Initial growth process and surface structure of Ag on Si(111) studied by low-energy Ion-Scattering Spectroscopy (ISS) and LEED-AES

The growth process of silver on a Si(111) substrate has been studied in detail by low-energy ion-scattering spectroscopy (ISS) combined with LEED-AES. Neon ions of 500 eV were used as probe ions of ISS. The ISS experiments have revealed that the growth at room temperature and at high temperature are quite different from each other even in the submonolayer coverage range. The following growth models have been proposed for the respective temperatures. At room temperature, the deposited Ag forms a two-dimensional (2D) island at around 2/3 monolayer (ML) coverage, where the Ag atoms are packed commensurately with the Si(111)1 substrate. One third of the substrate Si surface remains uncovered there. Then it starts to develop into Ag crystal, and at a few ML coverage a 3D island of bulk Ag crystal grows directly on the substrate. An intermediate layer, which covers uniformly the whole surface before the growth of Ag crystal, does not exist. At high temperatures (>~200°C), the well-known Si(111)√3-Ag layer is formed as an intermediate layer, which consists of 2/3 ML of Ag atoms and covers the whole surface uniformly. These Ag atoms are embedded in the first double layer of the Si substrate. It is concluded that the formation of the √3 structure needs relatively high activation energy which may originate from the large displacement of Si atoms owing to the embedment of the Ag atoms, and does not proceed below about 200°C. The most stable state of the Ag atoms on the outermost Si layer is in the shape of an island, both for the Si(111) surface and for the Si(111)√3-Ag surface.     

Electroabsorption spectroscopy of 6-hydroxyquinoline doped in polymer films: Stark shifts and orientational effects

Stark absorption spectroscopy was applied to 6-hydroxyquinoline (6-HQ) doped in polymer films of poly(methyl methacrylate) (PMMA) and poly(vinyl alcohol) (PVA) at temperatures of 50-300 K. The electroabsorption (E-A) spectrum of 6-HQ markedly depends on temperature in a PMMA film. The polarization dependence as well as the temperature dependence of the E-A spectra reveals that 6-HQ is oriented along the direction of the applied electric field at room temperature in a PMMA film. As the temperature becomes lower, the field-induced orientation of 6-HQ is restricted, and only the Stark shift induced by a change in electric dipole moment and in molecular polarizability is observed. On the other hand, E-A spectra of 6-HQ doped in a PVA film are essentially independent of temperature, suggesting that 6-HQ is not oriented along the electric field even at room temperature in PVA. These results show that the molecular motion of 6-HQ in a polymer film is very sensitive to the microenvironment of the surrounding matrix.     

Oxygen isotope effect in optimally doped Bi2Sr2CaCu2O8+δ studied by low-energy ARPES

Using angle-resolved photoemission spectroscopy (ARPES) with low-energy tunable photons, we studied the oxygen isotope effect in optimally doped Bi₂Sr₂CaCu₂O_8+δ (Bi2212). We found the oxygen isotope shift in the real part of the electron self-energies [ReΣ(ω)s] along the nodal direction derived not only from the momentum distribution curves (MDCs) but also from the energy distribution curves (EDCs). Present results indicate straightforwardly the coupling between the nodal electrons and the phonons.     

Degradation characteristics of YBCO coated conductors due to fault-current in power cable applications

In high temperature superconductor applications used in electric power devices, YBCO coated conductors may be subjected to short-circuit fault-currents that are 10–30 times the normal operating current. These over-currents cause heat generation, resulting in I_c degradation of the YBCO coated conductor. Therefore, it is necessary to fully investigate the degradation characteristics of YBCO coated conductors. We previously conducted preliminary experiments on the degradation of YBCO sample tapes resulting from the over-current pulse drive.     

Negative normal restitution coefficient found in simulation of nanocluster collisions

The oblique impacts of nanoclusters are studied theoretically and by means of molecular dynamics. In simulations we explore two models--Lennard-Jones clusters and particles with covalently bonded atoms. In contrast with the case of macroscopic bodies, the standard definition of the normal restitution coefficient yields for this coefficient negative values for oblique collisions of nanoclusters. We explain this effect and propose a proper definition of the restitution coefficient which is always positive. We develop a theory of an oblique impact based on a continuum model of particles. A surprisingly good agreement between the macroscopic theory and simulations leads to the conclusion that macroscopic concepts of elasticity, bulk viscosity, and surface tension remain valid for nanoparticles of a few hundred atoms.     

External electric field effects on fluorescence of pyrene butyric acid in a polymer film: concentration dependence and temperature dependence

Fluorescence spectra and electrofluorescence spectra (plots of the electric field-induced change in fluorescence intensity as a function of wavelength) have been measured at different temperatures for pyrene butyric acid (PBA) in a PMMA film at different concentrations. At a low concentration of 0.5 mol % where fluorescence emitted from the locally excited state of PBA (LE fluorescence) is dominant, LE fluorescence spectra show only the Stark shift in the presence of an electric field (F), which results from the difference in molecular polarizability between the ground and emitting states. At a high concentration of 10 mol % where the so-called sandwich-type excimer fluorescence (EX(1)) is dominant, both EX(1) and LE fluorescence are quenched by F. Another fluorescence assigned to a partially overlapped excimer (EX(2)) also exists at room temperature, and this emission is enhanced by F. As the temperature decreases, three fluorescence emissions whose electric field effects are different from each other become clear besides EX(1) and LE fluorescence, indicating that at least five fluorescence components exist at high concentrations at low temperatures. At a medium concentration of 5 mol % where EX(1) is comparable in intensity to the LE fluorescence, the intensity of EX(1) is not affected by F at any temperature, but LE fluorescence and EX(2) are markedly influenced by F at room temperature, and four fluorescence emissions are confirmed at low temperatures.     

Dirichlet principle using computers

In this article we shall give practical and numerical solutions of the Laplace equation on multidimensional spaces and show the numerical experiments by using computers. Our method is based on the Dirichlet principle by combinations with generalized inverses, Tikhonov's regularization and the theory of reproducing kernels.     

Subject Index to Volume 33

This paper reports the investigation of microdroplet sample preparation for phosphate, strontium and rubidium using X-ray fluorescence. Sample filter papers were prepared by drying under several different conditions and the front and the back sides of the filter papers were measured using X-ray fluorescence (XRF), scanning electron microscopy (SEM), X-ray diffraction (XRD), and electron-probe microanalysis (EPMA).

It was reported by Murata and Murokado that the elemental distribution difference between the front and the back sides after drying the filter paper led to erratic data.¹ It has been found that the intensity difference between the front and the back sides was due to the condensation of the material of interest on the surface of the filter papers and the amount of the condensed material on the filter paper was related to the temperature at which the filter paper was dried.

Optimum temperature at which a filter paper is dried and an appropriate internal standard are essential to reproducible measurements.