Energy losses of beryllium ions penetrating through thin films before the attainment of charge equilibrium

The dependences between the energy losses of beryllium ions penetrating through thin organic (celluloid) films and the initial ion charge i ₀ and target thickness t are calculated. The proposed modified method is used to determine the charge fractions and average charge of an ion beam and the half-width and skewness of the charge distributions before the attainment of charge equilibrium. Calculations are performed for Be ⁱ⁺ ions with a velocity of 8 × 10⁸ cm/s (E = 0.33 MeV/nucleon).     

Ein Beschleuniger für schwere Ionen

A heavy ion accelerator on the basis of the multiple-stage operation of a small tandem-generator is proposed. The ions will be accelerated in the first half of the tandem in a charge state equilibrated in a foil stripper and then slowed down in the second half of the tandem in a charge state equilibrated in a gas atmosphere where the average charge is much lower than in a solid. One passage through the tandem results in a gain of energy of (Z _solid-Z _gas)·eU MeV. The gain expected for the acceleration of iodine ions will be of the order of 4 MeV for potentials at the high voltage electrode of about 1 MV. The application of many of these systems in line or the application of a magnet system bending the ions many times through the same electric field and stripper will allow to accelerate very heavy ions up to energies of about 1000 MeV. The transmission of this accelerator as a function of scattering, solid angle and final particle energy is estimated.     

Acceleration of heavy multicharged ions up to 1 MeV from a cleaned solid target irradiated by a femtosecond laser pulse with an intensity of 10<Superscript>16</Superscript> W/cm<Superscript>2</Superscript>

A noticeable increase in the charge and energy of ions accelerated from a solid tungsten target irradiated by a femtosecond laser pulse with an intensity higher than 10¹⁶W/cm² has been found when the target surface is precleaned by a nanosecond laser pulse with an energy density of 3 J/cm². Tungsten ions with charges up to +29 and energies up to 1 MeV were detected in this case, while the charge and energy of tungsten ions from a target with an uncleaned surface do not exceed +3 and 12 keV, respectively.     

Ti4+ and Ge4+ ionic substitution in Cu-ferrite,electrical conductivity and thermoelectric power

Both the DC conductivity and the thermoelectric power of Cu_1+xGe_xFe_2−2xO₄ and Cu_1+xTi_xFe_2−2xO₄ ferrites, for 0⩽x⩽0.4, were measured in a wide range of temperature from RT up to 773 K. The measurements showed that the substitution of both tetravalent ions (Ge⁴⁺ and Ti⁴⁺) tend to convert Cu-ferrite from n- to p-type semiconductor. The results were analyzed on the basis of the small polaron model. The cation distribution for each system was proposed. The activation energy ΔE, Fermi energy E_F, the density of charge carriers n or p and the carriers mobility μ were determined for both systems. In addition, an energy band schemes of Cu–Ge and Cu–Ti ferrites were schematically represented.     

Generation of H− ions in a low-pressure xenon-hydrogen discharge. I

A theory of a low-pressure discharge in a xenon-molecular hydrogen mixture is developed. It is shown that, in such a discharge, at an interelectrode distance of L = 1 cm and a total plasma pressure of p ₀ ～ 1 Torr, the density of negative hydrogen ions produced via the dissociative attachment of thermal electrons to vibrationally excited molecules H₂ can reach a value as high as N_H ^? ≥ 10¹² cm^?3. According to calculations, the electron temperature in discharge operating regimes under study attains T _e ≈ 1?2 eV, which corresponds to the maximum of the e-v exchange rate constant of H₂ molecules. This ensures a relatively high rate of vibrational pumping of H₂ molecules in the discharge.     

Hyperfine interactions, charge compensation mechanisms, and the distribution of tin dopant cations in rare-earth orthochromites RCrO3 (R = Sm, Eu, Gd, Ho)

The reduction in the squared cosine of angle θ of the Cr-O-Cr bond in the Sm-Ho series in samples containing Sn⁴⁺ ions in the Cr³⁺ position in the crystallite bulk is accompanied by a linear increase in hyperfine field H _{T→0 K} at ¹¹⁹Sn nuclei. Upon annealing in H₂, tin attains oxidation state +2 occupying the Cr³⁺ and R ³⁺ positions on the surfaces of particles. Mössbauer measurements in situ at 100 K do not reveal the spin polarization of Sn²⁺, but this polarization does manifest itself for part of the daughter Sn⁴⁺ ions formed when samples come into contact with air.     

Structure and electrochemical performance of LiCoO2 cathode material in different voltage ranges

LiCoO₂ sample prepared by high-temperature solid state calcination shows a typical hexagonal structure with a single phase and fine particle size distribution. The high-voltage electrolyte with additive fluoroethylene carbonate (FEC) has been used. Electrochemical results show that the initial discharge capacities of the prepared LiCoO₂ cathode are 157.7, 169.5, 191.0, and 217.5 mAh g^?1 in the voltage ranges of 3.0–4.3, 3.0–4.4, 3.0–4.5, and 3.0–4.6 V, respectively. The capacity increases, while the initial coulombic efficiency and capacity retention decrease with increasing the charge cutoff voltage. The capacity retention is only 10.4 % after 200 cycles at 1C rate in the voltage range of 3.0–4.6 V. X-ray diffraction measurements confirm structural changes of the layered material in the different voltage ranges. A phase transition from the O3 to the H1-3 phase can be observed when LiCoO₂ is charged above 4.5 V. The AC impedance analysis indicates that the resistances (R _(sf+b), R _ct) of the prepared LiCoO₂ rapidly increase when the cell is charged to higher voltage. The amount of dissolved Co into the electrolyte also greatly increases with increasing the charge cutoff voltage.     

Charge exchange cross sections of carbon ions

Based on experimental data on the ion charge distributions, the cross sections of single electron loss σ _{i, i + 1} and single electron capture σ _{i, i ? 1} by carbon ions with velocities (2.7–8) × 10⁸ cm/s in different gaseous media (He, N₂, and Ar) have been obtained. Regularities of the cross section variation of the electron capture and loss by carbon ions as a function of the ion velocity, ion charge, and atomic number of the target have been for the first time studied in a wide range of the initial ion charge, from i = 0 to i = 6. A qualitative agreement of the obtained results with the published data has been established for a number of other ions. Theoretical calculations of the cross sections of single electron loss by carbon ions in helium have been carried out.     

Intensity and detuning dependence of fine structure changing collisions in a 85 Rb magneto-optical trap

In an experimental study, the multi-ionisation of metallic clusters (Na_n) has been analysed in collisions with light ions in low charge states (H⁺, He⁺, He²⁺, O³⁺) at collision velocities below 1 a.u. Cluster ions are produced in charge states up to 5+. The average charge of the nano-particles is found to increase linearly with the variation of projectile velocity and the square of the effective projectile charge, well in agreement with the electronic stopping power of the bulk material. A fraction of 50% to 30% of the total projectile energy loss (decreasing with velocity) is transferred into vibrational modes in good agreement with recent theoretical predictions. Received 8 November 2000 and Received in final form 26 January 2001     

Charge states of cobalt ions in nanostructured lithium cobaltite: X-ray absorption and photoelectron spectra

The charge states of ions in nanostructured lithium cobaltite prepared by severe plastic deformation under pressure have been determined using X-ray absorption spectroscopy and photoelectron spectroscopy, as well as calculations of the atomic multiplets with allowance for the charge transfer. It has been found that small deformations (pressures up to 5 GPa and angles of anvil rotation up to 30°) lead to the generation of lithium vacancies in the bulk of the nanostructured material and the formation of the Li₂O phase on the surface. The charge compensation occurs at the expense of holes in oxygen 2p states; the electronic configuration of cobalt ions is 3d ⁶ L, where L is a hole in oxygen 2p states. It has been shown that nanostructured lithium cobaltite belongs to the class of insulators with a negative charge transfer energy. An increase in the degree of deformation of lithium cobaltite (at a pressure up to 8 GPa) leads to the formation of Co²⁺ ions (with the electronic configuration 3d ⁷).     

A symmetry relating certain processes in 2-and 4-dimensional space-times and the value α0 = 1/4π of the bare fine structure constant

The symmetry manifests itself in exact relations between the Bogoliubov coefficients for processes induced by an accelerated point mirror in 1 + 1 dimensional space and the current (charge) densities for the processes caused by an accelerated point charge in 3 + 1 dimensional space. The spectra of pairs of Bose (Fermi) massless quanta emitted by the mirror coincide with the spectra of photons (scalar quanta) emitted by the electric (scalar) charge up to the factor e ²/ħc. The integral relation between the propagator of a pair of oppositely directed massless particles in 1 + 1 dimensional space and the propagator of a single particle in 3 + 1 dimensional space leads to the equality of the vacuum-vacuum amplitudes for the charge and the mirror if the mean number of created particles is small and the charge e = √ħc. Due to the symmetry, the mass shifts of electric and scalar charges (the sources of Bose fields with spin 1 and 0 in 3 + 1 dimensional space) for the trajectories with a subluminal relative velocity β₁₂ of the ends and the maximum proper acceleration w ₀ are expressed in terms of the heat capacity (or energy) spectral densities of Bose and Fermi gases of massless particles with the temperature w ₀/2π in 1 + 1 dimensional space. Thus, the acceleration excites 1-dimensional oscillation in the proper field of a charge, and the energy of oscillation is partly deexcited in the form of real quanta and partly remains in the field. As a result, the mass shift of an accelerated electric charge is nonzero and negative, while that of a scalar charge is zero. The symmetry is extended to the mirror and charge interactions with the fields carrying spacelike momenta and defining the Bogoliubov coefficients α^B,F. The traces trα^B,F, which describe the vector and scalar interactions of the accelerated mirror with a uniformly moving detector, were found in analytic form for two mirror trajectories with subluminal velocities of the ends. The symmetry predicts one and the same value e ₀ = √ħc for the electric and scalar charges in 3 + 1 dimensional space. Arguments are adduced in favor of the conclusion that this value and the corresponding value α₀ = 1/4π of the fine structure constant are the bare, nonrenormalized values. The text was submitted by the author in English.     

Antisite defects and valence state of vanadium in Na<Subscript>3</Subscript>V<Subscript>2</Subscript>(PO<Subscript>4</Subscript>)<Subscript>3</Subscript>

Electron paramagnetic resonance (EPR) studies have been performed with the aim of determining the valence state and local crystal structure of the nearest environment of vanadium ions in the initial, charged, and discharged samples of the cathode material Na_xV₂(PO₄)₃ (1 ≤ x ≤ 3). It has been found that the charged sample (x = 1) is characterized by an intense signal corresponding to V⁴⁺ ions located in a highly distorted octahedral crystal field. An EPR signal with the g-factor close to the g-factor of the V⁴⁺ ion has also been observed in the initial sample (x = 3), where the intensity of the resonance signal is one order of magnitude lower than that in the charged sample. It has been revealed that the resonance signal under consideration is associated with the formation of antisite defects when a part of vanadium ions are located in sites of sodium ions. It has also been found that the intensity of this signal increases after a complete charge–discharge cycle (x = 3).     

Test ion acceleration in a dynamic planar electron sheath

New exact results are obtained for relativistic acceleration of test positive ions in the laminar zone of a planar electron sheath evolving from an initially mono-energetic electron distribution. The electron dynamics is calculated against the background of motionless foil ions. The limiting gamma-factor γ_p∞ of accelerated ions is shown to be determined primarily by the values of the ion-electron charge-over-mass ratio μ=m_eZ_p/m_p and the initial gamma-factor γ₀ of the accelerated electrons. For μ> 1/8 a test ion always overtakes the electron front and attains γ_p∞> γ₀. For μ< 1/8 a test ion can catch up with the electron front only when γ₀ is above a certain critical value γ_cr, which for μ≪1 can most often be evaluated as . In this model the protons and heavier test ions, for which γ_cr> 10³⁹⁸ is enormous, always lag behind the front edge of the electron sheath and have γ_p∞< γ₀; for their maximum energy an appropriate intermediate asymptotic formula is derived. The domain of applicability of the laminar-zone results is analyzed in detail.     

Photoluminescence characteristics of energy transfer between Er and Bi in Gd2O3: Er, Bi

The phosphors, Bi³⁺- activated Gd₂O₃:Er³⁺, were prepared by sol-gel combustion method, and their photoluminescent properties were investigated under ultraviolet light excitation. The emission spectrum exhibited sharp peaks at about 520, 535, 545, 550 and 559 nm due to (²H_11/2, ⁴S_3/2)→⁴I_15/2 transitions of Er³⁺ ions. The luminescent intensity was remarkably improved by the incorporation of Bi³⁺ ions under 340 nm light excitation, which suggested very efficient energy transfer from Bi³⁺ ions to Er³⁺ions. The introducing of Bi³⁺ ions broadened the excitation band of the phosphor, of which a new strong peak occurred ranging from 320 to 360 nm due to the 6s²→6s6p transition of Bi³⁺ ions. There is significant energy overlap between the emission band of Bi³⁺ ions and the excitation band of Er³⁺ ions. Under 340 nm light excitation, Bi³⁺ absorbed most of the energy and transferred it to Er³⁺. The energy transfer probability from Bi³⁺ to Er³⁺ is strongly dependent on the Bi³⁺ ion concentration. Also, the sensitization effectiveness was studied and discussed in this paper.     

Role of methylene spacer in the excitation energy transfer in europium 1- and 2- naphthylcarboxylates

A series of compounds Ln(RCOO)₃·Phen (Ln=Eu, Gd, Tb; RCOO⁻-1- and 2-naphthoate, 1- and 2-naphthylacetate, 1- and 2-naphthoxyacetate anions, Phen-1,10-phenanthroline) was investigated by methods of optical spectroscopy. Compounds of composition Ln(RCOO)₃·nH₂O with the same carboxylate ligands are also considered. Results of studies of the effects of methylene spacer decoupling the π-π- or p-π-conjugation in the naphthylcarboxylate ligand on the structure of Eu³⁺ coordination centre, on the lifetime of ⁵D₀ (Eu³⁺) state, and on processes of the excitation energy transfer to Eu³⁺ or Tb³⁺ ions are presented. Introduction of the methylene bridge in the ligand weakens the influence of the steric hindrances in forming of a crystal lattice and results in lowering the distortion of the Eu³⁺ luminescence centre, and in elongation of the observed ⁵D₀ lifetime τ_obs. The latter is caused by decrease in contribution of the radiative processes rate 1/τ_r. This is confirmed by the correlation between the lifetimes τ_obs and the quantities “τ_r·const” inversely proportional to the total integral intensities of Eu(RCOO)₃·Phen luminescence spectra. The methylene spacer performs a role of regulator of sensitization of the Ln³⁺ luminescence efficiency by means of an influence on mutual location of lowest triplet states of the ligands, the ligand-metal charge transfer (LMCT) states, and the emitting states of Ln³⁺ ions. The lowest triplet state in lanthanide naphthylcarboxylate adducts with Phen is related to carboxylate anion. A presence of the methylene spacer in naphthylcarboxylate ligand increases the triplet state energy. At the same time, the energy of “carboxylic group-Eu³⁺ ion” charge transfer states falls, which can promote the degradation of excitation energy. In naphthylcarboxylates investigated a range of the carboxylate triplet state energies from 19 150 to 20 600 cm⁻¹ was demonstrated in dependence on the type of the carboxylate anion. The interligand energy transfer from Phen to carboxylate lowest triplet state was revealed in complexes with Phen ligand. The effect of OH-group inserted in 1- or 3-position of 2-naphthoate ligand on the excitation energy transfer is also analyzed.     

Synthesis and electrochemical performances of Li4Ti4.95Al0.05O12/C as anode material for lithium-ion batteries

Spinel compounds Li₄Ti_5−xAl_xO₁₂/C (x=0, 0.05) were synthesized via solid state reaction in an Ar atmosphere, and the electrochemical properties were investigated by means of electronic conductivity, cyclic voltammetry, and charge-discharge tests at different discharge voltage ranges (0-2.5 V and 1-2.5 V). The results indicated that Al³⁺ doping of the compound did not affect the spinel structure but considerably improved the initial capacity and cycling performance, implying the spinel structure of Li₄Ti₅O₁₂ was more stable when Ti⁴⁺ was substituted by Al³⁺, and Al³⁺ doping was beneficial to the reversible intercalation and deintercalation of Li⁺. Al³⁺ doping improved the reversible capacity and cycling performance effectively especially when it was discharged to 0 V.     

VUV-UV excited luminescent properties of LnCa4O(BO3)3:RE (Ln=Y, La, Gd; Re=Eu, Tb, Dy, Ce)

Calcium lanthanide oxyborate doped with rare-earth ions LnCa₄O(BO₃)₃:RE³⁺ (LnCOB:RE, Ln=Y, La, Gd, RE=Eu, Tb, Dy, Ce) was synthesized by the method of solid-state reaction at high temperature. Their fluorescent spectra were measured from vacuum ultraviolet (VUV) to visible region at room temperature. Their excitation spectra all have a broadband center at about 188 nm, which is ascribed to host absorption. Using Dorenbos’ and Jφrgensen's work [P. Dorenbos, J. Lumin. 91 (2000) 91, R. Resfeld, C.K. Jφrgensen, Lasers and Excite States of Rare Earth [M], Springer, Berlin, 1977, p. 45], the position of the lowest 5d levels E(Ln,A) and charge transfer band E_ct were calculated and compared with their excitation spectra.Eu³⁺ and Tb³⁺ ions doped into LnCOB show efficient luminescence under VUV and UV irradiation. In this system, Ce³⁺ ions do not show efficient luminescence and quench the luminescence of Tb³⁺ ions when Tb³⁺ and Ce³⁺ ions are co-doped into LnCOB. GdCOB doped with Dy³⁺ shows yellowish white light under irradiation of 254 nm light for the reason that Gd³⁺ ions transfer the energy from itself to Dy³⁺. Because of the existence of Gd³⁺, the samples of GdCOB:RE³⁺ show higher excitation efficiency than LaCOB:RE³⁺ and YCOB:RE³⁺, around 188 nm, which indicates that the Gd³⁺ ions have an effect on the host absorption and can transfer the excitation energy to the luminescent center such as Tb³⁺, Dy³⁺ and Eu³⁺.     

The peculiarities of the low-energy ion scattering by polycrystal targets

In the present work, experimental and computer simulation studies of low-energy (E₀ = 80-500 eV) Cs⁺ ions scattering on Ta, W, Re target surfaces and K⁺ ions scattering on Ti, V, Cr target surfaces have been performed for more accurate definition of mechanism of scattering, with a purpose of evaluation of an opportunity of use of slow ions scattering as a tool of surface layers analysis. The choice of the targets was based on the fact that the ratios of atomic masses of target atoms and ions μ = m₂/m₁ were almost the same for all cases considered and greater than 1 (direct mass ratio) however, the difference of binding energies of target atoms in the cases of Cs⁺ and K⁺ scattering was almost twice as much. It has been noticed that the dependencies of the relative energy retained by scattering ions at the maximum of energy distribution versus the initial energy E_m/E₀ (E₀) have a similar shape in all cases. The relative energy retained by scattering ions increases while the initial energy of incidence ions decreases. The curves are placed above each other relative to the binding energies of target atoms, to show what this says about the influence of binding energy on a process of scattering of low-energy ions. The correlation between value of energy change maintained by an ion for different values of E₀ in the case of scattering by targets with different masses of atoms and its binding energies is experimentally established. The contrary behavior of the E_m/E₀ (E₀) dependencies concerning the target atom binding energy quantity E_b for cases with direct (μ > 1) and inverse (μ < 1) mass ratio of colliding particles is established. The comparison of experimental energy distributions with calculated histograms shows that the binary collision approximation cannot elucidate the abnormally great shift in the maxima of relative energy distributions towards greater energy retained by scattering ions.     

Effect of Nb<Superscript>5+</Superscript> charge neutralization substitution on the electrochemical performance of lithium-rich layered oxides

The effect of the Nb⁵⁺ substitution with a charge-compensated strategy in lithium-rich layered oxides (LLOs) Li_1.2Ni_0.13+xCo_0.13-xMn_0.54-xNb_xO₂ (x?=?0, 0.01, 0.02, and 0.03) has been investigated systematically. A hydroxide co-precipitation method followed by a high-temperature solid-state reaction is adopted in the synthesis process. Structural characterization confirms that the low dose substituting of Nb⁵⁺ in the layered structures forms a solid solution, and the samples show low cation mixing and enlarged Li⁺-diffusing channels, which imply favorable high-rate capability. The initial charge/discharge measurements suggest that the oxygen loss from the network during the delithiation process has been suppressed by the substitution of Nb⁵⁺ due to the formation of robust Nb–O bonds and a decrease in TM-O (TMs are transition metals) covalence. Moreover, these Nb–O bonds contribute to the stabilization of the crystalline framework, resulting in an excellent cycle stability with a mitigated voltage decay.     

Role of Yb and Tm ions in upconversion emission of Tb under 798 and 980 nm laser excitations in Tb-Tm-Yb doped tellurite glass

Upconversion emission and energy transfer processes in singly, doubly and triply doped tellurite glasses have been studied under 798 and 980 nm laser excitations. Emissions have been observed at 482, 544, 584, 655 nm and at 477, 655, 698, 800 nm corresponding to Tb³⁺: ⁵D₄ → ⁷F₆, ⁷F₅, ⁷F₄, ⁷F_J (J = 0, 1, 2, 3) and Tm³⁺: ¹G₄ → ³H₆, ¹G₄ → ³F₄, ³F₃ → ³H₆, ³H₄ → ³H₆ transitions, respectively. Among Tm³⁺, Yb³⁺and Tb³⁺ ions only Tm³⁺ has a ground state absorption at 798 nm excitation due to ³H₄ ← ³H₆ transition. For 980 nm excitation only Yb³⁺ can absorb the incident radiation. However, for both types of excitations, emission from all the three ions Tb, Yb and Tm has been observed. Possible mechanisms are proposed as follows: under 798 nm excitation Tm³⁺ ions are excited which excite Yb³⁺ ions through energy transfer. Finally “cooperative energy transfer” from a pair of Yb³⁺ ions to Tm³⁺ and Tb³⁺ ions takes place. Under 980 nm excitation Yb³⁺ ions absorb the incident energy and excite Tm³⁺ and Tb³⁺ ions via cooperative energy transfer. Variation of emission intensity with the ion concentrations of Yb³⁺, Tm³⁺ and Tb³⁺ has been studied. The lifetime of the ¹G₄ level has also been measured.