一维磁性光子晶体的电磁场分析和数值计算

本文探讨一维磁性光子晶体的概念和结构.提出了一种分析一维磁性光子晶体的法拉第旋转效应的电磁场方法.分析计算表明:嵌于光子晶体中的一层很薄的磁性材料将可获得比单独一层同样厚度的磁性材料大得多的法拉第旋转效应,从而从理论上验证了文献上的相关实验.同时也分析了一维磁性光子晶体用作光子晶体结构下的光隔离器等器件中的法拉第旋转器的可能.     

Preparation and electronic structure of phase pure K3C60

Phase pure K₃C₆₀ films have been grown using vacuum distillation. The structure of such films could be shown to be face centered cubic consistent with X-ray diffraction studies. The electronic structure of the films has been studied using electron energy-loss spectroscopy in transmission. From C1s core excitation measurements the unoccupied density of states has been determined. Performing the dielectric function has been derived in a wide energy range (0–45 eV). It is shown that the low energy part of the optical conductivity cannot be understood within a simple free electron model but that interband transitions between the three conduction bands have to be taken into account. The spectral weight of interband transitions between valence and conduction bands shows strong momentum dependence due to optical selection rules demonstrating the molecular-like nature of the electronic states.     

Electronic structure and resonant X-ray emission spectra of carbon shells of iron nanoparticles

The electronic structure of carbon shells of carbon encapsulated iron nanoparticles carbon encapsulated Fe@C has been studied by X-ray resonant emission and X-ray absorption spectroscopy. The recorded spectra have been compared to the density functional calculations of the electronic structure of graphene. It has been shown that an Fe@C carbon shell can be represented in the form of several graphene layers with Stone-Wales defects. The dispersion of energy bands of Fe@C has been examined using the measured C Kα resonant X-ray emission spectra.     

Electronic structure of carbyne studied by X-ray photoelectron spectroscopy and X-ray emission spectroscopy

The electronic structure of amorphous carbyne has been investigated by X-ray photoelectron spectroscopy and X-ray emission spectroscopy. Carbyne band structure has been calculated semiempirically and the experimental data have been interpreted on the basis of the calculation results. The valence band width was found to be about 20 eV which is the same as that in all other condensed carbon structures. The fine satellite structure near the 1s line of carbon has been studied. It is shown that the energy bands in carbyne are arranged in a mirror-like way relative to the Fermi level. The real carbyne structure is susceptible to conformations which affect primarily the π-subband structure.     

Effect of the anisotropy of a conducting layer on the dispersion law of electromagnetic waves in layered metal-dielectric structures

The dispersion laws of electromagnetic waves in layered periodic metal-dielectric structures with anisotropic metal layers have been theoretically analyzed. It has been found that the anisotropy of metal layers is responsible for the appearance of additional allowed energy bands for photons. It has been shown that these bands correspond to plasma (Langmuir) waves propagating in anisotropic metal layers of the structure. Conditions under which the directions of group and phase velocities of Langmuir waves coincide or are opposite have been determined. It has been shown that the penetration of the electromagnetic field of Langmuir waves into dielectric layers is exponentially weak and this field is primarily concentrated in metal layers, where it oscillates in the direction perpendicular to the plane of the layers.     

Photon avalanche upconversion and pump power studies in LaF<Subscript>3</Subscript>:Er<Superscript>3+</Superscript>/Yb<Superscript>3+</Superscript> phosphor

Hexagonal LaF₃:Er³⁺/Yb³⁺ phosphor material has been synthesized by chemical precipitation method to obtain high near-infrared to green upconversion (UC) efficiency. Its thermal, structural and fluorescence properties have been studied. UC emission bands have been observed up to 315 nm in UV region. The effect of input pump power on the intensities of various emission bands has been studied in detail and photon avalanche UC mechanism has been identified. On increasing the excitation power, some bands have shown saturation in intensity. Also, at higher pump intensities two new UC bands were observed and their origin has been discussed. The phosphor has also been tested for possible UC-based fingerprint detection.     

应用于光隔离器的一维磁光光子晶体结构探索

采用传输矩阵方法分析了一维磁光光子晶体.对不同结构参量下的磁光多层膜的光学性质进行了数值计算.得到了一种新颖实用的磁光多层膜结构,可用作实现光集成应用中的光隔离器的元件.典型磁光材料的厚度仅为2.13 μm,一维磁性光子晶体的总厚度仅为7.03 μm.     

Formation of Nanodimensional SiO2 Films on the Surface of a Free Si/Cu Film System by $${\text{O}}_{2}^{ + }$$ Ion Implantation

Technical Physics - The composition and parameters of energy bands in thin SiO2 films grown on the surface of a free Si/Cu film system have been studied. It has been shown that unlike SiO2 films...     

Theoretical and experimental studies of the interatomic spectrum induced in the mixture Rb-Xe

We have studied the fluorescence of the “blue” satellite bands associated with the forbidden transition 5S-4D of rubidium perturbed by xenon. The experimental data have been compared with theoretical results arising from an estimate of the dipole intensity induced by collisions. These bands are shown to be well correlated with the 4D level. The observed intensities justify the interpretation we have suggested. The expected population inversion between the 4D and 5P levels, when the satellite bands are pumped, has been confirmed experimentally.     

含铅空位PbWO4晶体光学性质的模拟计算

为了研究钨酸铅晶体中铅空位对光学性质的影响,利用完全势缀加平面波局域密度泛函近似,按照能量最低原理采用共轭梯度方法,对含铅空位的PbWO4(PWO)晶体进行结构优化处理。计算了含铅空位的PWO晶体的电子结构、复数折射率、介电函数及吸收光谱,并与完整的PWO晶体进行了比较。结果表明：完整的PWO晶体在可见和近紫外区域内无吸收,而含铅空位的PWO晶体在可见和近紫外区域出现2个明显的吸收峰,这2个吸收峰可分解成4个高斯线型的吸收带,它们的峰值分别为350nm、405nm、550nm和670nm。可以得出这样的推论：PWO晶体中350nm、420nm、550nm和670nm吸收带的出现都与铅空位的存在有关。     

An infrared spectroscopic study of tert-butyl peroxoesters

The infrared spectra of peroxoesters based on tert-butyl hydroperoxide and aliphatic acids, tert-butyl peroxobenzoate, and their nonperoxo analogs have been studied. The observed absorption bands have been assigned to the vibrations of individual bonds, the characteristic features of the structure of the peroxoester molecules have been investigated, and the force constants have been calculated. A set of absorption bands suitable for the identification and analysis of tert-butyl peroxoesters based on aliphatic acids has been proposed.     

Photoemission from InAs/GaAs quantum dots decorated with cesium adatoms

An array of non-overgrown InAs/GaAs quantum dots has been decorated with adsorbed metal atoms in situ in ultrahigh vacuum. Their electron and photoemission properties have been studied. The radical modification of the spectra of the threshold emission from the quantum dots with increasing cesium coating has been found. Two photoemission channels have been established; they are characterized by considerably different intensities, spectral locations, and widths of the selective bands. It has been shown that the decoration of the quantum dots makes it possible to control the electronic structure and quantum yield of photoemission, the nature of which is related to the excitation of the electronic states of the GaAs substrate and InAs/GaAs quantum dots.     

An interpretation of decoupled bands by the weak coupling model

The band structure and mechanism of formation of odd-A decoupled rotational bands are studied using the weak coupling model of de-Shalit. The geometrical relation between the spin of the core and the particle can be shown explicitly because of the fact that the interaction matrix elements are written in terms of the angle between these two spins. This scheme is shown to be a good representation in describing decoupled bands and to have wave functions with large overlaps with those resulting from the coupling scheme introduced by Stephens.     

Vibration-rotation bands of hydrogen halides dissolved in liquefied noble gases

Fundamental absorption bands of hydrogen halides have been studied in dilute solutions in liquefied Ar, Kr, and Xe. The second band moments obtained from experimental profiles are in agreement with the theoretical values for vibration-rotation bands. Extensive rotational structure of the HCl and HF bands has been recorded in Kr and Xe solutions. The observed rotational lineshifts and linewidths are compared with the available gas phase data.     

The characteristic bands of the stretching vibrations of the nitro group in infrared absorption

Correlations have been established between the values of the frequencies and intensities of the bands due to the two stretching vibrations of the nitro group and the structure of molecules. The use of band intensities extends considerably the possibilities in structural analysis, and makes it possible to distinguish reliably saturated, unsaturated, and aromatic nitro compounds and to make a more detailed differentiation between compounds within classes. It has been shown that the intensities are additive and that the intensity of one of the vibrations is highly characteristic; quantitative determination of nitro groups in molecules of unknown structure is possible.     

Optics of circularly polarized light waves in one-dimensional magneto-photonic crystals: Theory

A theory is presented for propagation of electromagnetic waves through one-dimensional magnetic Bragg structures (magneto-photonic crystals). Within the self-consistent Green-function technique the transfer matrices and magneto-optical characteristics are derived in terms of circularly polarized waves propagating in periodical arrays of alternating magnetic and dielectric layers. For finite-thickness magneto-photonic crystals, the Faraday rotation and other magneto-optical responses are demonstrated to change considerably in the spectral range of stop-bands, the magnetic modulation of the in-plane reflection intensity being essentially enhanced.     

Serrated creep and spatio-temporal structures of macrolocalized plastic deformation

The dynamics and morphology of macrolocalized deformation bands have been investigated using a complex of high-speed in situ methods under the conditions of serrated creep of flat samples of the aluminum-magnesium alloy 5456 with different aspect ratios. It has been found that, at the front of a macroscopic plastic deformation jump, a complex structure of propagating deformation bands, which are considered as macrolocalized deformation “quanta,” is spontaneously formed in the material. It has been shown that, with an increase in the sample length, the deformation behavior of the alloy tends to the state of self-organized criticality.     

Losses in the Energy of Low-Energy Electrons in Fluorene, Fluorenone, and Diiodofluorenone Vapors

Electron energy loss spectra (EELS) of fluorene, fluorenone, and diiodofluorenone vapors excited by monokinetic electrons of energies 15–50 eV have been obtained. The singlet and triplet absorption bands of these molecules have been calculated. Comparison of these bands with the experimental EELSs and optical absorption spectra has shown that the forbiddenness of singlet-triplet transitions is not completely removed in the process of interaction of molecules with electrons. The presence of heavy iodine atoms in the diiodofluorenone molecule enhances singlet-triplet transitions. Bands of overtones of stretching vibrations of the CH groups of the benzene rings have been detected near the peak of elastic scattering of electrons of the molecules studied.     

Sensitized UV luminescence from single crystals of zinc oxide

The reflection, absorption, excitation, photoluminescence, and cathodoluminescence spectra have been studied for indium-doped single crystals of ZnO. The temperature quenching of the UV-radiation bands has also been studied. These studies have made it possible to establish that the UV-radiation bands are excited during quantum absorption corresponding to “band-band” transitions and also by exciton absorption. The studies have also made it possible to calculate the activation energy of the temperature quenching. In the photoluminescence spectrum of ZnO crystals there is a wide radiation band in the 3950–4050-Å region which could be described by transitions in donor-acceptor pairs. It is shown that the band of the equidistant series at 3834 Å is complex in character.     

New band systems of NiCl in the photographic infrared

High dispersion spectrograms of NiCl, in the photographic infrared (λ6350?λ8750Å) have shown the existence of five new band systems, designated as F, G, H, I and J. The bands in all the five systems are degraded to longer wavelengths. The F, G and I systems consist of single headed bands while H and J systems consist of double headed bands. Approximate vibrational constants have been determined from the vibrational analysis. The observed structure of the bands indicates doublet-doublet transitions, as in the visible band systems of NiCl.