Boltzmann spectral distribution or “infrared catastrophe” in the resonance radiation of a gas

The purely thermal infrared emission spectra of a resonance medium (sodium vapor) are investigated experimentally. It is shown that the emission intensity in the 2–3 μm range at temperatures of 600–1200 K is several orders of magnitude higher than the intensity obtained from the standard theory of resonance radiation transfer. This phenomenon can be conventionally termed an “infrared catastrophe.” The form of the recorded spectra and the absolute intensity of the emission in both the infrared and visible regions of the spectrum are in agreement with the theory developed by Yu. L. Zemtsov and A. M. Starostin, Zh. éksp. Teor. Fiz. 103, 345 (1993) [JETP 76, 186 (1993)], in which the Boltzmann spectral distribution of the population of the resonance level is proportional to exp(−ħω/T). Pis’ma Zh. éksp. Teor. Fiz. 65, No. 11, 807–811 (10 June 1997)     

Lasing on the resonance transition in sodium atoms under nonresonant optical excitation

Coherent emission on the 3P–3S resonance transition (D line) of nonresonantly excited sodium atoms in a buffer gas atmosphere is studied experimentally and theoretically. Both forward and backward coherent emission on the D lines is observed relative to the propagation direction of a pump beam whose frequency is blue-shifted from resonance. The divergence of the emitted radiation does not exceed that of the pump beam. The emission is due to the population inversion created on the “operating” transition when the pump is far detuned from resonance and the buffer gas pressure is sufficiently high. It is found that both emission intensity and the detuning range where this phenomenon is observed increase with the buffer gas pressure.     

The effect of electron irradiation on the optical properties of the natural armenian zeolite-clinoptilolite

Infrared (IR) absorption and luminescence in chemically and radiation-modified natural Armenian Zeolite (clinoptilolite) samples have been studied. The luminescence was studied in 390–450 nm and 620–710 nm wavelength bands, and the IR measurements were carried out in the 400–5400 cm⁻¹ range. It is shown that the luminescence intensity depends on the content of pure clinoptilolite in the samples and, probably on the distribution of “passive” luminescence centers over Si and Al sites that became “active” under radiation or chemical treatment. The samples of electron irradiated clinoptilolite have higher luminescence intensity than the chemically and thermally treated ones. A decrease in the intensity of IR absorption bands at 3550 cm⁻¹ and 3650 cm⁻¹ was found after irradiation.     

Nuclear resonant scattering using synchrotron radiation

A one-dimensional quantum model for nuclear resonant scattering using synchrotron radiation has been developed. This model gives a clear physical interpretation of the most prominent features of the coherent forward scattering process namely, the “speed-up” and “dynamical beat” effects. The form of the solution, for the time-dependent forward scattered intensity of the resonant radiation from the resonant medium after synchrotron radiation excitation, is a finite series. This unique solution can be interpreted in terms of a summation over all multiple forward scattering paths the radiation takes in reaching the detector. The resonant medium is represented by a linear chain of N effective resonant nuclei. The analysis starts from a coupled set of quantum mechanical equations for the relevant amplitudes in frequency space. Transformation to the time domain gives an analytical expression for the forward scattered intensity. The contribution of every order of the multiple scattering processes from the N effective nuclei appears naturally. The expression gives a clear physical understanding of all relevant aspects of resonant forward nuclear scattering. Furthermore, the present formalism allows the consideration of incoherent processes. This permits the study of processes in which there is gamma emission with recoil or emission of internal-conversion electrons. This revised version was published online in August 2006 with corrections to the Cover Date.     

Low-voltage low-temperature electroluminescence of CdF2-RE thin films

Different electroluminescence spectrums of the blueλ _max =420 nm wide-banded low-temperature low-voltage radiation of CdF₂-RE films at different levels of excitation in the region of temperatures of 77–300K are investigated. The kinetic characteristics and temperature dependence of this radiation are explored. An effect of the resonance interaction of the centers of luminescence of the wide-band and line radiation of the RE-centers is found. A model of the center of the wide-band radiation is suggested. It is shown that the “blue” radiation is caused by recombination of the carriers. Institute of Physics of Semiconductors of the National Academy of Sciences of Ukraine, Nauka Ave., 45, 252028, Kiev. Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 66, No. 1, pp. 127–132, January–February, 1999.     

Kinetics and Optical Properties of the Strongly Driven Gas Medium of Interacting Atoms

This paper investigates stimulated emission and absorption near resonance for a driven system of interacting two-level atoms. Microscopic kinetic equations for the density matrix elements of N-atom states including atomic motion are built, taking into account atom-field and atom-atom interactions. Analytical solutions are given for the resulting macroscopic equations in different limits, for a system composed of a strong coherent “pump” field and a weak counter-propagating “probe” field. It was shown that the existence of a dipole-dipole (long-range) interaction between atoms separated by distance less than the pump wave-length can cause the formation of periodic polarization and population structures (gratings in time and space) in the pumped medium without a probe field. The magnitude of pump induced population grating can have a strong dependence on the relation between the pump field detuning and the polarization decay rate. The “interaction” between pump and probe induced polarization/population gratings through a dipole-dipole interaction mechanism causes the absorption line shape asymmetry. Under certain conditions, this asymmetry is revealed in increasing probe gain for the “red”-shifted (relative to pump) probe and suppressing the gain for the “blue”-shifted probe field when pump is “red”-shifted relative to the ensemble averaged resonant frequency. The theoretical results are consistent with experimental data for the probe gain or absorption as the function of frequency and the dependance of the gain on atomic density for sodium vapor when the pump laser is tuned near the D ₂ line. Here the dependance of gain on particle density was explained in the terms of the long-range interaction between the atoms.     

Resonance luminescence of a nonuniformly heated dense vapor

The thermal luminescence spectra of a dense, nonuniformly heated resonance medium (sodium vapor) are investigated experimentally under conditions when the resonance corrections to the relative permittivity are not small compared to unity and the photon mean free path is comparable to the wavelength of the radiation. The shape of the recorded spectra agrees well with a previously developed general theory of resonance radiation transfer which predicts a strong asymmetry of the spectra. The prospects for performing more-sensitive measurements in order to make a quantitative check of the theoretically predicted anomalous intensity (an order of magnitude higher than in the standard theory of resonance radiation transfer) of the radiation from a dense nonuniform medium are discussed. Pis’ma Zh. éksp. Teor. Fiz. 65, No. 1, 15–19 (10 January 1997)     

Manifestation of outgoing resonance in stokes and anti-stokes spectra of ZnTe and ZnMgTe quantum wires

The spectra of resonant light scattering by ZnTe quantum wires have been measured at excitation energies of 2.18–2.72 eV. The quantum wires have been grown on Si(100) and GaAs(100) substrates by molecular beam epitaxy. The effect of outgoing resonance with the electron transition energy E ₀ on the intensity of phonon lines of the Stokes spectrum and on the intensity ratio of the Stokes and anti-Stokes spectral lines has been studied. The energy E ₀ has been determined in ZnTe and ZnMgTe quantum wires from the edge luminescence spectra.     

Ultraviolet gas-discharge lamp on iodine molecules

The emission characteristics of a pulsed-periodic UV radiation source are reported. The source excited by a pulsed-periodic capacitive discharge initiated in helium-iodine vapor, neon-iodine vapor, or krypton-iodine vapor mixtures radiates in the spectral range 200–450 nm. It is shown that most of the plasma radiation power concentrates in the integral line of the iodine atom (206.2 nm) and in the D′-A′ band of the iodine molecule with a maximum at 342 nm. The radiation intensity of the lamp is optimized in accordance with the partial pressure of the inert gases. The discharge plasma parameters that are of interest for simulating the process kinetics and the output characteristics of an UV source based on molecular iodine, atomic iodine, and xenon iodide are calculated in helium-iodine vapor and xenon-iodine vapor mixtures.     

Ultraviolet radiation sources on (H2O,D2O) water vapor

Emission characteristics of ultraviolet (UV) radiation from water vapor (H₂O, D₂O, and a mixture of H₂O and D₂O vapors) excited by pulse-periodic discharges with open electrodes, as well as electrodes outside the discharge tube (capacitive discharge), are presented. Radiation is studied in a spectral range of 175–350 nm. The emission characteristics of a UV radiation source based on vapors of ordinary and “heavy” water, as well as the results of optimization of brightness of radiation bands from the OH and OD radicals as functions of pressure and the composition of the He-H₂O and He-D₂O mixtures, are reported.     

Luminescence of fluctuation tails of disordered solid solutions

The form of the stationary luminescence spectra of excitons, localized by composition fluctuations, in disordered solid solutions under weak excitation is calculated. The tail states for which there are no nonradiative transition channels are distinguished by means of continuum percolation theory. Such states are responsible for the “zero-phonon” luminescence band. The shape of the short-wavelength luminescence band edge is determined mainly by the number of isolated localizing clusters and their smallest complexes, which decreases rapidly near the mobility threshold. The real luminescence spectrum is due to the simultaneous emission of phonons. The phonon emission determines the form of the long-wavelength wing of the emission band. The computed shape of the emission spectrum is compared with the experimental luminescence spectra of the solid solution CdS_(1−c)Se_c. Pis’ma Zh. éksp. Teor. Fiz. 65, No. 3, 274–279 (10 February 1997)     

Spectral and kinetic properties of fluorescence of immunoactive steroids in the gas phase

We have used steady-state fluorescence spectroscopy and pulsed kinetic fluorimetry with high time resolution to experimentally study the spectral and temporal characteristics of luminescence of immunoactive 8-aza-D-homogona-1,3,5(10), 13-tetraene-12,17a-dione (8-aza-D-homogonane) molecules in the gas phase. We have established the existence of several centers emitting long-wavelength and short-wavelength fluorescence. The fluorescence of high-temperature 8-aza-D-homogonane vapor (T = 550 K) when excited by radiation with λ_ex = 266 nm is represented by two spectrally separated emission bands with maxima λ _max ^fl = 465 nm and λ _max ^fl = 365 nm. Analysis of the distribution of fluorescence decay times for 8-aza-D-homogonane showed that in the spectral range of the emission wavelengths 360–590 nm, the fluorescence decay kinetics contains three components with average lifetimes <200 psec, 2.8 nsec and 13.5 nsec. The multicenter nature of luminescence of 8-aza-D-homogonane was confirmed by direct measurements of instantaneous fluorescence spectra in different stages of luminescence decay. __________ Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 73, No. 3, pp. 309–314, May–June, 2006.     

Multi-bubble sonoluminescence of phosphoric acid

Multi-bubble sonoluminescence spectra of 85% H₃PO₄ and the dependences of sonoluminescence intensity on the acid concentration and temperature are obtained. The spectra contain a weakly structured 300–600-nm band formed by the superposition of radiation from several emitters (presumably, oxygencontaining products of acid sonolysis, viz., PO, HOPO, and PO₂). Weak luminescence at a wavelength exceeding 600 nm can be due to emission from excited O* and Ar* atoms. The shape of the fundamental band changes upon a transition from multi-bubble sonolysis to sonolysis in the setup for one-bubble sonoluminescence, in which several clusters of cavitation bubbles are formed in a spherical flask at ultrasonic frequencies multiple of the first acoustic resonance frequency (multi-cluster sonoluminescence). The form of the temperature dependence of the sonoluminescence intensity depends on the detection regime: for natural heating of 85% acid under the action of ultrasound, a curve with a luminescence peak at 40°C is observed, while in detection with preliminary thermostating “over points,” only an inflection exists on a monotonic curve describing a decrease of intensity upon heating. An analogous curve for acids with a lower viscosity (hydrochloric and nitric acids) has neither a peak nor inflection irrespective of the detection regime. It is concluded that the viscosity of phosphoric acid plays a decisive role in the evolution of cavitation and in obtaining intense sonoluminescence.     

Photoluminescence and multiphonon resonant Raman scattering in Ni-and Co-doped Zn1−x MnxTe crystals

Low-temperature photoluminescence, exciton reflection, and multiphonon resonant Raman scattering spectra of Ni-and Co-doped Zn_1−x Mn_xTe crystals were investigated. Intense emission occurs in a broad spectral region (1100–17 000 cm⁻¹) in the crystals containing Ni atoms. It is caused by intracenter transitions involving Mn²⁺ ions and transitions between the conduction band and a level of the doubly charged acceptor. The features of the exciton photoluminescence and multiphonon resonant Raman scattering involving longitudinal-optical (LO) phonons at various temperatures are investigated. The insignificant efficiency of the localization of excitons on potential fluctuations in the Zn_1−x Mn_xTe:Co crystals is established. A temperature-induced increase in the intensity of the 5LO multiphonon resonant Raman scattering line due to the approach of the conditions for resonance between this line and the ground exciton state is observed in these crystals. Fiz. Tverd. Tela (St. Petersburg) 40, 616–621 (April 1998)     

Stimulated infrared emission under excitation of condensed molecular dielectrics with giant pulses of a ruby laser

Stimulated infrared (IR) emission from a condensed dielectric medium under exposure to a giant pulse of a ruby laser is reported. This effect was predicted in the theoretical paper [1]. Experimental studies were carried out for a number of molecular liquids in two experimental geometries. In the first case (“in transmission” geometry) the propagation direction of the detected IR radiation coincided with that of the exciting radiation. In the second case IR radiation generated was detected in the opposite direction. The angle of divergence of IR radiation was found to be of 10⁻² rad, while the conversion efficiency with respect to the pumping intensity depended on the type of molecular liquid and varied in the range of 0.05–0.6%. Possible microscopic mechanisms of generation of IR radiation under pumping of the dielectric medium with visible or ultraviolet (UV) radiation are analyzed.     

Intrinsic luminescence of amorphous and disordered crystalline systems

A unified method is developed for describing the steady-state luminescence of exciton fluctuation states for weak excitation in different disordered systems. The phononless luminescence band is found to be formed by “radiative” states of the fluctuation tail in the density of states, i.e., by states for which nonradiative states are either nonexistent or have a low probability. The shape of the emission spectra calculated including the phonon interaction is in good agreement with experimental luminescence spectra of α Si:H and of solid solutions of ZnSe_(1−c)Te_c and CdS_(1−c)Se_c. Fiz. Tverd. Tela (St. Petersburg) 40, 890–891 (May 1998)     

Wide colour gamut generated in triply lanthanide doped sol–gel nano-glass–ceramics

The generation of a wide colour gamut, based on up-conversion of cheap near-infrared photons into the visible range, is of great importance for general lighting appliances and integrated optical devices. Here, we report for the first time on up-conversion luminescence under infrared excitation at 980 nm in Yb³⁺–Er³⁺–Tm³⁺ triply doped sol–gel derived SiO₂–LaF₃ based nano-glass–ceramics (SOL-YET), containing LaF₃ nanocrystals with a size about 13 nm. Efficient simultaneous up-conversion emission of the three primary colours (blue, green and red) gives rise to a balanced white overall emission. The ratio between up-conversion emission bands can be varied by changing pump power intensity resulting in colour tuneable up-conversion phosphor.     

<Emphasis Type="Italic">Y</Emphasis> and <Emphasis Type="Italic">Z</Emphasis> luminescence of polycrystalline cadmium telluride

The properties of polycrystalline CdTe with a grain size of 5–30 μm have been investigated using the microphotoluminescence methods of spectral analysis and topography. This material has been prepared by direct synthesis in a vapor flow of components at a low temperature. The dominance of the Y and Z bands in the spectra reflects a nonequilibrium character of the crystallization processes. The superlinear dependences of the luminescence intensity on the level of the band-to-band excitation indicate the exciton nature of the corresponding transitions. The activation energies for temperature quenching of luminescence in the temperature range T = 100–150 K are found to be 120 meV for the Y luminescence and 180 meV for the Z luminescence, which correspond to the dissociation of excitons bound to defects with the transition of charge carriers to the conduction and valence bands. The monochromatic topography data indicate that Y and Z defects have different material bases.     

Luminescence and selective heat radiation of Yb<Subscript>2</Subscript>O<Subscript>3</Subscript> upon the resonant and thermal laser excitation

Yb₂O₃ polycrystals with a size of up to 10 mm are synthesized using the sintering and melting of the ultrapure Yb₂O₃ powders by the CO₂-laser radiation with the power P _L ≤ 100 W at the wavelength λ = 10.6 μm at the melting point T _m = 2703 K, forming due to surface tension in melt, and crystallization in air. The analysis of the polycrystal microstructure using the methods of optical and electron microscopy and X- ray diffractometry shows that perfect oxide crystallites are formed in the course of crystallization after melting-through. The transformation of the luminescence and selective heat radiation (SHR) spectra of the Yb₂O₃ polycrystals is studied under the resonant excitation at λ ≈ 975 nm using a laser diode and the laser heating at the wavelength λ = 10.6 μm. When the resonant excitation power of the Yb³⁺ ions increases from 0.15 to 4.5 W, the Stokes luminescence of the Yb₂O₃ polycrystals is sequentially transformed into SHR and the thermal radiation of the crystal lattice. The transformation of the emission spectra of the Yb₂O₃ polycrystals with an increase in the laser heating intensity by about four orders of magnitude can be represented as the low-temperature heat radiation, spectral burst of the thermodynamically nonequilibrium SHR of the Yb³⁺ ions, and the high-temperature radiation of the crystal lattice. The temperature dependence of the luminescence spectra and SHR of the Yb₂O₃ polycrystals on the intensity of the laser and laser-thermal excitation and the concentration quenching of the Yb³⁺ luminescence in oxides indicate the key role of the interaction of the f-electron shell of the Yb³⁺ ions with the natural oscillations of the crystal lattice in the processes of the multiphonon excitation and nonradiative (multiphonon) and radiative (vibronic) relaxation.     

Nonlinear Thomson scattering of an ultrashort laser pulse

The nonlinear scattering of an ultrashort laser pulse by free electrons is considered. The pulse is described in the “Mexican hat” wavelet basis. The equation of motion for a charged particle in the field of a plane electromagnetic wave has an exact solution allowing, together with the instant spectrum approximation, the calculation of the intensity of nonlinear Thomson scattering for a high-intensity laser pulse. The spectral distribution of scattered radiation for the entire pulse duration is found by integrating with respect to time. The maximum of the emission spectrum of a free electron calculated in 10¹⁹–10²¹ W/cm² fields lies in the UV spectral region between 3 and 12 eV. A part of the continuous spectrum achieves high photon energies. One percent of the scattered energy for the field intensity 10²⁰ W/cm² is concentrated in the range ħω > 2.7 × 10² eV, for a field intensity of 10²¹ W/cm² in the range ħΩ > 7.9 × 10² eV, and for an intensity of 10²² W/cm² in the range ħΩ > 2.45 × 10⁵ eV. These results allow us to estimate nonlinear scattering as a source of hard X-rays.