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     

Hyperfine structure and isotope shift of highly excited barium-I states

High-resolution laser-spectroscopy measurements of hyperfine structure and isotope shifts were performed for the 6snd ¹ D ₂ sequence of Ba-I in the regionn=12–24. Stepwise laser excitations of a collimated atomic beam were used. A strong influence on the hyperfine structure is observed at the perturbation atn=14, caused by interaction with the 5d7d configuration. Whereas the isotope shift for the even isotopes stays essentially constant with increasingn, the odd isotopes exhibit a strong change, indicating hyperfine-induced shifts.     

Measurement of isotope shifts,fine and hyperfine structure splittings of the lithium D lines

The lithium D lines were studied using a diode laser that was frequency modulated by an electro-optic modulator, to excite an atomic beam. The transmission of part of the laser beam through an etalon was monitored to correct for the nonlinearity of the laser scan. The results for the ^6,7Li 2 S _1/2 and 2 P _1/2 hyperfine splittings agree very well with the best existing data while those for the D1 isotope shift and ^6,7Li fine structure splittings disagree significantly from data obtained by a previous laser atomic beam experiment. Our result for the D1 isotope shift is very close to the latest value computed using Hylleraas variational theory. Received 8 April 2002 / Received in final form 26 June 2002 Published online 21 January 2003 RID="a" ID="a"e-mail: wvw@yorku.ca     

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     

Laser spectroscopy and mass measurements on alkali isotopes

Isotope shifts, spins, hyperfine structures and masses have been measured for the series of the alkali isotopes including the nuclei far from stability. The method of laser spectroscopy and its combinations with rf excitation are described. Some results are discussed, namely the first observation of the red doublet D₁-D₂ of francium, and the study of shell effects and changes of shape with mass and δ〈r ²〉 measurements for Rb and Na isotopes.     

High-resolution LIF measurements on hyperfine structure and isotope shifts in various states of Lu I using the second and third harmonic of a cw Ti:sapphire laser

With the second and third harmonic of a tunable single-mode cw Ti:S laser, generated inside external enhancement cavities, high-resolution LIF measurements on several states of Lu I in various parts of the electromagnetic spectrum are performed. From these measurements, hyperfine structure A and B constants for both ¹⁷⁵Lu and ¹⁷⁶Lu as well as isotope shifts have been determined for all levels observed in the single-step excitation process. From the measured A constants, the magnetic hyperfine structure anomaly has been derived for various states. Received 14 January 2002 Published online 19 July 2002     

Coherent population trapping involving Rydberg states in xenon probed by ionization suppression

We report the observation of pronounced coherent population trapping and dark resonances in Rydberg states of xenon. A weak two-photon coupling with radiation of = 250 nm is induced between the 5p^{6 1} S ₀ ground state of xenon and state 5p ⁵6p[1/2]₀, leading to (2+1) resonantly enhanced three-photon ionization. The state 5p ⁵6p[1/2]₀ is strongly coupled by radiation with ≃ 600 nm to 5p ⁵ ns[J _C]₁ or 5p ⁵ nd[J _C]₁ Rydberg states with principal quantum numbers n in the range 18 ?n? 23 and with the rotational quantum number of the ionic core J _C = 1/2 or J _C = 3/2. The ionization is monitored through observation of the photoelectrons with an energy resolution ΔE = 150 meV which is sufficient to distinguish the ionization processes into the two ionization continua. Pronounced and robust dark resonances are observed in the ionization rate whenever is tuned to resonance with one of the ns- or nd-Rydberg states. The dark resonances are due to efficient population trapping in the atomic ground state 5p^{6 1} S ₀ through the suppression of excitation of the intermediate state 5p ⁵6p[1/2]₀. The resolution is sufficient to resolve the hyperfine structure of the ns-Rydberg levels for odd xenon isotopes. The hyperfine splitting does not vary significantly with n in the given range. Results from model calculations taking the natural isotope abundance into account are in good agreement with the observed spectral structures. Pronounced dark resonances are also observed when the dressing radiation field with is generated from a laser with poor coherence properties. The maximum reduction of the ionization signal clearly exceeds 50%, a value which is expected to be the maximum, when the dip is caused by saturation of the transition rate between the intermediate and the Rydberg state due to incoherent radiation. This work demonstrates the potential of dark resonance spectroscopy of high lying electronic states of rare gas atoms. Received 7 May 2000 and Received in final form 25 June 2001     

New laser setup at the IRIS facility. Magnetic moments and mean squared charge radii of neutron deficient Tl isotopes

A new laser installation for the resonance ionization spectroscopy in a laser ion source and for rare isotope production has been put into operation at the IRIS mass-separator, working on-line with the 1 GeV proton beam of the Petersburg Nuclear Physics Institute synchrocyclotron. Isotope shift and hyperfine splitting of 276.9 nm atomic transition in the long chain of Tl isotopes and isomers have been measured. New data on the magnetic moments and changes in mean squared charge radius for ^{183,184,185,185m,186m2,195m,197m}Tl have been obtained.     

Measurement of hyperfine structure and isotope shifts in the 580.56nm line of 142－145,146,148,150Nd+

Isotope shifts and hyperfine spectrum of singly ionized neodymium ion was measured by collinear fast-ion-beam laser spectroscopy. The hyperfine A constants and B constants are obtained for the (23230)9/2^0 level and 4f^45d ^6K9/2 level, respectively. The optical isotope shifts between seven isotopes in the 580.56 nm of^142-145,146,148,150Nd^ line are determined. The configuration admixtures for (23230)9/2^0 level were quantitatively analysed to be 4f^46p, 4f^35d^2, and 4f^35d6p with mixing coefficients of 67%, 5%, and 28%, respectively.     

Isotope shift measurements and charge radii of152–158Yb

Isotope shifts have been measured for the neutron deficient even Yb isotopes up to the neutron shell closure at N=82. The isotope shifts were measured using the 556-nm atomic resonance transition from the¹ S ₀ ground state to the³ P ₁ level. The heavier isotopes of Yb have been investigated by Buchinger et al./1/. The change in (r ²) observed for Yb isotopes with N=82–90 has considerably different behavior than for the lighter rare earths.     

Hyperfine structure and isotope shift measurements on 4d10 1S0 → 4d9 5p J=1 transitions in Pd I using deep-UV cw laser spectroscopy

The 4 d ^{10 1} S₀ ground-state transitions to the 4 d ⁹ 5 p configuration of palladium (Pd) have been studied. For this purpose, a tunable, single-mode, deep-UV cw laser has been built to generate the sum frequency of a frequency-doubled Ti:S laser with a second Ti:S laser. The produced wavelengths range from 244 to 276 nm. From the measured spectra the frequency splitting due to hyperfine structure and isotope shift, the hyperfine structure A and B constants and the lifetimes of the states have been extracted. Received 3 October 2001     

Electronic and nuclear properties from the analysis of the isotope shifts in the spectral lines of lead

Isotope shifts in the 623.7 nm line of Pb I have been measured. Then, in a spectral range of nm the optical isotope shifts in 24 lines of neutral and singly ionized lead have been analyzed using a combined model-independent method. From the combination of the optical isotope shifts data with elastic electron scattering, muonic X-ray and electronic K_α X-ray data, we were able to determine the two contributions to the total isotope shift, namely the mass and the field shifts, and to obtain the values of several nuclear factors for a long chain of lead isotopes.     

Isotope shift studies in the first spectrum of dysprosium: confirmation of assignments to and new assignments to configuration

Isotope shifts (-) are reported for 221 spectral lines of the neutral dysprosium atom (Dy I) in the region 470-565 nm using a photoelectric recording Fabry-Perot spectrometer and highly enriched isotopic samples of and excited in liquid-nitrogen-cooled hollow-cathode lamps. Isotope shift data for 173 of these lines are being reported for the first time. Using the isotope shift data, term isotope shifts (-) have been evaluated for 99 even- and 68 odd-parity energy levels of Dy I. New values have been obtained for 24 odd and 36 even levels. These new values have enabled us to check some of the existing tentative assignments and also to suggest configuration assignments to a few unassigned energy levels. The earlier tentative assignments of 4 f10 5 d 6 p configuration to many high odd levels lying above have been presently confirmed. We could assign the 4f^95d6s6p configuration to 24 unassigned even levels. Received: 3 August 1998     

Inner-shell excited quartet states in Li-like O<Superscript>5+</Superscript> and Ne<Superscript>7+</Superscript> ions

First laser spectroscopic measurements of the 6s5d³D₁-6s6p¹P₁ and 6s5d³D₂-6s6p¹P₁ transitions in several isotopes of atomic barium have been performed. The hyperfine structure of these transitions was optically resolved and isotope shifts for even and odd isotopes were determined. The isotope shifts show a deviation from their expected behavior for odd isotopes in an analysis based on King-plots. This observation puts atomic structure calculations at test because available theories do not predict this. A profound understanding of the wavefunctions for heavy alkaline earth systems like barium (Ba) and radium (Ra) is essential for a theoretical evaluation of their sensitivity to fundamental symmetry breaking effects such as they could be observed, e.g., through permanent electric dipole moments. Further the absolute frequency of the 6s^{2 1}S₀-6s6p³P₁ intercombination line in ¹³⁸Ba was determined to be 12 636.6232(1) cm^-1.     

Hyperfine splitting and isotope shift in the atomic D2 line of 22,23Na and the quadrupole moment of 22Na

The hyperfine structure of the D₂ optical line in ²²Na and ²³Na has been investigated using high resolution laser spectroscopy of a well-collimated atomic beam. The hyperfine splitting constants A and B for the excited 3p ²P_3/2 level for both investigated sodium isotopes have been obtained. They are as follows: A(22) = 7.31(4) MHz, B(22) = 4.71(28) MHz, A(23) = 18.572(24) MHz, B(23) = 2.723(55) MHz. With this data, using the high precision MCHF calculations for the electric field gradient at the nucleus, the electric quadrupole moment of ²²Na has been deduced: Q_s(22) =+0.185(11) b. The sign of Q_s(22), determined for the first time, indicates a prolate nuclear deformation. A precise value of the isotope shift ^22,23Na in the D₂ line has also been obtained. Received: 26 February 1998 / Revised version: 25 June 1998     

Magnetic moments for lithium quartet S states

The fully correlated calculations of the Zeeman g_J factors for the first three quartet S states of lithium are presented, including relativistic and radiative corrections of orders α², α² m/M, and α³. The isotope shifts in g_J are predicted precisely for various isotopes of lithium. Received 4 December 2000 and Received in final form 26 September 2001     

On the Yrast levels of106–108Sn

The isotope shift in the Ca-intercombination line withλ=6,573 Å was measured for all isotopes between⁴⁰Ca and⁴⁸Ca with the only exception of 47Ca. The combination of the results with muonic x-ray data yields highly accurate values for the changes of the mean square nuclear charge radii. In addition, the nuclear quadrupole moments of the three isotopes⁴¹Ca,⁴³Ca and⁴⁵Ca have been determined from the hyperfine structure splitting of the 4s 4p ³ P ₁ state.     

Evolution from quasielastic to deep-inelastic transfer in the system132Xe+natFe§

The pronounced isotope shift of⁸⁷Sr versus⁸⁷Sr observed recently in 5sns¹S₀ Rydberg states reflects the singlet-triplet mixing solely caused by magnetic hyperfine interaction. Using semiempirical estimates for the hyperfine coupling constant a_{5 s} and the singlet-triplet splitting ΔE_ST (n) excellent agreement between experimental and calculated values is obtained.     

Isotope shifts and hyperfine structure of the 6s-7p transitions in the cesium isotopes 133, 135, and 137

The 6s-7p transitions in cesium at 459.3 nm (7² P _1/2) and 455.5 nm (7² P _3/2) have been investigated by saturation spectroscopy in vapor cells, using a laser spectrometer with 500 kHz bandwidth in the blue spectral range. Isotope shifts as well as hyperfine splittings were determined for the isotopes 133, 135 and 137.