Threshold and saturation properties of a solid-state XeF (C-A) excimer laser

A dielectric laser cavity of 1 cm length has been optimized for high gain (7 cm^–1) operation which is achieved in XeF doped Ar crystals. Mode structures on the C-A spectral distribution around 540 nm and far field transverse mode patterns are reported. Photchemical gain burning is observed in the spectral mode structures. The dependence of the laser threshold on pump energy, pumped length and on cavity losses is studied. XeF densities of 7×10¹⁷ cm^–3 and distributed losses of 1.2 cm^–1 are derived. The measured quantum efficiency of 14% and the saturation behaviour are consistently described. Losses by transient aborption and two photon absorption are discussed.     

Picosecond pulse generation in a benzene raman generator amplifier system

Picosecond ruby laser pulses generate simultaneously Stokes pulses of the 992 cm^–1 ring breathing mode and of the 3063 cm^–1 CH-stretching mode of benzene in a Raman generator cell by stimulated Raman scattering under self-focusing conditions. The Raman generator light is spectrally filtered, collimated, and amplified in three Raman amplifier cells pumped by ruby laser pulses. Both first Stokes lines have been selectively amplified to short, low divergence, intense light pulses.     

Far-infrared reflectivity of KI:Cl? and KI:Na+

The far-infrared reflectivity spectra of KI doped with 1% Cl^– and 2% Na⁺ were measured using a dual cavity technique. In addition to the observation of all previously-observed resonant and gap modes, several features were discovered in and near the optic band. A new gap mode at 90 cm^–1 in KI:Cl^– was discovered. In both systems sharp, narrow reductions in reflectivity at 98, 108, 116, and 139 cm^–1 were observed, as was a general reduction in reflectivity between 108 and 139 cm^–1. The structure at 98 and 116 cm^–1 is most-likely due to optical activity induced in normally inactive lattice modes by the high concentration of impurities. The features at 108 and 139 cm^–1 and the reduction in reflectivity between them were shown by a simple model calculation to be due to an increase in damping of the TO phonon.     

Estimation of the Optimum Concentration Interval of the Contents of Praseodymium, Neodymium, Europium, Holmium, and Erbium in a Solution

Based on the electronic absorption spectra of Pr³⁺, Nd³⁺, Eu³⁺, Ho³⁺, and Er³⁺ ions in 1 M aqueous solutions of chloric acid, calibration graphs have been constructed in a concentration of metals–optical density of a solution format for different frequencies. The band for praseodymium was used at 22,520 cm^–1, for neodymium at 17,380, 13,480, and 12,560 cm^–1, for europium at 25,380 cm^–1, for holmium at 18,580 and 15,580 cm^–1, and for erbium at 39,160, 26,480, and 19,160 cm^–1. The errors in determining the concentration of the indicated elements as a function of their content have been calculated. It is shown that for perchloric solutions of praseodymium it is possible to correctly determine its contents within the concentration range 0.1–1.5% at a frequency of 22,520 cm^–1; for neodymium the ranges are 0.4–1.0, 0.3–1.0, and 0.5–1.0% at 17,380, 13,480, and 12,560 cm^–1, respectively; for europium 0.4–1.5% at 25,380 cm^–1; for holmium — 0.2–1.5 and 0.4–1.5% at 15,580 and 18,580 cm^–1, and for erbium the range is 0.4–1.0% at frequencies of 39,160, 26,480, and 19,160 cm^–1.     

Tunable far-infrared solid-state lasers based on hot holes in germanium

The basic principles for achieving population inversion and stimulated emission in the far-infrared fromp-Ge are discussed. In the heavy-light hole lasing mode a broad gain region is found resulting in a broad multimode spectrum due to intracavity modes. By attaching external plates of germanium a single mode operation is realized. The obtained powers are in the W range with linewidths of 0.2 cm^–1. A single mode magnetically tunable coherent source is achieved with the light hole cyclotron resonance laser. With external mirrors a tuning range from 20 to 120cm^–1 with magnetic fields between 1 and 6 T is achieved. The intensity of the single mode is in the order of W, the linewidth below 0.2 cm^–1.     

Temperature effects on the phonon spectrum in YBa2Cu3O7 single crystals and thin films

We have performed detailed investigations on the temperature dependence of the 335 cm^–1 phonon in single crystals and thin films of the YBa₂Cu₃O₇ superconductor. The frequency of this phonon exhibits a downshift of about 5 cm^–1 on passing the superconducting transition from above. The shift of the phonon in thin epitaxial films on MgO or SrTiO₃ substrates is only about 2.5 cm^–1. The width of the asymmetric phonon line displays a slight increase belowT _c due to the electron-phonon interaction in these systems.     

Infrared absorption and far-infrared diffuse reflection spectra in Pb-doped Bi?Sr?Ca?Cu?O high-temperature superconductor

In this paper we study the room-temperature infrared transmission spectra (400–1600cm^–1) and far-infrared diffuse reflection spectra (50–450cm^–1) in Pb-doped Bi–Sr–Ca–Cu–O (2223) single phase (Tc=107k, sp1), multiphase (Tc=110k, sp2) and nonsuperconducting samples (sp3). The spectral features in superconductor are totally different from those in nonsuperconductor, which show the different crystal structure. The correlation existing between a factor group analysis of the phonons in (2223) and (2212) compounds affords a tentative assignment of ir-active modes in Pb-doped (2223) single phase by comparison with reported data in (2212) materials. The Cu–O stretching E_u vibration (605cm^–1) of CuO₂ layers is the characteristic vibrational mode related perovskitelike crystal structures. Two phonon coupling effect emerges in the infrared transmission spectra in Pb-doped superconductor. The Ca–O vibration A_2u (254cm^–1) might be related to superconductivity of Bi-based family.     

Ultrabroadband single-pulse CARS of liquids using a spatially dispersive Stokes beam

A double-channel spectrometer, which enables to acquire ultrabroadband single-pulse spectra of liquids by Coherent Anti-Stokes Raman Spectroscopy (CARS), is described. The method used to fulfill the phase-matching condition is based on the fact that the CARS efficiency in dispersive media is the largest when the interactive waves cross each other under frequency-determined angles. The dependence of the spatial separation between the pump and Stokes beam, in front of the crossing CARS lens, due to their frequency difference is analysed. It is shown that the different spectral components of an ultrabroadband Stokes source have phase-matched the CARS process when they are laterally shifted by a conjugated prism pair and focused into the sample. The method is tested in the spectral region 2800–3800 cm^–1 of a non-resonant medium (CCl₄) using an ultrabroadband dye laser (1000 cm^–1 FWHM). The influence of the Stokes beam spatial dispersion on the width of CARS generation is demonstrated. By this method, 1060 cm^–1 wide single-pulse spectra of the OH stretching vibration of liquid water are obtained for the first time. The ratio between the resonant and non-resonant part of the third-order susceptibility in water and methanol is determined.     

Intense tunable picosecond pulses generated by parametric amplification in β-BaB2O4

Amplified spontaneous emission of a dye cell is parametrically amplified in barium betaborate (BBO) crystals. Pumping the system by the third harmonic of a Nd:YAG laser a tuning range from 3500 to 25080 cm^–1 is accessible with energy conversion efficiencies of several percent. Properties of ultrashort light pulses in the visible and UV spectral range are presented. A spectral width of 10 cm^–1 and a pulse duration of approximately 20 ps are measured.     

Theoretical calculations and Raman spectrum of intercalation modes in LixInSe

By using an extended linear-chain model which includes the interlayer forces, we have calculated the new vibrational modes, of Li intercalated InSe. The dispersion curves along thek _z wavevector perpendicular to the layers for the -polytype are determined in the first Brillouin zone. Assuming that the interlayer interaction is not modified upon intercalation and the interaction between lithium atom and adjacent layers in the van der Waals plane has the same value than the interlayer one, the new modes are determined with the force constant given by the rigid layer mode of the, -polytype at 18 cm^–1. This model gives the variation of the acoustic branches and the appearance of two optical intercalation modes at higher frequencies. The Brillouin zone boundary modes of the acoustic branches at 18 and 41 cm^–1 in the pure material are calculated to be 22 and 50 cm^–1 respectively forx=1/2. The dispersion of the new optical branches is flat along thez-direction and frequencies are obtained at 96 cm^–1 for the Li mode perpendicular tok _z and at 218 cm^–1 for the Li mode parallel tok _z. We compare also our results with the Li mode frequencies obtained in a total energy calculation. Raman scattering experiments have been performed in intercalated sample in order to verify the proposed model.     

FTIR and Raman spectroscopic study of Fenugreek (<Emphasis Type="Italic">Trigonella foenum graecum L.</Emphasis>) seeds

The composition of Fenugreek seeds in the form of powder, ash, and oil is investigated through FTIR and FT Raman spectra measurements. The results indicate that Fenugreek seeds (powder) are rich in proteins. Fats (lipids) and starch are present in small amounts in the seeds. The FTIR absorption bands of seed powder appeared at: 3365 cm^–1 assigned as N-H stretching vibrations (amide A of protein), 1657 cm^–1 (C=O, amide I), 1540 cm^–1 (N-H bending vibration, amide II), and 1240 cm^–1 (N-H bending, amide III). In the FT Raman spectra the band at 1661 cm^–1 is ascribed to amide I (C=O) of proteins while the band at 1080 cm^–1 indicates the starch. The fenugreek oil Fourier transform infrared absorbance ratios A(3009 cm^–1)/A(2924 cm^–1), A(3009 cm^–1)/A(2854 cm^–1), and A(3009 cm^–1)/A(1740 cm^–1) were considered for measuring the iodine values. These ratios (0.3609, 0.4916, and 0.4129) revealed that the iodine value of fenugreek oil is higher than that of other oils. On the other hand, the ash of fenugreek is very rich in phosphate compounds. The spectra showed absorption bands at frequencies 1082, 1000, 618, and 566 cm^–1, and the FT Raman spectrum showed a strong absorbance band at 793 cm^–1, which is due to phosphate compounds. It could be concluded that the inorganic part of fenugreek consists mainly of phosphate compounds. The Fenugreek seed contains proteins, fat, fiber, and ash, which is in complete harmony with AACC, 1980.__________Published in Zhurnal Prikladnoi Spektroskopii, Vol. 72, No. 1, pp. 106–110, January–February, 2005.     

Rayleigh and raman scattering study of orientational and vibrational relaxation of carbon disulfide and chlorobenzene in solution

We have studied the line shape of the 655 cm^–1 Raman line in carbon disulfide and the 1002 cm^–1 line of chlorobenzene, from which we determine the orientational and vibrational relaxation times. We present results obtained on the vibrational relaxation of chlorobenzene in solution with heptane, dimethyl sulfoxide, acetone, and quinoline. Peculiarities in the behavior of the polarized line width in various solvents is related to molecular processes which depend on the dipole moment and density of the solvent.Samarkand State University. Translated from Izvestiya Vysshikh Uchebnykh Zavedenii, Fizika, No. 2, pp. 3–7, February, 1995.     

Laser isotope separation of titanium by two-step photoionization

Titanium isotopes were selectively excited and photoionized using a two-step photoionization method, and the isotope separation was demonstrated, in which a separation factor of around 15 for⁵⁰Ti was obtained. Spectroscopic parameters such as isotope shifts, photo-ionization cross section and excited state lifetimes were also measured. Isotope shifts up to 0.92 GHz were obtained for the transitions between 0 and 19938 cm^–1 or between 170 and 20006 cm^–1 among five isotopes. The cross section is 7.4×10^–17 cm² for the photo-ionization. The excited state lifetimes are 330±20 ns for 19938 cm^–1, 260±15 ns for 20006 cm^–1 and 250±15 ns for 20126 cm^–1.     

Far infrared and millimetre dielectric response of incommensurate and ferroelectric K2SeO4

Dielectric response of K₂SeO₄ in the spectral region 5–460cm^–1 was determined using transmissivity and reflectivity measurements as a function of temperature between 80 and 300K. The spectral features above 20cm^–1 are interpreted using results of lattice vibrational analysis in three known commensurate phases. The low-frequency dielectric anomaly in the incommensurate phase can be roughly described by critical slowing-down of a Debye relaxation given rise to by the overdamped infrared active phason mode which softens at the incommensurate-commensurate transition.     

The vibrational spectrum of crystalline KSCN

The spectrum is reported for the range 700 to 5000 cm^–1; the internal modes of the SCN^– ion are interpreted in terms of the C_s local symmetry group. The combinations of internal and external (lattice) modes are examined in terms of theD _2h factor group. The frequency of the translational mode is found to be 20 cm^–1.I am indebted to Academician A. N. Terenin for direction and encouragement, and to L. A. Gribov and D. S. Bystrov for discussions.     

Preparation and Raman scattering study of pore arrays on an InP (1 0 0) surface

Straight nanometer-sized pore arrays are formed on an n-InP (1 0 0) surface by electrochemical anodization in HCl-based electrolytes. Raman scattering spectra are measured and compared to those of the bulk InP. Two new peaks around 299 and 304 cm⁻¹ are observed for porous InP. The peak at 299 cm⁻¹ is attributed to a TO phonon mode observable due to a breakdown of polarization selection rule in the case of nanometer-sized crystallites. The peak at 304 cm⁻¹ is suggested to be a surface-related vibration mode. In addition, the Raman signals of the porous InP are intensified up to 20–25 times than that of the bulk InP. The reason for such strong enhancement is not clear and is under further investigation.     

Spectral Properties of Single Crystals of Synthetic Diamond

The half-width of the spectrum of Raman scattering (RS) of the first order of a diamond single crystal grown in a nickel-free system containing nitrogen getters is identical to all growth sectors (1.69 ± 0.02 cm^–1). The sectorial inhomogeneity is not reflected in the transmission spectra and birefringence of this crystal. The nitrogen concentration is 4·10¹⁷ cm^–3. For different growth sectors of the diamond crystal grown in the Ni–Fe–C system, the half-width of the Raman line varies from 1.74 to 2.08 cm^–1, differences in the transmission spectra and birefringence are observed, and photoluminescence is revealed. The concentration of nitrogen in the growth sectors {001} is 1.6·10¹⁹ cm^–3, the content of nickel is estimated to be at a level of 10¹⁹ cm^–3, and the content of nitrogen in the {¯111} sectors is 4·10¹⁹ cm^–3.     

Excited Even-Symmetry States of Metallocomplexes of Porphin and Its Derivatives

Based on calculations by the CNDO/S method, data on the excited molecular states of even parity of the magnesium complexes of porphin (P), tetraazaporphin (TAP), tetrabenzoporphin (TBP), and phthalocyanine (Phc) are obtained. It is only in MgP that the first excited g-state 1¹ B _2g (29,000 cm^–1) is located 300 cm^–1 higher than the B level (28,700 cm^–1). In MgTBP, the two states 1¹ B _1g (24,700 cm^–1) and 1¹ B _2g (25,500 cm^–1) are found to be near the B level (27,500 cm^–1), while the states 1¹ B _2g (25,500 cm^–1) in MgTAP and 1¹ B _2g (21,000 cm^–1) and 1¹ B _1g (23,100 cm^–1) in MgPhc are located much lower than the B level; the energy of the latter is 31,900 and 32,400 cm^–1 in MgTAP and MgPhc respectively. The results obtained are in good agreement with experimental data on two-photon absorption: in the zinc complex of tetraphenylporphin (TPhP), the g-state is detected in the region of the B level, while in ZnPhc, two bands at 20,400 and 21,700 cm^–1 show up.     

H2S : First Observation of the (70,0) Local Mode Pair and Updated Global Effective Vibrational Hamiltonian

The absorption spectrum of H₂S has been recorded by intracavity laser absorption spectroscopy in the spectral region 16 180–16 440 cm⁻¹ corresponding to an excitation of the (70^±, 0) local mode pair. Seventy-seven sublevels could be rotationally assigned and fitted with a rms of 0.009 cm⁻¹ by considering the (70^±, 0) local mode pair as isolated. The corresponding vibrational terms combined with all the levels reported in the literature were used to refine the effective vibrational Hamiltonian parameters of H₂³²S. The importance of the Fermi-type interaction is discussed.     

Optical studies on free-standing polypyrrole films by the photopyroelectric method

Optical spectra of free-standing polypyrrole films were investigated by a novel PhotoPyroElectric (PPE) method. The reflection and absorption spectra in the range 2000–25000 cm^–1 of TsO^–- and ClO ₄ ^su– -doped polypyrrole films were obtained with an experimental setup comprising two pyroelectric sensors. The absorption bands due to electronic transitions to the bonding and antibonding bipolaronic levels appear at 11 000 and 21 500 cm^–1, respectively. Some relevant details in the polypyrrole spectrum in the 2000–5000 cm^–1 range were observed. The absorption band located at 3400 cm^–1 is characteristic for NH stretching vibration. The bands in the 2300–2500 cm^–1 range are ascribed to the vibration of N⁺H groups containing positively charged nitrogen. The PPE spectra also reveal changes of the electronic and vibrational absorption bands after polymer reduction and HCl treatment.