Electron spin resonance in X-irradiated sodium sulphate

Reliable results are reported for the various triple-dipole dispersion energy coefficients needed to evaluate the (exact) triple-dipole dispersion energy for all three-body interactions involving He, Ne, Ar, Kr, Xe, H₂, N₂, CO, O₂ and NO, and at least one molecule. A total of 645 unique coefficients, corresponding to 185 unique interactions, are considered.     

Electronic and geometric structure of doped rare-gas clusters: surface, site and size effects studied with luminescence spectroscopy

The electronic and geometric structure of rare gas clusters doped with rare-gas atoms Rg = Xe, Kr or Ar is investigated with fluorescence excitation spectroscopy in the VUV spectral range. Several absorption bands are observed in the region of the first electronic excitations of the impurity atoms, which are related to the lowest spin-orbit split atomic ³P₁ and ¹P₁ states. Due to influence of surrounding atoms of the cluster, the atomic lines are shifted to the blue and broadened (“electronical cage effect”). From the known interaction potentials and the measured spectral shifts the coordination of the impurity atom in Ar_N, Kr_N, Ne_N and He_N could be studied in great detail. In the interior of Kr_N and Ar_N the Xe atoms are located in substitutional sites with 12 nearest neighbours and internuclear distances comparable to that of the host matrix. In Ne_N and He_N the cluster atoms (18 and 22, respectively) arrange themselves around the Xe impurity with a bondlength comparable to that of the heteronuclear dimer. The results confirm that He clusters are liquid while Ne clusters are solid for N≥ 300. Smaller Ne clusters exhibit a liquid like behaviour. When doping is strong, small Rg_m-clusters (Rg = Xe, Kr, Ar, m≤10 ²) are formed in the interior sites of the host cluster made of Ne or He. Specific electronically excited states, assigned to interface excitons are observed. Their absorption bands appear and shift towards lower energy when the cluster size m increases, according to the Frenkel exciton model. The characteristic bulk excitons appear in the spectra, only when the cluster radius exceeds the penetration depth of the interface exciton, which can be considerably larger than that in free Rg_m clusters. This effect is sensitive to electron affinities of the guest and the host cluster.     

Pressure-broadened iodine-laser-amplifier kinetics and a comparison of diluent effectiveness

An iodine laser kinetic model is used to investigate inversion parameters in highly pressure-broadened amplifier systems using i-C₃F₇I as the parent compound and CO₂, N₂, He, Ne, Ar, Kr, and Xe as the diluent gas. These data are used to calculate a diluent merit function for diluent pressures P_d = 1–100 atm. The most effective choices for buffer gases are as follows: P_d ? 1 atm, CO₂; 1 atm ? P_d ? 10 atm, Ar; and P_d ? 10 atm, Ne.     

Nonresonant third order hyperpolarizability of rare gases and N2 determined by third harmonic generation

The third order hyperpolarizabikity γ⁽³⁾₁₁₁₁(-ω₃;ω₁,ω₁,ω₁) of the rare gases He, Ne, Ar, Kr, Xe and of N₂ are determined by third harmonic generation involving picosecond light pulses of a Nd-glass laser. The results are compared with reported experimental and theoretical values.     

Charged clusters in liquid helium

The appropriateness of the experimental study of charged clusters in liquid helium has been supported. The interaction potential of negative ions (electron bubbles) with inert clusters formed by Ne, Ar, Kr, and Xe atoms or H₂ and N₂ molecules has been found. Small clusters levitate at a distance of 13–16 Å above the negative ion. The scalings laws for the properties of charged inert clusters have been discovered and grounded; the number of quantum levels and states of such clusters has been determined. The mobility measurement of charged clusters may provide a new technique of probing the properties of impurity nanoparticles in helium.     

Velocity dependence of total Penning ionization cross sections

The velocity dependence of the total Penning ionization cross sections,σ(v), is measured in the thermal relative velocity region, using a time of flight method.σ(v) curves are reported for the collision systems He(2¹ S)/Ar, Kr, Xe, N₂, Hg, He(2³ S)/Ar, Kr, Xe, N₂, Hg, Ne(³ P _{2, 0})/Kr, Hg, and Ar(³ P _{2, 0})/Hg. In a qualitative discussion it is shown that all features of the measuredσ(v) curves may be explained within the frame of the theory of Penning ionization, allowing to extract information on the physical quantities governing the process: on the interaction potentialV(R) and on the transition probabilityW(R). A theoretical calculation for the He(2³ S)/Ar system shows good agreement with our experimentalσ(v) curve. On the basis of the present results earlier data onσ(v), and on absolute cross sections and rate constants obtained at certain relative velocity distributions are discussed.     

Calculation of the pressure shift of the positronium hyperfine interval

We calculate the fractional positronium hyperfine pressure shift Δ(T) using a quantum mechanical thermal averaging and obtain for Δ(293 K)(±30%) in He, Ne, Ar, Kr, Xe, N₂ and SF₆ respectively; (-0.15, -0.34, -0.96, -1.41, -1.85, -1.12, -1.1) × 10^-7/torr (0°C).     

Is the critical Reynolds number universal?

This paper is devoted to checking whether the critical Reynolds number is universal in identical conditions for the flow of different fluids. The laminar-turbulent transition in a circular pipe flow has been tested experimentally. The flows of inert gases (He, Ne, Ar, Kr, Xe), molecular gases (N₂, CO, CO₂, SF₆), and two similar liquids (H₂O, D₂O) have been tested. A considerable, up to 40%, difference in critical Reynolds numbers was observed. The possible reasons for nonuniversality of the critical Reynolds number are discussed.     

Model of pulsed electric discharge expansion in dense gas, taking into account electron and radiative thermal conductivities. IV. Limiting brightness of discharge radiation

Based on the relation between the radiation brightness B _R of the pulsed high-current electric discharge in dense gas (Xe, Kr, Ar, Ne, He, N₂, and air at atmospheric pressure and above) and its temperature, the dependence of the limiting brightness B _LIM of discharge channel radiation on ionization potentials of atoms of mentioned gases was obtained, and the condition under which the brightness saturation is achieved was determined. It was shown that this dependence is in agreement with experimental data of various researchers.     

Na 32P-32D line broadening by Ne,Ar, and Xe

The normalized emission intensity in the wings of the optically thin Na 3²P-3²D lines broadened by Ne, Ar, and Xe has been measured in emission from a high-pressure discharge. A blended satellite occurs about 80 cm^-1 into the Na-Xe red wing and a progression of increasing red wing intensity from Ne to Ar to Xe is observed. Xe densities of 2.5 and 9.1 × 10¹⁹ cm^-3 were used, and the pressure dependence of the NaXe line shape indicates that multiple perturber interactions are important in the far wing at the higher noble gas densities.     

Infrared diode laser spectroscopy of the Kr–N2O van der Waals complex: the v 1 symmetric stretch region of N2O

The rovibrational spectra of four isotopomers of the Kr–N₂O van der Waals complex, namely ⁸²Kr–N₂O, ⁸³Kr–N₂O, ⁸⁴Kr–N₂O and ⁸⁶Kr–N₂O, were measured in the v ₁ vibrational band region of the N₂O monomer (～1285?cm^?1) using a tunable diode laser spectrometer to probe a pulsed supersonic slit jet. Rotational constants for both ground and excited vibrational states of these four isotopomers were accurately determined. The band-origin of Kr–N₂O was observed to shift by +0.1065?cm^?1 from that of the monomer. The band-origin shifts of Rg–N₂O (Rg?=?Ne, Ar, Kr) in the v ₁ vibrational band region could also be well explained by the model based on a Buckingham intermolecular potential [W.A. Herrebout, H.-B. Qian, H. Yamaguchi and B.J. Howard, J. Mol. Spectrosc. 189, 235 (1998)]. But the band-origin shift of He–N₂O was found to deviate significantly from this model. The possible reason is discussed and the band-origin shift of Xe–N₂O predicted.     

Spectral anomalies of the light-induced drift of rubidium atoms caused by the velocity dependence of transport collision frequencies

The spectral features of the light-induced drift (LID) velocity for rubidium atoms (⁸⁵Rb and ⁸⁷Rb) in an argon buffer medium and in binary buffer mixtures of noble gases (Ne + Ar, Ne + Kr, Ne + Xe, He + Ar, He + Kr, and He + Xe) have been investigated theoretically. A strong temperature dependence of the spectral shape of the LID signal for Rb atoms in an Ar atmosphere is predicted in the temperature range 450 K < T < 800 K. It is shown that the anomalous LID of Rb atoms in binary buffer mixtures of noble gases can be observed at almost any temperature (including the room one) depending on the fractions of neon or helium in these mixtures. The results obtained enable a highly accurate testing of the interatomic interaction potentials used to calculate the drift velocity for anomalous LID in LID experiments.     

Leading relativistic correction to the interaction coefficients between atoms and molecules using Borel integral II

Lower and upper bounds to the leading relativistic correction to the interaction coefficients between H, He, Ne, Kr, and Xe atoms, and H₂ and N₂ molecules have been evaluated by using Borel integral for the dynamic dipole polarizability. Our results for these bounds are in agreement with others.     

Effect of gas mixing on Xe ion currents from an ECR ion source

Gas mixing technique has been used in order to increase the current of highly charged ions of Xe at the TIFR-ECRIA. The He, N₂, O₂, Ne, and Ar are used as support gases, and their effect on output currents of Xe ions is studied. The effective ion charge and the total loss rate of ions are calculated from the measured currents. It is found that molecular gases, such as N₂ and O₂, exhibit better mixing effect in the enhancement of output of highly charged Xe ions. Furthermore, we describe this 14.5-GHz ECR ion source mounted on a high voltage (400 kV) deck, with its four beamlines, as well as the control system for the remote operation.     

Coincidence studies with polarisation analysis of the photon emission induced inK-inert gas collisions

The linear and circular polarisations of theK(4² P→4² S) transition detected in delayed coincidence with the inelastically scattered potassium atom are presented forK- He, Ne, Ar, Kr and Xe. For all systems the Stokes vector measurements have been performed as a function of the potassium scattering angle at a beam energy of 10³ eV. The coherence properties of the excitation process are studied with the help of the measured degree of polarisation. For He, Ne and Xe the excitation amplitudes (e.g. the parametersλ andχ) are deduced from the measured Stokes vector. For Ar and Kr the collisionally excited state is not a pure state, and it is concluded that both single excitation of theK atom and simultaneous excitation of both collision partners contribute toK(4² P) excitation. The results are compared with the predictions of the semiclassical treatment of the excitation process.     

The empirical Kestin model and the second order transport properties of binary mixtures of Ne,Ar, Kr and Xe

It is showed from the experimental α_T data for the dilute binary mixtures of Ne, Ar, Kr and Xe at 340 K that the law of corresponding states proposed by Kestin, Ro and Wakeham is able to predict the mentioned second order kinetic property altogether with the first order transport and thermodynamic properties of the examined mixtures.     

Totale Streuquerschnitte für den Stoß von H2, D2 und He an den Edelgasen Ne,Ar, Kr und Xe im thermischen Energiebereich

The velocity dependence of the total elastic cross section has been measured for the scattering of H₂, D₂, and He beams by Ne, Ar, Kr, and Xe gases. Velocity-selected beams were attenuated by gas in a scattering chamber. A universal detector, with a magnetic mass separator, was used in conjunction with lock-in techniques. The results are compared with quantum mechanical calculations using a Lennard-Jones-(12.6)-potential, and employing suitable averaging over experimental velocity distributions. Potential parameters are presented. These are in good agreement with those expected from other methods of measurement.     

UV photoemission from physisorbed atoms and molecules: Electronic binding energies of valence levels in mono- and multilayers

Angle-resolved UV photoemission spectra were measured for Ar, Kr, Xe, CO, O₂ and N₂ adsorbed on a Ni(110) surface at 20 K. The different gases were adsorbed also on the Ni(110) surface which had been precovered by mono- and multilayers of the same gases. Upon physisorbing one of these species onto the bare and precovered Ni surface, binding energy shifts up to 3 eV were found. These shifts will be explained by work function changes of the substrate onto which the gas is physisorbed. It will be shown that for the investigated gases the binding energy referred to the vacuum level is an atomic or molecular property which is independent of the substrate, to a first approximation. By physisorption of a known gas the work function of any substrate can be evaluated by UPS. The density of valence states for bulk Ar, Kr and Xe will be discussed. There is evidence that the conduction band can be seen in the secondary electron background of the UP spectra.     

Resonance Raman and fluorescence spectra of chlorine dioxide in argon,krypton, xenon,and nitrogen matrices at 16 K

Laser excitation studies of matrix-isolated ClO₂ at 16 K using the 4579, 4765, 4880, and 5145 Å argon ion lines and argon, krypton, xenon, and nitrogen matrices were conducted. Quenching of fluorescence by the matrix was evidenced by the observation of displaced bands in the Ar, Kr, and N₂ work and increased background in the Xe studies. An intense progression in ν₁ of ClO₂ with regularly decreasing intensities out to 6ν₁ observed in solid Ar with 4579 Å excitation was attributed to the resonance Raman effect. Shorter resonance Raman progressions were observed in Xe and N₂ matrices.     

Spectroscopic diagnostics of barrier-discharge plasma in mixtures of cadmium diiodide vapor with gases

The spectral characteristics of the emission of atmospheric-pressure gas-discharge plasma in mixtures of cadmium diiodide vapor with gases (Ne, Ar, Kr, Xe, and N₂) were investigated along with the time characteristics of the voltage and current. The gas-discharge plasma was produced and excited by a barrier discharge at a repetition rate of sine voltage pulses of up to 140 kHz. The discharge emission was analyzed in the spectral range 200–900 nm with a high resolution (0.05 nm). Radiation from exciplex CdI(B-X) molecules and excimer I₂* molecules was revealed, as well as the atomic lines of cadmium, iodine, and inert gases. In a mixture with xenon, radiation from exciplex molecules XeI(B-X, B-A) was also found. This radiation prevailed in the spectra at mixture temperatures up to 150°C. The further increase of the temperature leads to the prevalence of the CdI(B-X) radiation. It was found that the most intense CdI(B-X) radiation is observed in mixtures CdI₂/Xe(N₂)/Ne. Regularities in the spectral characteristics of the emission of the gas-discharge plasma are discussed.