Determination of the saturation parameter of electronic transition in a uranium-neon hollow-cathode discharge by optogalvanic spectroscopy

Summary The optogalvanic signal (OGS) induced in a uranium-neon hollow-cathode discharge was measured as a function of the laser power density for the 0→16900 cm⁻¹ (591.5 nm) uranium transition. Theoretical relations derived by solving a two-level system rate equations showed the OGS dependence on the laser photon flux, for a modulated c.w. light and for stimulated transitions starting from the ground state. A fitting of the theoretical relations to the experimental measurements allowed the determination of the σ₀ τ product, that is, the saturation parameter of the transition. The results showed good agreement between the σ₀ τ values obtained by the optogalvanic and the usual optical absorption processes.     

Two-color photoionization spectroscopy of uranium in a U–Ne hollow cathode discharge tube

A U–Ne hollow cathode discharge tube is used as a source of uranium atomic vapors as well as a photoelectron/photoion detector for carrying out two-color three-photon photoionization spectroscopy of uranium. Using the uranium excitation transition 0 cm⁻¹ (⁵L ₆ ⁰ ) → 16 900.38 cm⁻¹ (⁷M₇) at 591.5-nm laser wavelength as a first step transition and scanning the wavelength of a second laser from 558 to 568 nm, high-lying odd-parity atomic levels of uranium are studied in the energy region 34 500–34 813 cm⁻¹. All the expected 21 odd-parity atomic levels identified by various researchers in this region are observed in a single spectrum, demonstrating the high sensitivity achieved therein. In addition to this, we have identified eight autoionization resonances of uranium starting from its odd-parity atomic level at 33 801.06 cm⁻¹ pumped by two-photon excitation. Four out of these eight autoionization resonances are observed for the first time.     

Simple regge pole model for the reactionπ − p →η’n

The most recently measured differential cross-section data forπ ⁻ p → η’n has been fitted by using a simple Regge pole model with phenomenological residue functions. It has also been observed that this inelastic process has the scaling property.     

Infrared laser emission in two-photon pumped sodium vapour

We report infrared laser emission in the region of 3 to 5 μm from sodium vapour optically pumped by a pulsed dye laser with wavelengths ranging from 585 to 610nm. Twophoton excitation processes are believed to be responsible for the primary excitation. Both molecular transitions (4 to 5 μm) between high lying states, and atomic transitions (5² S _1/2−4² P _3/2,1/2 at 3.41 μm) have been identified.     

Optical absorption in early stage low temperature laser produced plasma

We describe a new technique to measure the UV/visible absorption spectrum of the ablated material during the laser pulse. The technique utilizes the continuum emission from one laser produced plasma as a light source to measure the absorption properties of a second laser produced plasma which is formed on a semi-transparent target with an array of 40 μm holes. A 6 ns, 1064 nm laser was used to ablate a Ag target and the plasma absorption was measured in the range 450–625 nm for a laser fluence of 1 J cm⁻². The total absorption cross-section is (0.5–1.5)×10⁻¹⁷ cm² in the range 450–540 nm. By comparing the measured absorption with a calculation using the plasma spectroscopy code FLYCHK it can be concluded that, in the wavelength region examined here, the absorption is mainly due to bound-bound transitions.     

Excited state absorption and stimulated emission of Nd3+ in crystals. Part 2: YVO4, GdVO4, and Sr5(PO4)3F

3+ ion in the crystals YVO₄, GdVO₄, and Sr₅(PO₄)₃F. The measurements were performed in the spectral region of the main laser transitions ⁴F_3/2→⁴I_9/2, ⁴F_3/2→⁴I_11/2, and ⁴F_3/2→⁴I_13/2by a continuous wave pump and probe technique. The calibrated gain and ESA spectra are presented and possible implications of ESA on the laser performance are estimated. It is shown that ESA can be a small loss factor to the laser emission near 1060 nm but does considerably diminish the effective emission cross sections near 1340 nm especially in Nd:YVO₄ and Nd:GdVO₄. Received: 29 January 1998/Revised version: 8 May 1998     

Laser optogalvanic spectroscopy of argon in the wavelength region 605–740 nm

Two-photon optogalvanic transitions in Ar glow discharge with Nd: YAG laser pumped dye laser excitation in the frequency range 13520–16520 cm⁻¹ has been studied using linear and circular polarization. The intensities of two-photon optogalvanic transitions are very sensitive to changes in the incident laser power which is not the case with one-photon transitions. Intensity ratio for circular and linear polarized light for two photon transitions 6s′[1/2]°1←4s[3/2]°2, 6s′[1/2]°0←4s[3/2]°2, and 5d[1/2]°0←4s[3/2]°2, 5d[1/2]°1←4s[3/2]°2 are quite different from the other two-photon transitions. This has been explained as due to near one photon resonance of 4p′[3/2]1 level for the first pair and 4p′[1/2]1 for the second pair of transitions. The ratio of optogalvanic intensity for circular to linear polarized light has been theoretically estimated and compared with the observed results.     

Measuring photoionization cross-sections of excited atomic states

A new method of photoionization cross-section measurement based on the observation of saturation in the ion yield as a function of radiation intensity has been proposed. The photoionization cross-sections for the 6²P_1/2 and 6²P_3/2 levels of Rb atoms of the fundamental and second harmonics of ruby laser radiation are measured, with a tunable pulsed dye laser used for excitation. The following values of cross-sections are obtained: (1.7±0.4)·10⁻¹⁷ cm² and (1.5±0.4)·10⁻¹⁷ cm² for the levels 6²P_3/2 and 6²P_1/2, respectively, ionized by radiation of v₂=14403 cm⁻¹, and (1.9±0.5)·10⁻¹⁷ cm² for the 6²P_3/2 level ionized by v₂=28806 cm⁻¹ radiation.     

Negative parity states in144Nd and multipolarity of gamma-transitions from 1− to 2+ states by beta-gamma-gamma angular correlation method

Some of the low-lying states in many isotopes¹⁴⁴Nd,¹⁴⁸Sm,¹⁵²Gd and¹⁵⁶Gd show a similar typical behaviour. The first 2⁺ is regarded as a single quadrupole phonon state and 3⁻ as a single octupole phonon state. The levels with the spins and parities 1⁻, 5⁻, 3⁻, 4⁻, etc. are considered due to the simultaneous excitation of quadrupole and octupole phonons. If this consideration is correct, then the transition fromJ ⁻ to 2⁺ states must contain an appreciableE3 content. Theβ-γ-γ angular correlation coefficients for the cascade ofβ-rays ofE _max 800 keV→γ-rays of 1489 keV→γ-rays of 696 keV are used to estimateE3 content inE1 transition in¹⁴⁴Nd.     

Wavelength modulation and cavity enhanced absorption spectroscopy using ～1.9?μm radiation produced by difference frequency generation with a MgO doped PPLN crystal

We have demonstrated the production of ∼1.9 μm near-infrared radiation by using difference frequency generation within a 5% MgO doped PPLN crystal by coupling ∼735 nm radiation from a tunable external cavity diode laser with relatively high powered 532 nm radiation from both Nd:YVO₃ and Nd:YAG lasers. The radiation produced is of low power, ∼15 μW, and was used in conjunction with the sensitivity enhancing techniques of wavelength modulation spectroscopy (WMS) and cavity enhanced absorption spectroscopy (CEAS). Experiments were carried out on rotationally resolved transitions in the combination bands of NH₃ and CO₂ in the 1.9 μm region. An α _min value of 3.6×10⁻⁶ cm⁻¹ Hz^−1/2 was achieved for WMS measurements on CO₂. A comparable α _min value of 2.2×10⁻⁶ cm⁻¹ Hz^−1/2 was achieved for NH₃ using CEAS. The low NIR power indicates that despite the level of MgO doping quoted for the crystal, under prolonged exposure photorefractive damage has occurred.     

Sensitivity and mass selectivity of NO detection by stepwise photoionization

State selective stepwise laser photoionization of nitric oxide molecules has been investigated using mass spectroscopic detection with a quadrupole filter. The ionization was carried out in two steps, the first being excitation with a tunable dye laser in the (A ²∑⁺,v′=0.1 state at wavelength around 226 nm and 215 nm, and the second being excitation beyond the ionization limit with a fixed frequency laser at 266 nm, i.e. the fourth harmonic of a Nd:YAG laser. The sensitivity of NO detection and the mass resolution of this method has been studied. The ion signal of NO⁺ was observed with linear pressure dependence at partial densities of NO down to 1×10⁵ cm⁻³. This corresponds to a density per state of about 2.5×10⁴ cm⁻³. The mass selectivity was investigated at the various isotopic components of natural nitric oxide¹⁴N¹⁶O,¹⁵N¹⁶O,¹⁴N¹⁸O and the isobare¹⁴N¹⁷O.     

650-nm laser emission under upconversion pumping at 1.064 μm in Tm<Superscript>+3</Superscript>: ZBLAN fiber laser

We report for the first time continuous wave (CW) red laser emission in Tm⁺³-doped ZBLAN fiber laser, operated at 650 nm (¹ G ₄ → ³ F ₄ transition of Tm⁺³). The excitation uses a three step upconversion scheme. The pump source is a Nd:YAG laser operated at 1.064 μm. A laser output power of CW 80 mW was obtained for 1.42 W of launched pump power. The slope efficiency with respect to launched pump power was measured to be 7.7%. The temporal behavior of the emitted laser is also addressed.     

Five Simultaneously Q-Switch Mode-Locked Passive Laser Modulators

Five types of passive Q-switched as well as simultaneously Q-switch mode-locked modulators: plastic dye sheets (Kodak 9850 cellulose acetate dye sheets), lithium fluoride crystals containing F₂ ⁻ color centers (LiF:F₂ ⁻), chromium-doped yttrium–aluminum–garnet crystals (Cr⁴⁺:YAG), ionic color filter glass (Schott RG1000 color filter glass), and the single crystal semiconductor wafers (GaAs, Fe-doped InP, Zn-doped InP, S-doped InP, etc.) used for modulation of the Nd:hosted(Nd:YAG, Nd:YVO₄, and Nd:LSB) lasers were investigated in detail in our research. We also investigated applications of the Q-switch mode-locked pulse train for the development of a higher resolution solid-state laser range finder.     

Nd: YAG laser annealing of gallium-implanted silicon

A Q-switched Nd: YAG laser with a pulse duration of 20 ns was used to investigate effects of laser annealing in gallium implanted silicon. Rutherford backscattering and Hall-effect measurements were performed to evaluate the annealed layer. Differential Hall-effect measurements were carried out to obtain carrier concentration profiles after annealing. It was found that a maximum sheet carrier concentration of 8×10¹⁵ cm⁻² can be obtained for a gallium implantation of 10¹⁶ cm⁻² by laser annealing with an energy density of more than 1.0 J cm⁻². Although the peak carrier concentration was found to be 8.0×10²⁰ cm⁻³, the annealed layer showed polycrystalline structures even after annealing with an energy density up to 4J cm⁻². The annealing took place in the solid phase in this energy density range.     

Narrow resonances of two-photon absorption of super-narrow pulses in a gas

First cw laser oscillation with thresholds below 1 mW was observed for various B¹П_u → X¹ ∑ _g ⁺ transitions of diatomic molecular sodium excited by different argon laser lines in the range of 454–488 nm. For pump powers of 0.5 W output powers up to 3 mW and single-pass gain up to 0.1 cm⁻¹ were obtained. Some properties of the heat pipe laser system are discussed.     

Luminescence detection of multiphoton ionization-fragmentation of the molecular CrO 4 2− anions adsorbed on the surface of dispersed SiO2

It is shown that luminescence detection of multiphoton ionization-fragmentation of the molecular CrO ₄ ²⁻ anions adsorbed on the surface of dispersed SiO₂ is possible under excitation with the fundamental frequency of a Nd:YAG pulsed laser (λ=1.064 μm). The structure and the process of formation of the adsorbed complexes under thermal activation of the surface and the nature of luminescence transitions in CrO ₄ ²⁻ anions are studied in detail. It is shown that luminescence is excited as a result of the recombination of photoelectrons and ionized chromate ions. Multiphoton ionization of the ions occurs under three-photon resonance conditions. The resonance level is an antibonding state of the adsorption complex formed with the participation of an oxygen vacancy on the SiO₂ surface. The dynamics of the multiphoton luminescence excitation process includes autoionization (stimulated by intercomplex electronic excitation) in superexcited states, fragmentation of chromate anions, and annealing of surface oxygen vacancies. The rate equations for three-photon-resonance multiphoton ionization are studied. The cross sections for two-and one-photon transitions on the nonresonance steps of multiphoton absorption are obtained. It is concluded that the nonlinear polarizability of the donor-acceptor adsorption bond in “chromate anion-oxygen vacancy” complexes is very important. Zh. éksp. Teor. Fiz. 111, 1748–1774 (May 1997)     

Electron-impact excitation cross-sections for the3 S 0−,3 P 0−, and3 D 0-States of a ruthenium atom

The excitation cross-sections of transitions of a ruthenium atom from the³ S ⁰−,³ P ⁰−, and³ D ⁰-levels are measured by the method of extended crossed beams. Based on the results of measurements, the excitation cross-sections of the states are calculated (ignoring cascade contribution). Moscow Power Engineering Institute, 14, Krasnokazarmennaya St., Moscow, E-250, 111250, Russia. Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 65, No. 1, pp. 9–13, January–February, 1998.     

Generation of coherent tunable deep UV radiation for detection and absorption studies of explosives RDX and TNT

We report a technique for the efficient generation of tunable coherent deep UV radiation and its application in studies of RDX and TNT at the ppm level on the basis of their absorption characteristics. The obtained experimental absorption data are compared with conventional spectrophotometric data. The UV radiation in the range 200–260 nm has been generated by the type-I noncollinear third harmonic of the dye laser radiation (600–700 nm) and also by sum frequency mixing (SFM) of Nd:YAG output (1064 nm) with the second harmonic of the dye laser in β-barium borate (BBO) crystal. The maximum conversion efficiency of the generated signal is estimated to be 57.5% at λ = 218.9 nm wavelength. Apart from measurements of the absorbance of RDX and TNT at different concentrations in their respective solutions, the minimum detection concentrations have also been ascertained. The estimated minimum detectable concentration of RDX is 8.47·10⁻⁹ M, whereas that for TNT is 35.7·10⁻⁹ M. The data were obtained using only ∼100 μJ/pulse of laser energy. Published in Zhurnal Prikladnoi Spektroskopii, Vol. 74, No. 6, pp. 516–521, July–August, 2007.     

Intermolecular energy transfer in mixed laser dyes: photophysical properties of triplet states

Triplet-singlet energy transfer in laser dyes have been studied in EPA at 77K using N₂ laser as an excitation source. Phosphorescence of the donor (D) and the delayed fluorescence of the acceptor (A) and their lifetimes have been measured for coumarin 102 (D)-rhodamine B(A) and 9(10H)-acridone (D)-rhodamine 6G(A) dye systems as a function of acceptor concentration. These data yield energy transfer rate constants of ∼10³ dm³ mol⁻¹ s⁻¹ for the donor acceptor combinations, consistent with the Forster mechanism. The phosphorescence quantum efficiency and other spectral parameters are also reported.     

Time-and-energy resolved measurement of the cascaded Auger decay in krypton

The cascaded Auger decay following ionization or excitation with 94 eV soft-X-ray pulses from the 3d subshell in krypton has been energy-and-time-resolved for the first time. The decay time of the 4s ⁻¹4p ⁻² nl → 4p ⁻³ + e and/or 4s ⁻¹4p ⁻¹ nl → 4p ⁻² + e transition is measured to be 74 ± 20 fs. Furthermore, our data shows that the electrons with a kinetic energy around 25 eV (generally assigned as 3d ⁻¹ np → 4s ⁻² n′p + e) emitted after core excitation are emitted in a second decay step suggesting an alternative assignment of the form 4s ⁻² np 4p ⁻² + e.