Energy spectrum and phase transitions in C70 fullerite crystals at high pressure

Measurements have been made of the Raman, optical absorption, and luminescence spectra of single crystals and pellets of the fullerite C₇₀ at T=300 K and at pressures up to 12 GPa. The baric shift dω/dP and the Grüneisen parameters of the Raman-active intramolecular phonon modes have been determined. It has been established that the d ω/dP value for certain phonon modes abruptly changes at pressures of P ₁≈2 GPa and P ₂≈5.5 GPa, as do the half-widths of the Raman lines. These features in the Raman spectrum are associated with phase transitions at high pressure. The baric shifts of the absorption and luminescence edges of C₇₀ crystals have been determined and are −0.12 eV/GPa and −0.11 eV/GPa, respectively, for absorption and luminescence. The baric shift of the absorption edge decreases significantly with increasing pressure and is −0.03 eV/GPa at 10 GPa. These data have been used to determine the deformation potential of the fullerite C₇₀, which is about 2.1±0.1 eV. Zh. éksp. Teor. Fiz. 111, 262–273 (January 1997)     

Spectroscopic study ofβ-Ni(OH)2 under pressure

Infrared absorption and Raman study ofβ-Ni(OH)₂ has been carried out up to 25 GPa and 33 GPa, respectively. The frequency ofA _2u internal antisymmetric stretching O-H mode decreases linearly with pressure at a rate of −0.7 cm⁻1/GPa. The FWHM of this mode increases continuously with pressure and reaches a value of ∼ 120 cm⁻¹ around 25 GPa. There was no discernible change observed in the frequency and width of the symmetric stretchingA _1g O-H Raman mode up to 33 GPa. The constancy of the Raman mode is taken as a signature of the repulsion produced by H-H contacts in this material under pressure. Lack of any discontinuity in these modes suggests that there is no phase transition in this material in the measured pressure range.     

Kilohertz high power extracavity KGW yellow raman lasers based on pulse LD side-pumped ceramic Nd: YAG

We report an efficient operation of a kilohertz nanosecond extracavity KGd(WO₄)₂ (KGW) crystal Raman yellow laser, which is pumped by a 532 nm lasers based on pulse laser diode (LD) side-pumped ceramic Nd: YAG, BBO electro-optical Q-switched and LBO crystal extracavity frequency doubling. With the 5 W, 10 ns and 1 kHz output power pumped at 532 nm, we obtained 2.58 W, 7.4 ns, 1 kHz second Stokes Raman laser output at 579.54 nm for 768 cm⁻¹ Raman shift of KGW crystal, corresponding to a conversion efficiency of 51.4%. By changing the KGW crystal orientation, we further obtained 3.18 W, 7.8 ns, 1 kHz Raman pulses at 588.33 nm for 901 cm⁻¹ Raman shift, corresponding to a conversion efficiency of 63.3%. The beam quality factors M² of 579.54 and 588.33 nm were (M _x−579.54² = 5.829, M _y−579.54² = 6.336) and (M _x−588.33² = 6.405, M _y−588.33² = 6.895), respectively.     

The infrared and laser Raman spectra of K2Zn(SO4)2 · 6H2O

The Raman spectra of the single crystal of K₂Zn(SO₄)₂·6H₂O belonging toC _2h ⁵ space group in the 40–1200 cm⁻¹ region in different scattering geometries and their spectra ofthe microcrystalline salt in the 1500-50 cm⁻¹ region have been reported. The dynamics of the crystal has been described in terms of 186 phonon modes under the unit cell approximation. The weak bands in the region 400–900 cm⁻¹ have been assigned to the libratory modes of H₂O molecules in contradiction to the assignments reported by Ananthanarayanan. The ambiguities existing in the literature about the assignments ofν ₂ ^c andν ₅ ^c modes of [Zn(H₂O)₆]²⁺ have also been removed. The translatory and libratory modes of different units of the crystal have been identified and assignments are made using farir and Raman data on various isomorphous tutton salts. It has been inferred that both SO ₄ ²⁻ tetrahedron and [Zn(H₂O)₆]²⁺ octahedron undergo linear as well as angular distortions from their free state symmetries in the crystal.     

Polarized Raman spectroscopy study of NiSi film grown on Si(001) substrate

We report on the growth of NiSi film on Si(001) substrate with an orientation of NiSi[200]//Si[001]. Polarized Raman spectroscopy was used to assign the symmetry of the NiSi Raman peaks. Raman peaks at 213 cm⁻¹, 295 cm⁻¹, and 367 cm⁻¹ are assigned to be A _g symmetry and peaks at 196 cm⁻¹, and 254 cm⁻¹ are B _3g symmetry.     

Four-wave mixing spectroscopy of aqueous suspensions of single-wall carbon nanotubes in the ranges of 0.1–10 and 100–250 cm<Superscript>−1</Superscript>

Distinctive optical properties of single-wall carbon nanotubes (SWNT) are highly sensitive to variations in the environment. Here, we have studied SWNT in aqueous suspensions at a low (less than 0.1 μg ml⁻¹) concentration by four-wave mixing (FWM) spectroscopy in the spectral bands of 0.1 to 10 cm⁻¹ (≈300 GHz) and 100 to 250 cm⁻¹ (3 to 7.5 THz). We directly investigated the hydration layers around SWNT. A comparison of the FWM spectra of an SWNT aqueous suspension and Milli-Q water shows a considerable increase in the intensity of low-frequency Raman modes, which are attributed to the rotational transitions of H₂O₂ and H₂O molecules. We explain the observed phenomenon by the hydrogen peroxide production and formation of a low-density depletion layer at the water-nanotube interface. We have observed several SWNT radial breathing modes ω _RBM =118.5, 164.7, and 233.5 cm⁻¹ in an SWNT aqueous suspension and estimated the corresponding SWNT diameters as ≈2.0, 1.5, and 1 nm.     

High pressure Raman spectra of L‐methionine crystal

Raman spectra of an L ‐methionine (C₅H₁₁NO₂S) crystal were obtained in the spectral region between 50 and 3200 cm⁻¹ for pressures up to 5 GPa. Pronounced changes of the Raman spectra were observed for bands associated to rocking of CO₂⁻; wagging of CO₂⁻; deformations of CO₂⁻, CH₃, and NH₃⁺; and stretching vibrations of SC, CC, CH, CH₂, and CH₃. Upon decompression to ambient pressure the original Raman spectrum prior to compression is recovered. These modifications were associated to a reversible phase transition undergone by the L ‐methionine crystal at about 2.2 GPa, with a hysteresis of ∼0.8 GPa. Pressure coefficients for most of the internal modes of the crystal are given. Copyright © 2008 John Wiley & Sons, Ltd.     

New χ (3)-nonlinear-laser manifestations in tetragonal LuVO4 crystal: more than sesqui-octave Raman-induced Stokes and anti-Stokes comb generation and cascaded self-frequency “tripling”

We report the experimental investigations of nonlinear-laser effects in LuVO₄ vanadate under one-micron picosecond Nd³⁺:Y₃Al₅O₁₂ pumping. In this tetragonal host-crystal for Ln³⁺ lasants for the first time we excited ultra-broad, more than one and half octave (13500 cm⁻¹) Raman induced Stokes and anti-Stokes generation combs and observed multi-step cascaded parametric χ ⁽³⁾-lasing in UV spectral region. All generation lines were identified and attributed to SRS-promoting modes of the crystal (ω _SRS1≈900 cm⁻¹ and ω _SRS2≈113 cm⁻¹). We classified this vanadate as a promising material for self-Raman laser converters.     

The pressure effect on the photoluminescence and Raman spectra of Nd(DBM)3·Phen

Photoluminescence and Raman spectra of rare earth complex Nd(DBM)₃·Phen (DBM, dibenzoylmethane; Phen, 1,10-phenanthroline) are measured at high pressures. A new Raman band appearing at 1070 cm⁻¹ indicates a second-order phase transition around 5.0 GPa. Although the crystal lattice is destroyed for pressures higher than 7.1 GPa, photoluminescence spectra show that the emission intensity of Nd³⁺ is enhanced dramatically with the pressure increasing up to 9.9 GPa, which is attributed to an efficient intramolecular energy transfer from the ligand to Nd³⁺. By analyzing the energy of the ground and excited states at 9.9 GPa, the ⁴H_11/2 energy level is considered as the main resonance energy level that efficiently accepts the transferred energy from the ligand.     

Raman scattering by hot polaritons in NaClO3

Summary By nonlinear mixing of IR and visible radiation,i.e. coherent Raman scattering by polaritons driven by a CO₂ laser, it has been possible to get high-resolution spectra for theF-modes of a NaClO₃ crystal in the region (907÷957) cm⁻¹, where several isotopic modes are present. The obtained independent measurement of the refractive index and absorbance allows an accurate determination of the polariton dispersion curve and its width inq-space. The experimental data confirm the existence of a localized isotopic mode at 931 cm⁻¹ and a strongly damped isotopic mode near 960 cm⁻¹. Finally, an accurate measurement of the dispersion of the second-order nonlinear polarizability in the same energy region has been obtained for the first time. This work was supported by the Italian Consiglio Nazionale delle Ricerche and Ministero della Pubblica Istruzione.     

Magneto-Raman scattering inp-type indium antimonide

We report for the first time stimulated magneto-Raman scattering inp-type InSb. Two different Raman scattering processes were observed. The first one has a Raman shift of about 2cm⁻¹/kG and is observed at magnetic fields up to 30kG. The other one is observable only at high magnetic fields above 30kG and shows Raman shifts between 1.2cm⁻¹ and 3.0cm⁻¹ with a tuning rate of about 0.2cm⁻¹/kG. The first process can be interpreted either as spin-flip Raman scattering by photo-excited electrons in the conduction band or as Raman scattering by holes in the valence band involving transitions from heavy to light hole states. The other Raman shift observed seems to occur on account of transitions between the heavy hole ladders.     

Variation in the fluorescent background in Raman spectra of distilled water purified by different methods

The contribution of impurity fluorescence was determined in the water Raman spectra excited by the second harmonic (λ = 532 nm) of a pulsed Nd:YAG laser. Water samples prepared by different techniques (tap water (undistilled), distilled water, Milli-Q water, water for injections, and water subjected to cavitation treatment) were investigated. The Raman (bands at ν ₂ ∼ 1550 cm⁻¹ and ν ₃ ∼ 3400 cm⁻¹) and fluorescence (Stokes shift 2500 cm⁻¹) signals were separated spectrally and according to the differences in the emission kinetics. It was established that all investigated samples, including distilled and specially purified water for injections, exhibit afterglow. The highest sensitivity to the presence of impurities was revealed near ∼ 2500 cm⁻¹. The least contribution to the fluorescence signal was found in the water for injections.     

Influence of high pressure on the electrical properties of amorphous chalcogenides of the Ag-Ge-As-S system

New AgGe_{1 + x} As_{1 − x} S₃ (x = 0.1, 0.4–0.9) silver chalcogenides are synthesized and certified. Their electrical properties are studied at pressures of up to 45 GPa by means of impedance spectroscopy. Regions of significant variations in electrical properties are detected via analysis of an impedance hodograph, the baric dependencies of resistance, and the dielectric loss tangent.     

Manganese energy level in <Emphasis Type="Italic">p</Emphasis>-InAs〈Mn〉 under pressure

Resistivity ρ and the Hall coefficient R _H at atmospheric pressure in the temperature range of 77–400 K and the dependences of these parameters (ρ(P) and R _H(P)) and magnetic susceptibility (χ(P)) on hydrostatic pressures of up to P ≤ 7 GPa at 300 K in p-InAs〈Mn〉 single crystals was investigated. The baric coefficients of the ionization energy of Mn impurity centers and the pressure dependence of the dielectric constant ɛ(P) were determined.     

Polarized absorption spectra of Co2+ in Na2Cd3Cl8 single crystals

Summary The polarized optical absorption spectra of Na₂Cd₃Cl₈: Co²⁺ in the range of 15 000 to 40 000 cm⁻¹ down to 15 K are reported. The Co²⁺ ion is found to occupy the Cd²⁺ sites in octahedral geometry and the spectra are interpreted satisfactorily in terms of a cubic ligand field model including spin-orbit coupling. The observed crystal field spectra are well reproduced withB=745 cm⁻¹,C=3410 cm⁻¹,Dq=700 cm⁻¹ and ζ (spin-orbit interaction) =520 cm⁻¹. No spectral evidence for tetragonal distortion is observed.     

Optical absorption spectrum of Ni2+ doped in ammonium zinc sulphate

The optical absorption spectrum of Ni²⁺ ion doped in ammonium zinc sulphate has been studied at room and liquid air temperatures. From the nature and the positions of the bands a successful interpretation of all the bands could be made assumingO _h symmetry for the Ni²⁺ ion in the crystal. The fine splitting of the³ T ₁ ¹ band at liquid air temperature has been successfully interpreted to be due to spin-orbit interaction. The crystal field and spin-orbit parameters derived areDq=1000 cm⁻¹;B=750 cm⁻¹;C=3.45B andξ=600 cm⁻¹.     

Realization of a heavily doped and fully compensated semiconductor state in a crystalline semiconductor with a deep impurity band

We use the data on the pressure (up to P=1.5 GPa) and field (up to H=17 kOe) dependence of the Hall coefficient and the resistivity at 77.6 and 300 K in p-CdSnAs₂〈Cu〉 to calculate the effective kinetic characteristics of the charge carriers, the density and mobility of the conduction electrons and the holes of the deep acceptor and valence bands, in an interval of excess-acceptor densities N _ext ranging from 10¹⁰–10¹⁷ cm⁻³. We establish that in a heavily doped semiconductor with a deep impurity band at the tail of the density of states of the intrinsic band, with unequal donor and acceptor densities, a a heavily doped and fully compensated semiconductor state is realized under hydrostatic compression. The threshold value of the pressure that initiates the transition into such a state, P _c, depends on the extent to which the impurity band is populated. In p-CdSnAs₂〈Cu〉 at N _ext=N _A, where N _A is the density of deep acceptors, and T⩽77.6 K the value of P _c amounts to 10⁻⁴ GPa. As the population of the deep acceptor band grows, P _c increases and in the limit becomes infinite. We discuss the special features of the electrophysical properties of p-CdSnAs₂〈Cu〉 arising from the absence of an energy gap between the states of the conduction band and those of the deep acceptor band. Zh. éksp. Teor. Fiz. 111, 562–574 (February 1997)     

Structural changes in chlorpropamide at high pressure

The crystalline structure of a molecular crystal of chlorpropamide C₁₀H₁₃ClN₂O₃S is studied by X-ray diffraction at high pressures of up to 4.2 GPa at room temperature. Under normal conditions the structure of chlorpropamide has orthorhombic symmetry with the space group P2₁2₁2₁. At high pressures P > 1.2 GPa, a polymorphic phase transition into the monoclinic phase with the space group P2₁ is observed. The baric dependences of the lattice parameters and unit-cell volumes are obtained for both phases of chlorpropamide.     

Properties of shock-compressed liquid krypton at pressures of up to 90 GPa

The following quantities of shock-compressed liquid krypton are measured behind a plane shock front at pressures up to 90 GPa: compressibility up to densities of 7 g/cm³, brightness (color) temperatures of 6000–24000 K, and electrical conductivities of 40–60000 (Ω·m)⁻¹. X-t diagram methods are used to estimate sound speeds of up to 5.5 km/s at pressures of 30–75 GPa. The optical absorption coefficients in the violet and red (30–300 cm⁻¹) are measured at pressures of 20–90 GPa from the rise in brightness of the shock front luminosity. The optical reflection coefficient of the shock front (∼13%) at a pressure of 76.1 GPa is measured for the first time. Zh. éksp. Teor. Fiz. 116, 551–562 (August 1999)     

Laser Raman and infra-red spectra of biomolecule: 5-aminouracil

Laser Raman (200–4000 cm⁻¹) and IR (200–4000 cm⁻¹) spectra of 5-aminouracil were recorded in the region 200–4000 cm⁻¹. Assuming a planar geometry and C_s point group symmetry, it has been possible to assign all the 36 (25a′ + 11a″) normal modes of vibration for the first time. The two NH bonds of the NH₂ group appear to be equivalent as the NH₂ stretching frequencies satisfy the empirical relation proposed for the two equivalent NH bonds of the NH₂ group. The two NH₂ stretching frequencies are distinctly separated from the CH/NH ring stretching frequencies. A strong and sharp IR band at 3360 cm⁻¹ could be identified as the anti-symmetric NH₂ mode whereas the band at 3290 cm⁻¹ with smaller density could be identified as the symmetric NH₂ stretching mode. All other bands have also been assigned different fundamentals/overtones/combinations.