Beam reconfigurable antenna for the THz band based on a graphene high impedance surface

In this paper a reconfigurable beam antenna is proposed for THz applications, based on a switchable Graphene High Impedance Surface (G-HIS) that acts as a reflector for a primary radiator. The Graphene-HIS structure composed of two layers of graphene cells arranged in a 5×5 array, the two planes of the array are separated by a thin silicon oxide layer; patches in the same row are connected together, to be biased by a common DC voltage to the entire row; this gives the ability to control the graphene conductivity σ. The results show that the shape of the radiation pattern can be changed by changing the voltage applied to each row of G-HIS array. The antenna was fabricated and characterized using a THz-TDS laser system. Measurements are in good agreement with simulations as far as the graphene surface impedance and the resonance frequency are concerned. The scanning reflection on the antenna surface due to the change on the applied voltage is presented to show the effect of biased graphene layer on the dipole properties.     

Sorption of Cypermethrin Diastereoisomers to Quartz,Corundum, Goethite,Kaolinite and Montmorillonite

Differential sorption and degradation of different pesticide stereoisomers in soil may result in accumulation of the most strongly sorbed and the slowest degradable isomers. In this work the pyrethroid cypermethrin (8 isomers) has been used for test of stereochemical interactions with surfaces of the minerals quartz, corundum, goethite, kaolinite and montmorillonite. The sorption of three diastereoisomeric fractions denoted Cis A, Trans C and Cis B + Trans D were quantified by use of GC-ECD in batch experiments with initial cypermethrin concentrations in the range 1-9 µg/L. Correction for cypermethrin sorbed to surfaces of the shaking flasks were accomplished to obtain net sorption isotherms for the minerals, all of which were well fitted by the Freundlich equation. Bonding affinities per unit surface area decreased in the order: corundum > quartz > kaolinite > montmorillonite > goethite. The isotherms for sorption of all diastereoisomeric fractions to quartz, corundum and goethite were all linear, whereas non-linear isotherms were found for sorption of Cis A and Trans C fractions to kaolinite and montmorillonite. Corundum, quartz and goethite showed a significantly stronger sorption of Cis A than the other fractions, while kaolinite sorbed Cis B + Trans D most strongly. The observed differences predict less leaching and slower degradation of the Cis A fraction in subsoils low in organic carbon.     

Artificial boundary conditions on polyhedral truncation surfaces for three-dimensional elasticity systemsConditions aux limites artificielles sur des surfaces polyhédrales de troncature pour des systèmes d'élasticité tridimensionalle

For a three-dimensional exterior problem in the framework of anisotropic elasticity, artificial boundary conditions are constructed on a polyhedral truncation surface. These conditions do not need an explicit formula for the fundamental matrix. An approach to adapt the shape of truncation surfaces to the shape of the enclosed cavity is discussed. To cite this article: S. Langer et al., C. R. Mecanique 332 (2004).     

Gas-sensing properties of perovskite La0.875Ba0.125FeO3 nanocrystalline powders

La_0.875Ba_0.125FeO₃ nanocrystalline powders have been prepared by a sol-gel method. The structure, conductance and gas-sensing properties were investigated. La_0.875Ba_0.125FeO₃ crystallizes as a perovskite phase with the orthorhombic structure. The La_0.875Ba_0.125FeO₃ based sensor shows good sensitivity and selectivity to alcohol gas. The highest sensitivity to 500 ppm alcohol gas reached was 58 at 170 °C. The adsorption of O₂ on the La_0.875Ba_0.125FeO₃ (0 1 0) surface was studied with the first-principles calculation based on the density functional theory. The results show that the surface states are near the Fermi energy level and that the Fe ion plays an important role in the process of oxygen adsorption, which affects the gas-sensing properties.     

Enhancement in hydrophobicity of silica films using metal acetylacetonate and heat treatment

Water is one of the most affecting chemicals that can cause damage to the solid surface. To protect the surface due to the action of water, the surface should be made hydrophobic. In the present study, the improvement in hydrophobicity of silica films using metal acetylacetonate (M-acac) by employing heat treatment to methyltrimethoxy silane (MTMS) based silica coatings is reported as a novel attempt. Instead of following the established trends of the surface derivatization or co-precursor method, iron acetylacetonate Fe(acac)₃, copper acetylacetonate Cu(acac)₂ and heat treatment were used to incorporate hydrophobicity with silica coatings. As M-acac is readily soluble in organic solvents, Fe(acac)₃ and Cu(acac)₂ were dissolved in methanol (MeOH) and their concentration was varied from 0 to 0.025 M. The coating solution was prepared by optimizing molar ratio of MTMS:MeOH:basic H₂O to 1:7.15:6.34, respectively. Gelation time (t_g) for Cu(acac)₂ containing silica sol and that containing Fe(acac)₃ were noted to be 30 and 55 min, respectively. The substrates were taken out after gelation and heat treated at 150 °C for 2 h. The heat treated films showed a dramatic increase in the static water contact angle from 82° to as high as 142°.     

Preparation and characterization of surface modified γ-Fe2O3 (maghemite)-silica nanocomposites used for the purification of benzaldehyde lyase

γ-Fe₂O₃ (maghemite)-silica nanocomposite particles were synthesized using a sol-gel method. The condensation products of 3-glycidoxy propyltrimethoxy silane (GPTMS) and nitrilotriacetic acid (NTA) were introduced onto the surfaces of the γ-Fe₂O₃-silica nanocomposite particles and subsequently, these modified surfaces were complexed with cobalt (Co⁺²) metal ions. A possibility of using these surface modified γ-Fe₂O₃-silica particles for the purification of 6×histidine tagged recombinant benzaldehyde lyase (BAL, EC 4.1.2.38) based on magnetic separation was investigated. X-ray diffraction (XRD), thermal analysis, and vibrating sample magnetometry (VSM) methods were used to characterize the surface modified superparamagnetic γ-Fe₂O₃ (maghemite)-silica nanoparticles. XRD (Scherer's equation) results indicate that the primary particle size of maghemite was around 11 nm. Magnetic characterization results confirmed that the γ-Fe₂O₃ (maghemite)-silica nanoparticles were superparamagnetic. According to sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) results, these superparamagnetic nanoparticles specifically capture 6×His-tagged BAL from crude extract of Escherichia coli (E. coli) BL21(DE3)pLysS/BAL_HIS. This study shows that the surface modified γ-Fe₂O₃ (maghemite)-silica nanoparticles are eligible for immobilized metal-ion affinity adsorption for histidine tagged recombinant proteins with its high capacity (3.16±0.4 mg/g) and selectivity.     

The stability of the fractional quantum Hall effect in topological insulators

With the recent observation of graphene-like Landau levels at the surface of topological insulators, the possibility of fractional quantum Hall effect, which is a fundamental signature of strong correlations, has become of interest. Some experiments have reported intra-Landau level structure that is suggestive of fractional quantum Hall effect. This paper discusses the feasibility of fractional quantum Hall effect from a theoretical perspective, and argues that while this effect should occur, ideally, in the n=0 and |n|=1 Landau levels, it is ruled out in higher |n| Landau levels. Unlike graphene, the fractional quantum Hall effect in topological insulators is predicted to show an interesting asymmetry between n=1 and n=−1 Landau levels due to spin-orbit coupling.     

A superstructural 2D-phase diagram for Ga on the Si(111)- 7x7 system

The structural modifications of an Si(111)- 7x7 reconstructed surface and the evolution of growth induced by Ga adsorption in the submonolayer regime at various substrate temperatures ranging from room temperature (RT) to 600 °C, with a low Ga flux rate of 0.1 ML/min (1 ML∼6.8×10¹⁴ atoms/cm²) have been studied in-situ in Ultra High Vacuum (UHV) using Auger Electron Spectroscopy (AES), Low Energy Electron Diffraction (LEED) and Electron Energy Loss Spectroscopy (EELS) as characterization probes. Ga grows in the Stranski-Krastanov (SK) growth mode for temperatures ranging from RT to 350 °C, where 3D-islands form after one and two flat monolayers of Ga adsorption, while for higher temperatures ranging from 450 to 550 °C, Ga grows in the Volmer-Weber (VW) growth mode. A comprehensive 2D-phase diagram for this Ga/Si(111) system for adsorption, which provides pathways to attain the observed superstructural phases, viz., √3x√3-R30°, 6.3x6.3, 6.3√3x6.3√3-R30° and 11x11, has been investigated. The characteristic EELS spectrum for each superstructural phase is also reported in this study.     

Reconstructed (1 1 0) surfaces of FCC transition metals

The energies of the ideal, missing row (MR) and missing column (MC) (1 1 0) surfaces have been calculated by using modified embedded atom method (MEAM) for seven face centered cubic (FCC) transition metals Au, Pt, Ag, Pd, Rh, Cu and Ni. The results, that the MC reconstruction can not be formed for all metals, while the MR reconstruction can be formed naturally for Au and Pt, inductively for Ag, Pd, Rh and Cu and difficultly for Ni, are better than EAM calculated results in comparing with experimental results. In addition to the surface energy explanation, the results are also related to the surface topography and valence electron structure.     

Observation of metastable erbium trihydride

The γ phase of the erbium-hydrogen system is a hexagonal trihydride that is not predicted to be stable at room temperature without an overpressure of hydrogen gas. Herein, we report the creation of both, a thin film and powder of erbium trihydride that is metastable at ambient conditions. The presence of the hexagonal γ phase was determined by X-ray diffraction (XRD). The ratio of the total moles of hydrogen isotopes (hydrogen and deuterium) to moles of erbium, (H + D):Er, have been confirmed by elastic recoil detection (ERD)/Rutherford backscattering spectroscopy (RBS). Auger electron spectroscopy (AES) depth profiles and X-ray photoelectron spectroscopy (XPS) revealed the presence of an oxide layer that may account for the metastable behavior of the thin film.