Ion induced secondary electron emission from single crystal surfaces

Yields of ion impact induced electrons from very pure Ni(110) and Ni(111) surfaces have been measured. In several tilt planes the angle of incidence of a 5 keV H⁺, H⁺₂ or H⁺₃ ion beam is varied from perpendicular to grazing incidence. Below = 75° the yield increases as sec but shows characteristic depressions when the beam is incident along crystallographically low indexed lattice directions. This is explained by kinetic electron emission with respect to the projectile transparency of the crystal lattice.     

Observation of parametric X-rays produced by 400 GeV/c protons in bent crystals

Spectral maxima of parametric X-ray radiation (PXR) produced by 400 GeV/c protons in bent silicon crystals aligned with the beam have been observed in an experiment at the H8 external beam of the CERN SPS. The total yield of PXR photons was about 10⁻⁶ per proton. Agreement between calculations and the experimental data shows that the PXR kinematic theory is valid for bent crystals with sufficiently small curvature as used in the experiment. The intensity of PXR emitted from halo protons in a bent crystal used as a primary collimator in a circular accelerator may be considered as a possible tool to control its crystal structure, which is slowly damaged because of irradiation. The intensity distribution of PXR peaks depends on the crystal thickness intersected by the beam, which changes for different orientations of a crystal collimator. This dependence may be used to control crystal collimator alignment by analyzing PXR spectra produced by halo protons.     

Surface size effects under plastic deformation of microcrystals and nanocrystals

The size effects associated with the crystal surface as an effective sink for moving dislocations in a thin crystal and as a barrier for these dislocations in the presence of a high-strength film or a special hardened layer on the surface, which favor the accumulation of dislocations in the crystal, have been considered theoretically in terms of the kinetic equation for the density of dislocations concentrated in the crystal in the critical lengths of single-ended (unipolar) dislocation sources. The theoretical results have been illustrated by the experimental data available in the literature for microcrystals and nanocrystals of copper and aluminum. It has been found in accordance with these data that the dependence of the yield stress ??_2% of the crystal on the crystal transverse size D has the form ??_2% ?? D ^?0.75 when there is a free crystal surface for the escape ofthe dislocations and ??_2% ?? D ^?0.5 when there is a high-strength layer on the lateral surface of the crystal..     

BaF2晶体的取向和入射束的剂量对溅射的影响

２７ｋｅＶ Ａｒ^＋离子束沿法向分别入射在ＢａＦ₂单晶（１１１），（１００）和（１１０）的晶面上，用捕获器方法和Ｒｕｔｈｅｒｆｏｒｄ背散射分析法测定了Ｂａ原子的溅射角分布和溅射产额。结果发现不同取向的晶体表面，它们的溅射产额有明显差异。当用剂量为５×１０¹⁷ｉｏｎ／ｃｍ²的Ａｒ^＋离子分别轰击这三种晶面时，其溅射产额的顺序Ｙ_１００＞ｙ_１１１＞ｙ_１１０．对已被上述剂量辐照过的晶面再作相同剂量轰击时，测得的溅射产额明显增大。这些结果被认为是由于在离子辐照过程中表面晶格受损逐步增大所致。 关键词：     

Magnetic structure of the Sr<Subscript>2</Subscript>Cu<Subscript>3</Subscript>O<Subscript>4</Subscript>Cl<Subscript>2</Subscript> two-subsystem antiferromagnet according to nuclear quadrupole resonance data

The magnetic structure of the Sr₂Cu₃O₄Cl₂ two-subsystem antiferromagnet is studied by the nuclear quadrupole resonance (NQR) method on the ^{63, 65}Cu and ³⁵Cl nuclei. The resonance spectrum above T _N2 = 40 K is determined by the Zeeman splitting of the levels of the ^{63, 65}Cu nuclei of the copper atoms at the Cu1 site with the first-order quadrupole perturbation. The magnetic field on the copper nuclei is equal to 93 kOe. The spectrum below n is significantly different: it includes a low-frequency part, which is associated with the ordering of the second magnetic subsystem Cu2. The splitting of the NQR lines of ³⁵Cl is observed above and below T _N2. This fact indicates the ferromagnetic ordering of the moments of the Cu1 subsystem, which are located along the c axis of the crystal, and makes it possible to determine the direction of the magnetic field on Cu1 copper as (110).     

Probing a cooled beam of decelerated highly-charged heavy ions extracted out of the ESR by a channeling experiment

A cooled beam of decelerated highly-charged heavy ions is slowly extracted out of the cooler and storage ring ESR, by combining the deceleration technique and the charge exchange extraction mode. The quality of the external ion beam is tested by a channeling experiment. Bare Au⁷⁹⁺ ions are injected into the ESR at an energy of 360 MeV/u, decelerated to 53 MeV/u, and finally cooled strongly in the electron cooler. By breeding of neighboring charge state ions via radiative recombination in the electron cooler H-like ions are produced. The H-like ion fraction is extracted out of the storage ring. This extracted Au⁷⁸⁺ ion beam is probed by a channeling experiment measuring the extinction rate of the projectile Kα X-ray yield around the [110] axis of a thin silicon crystal. This revised version was published online in August 2006 with corrections to the Cover Date.     

Potentiodynamic desorption spectra of metallic monolayers of Cu,Bi, Pb,Tl, and Sb adsorbed at (111), (100), and (110) planes of gold electrodes

The formation of metallic adsorption layers was studied in solutions of Cu²⁺, Bi³⁺, Pb²⁺, Tl⁺ and Sb³⁺ at (111), (100) and (110) planes of gold single crystal electrodes. Potentiodynamic desorption spectra were recorded with a sweep rate of 20 mV s^?1 for all systems. Characteristic peak structures were obtained which depend strongly on the nature of the adsorbate as well as on the substrate orientation. The half width of the peaks indicates attraction and repulsion respectively for various systems. In most systems more than one peak was observed. This is explained by the formation of various ordered structures. At low coverages peak charge data obtained by integration of current/time curves yield surface concentrations which fit those of ordered structures well, e.g. c(2×2) on (100) or $\text{p(}\text{3}\text{×}\text{3}\text{)}$ R 30° on (111). The adsorption behaviour of the (110) plane is similar in all systems because atomic chains seem to be generally stable. Near the equilibrium potential of the correspondent metal electrode, ?_r = 0, a “mono-molecular” adsorption layer was found for Cu²⁺, Pb²⁺ and Bi³⁺. In the case of the small copper atom, a 1:1 adsorption was found for all planes. Larger atoms like bismuth and lead form epitactic layers at low coverages; at high coverages they form close-packed monolayers with surface concentrations independent of the substrate structure but decreasing with increasing adsorbate radius. The coulometric data for antimony and thallium are not so conclusive. Measurements with various sweep rates show that the adsorption reaction is a slow potential dependent process in various systems. The underpotential/work function correlation of Kolb, Gerischer and Przasnyski is discussed with respect to these experiments. It follows that this concept developed for polycrystalline electrodes is qualitatively valid for (110), but not clearly so for (100) and (111).     

Depolarization of a neutron beam in Laue diffraction by a noncentrosymmetric crystal

The depolarization of a neutron beam executing Laue diffraction in a thick (～3.5 cm) noncentrosymmetric α-quartz crystal is observed. This effect was predicted by us earlier and suggested for measuring the electric dipole moment (EDM) of a neutron. The effect is due to an interaction of the magnetic moment of a moving neutron with a strong crystal electric field, as a result of which the neutron spin rotates in opposite directions for waves of two types excited in the crystal. The effect is studied for neutron diffraction by a system of crystallographic (110) planes at Bragg angles close to π/2, up to 87°. It is shown that, for a crystal of thickness L=3.5 cm, a direct beam initially polarized along the reciprocal lattice vector becomes depolarized upon diffraction, irrespective of the value of Bragg angle, whereas the beam polarized perpendicular to the diffraction plane retains its polarization. The Eτ value determining the sensitivity of the method to EDM is experimentally estimated.     

Coherent signal beam amplification in two-wave mixing experiments with photorefractive Bi12SiO20 crystals

The amplification of the input signal beam in two-wave mixing experiments with photorefractive Bi₁₂SiO₂₀ crystals is achieved when an additional phase shift is established between the photoinduced index modulation (phase volume hologram) and the incident fringe pattern. This stationary phase shift is introduced by either moving the crystal or the interference fringes at a constant speed. The transferred intensity is measured versus the applied electric field, fringe spacing and crystal velocity. The crystallographic orientation and the relative displacement with respect to the applied electric field polarity determine the amplitude of the energy transfer. For the first time in this crystal, signal beam amplification is reached for an applied field E₀ > 8 kV cm^?1 and a crystal or fringe displacement speed around 5 μm s^?1 at the green line (λ = 514 nm) of an argon laser.     

In the wonderland of ultra-parallel neutron beams

Bragg reflections from single crystals yield angular widths of a few arcsec for thermal neutron beams. The Bonse-Hart proposal to attain a sharp, nearly rectangular profile by Bragg reflecting neutrons multiply from a channel-cut single crystal, was realized in its totality three and a half decades later by achieving the corresponding Darwin reflection curves for 5.23 Å neutrons. This facilitated SUSANS (Super USANS) measurements in the Q ～ 10^?5 Å^?1 range. The polarized neutron option was introduced into the SUSANS set-up by separating the up- and down-spin neutron beams by ～10 arcsec with a magnetic (air) prism. The neutron angular width has recently been reduced further by an order of magnitude to ～0.6 arcsec by diffracting 5.3 Å neutrons from a judiciously optimized Bragg prism. This constitutes the most parallel monochromatic neutron beam produced to date. I present the first SUSANS spectra probing the Q ～ 10^?6 Å^?1 domain, recorded with this beam.     

Limitations in specular beam leed analysis due to measurement of the scattering angle: Examples from a study of Cu(110)

The I–V profiles for specular LEED beams from a clean Cu(110) surface have been measured for three selected angles of incidence of the primary electron beam with respect to the crystal orientation. A comparison of experimental and calculated profiles indicates that the first interlayer spacing is contracted by 8 ± 3%, a value in reasonable agreement with the result obtained by a previous study of non-specular beams. However, this study demonstrates some inherent limitations of LEED analyses due to difficulties in the precise measurement of the alignment of the primary electron beam.     

Effects of evolving surface morphology on yield during focused ion beam milling of carbon

We investigate evolving surface morphology during focused ion beam bombardment of C and determine its effects on sputter yield over a large range of ion dose (10¹⁷-10¹⁹ ions/cm²) and incidence angles (Θ = 0-80°). Carbon bombarded by 20 keV Ga⁺ either retains a smooth sputtered surface or develops one of two rough surface morphologies (sinusoidal ripples or steps/terraces) depending on the angle of ion incidence. For conditions that lead to smooth sputter-eroded surfaces there is no change in yield with ion dose after erosion of the solid commences. However, for all conditions that lead to surface roughening we observe coarsening of morphology with increased ion dose and a concomitant decrease in yield. A decrease in yield occurs as surface ripples increase wavelength and, for large Θ, as step/terrace morphologies evolve. The yield also decreases with dose as rippled surfaces transition to have steps and terraces at Θ = 75°. Similar trends of decreasing yield are found for H₂O-assisted focused ion beam milling. The effects of changing surface morphology on yield are explained by the varying incidence angles exposed to the high-energy beam.     

Synthesis, crystal structure, EPR and electrochemical studies of copper(II) dipicolinate complex with 2,2′-dipyridylamine ligand

The (2,2′-dipyridylamine)(pyridine-2,6-dicarboxylato)copper(II) trihydrate complex was synthesized and characterized by spectroscopic (IR, UV-vis, EPR), X-ray diffraction technique and electrochemical methods. The copper(II) center is surrounded by one bidentate 2,2′-dipyridylamine (dpa) and one tridentate dipicolinate (dpc) ligand, and exhibits a distorted square-pyramidal geometry. The crystal packing involves both hydrogen-bonding and π-π interactions. The solvent water molecules link monomers to one another through hydrogen-bonding interactions, forming ladder-type chains in the ab plane. π-π interactions also occur between the dpa rings of neighboring molecules and are responsible for interchain packing. Based on EPR and optical absorption studies, spin-Hamiltonian and bonding parameters have been calculated. The g-values, calculated for title complex in polycrystalline state at 298 K and in frozen DMF (110 K), indicate the presence of the unpaired electron in the d_x²-y² orbital. The evaluated metal-ligand bonding parameters showed strong in-plane σ- and π-bonding. The cyclic voltammogram of the title complex investigated in DMF (dimethylformamide) solution exhibits only metal centered electroactivity in the potential range ±1.25 V versus Ag/AgCl reference electrode.     

Hot microplasma in the channel of a solid target induced by a sequence of femtosecond laser pulses

The dynamics of the hard X-ray yield is studied as a function of the laser-shot number, and the maximum temperature of the hot electron plasma component in the channel formed by a sequence of tightly focused near-IR femtosecond laser pulses (τ = 110 fs, λ = 1.24 μm, and I = 10¹⁵–10¹⁶ W/cm²) in air at various pressures (P = 0.01–760.00 Torr) is analyzed. The dependence of the depth of the channel in which the hard X rays are generated with the highest efficiency on the air pressure and the laser focusing is obtained. The electron concentration in air plasma in the laser beam waist is estimated using the spectral shift of the second harmonic radiation that is back reflected from the target channel.     

First observation of multiple volume reflection by different planes in one bent silicon crystal for high-energy protons

Multiple volume reflection by different planes in a bent silicon crystal with its 〈111〉 axis orientation close to the beam direction was observed for the first time for 400 GeV/c protons at the CERN SPS. The proton beam was deflected to the side opposite to the crystal bend by an angle of about 67 μrad, which is five times larger than in a single volume reflection by the (110) bent planes. The registered efficiency of one side deflection was about 84%. It was shown that multiple volume reflection transforms to a single volume reflection when the orientation angle of the 〈111〉 axis relative to the beam direction is increased.     

质子在α-LiIO3单晶中的沟道效应研究

利用MeV能量的准直质子束,在不同的质子能量下,测定了α-LiIO₃单晶<001>向的轴沟道参数角度半宽度ψ1/2和产额极小值χ_min。在向静电场作用卞,首次观察到入射质子与表面处的Ⅰ原子沟道-背散射产额随电场作用时间而增加,并定量计算了表面无序Ⅰ原子数随静电场作用时间的关系。另外,入射质子与 ⁷Li原子沟道-核反应[⁷Li(p,α)⁴He]产生的α粒子产额也随电场作用时间而增加。 关键词：     

Molecular beam study of the apparent activation barrier associated with adsorption and desorption of hydrogen on copper

Molecular beam techniques are employed to study the adsorption and desorption of H₂ on the (100), (110), and stepped (310) crystal faces of copper. Each crystal is exposed simultaneously to a supersonic molecular beam of H₂ (energy variable from 1.6 to 10.7 kcal/mole) and a highly dissociated beam of deuterium. The majority of the H₂ molecules are scattered from the surface (i.e., are not adsorbed), while a portion of the remaining molecules adsorb dissociatively and react catalytically with adsorbed deuterium atoms to form HD molecules. These HD molecules desorb, and their angular distribution is measured by a rotatable mass spectrometer. For all three crystal faces, the distributions of desorbed HD deviate significantly from diffuse emission and are in excellent agreement with the results of our previous permeation study. From the dependence of the HD signal on the energy and incident angle of the H₂ beam, it appears that there are substantial energy barriers to adsorption, with these barriers depending on crystallographic orientation and acting essentially perpendicular to the surfaces. Both the energy dependence of the dissociative adsorption probability and the shapes of the HD angular distributions are nearly identical for the stepped (310) and (100) surfaces, thereby suggesting that ledge sites are not the principal regions responsible for adsorption of hydrogen on copper. The estimated adsorption probabilities versus energy are “S” shaped curves which appear to level off at values considerably less than unity. A comparison of our results with a very simple model with a single energy barrier to adsorption is qualitatively but not quantitatively satisfactory. An interpretation which includes a distribution of energy barriers is suggested.     

Adsorption and reaction of glycine on the rutile TiO2(011) single crystal surface

The adsorption and reaction of glycine on the surface of a rutile TiO₂(011) single crystal has been studied by X-ray Photoelectron Spectroscopy (XPS) and Temperature Programmed Desorption (TPD) techniques. Special attention was given to the formation and stability of the zwitterion structure (⁺NH₃–CH₂–COO^?) in comparison to that of the dissociated structure (NH₂–CH₂–COO^?). Both species have been observed on the surface at 300 K. The zwitterion structure was found less stable than the dissociated structure. This is in line with other experimental results related to proline on rutile TiO₂(110) single crystal [13, 14], glycine on rutile TiO₂(110) single crystal [17, 24] and computational results related to glycine on rutile TiO₂(110) single crystal [25]. By 500 K most of the zwitterion structure has been converted to the dissociated one. TPD results indicated that glycine reacts in a similar way to carboxylic acids on this surface with the main decomposition products being ketene (CH₂=C=O). Other masses left unassigned for were also observed during TPD. The most intense being m/e 55 that might be due to =CH–C(O)N=or C(O)N=CH fragments.     

X-ray induced electron stimulated desorption versus photon stimulated desorption: NH3 on Ni(110)

The X-ray induced desorption of H⁺ ions from NH₃ layers adsorbed at T = 90 K on Ni(110) has been compared to the corresponding total electron yield (TY) in the photon energy range 390 to 900 eV. The H⁺ yield exhibits a jump at the N K-edge and the Ni L-edge which inversely varies with the NH₃ layer thickness. The H⁺ Ni L-edge jump is closely correlated to the TY jump. Both vanish for the saturated NH₃ multilayer, indicating that the observed Ni L-edge jump in the H⁺ yield is exclusively due to X-ray induced electron stimulated desorption (XESD). At the N K-edge, the near edge absorption fine structure of the H⁺ yield and TY of the saturated NH₃ multilayer are distinctly different. This is interpreted as the H ⁺ yield being the superposition of direct photon stimulated ion desorption (PSID) and XESD. Based on the observed variation of the H⁺ yield near edge fine structure with varying NH₃ layer thickness, a deconvolution of the PSID and XESD contributions is used to derive the relative contribution of PSID versus XESD to be 40% versus 60%, respectively. The relevance of this result for future PSID-SEXAFS studies is discussed. For monolayer NH₃ on Ni(110) the polarization dependence of the N K-edge fine structure in the N(KVV) Auger yield indicates that the symmetry axis of NH₃, is perpendicular to the surface.     

NMR study of KCuF3 at low temperatures

The NMR of F¹⁹ nuclei in KCuF₃ has been measured in the a-type single crystal at 1.7 K. Two types of magnetic domains exist; one occupies most part of the crystal and has easy axis along <110>, and the other occupies the rest of the crystal and has easy axis along <100>. In both domains the moment directions are distributed around the easy axes over a considerable angular range. The spin-flop begins with nearly zero applied field in the <110>;-domain. When the magnetic field is rotated in the c-plane, an angular dependence has been observed for those F¹⁹ nuclei which lie on the c-axis. This dependence arises from the alternate stacking of the ground state wave functions of Cu²⁺ ions.