Atomic structure of two-dimensional binary surface alloys: Si(111)-√21 × √21 superstructure

The atomic structures of Au and Ag co-adsorption-induced √21 × √21 superstructure on a Si(111) surface, i.e., (Si(111)-√21 × √21-(Au, Ag)), where the Si(111)-5 × 2-Au surface is used as a substrate, have been investigated using reflection high-energy positron diffraction (RHEPD) and photoemission spectroscopy. From core-level spectra, we determined the chemical environments of Ag and Au atoms present in the Si(111)-√21 × √21-(Au, Ag) surface. From the rocking curve and pattern analyses of RHEPD, we found that the atomic coordinates of the Au and Ag atoms were approximately the same as those of the Au and Ag atoms in other Si(111)-√21 × √21 surfaces with different stoichiometries. On the basis of the core-level and RHEPD results, we revealed the atomic structure of the Si(111)-√21 × √21-(Au, Ag) surface.     

An analysis on the Frequency-dependent grounding impedance based on the ground current dissipation of counterpoises in the two-layered soils

Because of the increased usage of power conversion equipment and their susceptibility to lightning strikes, high frequency fault currents flowing through grounding systems are increased. As grounding systems change from individual groundings to common or integrated groundings, the improved performance of grounding systems against high frequency fault currents is urgently required. When regarding the common or integrated grounding systems, most of them are required to satisfy the ground resistance defined by standards or regulations. The grounding system performance against high frequency fault currents is defined by the grounding impedance. A number of studies have reported that grounding system performance is reduced due to the increase of the grounding impedance with increasing of the frequency of fault currents. In this paper, in order to investigate the characteristics of the frequency-dependent grounding impedances of counterpoises installed in the two-layered soils, the ground current dissipation rates in each 10 m section of the counterpoises were measured and analyzed as functions of the length of grounding electrodes and the current injection point. As a result, most of the ground currents above the frequency of 100 kHz are dissipated into the earth near the current injection point and the high frequency grounding impedance of long counterpoises is converged into that of short counterpoises. The high frequency grounding impedance measured at the low soil-resistivity end of the counterpoise buried in the two-layered soils is much lower than that measured at the high soil-resistivity end.     

Surface structure of low-coveraged Cs on Si(0 0 1)-() system

Alkali metals (AM) on semiconductors have been investigated as a simple model system for the metal-semiconductor interfaces due to their simple electronic structures. Especially, cesium (Cs) on Si(0 0 1) surface has been studied with various experimental techniques. In this study, we investigated the atomic structure of initial Cs adsorption on Si(0 0 1)-(2×1) surface using coaxial impact collision ion scattering spectroscopy. When Cs atoms are adsorbed on Si(0 0 1)-(2×1) up to 0.2 ML at room temperature, the initial adsorption site is on-top T3 site with poor periodicity and the length of Si dimer is reserved as in the clean Si(0 0 1) surface. It is also found that Cs atoms adsorbed on Si(0 0 1) surface with a height of 2.83±0.05 Å from the second layer of Si(0 0 1) surface.     

Measurement of the wrong-sign decays D0 --> K+ pi- pi0 and D0 --> K+ pi- pi+ pi-, and search for CP violation

Using 281 fb-1 of data from the Belle experiment recorded at or near the (4S) resonance, we have measured the rates of the "wrong-sign" decays D0 --> K+ pi- pi0 and D0 --> K+ pi- pi+ pi- relative to those of the Cabibbo-favored decays D0 --> K- pi+ pi0 and D0 --> K- pi+ pi+ pi-. These wrong-sign decays proceed via a doubly Cabibbo-suppressed amplitude or via D0-D0 mixing; the latter has not yet been observed. We obtain R(WS)(K pi pi0) = [0.229 +/- 0.015(stat)(+0.013)(-0.009)(syst)]% and R(WS)(K3pi) = [0.320 +/- 0.018(stat)(+0.018)(0.013)(syst)]%. The CP asymmetries are measured to be -0.006 +/- 0.053 and -0.018 +/- 0.044 for the K+ pi- pi0 and K+ pi- pi+ pi- final states, respectively.     

Evidence for muon neutrino oscillation in an accelerator-based experiment

We present results for nu(mu) oscillation in the KEK to Kamioka (K2K) long-baseline neutrino oscillation experiment. K2K uses an accelerator-produced nu(mu) beam with a mean energy of 1.3 GeV directed at the Super-Kamiokande detector. We observed the energy-dependent disappearance of nu(mu), which we presume have oscillated to nu(tau). The probability that we would observe these results if there is no neutrino oscillation is 0.0050% (4.0 sigma).     

Advantages of Adaptive Speckle Filtering Prior to Application of Iterative Deconvolution Methods for Optical Coherent Tomography Imaging

The axial resolution of optical coherence tomography (OCT) is closely related to the light source spectrum width. Unfortunately, most basic sources providing the required power for decent OCT image have narrow spectra, which generate a resolution loss. Assuming the OCT system is linear shift-invariant, we can consider the system output as the convolution of the theoretical signal with a system impulse response due to this spectrum narrowness. It becomes then possible to enhance this resolution through iterative deconvolution methods (IDM). However those methods have a significant drawback, as they usually significantly enhance speckle, which is another consequence of the source spectrum narrowness. To compensate this, we rely on preliminary speckle filtering, and especially the adaptative ones, which allow tackling the speckle without blurring the image. We first studied enhancement proposed by most popular IDMs on OCT images, and then the effect of preliminary adaptive speckle filtering (ASF) by different common adaptive methods. Then, among those methods, we combined Frost filter and Richardson-Lucy deconvolution in the appropriated way; this way we both enhanced resolution by 2 and reduced speckle (raising CNR from 0.7 to 1.3)     

Recoil-proton polarization in high-energy deuteron photodisintegration with circularly polarized photons

We measured the angular dependence of the three recoil-proton polarization components in two-body photodisintegration of the deuteron at a photon energy of 2 GeV. These new data provide a benchmark for calculations based on quantum chromodynamics. Two of the five existing models have made predictions of polarization observables. Both explain the longitudinal polarization transfer satisfactorily. Transverse polarizations are not well described, but suggest isovector dominance.     

Comment on “An enhanced polarization mechanism for the metal cations modified amorphous TiO2 based electrorheological materials” by Qing Wu, Bin Yuan Zhao, Chen Fang and Ke Ao Hu

Comments on a recent article on an enhanced polarization mechanism for the metal cations modified amorphous TiO₂ based electrorheological materials are presented, based upon an examination of the yield stress, which is a function of electric-field strength, of the materials. Using the deduced critical electric-field strengths, we find that the universal yield stress equation proposed collapses the data given by Qing Wu, Bin Yuan Zhao, Chen Fang, Ke Ao Hu, Eur. Phys. J. E 17, 63 (2005), onto a single curve.     

Simultaneous Determination of Acetylsalicylic Acid and Caffeine in Pharmaceutical Formulation by First Derivative Synchronous Fluorimetric Method

A sensitive, rapid, and specific assay has been developed for the simultaneous determination of acetylsalicylic acid and caffeine in commercial tablets based on their natural fluorescence. The mixture of these drugs was resolved by first derivative synchronous fluorimetric technique using two scans. At Δλ=106 nm, using first derivative synchronous scanning, only acetylsalicylic acid yields a detectable signal at 316 nm (peak to zero method) which is unaffected by caffeine. At Δλ=30 nm, the signal of caffeine at 288 nm (peak to zero method) is not affected by acetylsalicylic acid. The range of application is between 0.021 and 41.62 μg ml⁻¹ (correlation coefficient, R=0.9995) for acetylsalicylic acid and between 0.4486 and 44.86 μg ml⁻¹ (correlation coefficient, R=0.99786) for caffeine. The recovery range of 98.40–102% for acetylsalicylic acid and 90–100.5% for caffeine from their synthetic mixture was reported. Overall recovery of both compounds about 97–99% for acetylsalicylic acid and 97–98% for caffeine was obtained from real sample analysis. The detection limits are 0.0013 μg ml⁻¹ and 0.0306 μg ml⁻¹ for acetylsalicylic acid and caffeine, respectively. The relative standard deviation (n=10) for 20 μg ml⁻¹ of acetylsalicylic acid is 2.75% and for 2.2 μg ml⁻¹of caffeine is 1.7%.