Target-ion source unit ionization efficiency measurement by a method of stable ion beam implantation

At the IRIS facility a rather precise method of the target-ion source unit ionization efficiency measurement has been developed. The method exploits an off-line mass-separator for the implantation of the ion beams of selected stable isotopes into a tantalum foil placed inside a Faraday cup in the focal plane of the mass-separator. After the implantation of the required amount of the investigated species, tantalum foil has been inserted into the volume of the target-ion source unit prepared for the on-line utilization at the IRIS on-line separator. The first tests have ensured the ionization efficiency values (90±10)% for Rb and (85±10)% for Cs in the empty combined target-ion source unit, which was used as a reference one. For the target-ion source unit with UC target material inside the measured value of the ionization efficiency of Rb was (52±20)%.     

Application of the laser ion source for isotope shift and hyperfine structure investigation

The study of nuclei far from stability requires high sensitivity of the experimental technique. The method of Resonance Ionization Spectroscopy in a Laser Ion Source (RIS/LIS) allows one to carry out measurements of the isotope shifts and hyperfine splittings for isotopes at the production rate about 10² atoms per second. The sensitivity of this method is determined by the high efficiency of the laser ion source and the low background of the detection system afforded by characteristic α particle registration. The isotope shifts and hyperfine structures of ¹⁵⁵Yb, ¹⁵⁴Tm (I=9 and I=2) and ¹⁵³Tm (I=11/2) have been measured and the isotopic changes in mean square charge radii and nuclear electromagnetic moments have been determined. The further development of this experimental method – enhanced Target Ion Source system aimed to suppress thermionic background – enables direct detection of the photoions and widens the range of the applicability of the RIS/LIS method. This revised version was published online in August 2006 with corrections to the Cover Date.     

Isotope shift and hyperfine structure of the highly excited atomic uranium

The laser induced fluorescence method using atomic beam combined with Doppler-free two-photon absorption technique was applied for the measurement of isotope shifts and hyperfine structures of atomic uranium including ²³⁴U, ²³⁵U, ²³⁶U and ²³⁸U isotopes. The isotope shifts between ²³⁸U-²³⁴U, ²³⁸U-²³⁵U, ²³⁸U-²³⁶U, and the hyperfine structure of ²³⁵U were obtained in the high lying odd levels around 4 eV. Received 3 December 2001 / Received in final form 4 July 2002 Published online 29 October 2002 RID="a" ID="a"e-mail: oba@analchem.tokai.jaeri.go.jp     

Isotope shift and hyperfine structure of43Ca by laser spectroscopy

The isotope shift⁴⁰Ca-⁴³Ca in the 4s ^{2 1} S ₀-4s4p ³ P ₁ intercombination line as well as the hyperfine structure splitting of the 4s4p ³ P ₁ state of⁴³Ca have been remeasured by saturation spectroscopy with a tunable stabilizedcw dye laser and an atomic beam of natural Ca as absorber. The nuclear charge radius of⁴³Ca obtained here reconciles our result with the radius obtained from measurements in muonic Ca-atoms and in the Ca resonance line. It reconfirms the fact that the charge radius of⁴³Ca is considerably smaller than the ones of both neighbouring even isotopes. The discrepancy of our previous measurement for this charge radius was due to a wrong assignment of so far unobserved absorption lines of probably molecular origin occuring in the neighbourhood of the atomic resonances under study.     

Isotope shifts and hyperfine structure in the transitions of gadolinium

High-resolution resonance ionization mass spectrometry has been used to measure isotope shifts and hyperfine structure in all (J = 2-6) and the transitions of gadolinium (Gd I). Gadolinium atoms in an atomic beam were excited with a tunable single-frequency laser in the wavelength range of 422-429 nm. Resonant excitation was followed by photoionization with the 363.8 nm line of an argon ion laser and resulting ions were mass separated and detected with a quadrupole mass spectrometer. Isotope shifts for all stable gadolinium isotopes in these transitions have been measured for the first time. Additionally, the hyperfine structure constants of the upper states have been derived for the isotopes ^{155, 157} Gd and are compared with previous work. Using prior experimental values for the mean nuclear charge radii, derived from the combination of muonic atoms and electron scattering data, field shift and specific mass shift coefficients for the investigated transitions have been determined and nuclear charge parameters for the minor isotopes ^{152, 154} Gd have been calculated. Received 18 November 1999     

Isotope shifts and hyperfine structure in the transitions in calcium II

The isotope shift and hyperfine structure in the three - transitions in Ca II have been studied by fast ion beam collinear laser spectroscopy for all stable Ca isotopes. The metastable 3d states were populated within the surface ionization source of a mass separator with a probability of about 0.1%. After resonant excitation to the 4p levels with diode laser light around 850 nm the uv photons from the transitions to the ground state were used for detection. Hyperfine structure parameters A and B for the odd isotope ⁴³Ca, as evaluated from the splittings observed, agree well with theoretical predictions from relativistic many-body perturbation theory. Field shift constants and specific mass shift constants were extracted from the measured isotope shifts and are discussed in comparison with expectation values from theory. Received: 19 September 1997 / Revised: 5 December 1997 / Accepted: 27 January 1998     

Isotope shift and hyperfine structure measurements at the242f Am fission isomer

Istope shift and hyperfine structure measurements have been performed for the^242fAm fission isomer with target production rates of only a few per second. The method is based on resonance ionization spectroscopy (RIS) in a buffer gas cell with radioactive decay detection of the ionization process (RADRIS). A relative isotope shift ratioX _exp=IS^242f,241/ IS^243,241=41.7±0.9 has been measured for the 500.02 nm transition corresponding to a nuclear parameter ^242f,241=5.4±0.3 fm². The analysis of the quadrupole moment based on the deformed Fermi-model of the nuclear charge distribution including second order corrections results inQ ₂₀=38.2 ±1.4( _–0.8 ^+0.4 )_model eb. The measurement of the hyperfine structure splitting of the transition at 466.28 nm yields a negativeg-factor and a nuclear spin ofI=2 orI=3.Work supported by the Bundesministerium für Bildung und Forschung under contract 06 MZ 5661.     

Integrated target-ion source unit for on-line production of radioactive short-lived isotopes

A new version of integrated target-ion source unit (ionising target) has been developed for the on-line production of radioactive single-charged ions. The target is able to withstand temperatures up to 2500 ^°C and acts also as an ion source of the surface and laser ionisation. Off-line and on-line experiments with the ionising target, housing tantalum foils as a target material, have been carried out at the IRIS (Investigation of Radioactive Isotopes on Synchrocyclotron) facility. The off-line surface ionisation efficiency measured for stable atoms of Li, Rb and Cs was correspondingly 6% , 40% and 55% at the target temperature of 2000 ^°C and 3-10% for atoms of rare-earth elements Sm, Eu, Tm and Yb at a temperature of 2200 ^°C. The off-line measured values of the ionisation efficiency for stable Gd and Eu atoms by the laser beam ionisation inside the target were 1% and 7%, respectively. The radioactive beam intensities of neutron-deficient rare-earth nuclides from Eu to Lu produced by the integrated target-ion source unit have been measured at a temperature of 2500 ^°C. The results of the integrated target-ion source unit use for on-line laser resonance ionisation spectroscopy study of neutron-deficient Gd isotopes have been also presented.     

EUV and fast ion emission from cryogenic liquid jet target laser-generated plasma

A liquid jet of either nitrogen or argon of 20 μm diameter was exposed to intense laser fields with pulse durations between 70 fs and 250 ps, leading to intensities of 10¹⁶ W cm^-2 and 10¹³ W cm^-2, respectively. The emission of extreme UV light and soft X-rays shows the characteristic lines of hydrogen-like nitrogen and carbon-like argon. For nitrogen the emitted photon flux at 250 ps was about two orders of magnitude higher than for 70 fs pulses. A weak dependence on the laser polarization with respect to the liquid jet axis was found. The kinetic energy of the emitted ions easily exceeded 100 keV for nitrogen and 200 keV for argon for a pulse duration close to 2 ps. Received: 21 August 2000 / Revised version: 20 December 2000 / Published online: 22 March 2001     

Properties of isolated DNA bases, base pairs and nucleosides examined by laser spectroscopy

The vibronic spectra of laser desorbed and jet cooled guanine (G) adenine (A), and cytosine (C) consist of bands from four, two and two major tautomers respectively, as revealed by UV-UV and IR-UV double resonance spectroscopy. The vibronic spectrum of adenine around 277 nm consists of weak nπ^* and strong ππ^* transitions, based on IR-UV and deuteration experiments. Precise ionization potentials of G and A were determined with 2-color, 2-photon ionization. We also measured vibronic and IR spectra of several base pairs. GC exhibits a HNH ^... OH/NH ^... N/C=O ^... HNH bonding similar to the Watson-Crick GC base pair but with C as enol tautomer. One GG isomer exhibits non-symmetric hydrogen bonding with HNH ^... N/NH ^... N/C=O ^... HNH interactions. A second observed GG isomer has a symmetrical hydrogen bond arrangement with C=O ^... NH/NH ^... O=C bonding. Two CC isomers were observed with symmetrical C=O ^... NH/NH ^... O=C bonding and nonsymmetrical C=O ^... HNH/NH ^... N interaction, respectively. Guanosine (Gs), 2-DeoxyGs und 3-DeoxyGs each exhibit only one isomer in the investigated wavelength range around 290 nm with a strong intramolecular sugar(5-OH) ^... enolguanine(3-N) hydrogen bond. Received 16 June 2002 / Received in final form 15 July 2002 Published online 13 September 2002     

Thermal lensing measurements and thermal conductivity of Yb:YAB

By using holographic shear interferometry, we have measured the thermal lens in a diode-pumped Yb:YAB crystal, under lasing and non-lasing conditions, as a function of absorbed power. From these purely optical measurements we estimate the fractional thermal loading and the thermal conductivity of Yb:YAB. Knowledge of these thermal parameters is essential for the optimisation of Yb:YAB laser cavity designs. Received: 5 February 2002 / Final version: 22 November 2002 / Published online: 26 February 2003 RID="*" ID="*"Corresponding author. Fax +61-2/9850-8915, E-mail: Judith@ics.mq.edu.au     

Slope efficiency of up to 73% for Yb:Ca4YO(BO3)3 crystal laser pumped by a laser diode

Yb:Ca₄YO(BO₃)₃ (Yb:YCOB) crystal with good quality and large size has been grown by the Czochralski method. The polarization absorption and fluorescence spectra have been measured. The laser action of the Yb:YCOB crystal has been demonstrated when it is pumped by a fiber-coupled laser diode (LD) at the wavelength of 976.4 nm. The pumping threshold is 55 mW, the light-light conversion efficiency is 58.7%, and a slope efficiency of up to 73% is thus calculated. Received: 16 December 1998 / Revised version: 4 February 1999 / Published online: 7 April 1999     

Laser operation and Raman self-frequency conversion in Yb:KYW microchip laser

We present a diode-pumped Yb:KYW microchip laser. The passive Q-switchedand CW regimes of operation for the Yb:KYW microchip laser have been investigated. An efficiency for CW operation of up to 10% with regard to incident pump has been obtained. Raman self-frequency conversion in the Q-switched regime has been observed. Received: 27 May 2002 / Revised version: 4 July 2002 / Published online: 15 November 2002 RID="*" ID="*"Corresponding author. Fax: +375-17/2840-879, E-mail: asg@dragon.bas-net.by     

Temperature and excitation wavelength dependencies of 3-pentanone absorption and fluorescence for PLIF applications

The temperature and excitation wavelength dependencies of 3-pentanone absorption and fluorescence were studied in support of planar laser-induced fluorescence (PLIF) imaging of temperature and mixture fraction in flows of practical interest. The temperature dependencies (300–875 K) of absorption and fluorescence were measured for gaseous 3-pentanoneat atmospheric pressure in a nitrogen bath gas using 248, 266, and 308 nm excitation. The results indicate that the fluorescence signal per unit mole fraction using 248 nm excitation is highly temperature-sensitive below 600 K, while the signal from 308 nm excitation is not temperature sensitive below 500 K. For quantitative measurements over a broad range of temperatures, one must choose excitation schemes carefully to balance the trade-off between measurement sensitivity and the amount of signal at the expected conditions. As an example of such a choice and to show the capabilities of ketone PLIF techniques, we include temperature and mixture fraction images of a 300–650 K heated air jet using near-simultaneous 308 and 266 nm excitation. Received: 29 May 2002 / Revised version: 5 November 2002 / Published online: 26 February 2003 RID="*" ID="*"Corresponding author. Fax: +1-650/723-1748, E-mail: jkoch@stanford.edu RID="**" ID="**"E-mail: hanson@me.stanford.edu     

Frequency measurement, isotope shift and hyperfine structure of the transition in atomic silver

The frequency of the centroid of the transition in Ag I has been determined by laser spectroscopy of a collimated metastable thermal atomic beam. We find MHz. The isotope shift MHz. For the magnetic hyperfine structure constant of the state, assuming IJ coupling, we find, MHz and MHz. Received 16 July 1999 and Received in final form 7 October 1999     

A high-sensitivity in situ optical diagnostic technique for laser cleaning of transparent substrates

A differential optical transmission technique has been used to monitor in situ the efficiency of laser cleaning for the removal of sub-micrometer-sized particles on substrates transparent at the monitoring wavelength. This technique has been applied to the removal of sub-micrometer polystyrene particles on polyimide substrates using laser pulses of 30 ps duration at 292 nm while probing the material transmission at 633 nm. The sensitivity achieved -1/10⁴ for the transmission changes induced upon single-pulse laser exposure – allows us to monitor the removal of just a few sub-micron-sized particles from the probed region inside the irradiated area. Received: 2 October 2002 / Accepted: 7 October 2002 / Published online: 29 January 2003 RID="*" ID="*"Corresponding author. Fax: +33-3/87844082, E-mail: nchaoui@iut.univ-metz.fr RID="**" ID="**"Present address: Laboratoire de Chimie et Applications, Institut Universitaire de Technologie de Metz, Département Chimie, Rue Victor Demange, 57500 Saint-Avold, France     

Droplet velocity and acceleration measurements in dense sprays by laser flow tagging

The feasibility of liquid-phase velocity measurements in dense sprays by 2D laser-based flow tagging is demonstrated. Velocity measurements in dense sprays are difficult with conventional techniques because of the high number densities of droplets, the optical thickness of the medium, and multiple light-scattering effects. The present flow-tagging technique is based on phosphorescent tracer molecules, which are excited by a grid of pulsed ‘write’ laser beams. The motion of the tagged droplet groups can be observed by a CCD camera in this way. In addition, multiple consecutive velocity measurements are performed by ‘droplet-group tracking’. This yields the acceleration along the trajectory of individual groups of droplets in unsteady sprays. Received: 5 June 2000 / Revised version: 28 July 2000 / Published online: 6 September 2000     

Observation of Doppler sidebands of a laser-cooled Ca+ ion by using a low-temperature-operated laser diode

1/2 -D_5/2 electric-quadrupole-allowed transitions of a laser-cooled Ca⁺ ion in a small rf trap. The electron shelving method was used to measure the absorption spectrum of the electric-quadrupole-allowed transitions, and the motional sidebands due to the secular motion of the ion in the harmonic potential well of the rf trap were completely resolved. The effective temperature of the ion, estimated by comparing the observed sideband intensities with the theoretical ones, was less than 4.4 mK. This result is in good agreement with that obtained from the analysis of the linewidth measurement. Received: 18 March 1998     

Production of biologically inert Teflon thin layers on the surface of allergenic metal objects by pulsed laser deposition technology

Allergic-type diseases are current nowadays, and they are frequently caused by certain metals. We demonstrated that the metal objects can be covered by Teflon protective thin layers using a pulsed laser deposition procedure. An ArF excimer laser beam was focused onto the surface of pressed PTFE powder pellets; the applied fluences were 7.5–7.7 J/cm². Teflon films were deposited on fourteen-carat gold, silver and titanium plates. The number of ablating pulses was 10000. Post-annealing of the films was carried out in atmospheric air at oven temperatures between 320 and 500 °C. The thickness of the thin layers was around 5 μm. The prepared films were granular without heat treatment or after annealing at a temperature below 340 °C. At 360 °C a crystalline, contiguous, smooth, very compact and pinhole-free thin layer was produced; a melted and re-solidified morphology was observed above 420 °C. The adhesion strength between the Teflon films and the metal substrates was determined. This could exceed 1–4 MPa depending on the treatment temperature. It was proved that the prepared Teflon layers can be suitable for prevention of contact between the human body and allergen metals and so for avoidance of metal allergy. Received: 12 June 2002 / Accepted: 13 June 2002 / Published online: 4 November 2002 RID="*" ID="*"Corresponding author. E-mail: bhopp@physx.u-szeged.hu