Neutralization of H− ions in collisions with fast, multiply charged ions

The neutralization of H⁻ ions in collisions with fast, multiply charged ions is considered in the parameter region where the Born approximation applies. An analytical formula is obtained for the H⁻ neutralization cross section in such collisions. Zh. Tekh. Fiz. 69, 1–4 (July 1999)     

Quasichanneling of ions in crystals. I. Elastic scattering of ions on atomic “chains” and planes

The scattering of quasichanneled particles on atomic chains and planes is studied by computer simulation for the crystals of chemical compounds. It is shown that quasichanneling is the specific regime of ion motion in the lattice. Its main features are: (1) a sharp increase of the backscattering probability; (2) transition of the ions from the quasichanneled component into a random one; (3) high sensitivity to the structure and the composition of the atomic “chain”; (4) dependence on the value and the direction of the atomic displacements.     

Detection of parametric resonance of trapped ions for micromotion compensation

We have detected excess micromotion of trapped ions by modulating the trapping voltage. This radio-frequency (rf) modulation induces parametric resonance and excites secular motion of the trapped ions when they possess excess motion. This technique has been applied to laser-cooled ions in a linear rf trap and it provides optimum values for compensating the trapping field. We found that the technique has sensitivity equal to or greater than the conventional method for detecting excess micromotion. Because any laser propagation direction can be used, this method is expected to be applied to surface-electrode traps.     

Coulomb predissociation rates of He dµ molecular ions

The predissociation or particle emitting decay rates of muonic molecular ions³He dµ and⁴He dµ are estimated by means of the complex rotation method. We use a highly accurate variational three-bodyP-wave function based on random-tempered Slater-type exponential expansion. A resonance eigenvalue ofE=–48.420 89 eV and =0.348 × 10^–3 eV for the³He dµ ion and a resonance eigenvalue ofE=–58.225 303 eV and =0.118 × 10^–3 eV for the⁴He dµ ion have been obtained. These results are in a good agreement with the ones previously obtained by Kino and Kamimura by scattering calculation with the non-adiabatic coupled-rearrangement-channel method.     

Substitution mechanism of Zn ions in β-tricalcium phosphate

Zn-doped β-tricalcium phosphate (β-TCP) is synthesized by the solid-state reaction method. The substitution mechanism of Zn ions in β-TCP synthesized here is investigated by carrying out a combination of near-edge X-ray absorption fine structure (NEXAFS) measurements and first-principles calculations. From the results of the present study, the substitution site for Zn ions in β-TCP is successfully determined.     

Towards sympathetic cooling of trapped ions with laser-cooled Mg + ions for mass spectrometry and laser spectroscopy

Sympathetic cooling by laser cooled Mg ions has been proposed as a method for fast cooling of highly charged ions to a very low temperature. The paper describes the construction of the solid state laser system at 279.63 nm required for laser cooling of the Mg ions. The laser system is composed of a fiber laser at 1,118.54 nm and two successive second harmonic generation (SHG) ring cavities for frequency quadrupling. In the first SHG cavity, non-critical phase matching of a lithium triborate (LBO) crystal is used for doubling from 1,118.54 to 559.27 nm. The second SHG cavity uses critical phase matching of a β-barium borate (BBO) crystal for doubling from 559.27 to 279.63 nm. With the aid of Boyd–Kleinmann theory, optimum experimental parameters are calculated and used for an efficient SHG. Besides this, the paper intends to be a shortcut for practical applications of the Boyd–Kleinmann theory for SHG.     

Adsorption of sodium ions and hydrated sodium ions on a hydrophobic graphite surface via cation-π interactions

Using density functional theory computation, we show that sodium ions and hydrated sodium ions can be strongly adsorbed onto a hydrophobic graphite surface via cation-π interactions. The key to this cation-π interaction is the coupling of the delocalized π states of graphite and the empty orbitals of sodium ions. This finding implies that the property of the graphite surface is extremely dependent on the existence of the ions on the surface, suggesting that the hydrophobic property of the graphite surface may be affected by the existence of the sodium ions.     

Influence of additional metal ions on the ratio of the rates of intermediate product transformations in the hydrolysis of adenizine-5′-triphosphoric acid catalyzed by divalent Cu ions

It was shown earlier that the hydrolysis of the (CuATP²⁻)₂ dimeric complex to CuADP⁻ and inorganic phosphate P _i was an irreversible reaction. The main intermediate hydrolysis product, the formation of which should be taken into account at comparatively early hydrolysis stages, was the IntK pentacovalent intermediate. It was formed in parallel with hydrolysis to CuADP⁻ and P _i through the common intermediate product (CuATP²⁻)₂OH⁻ — DOH⁻. We studied the influence of the addition of various concentrations of Mg²⁺ ions to the reaction mixture at pH 7.1–7.2, a range for which the kinetics of hydrolysis is sensitive to the rate constants of deactivation of DOH⁻ active centers (conjugated with CuADP⁻ formation and occurring via the formation of IntK). The conversion of ATP above which stationary hydrolysis regime was observed decreased as the concentration of Mg²⁺ grew. The DOH⁻ $ \underset{{OH^ - }}{\overset{{OH^ - }}{\longleftrightarrow}}$ \underset{{OH^ - }}{\overset{{OH^ - }}{\longleftrightarrow}} IntK equilibrium according to the conversion of ATP was established more rapidly, and it was to a greater extent shifted toward IntK. It was assumed that hydrated Mg²⁺ linked as a second metal ion with ATP β and γ phosphate groups hydrated IntK much stronger than DOH⁻. The Cu · OH₂ · AMP complex played the role of a common acid catalyst and hydrated DOH⁻ better than Mg²⁺ · OH₂. The selective hydration of DOH⁻ by the CuOH₂ · AMP complex at early hydrolysis stages directed the process toward the formation of IntK, which caused the appearance of an induction period in the formation of CuADP⁻.     

Techniques of laser spectroscopy in investigations of lanthanides’ free atoms and ions

Various experimental methods, used in Chair of Quantum Engineering and Metrology for determination of the hyperfine structure of electronic levels in lanthanides atoms and ions, are presented. In turn the spectroscopic methods on an atomic beam (laser induced fluorescence and laser-rf double resonance ABMR-LIRF), laser-rf double resonance in a Paul trap and spectroscopic methods in a hollow cathode discharge (optogalvanic detection and laser induced fluorescence) are presented. Each method has been characterized with its potential accuracy and domain of application. The results achieved for the atoms and the ions of lanthanum, praseodymium, neodymium and europium have been published in numerous articles (compiled in the reference list).     

K-shell photoionization of boron-like carbon ions： analysis of ls-2p resonances

Close-coupling calculations based on an R-matrix formalism are performed for the 1s--2p resonance photoionizations from the low-lying states of boron-like carbon ions. The resonance energies, widths and oscillator strengths of 1s-2p core excitations are determined by analysing the calculated photoionization cross sections. Our calculations are in reasonable agreement with the experimental and theoretical results presented by other authors. The present numerical values may help to analyse the astrophysical and laboratory plasmas.     

Calculation of ion energy distributions of argon excimer ions generated in helicon plasma

A program is developed to calculate the ion energy distributions （IEDs） of Ar2^＋ making use of a simplified kinetic model with a combination of Monte Carlo method. Several coefficients are used to realize good match between the calculated and measured results. Some important assumptions are confirmed： argon excimer ions have short lifetime, hence they are formed in a short range before the collecting electrode. The excimer ions that encounter collisions will be discarded because they turn to other ion species after they collide with argon atoms. From the calculated results some plasma parameters such as the cross section or neutral density in discharge could be evaluated.     

Influence of alkali metal ions on thermal stability of Bi-activated NIR-emitting alkali-aluminoborosilicate glasses

We study the influence of alkali oxides on the near-infrared（NIR）-emitting thermal stability of Bi-doped R2O–Si O2–B2O3–Al2O3（R = Li, Na, K） glasses below Tg. Results show that undergoing heat treatment, remarkable luminescence quenching occurs for the glasses containing Na2 O and K2 O due to the formation of Bi metallic colloids, whereas the glass with Li2 O shows much better thermal stability. These changes can be understood by the tendency of modifier cations with lower mobility and higher tightness network to restrain the transport of Bi-related NIR-emitting centers. The results provide a scientific reference for composition design of Bi-doped optical fiber.     

Average kinetic energy of ions ejected from pure Coulomb explosions of methane clusters

We use an electrostatic model to study the average kinetic energy of ions ejected from the pure Coulomb explosions of methane clusters(CA_4)_n(light atom A=H and D).It is found that the ratio of the average kinetic energy of the ions to their initial average electrostatic potential energy is irrelevant to the cluster size.This finding implies that as long as the ratio is given,the average kinetic energies of the ions can be simply estimated from their initial average electrostatic potential energies,rather than from the time- consuming simulations.The ratios for the different charge states of carbon ions are presented.     

Theoretical study of LiCl− and LiBr− molecular ions

The molecular structures and spectroscopic constants of the ground electronic states of LiCl^? and LiBr^? are investigated with the coupled-cluster method. To improve the accuracy of our calculations, we have employed the extrapolation schemes as well as corrections of the core–valence correlation and scalar relativistic effect. The equilibrium parameters, potential energy curves, force constants, vibrational energy levels and spectroscopic parameters of both molecular ions are derived, in which those of LiBr^? are reported for the first time. The electron affinities and vertical detachment energies of neutral and anionic LiCl and LiBr are also evaluated.     

Loss of electrons by fast H− ions in gases

The characteristic angles and cross sections for a (\mathop 1^- 0) + (\mathop 1^- 1)(\mathop 1\limits^ - 0) + (\mathop 1\limits^ - 1) reaction in which H⁻ atoms with an energy of 0.1–10 000 MeV lose electrons when scattered on C, N, or O atoms were calculated for the relativistic case of the Bethe scattering theory. The cross sections for N₂, O₂, and CO₂ molecular targets were obtained using the additivity rule. The results presented are compared with known experimental and theoretical data.     

Mössbauer study of the dynamics of iron ions in bipyramidal positions of strontium hexaferrite

The dynamics of Fe³⁺ ions in bipyramidal 2b positions of a type M hexaferrite are studied on single-crystal and polycrystalline SrFe₆Ga₆O₁₉ samples in the paramagnetic temperature range. We show that when the angle between the c axis of the crystal and the direction of -ray emission varies from 0 to 32 the area under the resonance lines corresponding to Fe³⁺ ions in 2b positions increases by a factor of roughly 1.5. The effect is more pronounced upon passing from a single-crystal sample (=0) to a polycrystalline sample. A comparison of the line intensities under different experimental conditions served as a basis for an evaluation of the difference between the mean-square displacements of the Fe³⁺ ions in 2b positions along the c axis in the perpendicular plane.Translated from Izvestiya Vysshikh Uchebnykh Zavedenii, Fizika, No. 1, pp. 5–8, January, 1991.     

Role of copper ions in dielectric and structural investigations of lead– borate glasses

Glasses in the system 0.1CuO-(x-0.1)PbO-(1-x)B₂O₃ (0.3≤ x ≤ 0.7) were synthesized by using the melt quench technique. A number of studies such as X-ray diffraction (XRD), differential scanning calorimetry (DSC), fourier-transform infrared (FTIR) and Raman spectroscopy, electron paramagnetic resonance (EPR) and dielectric properties (viz., dielectric constant ??, dielectric loss and ac conductivity σ_ac) are employed to characterize the glasses. The amorphous nature of the glasses was confirmed using XRD while the glass transition temperature (T_g) of glass samples have been estimated from DSC investigation and found that the T_g decreases with increasing PbO content. Raman and FTIR spectroscopy reveals that when increasing lead ions, the tetrahedral [BO₄] units are gradually replaced by trigonal [BO₃] units. The EPR study leads to determine the local site of Cu²⁺ ions and its transformation with the Pb content in the studied glasses.     

Substitutional effect of Cr ions on the properties of Mg–Zn ferrite nanoparticles

The effect of Cr³⁺ substitution in Mg–Zn ferrite, with a chemical formula Mg_0.5Zn_0.5Cr_xFe_2−xO₄ (x=0.0–1.0), synthesized by a sol–gel auto-combustion reaction is presented in this paper. The resultant powders were investigated by various techniques, including X-ray diffractometry (XRD), transmission electron microscopy (TEM), infrared spectroscopy (IR), vibrating sample magnetometry (VSM), and DC resistivity. The XRD pattern revealed that the cubic spinel structure is maintained for the all the compositions. The particle sizes measured from XRD and TEM are in good agreement with each other. The cation distribution suggests that Mg²⁺, Cr³⁺ and Fe³⁺ have strong preference towards octahedral B-site. The theoretical lattice constant and experimental lattice constant match each other very well. The IR analysis supports the presently accepted cation distribution. The saturation magnetization decreases linearly with increasing Cr³⁺ content. Curie temperatures are obtained by the Laoria and AC susceptibility techniques. The dc resistivity has been investigated as a function of temperature and composition.     

Influence of second sideband excitation on the dynamics of trapped ions in a cavity

We study the dynamics of a trapped ion placed at an antinode of the standing wave inside a high finesse cavity with consideration of the second sideband excitation between the ionic internal levels and the light field. We investigate the entanglement of the three subsystems embodying the ionic internal levels, the vibrational mode of the ion and the cavity field.     

Conductivity of La1−x CaxMnO3 under magnetic resonance of Mn ions

A change in the electrical conductivity, σ, is observed in the manganese perovskite La_1?x Ca_xMnO₃, with x=0 and 0.3 under saturation of the magnetic resonance transitions of Mn ions. This effect has a maximum in the temperature range of the magnetic phase transition of the compounds. Two contributions to the change in σ are found. The first, dominating in LaMnO₃, is an increase in σ caused by heating of the sample under magnetic resonance. The second is a σ decrease due to reorientation of the Mn spins, observed in La_0.7Ca_0.3MnO₃.