High-resolution investigation of the excited electronic states of CaSH and SrSH by laser excitation spectroscopy – ARTICLE WITHDRAWN

WITHDRAWN TO APPEAR IN SPECIAL ISSUE IN 2007     

Theoretically study on measurement of velocity distribution by means of laser induced fluorescence

Based on two-level atomic density matrix movement equation and emitting operator, the physical model is established for laser induced moving atomic resonant fluores cence. Theoretically study showsthat the measurement of atomic velocity distribution by means of laser induced fluorescence is only valid when the physical factors, such as atomic natural line width, laser power, laser line width, is suitably selected.     

Spin-orbit splitting in the X2Π, a4Π, B2Π and H2Π electronic states of the NS radical

A model calculating the laser fields at a flat structureless surface taking into account the surface photoelectric effect is presented. The photon is p or transverse magnetic linearly polarized, continuous and its wave length is long, i.e. λ _vac  ≥ 12.4 nm. The sharp rise of the electron density at the interface generates an atomic scale spatial dependence of the laser field. In real space and in the temporal gauge, the vector potential A of the laser is obtained as a solution of the classical Ampère-Maxwell and the material equations. The susceptibility is a product of the electron density of the material system with the surface and of the bulk tensor and non-local isotropic (TNLI) polarizability. The electron density is obtained quantum mechanically by solving the Schrödinger equation. The bulk TNLI polarizability including dispersion is calculated from a Drude-Lindhard-Kliewer model. In one dimension perpendicular to the surface the components \hbox{$\mathcal{A}_x(z,\omega)$} ?? _x (z,ω) and \hbox{$\mathcal{A}_z(z,\omega)$}?? _z (z,ω) of the vector potential are solutions of the Ampère-Maxwell system of two coupled integro-differential equations. The model, called vector potential from the electron density-coupled integro-differential equations (VPED-CIDE), is used here to obtain the electron escape probability from the power density absorption, the reflectance, the electron density induced by the laser and Feibelman’s parameters d _∥ and d _⊥. Some preliminary results on aluminium surfaces are given here and in a companion paper the photoelectron spectra are calculated with results in agreement with the experiment.     

Study of the electric field and wall voltage in a high pressure ac-PDP cell by laser induced fluorescence spectroscopy

The electric field in a surface discharge type ac-PDP cell with He or He/Xe(0.1%) mixture has been measured over a wide range of pressure (5－50 kPa) using laser induced fluorescence detection. The wall voltage was estimated from the measured electric field. The Stark manifolds of triplet atomic helium Rydberg state (2s^3S) with principal quantum numbers (n=8 and 9) have been used to measure the electric field, as the lifetime of 2s^3S is longer than the single atomic helium Rydberg state (2s^1S) in high pressure discharge. Comparison of the Stark manifolds between the n=9 and n=8 shows that the measurement accuracy of electric field can be increased by 10%. The maximum electric field strength during discharge and the wall voltage at the end of pulse decreases with the increase of pressure. The comparison of He and He/Xe(0.1%) discharge at 13 kPa showed that He/Xe gas mixture discharge can accumulate more wall charge on MgO surface and the electric field was somewhat higher than those of pure helium discharge during pulse off period under the same discharge conditions.     

Transition probabilities of the X1Σ+, A1Π, B1Δ, C1Σ+, and D1Π states of the AlO+ cation

ABSTRACT

This study computes the potential energy curves of the X¹Σ⁺, A¹Π, B¹Δ, C¹Σ⁺, and D¹Π states of AlO⁺ cation and the transition dipole moments between them. The orders of the rotationless radiative lifetimes are 10–100?μs for the A¹Π state, 1–1000?ms for the B¹Δ state, 10?ns for the first well and 100?ns for the second well of the C¹Σ⁺ state, and 1?μs for the D¹Π state. Emissions of the B¹Δ–A¹Π and D¹Π–C¹Σ⁺ systems are so weak that they are hardly measured via spectroscopy, the emissions of the C¹Σ⁺–X¹Σ⁺, C¹Σ⁺–A¹Π, and D¹Π–X¹Σ⁺ systems are so strong that they can be detected readily, and emissions of the A¹Π–X¹Σ⁺ and D¹Π–A¹Π systems can be observed through spectroscopy only by a significant effort. There is a strong great similarity between spontaneous emissions of the A¹Π–X¹Σ⁺ system of the AlO⁺ cation and the A²Π–X²Σ⁺ system of the AlO radical. The emissions of the A²Π–X²Σ⁺ system of the AlO radical have been measured in outer space Therefore, it is highly possible that the emissions of the A¹Π–X¹Σ⁺ system of the AlO⁺ cation can be detected in the astrophysical media.     

Vibrational Analysis of the A3Π0−X1Σ+ and B3Π1−X1Σ+ Subsystems of the GaBr Molecule

Abstract

The emission band spectrum of gallium monobromide has been excited in a dc hollow cathode discharge. bands of the ³Π_0,1?X¹Σ⁺ system, lying in the range from 340 to 370 nm have been recorded at high resolution and measured. The previous vibrational analysis has been revised and corrected. New vibrational assignment has been proposed and improved vibrational constants of the upper and lower electronic states have been determined.     

Expansion velocities of 0.5 ps KrF excimer laser induced plasma by Doppler-shift analysis of pump and probe measurements

High gradient laser plasma is formed by focused KrF laser pulses (248.3 nm, 450 fs, 10¹³ W/cm²) on liquids (water, styrene) and solids (silicon, aluminum, and polyimide). The hydrodynamic expansion of the plasma was studied by measuring the blue Doppler-shift of reflected probe pulses which was produced by a delayed dye laser (496.6 nm, 450 fs). The Doppler-shift corresponds to the velocity of the reflecting surface of the plasma which is defined by the critical electron density. Expansion is investigated as a function of delay time and laser intensity. The reflecting surface of the plasma accelerates over 1–2 ps after the onset of the ablating laser pulse. With increasing intensity up to 2×10¹³ W/cm² the maximum average velocities are monotonously increasing up to 1–2×10⁵ m/s. PACS 52.38.Kd; 52.50.Jm, 52.70.Kz     

Characterization of the [Xtilde] 1Σ+ à 3Π and à 1Π electronic states of BBO

The three lowest-lying electronic states, [Xtilde] ¹Σ⁺, à ³II and à ¹II, of the linear BBO molecule have been systematically investigated using ab initio electronic structure theory. The equilibrium structures and physical properties including dipole moments, vibrational frequencies and associated infrared intensities, Renner parameters and energetics for the three states of BBO have been determined employing SCF, CISD, CCSD and CCSD(T) levels of theory and a wide range of basis sets. The ground state of BBO presents a degenerate real bending frequency, while the à ³II and à ¹II states show two distinct real bending frequencies due to the Renner-Teller interaction. The bending motion of the à ¹II state was analysed using the equation-of-motion (EOM)-CCSD and EOM-CC3 techniques in order to avoid possible variational collapse to a lower-lying state. The [Xtilde] ¹Σ⁺-à ³II separation was predicted to be T ₀ = 16.6 kcal mol^?1 (5800 cm^?1, 0.719 eV) at the cc-pVQZ CCSD(T) level of theory. With the cc-pVQZ EOM-CC3 method the [Xtilde] ¹Σ⁺-à ¹II splitting was predicted to be T ₀ = 48.0 kcal mol^?1 (16 800 cm^?1, 2.08 eV), which is in good agreement with the experimental value of T ⁰ = 46.6 kcal mol^?1 (16 300 cm^?1, 2.02 eV). The Renner parameters and averaged harmonic frequencies of the bending mode were determined to be ? = 0.184 and ω₂ = 363 cm^?1 for the à ³II state, and ? = 0.246 and ω₂ = 383cm^?1 for the à ¹II state. The theoretical [Xtilde] ¹Σ⁺ state harmonic B-B stretching frequency ω₃ = 636 cm^?1 is somewhat higher than the experimental estimate of 582 cm^?1 and the predicted à ¹II state harmonic B-B stretching frequency ω₃ = 861 cm^?1 is significantly higher than the experimental estimate of 440 cm^?1     

Robustness self-testing of states and measurements in the prepare-and-measure scenario with 3 → 1 random access code

Recently, Tavakoli et al.proposed a self-testing scheme in the prepare-and-measure scenario, showing that self-testing is not necessarily based on entanglement and violation of a Bell inequality [Phys.Rev.A 98 062307(2018)].They realized the self-testing of preparations and measurements in an N → 1(N ≥ 2) random access code(RAC), and provided robustness bounds in a 2 → 1 RAC.Since all N → 1 RACs with shared randomness are combinations of 2 → 1 and 3 → 1 RACs, the3 → 1 RAC is just as important as the 2 → 1 RAC.In this paper, we find a set of preparations and measurements in the3 → 1 RAC, and use them to complete the robustness self-testing analysis in the prepare-and-measure scenario.The method is robust to small but inevitable experimental errors.     

The vibrational structure of bromocyanoacetylene cation in the X̃2π and Ã2π electronic states studied by emission and laser exci

The vibrational frequencies of bromocyanoacetylene cation in its ground and first excited electronic states have been obtained by recording and analysing the emission and laser excitation spectra of the òπ-X̃²π transition. In the emission experiments the ions are produced rotationally cooled to ca. 10 K by means of a supersonic free jet and in the laser excitation measurements to ca. 100 K by Penning ionisation followed by collisional relaxation. The resulting narrowing of the vibronic bands in the spectra is such that the vibrational frequencies of most of the fundamentals could be inferred to within ± 2 cm⁻¹.     

Calculation of molecular constants for the X 1Σ g + , A 1Σ u + , B 1Πu, and a 3Σ u + electronic states of 39K2

The molecular constants are calculated for the X ¹Σ _g ⁺ , A ¹Σ _u ⁺ , B ¹Π_u, and a ³Σ _u ⁺ and electronic states of a potassium dimer. The wave functions and vibrational energies necessary for calculating the molecular constants are determined by solving the radial wave equation with the use of potential energy curves constructed by the semiempirical method. The vibrational terms, the rotational constants, and the centrifugal distortion constants calculated from the potential curves are compared with those determined from the experimental data.     

Enhancement of stimulated Raman scattering of acetone and the generation of three-color laser by using fluorescence dye RB

The enhancement of stimulated Raman scattering (SRS) of acetone (C3H6O) and the generation of three color lasers in lasing dye rhodamine B (RB) were reported. The first-order Stokes wave (629.9 nm) of SRS of C3H6O was amplified by 2.83 times than that of pure C3H6O. At the same time, a dye laser of RB at the wavelength from 575 to 598 nm can be generated in a suitable concentration of RB between 3×10-5 and 2×10-4 mol/L. Thus the green pump laser, yellow dve laser, and red Stokes wave concurred.     

Formation of N2 C3Πu and B3Πg by dissociative recombination of Ar 2 + in Ar+N2 early afterglow

The hf pulse excited Ar + N₂ mixtures and early afterglow are investigated at total pressures from 266 to 1995 Pa using nitrogen of 0·05–0·5% concentration. The time-resolved intensity of Ar I atomic lines and N₂ (2nd pos., 1st pos. and 1st neg.) band systems exhibit an intense early afterglow (0·3 ms). Both the decay of electron densityn _e and that of molecular Ar ₂ ⁺ ions and enhancement of coefficient of dissociative recombination due to electron temperature decrease after the pulse lead to the formation of characteristic secondary maximum of Ar I spectral line and N₂ molecular band intensities in the momentt _m after cut-off the pulse. The values oft _m(B³_g)>t _m(C³_u)>t _m(Ar I) decrease with increasing total pressure and increase with growing concentration of N₂ in Ar. In the afterglow period the Ar ₂ ⁺ dissociatively recombine in 5p and 4p Ar states. As a result of radiative transitions the metastable Ar (³P_2,0) atoms are formed which consequently due to collisions with N₂ molecules create electronically excited N₂. With increasing nitrogen concentration this effect becomes less pronounced and at concentration of N₂ greater than 0·5% it is negligible.     

Near-resonant electronic energy transfer induced by first- and second-order long-range potentials between the two states A1Σu+ and X1Σg+ of Li2 and Na2

Collision-induced rotational transitions between different electronic states are treated theoretically in the Born approximation for a second-order long-range interaction potential. It is shown that the experimentally observed cross sections for resonant channels in the A → X transfer of Li₂ are reproduced by this simple calculation taking the two terms' first-order dipole-dipole and second-order interaction potentials into consideration.     

Calculation of spectroscopic constants and radiative parameters for the B 1Π-X 1Σ+ electronic transitions of NaK,NaRb, and NaCs molecules

The vibrational, rotational, and centrifugal spectroscopic constants and the radiative parameters (the Einstein coefficients, oscillator strengths, Frank-Condon factors, r _v′v″ centroids, and wavenumbers of rotational lines) of electronic-vibrational-rotational transitions in the systems of bands B ¹Π -X ¹Σ⁺ of NaK (0 ≤ v′ ? 14, 0 ≤ v″ ≤ 52, j = 0, 30, 50, 70, 80, and 100), NaRb (0 ≤ v′ ≤ 12, 0 ≤ v″ ≤ 51, j = 0, 20, 30, 50, 70, 90, 100, and 120), and NaCs (0 ≤ v′ ≤ 10, 0 ≤ v″ ≤ 44, j = 0, 30, 50, 70, 90, 100, and 120) molecules, as well as the radiative lifetimes of excited electronic states, are calculated. Calculations are performed based on semiempirical potential curves constructed in this work. The calculated spectroscopic constants and the radiative lifetimes are compared with experimental values.     

Microstructure and properties of plastic deformed martensite induced by laser shock processing

Firstly, 45# steel was quenched by the NEL-2500A rapidly axial flow CO2 laser. The experimental parameters were the laser power of 750 W, the laser beam diameter of 4 mm, the scanning velocity of 7 mm/s. The thickness of coating layer was 0.1 mm and the width was 8 mm. Secondly, the martensite induced by laser quench was shocked by Nd:YAG laser. The parameters of laser shock processing were the wavelength of 1.06 μm, the pulse duration of 23 ns, and the output energy of 16-20 J. The laser was focused on a spot of φ7 mm. K9 optical glass was used as confinement. The sample was coated with black paint 86-1 (the thickness is about 0.025 mm). By testing and analysis of samples which were treated by laser quench and laser quench+shock with transmission electron microscope (TEM), it was discovered that the surface layer of martensite was deformed plastically by laser shock processing. In the secondary hardened zones, there were a lot of slender secondary twin crystal martensites, dislocation tangles, and cel     

High-resolution infrared Fourier transform spectroscopy of SO in the X3Σ− and a1Δ electronic states

The v = 1 ← 0 vibration-rotation absorption bands of ³²S¹⁶O, ³⁴S¹⁶O, and ³²S¹⁸O in the ground electronic state, X³Σ⁻, and the v = 1 ← 0 vibration-rotation band of ³²S¹⁶O in the first excited electronic state, a¹Δ, were measured at 0.004 cm⁻¹ unapodized resolution with a high-resolution Fourier transform spectrometer coupled to a long path absorption cell. The v = 2 ← 0 vibration-rotation band of ³²S¹⁶O in the X³Σ⁻ state was also observed. Line positions for P- and R-branch transitions up to N = 44 for ³²S¹⁶O have been measured and analyzed yielding improved molecular parameters. The present measurements are compared with previous infrared and microwave measurements.