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The transmissions of oxygen ions through Al2O3 nanocapillaries each 50 nm in diameter and 10 μm in length at a series of different tilt angles are measured, where the ions with energies ranging from 10 to 60 keV and charge states from 1 up to 6 are involved. The angular distribution and the transmission yields of transported ions are investigated. Our results indicate both the existence of a guiding effect when ions pass through the capillary and a significant dependence of the ion transmission on the energy and the charge state of the ions. The guiding effects are observed to be enhanced at lower projectile energies and higher charge states. Meanwhile, the results also exhibit that the transmission yields increase as the tilt angle decreases at a given energy and charge state.

This paper reports that the K x-ray spectra of the thin target (47)Ag, (48)Cd, (49)In and (50)Sn were measured by an HPGe semi-conductor detector in collisions with 84.5 MeV (6)C(4+) ions. Our experiment revealed the K alpha x-ray energy shifts were not obvious and the K beta(1) x-ray energy shifts were about 90 similar to 110 eV. The simple model of Burch et al has been previously used to calculate the K x-ray energy shifts due to an additional vacancy in 2p orbit. The present work extends the model of Burch to calculate the x-ray energy shifts of multiple ionized atoms induced by heavy ions with kinetic energy of MeV/u. In addition to our experimental results, many other experimental results are compared with the calculated values by using the model.

This paper reports that at a newly constructed small-angle x-ray scattering station of Beijing Synchrotron Radiation Facility, the topological shape of ligand-free bovine serum albumin in solution has been investigated. An appropriate scattering curve is obtained and the calculated value of the gyration radius is 31.2A±0.25A (1A=0.1 nm) which is coincident with other ones' results. It finds that the low-resolution structure models obtained by making use of ab initio reconstruction methods are fitting the crystal structure of human serum albumin very well. All of these results perform the potential of the beamline to apply to structural biology studies. The characteristics, the defects, and the improving measures of the station in future are also discussed.

The values of direct double-to-single ionization ratio R of helium atoms induced by Cq+, Oq++ (q = 1–4) ions at incident energies from 0.2 to 8.5MeV are measured. Based on the existing model (Shao J X, Chen X M and Ding B W 2007 Phys. Rev. A 75 012701) the effective charge of the projectile is introduced to theoretically estimate the value of R for the partially stripped ions impacting on helium atoms. The results calculated from our 'effective charge' model are in good agreement with the experimental data, and the dependence of the effective charge on the ionization energy of the projectile is also discussed qualitatively.

This paper reports that the ratios of double to single electron loss cross-section (R) of O2+ in collision with Ar and He at the velocity of 1–4ν0 (ν0 is the Bohr velocity) have been obtained by the coincidence technique. The trend of R – V in the experiment indicates that the effective charge varies with injected velocity. The effective charge can be obtained by the n-body classical trajectory Monte Carlo method, which is interpreted by the molecular Coulomb over barrier model.

The L-shell x-ray yields of Zr and Mo bombarded by slow Ar16+ions are measured. The energy of the Ar16+ions ranges from about 150 keV to 350 keV. The L-shell x-ray production cross sections of Zr and Mo are extracted from these yields data. The explanation of these experimental results is in the framework of the adiabatic direct-ionization and the binding energy modified BEA approximation. We consider, in the slow asymmetric collisions such as Ar and Mo/Zr, the transient united atoms (UA) are formed during the ion-surface interaction and the direct-ionization is the main mechanism for the inner-shell vacancy production. Generally, the theoretical results are in good agreement with the experimental data.

The ratios of transfer ionization (TI) to single-electron capture (SC) cross sections have been measured for the collisions of partially stripped Cq+ ions (q = 1-4) with He. The collision velocity ranges from 0.7 to 4.4v(0) (v(0) is the Bohr velocity). The projectile-ion and recoil-ion coincidence technique is used to separate the processes of TI and SC. The ratios reach the maximum when the velocity is about 3.7 v(0). This can be explained qualitatively based on the two-step mechanism. The experimental results are also compared with the results calculated using the classical trajectory Monte Carlo (CTMC) method. The CTMC results are in agreement with the experimental data basically. The discrepancies in higher velocity region are interpreted by the effective charge effect.

The relative partial cross sections for 13C6+–Ar collisions at 4.15–11.08 keV/u incident energy are measured. The cross-section ratios σ2E/σSC, σ3E/σSC, σ4E/σSC and σ5E/σSC are approximately the constants of 0.51±0.05, 0.20±0.03, 0.06±0.03 and 0.02±0.01 in this region. The significance of the multi-electron process in highly charged ions (HCIs) with argon collisions is demonstrated (σME/σSC as high as 0.79±0.06). In multi-electron processes, it is shown that transfer ionization is dominant while pure electron capture is weak and negligible. For all reaction channels, the cross-sections are independent of the incident energy in the present energy region, which is in agreement with the static characteristic of classic models, i.e. the molecular Coulomb over-the-barrier model (MCBM), the extended classical over-the-barrier model (ECBM) and the semiempirical scaling laws (SL). The result is compared with these classical models and with our previous work of 13C6+-Ne collisions [Chin. Phys. Lett. 23 (2006) 95].

The cross-section ratios of double-, triple-, quadruple-, and the total multi-electron processes to the single electron capture process (σDE/σSC, σTE/σSC, σQE/σSC and σME/σSC) as well as the relative ratios among reaction channels in double-electron active, triple-electron active and quadruple-electron active are measured in 13C6+–Ne collision in the energy region of 4.15–11.08 keV/u by employing position-sensitive and time-of-flight coincident techniques. It is determined that the cross-section ratios σDE/σSC, σTE/σSC, σQE/σSC and σME/σSC are approximately the constants of 0.20±0.03, 0.16±0.04, 0.06±0.02 and 0.42±0.05. These values are obviously smaller than the predictions of the molecular Coulomb over-the-barrier model (MCBM) [J. Phys. B 23 (1990) 4293], the extended classical over-the-barrier model (ECBM) [J. Phys. B 19 (1986) 2925] and the semiempirical scaling laws (SL) [Phys. Rev. A 54 (1996) 4127]. However, the relative ratios among partial processes of DE, TE and QE are found to depend on collision energy, which suggests that the collision dynamics depends on the collision velocity. The limitation of velocity-independent character of ECBM, MCBM and SL is undoubtedly shown.

In this paper we report the measurements of the K x-ray relative transition probabilities as follows: K-beta/K-alpha for the atomic numbers Z = 39, 51, 62, 63, 64, 66, 67 and 68; and K-alpha2/k(alpha1), k(beta1)(1)/k(alpha1), k(beta2)(1)/k(beta1)1, and k(beta3)/k(beta2) for the atomic numbers Z = 62, 63, 64, 66, 67 and 68 as induced by protons at an energy of 3 MeV. The experimental results obtained are then compared with relativistic Hartree-Fock calculations.

We investigate angular distributions of the transmitted 60 keV and 120 keV O3+ ions through nanocapillaries with 50nm diameter and 10μm length. The experimental results are in agreement with the 'guiding effect' found by Stolterfoht et al. For different tilted angles of the nanocapillary membrane with respect to the beam, the angular distributions of the transmitted ions are measured by a one-dimensional micro-channel plate (MCP) detector. Moreover, the dependence of this guiding effect on the projectile energy is studied.

The Cu films are deposited on two kinds of p-type Si (111) substrates by ionized cluster beam (ICB) technique. The interface reaction and atomic diffusion of Cu/Si (111) and Cu/SiO2/Si (111) systems are studied at different annealing temperatures by x-ray diffraction (XRD) and Rutherford backscattering spectrometry (RBS). Some significant results are obtained: For the Cu/Si (111) samples prepared by neutral clusters, the interdiffusion of Cu and Si atoms occurs when annealed at 230?C. The diffusion coefficients of the samples annealed at 230?C and 500?C are 8.5 ? 10-15 cm2?s-1 and 3.0 ? 10-14 cm2?s-1, respectively. The formation of the copper-silicide phase is observed by XRD, and its intensity becomes stronger with the increase of annealing temperature. For the Cu/SiO2/Si (111) samples prepared by neutral clusters, the interdiffusion of Cu and Si atoms occurs and copper silicides are formed when annealed at 450?C. The diffusion coefficients of Cu in Si are calculated to be 6.0 ? 10-16 cm2?s-1 at 450?C, due to the fact that the existence of the SiO2 layer suppresses the interdiffusion of Cu and Si.

A simple model for the direct ionization and transfer ionization probabilities in A2+ +He collisions in a wide projectile energy range is proposed based on the Bohr–Lindhard model and the classical statistical model. The calculated cross sections are in satisfactory agreement with the experimental data available.

The multi-electron processes are investigated for 17.9–120 keV/u C1+, 30–323 keV/u C2+, 120–438 keV/u C3+, 287–480 keV/u C4+ incident on a helium target. The cross-section ratios of double electron (DE) process to the total of the single electron (SE) and the double electron process (i.e. SE+DE), the direct double electron (DDI) to the direct single ionization (DSI) as well as the contributions of DDI to DE and of TI to DE are measured using coincidence techniques. The energy and charge state dependences of the measured cross-section ratios are studied and discussed.

The cross section ratios of the double, triple and quadruplicate ionization to the single ionization of argon by 1.5-7.5 MeV partially stripped carbon ions are measured by using time-of-flight technique. The Auger transition and the charge exchange process in the multiple ionization of argon are studied. The ratios of cross sections of the direct multiple ionization to those of the direct single ionization are obtained by subtracting the parts of the Auger transition and the charge exchange process from the measured data. It is found that the cross section ratios of the direct multiple ionization to those of the direct single ionization are in good agreement with the predicted multi-step (ν/qeff)-2n+2 law.

The isotopic bare ion 13C6+ was employed to collide with helium at 4.15–11.08 keV/u. The relative partial cross sections were measured by position-sensitive and time-of-flight coincident techniques. It is shown that the direct-ionization (DI) process can be completely ignored in this region, the transfer ionization (TI) process is the most important double-electron channel, and the probability of the pure double-electron capture (DC) process is quite small. The cross-section ratio of the total double-electron (DE) process (i.e. DC+TI) to the single-electron capture (SC) process is experimentally determined to be approximately a constant of 0.09±0.03 in this region, and this value is obviously smaller than the predictions of the classical over-barrier models and the semi-empirical scaling laws. It is found that the cross-section ratio of pure DC to DE decreases obviously as the projectile velocity increases. Because the pure DC process only comes from the radiation de-excitation following the DC process and are competed by the TI process (comes from the auto-ionization following the DC process), this implies that the population of the two captured electrons depends distinctly on the collision velocity. Comparison with works on Ar16+–He by Wu et al. [Phys. Rev. A 48 (1993) 3617] reveals that the strong projectile-dependent character of the pure DC process exists.

We study the L x-ray emission from Zr, Mo and In targets and M x-ray emission from Pb target under bombardment of low energy Arq+ (q = 13,14,15,16) ions. The relative x-ray yields were measured in the projectile kinetic energy range 210–360 keV. It is found that the relative x-ray yields from Zr, Mo and Pb targets increase with the increasing projectile kinetic energy for Ar14+ and Ar16+ projectiles and depend on the potential energy of the projectile remarkably.

In this paper, we present a simple theoretical approach to calculate the multiple ionization of big atoms and molecules induced by very high-q fast projectiles in a strong coupling regime (q/v > 1). The results obtained from this approach are in excellent agreement with the available experimental data. A probable scenario of molecular multiple ionization by fast and very high-q projectiles is discussed. The very small computational time required here and the good agreement with the existing experimental data make it a good candidate for studying the multiple ionization of complex molecules under high linear energy transfers.

We have measured the cross-section ratios of helium induced by Cq+ and Oq+ (q = 1?4) in an energy range from 20 keV/amu to 500 keV/amu, and obtained the two-dimensional spectra by employing the coincidence method combined with the MPA-3 data acquisition system. Hence, we obtain the ratios of total single-ionization cross-sections (SI, SC, SLSI, and DLSI), total double-ionization cross-sections (DI, DC, TI, SLDI, and DLDI) and cross-sections of every process (SI, SC, SLSI, DLSI, DI, DC, TI, SLDI, and DLDI), which induce the single-ionization and double-ionization, to the total cross sections respectively. The competitive relations between the reaction-channels and the experimental data law of each reaction-channel are revealed explicitly, and the qualitative explanations involved in those results are also presented accordingly.

In this paper a projectile ion-recoil ion coincidence technique is used to investigate the transfer ionization processes in collisions of 0.22–6.30 MeV Cq+ ions and 0.25–6.35 MeV Oq+ ions (q = 1, 2, 3, 4) with the He atom separately. The cross section ratio f of transfer ionization to single electron transfer is measured, and the dependence of f on both charge state q and energy E of the projectiles is investigated. The electron-structure and the mechanisms leading to transfer ionization affect the dependence of f on q and E. Our measurements, along with other data published previously, suggest a similar dependence of f on charge state and energy of projectile for partially stripped ions over a large energy range. The maximum value of f is approximately 0.17q0.60; the energy corresponding to maximum f is about 160q0.60 keV/u.

The properties of the Z = 117 isotopic chain are studied within the framework of the axially deformed relativistic mean field theory (RMFT) in the blocked BCS approximation. The ground-state properties, such as binging energies, deformations as well as the possible.. decay energies and lifetimes are calculated with the parameter set of NL-Z2 and compared with results from the finite range droplet model. The analysis by RMFT shows that the isotopes in the range of mass number A = 291 similar to 300 exhibit higher stability, which suggests that they may be promising nuclei to be hopefully synthesized in the lab among the nuclei Z = 117.

Cu thin films are deposited on p-type Si (100) substrates by magnetron sputtering at room temperature. The interface reaction and atomic diffusion of Cu/SiO2/Si (100) systems are studied by x-ray diffraction (XRD) and Rutherford backscattering spectrometry (RBS). Some significant results can be obtained. The onset temperature of interdiffusion for Cu/SiO2/Si(100) is 350 °C. With the annealing temperature increasing, the interdiffusion becomes more apparent. The calculated diffusion activation energy is about 0.91 eV. For the CU/SiO2/Si (100) systems copper silicides are not formed below an annealing temperature of 350 °C. The formation of the copper silicides phase is observed when the annealing temperature arrives at 450 °C.