Secondary emission of carbon ions from graphite nanocrystallites

Emission of secondary C⁺ ions from the surface of well-oriented graphite nanocrystallites irradiated with 10 keV Ar⁺ ions has been studied. The energy distribution of emitted secondary ions has been measured. It has been found that the form of energy distribution and the energy corresponding to the maximum of distribution E_max depend on the polar angle θ of C⁺ ion emission. The linear dependence of energy in the maximum of energy spectrum of single-charged secondar y carbon ions on the polar angle of their emission E_max(θ) has been obtained. The mechanism responsible for the observed features of the energy spectra is discussed.     

Spectroscopic characteristics of anionic centers in α-Al<Subscript>2</Subscript>O<Subscript>3</Subscript> crystals bombarded by Cu<Superscript>+</Superscript> and Ti<Superscript>+</Superscript> ions

We have studied the effect of bombardment by Cu⁺ and Ti⁺ ions with energy 30 keV on the optical absorption and luminescence of F centers in oxygen-deficient aluminum oxide. We have shown that in the induced optical absorption spectra there are six components of gaussian shape, which can be assigned to absorption bands of F⁺, F², and F₂⁺ centers. We have established that bombardment of the samples by ion beams has a weak effect on the thermoluminescence parameters in the 3.0 eV and 2.4 eV bands, while in the 3.8 eV luminescence band for F⁺ centers, the thermoluminescent response increases considerably. __________ Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 75, No. 3, pp. 422–424, May–June, 2008.     

Origin of grey spots on the surface of metallic glasses under Ar ion irradiation: The surface and volume properties

The nature of grey spots on the surface of amorphous Fe₆₇Cr₁₈B₁₅ metglass ribbons irradiated by 30 keV Ar⁺ ions is investigated. Changes in the surface and volume properties of samples are analyzed bearing in mind the presence of competitive processes of ordering and disordering in the structure under irradiation at initial stage of crystallization (T = 500 °C). Changes in the volume properties of the samples become apparent in their structure, electrical and magnetic properties and are caused by radiation-enhanced diffusion at high gradients in the concentration of defects generated by Ar⁺ irradiation. It is established that grey spots are shown by decrease in the reflection coefficient in a visible range. They emerge as a result of reorganization in the electronic structure of irradiated ribbons due to damage in the short-range order and formation of non-uniformly scaled atomic structure during transition from the medium-range to the long-range atomic order. Experimental data are in accord with the calculations in the framework of the free electrons model.     

Study on the dynamic energy spectra of mev heavy ions penetrating biological sample

In order to study the probability for heavy ions to have a long projectile range in botanic sample, transmission energy spectra of 1.5 MeV F⁺, 3 MeV F²⁺ and 1.5 MeV H⁺ penetrating 100 µm seed cotyledon samples were measured as a function of ion dose. Results show that very fewer ions can penetrate through the samples, though their theoretical ranges are much shorter than sample thickness. Besides, the measured energy spectra of 1.5 MeV and 3.0 MeV F ions change dynamically while increasing the ion dose, they extend to the high energy direction and the count rates of the transmission ions increases quickly. These phenomena can be understood with the special composition and structure of the biological material.     

Local structure of amorphous and microcrystalline Fe-B alloys

Amorphous and microcrystalline Fe-B alloys in the composition range (4–25) at % B, fabricated by melt spinning, were investigated by pulse nuclear magnetic resonance (NMR) on ¹¹B nuclei at 4.2 K. Alloy samples were prepared both from a natural mixture of isotopes and an isotope mixture ⁵⁶Fe-¹¹B. The NMR spectra were measured at different boron contents. The local atomic structure of amorphous Fe-B alloys has been determined. The amorphous alloys consist of microregions (clusters) with short-range order of the tetragonal and orthorhombic Fe₃B-phase types, as well as of the α-Fe type.     

Physical and Spectral Investigations of Cu<Superscript>2+</Superscript>-Doped Alkali Zinc Borate Glasses

Physical and spectral studies on 20ZnO + xLi₂O + (30-x)Na₂O + 50B₂O₃ (5 ≤ x ≥ 25) doped with 0.1 mol% of paramagnetic CuO impurity are carried out. Powder X-ray diffraction patterns of the glass samples confirm the amorphous nature. The physical parameters of all the glasses were also evaluated with respect to the composition. The electron paramagnetic resonance spectra of all these glasses exhibit resonance signals that are characteristic of Cu²⁺ ions. The optical absorption spectra also confirm the Cu²⁺ ion in tetragonally elongated octahedral site. Various crystal field, spin-Hamiltonian and bonding parameters are evaluated. It is observed that the mixed alkali effect is significant.     

Photofragmentation of mass-selected titanium oxide cluster cations

In this paper we present the photofragmentation spectra of mass-selected positive titanium oxide cluster ions Ti _x O _y ⁺. The clusters are generated by the combination of laser ablation of a titanium target and the supersonic nozzle expansion of oxygen and are detected by time-of-flight mass spectrometry. Small clusters are mass-selected and photodissociated at a wavelength of 308 nm. The recorded photofragmentation spectra indicate that for all parent clusters the main fragment is TiO⁺ and, in some cases, Ti₂O₃ ⁺ is also observed. This is consistent with the assumption that small Ti _x O _y ⁺ clusters are built from a TiO⁺ core with TiO₂ building blocks.     

Secondary ion emission from a GaAs single crystal upon bombardment with Bi<Stack> <Subscript> <Emphasis Type="Italic">m</Emphasis> </Subscript> <Superscript>+</Superscript> </Stack> cluster ions

Secondary-ion mass spectra and energy distributions upon bombarding a gallium arsenide single crystal using Bi_m⁺(m = 1–5) cluster ions with energies of 2–12 keV are investigated. The gallium cluster ion yield grew nonadditively with the number of atoms in the cluster projectiles. A quasi-thermal component found in the energy spectra of secondary Ga⁺ and Ga₂⁺ ions is indicative of the occurrence of the thermal spike mode upon cluster ion bombardment. The quasi-thermal component in the yield of atomic Ga⁺ ions upon bombardment with Bi₂⁺–Bi₅⁺–ions is 35–75%.     

Ion-beam sputtering of quartz samples: Material properties observed in the mass spectra of secondary ions

Matrix effects are analyzed in the secondary ion mass spectra of quartz samples and SiO₂ and SiO _x films. The spectral relations between Si⁺, O⁺, and Si _n O _m ⁺ ions and the corresponding atomic fragments of the matrix are discussed. Previously revealed correlations between the mass spectrum and the structural features of SiO₂ and SiO _x are analyzed via the kinetic models of ion mixing.     

Molecular effects in ion-induced secondary electron spectra

The energy spectra of slow secondary electrons from a copper surface under bombardment with H⁺, H⁺₂, and H⁺₃ ions have been measured at an energy of 200 keV/atom. Distinct molecular effects are revealed in the ratios of the respective distribution curves for molecular ion and proton impact.     

Optical absorption behavior of Tl<Superscript>+</Superscript> DOPED Rb(Br<Subscript>1–<Emphasis Type="Italic">x</Emphasis></Subscript>I<Subscript><Emphasis Type="Italic">x</Emphasis></Subscript>) system

The optical absorption behavior of Tl⁺ doped Rb(Br_1–x I _x ) mixed crystals (with x = 0.00, 0.05, and 0.10) grown under vacuum by slow cooling from the melt has been studied. Absorption spectra of the mixed crystals recorded at room temperature showed that the characteristic A-absorption band of Tl⁺ ions in the Rb(Br_1–x I _x ) system (0.1 mol. %) with x = 0.00 (i.e., RbBr:Tl⁺) broadened with the iodine content towards the low energy side. Changes in the absorption spectra of the mixed crystals are due to creation of some complex centers involving Tl⁺, Br^–, and I^- ions with energy levels inside the band gap while forming the mixed crystal. The absorption spectra of gamma-irradiated mixed crystals showed the F-band, which shifted towards the low energy side due to the existence of iodine ions in the mixed crystals.     

Anisotropy of secondary ion emission from a Ni4Mo single crystal

The azimuthal and polar angle distribution of Ni⁺ and Mo⁺ ions emitted from an ordered Ni⁴ Mo single crystal irradiated with 10-keV Ar⁺ ions was studied. Different azimuthal distributions for Ni⁺ and Mo⁺ ions emitted from the (001) Ni₄Mo face were detected; emission maxima were observed in 〈 011 〉 and 〈 001 〉 directions for Ni⁺ and Mo⁺ ions, respectively. It was shown that polar distributions of nickel’s secondary ions vary with its energy. The observed systematic features were explained by correlated collisions in the upper layers of a Ni₄Mo single crystal.     

Secondary ion mass spectra of alkali halides

Mass spectra of positive and negative secondary ions from various alkali halides have been measured in the Manitoba time-of-flight mass spectrometer. The ions were produced by Cs⁺ and K⁺ bombardment at primary ion energies of 3 to 19 keV for the positive spectra, and 11 to 28 keV for the negative spectra. The ions measured were those emitted within a time interval ～ 20 ns after the primary ion impact. The secondary ion yields are strongly dependent on the sample composition and treatment; prior irradiation may change the yield by an order of magnitude or more. The secondary ion yields also depend strongly on the energy loss of the primary ion, but the ratio of yields of different cluster ions from a given target is almost independent of this parameter. The results appear to be consistent with models in which the clusters are ejected directly from the target, but do not determine whether or not they possess the original surface structure. The results may also be described by a recombination model if the recombination is essentially complete.     

Li3VO4-Li4TO4(T=Ge,Si)固溶体离子导体7Li的NMR研究

在150—573K温度范围内,研究了固溶体Li₃VO₄-Li₄TO₄(T=Ge,Si)系统不同成分的⁷Li的NMR谱。发现γ_II相固溶体室温⁷Li的NMR线宽和自旋晶格弛豫时间T₁的值都比Li₄GeO₄,Li₄SiO₄和Li₃VO₄小约一个数量级。这表明在γ_II相固溶体离子导体中,Li⁺离子运动有可能比固溶前有数量级增长。同时还发现⁷Li的电四极分裂伴线数随成分和温度而异,以及伴线强度百分比依赖于温度。这反映γ_II相的不同成分中,间隙Li⁺离子占有的不等价位置个数不同,而Li⁺离子在每个不等价位置上的占有率又随温度而变化。 关键词：     

Photoluminescence and structural defects in silicon layers implanted by iron ions

The photoluminescence spectra of silicon samples implanted by ⁵⁶Fe⁺ ions [energy, 170 keV; dose, 1×10¹⁶, (2–4)×10¹⁷ cm^?2] and annealed at temperatures of 800, 900, and 1000°C are measured. The structure of the samples at each stage of treatment is investigated using transmission electron microscopy (TEM). It is found that the phase formation and morphology of crystalline iron disilicide precipitates depend on the dose of iron ions and the annealing temperature. A comparison of the dependences of the intensity and spectral distribution of the photoluminescence on the measurement temperature, annealing temperature, and morphology of the FeSi₂ phase revealed the dislocation nature of photoluminescence.     

Theory of Isotope Effects on He+ Trapping in Solid Hydrogen

We are currently investigating the influence of vibrational effects on the strength of trapping of He⁺ in solid hydrogen. Such effects can lead to an isotope dependence of the trapping energy associated with the hydrogen molecules and He⁺ ion. At the present time, our focus is on the isotope effect for ³He⁺ and ⁴He⁺, which we are studying through the vibrational motions of the trapped He⁺ ions in the potential they experience as they move about their equilibrium positions. The potential governing the vibrations has been obtained from Hartree–Fock cluster calculations of the total energy of the cluster composed of the He⁺ ion and up to the third nearest neighbor hydrogen molecules as a function of the displacement of the He⁺ ion from its trapped position. The energy eigenvalues for the ground vibrational states of ³He⁺ and ⁴He⁺ in this potential come out as 1.29 and 0.96 meV, respectively, leading to corresponding reductions by these amounts in the binding energy of 8.6 eV for both ions without vibrational effects. The difference of these reductions can be considered as an isotope shift, its value for this case being 0.33 meV. From the analysis for these results, it is suggested that isotope shift effects for deuteron and triton in solid D–T would have the same order of magnitude. A procedure for more accurate investigations of the isotope shifts is discussed. This revised version was published online in August 2006 with corrections to the Cover Date.     

High resolution diffraction and small angle scattering neutron investigations of LaCo<Subscript>0.5</Subscript>Mn<Subscript>0.5</Subscript>O<Subscript>3+</Subscript><Subscript>δ</Subscript>: effect of oxygen content

We have investigated LaCo_0.5Mn_0.5O_{3+ δ} compounds with different oxygen content by means of magnetization, high resolution and small-angle neutron diffraction measurements. Oxygen content decrease down to stoichiometric composition leads to an essential increase of T_C and magnetic moment while Co/Mn ionic ordering degree is kept almost constant. It is assumed that upon oxygen reduction Co³⁺ ions change their valence state down to 2+ one that leads to dominating of Co²⁺-Mn⁴⁺ ferromagnetic interactions as well as T_C increase. Magnetic properties can be explained in terms of coexistence of long-range ferromagnetic order and short-range clusters with antiferromagnetic interactions prevailing. Size distribution of the mentioned short-range magnetic inhomogeneities is rather mild within the samples but it is strongly temperature dependent.     

Secondary ion emission under the bombardment of Si by multiply charged Si q+ ions

The spectra of secondary ion emission under the bombardment of a B-doped Si target by multiply charged Si ^q+ ions (q = 1?C5) have been studied in the energy range of 1 to 10 keV per unit of charge. A multifold increase in the yield of secondary cluster Sk _n ⁺ ions, multiply charged Si ^q/+ ion (q = 1?C3), and H⁺, C⁺, B⁺, Si₂N⁺, Si₂O⁺ is observed as the charge of the multiply charged ions increases. The increase in the yield of secondary ions with increasing charge of the multiply charged-ion charge is most significant for ions with relatively high ionization potentials.     

Luminescence in collisions of low-energy ions with graphite and Al<Subscript>2</Subscript>O<Subscript>3</Subscript>

Excitation of H⁺, H₂ ⁺, H₃ ⁺, He⁺, and Ar⁺ ions by impact on graphite and Al₂O₃ was investigated by means of emission spectroscopy in the 50–1000 eV energy range of the projectiles. Emission of Balmer series from excited neutral hydrogen is observed for both targets. In addition, for the Al₂O₃ target a continuum emission is observed. The continuum probably originates from excited M_nO_m molecules produced in the collision cascade, when surface atoms bound by ionic bonds are released after the bond breaking caused by neutralization. The spectra obtained under Ar⁺ -bombardment show Ar II lines emitted by backscattered ions.     

On the energy spectra of secondary ions emitted from silicon and graphite single crystals

Secondary ion emission from silicon and graphite single crystals bombarded by argon ions with energies E ₀ varied from 1 to 10 keV at various angles of incidence α has been studied. The evolution of the energy spectra of C⁺ and Si⁺ secondary ions has been traced in which the positions of maxima (E _max) shift toward higher secondary-ion energies E ₁ with increasing polar emission angle θ (measured from the normal to the sample surface). The opposite trend has been observed for ions emitted from single crystals heated to several hundred degrees Centigrade; the E _max values initially remain unchanged and then shift toward lower energies E ₁ with increasing angle θ. It is established that the magnitude and position of a peak in the energy spectrum of secondary C⁺ ions is virtually independent of E ₀, angle α, and the surface relief of the sample (in the E ₀ and α intervals studied). Unusual oscillating energy distributions are discussed, which have been observed for secondary ions emitted from silicon (111) and layered graphite (0001) faces. Numerical simulations of secondary ion sputtering and charge exchange have been performed. A comparison of the measured and calculated data for graphite crystals has shown that C⁺ ions are formed as a result of charge exchange between secondary ions and bombarding Ar⁺ ions, which takes place both outside and inside the target. This substantially differs from the ion sputtering process in metals and must be taken into account when analyzing secondary ion emission mechanisms and in practical applications of secondary-ion mass spectrometry.