Photoionization cross-section measurements from the 2p, 3d and 3s excited states of lithium

The photoionization cross-sections from the 2p²P_{1/2, 3/2}, 3d²D_{3/2, 5/2} and 3s²S_1/2 excited states of lithium have been measured at different ionizing laser wavelengths, above the first ionization threshold. The experiments are performed by using a thermionic diode working in the space charge limited mode and the cross-sections are measured by employing the saturation technique. By changing the ionization photon energy, a smooth frequency dependence of the cross-sections has been observed for the 2p and 3d states. The cross-section from the 3s excited state has been measured at a single photon energy. The measured values of the photoionization cross are compared with the available data.     

Partial cross sections for Rb− photodetachment in the region of the Rb(5p 2 P 1/2 3/2) thresholds and their analysis by multichannel quantum defect theory

A crossed ion-laser beam apparatus has been used to measure accurate relative total and partial cross sections for photodetachment from Rb^? ions with high photon energy resolution (0.1–0.6 cm^?1) in the region of the Rb(5p ² P _1/2,3/2) thresholds (photon energy range 16,350–16,820 cm^?1). Satisfactory fits to these data by multichannel quantum defect theory (MQDT) have been obtained, resulting in a reliable set of seven MQDT parameters. The electron angular distribution parameter for the Rb(5_s) channel was found to beβ(5s)=2, independent of photon energy. MQDT predicts a sharp, window-type variation of?(5s) around the minimum of the 5s-cross section below the Rb(5p ² P _1/2) threshold (where an accurate experimental measurement ofβ(5s) was not possible) and a similar behaviour ofβ(6s) in the case of Cs^?photodetachment below the Cs(6p ² P _1/2) threshold.     

甲醛的态选择性多光子电离研究

我们在XeCl准分子激光多光子电离甲醛分子的研究中,获得了甲醛经过2+1和2+2光子共振激发过程而产生的母体离子和高能离解通道的离子CO⁺。在电子轰击和单光子电离中占优势的低能阈离解通道离子HCO⁺,由于态选择性激发的结果而未出现。 关键词：     

Optically pumped high-pressure DF-CO2 transfer laser

Pulsed sealed off CO₂ laser operation at 19 atm gas pressure has been demonstrated by pumping DF/CO₂/He mixtures with radiation from a pulsed DF laser. DF acts as an absorber for the pumping radiation, and the CO₂ upper laser level is populated via subsequent energy transfer. CO₂ pulse energy at 19 atm was 0.5 mJ corresponding to a photon conversion efficiency of 4% measured relative to the number of absorbed pumping photons.     

The temperature dependence of penning ionization electron energy spectra: He(23S)—ar,N2, NO,O2, N2O,CO2

Using two intense thermal energy He(2³S) sources of different temperatures (≈400 and ≈ 1000 K, resp.) and a transmission-calibrated electron energy analyzer with about 30meV resolution, the dependence of He(2³S) Penning ionization electron spectra on collision energy for the target species Ar, N₂, NO, O₂, N₂O and CO₂ have been studied. The energy shifts of the Penning electron energy distributions and the branching ratios for the population of different electronic states in the molecular ions are determined quantitatively and compared for the two different collision temperatures. These results and the shapes of the observed Penning electron energy distributions are discussed in the light of current models for the Penning procen; the observed temperature dependences are correlated with the nature of the ionized orbitals in cases of only one entrance channel (closed shell targets) and, in addition, to the existence of qualitatively different entrance channels (open shell targets).     

Photodesorption from powdered zinc oxide

Mass spectrometric measurements of photodesorption from powdered ZnO under controlled radiation are reported. Neutral carbon dioxide and atomic oxygen prevail as the desorbing species. From photodesorption rate decay curves we obtain cross sections for photodesorption of ~ 2 × 10^?17 cm² for O and ~4 × 10^?19 cm² for CO₂. Both species desorb only when the incoming photon energy exceeds the ZnO band gap energy (3.2 eV). The desorption rate is linear with incoming photon flux. All the data seem to support a substrate dependent process of photodesorption by neutralization of chemisorbed species by photogenerated holes. The temperature dependence of the photodesorption rate for CO₂ yields a value of 0.26 eV for the apparent binding energy of the physisorbed CO₂ molecule.     

Characterization of a Br(2P1/2)–CO2(1001-1000) transfer laser driven by photolysis of iodine monobromide

2 laser operating on the 10⁰1-10⁰0 transition at λ=4.3 μm and pumped by E –V energy transfer from Br(²P_1/2) has been demonstrated. The dynamics and performance of this device were characterized by observing the time-resolved stimulated emission and the steady-state spontaneous side fluorescence after photolysis of IBr or Br₂ by a frequency-doubled Nd:YAG laser or Ar⁺ laser, respectively. Although the E –V excitation kinetics are favorable, rapid vibrational relaxation limits laser action to CO₂ pressures of less than 1 Torr. Numerical modeling of laser pulse shapes and the dependence on IBr and CO₂ pressure and photolysis energy establish a relatively high gain of 0.33%/cm, a CO₂-pressure-dependent optical loss of 0.04–0.06%/cm, and an efficiency of 2×10^-5 4.3-μm-laser photons per incident photolysis photon. The CO₂ fluorescence after photolysis of a fixed Br₂/CO₂ gas mixture decreases as a function of photolysis time by about 30%/h, indicating the photolytic production of an important quencher. Received: 23 June 1997/Revised version: 23 September 1997     

Pulsed optoacoustic detection of multiple photon excitation in molecules

Multiple photon excitation, saturation, and linear absorption of SF₆-argon mixtures when irradiated by a high power CO₂ TEA laser is investigated using a pulsed optoacoustic technique. At low intensities the expected linear dependence of the absorption on laser intensity is observed. At intermediate intensities the absorption exhibits a square root dependence on the incident laser intensity, a dependence which is typical for saturation of an inhomogeneously broadened absorption. At even higher intensities, the absorption shows an intensity dependence typical of multiple photon excitation. The laser intensity was varied between 0.016 kW/cm² and 5 MW/cm², values lower than that needed to produce multiple photon dissociation of SF₆. Increasing the collision frequency of the absorbing molecules with an inert buffer gas is observed to quench the multiple photon excitation.     

Chemisorption,photodesorption and conductivity measurements on ZnO surfaces

Experimental results of a mass-spectro metric analysis of photodesorption from ZnO single crystals at different temperatures are reported. They provide direct evidence that CO₂ is the only photodesorbed species from both the single crystal and powder samples studied. The CO₂ photodesorption occurs only when the incident photon energy exceeds the ZnO band gap energy. Excellent agreement between the illumination time dependence of the CO₂ photodesorption and surface conductivity data in both single crystals and powder samples strongly suggests a substrate dependent mechanism in which photodesorption occurs by the neutralization of chemisorbed CO₂^? “ion-molecules” by photogenerated holes. In addition, measurements of the chemisorption kinetics of oxygen on ZnO single crystal and powder surfaces are reported. The results are compared with CO₂ and CO chemisorptiun experiments to show that, of these gases, only oxygen chemisorbs from the gas phase. Auger analysis of oxygen saturated and photodesorbed surfaces of ZnO show a significant relation between the carbon content and the photo-desorptive and conductive activities of those surfaces. These observations indicate that impurity carbon atoms on ZnO surfaces can be oxidized by electron capture to produce chemisorbed CO₂^? “ion-molecules’ which will then readily photodesorb by bandgap radiation. This proposed process is discussed together with further supporting evidence.     

Reflection measurements in CO2 laser solid deuterium target interaction

Using a 60 nsec, 300 MW CO₂ TEA laser reflection measurements from solid deuterium targets have been investigated. Energy, reflected and scattered pulse shape are recorded at various angles: 0°, 45°, 90°, 135°. Reflection, X-ray measurements and ion mean kinetic energy are correlated at the focussing lens position with respect to the target position. The maximum plasma temperature varies from 20 to 35 eV for incident laser fluxes ranging from 5 × 10¹⁰ up to 5 × 10¹¹ W/cm². The cut-off density inside the deuterium ice has been observed and located. In each case reflection has been found to be weak less than 5% for each direction. For the maximum fluxes X-ray energies greater than 0.5 keV have been observed.     

New intraband magneto-optical studies on n-InSb

A highly sensitive photoconductive technique has been used to provide the first direct evidence of emission of five optical phonons during the energy relaxation process of the photoexcited electrons induced by a CO₂ laser in n-InSb. The CO₂ laser-induced magnetophotoconductivity exhibits a number of very sharp resonances whose positions depend strongly upon photon energy. All observed transitions can be described with one single set of band parameters.     

Fundamental and combination bands of CO2–C2H2 and CO2–C2D2 in the mid-infrared region

Spectra of the weakly bound CO₂–C₂H₂ and CO₂–C₂D₂ complexes are observed in the regions of CO₂ ν₃ (≈ 2349 cm^?1) and C₂D₂ ν₃ (≈ 2440 cm^?1) fundamental vibrations, using an infrared optical parametric oscillator to probe a pulsed supersonic slit-jet expansion. Five bands are measured and analysed: the fundamental asymmetric stretch of the C₂D₂ component, two combination bands involving the out-of-plane torsional vibrations (C₂D₂ ν₃ + torsion and CO₂ ν₃ + torsion) for CO₂–C₂D₂, and two combination bands involving an intermolecular in-plane bending vibration for CO₂–C₂H₂ and CO₂–C₂D₂. The resulting intermolecular frequencies are 61.408(1), 54.5(5), 39.9(5), and 39.961(1) cm^?1 for CO₂–C₂H₂ and CO₂–C₂D₂ in-plane vibrations, and CO₂–C₂D₂ out-of-plane torsional vibrations in CO₂ and C₂D₂ regions, respectively. This is the first experimental determination of these intermolecular vibrational frequencies.     

A photoelectron spectroscopic study of the adsorption of CO and CO2 on platinum

The adsorption of CO and CO₂ on platinum has been studied by UV photoelectron spectroscopy using both He I and He II radiation. The modulation of the intensity of the spectral features observed for adsorbed CO as the photon energy is changed is used to assign the observed levels. The results are in reasonable agreement with recent theoretical and experimental work. The levels are observed to shift by different amounts compared to gas phase CO because of chemical binding effects. The adsorption of CO₂ produces spectral features that are shifted by the same amount compared to gas phase CO₂. This, together with the absence of any localized attenuation of the platinum valence band and the low heat of adsorption, indicates that CO₂ is physisorbed on platinum.     

Fast particle emission from CO2 laser produced plasmas

Spatial distributions and spectra of non thermal particles emitted from CO₂ laser aluminum plasmas have been recorded. With laser fluxes greater than 10¹³ W/cm² ions with MeV maximum kinetic energy have been detected as well as fast electrons in the range of 50 to 500 keV. The results are discussed in terms of resonant absorption as a function of different parameters s such as laser flux and angle of incidence.     

Photoelectron asymmetry parameters and branching ratios for sulfur dioxide in the photon energy range 14–25 eV

Triply differential photoelectron spectroscopy has been performed in the photon energy range 14–25 eV for sulfur dioxide. The results are presented in the form of electronic branching ratios and asymmetry parameters, and are discussed briefly in the context of similar data for CO₂ and of the inner-shell spectra of SO₂.     

Optoacoustic detection of multiple photon molecular absorption in a strong IR field

A new method based on the optoacoustic effect has been proposed to measure multiple photon absorption at vibrational molecular transitions in a strong IR laser field. Comparison measurements of the average absorbed energy have been done by this method for molecules with different dissociation limits in a strong CO₂-laser field, the field intensity changed therewith by four orders. For the poly-atomic molecules C₂H₄ and SF₆ having a comparatively low dissociation limit, the absorption increases monotonously as the power density of laser radiation P increases up to the dissociation limit. For three-atom molecules, such as D₂O and OCS, absorption saturation takes place with P ? 10 MW/cm².     

Luminescence studies on gamma irradiated KCl: Ce crystals

This paper reports thermoluminescence(TL), optical absorption and TL emission studies that are made on Ce³⁺ doped KCl single crystals irradiated at room temperature. The glow curve and optical absorption studies indicate the participation of Ce³⁺ ions in the TL process. The TL study suggests the presence of low concentration of Ce³⁺ ions which reduces the TL efficiency with respect to pure KCl samples. On F bleaching γ irradiated crystals Z₁ centers are observed. A broader and strongly intense violet blue emission at 290, 370, 423 and 488 nm has been observed with 240 nm excitation. This emission has been attributed due to the transition from 5d(2D) excited energy level to the 4f¹ ground stable energy level (2F_5/2 and 3F_7/2) of Ce³⁺ doped KCl crystals.     

Effect of pressure on pressed pellets in XRS

In this study, the absorption experiments which are an application area in XRS are discussed. The effect on the absorption parameters of the pressure applied to make pellet powder samples was investigated. The mass attenuation coefficients ( μ _m ), mean free paths and half-value layers of samples prepared at different pressures were experimentally determined. C₆H₁₀O₅, VF₄, CaO and Y₂O₃ samples were pressed at 1.91, 3.82, 5.72 and 7.63 tons/cm². A variable energy x-ray source from Amersham (AMC.2084) was used in order to irradiate the samples at energies 13.39, 19.63, 24.90, 32.06, 36.39, 44.48, 51.70 and 59.54 keV. The photon intensities were measured by using an HPGe detector with a resolution of 182 eV at 5.9 keV. The theoretical radiation absorption parameters were calculated by WinXCOM program. The calculated values were compared with the experimental values. Good agreement has been observed within experimental uncertainties for low pellet pressure. The obtained results show that the radiation absorption parameters change with the amount of pressure applied to the sample.     

Differential elastic and quenching cross sections for Ar*(3P) and CO2(X1 ∑ g +)

The energy dependence of the differential scattering of metastable Ar*(³P) by ground-state CO₂(X¹ ∑ _g ⁺) has been studied at relative kinetic energies from 58 to 126 meV over an angular range of 5–160° c.m. using crossed molecular beams. The position and curvature of rainbow maxima, which are observed at each energy, are used to obtain parameters for a Lennard-Jones (12, 6) spherically symmetric potential. The position of the minimum, r _m = 5·02 ± 0·65 Å, is identical to that for K + CO₂ and the well depth, ε = 16·3 ± 0·8 meV, is about 10 per cent greater. The scattered intensity shows a distinct fall-off on the dark side of the rainbow compared to that expected for elastically scattered Ar*. This depletion, caused primarily by the quenching of Ar*, is analysed in terms of the optical-shadow model to determine the energy dependence of the observed quenching cross section, which is predicted to have a maximum of 67 Ų at 193 meV.     

Relative partial photoionization cross-section of methylacetylene to the X2E ion state over the photon energy range 11–26 eV

Relative partial cross-sections for photoionization to the X²E ground state of the methylacetylene ion over the photon energy range 11–26 e V have been determined using synchrotron radiation. The observed cross-sections show a broad resonance feature similar to the results for photoionization to the X²II_u ground state of the acetylene ion. An explanation involving autoionization from a π^* (e) excited state is proposed.