Zur Bildungskinetik der F-Folgezentren in KCl

Following the same procedure as in part I the formation of Z₁-centers under Flight irradiation was investigated in additively colored KCl crystals doped with Ca⁺⁺ and Sr⁺⁺ ions. The measurements show that again F′-centers and empty anion vacancies are the first reaction product and determine the rate of Z₁-center formation. The temperature dependence and rate of the Z₁-center formation is in agreement with the corresponding results on F _A -center formation, demonstrating that Z₁-centers are formed as the consequence of an ionic process and not a mere electronic transfer. It is concluded that again empty anion vacancies or F′ centers diffuse randomly in the lattice (activation energy 0.6 eV) until they are captured at an impurity site. Arguments are presented that these impurities are divalent cation/vacancy complexes, so that the model of the Z₁-center should be a combination of the F-center with this complex. The independence of the Z₁-band of the nature of the divalent cation indicates the assoziation of the F-center to the vacancy-side of the complex. A characteristic delay period in the Z₁-center formation can be accounted for by a non-statistical distribution of F-centers and divalent cations to each other. This is a necessary consequence of the high temperature dynamical equilibrium between these imperfections which is frozen in by the quenching of additively colored crystals. A direct proof for this interpretation is the absence of the delay period in crystals where the F-centers are formed by x-irradiation at room temperature.     

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.     

Elektronenspinresonanz- und optische Untersuchungen zur FarbzentrenreaktionF⇄F′ in KCl-Kristallen

Simultaneous measurements of optical absorption and electron spin resonance of additively colored KCl crystals have been carried out during the optical bleaching ofF-centers at ?90°C. TheF-center resonance signal does not change in its significant properties e.g. line shape, line width,g-value, and saturation behavior, but it decreases proportional to the decrease of the opticalF-center absorption band. No ESR-signal due to theF′-center could be observed. The time dependence of theF?F′-center conversion has been investigated by ESR and optical measurements. It does not give any indication of a paramagnetism of theF′-center, too. The kinetics of the thermal decay of theF′-center at ?90°C have been studied. One can interpret the time dependence of this process, if one assumes that the mean lifetime of anF′-center depends on the distance of the nearest halogen ion vacancy. The expectation of life of theF′-centers therefore increases during the thermal decay, as the mean distance between remainingF′-centers and vacancies increases.     

Farbzentrenassoziate mit (100)-Symmetrie (A und B-Zentren)

By light absorption in additively colored KCl A-centers can be developped under certain conditions. Irradiation with (100) polarized F-light produces a reorientation of these centers, which is observed by a characteristic dichroic absorption. From these measurements the symmetry and the two optical transitions A₁ und A₂of the A-center are derived. Experiments with Na-doped crystals suggest as a model for the A-centeran F-center assoziated to a single Na ⁺ ion in the KCl lattice. From A-centers a new center can optically be developped, which has again (100) symmetry and two optical transitions. This ?B-center“ is interpreted as the assoziation oftwo F-Centers to a Na ⁺ion in KCl.     

Mechanism of <Emphasis Type="Italic">F</Emphasis>-center luminescence in anion-defective aluminum oxide single crystals

New experimental data illustrating the effect of deep traps on the luminescence properties of anion-defective α-Al₂O₃ single crystals are presented. It was established that deep traps have electronic nature and their filling occurs through photoionization of F centers and is accompanied by F → F⁺-center conversion. Model concepts were developed that describe the luminescence mechanism in anion-defective aluminum oxide single crystals with inclusion of thermal ionization of the excited F-center states. The validity of the model was supported by experimental data obtained in a study of thermoluminescence, thermally stimulated exoelectron emission, and thermally stimulated electrical conductivity.     

M-Zentrenbildung in röntgenbestrahlten KCl-Kristallen

The production of F- and M-centres in KCl by X-irradiation has been studied at temperatures between ?20 °C and 50 °C. The optical absorption measurements could be conducted without interrupting the X-irradiation. The results can be summarized as follows: 1. In Harshaw KCl crystals the number of F-centres created by the so-called fast coloration process was proportional to the height of the absorption band at 204 mμ prior to the irradiation. 2. The F-centres formed by the fast process did not contribute to the formation of M-centres. 3. In crystals with a strong absorption band at 204 mμ unstable M-centres were observed, which decayed rapidly after the cessation of the X-irradiation. Their concentration was found to be independent of the F-centre concentration. 4. At temperatures below 0 °C the relation between the concentration of the stable M-centres and the F-centre concentration could not any longer be represented by [M]=k ₁₂·[F₁]·[F₂]+k ₂₂·[F₂]², F₁ and F₂ referring to the F-centres created respectively by the fast and the slow coloration process. Except at very low F₂-centre concentrations however the relationship [M]=k ₀+k ₂·[F₂]² represented the experimental data at all temperatures between ?20 °C and 50 °C. At constant temperaturek ₂ varied withL, the X-ray energy absorbed per unit time and unit volume, according to 1/k ₂=a+bL+cL ². The temperature dependence ofa ^?1 b ^?1 andc ^?1 could be approximated by Boltzmann factors. The corresponding activation energies wereE _a=0.12 eV,E _b=0.53 eV,E _c=0.97 eV.     

H-center interactions during thermal annealing in KBr

Formation of the V₄-center and the H_A-center during thermal annealing in pure and Na⁺- and Li⁺-doped KBr, X-irradiated at low temperatures, is studied. It is found that these centers are produced accompanied with the annealing of the H-center at the second stage, of which the reaction order is two. The dependence of the concentration of Na⁺ impurity on the formation yield of the V₄-center by thermal annealing is studied and it is shown that the yield of the V₄-center formation is proportional to the square of the concentration of the H-center annealed at the second stage. This result confirms the former di-H-center model of the V₄-center.     

Die Hyperfeinstruktur des angeregten 32P3/2-Zustandes von Natrium

The hyperfine structure of the 3²P_3/2-state in the Na(I)-spektrum was investigated by optical double resonance. Three zero fieldrf-transitions (ΔF=±1, Δm_F=0) were detected and thus the unambiguous interpretation of therf-spectrum was made possible. From an analysis of therf-spectrum one obtains the magnetic hyperfine structure splitting constant a=(18.5 _?0.2 ^+0.6 ) Mc/sec the electric quadrupole interaction constantb=(3.2±0.5) Mc/sec which yields an electric quadrupole moment Q(Na²³)=(0.138±0.025)·10²⁴cm².     

Vibrational properties of the F A (Li+) center in alkali halides

Abstract

The on- or off-axis behavior and the vibrational properties of the F _A (Li⁺) center are investigated in several alkali halides by means of polarized resonant Raman scattering. The observed Raman modes are interpreted and classified according to their nature and frequency. A comparison between on- and off-axis systems and between the vibrational modes of the isolated Li⁺ and the F _A (Li⁺) center reveals a displacement of the Li⁺ equilibrium position parallel to the F _A (Li⁺) defect axis and, due to the small impurity size, away from the adjacent F center.     

Electronic polarisabilities of ions in alkali halide crystals

Tessman, Kahn and Shockley calculated the electronic polarisabilities of ions in alkali halide crystals using the long wavelength limiting values of the visible light dielectric constants. We have recalculated these widely used polarisabilities using the more accurate room-temperature dielectric constant data of Lowndes and Martin and a better minimisation procedure of Pirenne and Kartheuser. We have also calculated for the first time the low temperature values of these polarisabilities. The computed values of the polarisability in ų are Li⁺ 0·029, Na⁺ 0·285, K⁺ 1·149, Rb⁺ 1·707, Cs⁺ 2·789, F^? 0·876, Cl^? 3·005, Br^? 4·168, I^? 6·294 at 300°K and Li⁺ 0·029, Na⁺ 0·290, K⁺ 1·133, Rb⁺ 1·679, Cs⁺ 2·743, F^? 0·858, Cl^? 2·947, Br^? 4·091, I^? 6·116 at 4°K. The relative standard deviations for all the alkali halides are 1·20 and 1·43 per cent at 300°K and 4°K respectively justifying the additive nature of the individual ion polarisabilities.     

Zerfallsschema und Matrixelemente für denβ-Übergang Ag110m→Cd110

Theβ decay Ag^110m→Cd¹¹⁰ has been investigated with a double lens spectrometer and aβ-γ circular-polarization correlation setup. The shape of the 6⁺→6⁺ β spectrum withE ₀=529 keV was found to be allowed, in disagreement with earlier work. The constantA of theβ-γ circular-polarization correlation was measured to beA=0·07±0·02. This implies a ratioX of Fermi to Gamow-Teller contribution to the decay ofX ₁=?0·02±0·03 orX ₂=?10·3 _?4·1 ^+2·3 . Qualitative shell model considerations favor the valueX ₁. Additional information is given for the disintegration schemes of Ag^110m and Ag¹¹⁰.     

Red-shift in the photostimulation of the X-ray storage phosphor RbBr:Ga+

Abstract

By means of magnetic circular dichroism of the optical absorption and photostimulated luminescence (PSL) the X-ray induced formation of F_A and F centres in RbBr:(Ga⁺, Li⁺) was investigated. It turnes out that RbBr:Ga⁺ co-doped with 1% Li⁺ in the melt reveals the largest red-shift of the PSL excitation bands to 790 nm, whereby the F_A to F ratio increases up to about 10% with decreasing X-ray dose. This is more than statistically expected (6%). High X-ray doses destroy F_A centres. However, up to 15% of the simultaneously generated F centres could be converted into the F_A species by appropriate bleaching with 633 nm light into the F centre absorption band.     

Über die mathematische Struktur und eine Klasse strenger Lösungen der Jordanschen erweiterten Gravitationstheorie

Theβ-α. angular correlationW(Θ)=1+a cosΘ+cos² Θ of the decay of Li⁸ was measured for average electron energies ofE _β ≈5 MeV, 11 MeV and 12 MeV. The experiment yields an anisotropyA=(0·0036±0·0011)·E _β (MeV)^?1. This result is in good agreement with the results of the other groups. The measurements were performed in a counting chamber separated from the activation room simultaneously for two sealer positionsΘ=90° and 180°. The result is discussed in terms of the CVC-theory, taking into account the second forbidden Fermi-matrixelements (‖M1‖) and (‖E2‖).     

Bestimmung des elektrischen Kernquadrupolmomentes des ungeraden stabilen Strontium-87-Kerns

In order to determine the electric quadrupole moment of Sr⁸⁷ (I= 9/2) the hyperfine structure-splitting of the 5s5p ³ P ₁-state of the SrI-spectra was investigated by optical double resonance. By detection of high frequency transitions (ΔF=±1,Δm _F=0,±1) in an external magnetic fieldH ₀≈0 one obtains the hyperfine structure separations asv _F=11/2?F=9/2=1463·149 (6) Mc/sec andv _F=9/2?F=7/2=1130·264 (6) Mc/sec. From these frequencies one calculates the magnetic hyperfine structure-splitting constantA=?260·084 (2) Mc/sec and the electric quadrupole interaction constantB=?35·658 (6) Mc/sec. B leads to an electric quadrupole moment ofQ(Sr⁸⁷)=+0·36 (3)·10^?24 cm².     

Rotational analysis of the B-X band system of the SbO molecule

Rotational analyses of the two 0-0 bands of theB ²ΣX ²Π_reg system of SbO were carried out for the first time from spectrograms taken in the second order of a 21 ft. concave grating spectrograph having a dispersion of 1·25 Å/mm. The rotational constants of the ν=0 vibrational levels of the upper and lower states, and of the coupling constant A₀ of the lower²Π_reg state were deduced. These values are summarised below. v₀₀=25 334·93 cm^?1 B′₀=0·3190 cm^?1 B″₀=0·3490 cm^?1 A ₀=2276 cm^?1 r′₀=1·933 Å r″₀=1·848 Å.     

Raman spectroscopy of crystalline,glassy, and molten states of lead diborate

Polarized Raman spectra of single crystals of lead diborate, PbB₄O₇ (PBO), are studied in detail at 300 K. The TO-, LO-, and IO-phonon lines of the A ₁, A ₂, B ₁, and B ₂ symmetries in the Raman spectra of this compound are assigned. Changes in the Raman spectra of the internal vibrations of boron–oxygen complexes upon transition from the crystalline to the glassy and the molten states of PBO are observed. On the basis of the obtained results, the regularities in the formation of boron–oxygen complexes in glasses, melts, and crystals of the PbO · 2B₂O₃, SrO · 2B₂O₃, and Li₂O · 2B₂O₃. diborate compositions are analyzed.     

A new emission band spectrum of sulphur

A new emission band system of S₂ has been obtained in the region λ 3050–λ 2670 when sulphur is excited in a 30 mc/S. high frequency discharge from a 1/2 kW oscillator. The bands appear single sharp headed and are degraded towards red. Analysis of these new bands as belonging to a single system has led to the following vibrational formula.ν=36624·7+428·5(v′+1/2)?3·45(v′+1/2)² ?699·2(v″+1/2)+3·2(v″+1/2)². This system disignated as (b?x) is tentatively assigned to the electronic transition¹∑ _u ⁺ ?¹∑ _g ⁺ . The¹∑ _g ⁺ (x) state is found as the common lower state of three of the far ultraviolet systems of S₂ recently reported byTanaka andOgawa.     

Das magnetische Moment des 2,083 MeV-Zwei-Protonen-Niveaus des gerade-gerade-Kerns Ce140

The nuclearg-factor of the 2·083 MeV-state of Ce¹⁴⁰ has been determined as:g=1·11±0·04 This value suggests the interpretation of the level as the (g7/2,d5/2)₄ two proton shell model configuration. The investigation implies an integral measurement as well as a time dependent differential measurement (spin rotation method) of the rotation of the 329 keV-487 keVγγ-angular correlation in strong external magnetic fields. Liquid sources of lanthanum nitrate solved in 3n HNO₃ were used in these experiments. Some cerium (IV)nitrate was added to make sure that the 4f;-electronic shell remained empty after theβ ^?-decay. This prevented paramagnetic effects. Additional runs were performed without adding cerium (IV)nitrate and finally by using liquid sources of lanthanum chloride solved in 2n HCl with some iron (II)-chloride added. It was expected that the Fe⁺⁺ ions would reduce the primarily formed Ce⁺⁺⁺⁺ ions into the Ce⁺⁺⁺ state. The Ce⁺⁺⁺ shell is paramagnetic and enlarges the effective magnetic field at the position of the nucleus by about 36%. As no definitely faster rotation could be observed, one has to conclude that the ion reaction Ce⁺⁺⁺⁺+Fe⁺⁺?Ce⁺⁺⁺+Fe⁺⁺⁺ takes more than about 10^?8s. The half life of the 2·083 MeV state has been redeterminded asT _1/2=(3·41±0·04)·10^?9s. Differential measurements of the angular correlation of the 329 keV-487 keV cascade as a function of the time delay showed that perturbations by internal fields were very small. The coefficientsA ₂ andA ₄ of the angular correlation and the attenuation parameterλ ₂ were determined from measurements with sources of the first type as:A ₂=?0·105±0·003A ₄=?0·001±0·002 andλ ₂=(0·0065±0·0040)·10⁹S^?1=(0·032±0·020)·λ A comparison with the theoretical coefficients of a (3-4-2)-cascade shows that the multipolarity of the 329 keV radiation is a mixture of 99·83%M1 and (0·17±0·03) %E2.     

Das β+-Spektrum des Na22

Theβ ⁺-spectrum of Na²² was measured with a scintillation spectrometer. To avoid source absorption and scattering troubles the Na²² source was built in in the lattice of NaJ(Tl)-crystals. The observedβ ⁺-spectrum of Na²² has a statistical shape. The Fierz termb is obviously zero the value obtained in this paper is (+0,8±6,0)·10^?3 m ₀ c ².     

Der Quartett-Zustand desR-Zentrums in Kaliumchlorid-Kristallen

Optical absorption and paramagnetic resonance of KCl crystals containing preferentiallyR-centers have been studied during and after excitation with 430 mμ or 365 mμ light at 90 °K. A partly metastable, partly stable state has been detected and identified as the quartet state of theR-center, which proves to be an association of threeF-centers forming an equilateral triangle in the (111) plane of the crystal as proposed byvan Doorn andHaven andPick. — The crystals used were additively colored to 6.6·10¹⁷ F-centers/cm³ and illuminated withF-band light at room temperature until theR/M-ratio reached its maximum value. During light excitation the optical spectrum in the region of theR-bands shows characteristic small changes. A part of these changes disappears spontaneously with a time constant τ=14.5 sec when the light excitation is removed (“temporary bleaching”). The remaining part has a similar spectral distribution. It is completely stable in the dark, but can be bleached within a few seconds by illumination with 840 mμ light. — Electron spin resonance of the crystal under light excitation shows in addition to theF-center line a seven-line spectrum with strong angular dependence, if the field is rotated in a (110) plane. The maximum splitting is 674 G, the width of the individual lines 35.5 G. The angular dependence of the spectrum can be fitted to a fine-structure spin Hamiltonian

$$H = g\mu _B \vec H_0 \vec S + D[S_z^2 - \tfrac{1}{3}S(S + 1)]$$