Fluorescence of N,N-di(2-carboxyethyl)-<Emphasis Type="Italic">p</Emphasis>-anisidine in solution and crystalline states

The fluorescence properties of N,N-di(2-carboxyethyl)-p-anisidine (I) in solvents of various nature and in the crystalline state have been studied at room temperature (273 K) and at the boiling point of liquid nitrogen (77 K). Fluorescence in aqueous solutions of I with protonated (λ _ex /λ _fl ^max = 225/290 nm) and unprotonated (λ _ex /λ _fl ^max = 270/380 nm) amino nitrogen has been detected. On going from aqueous solutions to nonaqueous, the fluorescence band of unprotonated I experiences a blue shift and its intensity rises. The fluorescence intensity of the band in aprotic polar solvents is higher than that in protic solvents. A linear dependence of the fluorescence intensity of deprotonated I on Cu(II) concentration (ranging from 1.0 to 5.0 mg/dm³) in aqueous solution has been found. The fluorescence intensity of I in aqueous solutions at 77 K and pH 1–6 has been shown to increase in the presence of Zn(II) (1–170 mg/dm³) and Cd(II) (2–330 mg/dm³) although a similar dependence is not observed at 293 K.     

Optical absorption behavior of Tl<Superscript>+</Superscript> DOPED Rb(Br<Subscript>1–<Emphasis Type="Italic">x</Emphasis></Subscript>I<Subscript><Emphasis Type="Italic">x</Emphasis></Subscript>) system

The optical absorption behavior of Tl⁺ doped Rb(Br_1–x I _x ) mixed crystals (with x = 0.00, 0.05, and 0.10) grown under vacuum by slow cooling from the melt has been studied. Absorption spectra of the mixed crystals recorded at room temperature showed that the characteristic A-absorption band of Tl⁺ ions in the Rb(Br_1–x I _x ) system (0.1 mol. %) with x = 0.00 (i.e., RbBr:Tl⁺) broadened with the iodine content towards the low energy side. Changes in the absorption spectra of the mixed crystals are due to creation of some complex centers involving Tl⁺, Br^–, and I^- ions with energy levels inside the band gap while forming the mixed crystal. The absorption spectra of gamma-irradiated mixed crystals showed the F-band, which shifted towards the low energy side due to the existence of iodine ions in the mixed crystals.     

Beat frequency intercomparisons of127I2 stabilized ion lasers at 514.5 nm

International comparisons of I₂ stabilized ion lasers operated at 514.5 nm have shown a laser frequency reproducibility of 2·10⁻¹⁰ v to 5·10⁻¹² v. These results encouraged the international acceptance of the wavelength value λ_vac=514.673467 for thea ₃ hyperfine component of the¹²⁷I₂ line 43-0P(13).     

Multi-Hamiltonian structure of kdv hierarchy by Drienfeld-Sokolov formalism

Conserved quantities and the multi-Hamiltonian structure for the integrable coupled kdv system which is associated with the isospectral flow [(∑ _i=0 ^N−1 ε _i λ ⁱ )∂² + ∑ _i=0 ^N−l V ₁λ ⁱ ]φ=λ ^N φ are deduced by the Drienfeld-Sokolov formalism.     

Temperature dependence of surface impedance of Tl2Ba2CaCu2O8−δ and YBa2Cu3O6.95 single crystals measured in the microwave band

The real part R _s and the imaginary part X _s of the surface impedance Z _s=R _s+ iX _s of Tl₂Ba₂CaCu₂O_8−δ and YBa₂Cu₃O_6.95 single crystals have been measured with high precision at frequency ω/2π=9.4 GHz in the temperature range 0<T<140 K. In the Tl₂Ba₂CaCu₂O_8−δ crystal a linear temperature dependence R _s(T) has been found for T⩽50 K, and the magnetic field penetration depth λ(4.2 K)=X _s(4.2 K)/ω μ ₀≈3760 Å has been measured. Along with well known features of the function Z _s(T) in high-quality YBa₂Cu₃O_6.95 single crystals, such as the linearity of λ(T) and R _s(T) for T<T _c/3 and a maximum of R _s(T) at T∼T _c/2, the linearity range of λ(T) extends to T≃50 K, and this curve has a plateau in the range 60<T<85 K. The curve of R _s(T) in both the superconducting and normal states of YBa₂Cu₃O_6.95 is well described by a two-fluid model with the electron-phonon mechanism of quasiparticle relaxation. A formula describing the curve of λ ²(0)/λ ²(T) throughout the studied temperature range is also given. Zh. éksp. Teor. Fiz. 112, 2210–2222 (December 1997)     

Non-steady-state photo-EMF in nanostructured GaN and polypyrrole within porous matrices

We report an experimental investigation of the non-steady-state photoelectromotive force in nanostructured GaN within porous glass and polypyrrole within chrysotile asbestos. The samples are illuminated by an oscillating interference pattern created by two coherent light beams and the alternating current is detected as a response of the material. Dependences of the signal amplitude versus temporal and spatial frequencies, light intensity, and temperature are studied for two wavelengths λ=442 and 532 nm. The conductivity of the GaN composite is measured: σ=(1.1–1.6)×10⁻¹⁰ Ω⁻¹ cm⁻¹ (λ=442 nm, I ₀=0.045–0.19 W/cm², T=293 K) and σ=(3.5–4.6)×10⁻¹⁰ Ω⁻¹ cm⁻¹ (λ=532 nm, I ₀=2.3 W/cm², T=249–388 K). The diffusion length of photocarriers in polypyrrole nanowires is also estimated: L _D=0.18 μm.     

High-spin states in 160Lu

High-spin states of ¹⁶⁰Lu have been studied through the ¹⁴⁴Sm( ¹⁹F, 3n) reaction. The previously known πh _11/2⊗υi _13/2 yrast band is extended from I ^π = 21^- to 25^- and a four quasiparticle band with configuration πh _11/2[523]7/2 ^-⊗υh _9/2[521]3/2 ^-⊗ (υi _13/2)² is reported. Received: 21 May 2001 / Accepted: 19 July 2001     

Ionic photoconductivity of RbAg4I5 superionic crystals

A new effect of illumination on ionic conductivity and activation energy of migration of mobile Ag⁺ cations in RbAg₄I₅ superionic crystals has been detected and studied. Reversible changes in the ionic conductivity due to illumination of superionic crystals are caused by reversible changes in the structure of electronic centers caused by elastic strain around these centers. The effect of elastic deformation on the process of ionic transport and activation energy for diffusion of mobile silver cations has been studied. Photostimulated recovery of the ionic conductivity after its change due to preliminary illumination of a RbAg₄I₅ superionic crystal with light of wavelength λ≃430 nm has been detected. This recovery of the ionic conductivity is due to excitation of centers in complexes generated by previous illumination of tested samples. Zh. éksp. Teor. Fiz. 112, 698–706 (August 1997)     

Oscillator rule of the trap activation energies in NaCl crystals

The energy spectra of traps in NaCl crystals have been studied in detail by the method of thermoluminescence. Crystals of NaCl were undoped but treated thermally in different ways. The activation energies of traps form a single oscillator series, E _n =ℏω _TL (n+1/2), ℏω _TL =903 cm^-1. Contrary to other previously studied crystals with complex lattices, the corresponding line ℏω _Ram =ℏω _TL was not found in Raman spectra of NaCl. It is assumed that the oscillator rule is governed by the polaron nature of traps. The trap activation energy is determined by the vibration level from which the transition of the charge carrier to the excited luminescence centre is made possible and depends on the distance between these centres.     

The nonlinear optical susceptibility and electro-optic tensor of ferroelectrics: first-principle study

The nonlinear optical properties of some ABO₃ materials (BaTiO₃, KNbO₃, LiTaO₃ and LiNbO₃) are studied by density functional theory (DFT) in the local density approximation (LDA) expressions based on first-principle calculations. Our goals are to give the details of the calculations for linear and nonlinear optical properties, including the linear electro-optic (EO) tensor for some ABO₃ structures with oxygen octahedral structures using first-principles methods. These results can then be used in the study of the physics of ferroelectrics, specifically, we present calculations of the second harmonic generation response coefficient X _ijk ⁽²⁾ (−2ω, ω, ω) over a large frequency range for ABO₃ crystals. The electronic linear EO susceptibility X _ijk ⁽²⁾ (−ω, ω,0) is also evaluated below the band gap. These results are based on a series of the LDA calculations using DFT. Results for X _ijk ⁽²⁾ (−ω, ω,0) are in agreement with experiments below the band gap. The results are compared with the theoretical calculations and the available experimental data.     

Light induced phenomena in superionic crystals

The phenomena of the reversible transformation of concentration and a structure of luminescence centers and of the concentration of mobile silver ions in local irradiated region of RbAg₄I₅ superionic crystals are studied. A new effect of illumination on ionic conductivity and activation energy of migration of mobile Ag⁺ cations in RbAg₄I₅ superionic crystals are observed. Reversible changes in the ionic conductivity due to illumination of superionic crystals are caused by reversible change in the structure of electronic centers caused by elastic strain around these centers. The effect of elastic deformation on the process of ionic transport and activation energy for diffusion of mobile silver cations are studied. Photostimulated recovery of the ionic conductivity after its change due to preliminary illumination of a RbAg₄I₅ superionic crystal with light of wavelength λ=430 nm are detected. This recovery of the ionic conductivity is due to excitation of centers in complexes generated by previous illumination of tested samples.     

Theoretical investigations of rotational phenomena and dielectric properties in a nematic liquid crystal

The molecular dynamics (MD) simulation, based on a realistic atom-atom interaction potential, was performed on 4-n-pentyl-4'-cyanobiphenyl (5CB) in the nematic phase. The rotational viscosity coefficients (RVCs) γ _i, (i = 1, 2) and the ratio of the RVCs λ = - γ ₂/γ ₁ were investigated. Furthermore, static and frequency-dependent dielectric constants and ε were calculated using parameters obtained from the MD simulation. Time correlation functions were computed and used to determine the rotational diffusion coefficient, D _⊥. The RVCs and λ were evaluated using the existing statistical-mechanical approach (SMA), based on a rotational diffusion model. The SMA rests on a model in which it is assumed that the reorientation of an individual molecule is a stochastic Brownian motion in a certain potential of mean torque. According to the SMA, γ _i are dependent on the orientational order and rotational diffusion coefficients. The former was characterized using: i) orientational distribution function (ODF), and ii) a set of order parameters, both derived from analyses of the MD trajectory. A reasonable agreement between the calculated and experimental values of γ _i and λ was obtained. Received 22 March 2000 and Received in final form 8 October 2000     

Continuous frequency up-conversion in a double-Λ scheme of Na2

 In a double-Λ level configuration of Na₂ molecules, involving rotational–vibrational levels of the X, A and B bands, continuous resonant frequency mixing ω₄=ω₁−ω₂+ω₃ is demonstrated. A DCM dye laser at 661 nm (λ₁) pumps a molecular Raman laser at 746 nm (λ₂) in a sodium heatpipe, which is used to generate the molecular vapour. In the same heatpipe, both fields are mixed with the radiation of an argon-ion laser at 514 nm (λ₃) to generate up-converted laser radiation at 473 nm (λ₄). For laser powers of 200 mW (λ₁), 700 mW (λ₂, internal power) and 140 mW (λ₃), an output power of 120 μW (λ₄) has been achieved. Dependences of the generated radiation on the pump fields (powers and detunings) and polarization features are presented; influences of coherent coupling and population transfer mechanisms are discussed. Received: 7 October 1996     

Laser-initiated ignition of hydrogen-air mixtures

The subject of investigation is the kinetic mechanisms intensifying chain reactions that proceed in a hydrogen-air mixture when O₂ molecules dissociate under the action of laser radiation with wavelength λ _I = 193.3 nm and are excited into the b ¹Σ _g ⁺ electron state by radiation with λ _I = 762.346 nm. The efficiencies of both methods to initiate ignition are compared. Numerical simulation shows that the ignition temperature for the laser-induced excitation of O₂ molecules into theb ¹Σ _g ⁺ state is lower than for the dissociation of O₂ molecules by UV laser radiation, with the energy supplied to the mixture being the same. However, both photochemical methods are much more efficient than mere heating of the mixture by laser radiation or another source of heat.     

Parametrical conversion of the frequency of organic lasers into the middle-IR range of the spectrum

The possibility of parametrical conversion of visible radiation of solid-state organic lasers into the middle-IR range of the spectrum in nonlinear GaSe_1–x S _x (x = 0‒0.13) crystals is investigated. Generation at the difference frequency (wavelength λ₃ = 9.43 μm) of induced oxazine-1 (at λ₁ = 740 nm) and rhodamine-800 (λ₂ = 803.4 nm) radiation is excited. The conversion efficiency is estimated, and prospects for its further increase are demonstrated.     

Two-electron excitations in helium-like ions by inelastic photon scattering

Inelastic photon scattering by helium atoms and helium-like ions with simultaneous excitation of the two-electron transition 1s ²→2s ² is examined in the nonrelativistic energy range I≪ω≪m (I is the ionization potential, ω is the photon energy, m is the electron mass, and ℏ=c=1). The electrons are assumed to be moving in the Coulomb field of the nucleus, and the electron-electron interaction is taken into account in the lowest perturbation order. The differential and total cross sections of the process and the autoionization width of the 2s ² energy level are calculated. The numerical value of the autoionization width is found to agree with the results of the more rigorous calculations of other researchers. Zh. éksp. Teor. Fiz. 113, 539–549 (February 1998)     

Magnetism,exchange and crystal field parameters in the orbitally unquenched Ising antiferromagnet FePS3

FePS₃ is a layered antiferromagnet (T _N=123 K) with a marked Ising anisotropy in magnetic properties. The anisotropy arises from the combined effect of the trigonal distortion from octahedral symmetry and spin-orbit coupling on the orbitally degenerate⁵ T _2g ground state of the Fe²⁺ ion. The anisotropic paramagnetic susceptibilities are interpreted in terms of the zero field Hamiltonian, ℋ=Σ_i [δ(L _iz ² −2)+|λ|L _i .S _i ]−Σ _ij J _ij S _i .S _j . The crystal field trigonal distortion parameter Δ, the spin-orbit coupling λ and the isotropic Heisenberg exchange,J _ij, were evaluated from an analysis of the high temperature paramagnetic susceptibility data using the Correlated Effective Field (CEF) theory for many-body magnetism developed by Lines. Good agreement with experiment were obtained for Δ/k=215.5 K; λ/k=166.5 K;J _nn k=27.7 K; andJ _nnn k=−2.3 K. Using these values of the crystal field and exchange parameters the CEF predicts aT _N=122 K for FePS₃, which is remarkably close to the observed value of theT _N. The accuracy of the CEF approximation was also ascertained by comparing the calculated susceptibilities in the CEF with the experimental susceptibility for the isotropic Heisenberg layered antiferromagnet MnPS₃, for which the high temperature series expansion susceptibility is available.     

Amplitude gratings generation by selective defect bleaching in KCl:CO<Subscript>3</Subscript>K<Subscript>2</Subscript> crystals

Volume grating formation by spatially-selective defect bleaching is demonstrated in coloured KCl:CO₃K₂ crystals. The sample is coloured by a train of pulses with a wavelength of λ= 266 nm and bleached with a cw Ar-laser with a wavelength of λ= 514.5 nm. Diffraction efficiency for a 1.6 μm grating period is studied both experimentally and theoretically, using the evolution of colour centre concentration. Hologram recording parameters are obtained and the evolution of the spatial grating profile is discussed. Diffraction efficiencies three times higher than previously published efficiencies are obtained. PACS 42.40.Ht; 42.40.Lx; 42.70.Ln     

Breit–Wigner Approximation and the Distribution¶of Resonances

For operators with a discrete spectrum, {λ _j ²}, the counting function of λ _j 's, N (λ), trivially satisfies N ( λ+δ ) −N ( λ−δ ) =∑ _j δ_{λ j} ((λ−δ,λ+δ]). In scattering situations the natural analogue of the discrete spectrum is given by resonances, λ _j ∈ℂ₊, and of N (λ), by the scattering phase, s(λ). The relation between the two is now non-trivial and we prove that

Photoluminescence of ZnS:Cu crystals at various concentrations of copper

Doping of ZnS crystals with background impurities and ZnS:Al crystals by various concentrations of copper from a bismuth melt has been carried out. The photoluminescence spectra of the starting ZnS crystals annealed in the bismuth melt and doped by copper have been investigated. Interpretation of the experimental results according to the model in which the associates (Cu _Zn ^′ Cu _i ^● ) are responsible for the B-Cu band (≈460 nm) and the donor—receptor pairs [Cu _i ^● -(Cu _Zn ^′ Cu _i ^● )] are responsible for the G-Cu band (≈505 nm) is given. It is assumed that doping by copper from a bismuth melt is accompanied by the separation of a Cu_xS-type phase. It has been shown that heat treatment of ZnS crystals in the Bi melt does not lead to the appearance of luminescence centers based on Bi_Zn, Bi_S, and Bi_i. __________ Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 72, No. 6, pp. 794–798, November–December, 2005.