Bestimmung des elektrischen Kernquadrupolmomentes des ungeraden stabilen Strontium-87-Kerns

In order to determine the electric quadrupole moment of Sr⁸⁷ (I= 9/2) the hyperfine structure-splitting of the 5s5p ³ P ₁-state of the SrI-spectra was investigated by optical double resonance. By detection of high frequency transitions (ΔF=±1,Δm _F=0,±1) in an external magnetic fieldH ₀≈0 one obtains the hyperfine structure separations asv _F=11/2?F=9/2=1463·149 (6) Mc/sec andv _F=9/2?F=7/2=1130·264 (6) Mc/sec. From these frequencies one calculates the magnetic hyperfine structure-splitting constantA=?260·084 (2) Mc/sec and the electric quadrupole interaction constantB=?35·658 (6) Mc/sec. B leads to an electric quadrupole moment ofQ(Sr⁸⁷)=+0·36 (3)·10^?24 cm².     

Variation Angulaire,Transitions Interdites Dans Le Spectre De R.P.E. Des Ions Mn2+ Dans L'alumine α

The spin Hamiltonian with trigonal symmetry for Mn²⁺ in Al₂O₃ has been derived. The line positions have been calculated using perturbation theory up to third order. Three groups of forbidden transitions ΔM = ± 1 Δm = ± 1 have been investigated. Q′ and γ have been deduced from for forbidden hyperfine doublets. The two evaluations of the spin Hamiltonian parameters from allowed (Δm = 0) and forbidden lines (Δm = 1) are discussed.     

Relaxationserscheinungen im 63 P 2-Zustand des Quecksilber-Isotops199Hg bei Stößen mit Quecksilberatomen im Grundzustand

The decay ofrf resonance signals (Δm _F =± 1, ΔF=0) in the hfs-states (F=3/2, 5/2) of the 6³ P ₂-state of¹⁹⁹Hg has been observed by means of a sampling method. By comparing the relaxation times to those of the even isotopes, the cross section σ₂(F) for the destruction of an alignment in the hfs-states by collisions with ground state Hg-atoms could be measured. The following ratios were obtained: σ₂(F=3/2)/σ₂=1.04±0.06 and σ₂(F=5/2)/σ₂=0.90± 0.03. The cross section σ₂ for the even isotopes was found to be (2.620±0.265) 10^?14cm². Assuming total decoupling of nuclear spinI and electronic angular momentumJ during the collision, the cross sections for the destruction of an orientation (σ₁) and an “octupolarisation” (σ₃) could be calculated. For the even isotopes the following ratios were derived: σ₁/σ₂=0.76 ± 0.07 and σ₃/σ₂=1.08 ± 0.09.     

E1,ΔK=0−Übergänge in deformierten Kernen ungerader Massenzahl

The half lives of the 5/2 5/2^?[523] level at 25.7 keV in ₆₆ ¹⁶¹ Dy and the 5/2 5/2⁺[642] level in ₆₈ ¹⁶³ Er, found in this work to lie at 69.2 keV, have been determined by the delayed coincidence method to be T_1/2=27.8± 1.5 nsec, and T_1/2=8.8± 0.5 nsec, respectively. The following hindrance factors relative to the single particle Weisskopf estimate (F _W and the Nilsson estimate (F_N were obtained: ₆₆ ¹⁶¹ Dy 5/2 5/2^?[523] → 5/2 5/2⁺[642]:F_W=(6.6± 1.3) × 10³, F_N=0.48± 0.10 ₆₈ ¹⁶³ Er 5/2 5/2⁺[642] → 5/2 5/2^?[523]:F_W=(2.4± 0.5)× 10⁴, F_N=1.8 ± 0.4 A systematic difference between transitions in odd proton nuclei and odd neutron nuclei was found: E1, ΔK=0 transitions in odd neutron nuclei have hindrance factors F_N from 2.9 to 0.16, this means, these transitions are in agreement with the predictions of the Nilsson model within a factor of 10. For transitions in odd proton nuclei one has hindrance factors F_N from 75 to 9.9 × 10^?4. It is shown that a small difference between the deformation of the initial and the final state changes the transition probability of both, proton and neutron transitions, considerably.     

Die Hyperfeinstrukturaufspaltung des Grundzustandes2 S 1/2 und das magnetische Kerndipolmoment von Au197

The hyperfine structure of the groundstate 6s ² S _1/2 and the nuclear magnetic dipole moment of gold 197 have been studied by the atomic beam magnetic resonance technique. A special high frequency arrangement is described. The hyperfine structure separationΔ v was determined fromΔF=1 transitions. The magnetic dipole momentμ _I was measured by a direct method. The experiments yield the following results:Δv (²S_1/2)=(6099,309±0,010) Mc/secμ _I (Au¹⁹⁷)=+(0,1445±0,0014)μ _K.     

Bestimmung der Lebensdauer des 3d 9 4s 4p 4 P 3/2-Terms im Cu I-Spektrum mit optischer Doppelresonanz

The lifetime of the 3d ⁹ 4s 4p ⁴ P _3/2 state of Cu has been determined with optical double resonance by observation of radiofrequency transitions ΔF=0, Δm _F =±1 between hfs-Zeeman levels of the stable odd isotopes. The result is τ(3d ⁹ 4s 4p ⁴ P _3/2, Cu)=3.18(16)·10^?7 sec.     

Half-life measurements of intrinsic states in deformed odd-mass nuclei

The half-lives of the following intrinsic states in deformed odd-mass nuclei has been measured by delayed coincidences with a time-to-amplitude converter:

1. 5/2 5/2⁺[642] at 86.5 keV in¹⁵⁵Gd:T _1/2=6.7±0.3 ns, which results in the determination of theE1,ΔK=1 transition probability to the ground state 3/2 3/2^?[521] and first rotational state 5/2 3/2^?[521], yielding hindrance factors ofF _N ≈5.5 and ≈1.8 (F _W =3.1×10⁴ and 2.3×10⁴) respectively.
2. (3) 5/2 5/2^?[512] at 191.4 keV in¹⁶⁹Yb:T _1/2=3.35±0.15 ns and at 122.39 keV in¹⁷¹Yb:T _1/2=265±20 ns which results in the determination of the transition probabilities of theE1,ΔK=1 transitions to the ground states 7/2 7/2⁺[633], of theK-forbiddenM1 transitions to the 5/2 and 3/2 1/2^?[521] and of theE2 transitions to the 5/2, 3/2 and 1/2 1/2^?[521] states in both nuclei.

TheE1 transition probabilities are compared to the transitions between the same Nilsson states in¹⁷³Yb and¹⁷⁵Hf discussing the influence of the position of the Fermi surface — obtained from recent stripping and pick-up reactions — on these transition probabilities. Additional information on the decay scheme of¹⁷¹Lu→¹⁷¹Yb is obtained by delayed coincidence measurements. For testing the used time-to-amplitude converter the well known half-lives of the 482 keV level in¹⁸¹Ta (T _1/2=10.4±0.3 ns) and of the 279 keV level in²⁰³Tl (T _1/2=0.285 ±0.015 ns) were measured, in good agreement with other measurements.     

The F+ center in reactor-irradiated aluminum oxide

A point-ion calculation has been performed for the F⁺ center in α-Al₂O₃ (one electron in an O^2? vacancy). Optical transitions are predicted at 2·26, 3·39 and 5·15 eV. Contact hyperfine interactions with the two nearest pairs of Al³⁺ ions are calculated to be 151 and 39 G. Single crystals of α-Al₂O₃ were reactor-irradiated up to doses of 10²⁰ fast neutrons per cm², and studied by electron spin resonance (ESR). A broad ESR spectrum with 13 resolved components at g=2·0029±0·0005 was interpreted as the interaction of an unpaired electron with two pairs of Al³⁺ nuclei with hyperfine constants of 49·2 and 13·5 G. These values are in the same ratio as the values calculated for the F⁺ center, to which this ESR spectrum is attributed. The discrepancy of a factor of three is typical of point-ion calculations. The optical absorption spectrum for heavily-irradiated samples is not available for comparison with calculated transition energies.     

Blue laser cooling transitions in Tm I

We have studied possible candidates for laser cooling transitions in ¹⁶⁹Tm in the spectral region of 410–420 nm. By means of saturation absorption spectroscopy, we have measured the hyperfine structure and rates of two nearly closed cycling transitions from the ground state 4f¹³6s²(²F₀)(J_g=7/2) to upper states 4f¹²(³H₅)5d_3/26s²(J_e=9/2) at 410.6 nm and 4f¹²(³F₄)5d_5/26s²(J_e=9/2) at 420.4 nm and evaluated the life times of the excited levels as 15.9(8) ns and 48(6) ns, respectively. Decay rates from these levels to neighboring opposite-parity levels are evaluated by means of Hartree–Fock calculations. We conclude that the strong transition at 410.6 nm has an optical leak rate of less then 2×10^-5 and can be used for efficient laser cooling of ¹⁶⁹Tm from a thermal atomic beam. The hyperfine structure of two other even-parity levels, which can be excited from the ground state at 409.5 nm and 418.9 nm, is also measured by the same technique. In addition, we give a calculated value of 7(2) s^-1 for the rate of magnetic-dipole transition at 1.14 μm between the fine structure levels (J_g=7/2)↔(J’_g=5/2) of the ground state which can be considered as a candidate for applications in atomic clocks. PACS 32.70.Cs; 32.10.Fn; 32.80.Pj     

Hyperfine structure investigations in the4F9/2 atomic ground state of191Ir and193Ir

The5d ⁷6s^{2 4}F_9/2 atomic ground state of¹⁹¹Ir and¹⁹³Ir has been studied using the atomic-beam magnetic-resonance method. The results are:¹⁹³Ir:g _J(⁴F_9/2)=1.29694 (3)¹⁹¹Ir:Δv(⁴F_9/2; F=6?F=5)=659.26496 (12) MHzΔv( ⁴F_9/2; F=5?F=4)=189.44002 (09) MHzΔv( ⁴F_9/2; F=3?F=4)=84.05040 (80) MHzA=57.52148 (04) MHzB=471.20425 (57) MHzC=?0.020 (30) kHz¹⁹³Ir:Δv( ⁴F_9/2; F=6?F=5)=660.09043 (12) MHzΔv( ⁴F_9/2; F=5?F=4)=224.47848 (13) MHzΔv( ⁴F_9/2; F=?F=4)=33.53453 (89) MHzA=62.65556 (05) MHzB=426.23546 (64) MHzC=0.020 (30) kHz Using the magnetic dipole moments known by NMR-technique [1] we obtained for the electric quadrupole moments as calculated from the hyperfine interaction constantsA andB:Q(¹⁹¹Ir)=0.78 (20) barns,Q(¹⁹³Ir)=0.70 (18) barns (uncorrected for core polarization effects). A calculation of the hyperfine anomaly yields:₁₉₁ Δ ₁₉₃=?0.00023 (10). The ratio of theB factors which should be the same as for the quadrupole moments turned out to be:B(¹⁹¹Ir)/B(¹⁹³Ir)=Q(¹⁹¹Ir)/Q(¹⁹³Ir)=1.105502(3).     

Atomic beam magnetic resonance investigations in the3 F 2 Ground State of177Hf,179Hf and180Hf

The 5d ²6s ^{2 3} F ₂ ground state of¹⁷⁷Hf,¹⁷⁹Hf and¹⁸⁰Hf has been studied using the atomic beam magnetic resonance method. The atomic beam was produced by an universal evaporation technique described in a previous paper. The results are¹⁸⁰Hfg _j (³ F ₂)=0.695812 (10)¹⁷⁷Hf Δv(³ F ₂;F=11/2?F=9/2)=991.7917 (10) MHz Δv(³ F ₂;F=9/2?F=7/2)=477.0081 (10) MHz Δv(³ F ₂;F=7/2?F=5/2)=162.8890 (10) MHz¹⁷⁹HfΔv(³ F ₂;F=13/2?F=11/2)=82.1320 (10) MHz Δv(³ F ₂;F=11/2?F=9/2)=392.8498 (10) MHz. The magnetic dipole and electric quadrupole moments of the¹⁷⁷Hf and¹⁷⁹Hf nuclear ground states as calculated from these hyperfine structure measurements are the following: μ(177)=0.75(8)μ _k , Q(177)=4.34 (65) barns μ(179)=?0.61 (6)μ _k , Q(179)=4.90 (75) barns.     

Thermal evidences for successive CDW phase transitions in 1T-TaS2

The heat capacity of 1T-TaS₂ has been measured over the temperature range including the successive phase transitions (140 K–370 K) by an adiabatic calorimeter. There are three transitions in the measured temperature range, two first-order transitions (at about 226 K (T₁) and about 353.5 K (T₃)) and one small anomaly at about 283 K (T₂) with a broad peak. The transition enthalpies are as follows; ΔH₁=52±5 cal·mol^-1, ΔH₂=7.5±2 cal· mol^-1 and ΔH₃=122±8cal·mol^-1.     

Hyperfine structure investigations of some odd levels of Co I by level crossing and optical methods

Using the level crossing technique the ratios and absolute values of the hyperfine structure (hfs) constants of the levelsz ⁴F_9/2 andz ⁴F_7/2 of the configuration 3d ⁷4s4p of Co I were measured:z ⁴ F _9/2: ¦A¦=(811±12)MHz; ¦B¦=(48±93) MHz;B/A=?0.06±0.11 A>0; B<0z ⁴ F _7/2: ¦A¦ = (659 ±11)MHz; ¦B¦=(33±84)MHz;B/A=?0.05±0.13 A>0; B<0. In addition the hfs constants of three other excited levels of Co I could be determined by optical methods:z ⁴ F _9/2:A=525±26 MHz;B=200 MHzy ⁴ F _9/2:A=300±30 MHz;B=?500 MHzy ⁴ G _11/2:A=315±20 MHz;B=400 MHz. The experimental results are compared with known experimental and also with theoretical values which where calculated using the parametric potential method.     

Die Hyperfeinstruktur des angeregten 32P3/2-Zustandes von Natrium

The hyperfine structure of the 3²P_3/2-state in the Na(I)-spektrum was investigated by optical double resonance. Three zero fieldrf-transitions (ΔF=±1, Δm_F=0) were detected and thus the unambiguous interpretation of therf-spectrum was made possible. From an analysis of therf-spectrum one obtains the magnetic hyperfine structure splitting constant a=(18.5 _?0.2 ^+0.6 ) Mc/sec the electric quadrupole interaction constantb=(3.2±0.5) Mc/sec which yields an electric quadrupole moment Q(Na²³)=(0.138±0.025)·10²⁴cm².     

Hyperfine-structure and isotope-shift measurements in the 6s 5d↔6p 5d transitions of Ba I in the far-red spectral region

Measurements of the hyperfine structures in the 6p5d ¹ D ₂,³ D ₁ and³ F _{2, 3, 4} states of¹³⁵Ba and¹³⁷Ba, and isotope-shifts in several far-red transitions between the 6s 5d and 6p 5d configurations, as well as the transition 6s ^{2 1} S ₀→6s6p ³ P ₁ at 7,911 Å have been performed using high-resolution laser spectroscopy on a collimated atomic beam of natural barium. An analysis of the magnetic-dipole interaction in the 6p 5d configuration using effective one- and two-body hyperfine operators is presented. In particular the contact interaction was studied with respect to the correlation between the two valence electrons. Effects of strong configuration interaction were found. From a King-plot analysis of the isotope shift term- andJ-dependence of the field shift have been evaluated for the transitions between the 6s 5d and 6p 5d configurations. Relativistic Hartree-Fock (RHF) calculations have been performed of electron densities at the nucleus for six different configurations in Ba I and Ba II. The RHF calculations reproduce the experimental King-plot slopes quite well, while the absolute values, of the changes in electron density at the nucleus for the studied transitions, are found to be 9% lower than the results derived from a muonic experiment.     

Mode-crossing signals of high order on the 4d 95s 2 2 D 5/2 state of Cd II isotopes

In the linearly polarized radiation field of a 442 nm He-Cd laser containing a natural isotope mixture, saturation-induced mode-crossing signals of the 4d ⁹5s ^{2 2} _5/2 state of Cd II are observed due to the even as well as the odd isotopes. The signal width of about 10^?4 T yields high resolution. Thus the signal splitting respective to the magnetic quantum number can be resolved. Theg _J - andg _F -factors of the² D _5/2 state are determined as follows:g _J=1.1980±0.0036,g _F(F=2)=1.397±0.008,g _F(F=3)=1.002±0.009.     

Investigation of hyperfine structure and isotope shift of the 605.5 nm-line of Lu176 by laser spectroscopy

Using a tunable single mode dye laser the hyperfine structure of the transition 5d6s ^{2 2} D _5/2 — 5d6s6p ⁴ F _5/2 has been investigated for the Lu-isotopes Lu¹⁷⁵ and Lu¹⁷⁶. From our measurements the following values for the hyperfine constantsA andB could be deduced Lu¹⁷⁶ 5d6s6p ⁴ F _5/2:A=698.4 (0.4) MHz,B=1,564 (10) MHz 5d6s ^{2 2} D _5/2:A=104.1 (0.3) MHz.B=2,631 (6) MHz Lu¹⁷⁵ 5d6s6p ⁴ F ^5/2:A=987.2(0.4) MHz,B=1,117(6) MHz. The isotope shift between the line centers has been determined to be IS(176-175, 605.5 nm)=?420(10) MHz.     

Submillimeter-wave spectroscopy of VN (XΔr) and VO (XΣ): A study of the hyperfine interactions

The pure rotational spectra of VN (X³Δ_r) and VO (X⁴Σ⁻) have been recorded in the frequency range 290-520 GHz using direct absorption spectroscopy. These radicals were synthesized in the gas-phase from the reaction of VCl₄ with either N₂ or H₂O in an AC discharge. Seven rotational transitions were recorded for each molecule; in both sets of spectra, fine and hyperfine structures were resolved. The data sets for VN and VO were fit with Hund’s case (a) and case (b) Hamiltonians, respectively, and rotational, fine structure, and hyperfine constants determined. For VN, however, an additional hyperfine parameter, Δa, was necessary for the analysis of the Ω = 2 sublevel to account for perturbations from a nearby ¹Δ state, in addition to the usual Frosch and Foley constants. Determination of Δa suggests that the ¹Δ state lies ∼3000 cm⁻¹ above the ground state. In VO, the hyperfine structure in the F₂ and F₃ components was found to become heavily mixed due to an avoided crossing, predicted by previous optical studies to be near the N = 15 level. The hyperfine constants established for these two molecules are consistent with the proposed σ¹δ¹ and σ¹δ² electron configurations.     

Optical pumping of free atomic ions with hyperfine structure

Free atomic ions with hyperfme structure have been oriented m He buffer gas by absorption of circularly polarized light. ΔF=±1 hyperfine transitions have been measured in the 6² S _1/2 ground state of¹³⁵Ba⁺ and¹³⁷Ba⁺ with an accuracy of 1 part in 10⁷.     

Effect of cascading of higher-lying states on a delayed 1s-2p transition after beam-foil excitation of 56 MeV hydrogen-like oxygen and fluorine

The delayed fluorescence of the soft X-ray (1s-2p) transition was observed for H-like ions (O⁷⁺ and F⁸⁺) between 1.3 ns and 20 ns decay time after beam-foil excitation. The delayed X-ray fluorescence was found to decay with at ^Δ power law time dependence. The non-exponential decay is attributed to cascading through higher lying states. We found thatΔ ₀=1.40±0.08 andΔ _F =1.44±0.02 for H-like oxygen and fluorine, respectively. Present results are in fair agreement with the previously reported exponent,Δ ₀=1.5, measured over 3 ns after excitation.