Determination of theg j -factor in the72 P 3/2-state of133Cs by optical double resonance in a strong magnetic field

The hfs in the 7² P _3/2-state of¹³³Cs has been investigated by optical double resonance in a strong magnetic field. From the positions of the magnetic dipole transitions Δm _j =± 1, Δm _i =0 the magnetic hfs coupling con slanta (7² P _3/2)=16.591(25) MHz and theg _j -factorg _j (7² P _3/2)=1.33410(15) could be derived. Contrarily to recent measurements,g _j agrees well with the value calculated from the Lande formula.     

Level crossing investigation of the 6p 2 P 3/2 and 7p 2 P 3/2 levels of Cs133, Cs135, and Cs137

The level crossing method has been used for the investigation of the hyperfine structure of the 6p²P_3/2 and 7p²P_3/2 levels of the isotopes Cs¹³³, Cs¹³⁵, and Cs¹³⁷. For the hyperfine coupling constants a and b and for the lifetimes Τ we find: a(6p Cs¹³³)=50.72(3) g_J/?1.345, b(6p Cs¹³³)=?0.38(18) g_J/?1.345 a(7p Cs¹³³)=16.610(6) g_J/?1.3349, b(7p Cs¹³³)=?0.15(3) g_J/?1.3349 a(6p Cs¹³⁵)=53.64(4) g_J/?1.345, b(6p Cs¹³⁵)=7.41(32) g_J/?1.345 a(7p Cs¹³⁵)=17.570(6) g_J/?1.3349, b(7p Cs¹³⁵)=2.35(7) g_J/?1.3349 a(6p Cs¹³⁷)=55.80(4) g_J/?1.345, b(6p Cs¹³⁷)=7.54(20) g_J/?1.345 a(7p Cs¹³⁷)=18.274(6) g_J/?1.3349, b(7p Cs¹³⁷)=2.37(4) g_J/?1.3349 (MHz), Τ(6p²P_3/2)=29.7(2) ?1.345/g_J ns, Τ(7p²P_3/2)=135(1) ?1.3349_Jns. From a comparison with double resonance results the g_J factor of the 7p²P_3/2 level was deduced: g_J(7p²P_3/2=?1.3349(10). Level crossing measurements in the 8p²P_3/2 state of Cs¹³³ give for the g_J factor and the lifetime the following results: g_J(8p²P_3/2)=?1.3353(14), Τ(8p²P_3/2)=310(15) ns. Using recently calculated relativistic correction factors and applying corrections for core polarization and the Sternheimer effect, we obtain for the quadrupole moments: Q(Cs¹³³)=?0.0030 b, Q(Cs¹³⁵)=+0.052 b, Q(Cs¹³⁷)=+0.052 b.     

Optical double resonance and zero field level crossing spectroscopy applied to the 5p 3 6s 5 S 2 level in the Te-I spectrum

As a first application of optical double resonance and zero field level crossing spectroscopy to the elements of the sixth group in the periodic table of the atoms, the 5p ³6s ⁵ S ₂ level in the Te-I spectrum was investigated using natural tellurium in a high temperature quartz cell. For the electronic Landé-factor and the natural radiative lifetime the following values were obtained: $$g_J \left( {5p^3 6s^5 S_2 } \right) = - 1.9657\left( {12} \right),\tau \left( {5p^3 6s^5 S_2 } \right) = 71.8\left( {2.2} \right)ns.$$      

Calculation of the hyperfine structure constants in 85Rb and 133Cs

For heavy atoms or ions, such as, Rb and Cs et al., relativistic effect must be considered in the calculation. In this paper, the relativistic many-body perturbation theory is used to solve the Dirac equation. And the zeroth-order hyperfine constants are evaluated with Dirac-Fock wave function. The finite basis sets of dirac equation are constructed by B-splines. With the finite basis sets the core polarization and the correlation diagrams are calculated. The hyperfine structure constants of the 5S1/2 and 6S1/2 states of 85Rb as well as the 6S1/2 and 7S1/2 states of 133Cs are evaluated.     

Orientation of Cs 6p 2P3/2 atomic photofragments in a magnetic field: interference in the photodissociation of diatomic molecules

In a magnetic field, Cs₂ molecules were excited from the ground X¹Σ⁺_g(v_X=0,J_X=55) level to the D ¹Σ⁺_u(v=46,J=54) level by dissociation laser light linearly polarized parallel to the field, for which the magnetic sublevels were degenerated and thus all the transitions between them were simultaneously stimulated. Probe laser light excited the dissociated Cs 6p²P_3/2 atomic fragments to 6p²D_3/2 level and the resultant 6p²P_1/2 - 6d²D_3/2 emission was detected as the function of the wavelength of the probe light. The populations of the 6p²P_3/2,mj magnetic sublevels were determined from the relative strengths of the 6p²P_3/2,mj - 6d²D_3/2,m'j transitions induced by the probe light. Non-zero orientation O₀ was found in the ensemble of dissociated Cs 6p²P_3/2 atomic fragments. The orientation O₀ increased as the magnetic field strength increased. It was demonstrated both experimentally and theoretically that the orientation O₀ was induced through the interference in the excitation and dissociation paths in the presence of an external magnetic field, even when all degenerated transitions between the magnetic sublevels of the molecules are simultaneously excited by the light linearly polarized parallel to the field.     

Bestimmung derg J-Faktoren in den Zuständen 62 P 3/2 und 82 P 3/2 von133Cs

The hyperfine structures of the 6² P _3/2- and 8² P _3/2-states of¹³³Cs have been investigated by optical double resonance in a strong magnetic field. The Landé-g-factors and the hfs coupling constants were found to be:g _J(6² P _3/2)=1.3340(3)g _J(8² P _3/2)=1.3342(2)a(6² P _3/2)=50.02(25) MHza(8² P _3/2)=7.644(25) MHz. Contrarily to recent measurements, theg _J-factors agree well with the value calculated from the Landé formula.     

Hyperfine structure of the 8p 2 P 3/2 and 8p 2 P 1/2 levels of115In

The hyperfine structure of the 8p ² P _3/2 and² P _1/2 levels of¹¹⁵In was measured using high-resolution laser spectroscopy on a collimated indium atomic beam. Step-wise excitations from the metastable 5² P _3/2 state via the shortlived 6s ² S _1/2 state were employed. For the magnetic-dipole and electric-quadrupole interaction constantsa andb, respectively, the following results were obtained:a(8p ² P _3/2)=16.3 (3) MHz,b(8p ² P _3/2)=11 (3) MHz anda(8p ² P _1/2)=44.0 (5) MHz. The magnetic hyperfine structure is shown to be strongly influenced by core polarization. For the electric-quadrupole moment of¹¹⁵In the valueQ=0.79 (20) barn is deduced.     

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.     

Core polarization of the133Cs atom by the 7p electron

The hfs of the 7² P _1/2 state of Cs has been measured by optical double resonance yieldingA(7² P _1/2,¹³³Cs)=94.35 (4) MHz. The core polarization contribution to the hfs and the value 〈r ^?3〉 _j =2.54 · 10⁺²⁴ cm^?3 of the 7p electron of Cs has been calculated from the experimental data and was compared with current theories indicating still an appreciable uncertainty in the atomic wave functions of this one-electron atom.     

Isotope shift and hyperfine structure of the transition5d6s 2 2 D 3/2-5d6s6p 4 F 3/2 of Lu175 and Lu176

Using a tunable single mode dye laser the isotope shift of the 573.7 nm-line between the isotopes Lu¹⁷⁵ and Lu¹⁷⁶ has been determined to be IS(176?175, 573.7 nm)=?394(5) MHz yielding a change of mean square nuclear radii ofδ〈r ²〉=0.022(5) fm². In addition from our measurements the following values of the hyperfine splitting constantsA andB could be deduced Lu¹⁷⁶ 5d6s6p ⁴ F _3/2:A=?651.4(0.3) MHz,B=2,494(4) MHz 5d6s ^{2 2} D _3/2:A=138.0(0.3) MHz,B=2,131(3) MHz Lu¹⁷⁵ 5d6s6p ⁴ F _3/2:A=?924.7(0.5) MHz,B=1,767(4) MHz.     

Analysis of the isotope shifts and hyperfine structure in the 3 988 Å (6s6p 1 P 1↔6s 2 1 S 0) YbI line

High-resolution laser spectroscopy using a pulsed dye-laser acting on a collimated atomic beam has been used to determine the isotope shifts in the 3 988 Å YbI line. The following results have been obtained:Δσ(176, 174)=?509(4)MHz,Δσ (174, 173)=?291(10) MHz,Δσ(174, 172)=?530(4) MHz,Δσ(172, 171)=?414(5) MHz andΔσ(172, 170)= ?665(10) MHz. The sign of the magnetic dipole interaction constant in the¹ P ₁ state for¹⁷¹Yb is found to be negative,a(¹ P ₁, 171)=?213.4(3.0) MHz. The electric quadrupole interaction constant for¹⁷³Yb in the¹ P ₁ state is found to beb(¹ P ₁, 173)=605(20) MHz.     

Precise measurement of hyperfine structure in the 52P1/2 state of Rb

We have measured hyperfine structure in the 5 ²P_1/2 state of Rb using a frequency-stabilized diode laser, which is locked to one hyperfine transition, and an acousto-optic modulator, whose frequency is locked to the interval of interest. We check for optical-pumping errors by repeating the measurement at different values of pump power in the saturated-absorption spectrometer. We obtain precise values of the hyperfine constant: A=120.645(5) MHz for ⁸⁵Rb and A=406.119(7) MHz for ⁸⁷Rb. The values resolve a large discrepancy between two earlier high-accuracy measurements on this state.     

Calculation of the hyperfine structure of the 42 S 1/2, 42 P 1/2, 42 P 3/2 states in the 3d 10 nl configuration of Cu

The hyperfine structure of the 4² S _1/2, 4² P _1/2, 4² P _3/2 states in the 3d ¹⁰ nl configuration of Cu has been evaluated using many-body perturbation theory. Polarisation effects were included in all orders and correlation to third-order. By the use of iteration methods, a large number of higher order diagrams were also included. The correlation effects between the valence electron and the 3d shell were found to be very important. The results forA(² S _1/2) andA(² P _1/2) 5827MHz and 440 MHz, respectively, are in good agreement with the experimental results, whereas the result forA(² P _3/2)=83 MHz is far from the experimental value. No explanation was found for the discrepancy. The quadrupole values were found to be ?206 mb for⁶³Cu and ?185 mb for⁶⁵Cu.     

Isotope shift in the resonance lines of the arc spectrum of133Cs,135Cs,and137Cs

Reactor Cs and mixtures of electromagnetically enriched Cs were used to investigate the isotopic shift of the two resonance lines. By a digital evaluation method anomalies in the isotope shift were found.     

Study of the formation of Cs inclusions in refractory bcc metals by133Xe(Cs) Mössbauer resonance

The formation and properties of Cs inclusions in Mo and W are observed through a preimplanted¹³³Xe(Cs) local probe, which is found to reside in three sites: a substitutional site, an interfacial one and a further site which is not detectable directly, but the presence of which can be inferred from the Mössbauer measurements. The location of the probe at the interface of small Cs inclusions is characterized by large Debye temperatures of around 200 K, a quadrupole interaction of +1.86(15) mms^–1, which is close to known surface site values, and an isomer shift of –0.33(12) mms^–1. From the latter value an approximate local pressure of 5 GPa is deduced. In W the site populations are followed as a function of Cs dose. The observed interchange of populations in the low dose range is thought to represent the initial formation of the second phase inclusions.     

Electron paramagnetic resonance spectroscopy of Cr 3+ in hexagonal Cs 2 NaGaF 6 crystals

Powder samples of hydrothermally grown Cr 3+ -doped Cs 2 NaGaF 6 crystals have been investigated with electron paramagnetic resonance spectroscopy at X - (9.5 v GHz) and Q -band (34 v GHz). Analysis of the spectra clearly demonstrates that there are two distinct Cr 3+ centres in the Cs 2 NaGaF 6 crystal, having nearly identical g factors, but differing largely from the viewpoint of their zero field splitting. By using the 53 Cr hyperfine spectra observed with electron nuclear double resonance spectroscopy, it is deduced that these centres have opposite signs for the zero field splitting. The spectroscopic properties of the Cr 3+ centres in the isostructural Cs 2 NaGaF 6 and Cs 2 NaAlF 6 crystals are compared and discussed.