Effects of passage of 200 MeV Ag9+ ions in indium phosphide at different depths

Indium phosphide sample was irradiated with 200?MeV Ag⁹⁺ ions for the fluence of 2?×?10¹³?ions?cm^?2. The sample was chemically etched down up to 240?nm depth to investigate the distribution of defects at different regions. Raman scattering and glancing incidence X-ray diffraction spectra were recorded at different depths. The stress estimated from Raman shift was found to increase with depth up to 160?nm and thereafter it decreased and at a depth of 224?nm sample did not show any stress. Phonon coherence length estimated from the Phonon Confinement Model was found to vary between 43 and 18?nm with respect to depth. Glancing incidence X-ray diffraction results revealed the decrease in crystallite size from 16.12 to 1.00?nm in different depth regions.     

Photodissociation spectroscopy of OH+ molecular ions at the TSR storage ring

When infrared active molecular ions are stored in a heavy ion storage ring, a fast beam of vibrationally and rotationally relaxed molecules can be obtained. This opens up new opportunities for various experimental studies in molecular ion physics, particularly those involved with spectroscopy and dissociation dynamics of excited states. The analysis of such experiments is facilitated by the fact that the information on the initial states is able to identify and, therefore, eliminate them from the assignment problem. Moreover, when the intensity of the measured transitions is monitored as a function of storage time, the dependence of these processes on the degree of internal relaxation is revealed. We demonstrate these general principles by application to near threshold dissociation spectroscopy of the OH⁺ molecular ion. The structure of quasibound levels near the dissociation limit of OH⁺ and its dissociation energy are deduced. This revised version was published online in August 2006 with corrections to the Cover Date.     

Triatomic wake effect and the determination of the molecular structure of HD2+ from the Coulomb explosion

A new theoretical model of the triatomic molecular wake effect is proposed and applied to molecular ions D+ 3 and HD+ 2 while passing through a solid.The wake effects resulting from the reactions of the two similar ions with thin carbon foil are also investigated by using the Coulomb explosion technique.The experimental results are in good agreement with theoretical estimates and the molecular structure of HD+ 2 is determined by using the model.     

Deep inelastic collisions of32S +27Al reaction at 130 MeV bombarding energy

The³²S +²⁷Al reaction was studied to investigate the deep inelastic collisions at a bombarding energy of 130 MeV which is well above the Coulomb barrier. The energy distributions of the binary decay products of 6⩽Z⩽10 were determined using a large area position sensitive ionization chamber. The average kinetic energies of the reaction products indicate that the exit shapes correspond to highly stretched scission configurations in the deep-inelastic processes.     

Optical model potential of 800 MeV/c K+ meson for12C and40Ca by the method of inversion

The elastic scattering differential cross-sections of 800 MeV/c K⁺ mesons from¹²C and Ca have been analyzed using the Ericson’s parametrization for the phase shift. It is found that the parameter values obtained by our analysis are significantly different from those obtained from the closed expression for K⁺-nucleus amplitude derived by the strong absorption approximation. Next, using the phase shift obtained from the present analysis we calculate the K⁺ optical model potentials for¹²C and⁴⁰Ca by the method of inversion. The calculated potentials are compared with the recently determined phenomenological ones.     

Absorption and EPR spectra of Cr3+ ions in a LaBeAl11O19 crystal

Electron spectra of optical absorption and EPR of Cr³⁺ ions in a LaBeAl₁₁O₁₉ crystal are investigated. It is shown that the Cr³⁺ ions occupy, three different octahedral positions of Al³⁺ in the LaBeAl₁₁O₁₉ structure, namely, 12k, 2a, and 4f₂; the ratio of their intensitites is 1∶2∶30, respectively. Parameters of the Cr³⁺ centers are determined and its is shown that the optical absorption spectra in the visible region are practically determined by the Cr³⁺ (III) occupying the 4f₂-positions. Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 66, No. 2, pp. 275–277, March–April, 1999.     

自受激拉曼晶体Nd3+:SrMoO4的光谱性质研究

通过拉曼散射光谱，吸收光谱，荧光发射寿命和808 nm LD激发下的红外荧光光谱的实验测量，系统研究了Nd³⁺:SrMoO₄晶体的自受激拉曼光谱性质.分析指认了拉曼散射光谱中各拉曼峰所对应的晶格振动模式，得出了其SRS活性最强的声子频率约为898 cm^-1，对应于(MoO^2-₄)离子团的完全对称光学伸缩振动A_g模；通过J-O理论对晶体的吸收谱进行了全面的光谱参数计算，得出⁴F_3/2→⁴I_11/2跃迁的积分发射截面达0.57×10^-18 cm²，自发辐射概率为141.06 s^-1；同时，实验测得该跃迁的荧光发射寿命约为0.2 ms.最后，结合808 nm LD激发下的红外波段荧光光谱，论证了SrMoO₄晶体中Nd³⁺离子1068 nm发射通过拉曼频移获得1180 nm一级斯托克斯激光发射的可能性，为Nd³⁺:SrMoO₄晶体的自受激拉曼激光器研究提供了理论依据. 关键词： 3+离子')" href="#">d³⁺离子 4 晶体')" href="#">SrMoO₄ 晶体 自受激拉曼散射     

Zeros of the helicity amplitudes of Σ+-p elastic scattering

Optimally exploiting the analytic structure of the helicity amplitudes of Σ⁺-p scattering we locate their zeros by making a fit to the differential cross-section curves at 40, 100 and 150 MeV energies. Minute changes in the positions of the zeros produced detectable noises in the fit. It was observed that quite reliable predictions for the phase shifts can also be obtained from this analysis.     

Kinetic energy and charge state effects in the X-ray emission of Mo surface induced by Xe q + ( q = 25, 29) ions

L-shell X-ray spectra of Mo surface induced by Xe²⁵⁺ and Xe²⁹⁺ were measured. The X-ray intensity was obtained in the kinetic energy range of the incident ions from 350 to 600 keV. The relationship of X-ray intensity with kinetic energy of the projectile and its charge state were studied, and the simple explanation was given. Supported by the Science and Technology Ministry Foundation of China (Grant No. 2002CCA00900) and the Foundation of National Key Laboratory of Vacuum & Cryogenics Technology and Physics     

Unified calculations of spin-Hamiltonian parameters and optical band positions for Ni+ ion in AgGaSe2 crystal

The complete diagonalisation (of energy matrix) method based on the two-spin-orbit-parameter model is applied to unifiedly calculate the spin-Hamiltonian parameters (g factors g_//, g_⊥ and hyperfine structure constants A_//, A_⊥) and optical band positions for Ni⁺ ion in silver gallium selenide (AgGaSe₂) crystal. In the model, besides the contribution due to the spin-orbit parameter of central dⁿ ion (i.e., the one-spin-orbit-parameter model in the traditional crystal-field theory), that of ligand ions are taken into account. The calculated results are reasonably consistent with the experimental values. The local structure of Ni⁺ centre in AgGaSe₂ is estimated through the calculation. The complete diagonalisation method based on the one-spin-orbit-parameter model is also applied to calculate these electron paramagnetic resonance and optical data. It is found that although the calculated optical band positions are close to those based on the two-spin-orbit-parameter model and hence to the experimental values, the calculated spin-Hamiltonian parameters (in particular, the g factors) are in disagreement with the experimental values. The latter point is further confirmed from the calculations with the perturbation method. So, for the rational calculations of spin-Hamiltonian parameters of dⁿ clusters with ligand having large spin-orbit parameter, the contributions due to spin-orbit parameters of both the central dⁿ ion and ligand ion should be contained.     

New expressions for g—factors of the mixed ground state of 3d^9 ions with a compressional tetragonal symmetry and its application to NaCl：Ni^＋（I）

We deduce new expressions for g-factors of the 3d⁹ ions with a compressional tetragonal symmetry, in which we consider not only the contribution from the spin-orbit coupling of the central transition metal ion but also that of the ligand orbits as well as the admixture of ²B_1g into ²A_1g (ground state). By using the new formulae, the electron paramagnetic resonance g-factors for NaCl:Ni⁺(I) are studied. Thus, the puzzle that the g_‖-shift is positive is reasonably explained.     

Investigations on the g factors of the ground and excited states for Cu2+ ions in ZnO crystal

The g factors g _// and g _⊥ of the ground Γ₆(² T ₂) and excited Γ_4,5(² E), Γ₆(² E) states for trigonal Cu²⁺ centres in ZnO crystals are calculated from three theoretical methods, the complete diagonalization (of the energy matrix) method, the second-order perturbation method (PTM-I) and the simplified second-order perturbation method (PTM-II, this method was described in an earlier paper). These methods are based on the cluster approach in which the spin-orbit coupling parameters ζ, ζ′ and the orbital reduction factors k, k′ are calculated from a semi-empirical molecular orbital method. The crystal-field parameters used in the calculations are obtained from the superposition model and so the defect structure of Cu²⁺ centres in ZnO can be acquired. The calculated g factors from the three methods are in reasonable agreement with the experimental values and the defect structure of Cu²⁺ centres in ZnO is acquired. It appears that in some cases the approximate PTM can be applied in the studies of g factors of various states. The conditions that the PTM are ineffective are discussed.     

Unified calculations of the optical band positions and spin-Hamiltonian parameters for V2+ ions in CdCl2 crystal

The eight optical spectral band positions and three spin-Hamiltonian parameters (g factors g_//, g_⊥ and zero-field splitting D) of V²⁺ ions in trigonal CdCl₂ crystal are calculated together from the complete diagonalisation (of energy matrix) method (CDM) based on the two-spin-orbit-parameter model (also called the cluster approach). In the model, differing from the usual one-spin-orbit-parameter model in the conventional crystal-field theory (where only the contribution to spin-Hamiltonian parameters due to the spin-orbit parameter of central dⁿ ion is considered), both the contributions from the spin-orbit parameter of central dⁿ ion and that of ligand ions are taken into account. The calculated results show reasonable agreement with the experimental values. The local lattice relaxation in the vicinity of V²⁺ ion due to the introduction of V²⁺ impurity is acquired from the calculations. The calculations of spin-Hamiltonian parameters from the CDM based on the one-spin-orbit-parameter and those from the perturbation theory method based on the two-spin-orbit-parameter model are also made for comparison. The results are discussed.     

低速高电荷态离子40Ar16+与云母表面作用中的电子发射研究

报道了由兰州ECR源提供的低速高电荷离子40Ar16 入射到云母表面产生的电子发射的实验测量结果.结果发现,电子发射产额Y与离子入射角ψ有近似1/tanψ的关系.基于经典过垒模型,我们对这一关系进行了理论分析.实验结果和理论结果相当符合,这就间接说明势能电子发射是低速高电荷态离子作用于表面发射电子的一个主要途径.     

Calculations of the optical and EPR spectral data for Cr3+ ion in Y3Ga5O12 crystal from the complete diagonalisation method

The complete diagonalisation (of energy matrix) method is applied in this paper to calculate together the optical and electron paramagnetic resonance (EPR) spectral data for Cr³⁺ ion at the trigonal Ga³⁺ site of Y₃Ga₅O₁₂ crystal. The method is founded on the two-spin-orbit-parameter model where in addition to the contributions from the spin-orbit parameter of central dⁿ ion (i.e., one-spin-orbit-parameter model) in the traditional crystal field theory, those from the spin-orbit parameter of ligand ion via covalence effect is also considered. The calculated results propose that by using only four adjustable parameters, the 12 observed spectral data (nine optical band positions and three EPR parameters g_//, g_⊥ and D) in Y₃Ga₅O₁₂: Cr³⁺ are reasonably explained. The impurity-induced local lattice distortion of Cr³⁺ in Y₃Ga₅O₁₂ crystal is also estimated through the calculations. The results are discussed.     

Electron paramagnetic resonance parameters of Mn<Superscript>4+</Superscript> ion in h-BaTiO<Subscript>3</Subscript> crystal from a two-mechanism model

The EPR parameters (g factors g _‖, g _⊥ and zero-field splitting D) of Mn⁴⁺ ion in h-BaTiO₃ crystal are calculated from the complete high-order perturbation formulas based on a two-mechanism model for the EPR parameters of 3d ³ ions in trigonal symmetry. In the model, not only the widely used crystal-field mechanism, but also the charge-transfer mechanism (which is not considered in crystal-field theory) are included. The calculated results are in reasonable agreement with the experimental values. The relative importance of charge-transfer mechanism to EPR parameters and the defect structure of Mn⁴⁺ centre in h-BaTiO₃ crystal obtained from the calculations are discussed.