Relativistic J-dependence of the isotope shift in the 6s-6p doublet of Ba II

The collinear laser-ion beam technique has been used to measure the isotope shift and hyperfine structure in the 6s-6p doublet (4,934Å, 4,554Å) of Ba II for all seven stable isotopes. The influence of the excited² P _1/2 and² P _3/2 states on the field shift leads to a difference of 2.5(3)% in the electronicF factors. The specific mass shifts differ by {A′-A} 2.2(3) MHz which corresponds to about 12% of the normal mass shift.     

Laserspectroscopic studies of collective properties of neutron deficient Ba Nuclei

Isotope shifts and hyperfine structure of the BaI resonance-line (λ=553.6 nm) have been measured by dye laser induced resonance fluorescence on an atomic beam for^{135m, 129g, 129m, 126}Ba thus extending previous high resolution measurements of neutron deficient Ba nuclides (N<82). The experimental results, now available for 16Ba isotopes and isomers withA=140?126, are used to deduce differences of rms charge radii, magnetic dipole and electric quadrupole moments. While the groundstates display a pronounced odd-even staggering the h 11/2^? isomers^135mBa and^133mBa show a decreased staggering. Conspicuously the isomer shift of theg 7/2⁺ isomer^129m Ba proves to be negative. The nuclear structure information is discussed in the context of gammaspectroscopic studies of transitional nuclei with 50<N,Z<82 and on the basis of a quasi-particle-plus-triaxial rotor model. The isotope shift discrepancy observed is fairly well described by the droplet model.     

Isotope shift in the Ca I resonance line and changes in mean-square nuclear charge radii of the stable Ca isotopes

The isotope shift of all stable Ca isotopes was studied in the Ca I resonance line. Enriched isotopes were used in an atomic beam, passing through the center of a spherical Fabry-Perot interferometer. The measured isotope shifts were separated into mass shift and field shift by comparing the optical isotope shift with δ〈r ²〉 values derived from recent muonic x-ray measurements. The results are discussed together with known data on the isotope shift in the Ca I intercombination line and data from Hartree-Fock calculations. The following mean values are obtained for the change in nuclear charge distribution δ〈r ²〉 [fm²]∶ [40, 42] 0.23(3); [40, 43] 0.13(3); [40, 44] 0.28(4); [40, 46] 0.14(7); [40, 48] 0.00(2).     

Hyperfine structure and isotope shift of the neutron-rich barium isotopes139–146Ba and148Ba

The hyperfme structure and isotope shift in the 6s ² S _1/2?6p ²P_3/2 line of Ba II (455.4 nm) have been measured by collinear fast-beam laser spectroscopy for the neutron-rich isotopes^139–146Ba and¹⁴⁸Ba. Nuclear moments and mean square charge radii of these isotopes have been recalculated. The isotope shift of the isotope¹⁴⁸Ba (T_1/2=0.64 s) could be studied for the first time, yieldingδ〈r²〉^138,148=1.245(3) fm².     

Isotopieverschiebung der natürlichen geraden und ungeraden Sm- und Nd-Isotope

The isotope shift of the natural isotopes of Sm and Nd was investigated by a digital recording Fabry-Perot spectrometer using highly enriched samples. By the accuracy achieved in the measurements it was possible to verify earlier results indicating different relative isotope shifts for lines with positive and negative displacements, and to show that also lines with the same sign of the displacement may have different relative isotope shifts. It is shown that these non-constant relative isotope shifts can be explained for the even isotopes by the different contributions of the mass and volume effect to the isotope shifts in the different lines, but this explanation seems only to be partly valid for some distances between even and odd isotopes. The size of the mass effect is estimated and its influence especially on the results of the odd-even staggering is considered. The odd-even staggering is compared to earlier results for Hg. The estimation of the mass effect shows that the results forδ〈r ²〉 determined from the measured isotope shifts without correcting for the mass effect may be considerably wrong. Nevertheless it is possible by a suitable combination of the measured distances to calculate a quantity which only depends on nuclear properties and which therefore enables to check the known theories of the volume dependent isotope shift also without calculating the probability density of thes-electrons at the nucleus.     

Precision ground state Hfs-separation of137Ba

High resolution two-photon spectroscopy was applied to investigate isotope shifts of Ssns S₀ Rydberg states of natural strontium in the range 10 ≤ n ≤ 70. While the isotope shifts between the even isotopes 84, 86, and 88 showed no change, a dramatic increase of the shift with increasing principal quantum number was found for the odd isotope Sr-87.     

Isotope shift in Ni I and changes in mean-square nuclear charge radii of the stable Ni isotopes

The isotope shift in the Ni I spectrum was studied in 17 lines for all stable isotopes by means of a photoelectric recording Fabry-Perot spectrometer with digital data processing. The measured isotope shifts were separated into mass shift and field shift by comparing the optical isotope shift with model-independent δ〈r ²〉 values derived from a combined elastic electron scattering and muonic x-ray data analysis. The ratios of the observed field shifts in different types of transitions could be explained quantitatively by Hartree-Fock calculations. The relative changes in mean-square nuclear charge radii were found to be: [58, 60] 1.293(15); [60, 62]1; [62, 64] 0.641(16); [60, 61] 0.382(9). The absolute value δ〈r ²〉^60,62=0.170(35) fm² was derived using fine structure as well as hyperfine structure data for the determination of the change in the electron charge density at the nucleus in 4s-4p transitions.     

Hyperfine structure in the 6p5d configuration and isotope shifts in transitions between the 6s5d and the 6p5d configurations in Ba I

High-resolution laser fluorescence spectroscopy, using a single-mode dye laser acting on a collimated atomic beam, has been performed to determine the hyperfine-structure (hfs) constants in six states of the 6p 5d configuration of¹³⁵Ba and¹³⁷Ba. Isotope shifts (IS) for eleven transitions between the 6s 5d and the 6p 5d configurations have also been measured. From an analysis of the energy levels, intermediate angular wavefunctions have been deduced. The wavefunctions are used to evaluate experimental hyperfine parameters from the experimental hfs constants. The parameters are, for the magnetic-dipole interaction compared with theoretical values, and for the electricquadrupole interaction used to estimate the nuclear quadrupole moments for the odd isotopes. The IS in the measured transitions are analysed using a King-plot, with the first resonance line in Ba II as the reference. Specific mass and field shifts are evaluated for the measured transitions. The field shifts have been used to determine the change in mean-square radius between the natural abundant Ba-isotopes.     

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.     

Changes in nuclear mean square charge radii of stable Krypton isotopes

The isotope shifts of stable even Kr isotopes (A=78 throughA=86) in the optical transitions at 432 nm and 557 nm were measured by means of polarization laser spectroscopy. The observed shifts are consistent with earlier results for other transitions. From the isotope shifts the changes in the nuclear mean square charge radiiδ〈r ²〉 were inferred using preliminary muonic isotope shift data. Starting from⁷⁸Kr, a monotonic decrease of 〈r ²〉 with increasing mass number is found throughout theg _9/2 neutron shell. The effect onδ〈r ²〉 of nuclear deformations as well as possible contributions due to changes in the skin thickness of the nuclear charge distribution are discussed.     

Isotope shifts in the atomic spectrum of xenon and nuclear deformation effects

Optical isotope shifts of four lines in the atomic spectrum of xenon have been measured using enriched samples of all stable xenon isotopes. The spectrograms were recorded with the aid of a pressure-scanned Fabry-Pérot interferometer and analysed by digital data techniques. The measured isotope shifts are shown to be self-consistent by means of a King plot. An estimate of the specific mass effect is given and the changesδ 〈r ²〉 of the mean square radius of the nuclear charge distribution are extracted from the measured shifts. These changesδ 〈r ²〉 are discussed in terms of the nuclear deformation parameterβ ². The results for the deformation of the stable even xenon isotopes are shown to be in good agreement with the systematic of deformation found for the neighbouring elements from Coulomb excitation experiments.     

Isotope shifts of the ground state of neon: Refining the measurement results

Abstract—It has been revealed that the published results of measurements of the isotope shift of the ground state of even neon isotopes contain systematic errors. The errors are caused by the use of erroneous data regarding the absolute values of specific mass shifts of excited states and by the measurement errors of the isotope shifts themselves for transitions to the ground state. The isotope shift of the 2p⁵4s[3/2]₁ → 2p⁶(¹S₀) transition has been measured to be 2305 ± 20 MHz, the absolute specific mass shift of the 3p[3/2]₂: (2_р9) level has been determined to be 647 ± 10 MHz, and the isotope shift of the ground state has been found to be–3156 ± 30 MHz.     

Isotope shift of182Hg and an update of nuclear moments and charge radii in the isotope range181Hg-206Hg

The technique of collinear fast-beam laser spectroscopy has been used to measure the isotope shifts of the even-even isotopes of Hg (Z=80) in the mass range 182≤A≤198 at the on-line mass separator ISOLDE at CERN. The atomic transition studied (6s 6p ³ P ₂- 6s7s ³ S ₁,λ=546.1 nm) starts from a metastable state, which is populated in a quasi resonant charge transfer process. The resulting changes in nuclear mean square charge radii show clearly that¹⁸²Hg follows the trend of the heavier, even, weakly oblate isotopes. Correspondingly the huge odd-even shape staggering in the light Hg isotopes continues and the nuclear shape staggering and shape coexistence persists down to the last isotope investigated,¹⁸¹Hg. An update of isotope shift and hyperfine structure data for^181–206Hg is given, with a revised evaluation of the differences in nuclear mean square charge radii and of spectroscopic quadrupole moments.     

Isotope shift measurements of muonic X-rays in134, 136, 138Barium

The isotope shifts of muonic X-rays for the three stable Ba-isotopes^{134, 136, 138}Ba have been measured with high accuracy. Especially the differences in the rms radiiΔ〈r ²〉 have been determined in a model independent way and have been used to calibrate optical isotope shift data.     

Ba原子6s5d~3 D与6p5d~3 F态的超精细结构及态间跃迁的同位素移动的直接确定

提出并演示了一种光泵预选态的原子光谱测量方法,并对Ba原子的6s5d3 D态与6p5d3 F态的超精细结构及该跃迁的同位素移动进行了直接测量。首先利用791nm的激光激发Ba原子特定同位素及特定超精细结构的6s6s 1 S0→6s6p3 P1跃迁,并利用6s6p3 P1→6s5d3 D2的自发辐射有选择地分别将这些同位素制备到6s5d3 D2态不同的超精细能级上,再用778nm的激光扫出对应的6s5d3 D2→6p5d3 F2跃迁的荧光光谱,通过这几组光谱之间的对比直接实现了对22条超精细谱线的认定和归属,从而得到了135 Ba和137 Ba的6s5d3 D2能级与6p5d3 F2能级的超精细结构常数及该跃迁的同位素移动。     

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     

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.     

Laser-atomic-beam spectroscopy in Sm: Isotope shifts and changes in mean-square nuclear charge radii

A systematic investigation of the isotope shifts of all natural Samarium isotopes was performed in 15 lines of the Sm I spectrum using the laser-atomic-beam technique. The observed lines correspond to transitions between the ground configuration 4f ⁶6s ² and the upper configurations 4f ⁶6s6p and 4f ⁵5d6s ². In one line a contribution of hyperfine-structure second-order effects to the isotope shift of the odd isotopes could be demonstrated. The measured isotope shifts have been separated in all lines into field shift and mass shift contributions assuming the specific mass shift to be zero in pures ²-sp transitions. From the field shift of the pures ²-sp transitions the changes in mean-square nuclear charge radii, δ<r ²>, have been evaluated for all natural Sm isotopes (in fm²): [144, 148] 0.517(27); [148, 150] 0.303(16); [150, 152] 0.423(22); [152, 154] 0.230(12); [147, 148] 0.152(8); [148, 149] 0.092(5). There is good consistency with recent muonic x-ray measurements of the changes in the Barrett nuclear charge radii,δR _k , of the even Sm isotopes.     

Laser Spectroscopy Programme at the Jyväskylä IGISOL

This paper reviews the status of the laser spectroscopy programme being carried using the IGISOL mass separator in combination with an RFQ cooler-buncher. Measurements in the zirconium region are being extended to the yttrium isotopes. Two K = 8 isomers, in ¹⁷⁶Yb and ¹³⁰Ba, are found to have smaller mean square charge radii than their ground states, and the isotope shifts of stable osmium isotopes have been measured off-line by collinear laser spectroscopy.     

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