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.     

Hyperfine-structure investigation in the 6s5d configuration of135Ba and137Ba

The hyperfine structure of the metastable states of the 6s5d configuration of¹³⁵Ba and¹³⁷Ba has been studied by the atomic-beam magnetic resonance (ABMR) method. The metastable barium states were populated in a plasma-discharge inside the atomic-beam oven. The atoms emerging from the ABMR-apparatus were detected by the use of a dyelaser. Compared to conventional methods this technique has the advantage of being state selective. The following magnetic dipole and electric quadrupole interaction constantsa andb have been obtained:¹³⁷Ba:a(³ D ₁)=?520.536 (3) MHzb(³ D ₁)=17.890 (3) MHza(³D₂=415.928 (3) MHzb(³D₂)=25.899 (13) MHza(³D₃)=456.559 (4) MHzb ³D₃=47.390 (16) MHz¹³⁵Ba:a ³ D ₁=?465.166 (4) MHzb(³D₁)=11.642 (4) MHza(³D₂)=371.736(4) MHzb ³ D ₂=16.745 (14) MHza(³D₃)=408.038 (6) MHzb(³D₃)=30.801 (24) MHz Using these constants and the earlier known ones for the¹ D ₂ state the hyperfine structure for the 6s5d configuration has been analyzed with an effective hyperfine hamiltonian. Hyperfine parameters obtained from the analysis have been compared with theoretical values calculated with relativistic self-consistent-field (SCF) wavefunctions. The quadrupole moments have been evaluated with the following result Q(¹³⁵Ba) =0.20(3)b and Q(¹³⁷Ba) = 0.34(4)b uncorrected for the quadrupole shielding.     

Präzisionsmessung der Kerndipolmomente von Ba135 und Ba137 mit optischem Pumpen

The nuclear Zeeman levels of the ground state of Barium (6s^{2 1}S₀, F=I=3/2) were polarized by means of optical pumping with the resonance line (6s^{2 1}S₀?6s 6p¹P₁, λ=5535 Å). The magnetic field was calibrated by means of optical pumping of sodium. The magnetic moments, calculated from the nuclear Hf-Zeeman-transitions at 228 Gauss are μ₁₃₅=0,83651 (6) μ_N μ₁₃₇=0,93573 (6) μ_N (with diamagnetic correction). With the results of nuclear induction in BaCl₂ we calculate the chemical shift to be (8.6±1.0)·10^?4. The ratio of the nuclear moments is μ₁₃₇/μ₁₃₅=1.11862 (3) in agreement with the measurements in BaCl₂.     

Molecular motions in chloramphenicol studied by35Cl nuclear quadrupole and1H nuclear magnetic resonance spectroscopy

The³⁵Cl nuclear quadrupole resonance (NQR) frequency (v_Q), nuclear quadrupole spinlattice relaxation time (T_1Q),¹H nuclear magnetic resonance second moment (M₂) and nuclear magnetic spin-lattice relaxation timeT ₁) were measured for polycrystalline chloramphenicol (drug) as a function of temperature. Hindered rotation of the CHC1₂ group and the phenyl ring was detected, the relevant activation energies were determined. The rotations are discussed in detail.     

Nuclear quadrupole interaction at133Ba (EC)133Cs in Eu1Ba2Cu3O7−°

We studied the nuclear quadrupole interaction (NQI) at¹³³Ba(EC)¹³³Cs in Eu₁Ba₂Cu₃O_7–6 by time differential perturbed angular correlation between 11 K and 300 K. No anomalies in the NQI parameters around T_c were detected. All Ba sites appear to be identical and the precession frequency is ω=80(2) Mrad/s (assuming axial symmetry), independent of temperature.     

Nuclear magnetic order in PrF3

PrF₃ is an enhanced nuclear paramagnet for which the resonance parameters have been determined both by acoustic resonance (Al’tshuleret al., 1979 [1]) and by conventional nuclear magnetic resonance (Nielsen, 1983 [2]). In this paper, the temperature at which the nuclei of the single stable isotope¹⁴¹Pr,I=5/2, enter an ordered state is estimated to beca. 0.1 mK, smaller than the overall nuclear electric quadrupole splitting 6P/h=1.2 mK. Possible arrangements of the nuclear moments in the ordered state are discussed, together with the requirements for a neutron diffraction measurement.     

Double resonance experiments in low magnetic field: Dynamic polarization of protons by N and measurement of low NQR frequencies

The possibilities of dynamically polarizing proton spin system via the quadrupole ¹⁴N spin system in low magnetic field are analyzed. The increase of the proton magnetization is calculated. The polarization rate of the proton spin system is related to the transition probabilities per unit time between the ¹⁴N quadrupole energy levels and proton energy levels. The experiments performed in 1,3,5-triazine confirm the results of the theoretical analysis. A new double resonance technique is proposed for the measurement of nuclear quadrupole resonance frequencies ν_Q of the order of 100 kHz and lower. The technique is based on magnetic field cycling between a high and a low static magnetic field and observation of the proton NMR signal in the high magnetic field. In the low magnetic field the quadrupole nuclei and protons resonantly interact at the proton Larmor frequency ν_H = ν_Q/2. The quadrupole nuclei are simultaneously excited by a resonant rf magnetic field oriented along the direction of the low static magnetic field. The experimental procedure is described and the sensitivity of the new technique is estimated. Some examples of the measurement of low ¹⁴N and ²H nuclear quadrupole resonance frequencies are presented.     

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.     

Messung der magnetischen Kerndipolmomente an freien43Ca-,87Sr-,135Ba-,137Ba-,171Yb- und173Yb-Atomen mit optischem Pumpen

As previously reported^3,4 the optical pumping method was succesfully used to determine the nuclear magnetic moments of¹³⁵Ba,¹³⁷Ba,¹⁷¹Yb and¹⁷³Yb. This method has now been extended to⁴³Ca and⁸⁷Sr. The nuclear moments of the Ba- and Yb-isotopes have been remeasured by means of an improved experimental technique. Especially the influence of the light shift has been investigated and the nuclear moments have been corrected by eliminating this shift. The magnetic field has been calibrated by means of optical pumping of²³Na. The nuclear magnetic moments obtained from the rf-transitions between the Zeeman-levels of the ground state¹ S _o are: μ(⁴³Ca)=?1.3172 (6)μ _N ; μ⁸⁷Sr)=?1.0924 (7) μ _N ; μ(¹³⁵Ba)=0.83656(2)μ _N ; μ(¹³⁷Ba)=0.93582(2)μ _N ; μ(¹⁷¹Yb)=0.491889 (8)μ _N ; μ(¹⁷³Yb)=?0.67744 (3) μ _N (diamagnetic correction was applied). The ratios of the nuclear moments of the elements with two odd isotopes are: μ(¹³⁷Ba)/(¹³⁵Ba)=1.11865 (3); μ(¹⁷³Yb)/μ(¹⁷¹Yb)=?1.37723 (7). In comparison with the results of nuclear induction the chemical shifts have been calculated to be: δ(Ca)≦± 5 · 10^?4 δ(Sr)=?6(7) ·10^?4 δ(Ba)=?7.8(4) ·10^?4 δ(Yb)=?23(10) · 10^?4.     

Hyperfine structure of the 5d26s23F3,4 metastable atomic levels of 179Hf and the nuclear quadrupole moments of 177Hf and 179Hf

From hyperfine structure measurements in the ground multiplet ³F of ¹⁷⁹Hf performed with the atomic beam magnetic resonance method effective radial parameters have been determined and new spectroscopic values of the nuclear quadrupole moments of ¹⁷⁷Hf and ¹⁷⁹Hf are evaluated.     

73Ge NMR spectra in germanium single crystals with different isotopic composition

We have studied the influence of isotopic disorder on the local deformations in Ge single crystals from both experimental and calculation points of view. The nuclear magnetic resonance (NMR) spectra of⁷³Ge nuclei (the nuclear spin equals 9/2) in perfect single crystals of germanium with different isotopic content were measured at temperatures 80, 300 and 450 K. Abnormal broadening of the spectrum was found to occur when the magnetic field was aligned along the [111] axis of a crystal. The observed specific angular dependence of the quadrupole broadening was attributed to isotopic disorder among atoms of germanium sited around the⁷³Ge NMR probe. Local lattice deformations in germanium crystal lattice due to isotopic impurity atoms were calculated in the framework of the adiabatic bond charge model. The results obtained were applied to study random noncubic crystal field interactions with the nuclear quadrupole moments and corresponding effects in NMR spectra. Simulated second and fourth moments of resonance frequency distributions caused by the magnetic dipole-dipole and electric quadrupole interactions are used to analyze the lineshapes, theoretical predictions agree qualitatively with the experimental data.     

Nuclear moments around the Z=40 shell closure:91mY,95Zr and97Nb

Magnetic moments around the Z=40 shell closure have been established using nuclear magnetic resonance on oriented nuclei (NMR/ON) in iron. From the resonance frequencies we established |μ(⁹¹Y;9/2⁺)|=5.96(6)μ_N, |μ(⁹⁵Zr;5/2⁺)|= 1.103(23)μ_N, | μ(⁹⁷Nb;9/2⁺)| = 6.153(5)μ_N. From the electric quadrupole alignement of⁹⁵Zr+⁹⁵Nb in a Zr single crystal Q(⁹⁵Zr)=+0.29(5)b and Q(⁹⁵Nb)<0 have been derived. The results obtained are discussed using the Nilsson deformed single particle model. It is shown that for certain deformation regions, a measurement of the magnetic moment can give information on the nuclear quadrupole deformation. the NICOLE-ISOLDE Collaboration, CERN     

Oxidation and magnetic states of chalcopyrite CuFeS2: A first principles calculation

The ground state band structure, magnetic moments, charges and population numbers of electronic shells of Cu and Fe atoms have been calculated for chalcopyrite CuFeS₂ using density functional theory. The comparison between our calculation results and experimental data (X-ray photoemission, X-ray absorption and neutron diffraction spectroscopy) has been made. Our calculations predict a formal oxidation state for chalcopyrite as Cu¹⁺Fe³⁺S ₂ ^2? . However, the assignment of formal valence state to transition metal atoms appears to be oversimplified. It is anticipated that the valence state can be confirmed experimentally by nuclear magnetic and nuclear quadrupole resonance and Mössbauer spectroscopy methods.     

139La and63Cu-NQR of high-T c oxide superconductors

Nuclear quadrupole resonances (NQR) of¹³⁹La in La_2−xM_xCuO₄ (M=Ba, Sr) and⁶³Cu in YBa₂CU₃O₇ have been investigated with substitution of Cu by magnetic impurities. For La-system, the strong enhancement of the nuclear relaxation rate, 1/T ₁ atT _c ^*≈10 K (suggesting the occurrence of magnetic instability with hole-doping), is suppressed by 3D-antiferromagnetism induced by magnetic impurities. In the superconducting region, fluctuations of Cu moments at low temperatures remain extremely fast as at high temperatures. For Y-system, Fe-ions are substituted for both Cu(1) and Cu(2) sites, But Co-ions are preferentially substituted to Cu1 sites. The peaks in the relaxation rate of Cu indicate the appearance of magnetic ordering without destroying superconductivity for the 0.5%-Fe doped sample.     

Fe-induced magnetic transition in YBa2(Cu1−x 57Fe x )3O6 by NQR and Mössbauer spectroscopy

Nuclear quadrupole resonance spectroscopy (around 30 MHz) on the chain site Cu(1) nuclei in oxygen deficient YBa₂(Cu_1?x Fe _x )₃O₆ doped with different amounts of⁵⁷Fe (x≤0.01) reveal an onset of magnetic order at low temperatures represented by a symmetrical doublet contribution to the nuclear quadrupole resonance (NQR) spectrum. The onset temperatureT _N2 depends on the concentration of Fe reaching 130 K forx=0.01. The splitting forx=0.01 at 100 K corresponds to a net internal field of 0.09 T with a distribution of ≈0.08 T representing about 70 percent of the Cu(1) nuclei.⁵⁷Fe and⁵⁷Co Mössbauer spectroscopy at 4.2 K with and without an external magnetic field of 5 T revealed that belowx=0.00015 Fe spins are decoupled from the Cu(2) moments in the antiferromagnetic state. Results are interpreted in terms of the magnetic model structure suggested by Kadowaki et al. [1].     

Magnetic structure of the Sr<Subscript>2</Subscript>Cu<Subscript>3</Subscript>O<Subscript>4</Subscript>Cl<Subscript>2</Subscript> two-subsystem antiferromagnet according to nuclear quadrupole resonance data

The magnetic structure of the Sr₂Cu₃O₄Cl₂ two-subsystem antiferromagnet is studied by the nuclear quadrupole resonance (NQR) method on the ^{63, 65}Cu and ³⁵Cl nuclei. The resonance spectrum above T _N2 = 40 K is determined by the Zeeman splitting of the levels of the ^{63, 65}Cu nuclei of the copper atoms at the Cu1 site with the first-order quadrupole perturbation. The magnetic field on the copper nuclei is equal to 93 kOe. The spectrum below n is significantly different: it includes a low-frequency part, which is associated with the ordering of the second magnetic subsystem Cu2. The splitting of the NQR lines of ³⁵Cl is observed above and below T _N2. This fact indicates the ferromagnetic ordering of the moments of the Cu1 subsystem, which are located along the c axis of the crystal, and makes it possible to determine the direction of the magnetic field on Cu1 copper as (110).     

Incommensurate helical magnetic order in LiCu<Subscript>2</Subscript>O<Subscript>2</Subscript> and NaCu<Subscript>2</Subscript>O<Subscript>2</Subscript> quasi-one-dimensional compounds

The results of the measurements of the ^{6, 7}Li and ²³Na nuclear magnetic resonance (NMR) and ^{63, 65}Cu nuclear quadrupole resonance in LiCu₂O₂ and NaCu₂O₂ quasi-one-dimensional compounds with a spin chains in the paramagnetic and magnetically ordered states are presented. The shape of the NMR line below T _c = 24 and 13 K for LiCu₂O₂ and NaCu₂O₂, respectively, is characteristic of the incommensurate static modulation of the local magnetic field matching with the incommensurate spiral modulation of the magnetic moments. The differences in the shape of the NMR spectra of ²³Na and ⁷Li are discussed in terms of the features of the crystal structure of LiCu₂O₂ and NaCu₂O₂.     

Evidence for low-temperature internal dynamics in Cu12As4S13 according to copper NQR and nuclear relaxation

^63,65Cu nuclear quadrupole resonance (NQR) was applied to study the natural mineral Cu₁₂As₄S₁₃ (tennantite) in the temperature range 4.2–210 K. The obtained results point to the presence of field fluctuations caused by internal motions in tennantite. Consistently with the crystal structure, the experimental data can be described by an occurrence of a magnetic phase transition, which takes place near 65 K. The low-temperature phase is characterized by Cu(II) electron magnetic moments freezing in the form of a spin-glass-like constitution.     

Hyperfine structure and nuclear moments of99Ru and101Ru

The atomic-beam magnetic-resonance method in combination with the triple resonance technique has been used to determine the nuclear magnetic dipole moments of⁹⁹Ru and¹⁰¹Ru. The moments are deduced fromrf transition measurements in the⁵F₅ and⁵F₄ states at magnetic fields between 770 and 2400 Oe. In order to reduce the part of the uncertainty of the moments which arises from the uncertainty of the hyperfine structure constants more precise values of the constants than those available up to now were determined from low field measurements. After making corrections for hyperfine and Zeeman interactions with neighbouring atomic states we obtain the following values for the magnetic dipole moments:μ ₉₉=?0.6381 (51)μ _N andμ ₁₀₁=?0.7152 (60)μ _N (uncorrected for diamagnetic shielding). The results of the present work combined with the results of an earlier hyperfine structure investigation in the⁵F multiplet are analysed with respect to the effective-operator formalism. From this analysis we obtain the following values for the electric quadrupole moments:Q ₉₉=0.076 (7) b andQ ₁₀₁=0.44 (4) b (uncorrected for Sternheimer shielding or antishielding).     

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.