Spectra of optically pumped superradiant and cavity NH3 far-infrared laser

Based on the density matrix theory of quantum system, the spectra of optically pumped superradiant and cavity NH₃ far-infrared (FIR) lasers were calculated by means of iteration method. The calculation showed that, compared with the optically pumped superradiant FIR laser, the cavity laser had a wider band spectrum of FIR emission and a higher output power under certain condition, moreover, the spectra of cavity laser had multi longitudinal-mode structure. Supported by the Research Foundation of Hubei Province Education Committee, PRC     

A twin optically-pumped far-infrared CH3OH laser for plasma diagnostics

A twin optically-pumped far-infrared CH₃OH laser has been constructed for use in plasma diagnostics. The antisymmetric doublet due to the Raman-type resonant two-photon transition is reproducibly observed at 118.8 m. With the 118.8-m line, it is obtained from the frequency separation of the anti-symmetric doublet that CH₃OH absorption line center is 16±1 MHz higher than the pump 9.7-m P(36) CO₂ laser line center. It is shown that the Raman-type resonant two-photon transition is useful in order to get several-MHz phase modulation for the far-infrared laser interferometer. Some preliminary performances of this twin laser for the modulated interferometer are described.This work was carried out under the collaborating research program at the Institute of Plasma Physics, Nagoya University, Nagoya 464, Japan.     

Infrared and far-infrared laser emissions from a TE CO2 laser pumped NH3 gas

In this paper, infrared (IR) and far-infrared (FIR) laser emissions from a TE CO₂ laser pumped NH₃ gas are reported. 8 IR laser emissions near the wavelength of 12 μm were observed by using 4 different CO₂ laser lines for the pumping. 3 IR laser emissions in P-branch of vibrational-rotational band (ν₂ → G) oscillated simultaneously in two pumping cases, i.e. pumping with the R(30) or R(16) line of 9.4 μm band from the CO₂ laser. 26 FIR laser emissions (26.45 μm ～ 281.0 μm) were observed by using 12 different CO₂ laser lines, and the 10 FIR emissions of them may be new laser emissions as far as we know.     

New NH2H4 far-infrared laser lines and their frequencies

We report 25 new far-infrared laser lines and 26 heterodyne frequency measurements in hydrazine. The frequencies range from 1.0 to 5.5 THz with most of the frequencies between 2.5 and 4.0 THz. The lines were generated in a high frequency, far-infrared Fabry-Perot laser cavity pumped by a CO₂ laser. The cavity has a high Q for wavelengths below 150 µm and uses variable coupling to optimize the power for each line.This work has been financed by the Brazilian Government - Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), and by the United States Government - NASA grant W-18, 623.Contribution of NIST, not subject to U.S. copyright.     

A high-power far-infrared NH3 laser pumped in a three-mirror CO2 laser cavity with optically-switched cavity-dumping

Results are reported of cavity-dumping a submillimeter radiation high-Q, zig-zag optically-pumped resonator which utilizes a silicon optical switch photo-excited by a NdYAG laser. Peak powers at 152 m approaching 10 kW in temporally smooth pulses of 5 ns (FWHM) duration have been obtained at a pulse repetition rate of 12 Hz. The far-infrared laser radiation, as measured with a scanning metal-mesh Fabry-Perot interferometer and averaged over many pulses, is, upon deconvolution of the 125 MHz instrumental linewidth, found to oscillate in a predominantly single longitudinal mode of width 250 MHz. Theoretical investigations of the transient far-infrared reflectivity of the silicon optical switch predict a rise in the Brewster-angle reflectivity from 0% to nearly 80% in 1 ns, when activated by a Q-switched, frequency-doubled NdYAG laser providing an incident energy density of 50 mJ/cm² in a pulsewidth of 10 ns.     

RF generator for compact CO2 waveguide lasers

This letter reports the fabrication and testing of a compact Radio Frequency Generator (Oscillator-Amplifier) for its integration in a CO₂ waveguide laser. The circuit uses a common source MOSFET transistor that has been modified for self-sustained oscillations impedance-matched to 50 Ω. RF power is supplied to the laser resonant cavity made of a ceramic-metal slab which is placed between a negative branch unstable optical resonator.     

(NH4)2SO4，NH4NO3和(NH4)2SO4/NH4NO3混合气溶胶吸湿质量增长因子的快速测量方法

气溶胶颗粒的吸湿性决定了其尺寸、浓度、化学组成以及相态,从而显著影响着全球气候、大气异相化学以及人类健康。运用在线、原位、连续扫描衰减全反射傅里叶变换红外光谱（ATR-FTIR）技术, 结合线性湿度（RH）控制系统,实现了RH连续变化条件下气溶胶FTIR-ATR光谱的快速测量。根据水弯曲振动谱带（~1 640 cm-1）峰面积随RH的变化,得到了(NH₄)₂SO₄,NH₄NO₃和(NH₄)₂SO₄/NH₄NO₃混合气溶胶的质量增长因子（MGFs）、潮解点（DRH）和风化点（ERH）。与气溶胶的E-AIM模型预测值相比较,实验结果表现出良好的一致性,证实该方法是一种测量大气气溶胶MGFs,ERH和DRH的快速测量方法。     

NMR spectral densities and two dimensional diffusion in TiS2(NH3)1.0 and TaS2(NH3)x

NMR measurements of proton spin-lattice relaxation times T₁ and T_1? in the layered intercalation compounds TiS₂(NH₃)_1.0 and TaS₂(NH₃)_x (x = 0.8, 0.9, 1.0) are reported as functions of frequency and temperature (100 K – 300 K). These observations probe the spectral density of magnetic fluctuations due to motions of the intercalated molecules at frequencies accessible to the T₁ (4–90 MHz) and T_1? (1–100 kHz) measurements. Since the average molecular hopping time (τ) can be changed by varying temperature, different regions of the spectral density can be examined. For T > 200 K, both T^?1₁ and T^?1_1? vary logarithmically with frequency, reflecting the two dimensional character of the molecular diffusion. The temperature dependence of T₁ suggests that a more accurate picture of the short time dynamics is required. No dependence of relaxation rate on vacancy concentration is found.     

Partly tunable mid-infrared NH3 laser

Using a continously tunable pulsed 20-atmosphere CO₂ laser as a pump source, we generated pulses of mid-infrared radiation, partly tunable in frequency intervals in the range between 200 and 900 cm^–1 via stimulated Raman scattering in gaseous ammonia. As a Raman cell we used a multiple pass cell. We observed for¹⁴NH₃ and¹⁵NH₃ laser lines at 52 different frequencies with 39 lines observed for the first time. Tuning ranges up to 150 GHz and peak powers of several MW were achieved. The quantum efficiency reached 40 %.     

Integrated infrared intensities in NH3

The integrated infrared intensities of the fundamental modes of NH₃ have been measured by the Wilson-Wells-Penner-Weber method. The intensities were found to be 43.9 ± 0.6, 567.6 ± 9.4 and 110.5 ± 2.0 atm^-1 cm^-2 (standard temperature and pressure) for the ν₁ + ν₃, ν₂ and ν₄ bands, respectively.     

Chlorine K X-ray absorption-edge structures of CIS-[Pt(NH3)2Cl2], trans-[Pt(NH3)2Cl2], trans-[Pd(NH3)2Cl2] and (NH4)2PdCl4

The K absorption-edge spectra of the ligand chlorine ion in square-planar complex compounds cis- and trans-[Pt(NH₃)₂Cl₂], trans-[Pd(NH₃)₂Cl₂], and (NH₄)₂PdCl₄ are reported and discussed in connection with the chlorine K absorption spectra of K₂PtCl₄ and K₂PdCl₄, reported previously. The observed chemical shift of a white line at the absorption threshold is interpreted in terms of the difference of the ligand-field splitting of electronic states for metal ions. The white line is attributed to the electronic transition from the Cl^? ls level to the lowest unoccupied antibonding molecular orbital (MO), which is specified by a $\text{MO}\text{b}{}_{\mathrm{1g}}\text{(σ}{}^1\text{)}$ in the square-planar complex with D_4h symmetry. The other absorption structures are regarded as continuum “shape resonances” of the outgoing electron trapped by the cage of the surrounding atoms. The effect of geometrical isomerism is found in the chlorine K absorption spectra of cis- and trans-[Pt(NH₃)₂Cl₂].     

Calorimetric and x-ray diffraction studies of the (NH4)3WO3F3 and (NH4)3TiOF5 perovskite-like oxyfluorides

The heat capacity and unit cell parameters of the (NH₄)₃WO₃F₃ and (NH₄)₃TiOF₅ perovskite-like oxyfluorides were measured in the temperature interval from 80 to 300 K; the existence of two and one phase transitions in these compounds, respectively, was demonstrated, and their thermodynamic parameters were determined. The effect of a hydrostatic pressure of up to 0.5 GPa on the phase transition temperatures was studied. Triple points and high-pressure phases were found in the T vs. p diagrams. An analysis of entropy changes suggests that all the structural transformations revealed are associated with the ordering of structural blocks. __________ Translated from Fizika Tverdogo Tela, Vol. 46, No. 5, 2004, pp. 888–894. Original Russian Text Copyright ? 2004 by Flerov, Gorev, Fokina, Bovina, Laptash.     

Acoustooptic extension of the frequency tunability of CW CO2 lasers: New FIR lasers emissions from CH3OH and13CH3OH

We have increased the frequency tunability of our CW waveguide CO₂ lasers by means of an acoustooptic amplitude modulator, operating at the fixed frequency of 90 MHz. The up-shifted, or down-shifted, laser optical sideband can be generated independently by adjusting the orientation of the modulator. The efficiency is larger than 50%. The frequency tunability of the CO₂ laser around each laser line is thus increased by 180 MHz. To demonstrate the possibilities of this method, a source composed of the above modulator and of a CW, 300 MHz tunable waveguide CO₂ laser has been used for the search of new large offset FIR laser lines from optically pumped CH₃OH and¹³CH₃OH molecules. As a result 15 and 10 new large offset laser lines were discovered respectively. New assignments of some laser lines are also proposed. We have also measured the Stark effect, the offset, and the polarization of other already known lines. In particular a Stark effect frequency tuning of about 1 GHz is demonstrated for a laser line at 208.399 m.     

Mode structure in wideband waveguide radiofrequency CO2 lasers

We have analysed the mode structure of a wideband radiofrequency excited waveguide CO₂ laser by using different waveguide diameters and optical cavities. In particular we have observed the phase shift of some linear polarized waveguide modes in the transition region between the guided and the free Gaussian propagation.     

Line Broadening and Mixing in NH3 Inversion Doublets Perturbed by NH3, He, Ar, and H2

Measurement of absorption by pure ammonia and NH₃–(H₂, He, and Ar) mixtures in the P branch of the ν₄ band at room temperature have been made with a high-resolution Fourier transform spectrometer. Least squares fits of the spectra using different techniques are used for the analysis of the evolution with pressure of the absorption shape for a number of ^PP inversion doublets. Intensities, half-widths, and line-coupling parameters are determined, demonstrating the great importance of line-mixing effects. The results are compared with values calculated using a semiclassical model. The latter explains most of the features of the line-broadening and the J and K dependencies of line-coupling for pure NH₃, whereas poorer results are obtained for line-mixing in mixtures. The most striking and original result is the very large amount of coupling between the symmetric and antisymmetric components, which can reach up to 80% of the width in the case of pure NH₃. Also remarkable is the very strong influence of the rotational quantum number K.     

Vibration-inversion-rotation spectra of ammonia: Centrifugal distortion, Coriolis interactions, and force field in NH3, NH3, ND3, and NT3

An effective inversion-rotation Hamiltonian has been developed for NH₃ which avoids the necessity of having to include high powers of the inversion motion coordinate in the Taylor expansions of the potential energy and the inverse moment of inertia tensor. This nonrigid bender Hamiltonian describes the centrifugal distortion and the Coriolis interactions in the ground and excited inversion states. It also describes the inversion doublings in the ground and excited vibration-inversion states of ammonia. A least-squares procedure that includes the numerical integration of the Schrödinger wave equation has been used to determine the harmonic force field and the double-minimum inversion potential function for (¹⁴NH₃, ¹⁵NH₃) and for (¹⁴ND₃ and ¹⁴NT₃).The anomalous rotational dependence of the inversion doublings in the (±l) components of the v₄ = 1 state of ¹⁴NH₃ has been explained by the Coriolis interactions between v₂=1, v₄ = 1, v₂ = 2, v₂ = 1, v₄ = 1, and v₂ = 3 vibration-inversion states.     

Magnetic phase diagram of Ni(NO3)2 6NH3

The magnetic phase diagram of Ni(NO₃)₂6NH₃ was determined from the field and temperature dependence of the magnetic susceptibility. The zero temperature exchange and anisotropy fields were determined to be H_E(0) ≈ 26 kOe and H_A(0) ≈ 0.7 kOe respectively.     

The electrooptic effect in NH4IO3

The static electrooptic coefficients of NH₄IO₃ at room temperature are r₄₃ = 4.9, r₆₁ = 1.0, r₁₂n²₁ ? r₃₂n³₃ = 59.6, r₂₂n³₂ ? r₃₂n³₃ = 116.8 [ X 10^-12m/V]. The electrooptic effect depends on temperature and shows two ph ase transitions at 82.5°C and near 120°C.     

Classical theory of the dielectric loss for NH3 and ND3

A formula for the frequency dependent dielectric loss in dilute gases of NH₃ and ND₃ describing the deviation of the nonresonant spectrum from the Debye shape and demonstrating the importance of dipole reorientation memory loss effects in lineshift calculations has been developed.     

Kinetic study of NH3/ND3 exchange in TaS2 by neutron diffraction

Tracer exchange of TaS₂·NH₃ by liquid ND₃ was investigated at 215 and 223 K by neutron diffraction. The results suggest only a molecular exchange on the time-scale of quasielastic neutron scattering measurements.