Control of radiation spatial coherence under synchronous amplification in crystalline LiF:F 2 − amplifier

A technique of spatial coherence control, based on the synchronous amplification of a radiation in LiF crystals with F ₂ ^? color centers, is demonstrated. Spatial radiation distributions of stimulated Raman scattering (SRS) in oxide crystals were investigated under picosecond laser excitation. Low spatial radiation coherence was revealed for both the transient and quasi-stationary SRS. Spatially incoherent SRS was transformed to spatially coherent radiation as a result of phase—locked picosecond synchronous laser pumping of nonlinear Raman and LiF: F ₂ ^? crystals and the Stokes radiation amplification in the color center crystal.     

Application of LiF crystals with F 2 − colour centers

It is shown that LiF crystals with F ₂ ^? colour centers may be used in lasers for cavity Q-switching and in high-power Nd: glass laser systems for, increasing the contrast and the self-excitation threshold. Also Lif crystals with F ₂ ^? centers are successfully used for the generation of ultrashort pulses, for the generation of difference frequencies in the ir spectral range and in intracavity spectroscopy experiments.     

Tunable laser via F 2 + and F 2 − colour centers in the spectral region 0.88–1.25 μm

Frequency-tunable generation by means of F ₂ ⁺ and F ₂ ^? colour centers in a LiF crystal is reported. Colour centers were created by illuminating LiF crystals with electrons of 3 meV energy at the electron current density of 1 μA/cm². The pumping source was a ruby laser with a peak power of 20 MW, a pulse duration of 20 ns, and a repetition rate of 1 Hz. The frequency tuning is obtained in the range of 0.88–1.25 μm. Discussed are the ways of pumping of colour centers and the possibility of lasing in the spectral region of 0.85 to 2 μm in the type of colour centers under investigation.     

Radioluminescence of ionized electron color centers in LiF crystals

Photoluminescence (PL) and temporal variation of optical absorption and radioluminescence (RL) of LiF crystals after irradiation with an electron impulse are investigated by pulse spectrometry methods using different irradiation regimes and different degrees of initial radiation damage. The difference in the RL and PL characteristics of ionized F ₂ ⁺ and F ₃ ⁺ centers is revealed. Several mechanisms for inducing these centers by irradiation, which differ in energy and kinetic parameters and in temperature dependence, are proposed. It is established that the ionized centers in the radiation active state are created due to the interaction of the respective neutral centers with holes of different thermalization extent. A mechanism for the excitation of these radiation-active centers is proposed.     

Electronic color centers in SrF2-Na crystals

It was shown that optical bleaching of M _A ⁺ color centers at 80 K in SrF₂-Na crystals causes the core of an M _A ⁺ -center to transform into the V _a ⁺ Me ⁺ V _a ⁺ configuration, in which all three point defects are arranged diagnonally in the cube cell. Reirradiation of an optically bleached crystal by x-rays generates F _D centers in it: V _a ⁺ Me ⁺ V _a ⁺ + e ^? → V _a ⁰ Me ⁺ V _a ⁺ ≡ F _D. The F _D → M _A ⁺ transformation in SrF₂-Na crystals proceeds at T = 135 K, in contrast to the F _A → M _A ⁺ transformations, which take place at T > 200 K.     

Dual nature of RN-centers in LiF crystals

An alternative model of the N_c-center as a complex defect consisting of the F ₂ ⁺ -center perturbed by the F_L defect (where F_L is Li⁰ in the F-center) is confirmed by the methods of optical spectroscopy and X-ray diffraction analysis of LiF crystals. Upon selective optical excitation, these centers are decomposed into F₂ and F_L defects.     

Relaxation processes in colored crystals of LiF after the coaction of UV radiation and a shock wave

The relaxation of F ₂ ⁺ centers in radiation-colored crystals of lithium fluoride starting from the moment of the coaction of pulsed UV irradiation and a shock wave is investigated. It is shown that the annealing curve of these centers displays a nonmonotonic character at room temperature and is a consequence of three + processes. The first two are the processes of disintegration of unstable (short-lived) and stable F ₂ ⁺ centers, and the third process involves the formation of stable centers upon a random encounter of appropriate constituents in the course of their diffusive wandering over the lattice.     

Mechanisms of ionization of <Emphasis Type="Italic">F</Emphasis><Subscript>2</Subscript>-centers in laser media on the basis of LiF crystals

F₂ color centers with a superhigh concentration (5000-cm^–1 absorption coefficient at 450 nm) were formed by high-density electron beams in a layer of LiF crystals of micrometer thickness. The F₂-centers excited by high-power nanosecond wide-band optical pulses (the “soft” pumping regime) efficiently amplified the laser radiation and showed high stability under these conditions. A low stability of F₂-centers to laser radiation (the “hard” excitation regime) is explained by the dissociation of (F ₂ ⁺ , F^–) pairs induced by two-step ionization of F₂-centers: (2hν > 4.5 eV) → F₂ → (F₂)* → F ₂ ⁺ + e; F + e → F^–; F ₂ ⁺ + F^– → 3F.     

Near resonance charge transfer from a laser excited donor state

A laser induced charge transfer from Na(3p) to hydrogen-ions at different kinetic energies has been studied. An enhancement factor of about 90% in the production rate of Lyman-α radiation has been demonstrated to occur only with H⁺ and Na(3p) atoms reaction; no enhancement was observed with either H ₂ ⁺ or H ₃ ⁺ ions. Absolute cross-section for the production of Lyman-α radiation during the collision of H⁺, H ₂ ⁺ and H ₃ ⁺ ions and Na(3p) and Na(3s) atoms have been measured in the energy range 1–600eV. The charge exchange reactions involving hydrogen-ions and Na(3p) atoms created by two different methods have also been compared.     

Radiation phenomena in microinhomogeneous structures of flouroaluminate glass-like materials

The simulation of the fluoroaluminate matrix with small additives of phosphates has made it possible to create low-scattering glasses with a wide transparency window in the infrared region and to study the fundamental problem on the formation of radiation defects typical for the phosphate matrix (PO ₃ ^2? hole, PO ₃ ^2? electron, and PO ₄ ^2? hole defects). By comparing the spectra of induced optical absorption, electron paramagnetic resonance, and Raman scattering, it has become possible to investigate the generation of defects in the course of the successive formation of the phosphate matrix in fluoroaluminate glass. The feasibility of the formation of PO ₄ ^2? hole centers both in single tetrahedra and upon rupture of P-O-P bridge bonds with the simultaneous formation of PO ₃ ^2? electron centers has been shown. As a result of the revision of the nature and mechanisms of formation of radiation color centers in the studied glasses, it appears promising to introduce cerium (Ce³⁺) and europium (Eu³⁺) as protectors into these glasses.     

Electric properties of levels of 156Dy rotational bands

The nonadiabaticity of E0 transitions from 0 ₂ ⁺ states and 2 ₁ ⁺ bands in ¹⁵⁶Dy is examined within a phenomenological model that takes into account the mixing of K ^π = 0 ₁ ⁺ , 0 ₂ ⁺ , 0 ₃ ⁺ , 2 ₁ ⁺ states and 1⁺-bands. It is shown that the nonadiabaticity of E0 transitions is due primarily to the mixing of 0 ₂ ⁺ and 0 ₃ ⁺ bands.     

Pion photoproduction on197Au to ground and isomeric states in197Hg

The lifetime of the 331.3 keV 0 ₂ ⁺ state in¹⁰⁰Zr has been measured at the gas-filled recoil separator for fission products JOSEF. By observing the delayed coincidences between theβ-particles populating the level and theE0 conversion electrons from its decay into the ground state, a half-life of 3.37±0.30 ns has been obtained. From the measured lifetime and the relative intensities of the 0 ₂ ⁺ →0 ₁ ⁺ and 0 ₂ ⁺ →2 ₁ ⁺ transitions, values of 0.493±0.015 for theE0 strength parameterρ, and of 16 single particle units forB(E2,2 ₁ ⁺ → 0 ₂ ⁺ ) have been deduced. The enhanced nature of theE0 transitions suggests mixing of the 0 ₁ ⁺ and 0 ₂ ⁺ states which may be estimated by comparing the experimentalB(E2) values for the 2 ₁ ⁺ →0 ₁ ⁺ and 2 ₁ ⁺ →0 ₂ ⁺ transitions with the predictions of the asymmetric VMI model.     

Luminescence centers in silicate and germanate glasses activated by bismuth

Concentration series of silicate and germanate glasses activated by bismuth are studied. It is shown that luminescence in the IR region is controlled by several active centers related to bismuth. Based on a comparison of spectroscopic characteristics of the studied glasses with the data previously obtained for chloride glass, the observed centers were identified as Bi⁺, Bi ₂ ⁴⁺ , and Bi ₅ ³⁺ in germanate glass and Bi⁺, Bi ₂ ⁴⁺ in silicate glass.     

Comparison of electron spin polarization of P 870 + Qa a − observed in Zn2+-containing and Fe2+-depleted bacterial reaction centers

Recently, a general model has been developed to explain electron spin polarized (ESP) electron paramagnetic resonance (EPR) signals found in systems where radical pairs are formed sequentially. The photosynthetic bacterial reaction center (RC) is such a system in which we can experimentally vary parameters (lifetime, structure, and magnetic interactions in the sequentially formed radical pairs) that affect ESP development in order to test this model. In Fe²⁺-depleted transfer step from intermediate radical pair, P ₈₇₀ ⁺ Q _a ^? which is produced in an electron transfer step from intermediate radical pair, P ₈₇₀ ⁺ I^?. (P ₈₇₀ ⁺ is the oxidized primary donor, a special pair of bacteriochlorophyll molecules, I^? is the reduced bacteriopheophytin acceptor, and Q _a ^? is the reduced primary quinone acceptor.) The lifetime of P ₈₇₀ ⁺ I^? can be shortened relative to the lifetime of P ₈₇₀ ⁺ I^? in Fe²⁺-depleted RCs by substitution of Zn²⁺. We report the first observation of X-band and Q-band ESP EPR signals due to P ₈₇₀ ⁺ Q^? from bacterial reaction centers that contain Zn²⁺. Comparison of these signals to those observed from Fe²⁺-depleted bacterial reaction centers shows intensity differences and g-factor shifts. The results are discussed in terms of the general sequential radical pair model.     

A method for studying the multipolarity and orientation of elementary oscillators in cubic crystals on the basis of axially periodic dependence of the luminescence intensity

A new method for determining the multipolarity and orientation of elementary quantum oscillators in cubic crystals is proposed. This method is based on studying the spatially periodic dependences of the intensity of luminescence observed in crystals with an induced anisotropy. The method was experimentally verified on LiF crystals containing F ₂ and F ₃ ⁺ color centers. It is shown that the observed spatially periodic dependences are in good agreement with the calculated dependences. The proposed method supplements the known methods for studying polarized luminescence (the methods of azimuthal dependences and polarization ratios and their various modifications). However, the new method, in contrast to the known ones, does not require measurements of the polarization ratios (for example, the degree of luminescence polarization), which in some cases significantly simplifies the experiment. Another advantage of the proposed method is its universality; i.e., it can be applied with equal success to both anisotropic and cubic crystals.     

Formation of Color Centers and Molecular Complexes with a Weak Hydrogen Bond in Lithium Fluoride Crystals Depending on the Form of OH<Superscript>¯</Superscript> Inclusion

The form of oxygen-containing inclusions in the LiF crystal was shown to be determined by the laws of isomorphic substitution and impurity accumulation in a melt during crystal growth in open air. Color centers and hydrogen-bonded complexes of different types appear in the LiF crystal after irradiation depending on the form of OH^– and Mg²⁺ inclusions. The radiative decay of OH^– ions and the properties of molecular complexes (MCs) with a weak hydrogen bond are responsible for the decreased efficiency of formation of the F- and F₂-color centers and increased concentration of the positively charged F ₂ ⁺ - and F ₃ ⁺ -centers. Radiochemical reactions involving hydrogen and fluorine atoms and ions that compete with the formation of color centers were presented.     

Gyromagnetic ratios of excited states in186W

The gyromagnetic ratios of the 4 ₁ ⁺ , 6 ₁ ⁺ , and 2 ₂ ⁺ states in¹⁸⁶W were measured relative to that of the 2 ₁ ⁺ level by means of the transient field implantation perturbedγ-ray angular distribution technique. The nuclei in the states of interest were Coulomb excited using a beam of 220-MeV⁶³Cu projectiles and recoiled swiftly through a thin, polarized Fe foil. The present measurements yielded ratiosg(4 ₁ ⁺ )/g(2 ₁ ⁺ )=1.04±0.07,g(6 ₁ ⁺ )/g(2 ₁ ⁺ )=1.03 ±0.20 andg(2 ₂ ⁺ )/g(2 ₁ ⁺ )=0.63±0.13. The sizable disparity between the measuredg-factors of the ground- and excited-band is examined within the context of the interacting boson approximation model.     

Untersuchung des Zerfalls von134Cs durch γ-γ-Winkelkorrelationsmessungen

γ-γ-angular correlation measurements with Ge(Li) detectors and NaJ(Tl) detectors provided theE2/M1 mixing ratios of the following gamma transitions: 3 ₁ ⁺ →2 ₂ ⁺ (475.3 keV), 2 ₂ ⁺ →2 ₁ ⁺ (563.3 keV), 4 ₂ ⁺ →4 ₁ ⁺ (569.4 keV), 3 ₁ ⁺ →2 ₁ ⁺ (1,039 keV). The angular correlation measurements were only consistent with spin 3 of the 1,643 keV level. The half life of the 1,401 keV level was determined by delayed coincidence techniques to beT _1/2 (1,401 keV)≦30 ps.