Self-diffusion of potassium in potassium azide

The tracer sectioning technique was used to study the diffusion of potassium ions in melt grown single crystals of potassium azide. The temperature dependence of the diffusion coefficients in the range 85–254°C can be represented by D=(0·19±0·03) exp [(?0·80±0·06) eV/kT] cm²/sec. It appears that the cations are the predominant mobile species and that they diffuse by a vacancy mechanism with an enthalpy of migration of 0·80±0·06 eV.     

Space-charge-limited-trap-limited-currents in anthracene crystals

Space-charge-limited-trap-limited hole currents in anthracene crystals are interpreted in terms of a trap distribution which starts at a discrete trap level at 0·6–0·8 eV and in which the trap density falls off exponentially with energy relative to this level. It is suggested that exponential hole trap distributions are produced by physical perturbations of the crystal lattice introduced by the same impurities which give rise to the discrete hole trap level at 0·6–0·8 eV (revealed by thermally stimulated current studies). The results indicate that a perturbed molecule is introduced for every 10,000 impurity molecules and the total number of perturbed molecules is constant at 10¹⁷ m^?3 for melt-grown and vapor-grown crystals. The parameter kT_c varies from crystal to crystal, indicating that the relative contributions of highly perturbed and slightly perturbed molecules is influenced by crystal growth conditions.     

Optical absorption edge in SnS

Optical absorption in single crystals of tin sulfide has been studied at many temperatures between 100 and 300 °K, in the wavelength range 2·2–0·8 μ. From the interference fringe patterns the absorption coefficient, reflection coefficient and index of refraction as a function of wavelength were determined for two light polarizations (ε∥a and ε∥b). From an analysis of the data, indirect band gaps of 1·142 and 1·095 eV were found for the two directions of polarization. Also it was found that the phonon assisted transitions required the participation of two phonons at different energy thresholds with energies 0·033 or 0·038 eV and 0·082 or 0·113 eV, with reference to the two axis. The temperature dependence of the indirect band gap for each direction of light polarization is linear with a slope ?4·05 × 10^?3eV and ?4·37 × 10^?3 eV respectively.     

Diffusionskonstante und charakteristische Absorption vor der Bandkante von Mn in ZnO-Kristallen

ZnO single crystals were doped with Mn and Co by diffusion. In the temperature range from 1400–1600 K the Mn and Co-diffusion-constants were determined:D _Mn=3.2 · 10^?3 exp (?2.87 eV/kT) cm² sec^?1 andD _Co=1·10exp(?3.98 eV/kT) cm² sec^?1. The Mn doped ZnO crystals show a characteristic colour due to an absorption near the intrinsic absorption edge. The corresponding absorption spectra were measured forE⊥c andE∥c. A discussion of different absorption mechanism shows that a charge-transfer transition is responsible for this absorption.     

Migration and stabilization of hydrogen atoms in KCl

Stabilities of hydrogen atoms at the interstitial (H⁰_i), cation and anion sites (H⁰_sc and H⁰_sa) in KCl have been studied with ESR and thermoluminescence. The close pair between H⁰_i and S^? formed by UV-irradiation of KCl:SH^? recombines first with the activation energy of 0.17±0.02 eV following the emission of light and then H⁰_i becomes mobile with the energy of 0.20±0.02 eV. The energies determined from the decay of ESR signal intensity of H⁰_sc and H⁰_sa are 0.24±0.02 eV and 0.43±0.03 eV, respectively.     

The thermal activation energy of crystalline As2Se3

The conductivity of As₂Se₃ single crystals has been measured, both 6 b and ⊥ b, in the temperature range 300–400°K. Thermal activation energies of 0.94 and 1.1 eV were obtained for H₂ and I₂-grown crystals, respectively.     

Study of cation tracer diffusion in NaF

Cation tracer diffusion coefficients were measured in pure NaF crystals in the intrinsic ionic conductivity range (876–970 °C). The results can be rationalized satisfactorily in terms of contributions to the observed Na tracer diffusivities arising from both free vacancies and neutral vacancy pairs, the latter contribution amounting to about 53 per cent of the total Na diffusion at the highest measuring temperature. The best-fit defect parameters derived in an earlier conductivity study [21] from this laboratory on similar NaF crystals give for the free vacancy contribution D_v^*(Na) = 4·25 exp (?2·21 eV/kT) cm²s^?1. A combination of these D_v^*(Na) values with the present diffusion data yields for the vacancy-pair contribution D_p^*(Na) = 1·15 × 10⁸exp (?4·04 eV/kT) cm²s^?1. Comparison of the present findings with published values of the anion tracer diffusion coefficient in NaF showed that D_p^* (F) is 2·3 to 4·4 times larger than D_p^*(Na) over the temperature range of our observations, the difference between the two contributions increasing with decreasing temperature. When approximate account is taken of the temperature-dependence of the two pair correlation factors, this last result indicates that the anion jumps into the vacancy pair occur with a higher frequency, and increasingly so at lower temperatures, than do those involving the cations.     

Microwave electrophysical properties of superionic crystals Ag2HgI4

The paper concerns itself with the investigation results of temperature dependencies of electric conduction and dielectric properties of Ag₂Hgl₄ crystals in the frequency range of 10⁷–7,8·10¹⁰ Hz. The obtained data have shown that in α-phase at T=326 K, the electric conductivity σ is proportional v^0,28 in the frequency range of 10⁷–10⁹ Hz and σ is proporti onal v^0,5 in the range of (1,1–78)·10⁹ Hz. The dependence σ(v) in the range of (1,1–78)·10⁹ Hz may be conditioned by the jumping mechanism of the conductivity and low frequency oscillations of the crystal lattice. It is believed, tha in the σ-phase of Ag₂Hgl₄ a condition of the existence of the ionic polaron is satisfied. The activation energy of the polaron is ΔE_p=0,09 eV.     

Copper and native defects in zinc telluride

Zinc telluride crystals were grown from tellurium-rich solutions containing 10¹⁷–10²⁰ cm^?3 atoms of copper. The copper concentrations in these crystals were measured by activation analysis. Hall effect and resistivity measurements were performed. Photoluminescence spectra were also determined. Our interpretation of the different results is that copper brings about both acceptor defects Cu_Zn with a 0·12–0·13 eV ionization energy, and donor defects. The second acceptor level of the zinc vacancy was found to be at 0·15 eV.     

Effect of the ionic radius on jump frequencies of alkaline earth cations in NaCl crystals

By comparing diffusion coefficientsD of bivalent cations Ba²⁺, Ca²⁺, Sr²⁺ in NaCl crystals it was shown that in the temperature range above 550 °CD (Ba²⁺)>D (Sr²⁺)>D (Ca²⁺) is valid. Temperature dependences of jump frequenciesw ₂ of these cations are described byw ₂ (Ba²⁺)=(2·15±0·55) × 10¹² × exp {?(0·817±0.007)/kT};w ₂ (Sr²⁺)=(2·9±1·1) × 10¹² × exp {?(0·84±0.02)/kT} andw ₂ (Ca²⁺)=(5·5±6·5) × 10¹⁰ × exp {?(0·51±0·07)/kT}. It was demonstrated that in NaCl crystals the activation enthalpy and the preexponential factor of the jump frequencyw ₂ increase with increasing ionic radius and mass of the bivalent alkaline earth cation.     

Influence of the surface on the quantum P.E.M. effect in InP

The photoelectromagnetic effect of InP is studied in quantizing magnetic fields at 4·2 K in an energy range 1·4–1·5 eV for linearly polarized light. Depending on the sample surface condition two types of spectral oscillations may appear, those associated with interband transitions between Landau levels or the LO phonon type usually seen in photoconductivity. An analysis of the spectral oscillations gives: E₀ = 1·423±0·001 eV; Δ₀ = 0·102±0·006 eV; hω_L = 0·036 eV.     

Experimental determination of the electron screening potential energy for the d(d, n)3He Reaction in ZrD2 and D2O in the ultralow energy region

This work is devoted to measuring of the values of the astrophysical S-factors and electron screening potential energy for a d(d,n)³He reaction occurring at ultralow energies in zirconium deuteride ZrD₂ (3.5–7.0 keV) and heavy water D₂O (2.2–6.0 keV). The experiment was performed on the Hall pulsed plasma accelerator at the TPU Nuclear Physics Institute (Tomsk) with ZrD₂ and D₂O targets produced by the magnetron sputtering of zirconium in a deuterium environment and heavy water freezing-out on a copper support, respectively. A χ ² analysis of the dependence of the neutron yields and astrophysical S-factors for the dd reaction on the deuteron collision energy E revealed that the upper bounds of the electron screening potential energy for interacting deuterons in ZrD₂ and D₂O and of the astrophysical S-factors at the deuteron collision energy E = 0 were U _e (ZrD₂) < 30 eV, U _e (D₂O) < 25 eV, S(0) = (57.2 ± 3.9) keV · b (ZrD₂), S(0) = (58.6 ± 3.6) keV · b (D₂O) at the 90% confidence level.     

Indirect electronic transitions in alkali halate crystals-I (sodium and potassium chlorate crystals)

The long wavelength tail of the fundamental absorption in NaClO₃ and KClO₃ crystals has been analysed based on the theory of band to band transitions of Bardeen et al.[8] developed in the case of semi-conducting crystals. Evidence of phonon involvement in the transitions giving an indirect band gap is observed. The energies of the phonons involved in the process are the same for both the crystals, and agree well with combinations of prinicple frequencies of ClO₃^? ion, their overtones and also lattice phonons. The indirect band gap in these crystals varies with temperature more or less linearly and the rate of variation is ?3·8 × 10^?4 eV/K and ?5·0 × 10^?4 eV/K for sodium chlorate and potassium chlorate respectively.     

Dissociation energies for the electronic ground states of BeCl,GaH and LiH

The dissociation energies of the diatomic molecules BeCl, GaH and LiH have been computed by fitting empirical potential functions to the true potential energy curves for the electronic ground states of the molecules. The Lippincott three-parameter potential function, the five-parameter Hulburt-Hirschfelder potential function and the Szöke and Baitz electronegativity potential function have been used. The estimated dissociation energiesD ₀ ⁰ are 4·50, 3·09 and 2·94 eV for BeCl, GaH and LiH respectively. These values compare well with the experimental values.     

Gas-surface scattering from W(100): Kinetic energy dependence of the effective corrugation

Angular and velocity distributions have been obtained for the scattering of argon and N₂ from a W(100) surface for incidence energies, E_i, in the range 0.03–5.5 eV, and surface temperatures, T_s, from 90 to 1700 K. For E_i < 0.1 eV, we find broad angular distributions (> 60° FWHM) which are relatively insensitive to T_s and velocity distributions which are inconsistent with parallel momentum conservation, indicating a relatively corrugated interaction potential. Increasing E_i first causes a rapid narrowing in these distributions, but as E_i exceeds ~ 2 eV, they broaden again, as the effective corrugation again becomes large.     

Ionization function of magnesium for electron impact

Ionization cross sections for electron impact are measured with crossed beams of Mg atoms and pulsed electrons. Total numbers of particles are determined by the light emission of excited atoms. The ionization cross section obtained for electron energies from 7 eV to 60 eV has its maximum valueq _i (max)=7.8 · 10^?16 cm² at 12 eV electron energy.     

Lineshift and linewidth in optical spectra of europium salts

The lineshift and the linewidth of the transition⁵ D ₀ →⁷ F ₀ has been measured in EuCl₃ · 6H₂O, Eu(NO₃) · 6H₂O and Eu₂O₃ as a function of temperature between 4.2 and 300 °K. In all cases the lines are shifted to the blue (shorter wavelength) with increasing temperature. A linear relationship is found between the lineshifts and the internal energies of the compounds.—In Eu(C₂H₅SO₄)₃ · 9H₂O the linewidth of several transitions from the⁵ D ₀ state to the crystal field states of the⁷ F _i levels have been measured at 4.2 °K. The linewidths are compared with those expected for a depopulation of the⁷ F _i states by phonons.     

Synthesis,magneto-optics and fluorescence of the ferromagnetic semiconductor Eu3(II)SiO5

Small single crystals of the transparent ferromagnet Eu₃SiO₅ have been synthesized by high temperature chemical transport. Magnetic measurements indicate T_c = 9°K and a saturation magnetization very close to 7 μ_B/Eu ion. Crystalline samples show a very low residual optical absorption and an absorption edge near 2 eV which displays a small red shift of 20 meV on cooling below T_c. Samples, containing a small percentage of dissolved EuO clusters, show in addition an absorption band at lower energies with a temperature dependence and magnetic behavior typical for EuO. The photoluminescence of the pure compound has a single emission band near 1·9 eV with a high quantum yield. At low temperatures also the fluorescence displays a red shift similar to that of the absorption edge. The fluorescence is accompanied with photoconductivity.