Synthesis of silica supported titania nanocomposite in controllable phase content and morphology

The silica supported titania nanocomposite thin films with controllable particle size and phase content were successfully prepared by a convenient post annealing approach involving in solid-solid interfacial reaction. The effects of growth conditions, such as the annealing temperature and silicon concentration on the particle size and phase content, were systematically studied by using Atomic force microscopy (AFM), Raman spectroscopy, X-ray diffraction (XRD), and X-ray spectroscopy (XPS). The results indicate that the silicon concentration is a dominant factor in the morphology, crystallization and phase transformation of these nanocomposites. A mechanism for the high temperature phase transformation is also proposed based on the migration of the oxygen vacancies.     

Formation of surface stabilized Si nanocrystal by pulsed laser ablation in hydrogen gas

We prepared silicon nanocrystallites by pulsed laser ablation (PLA) of a Si target in hydrogen background gas. A mixture of hydrogen and helium was used as a background gas and the hydrogen partial pressure was varied. The deposited nanocrystal-film system shows a hierarchical structure composed of surface hydrogenated silicon nanocrystallites as the primary structure and aggregates of the nanocrystallites as the secondary structure. The size of the primary particles was not sensitive to the hydrogen partial pressure, while the porosity of the secondary structure constituted by the aggregation of the primary particles increased with increasing hydrogen partial pressure. This indicates that the surface is stabilized and that aggregation of the primary structure is depressed by surface hydrogenation. The optical gap energy of the deposits shifted to higher energy with increasing hydrogen partial pressure due to the formation of well-isolated nanocrystallites by surface stabilization. These results indicate that PLA in hydrogen gas is a promising technique to prepare surface stabilized and controlled silicon nanocrystallites.     

Magnetic-dichroism study of iron silicides formed at the Fe/Si(100) interface

The interplay between the phase composition, electronic structure, and magnetic properties of the Fe/Si(100)2×1 interface has been studied at the initial stages of its formation (at Fe doses up to 8 Å). The experiments were carried out in ultra high vacuum by using high-resolution photoelectron spectroscopy with synchrotron radiation. The interface magnetic properties were examined in terms of magnetic linear dichroism in angle-resolved Fe 3p core-level photoemission. It was found that at room temperature a disordered Fe–Si solid solution is formed at the first stage of Fe deposition (≤3.4 Å). In the coverage range of 3.4–4.3 Å the solid solution transforms into Fe₃Si. However, the in-plane ferromagnetic ordering of the silicide occurs only at 6.8 Å Fe that demonstrates the thickness dependence of the magnetic properties of Fe₃Si. The subsequent sample annealing to 150°C transforms Fe₃Si to ε-FeSi, leading to the disappearance of ferromagnetic behavior.     

Large scale highly organized single-walled carbon nanotube networks for electrical devices

Large-scale room-temperature liquid-phase directed assembly of highly organized single-walled carbon nanotubes (SWNT) over large areas is demonstrated. The presented process utilizes lithographically patterned template to guide the fluidic self-assembly of SWNTs on a silicon-dioxide substrate. The width of these highly organized SWNT structures are in the micron range while their heights are in orders of nanometers. Room temperature electrical I–V characterization of these fabricated high coverage SWNT wires show linear ohmic behavior. The resistivity of these assembled SWNT network is in the order of 10⁻⁶ Ω m demonstrating their metallic characteristics during conductance. Scaling of the assembly processes on a wafer level with high yield is demonstrated. Our developed assembly process is compatible with complimentary metal oxide semiconductor (CMOS) processes and provides a simple and flexible way of building SWNT nanotube-based electronics in a large scale.     

Open-system density matrix description of an STM-driven atomic switch: H on Si(100)

Previous experiments indicate that an STM (scanning tunnelling microscope) can be used to switch a hydrogen atom at a partially hydrogen-covered Si(100)-2×1 surface, from one Si atom of a Si dimer to a neighbouring, empty Si site [U.J. Quaade et al., Surf. Sci. 415, L1037, 1998]. It has been suggested that the switching occurs via a transient positive ion resonance state. In an earlier paper, we have examined the switching process for the “above threshold” regime when the bias is large enough to directly populate the positive ion resonance. In the present paper we study the “below threshold” regime instead, where the switching is more appropriately modelled as a ladder climbing over the barrier, in the ground electronic state. For this purpose we solve the Liouville–von Neumann equation in Lindblad form, describing a switching H atom on a Si dimer. STM-induced transition rates between vibrational levels are estimated from cluster calculations, assuming contributions both from a dipole and a resonance scattering mechanism. Vibrational relaxation is also included, as well as finite temperature and field effects. The switching rate in a current regime of about 1 to 10 nA scales highly non-linearly with current, and it is found to be governed by vibrational “ladder climbing” and subsequent tunnelling through the top of the ground state barrier. Multi-phonon processes also play a role. As a result of tunnelling, pronounced isotope effects are observed when replacing H with D. It is further argued that resonance-mediated inelastic scattering dominates over dipole excitation, and that the STM switch is stable also at room temperature.     

Er<Superscript>3+</Superscript> as glass structure modifier of Ga–Ge–S chalcogenide system

Er³⁺ clustering phenomenon in Ga–Ge–S chalcogenide system is studied using Raman spectroscopy. The Raman spectra from 10 to 500 cm⁻¹ for glasses (100−y)[15Ga₂S₃–85GeS₂]–yEr₂S₃ (y=0.08−5.00 mol. %) have been analyzed. To reveal the influence of the chemical composition on the glass structure the intensity of the peak corresponding to Ge–Ge (Ga–Ga) homopolar bonds has been examined. The peak intensity increase with Er₂S₃ concentration change in the region 0<C(Er₂S₃)<2 mol. % has been interpreted in terms of the sulphur deficiency in the glass resulting in the formation of S₃Ge–GeS₃ (S₃Ga-GaS₃) structural units. The further increase in concentration beyond 2 mol. % reduces the sulphur deficiency, which can be attributed to the formation of the ternary compound Er₃GaS₆. The structural units Er₃GaS₆ contain a large mol. fraction of Er³⁺ or, in other words, Er³⁺ clusters. The data obtained from the low-frequency Raman spectra (boson band) indicate strong variations of the medium-range order (MRO) in the glasses induced by Er³⁺. The observed behavior of the MRO size (the correlation length) with increasing of Er₂S₃ concentration provides for additional evidence of the Er³⁺ clustering.     

Refractive index change mechanisms in femtosecond laser written ceramic Nd:YAG waveguides: micro-spectroscopy experiments and beam propagation calculations

The effect that femtosecond laser filamentation has on the refractive index of Nd:YAG ceramics, and which leads to the formation of waveguide lasers, has been studied by micro-spectroscopy imaging, beam propagation experiments and calculations. From the analysis of the Nd³⁺ luminescence and Raman images, two main types of laser induced modifications have been found to contribute to the refractive-index change: (i) a lattice defect contribution localized along the self-focusing volume of the laser pulses, in which lattice damage causes a refractive-index decrease, and (ii) a lattice strain-field contribution around and inside the filaments, in which the pressure-driven variation of the inter-atomic distances causes refractive-index variations. Scanning near-field optical-transmission and end-coupling experiments, in combination with beam propagation calculations, have been used to quantitatively determine the corresponding contribution of each effect to the refractive-index field of double-filament waveguides. Results indicate that the strain-field induced refractive-index increment is the main mechanism leading to waveguiding, whereas the damage-induced refractive-index reduction at filaments leads to a stronger mode confinement.     

Charge transfer and polarization screening in organic thin films: phthalocyanines on Au(100)

Core hole screening effects at organic/metal interfaces were studied by core level X-ray photoemission spectroscopy (XPS), X-ray excited Auger electron spectroscopy (XAES), and valence band ultraviolet photoemission spectroscopy (UPS). The comparison of energetic shifts in XPS and XAES enables the estimation of electronic relaxation energy (screening ability). Magnesium phthalocyanine (MgPc) and zinc phthalocyanine (ZnPc) evaporated on single crystalline Au(100) were used as model molecules. Two different features in the Mg KLL spectra can be clearly separated for (sub-)monolayer coverages, while only minor changes of the shape of Mg 1s are observed. Applying a dielectric continuum model, the major screening mechanism cannot be described sufficiently by polarization screening due to mirror charges, significant contributions by charge transfer screening have to be considered. In contrast, small screening effects in the bulk material can be explained by surface polarization.     

Monte carlo simulations of growth modes of Pb nanoislands on Si(111) surface

The growth of Pb islands on a Si(111) surface exhibits many interesting properties. For example, the self-assembled process results in a homogeneous distribution of Pb islands with uniform height. The dependence of this height on coverage and temperature can be expressed as a phase diagram [1]. In this paper we develop a model of the growth process that reflects the main features of the experimental observations and determines the key processes of quantum dot formation in a Pb/Si(111) system. The growth of islands is simulated by the Monte Carlo method. With suitably chosen parameters the model is able to reconstruct the phase diagram, via the dependence of the dynamics of Pb atoms on area and height. These dependencies are attributed to stress energy and quantum size effects.     

Square-pyramidal iron coordination modules as potential spin switches for the chemisorption on gold

Octahedral iron(II) complexes of a unique pyridine-derived tetrapodal pentadentate polyamine ligand, 2,6-C₅H₃N(CMe[CH₂NH₂]₂)₂, show temperature-dependent spin crossover (SCO) depending on the nature of a sixth monodentate ligand L (imidazol or pyridine derivative). For L = 1-methylimidazol, the redox behaviour of the complex, as determined by cyclic voltammetry, suggests an accompanying ligand exchange. Pyridine-4-thiol and the disulphides: 4-(2-methyldisulphanyl)pyridine, 4-(2-hexadecyldisulphanyl)pyridine and 1,2-bis([pyridine-4-yl]methyl)disulphane, were studied as mono-dentate ligands L, with a view to enable chemisorption of iron(II) complexes on a gold surface. In the case of pyridine-4-thiol, the participation of the thiolate functional group in iron coordination is difficult to suppress, whereas the disulphides enter into yet unrecorded redox chemistry with iron(II), yielding a di-iron(III) complex containing a persulphide bridge (S ₂²⁻).     

Material processing of dielectrics with temporally asymmetric shaped femtosecond laser pulses on the nanometer scale

Laser material processing of dielectrics with temporally asymmetric femtosecond laser pulses of identical fluence, spectrum, and statistical pulse duration is investigated experimentally. To that end single shot structures at the surface of fused silica as a function of fluence and pulse shape are analyzed with the help of scanning electron microscopy. Structures for the bandwidth limited pulses show the known expansion in structure size with increasing laser fluence approaching the diffraction limit, which is 1.4 μm for the 0.5NA microscope objective used. In contrast, structures from the asymmetric pulses are remarkably stable with respect to variations in laser fluence and stay below 300 nm despite doubling the fluence. Different thresholds for surface material modification with respect to an asymmetric pulse and its time reversed counterpart are attributed to control of different ionization processes.     

LSP spectral changes correlating with SERS activation and quenching for R6G on immobilized Ag nanoparticles

In terms of chemical enhancement in Surface Enhanced Raman Scattering (SERS), we investigated the effect of halide and other anions to rhodamine 6G (R6G) adsorbed Ag particles that were immobilized on the substrates. The residual species on chemically prepared Ag particles such as citrate or a-carbon were thoroughly substituted by various anions, e.g., Cl⁻, Br⁻, I⁻, SCN⁻, CN⁻, or S₂O₃ ²⁻ anions, whose adsorption features are elucidated by the formation constants for AgX₂ ^(m−1)−, here X denotes the above anions. In particular, Cl⁻, Br⁻, or SCN⁻ ions activated SERS of R6G via intrinsic electronic interaction with Ag, whereas CN⁻, S₂O₃ ²⁻, or I⁻ anions quenched it due to their exclusive adsorption onto the Ag surfaces. We found that the activation process with the anions commonly yields a marked blue-shift of the coupled plasmon peak from ca. 650–700 to 500–550 nm in elastic scattering. It is rationalized by slight increase of the gap size between adjacent Ag nanoparticles by only ca. 1 nm based on theoretical simulations. This is probably caused by slight dissolution, oxidative etching, of the particles according to large formation constants of the complexes. Consequently, partly remaining negative charges on the Ag surface, and a slight increase in the gap size, providing huge electric field, facilitated R6G cations to adsorb on the nanoparticles, especially at the junction.     

Structural and electronic properties of Ren (${\sf n} \leq$ 8) clusters by density-functional theory

The structures, stabilities and electronic properties of small-sized Re_n (n ≤ 8) clusters have been systematically investigated by density-functional theory. The lowest-energy structures of Re_n clusters favor 3-dimensional configuration. The results of second-order difference of energies indicate that Re₄ and Re₆ possess relatively higher stability in structure. Importantly, our theoretical results of electron affinity are in agreement with experimental values, which can be responsible for the reliability of the structures.     

Preparation of conventional thermoelectric nanopowders by pulsed laser fracture in water: application to the fabrication of a pn hetero-junction

The technique of laser fracture in a liquid medium has been applied to the synthesis of n-type (Bi_0.95Sb_0.05)₂ (Te_0.95Se_0.05)₃ and p-type (Bi_0.2Sb_0.8)₂Te₃ semiconducting nanopowders which are the best conventional materials currently used for thermoelectric applications at ambient temperature. The nanopowders have been prepared with a high yield in an especially built-up cell. Laser fracture in water of micronsized powders has been applied, using a nanosecond Nd:YAG laser working at 532 nm. The obtained powders have been characterized by scanning and transmission electron microscopy and by X-ray diffraction. The mean diameter is about 10 nm and the phase of the initial powders is kept. To test the potentiality of these nanosized materials, we have shown the feasibility to produce a pn hetero-junction.     

The development of a TESLA recirculator with superconducting accelerating structures in Ukraine

The recirculator project, which is to be built at the National Science Center, Kharkov Institute of Physics and Technology (NSC KIPT), is presented. The basic solutions incorporated in the design are given. The TESLA superconducting section is chosen as the accelerating structure of an accelerating complex. The text was submitted by the authors in English.     

New optical diagnostics of the VEPP-4M collider

The experiments in measuring the dynamic aperture and beam energy spread of the VEPP-4M collider [1] are described. The optical diagnostics of the accelerator were applied for these purposes. The text was submitted by the authors in English.     

DAΦNE status and upgrade plans

The Frascati Φ-factory DAΦNE has successfully completed experimental runs for the three main detectors, KLOE, FINUDA and DEAR. The best peak luminosity achieved so far is 1.6 × 10³² cm⁻² s⁻¹, while the best daily integrated luminosity is 10 pb⁻¹. At present the DAΦNE team is preparing an upgrade of the collider based on the novel crab waist collision scheme. The upgrade is aimed at pushing the luminosity towards 10³³cm⁻²s⁻¹. In this paper we describe present collider performance and discuss ongoing preparatory work for the upgrade. for DAΦNE Collaboration Team [1] The text was submitted by the author in English.     

VEPP-2000 collider commissioning

Construction of the VEPP-2000 construction was completed at the end of 2006. The first beam was captured in a special regime without final focus solenoids. In this regime, all systems of power supplies and machine control were calibrated and tuned. In the same mode vacuum chamber treatment by synchrotron radiation was performed with an electron beam current of up to 150 mA. The first test of the round beam option was performed at an energy of 508 MeV with a solenoidal field of 10 T in two straight sections of interaction. The text was submitted by the author in English.     

Femtosecond-laser nanofabrication onto silicon surface with near-field localization generated by plasmon polaritons in gold nanoparticles with oblique irradiation

Nanohole fabrication process with gold nanoparticles irradiated by femtosecond laser at different incident angles is investigated. Nanoparticles with diameter of 200 nm and laser irradiation with center wavelength of 800 nm are used in the present study. The analysis of the electromagnetic field distribution in the near-field zone of the particle is made by simulations based on finite-differential time domain (FDTD) method. It is shown that when gold nanoparticle is irradiated by laser pulse surface plasmon excitation can be induced, and associated with it, high-intensity near field is produced in a limited area around the particle. It is found that the change of the irradiation conditions by means of irradiation from various incident directions gives a possibility of laser nanoprocessing with tunable characteristics. Our results show that enhanced optical intensity is able to be induced on the substrate surface regardless of incident direction of the laser due to the image charge interaction with the substrate. Furthermore, the use of p-polarized laser irradiation at a certain angle gives a minimum of the spatial dimensions of the enhanced zone on the substrate which is about two times smaller than that obtained at normal incidence.