Iodine magnetic moments measured by on-line nuclear orientation

On-Line measurements of magnetic dipole moments of^117–122I are interpreted using coupling of the odd particles to a deformed core. The results show interesting effects of g_7/2, d_5/2 orbital admixtures in the odd-A isotopes, which are close to spherical. The odd-odd isotopes^{118, 120}I show clear examples of shape co-existence.     

Nuclear magnetic moment of the 9.7 h 12− isomer 196mAu

The magnetic hyperfine splitting v_M=|gμ_NB_HF/h| of ^196mAu (j^π=12^?; configuration ¦(π$\text{11}\text{2}$($\text{v}\text{13}\text{2}{}^{\mathrm{+}}\text{)〉}{}_{12}{}^{\mathrm{?}}$; $\text{T}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}\text{= 9.7}\text{h}\text{)}$ as dilute impurity in Ni has been determined with nuclear magnetic resonance on oriented nuclei as 96.0(2) MHz. With the known hyperfine field B_HF = ?264.4(3.9) kG corrected for hyperfine anomalies the g-factor and magnetic moment of ^196mAu are deduced to be |g| = 0.476(7) and |μ| = 5.72(8) μ_N. Taking into account the known magnetic properties of $\text{π}\text{1}\text{2}{}^{\mathrm{?}}$ and $\text{v}\text{13}\text{2}{}^{\mathrm{+}}$ isomeric states in the neighbouring odd Pt, Au and Hg nuclei the structure of the 12^? state is discussed.     

Measurement of isotope shift and hyperfine splitting of190, 191, 193, 197Pb isotopes by collinear laser spectroscopy

We report here on the measurement of isotope shift and hyperfine splitting of^{190, 191, 193, 197}Pb for the 723 nm atomic optical transition. Detailed analysis of the optical data has been done by combining them with the available muonic and electronicx-ray isotope shift data. The magnetic dipole moments and the electric quadrupole moments of the odd isotopes have been extracted from the hyperfine coupling constants of the atomic states involved in the optical transition used.     

The magnetic moments of (vg 9/2)-levels in odd Zn isotopes

^69m,71mZn have been implanted with an isotope separator on-line into a cold iron host matrix. Nuclear magnetic resonance of the low-temperature oriented isotopes has been observed. The resonance frequencies for zero external magnetic field are v_L(^69mZnFe@#@) =36.814(35) MHz andv _L (^71mZnFe)=33.47(19) MHz. From these the magnetic moments of the 9/2⁺ iosmeric states have been derived as μ(^69mZn)=(?)1.138(18) n.m. andμ(^71mZn)=(?)1.035(18) n.m. The experimentally known magnetic moments of (vg _9/2)-levels in odd zinc isotopes are compared to theoretical estimates.     

Mean square charge radii of radium isotopes and octupole deformation in the 220–228Ra region

The first investigation of isotope shifts in both the atomic and ionic resonance lines of radium has been carried out using the technique of on-line collinear fast-beam laser spectroscopy at the ISOLDE facility at CERN. The measurements cover 19 isotopes in the mass range 208⩽A⩽232 with half-lives between 23 ms and 1600 y. The differences in the nuclear mean square charge radii δ〈r²〉 have been evaluated and - together with earlier published spins and moments from the hyperfine structure - related to nuclear deformation. In particular the inversion of the odd-even staggering effect for the isotopes ²²¹Ra, ²²³Ra and ²²⁵Ra can be interpreted by the presence of octupole instability and adds weight to the concept of near-stable octupole deformation in the odd-A isotopes which already explained their spins and magnetic moments.     

On-line nuclear orientation of the deformed neutron-deficient Eu,Sm and Pm isotopes

Low-temperature nuclear orientation measurements made on-line at the SERC Daresbury Laboratory on^142m Eu,^141m Sm, and¹⁴¹Pm, with known magnetic dipole moments, have yielded the magnitude of the hyperfine fields of these isotopes in an iron host lattice. Thus measurements for the isotopes^{139, 138}Eu,^139m Sm, and¹³⁸Pm yielded values for the respective magnetic moments. Limits on the thermal relaxation times of Eu and Sm isotopes in Fe were also deduced. The results for¹³⁸Eu appear to contradict the earlier πh_11/2⊗νh_11/2 ground-state configuration assignment.     

Magnetic moment of the 5/2−1/2[541] ground state of 14h 185Ir

The magnetic and electric hyperfine splitting frequencies ¦gμ _N B _HF/h¦ ande ² qQ/h of the 5/2^?1/2[541] ground state of 14h ¹⁸⁵Ir in Ni were measured with nuclear magnetic resonance on oriented nuclei to be 360.8(7) MHz and +6.7(2.0) MHz, respectively. The ground state magnetic dipole moment and electric quadrupole moment of¹⁸⁵Ir are deduced to be ¦μ¦=2.601 (14)μ _N andQ=?1.9(5)b, taking values for the hyperfine field and electric field gradient of B_HF=?454.9 (2.3) kG and eq=?0.151(4) × 10¹⁷ V/cm², respectively. The negative quadrupole moment is in agreement with nuclear-orientation data and proves again theI ^π K=5/2^? 1/2 ground state configuration.     

Nuclear magnetic resonance on oriented194Ir (T 1/2=19.4 h) in Fe and Ni

The hyperfine interaction of¹⁹⁴Ir (j ^π =1^?;T _1/2=19.4 h) in Fe and Ni has been investigated with the technique of nuclear magnetic resonance on oriented nuclei. For both systems the electronic-orbital-momentum induced electric quadrupole splitting could be resolved. The magnetic and electric hyperfine splitting frequencies,v _M =¦gμ _N ^B _HF/h¦ andv _Q =e ² qQ/h, respectively, were measured as:¹⁹⁴IrFe:v _m =408.54 (23) MHz;v _q =?2.47(20) MHz;¹⁹⁴IrNi:v _M =135.24(5) MHz;v _q =?1.23 (3) MHz. Taking into account a 3% uncertainty arising from hyperfine anomalies theg-factor is deduced as ¦g¦=0.39 (1). The electric quadrupole moment,Q=+0.352 (18)b, is slightly smaller than expected from the known systematics of deformation parameters in this mass region.     

Hyperfine magnetic anomaly in isotopic pairs <Superscript>151, 152</Superscript>Eu and <Superscript>152, 153</Superscript>Eu

High-resolution laser spectroscopy measurements of optical hyperfine splitting on the ^{151, 152, 153}Eu isotopes were performed on the atomic transition 4f ⁷6s ^{2 8} S _7/2 → 4f ⁷6s6p ⁶ P _5/2 at λ ≈ 564.58 nm. Values of the nuclear magnetic dipole and electric quadrupole moments are obtained from the measured hyperfine splitting and the magnetic hyperfine anomalies in the isotope pairs ^{151, 152}Eu and ^{152, 153}Eu are deduced. The absolute values of the hyperfine anomaly in both cases are unusually large: 5 (1)%. The possible sources causing these anomalies are discussed.     

Collinear laser spectroscopy on108g, 108m In using an ion source with bunched beam release

The hyperfine structure and isotope shift of^108gIn and^108mIn have been investigated by means of collinear fast-beam laser spectroscopy in the resonance line atλ=451 nm. The indium isotopes were prepared at the GSI on-line mass separator following a fusion evaporation reaction. For the first time, a FEBIAD ion source with bunched release of indium was used. Magnetic dipole moments, electric quadrupole moments and isotope shifts were determined. The present results lead us to assign the spinI=2 to the¹⁰⁸In (T _1/2=40 min) state. Spins and moments are discussed in the framework of thejj-coupling model.     

EPR of Er3+, Nd3+, and Ce3+ ions in YAlO3 single crystals

EPR spectra of the Er³⁺, Nd³⁺, and Ce³⁺ ions substituting for the Y³⁺ ion in the YAlO₃ yttrium orthoaluminate lattice are studied. The EPR spectra of these rare-earth ions are described by a spin Hamiltonian of rhombic symmetry with an effective spin S=1/2. The principal values of the g tensors were determined from an analysis of the angular dependences of the EPR spectra. The orientation of the local magnetic axes of paramagnetic centers relative to the YAlO₃ crystallographic directions are shown to depend on the actual rare-earth species. The EPR spectra exhibit a hyperfine structure due to the ¹⁶⁷Er, ¹⁴³Nd, and ¹⁴⁵Nd odd isotopes, which permitted unambiguous identification of these spectra. The hyperfine coupling constants for the odd erbium and neodymium isotopes are determined.     

Nuclear magnetic resonance on oriented109In(4.2h) and110In(4.9h) after recoil implantation into Fe

Radioactive¹⁰⁹In(j ^π=9/2⁺;T _1/2=4.2h) and¹¹⁰In(j ^π=7⁺;T _1/2=4.9h) were produced via the¹⁰⁹Ag (α, xn) reactions and recoil-implanted into Fe foils. With the technique of nuclear magnetic resonance on oriented nuclei the magnetic hyperfine splittings were investigated in external magnetic fieldsB ₀=0.5...4.2 kG. The zero-field splitting were measured as 268.9(2)MHz and 147.3(3)MHz for¹⁰⁹InFe and¹¹⁰InFe, respectively. With the known hyperfine fieldB _HF(InFe)=?286.6(5) kG the nuclearg-factors are deduced asg(¹⁰⁹In)=1.231(3) andg(¹¹⁰In)=0.674(2). Our result for¹⁰⁹In shows that theπ g _9/2 g-factors vary by only ～0.1% betweenA=109 and 115. For the |π _9/2 vd _5/2〉₇₊ of¹¹⁰In the additivity relation of magnetic moments is fulfilled to on accuracy of 0.3(3)%.     

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.     

Transient magnetic fieldg-factor measurements of 2 1 + in64, 66, 68, 70Zn

The implantation perturbed angular correlation technique (IMPAC) has been used to determine the magnetic dipole moments of the first excited 2⁺ states in the stable even-even Zn-isotopes. Transient magnetic field measurements for⁵⁶Fe in ferromagnetic Gd at 77 K have been performed for recoil velocities up tov/v ₀～8. The result confirms the earlier reported linear velocity dependence. Theg-factors are deduced to be 0.46±0.10, 0.47±0.11, 0.46±0.14 and 0.30±0.07 for^{64, 66, 68}Zn and⁷⁰Zn respectively. The results are compared with theoretical predictions.     

In-beam studies of203, 205Bi and shell-model features of odd-a bismuth isotopes

States in^{203, 205}Bi are populated using the reaction^{203, 205}Tl(³He,3n). Theπi _13/2 single-proton states and all the members of thev(2 ₁ ⁺ )?π h _9/2 quintuplet are identified in both nuclei. The half-lives of the isomericJ ^π=21/2⁺ states in both isotopes are measured and found to be 90±7 ns and 100±6 ns, and from these values suggestions for the half-lives of the previously reportedJ ^π=25/2⁺ isomers are made. The structures of the multiplets of the formv(Pb)?π h _9/2 are calculated in the framework of the shell model and it is shown that the main features can be derived from theπ?v ^?1 effective interaction. The wave functions of the 4 ₁ ⁺ and 4 ₀ ⁺ states in^{202, 204}pb are deduced indirectly from the calculation in^{203, 205}Bi.     

Laser spectroscopy of radioactive lead and thallium isotopes

By collincar fast beam laser spectroscopy hyperfine structure and isotope shift have been measured of neutron deficient radioactive isotopes of lead (¹⁹⁰Pb,¹⁹¹Pb,¹⁹²Pb,¹⁹³Pb,¹⁹⁴Pb,¹⁹⁵Pb,¹⁹⁶Pb,¹⁹⁷Pb) and thallium (¹⁸⁸Tl¹⁹⁰Tl,¹⁹¹Tl,¹⁹²Tl,¹⁹⁴Tl,¹⁹⁶Tl). Therefrom nuclear magnetic dipole moments, electric quadrupole moments, changes of the mean square charge radii and deformation parameters are deduced and compared with predictions from theory.     

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).     

Probabilities of rovibronic transitions in the I 1Π g − , J 1Δ g − →C 1Π ± u systems of bands of the deuterium molecule

Probabilities of spontaneous rovibronic transitions I ¹Π _g ^? , v′ J′, J ¹Δ _g ^? , v′, J′→C ¹Π _u ^± , v″, J″ of the D₂ molecule (for vibrational and rotational quantum numbers v′=v″=0–3 and J′=1–9, J″=J′±1) have been obtained for the first time. They were determined using (1) the previously proposed nonadiabatic model, which takes into account the electron-rotational interaction of the upper levels; (2) the coefficients of expansion of wave functions of perturbed states in the Born-Oppenheimer basis, which were found from the experimental data on rovibronic terms; and (3) semiempirical b initio data on electronic transition dipole moments of the 3dπ¹Π_g→2pπ¹Π_u and 3dπδ¹Δ_g→2pπ¹Π_u transitions. The dependences of the transition probabilities on J′ for the same bands of both hydrogen isotopomers H₂ and D₂ were found to be identical. They represent monotone functions for R and P branches and functions with a maximum (minimum) for Q branches. The ratios of transition probabilities of different isotopomers for different branches of the same systems of bands and for the same branches of different systems of bands were found to be correlated. The semiempirical values obtained in the paper agree with the experimental values within the limits of the errors of their determination. The nonempirical values of transition probabilities agree with the experiment considerably worse.     

Hyperfine splitting constants in the optical transition \boldsymbol{{4{f}^{7}} {6{s}^{2}} \;{^{8}{\rm S}_{7/2}} \to {4{f}^{7}} {6{s}6{p}}\; {^{6}{\rm P}_{5/2}} \ {\rm of} \ {^{151-155}{\rm Eu}}} isotopes and hyperfine anomaly

Using the method of laser-induced fluorescence in an atomic beam we have measured the hyperfine splitting constants, A and B, of the ground and excited states of the optical transition 4f ⁷6s ^{2 8}S $_{1/2}\to 4f^{7}$ 6s6p ⁶P_5/2 (564.58 nm) for ^151???155Eu isotopes. For all isotopes, the magnetic dipole constants of the ⁶P_5/2 atomic level are determined to a precision better than 0.04%. The A and B constants for the ground state ⁸S_7/2 of the radioactive ^152,154,155Eu were obtained for the first time with a precision better than 0.5%. Our data along with previous ground state hyperfine structure measurements for the stable europium isotopes allow us to determine the hyperfine anomaly for mentioned Eu isotopes.     

Investigation of N 2 + (C 2Σ u + → X 2Σ g + fluorescence excited through auger decay of the 1s −1π* resonance

A theoretical investigation of N ₂ ⁺ (C ²Σ _u ⁺ → X ²Σ _g ⁺ molecular fluorescence excited through the Auger decay of the 1s ^?1π* resonance is carried out. The fluorescence cross sections are calculated with due regard for the dependence of the matrix element of the C → X dipole transition on the internuclear distance, the interference between channels of excitation via different vibrational levels v _r of the 1s ^?1π* resonance, the rotational structure of the fluorescence band, and the predissociation of the N ₂ ⁺ C ²Σ _u ⁺ v′ ≥3) states. The calculated cross sections are in good agreement with the experimental results of recent measurements. The results of the calculations have demonstrated that the observed dependence of the cross section of the (C ²Σ _u ⁺ (v′) → X ²Σ _g ⁺ (v″) fluorescence on the excitation energy and the fluorescence wavelength for a group of bands with equal values of the difference Δv = v′ ? v″ is associated with transitions between the vibrational levels of the electronic states involved in the excitation and subsequent cascade decay of the 1s ^?1π* resonance: N₂ (v ₀ = 0) → N*₂(1s ^?1π*(v _r)) ? N ₂ ⁺ : (C ²Σ _u ⁺ (v′) → X ²Σ _g ⁺ (v″).