Interactions hyperfines magnetiques et mecanisme de compensation de la charge pour les ions d'impurete 119Sn4+ dans Cr2O3

Mössbauer spectra of Cr₂O₃ sesquioxide doped with ¹¹⁹Sn⁴⁺ ions lead to the hypothesis of three non-equivalent magnetic sites for Sn⁴⁺. The identification of these sites has allowed to estimate the relative importance of exchange interactions between Cr³⁺ ions along [111] axis and in (111) plane.     

Outside dislocations generated from phosphorus implanted silicon layers

The growth, movement and nature of outside dislocation, which propagate from heavily phosphorus (>10¹⁵ ions/cm²) implanted (111), (100), and (110) silicon layers into unimplanted outside regions by a compressive strain induced during 1100° C wet O₂ annealing, are investigated using transmission electron microscopy and x-ray diffraction topography. Outside dislocations are formed, mainly on (111) planes., by the glide motion of dislocation networks formed in implanted layers during early annealing. This results in dislocations extending into the unimplanted areas to different degrees, in the order of, from the largest to smallest, (111), (110), and (100) wafers. In (110) wafers, the [001] oriented dislocations in the implanted regions rise to the surface at the implant and unimplant boundary. On the other hand, the [110] dislocations penetrate into the unimplanted region. Two sets of orthogonal 〈110〉 oriented dislocations generated in (100) implanted wafers behave in the same manner as the [001] dislocations in (110) wafers. Some sources of the compressive strain related to the generation of these dislocations are discussed.     

Growth and photoluminescence properties of inclined ZnO and ZnCoO thin films on SrTiO_3（110） substrates

ZnO thin film growth prefers different orientations on the etched and unetched SrTiO 3（STO）（110） substrates.Inclined ZnO and cobalt-doped ZnO（ZnCoO） thin films are grown on unetched STO（110） substrates using oxygen plasma assisted molecular beam epitaxy,with the c-axis 42 inclined from the normal STO（110） surface.The growth geometries are ZnCoO[100]//STO[110] and ZnCoO[111]//STO[001].The low temperature photoluminescence spectra of the inclined ZnO and ZnCoO films are dominated by D 0 X emissions associated with A 0 X emissions,and the characteristic emissions for the 2 E（2G）→ 4A2（4F） transition of Co 2＋ dopants and the relevant phonon-participated emissions are observed in the ZnCoO film,indicating the incorporation of Co 2＋ ions at the lattice positions of the Zn 2＋ ions.The c-axis inclined ZnCoO film shows ferromagnetic properties at room temperature.     

Field-induced splitting of the OH-Stretch absorption line in KTaO3 and KTaO3 :Li

Abstract

We have studied the electric field-induced splitting of a single OH stretch mode in KTaO₃ and KTaO₃ :Li. For the three prominent directions [100], [110] and [111] we observed polarized splitting patterns with up to six components. The line positions exhibit no mirror symmetry with respect to the zero-field frequency. This behaviour can be interpreted by taking into account a field-dependent shift of the Ta⁵⁺ ion and a change of the covalent character of the bond. Li-doped KTaO₃ samples show for [Li] < 2mol% a line broadening, while for [Li] < 3.5 mol% a field dependent phase transition has been observed with evidence for a 90 degree domain structure.     

Anisotropy of the 15 eV volume plasmon dispersion in A1

A dependence of plasmon dispersion for epitaxial aluminum films has been found for the directions [100], [110] and [111]. A differene of about 0.5 eV has been observed between the directions [100] and [110] at q = 1.4 Å^?1. This effect is due to the influence of lattice on the electron gas.     

Magnetic characteristics of PrCd single crystal

Magnetic measurements have been made along the [100], [110] and [111]-axes of PrCd single crystal in magnetic fields up to 70 kOe in the temperature range from 4.2 to 300 K. PrCd shows metamagnetism below T_t = 25 K in which two critical fields are observed in the magnetization processes along the [110] and [111]-axes and a critical field along the [100]-axis. The metamagnetic behaviour is interpreted by a noncollinear antiferromagnetic model with the Pr moments of ～ 2μ_B directed to the 〈111〉-axes.     

Monazite (monoclinic LaPO4) slip systems at room temperature

Polycrystalline monazite (monoclinic LaPO₄) was deformed by spherical indentation at room temperature. Slip systems were identified using TEM of thin sections prepared parallel and close to the indented surface. Dislocation Burgers vectors (b) were identified by Burgers circuit closure in high resolution TEM images, supplemented by diffraction contrast where possible. A total of 441 b determinations were made in 97 grains. The most common slip systems were [001]/(010), [100]/(010) and [010]/(100). Slip on (001) was less common. Many other less common slip systems and Burgers vectors were also identified, including b = [101], [101], [011], [110] and [111]. b = [101] dislocations dissociate into ½[101] partials, and b = [101] dislocations are inferred to dissociate to ½[101] partials, with a low energy stacking fault of ～30 mJ/m². b = [100] dislocations may dissociate into ¼[210] + ¼[210] partials. b = [010] may sometimes dissociate to ½[010] + ½[010] partials. Other types of partial dislocations were also observed and discussed. All partial dislocations were climb dissociated. The line energies of monazite dislocations and their partials were calculated, and stacking fault structures for partial dislocations are analyzed. Satisfaction of the Von Mises criterion for full ductility most likely involves [101]/(111) and ?011?/{011} or {111} slip, but other combinations that require both b = [101] and ?011? or ?110? are possible. If deformation twinning is active, slip systems with b = ?011? or ?110? may not be necessary for full ductility.     

Cr<Superscript>3+</Superscript> spectroscopy study in ZnO-codoped and Zn-in-diffused congruent LiNbO<Subscript>3</Subscript>:Cr crystals

This paper reports on the spectroscopy properties, absorption and luminescence, of Cr³⁺ ions in singly doped, ZnO-codoped, and Zn in-diffused LiNbO₃:Cr crystals. In addition to the broad absorption, inter-ionic transitions ascribed to Cr³⁺ ions located in Li⁺ and Nb⁵⁺ sites; [Cr]_Li and [Cr]_Nb centres two absorption bands at higher energy are reported and ascribed to the charge transfer transitions of the Cr³⁺ ions of the two defect centres. The charge transfer transitions are used as optical probe to study the role of the Zn ions in the Zn in-diffused LiNbO₃:Cr samples. It has been observed that the Zn-in-diffused processes created [Cr]_Nb centres in the diffusion zone. The location of the diffused Zn²⁺ ions is considered to be in Li⁺ site, displacing the Cr³⁺ ions from the Li⁺ sites, [Cr]_Li, to the Nb⁵⁺ positions, [Cr]_Nb.     

An NMR Analysis of Transitions in FexNbxV2-2xO4

The first order semiconductor - metall phase transition with the lattice symmetry change from monoclinic to tetragonal and the conductivity jump of several orders of magnitude is observed in pure vanadium dioxide and the dioxide doped by varios impurities [I]. Transition temperature T_t for pure VO₂ is 68°C and depends on the impurity. For example, the impurities which enter the insulating phase as pentavalent ions Nb⁵⁺ [2] give rise to a decrease in metal-semiconductor transition temperature at low concentrations and the trivalent ions Cr³⁺, Fe³⁺ [3,4] lead to an increase in T_t. In the latter case three different monoclinic phases are stabilized at a temperature below T_t. It has been already shown [5] that for double doping of vanadium dioxide by pentavalent Nb⁵⁺ and trivalent Fe³⁺ or Cr³⁺ ions three semiconductor phases exist (M_I, M₂, M₃) but the transition temperature decreases as the impurity concentration increases.     

Nuclear Spin-Lattice Relaxation of 82BrFe

The field dependence of the nuclear spin-lattice relaxation (SLR) of cold implanted ⁸²Br (T ≤ 25 mK) in α-Fe single crystals was investigated with nuclear magnetic resonance of oriented nuclei (NMR/ON) at low temperatures as experimental technique. The SLR at the lattice sites with the hyperfine fields found by earlier NMR/ON experiments was measured as a function of the applied external magnetic field B _ext parallel to the three principle axes [100], [110] and [111] of the iron single crystal. The data were evaluated with the full relaxation formalism in the single impurity limit and for comparison also with the often employed model of a single exponential function with an effective relaxation time T ₁′. With a phenomenological model the high field values of the relaxation rates r _{∞, [100]′} = 6.6(2) · 10⁻¹⁵ T²sK⁻¹, r _{∞, [110]} = 5.4(2) · 10⁻¹⁵ T²sK⁻¹ and r _{∞, [111]} = 5.2(1) · 10⁻¹⁵ T²sK⁻¹ were obtained.     

Magnetostrictive effects at a spin reorientation transition in a cubic crystal

Mössbauer studies of spin reorientation transitions in the high magnetostrictive materials RFe₂(R = rareearth) were performed. The transitions studied were [100] → [110] (Ho_0.9Tb_0.1Fe₂ at 240 K), [100] → [111] (Dy_0.7Tb_0.3Fe₂ at 220 K), [110] → [100] (Ho_0.5Er_0.5Fe₂ at 135 K and Ho_0.3Tm_0.7Fe₂ at 110 K), [111] → [100] (Dy_0.2Er_0.8Fe₂ at 140 K) and [110] → [111] (Ho_0.7Tb_0.3Fe₂ at 120 K). The first four transitions were found to be of second order, continuous reorientation of magnetization. In Dy_0.2Er_0.8Fe₂ and Ho_0.7Tb_0.3Fe₂ a sharp discontinuous first order transition is observed. In all systems the Mössbauer recoil free fraction, its anisotropy, the isomer shift and hyperfine interaction parameters change sharply through the spin reorientation transition. All phenomena observed can be understood in terms of changes in static magnetostrictive distortions combined with critical phonon softening at the spin reorientation phase transitions. The system Ho_1-xTb_xFe₂ is unique in behaviour as Ho_0.9Tb_0.1Fe₂ shows the highest magnetostrictive effects, whereas Ho_0.7 Tb_0.3Fe₂ shows almost none.     

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).     

Elastic constants of Cr3Si

Elastic constants of Cr₃Si have been measured on single crystals oriented along [110] and [100] as a function of temperature between 4.2 and 300 K. Their magnitudes at 4.2 K are in unit of 10¹¹ Nm^-2C₄₄ = 1.32C' = (C₁₁?C₁₂)/2 = 1.58B = 1.99 There is no peculiar behaviour as a function of temperature.     

Comment on “oscillatory indirect interaction between adsorbed atoms — Non-asymptotic behavior in tight-binding models at realistic parameters” by K.H. Lau and W. Kohn

A sensitive infrared reflectance accessory suitable for the study of surface films on medium size single crystals is described. Oxide films formed on the (100), (110) and (111) crystal faces of aluminum in air, at room temperature, display nearly identical behavior with films approximately 10 Å thick absorbing as a single band near 940 cm^?. After 10⁴ sec at 570 °C, in oxygen, films formed on these crystals begin to display differences in band characteristics and growth kinetics. Between 10⁴ and 4 × 10⁴ sec the rates of growth on the (110) and (111) crystal faces are much greater than on the (100) face. Beyond 4 × 10⁴ sec the growth rate on the (100) face increases while the (110) and (111) growth rates approach zero. Limiting thicknesses reached after 4 × 10⁵ sec approach 3.4 × 10², 2.1 × 10² and 2.2 × 10² Å for (100), (110) and (111) faces, respectively. Oxide compositional differences were reflected by the number and form of the infrared bands after 10⁴ sec of oxidation. After 5 × 10⁴ sec the (100) face oxide was composed of two and possibly three oxide species as evidenced by several bands. Differences in bandwidth and frequency were observed between the (110) and (111) oxide films. The significance of such differences is discussed.     

ESR of adsorbates on single crystal metal surfaces under UHV conditions

Angular dependent electron spin resonance measurements were taken for paramagnetic molecules adsorbed on metallic single crystal surfaces in UHV. For the hydrated Cu(NO₃)₂ complex on a Cu[111] surface an angular dependent ESR signal is recorded. The plane ofthe molecule is found to lie preferentially out of the surface plane. Experiments on chemisorbed molecular O₂ on Ag[110] at 25 K and NO on Pt[111] at 110 K show no sharp ESR signal characteristic for well localized moments. If one assumes that NO on Pt (respectively Pd) carries an unpaired spin, one can estimate a lower limit for the spin flip rate of π^?1>2×10⁹s^?.     

The adsorption of hydrogen on iron; A surface orbital modified occupancy — bond energy bond order calculation

A Surface Orbital Modified Occupancy — Bond Energy Bond Order (SOMO-BEBO) model calculation of hydrogen adsorption on iron is presented. This calculation represents a novel approach to the CFSO-BEBO method in that the calculation is correlated in a consistent way with the thermal desorption spectra of the hydrogen-iron system. Heats of molecular adsorption calculated are ?32.88, ?35.68 and ?49.57 kJ/mol for the iron (110), (100), and (111) surfaces, respectively. Heats of dissociative adsorption calculated are ?54.40, ?75.30 and ?87.90 kJ/mol for the three states on the iron (111) surface; ?51.21 and ? 73.62 kJ/mol for the two states on the iron (100) surface; and ?63.78 kJ/mol for the one state on the iron (110) surface. Activation energies for dissociative adsorption were found to be small or zero for the iron (111) surface while non-zero activation energies of 49.27 and 45.05 kJ/mol were calculated for the iron (100) and (110) surfaces, respectively. The FeH single-order bond energy has been calculated to be 298.2 kJ/mol. The radius of the hydrogen surface atom has been estimated to be 1.52 × 10^?10 m consistent with the expected size of an H^? ion. The elimination of certain surface sites for molecular adsorption as a result of the ferromagnetism of iron is suggested by the calculation. The reason for the absence of well defined LEED patterns for hydrogen adsorption on the iron (111) and (100) surfaces [Bozso et al., Appl. Surface Sci. 1 (1977) 103] is explained on the basis of the size of the H^? surface ion. The adsorption of hydrogen on the iron (110) surface is consistent with a relatively stable, small-sized H⁺₂ surface ion giving, therefore, a regular LEED pattern and a positive surface potential upon adsorption of hydrogen on this surface.     

Electron density distribution in Si and Ge using multipole, maximum entropy method and pair distribution function analysis

The local, average and electronic structure of the semiconducting materials Si and Ge has been studied using multipole, maximum entropy method (MEM) and pair distribution function (PDF) analyses, using X-ray powder data. The covalent nature of bonding and the interaction between the atoms are clearly revealed by the two-dimensional MEM maps plotted on (100) and (110) planes and one-dimensional density along [100], [110] and [111] directions. The mid-bond electron densities between the atoms are 0.554 e/?³ and 0.187 e/?³ for Si and Ge respectively. In this work, the local structural information has also been obtained by analyzing the atomic pair distribution function. An attempt has been made in the present work to utilize the X-ray powder data sets to refine the structure and electron density distribution using the currently available versatile methods, MEM, multipole analysis and determination of pair distribution function for these two systems.      

Theoretical investigation of the EPR parameters and the crystal lattice defects of the trigonal symmetry in RbCdF3:Cr3+

In this paper, the electron paramagnetic resonance (EPR) parameters in RbCdF₃:Cr³⁺ have been studied by means of energy matrices and the Newman superposition model, the theoretical results are in excellent agreement with the experimental ones. The existence of Rb⁺ vacancy and the lattice distortion have been verified. The EPR parameters arising from the Rb⁺ vacancy itself and the crystal lattice distortion are analyzed and calculated. We obtain that the six ligand F⁻ ions move to the central Cr³⁺ ion by Δ = 0.0013 nm, and the front three F⁻ ions rotate 2.98° away from the [111] axis while the back three F⁻ ions rotate 1.016° toward it.     

Output properties of diode-pumped passively Q-switched 1.06 μm Nd:GdVO4 laser using a [100]-cut Cr4+:YAG crystal

A passively Q-switched 1.06???m Nd:GdVO₄ laser with a [100]-cut Cr⁴⁺:YAG saturable absorber was demonstrated. The output characteristics were investigated when the anisotropic transmission of Cr⁴⁺:YAG crystal and the incident pump power level were considered. The experimental results showed that it was feasible to generate laser with narrower pulse width (?? _p ), higher pulse energy and peak power when the polarization direction of laser was parallel to the [001], [010], [ $00\overline{1}$ ], and [ $0\overline{1}0$ ] orientations of the Cr⁴⁺:YAG crystal. The different changes of ?? _p as a function of incident pump power was observed due to the anisotropy of transmission of Cr⁴⁺:YAG and the different gain levels (pump power levels). If the Cr⁴⁺:YAG was fully bleached as a result of high cavity gain or due to the laser polarization direction was parallel to the [001], [010], [ $00\overline{1}$ ], and [ $0\overline{1}0$ ] orientations, ?? _p was constant, otherwise ?? _p decreased when the gain increased.     

Longitudinal relaxation of Fe nuclei in Yb-doped YIG

Measurements of T₁ for ⁵⁷Fe nuclei in Yb-doped YIG are reported for the temperature range 0·7–140 K, with the magnetization along the [111], [100], [110], and [112] crystallographic directions respectively. The dependence of T₁ on Yb concentration and on the magnitude of the applied field was also studied. These results are interpreted in terms of the ‘slow relaxation theory’, and are correlated with the ferrimagnetic resonance work of Clarke, Tweedale, and Teale, whose data have been reanalyzed by us. Both sets of data can be represented fairly well by the theory, with a consistent set of relevant parameters. However, the tensor G which describes the splitting of the Yb ground-state doublet must be modified somewhat from that deduced by Clarke et al., the new principal values being G₁ = 29·0 cm⁻¹, G₂ = 20·4 cm⁻¹ and G₃ = 8·5 cm⁻¹ respectively. Below approximately 10 K, when the magnetization is in the [110] or [112] direction, the nuclear relaxation rate is higher than predicted. These anomalies correspond to those observed in ferrimagnetic resonance line width, which have been attributed to Yb ions on the octahedral lattice sites normally occupied by iron. Anomalously large values of T⁻¹₁ are also observed below approximately 4 K in the [111] and [100] directions, and these remain to be accounted for.