable bodies was computed. By numerical calculations stable structures for N = 6 and N = 8 particles were obtained.

A special mechanism of thermoelectric transport is described, consisting of pulses of charge carriers which "fly" periodically through the external circuit from the hot end of the sample to the cold end, with a determined duration of the "on" and "off" times of the electric contacts, while maintaining continuously the thermal contacts. It is shown that such a "resonant" ideal thermogenerator may work cyclically, with the same efficiency quotient as the ideal efficiency quotient of the thermoelectric devices operated in the usual stationary transport regime but the electric flow and power are increased, as a consequence of the concentration of the charge carriers on pulses of small spatial extent. The process is reversible, in the sense that it can be operated either as a thermoelectric generator or as an electrothermal cooler. (C) 2010 American Institute of Physics. [doi: 10.1063/1.3456037]

It is shown that the figure of merit of a thermoelectric couple can be appreciably improved by using a pulsed current transferred from the thermoelectric circuit. In the frame of this theory un unusual drop of temperature in a thermoelectric circuit is possible. An ultrafast process of thermoelectric conduction is described, whose increased performance is realized by minimizing the effects of thermal dissipation.

Within a one-dimensional model of off-centre diffusion it is shown that the diffusion coefficient depends on the number of off-centre sites and on their orientation relative to the host lattice.

The crystalline phases in the superconducting ceramic Bi:Sr:Ca:Cu2:O(x) exhibiting either low superconducting transition (almost-equal-to 80 K) or both, low and high superconducting transitions (almost-equal-to 110 K) are identified by X-ray and electron diffraction. Two types of modulated structures are observed and their relation to T(c) is discussed within the frame of the oxygen-displacive mode theory.