Relative vibrational transition probabilities in the (B 3 π g−A 3Σ u + ) system of nitrogen for Hulbert-Hirschfelder oscillator model

Hulbert-Hirschfelder (h-h) potential function has been used to obtain the relative vibrational transition probabilities for the observed bands of the first positive system of nitrogen molecule. The vibrational wavefunctions have been calculated by solving the Schrödinger equation by the method due to Langer, at low vibrational quanta and by thewkb method at high vibrational quanta. It is established that theh-h potential is superior to the often used Morse potential function for the transition under consideration.     

Observation of perturbations in the rovibronic transition probabilities for the (4d)r 3Π g − , (4d) s 3 Δ g − → (2p) c 3Π u ± band systems of the H2 molecule

The ratios of the radiative transition probabilities for the lines of the P, Q, and R branches of the (4d)r ³Π _g ^? , (4d)s ³Δ _g ^? → (2p) c ³Π _u ^± band systems of the H₂ molecule have been measured for the first time. Significant (to two orders of magnitudes) differences are found between the experimental values and the adiabatic theory predictions. It is established that the results of the nonadiabatic calculation performed by us in the pure-precession approximation taking into account the electronic-rotational interaction of the 4d ³Π_g and 4d ³Δ_g states are in agreement with the experimental data. The optimal energies of rovibronic levels of the r ³Π _g ^? , s ³Δ _g ^? , c ³Π _u ^? , and c ³Π _u ⁺ states have been found and reidentification of 11 from 54 spectral lines, assigned previously to the (0-0) and (1-1) bands, was performed.     

Improved lasing properties of the HêN 2 + system at 391 nm and 428 nm by H2 admixture

The He/N₂ system lasing on the N ₂ ⁺ (B)N ₂ ⁺ (X, 0) transition at 391 nm and on the N ₂ ⁺ (B)N ₂ ⁺ (X, 1) transition at 428 nm was investigated by e-beam excitation. By adding H₂ the lower laser state is efficiently quenched, which leads to a drastic improvement of the laser properties. A kinetic model is proposed which accounts for the experimental results. For a laser amplifier operated at 5 bar total efficiencies of 0.6% and 0.7% are predicted for the 391 nm and the 428 nm transitions respectively.     

Ordering of the O(2)…D… O(2) bonds near the phase transition in KD3(SeO3)2 single crystals by D nuclear magnetic resonance

Deuterium resonance investigations of KD₃(SeO₃)₂ single crystals have been performed near the phase transition temperature T _C . There are two types of deuterium bonds in these crystals with different behaviors at this phase transition. Our experimental results show that there are significant changes in the D spinlattice relaxation time T ₁ at T _C ; the abrupt decrease in T ₁ near T _C can be explained by the critical slowing down of an overdamped soft pseudospin-type deuteron mode. Further, the ordering of the O(2)…D… O(2) bonds is affected by the phase transition, whereas the ordering of the O(1)-D… O(3) bonds is unaffected. The D NMR measurements also show that the D(2) deuteron disordering above T _C is dynamic and not static.     

Z−Z′ mixing and oblique corrections in anSU(3)×U(1) model

We address the effects of the new physics predicted by theSU(3) _l ×U(1) _X model on the precision electroweak measurements. We consider bothZ–Z mixing and one-loop oblique corrections, using a combination of neutral gauge boson mixing parameters and the parametersS andT. At tree level, we obtain strong limits on theZ–Z mixing angle, –0.0006<0.0042 and="> 490$$ " align="middle" border="0"> GeV (both at 90% C.L.). The radiative corrections lead toT>0 if the new Higgs are heavy, which bounds the Higgs masses to be less than a few TeV.S can have either sign depending on the Higgs mass spectrum. Future experiments may soon place strong restrictions on this model, thus making it eminently testable.     

NH3-induced c(4 × 2) to (2 × 2) transition on the Ge(001) surface by a domino-like dimer flip

Under the conditions of thermodynamic adsorption-desorption equilibrium, the first strongly bound molecular adsorption state of ammonia on Ge(001) saturates at one molecule per Ge reconstruction dimer (1/2 ML). High-resolution electron diffraction studies show that this adsorption is accompanied by a structural transition from c(4 × 2) on the clean surface to a (2 × 2) structure which is already completed for a coverage of about 0.04 ML, far below saturation. We propose a model implying the formation of NH₃ islands locally covered with 1/2 ML and a (2 × 2) periodicity caused by a flip of the dimer tilt direction of every second dimer Beyond the edge of these islands, the dimer flip continues domino-like along the dimer rows over the clean parts of the surface. Elongated (2 × 2) domains about 280–330Å long and 30–65Å wide are formed, depending on coverage.     

氯分子Cl2激发态D’(2u3)势能函数的高阶修正

采用能量自洽法研究了Cl2分子D’(2u3)态的解析势能函数。结果表明,对于Cl2分子D’(2u3)态,传统的解析势能函数Morse势与基于实验的Rydberg–Klein–Rees (RKR)数据有明显偏差,普遍认为优秀的Murrell–Sorbie (MS)势的改进型Huxley–Murrell– Sorbie (HMS)却给出了与物理意义不符的势能行为。采用能量自洽法Energy Consistent Method (ECM)研究得到的三阶解析势能函数ECM(3)对HMS的势能行为虽有改进,但仍与RKR数据不符。我们对Cl2分子D’(2u3)态的解析势能函数进行了高阶修正,将ECM(3)势推广到五阶,得到的五阶解析势能函数ECM(5) 结果与RKR数据符合得很好,并且正确描述了包括渐近区和离解区在内的全程势能行为,而渐近区和离解区内的实验势能数据常常是缺乏的。     

A two-frequency He−Ne laser at the 3S 2→3P 4 transition in mutually orthogonal transverse magnetic fields

By taking as an example a He−Ne laser that operates at the 3S₂−3P₄ transition (λ=3.39 μm), we studied the specific features of nonlinear interaction of the waves of linear orthogonal polarizations in a transverse magnetic field. Using mutually orthogonal transverse magnetic fields on the neighboring portions of an active medium, we implemented a regime of two-frequency generation, which was investigated theoretically and experimentally. To whom correspondence should be addressed. B. I. Stepanov Institute of Physics, National Academy of Sciences of Belarus, 68, F. Skorina Ave., Minsk, 220072, Belarus. Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 66, No. 4, pp. 568–573, July–August, 1999.     

Study on the A~2Π_(3/2u), B~2Δ_(3/2u), and X~2Π_(3/2g) states of Cl_2~+ including its isotopologues

Adopting the experimentally available vibrational constants in a recent analysis of the strong perturbation between the A22Π3/2u and BΔ3/2u states of Cl+2in the A–X band system [Gharaibeh et al. 2012 J. Chem. Phys. 137 194317], an unambiguous vibrational assignment of the bands reported previously is carried out. The equilibrium rotational constants Be and α e of the X2Π3/2g and A2Π3/2u states for35Cl+2and35Cl37Cl+and those of the B2Δ3/2u state for35Cl+2are obtained by fitting the experimental values of Bυ. In addition, the values of Be and α e of these three states for the minor isotopologues35Cl37Cl+and37Cl+2are predicted by employing the isotopic effect. The values of equilibrium internuclear distance Re of the three states for the three isotopologues are calculated as well.     

Low-temperature phase transition in α′-(BEDT-TTF)2IBr2 single crystals detected by the ESR method

A hysteresis of electron spin resonance spectra, which indicates a first-order phase transition, has been revealed in α′-(BEDT-TTF)₂IBr₂ single crystals in the temperature range 15–30 K. Two lines corresponding to the high-temperature and low-temperature phases have been observed in the ESR spectra.     

Tunable UV radiation at short wavelengths (188–240 nm) generated by sum-frequency mixing in lithium borate

Sum-frequency mixing (₃=₁+₂) of UV laser radiation (₁=266 nm and 213 nm) and tunable coherent infrared light (₂=1.2–2.6 m) in lithium borate (LBO) generates radiation at short wavelengths (₃=188–242 nm). The UV radiation at ₁ is produced by the fourth and fifth harmonic of a pulsed Nd-YAG laser. The infrared light is generated with an optical parametric oscillator of beta barium borate. The phase-matching angle is measured as function of ₃ and compared with calculated values. For UV laser radiation at shorter wavelengths (173 nm₁213 nm) the calculations predict an extension of the tuning range of the sum-frequency generated at ₃ to wavelengths as short as the LBO transmission cutoff at 160 nm.     

The B̃2Σ−g (Πu) ← X̃2A1 system of nitrogen dioxide in neon matrices

The $\text{B}\text{?}\text{←}\text{X}\text{?}$ band system of NO₂, ${}^2\text{Σ}{}^{\mathrm{?}}{}_{\mathrm{g}}\text{(π}{}_{\mathrm{u}}\text{) ←}{}^2\text{A}{}_1$, has been measured in absorption in a neon matrix at 6 K, using ¹⁵NO₂ and N¹⁸O₂ in addition to the normal isotope. The spectrum consists essentially of a single, long progression of bands terminating on successive levels of the bending mode in the upper state. Transitions to odd- and even-v₂′ states occur with a uniform intensity distribution indicating that the rotation of the bent ground state of NO₂ about its near-prolate axis is hindered in the matrix. The observations strongly suggest that the top axis of the molecule coincides with a C₂ axis of neon crystals in the polycrystalline matrix. Relative to the vapor absorption the matrix spectrum is red shifted by about 150 cm^?1, the crystal field parameter V₂ and principal constants of the $\text{B}\text{?}$ state of ¹⁴N¹⁶O₂ in neon being

$\text{T}{}_{010}\text{14 571 cm}{}^{\mathrm{?1}}\text{: x}{}_{22}\text{, ?0.3 cm}{}^{\mathrm{?1}}\text{;}$

$\text{w}{}_2\text{460.2 cm}{}^{\mathrm{?1}}\text{: V}{}_2\text{, 80 cm}{}^{\mathrm{?1}}\text{.}$

     

On the nature of the valence transition in Eu(Pd1−xAux)2Si2

The intermediate valent compound series Eu(Pd_1−xAu_x)₂Si₂ has been studied by Mössbauer effect measurements on ¹⁵¹Eu(T = 4.2−300K) and ¹⁹⁷Au (4.2K) and by X-ray diffraction (10K, 300K). The temperature induced valence transition Eu²⁺ → Eu³⁺ for x < 0.175 is not of first order type, as suggested in a previous phase diagram [1]. The valence change of the Eu-ion is reflected also in the isomer shift of the ¹⁹⁷Au Mössbauer-resonance.     

The magnetic circular dichroism spectrum of the 1 B 2u ←1 A 1g transition of benzene in the vapour phase

The magnetic circular dichroism (MCD) spectrum of the ¹ B _2u ←¹ A _1g transition of benzene has been measured in the vapour phase. Many of the bands due to transitions between single vibronic levels display A terms. It has been shown that the angular momentum arises by vibronic mixing both of the ¹ E _1u state with the ¹ B _1u state and of the ¹ E _2g states with the ¹ A _1g ground state by e _2g vibrations. The magnitudes and signs of the experimental and calculated ratios, A/D, for the A ₀ ⁰ vibronic origin are in excellent agreement. Two strong MCD progressions of opposite sign with B-term dispersion have been observed in regions of low absorption. These are identified with vibronic origins due to the v ₈ and v ₉ e _2g modes. By contrast the MCD spectrum of hexadeuterobenzene vapour has a much lower magneto-rotational strength and displays none of the striking features of the benzene MCD spectrum.     

Laser oscillation by the F3− and F2− color centers in LiF crystal at room temperature

A stable, free-running LiF:F₃ ⁻ and LiF:F₂ ⁻ color center laser oscillation is achieved at room temperature by pumping with the 930-nm laser radiation. The LiF:F₃ ⁻ laser radiation has a peak at 1100 nm and shifts from the peak wavelength of the F₃ ⁻ luminescence band because of the absorption of the F₃ ⁻ luminescence by the F₂ ⁻ center, which co-exists with the F₃ ⁻ center. Received: 2 March 1999 / Revised version: 16 March 1999 / Published online: 12 May 1999     

Semiempirical investigation of perturbations of the g factors of electronic-vibrational-rotational levels of hydrogen: III. The r 3Π g − and s 3Δ g − states of the H2 and D2 molecules

The g factors of rovibrational levels of the (4d)r ³Π _g ^? and (4d)s ³Δ _g ^? states of the H₂ and D₂ molecules have been obtained for the first time. These values were found within the nonadiabatic model taking into account the interaction of the 4dπ³Π_g and 4dδ³Δ_g states in the pure precession approximation using semiempirical values of the expansion coefficients of the wave function in an adiabatic basis, which was obtained for the first time for the states of the triplet 4d complex of terms of the hydrogen molecules, and the results of numerical calculation of the overlap integrals of the vibrational wave functions of these states. It is established that the interference effects of the interaction between the 4dπ³Π _g ^? and 4dδ³Δ _g ^? states lead to significant (up to 7 times for the r ³Π _g ^? state of the H₂ and D₂ molecules and 70 and 8 times for the s ³Δ _g ^? state of the H₂ and D₂ molecules, respectively) differences between the nonadiabatic values of the g factors and the corresponding adiabatic values. It is found that the perturbed values of the g factors are much closer to the values corresponding to the case of Hund’s d coupling of angular momenta than to the values corresponding to the b coupling. It is established that the perturbations of the g factors of rovibrational levels of the states of the 4d complex of terms are much greater (up to 2 times for the ³Π _g ^? states and 350 times for the ³Δ _g ^? states) than the perturbations of the same characteristics for the 3d complex of terms of the hydrogen molecule with the same vibrational and rotational quantum numbers.