Hyperfeinstruktur- und Stark-Effekt-Untersuchungen der Terme 4d5s5p z 2 F 5/2 undz 2 F 7/2 im Yttrium I Spektrum

The hyperfine structure and the Stark effect shift of the 4d5s5p z ² F _5/2 states in the Y I spectrum were investigated by level-crossing technique. Between the Zeeman effect region and the Paschen-Back region of hyperfine structure states some of the levels cross. The resonance radiation of these coherently excited levels show an interference effect of the scattering amplitudes in the crossing region. The level-crossing signals give information about hfs splitting and lifetime of the excited states under investigation. The magnetic hfs splitting factorsA of the 4d5s5p z ² F _{5/2, 7/2} states and their lifetimes were deduced. $$\begin{gathered} |A (z^2 F_{5/2} )| = (23.8 \pm 0.04) MHz \frac{{g_J }}{{0.854}} \hfill \\ |A (z^2 F_{7/2} )| = (84.08 \pm 0.01) MHz \frac{{g_J }}{{1.148}} \hfill \\ \tau (z^2 F_{5/2} ) = (46 \pm 3) 10^{ - 9} s \frac{{0.854}}{{g_J }} \hfill \\ \tau (z^2 F_{7/2} ) = (44 \pm 4) 10^{ - 9} s \frac{{1.148}}{{g_J }}. \hfill \\ \end{gathered} $$ With an electric field parallel to the magnetic field a shift of the level-crossing signals of the 4d5s5p z ² F _{5/2, 7/2} states was observed, and the Stark constants β were deduced. $$\begin{gathered} |\beta (z^2 F_{5/2} )| = (0.0020 \pm 0.0002) MHz/(kV/cm)^2 \hfill \\ |\beta (z^2 F_{7/2} )| = (0.0025 \pm 0.0015) MHz/(kV/cm)^2 . \hfill \\ \end{gathered} $$      

Nuclear orientation and NMR/ON of205,207Po

^205,207Po have keen implanted with an isotope separator on-line into cold host matrices of Fe, Ni, Zn and Be. Nuclear magnetic resonance of oriented²⁰⁷Po has been observed in Fe and Ni, of²⁰⁵Po in Fe. The resonance frequencies for zero external field are $$\begin{gathered} v_L (^{207} Po\underline {Fe} ) = 575.08(20)MHz \hfill \\ v_L (^{207} Po\underline {Ni} ) = 160.1(8)MHz \hfill \\ v_L (^{205} Po\underline {Fe} ) = 551.7(8)MHz. \hfill \\ \end{gathered} $$ From the dependence of the resonance frequency on external magnetic field theg-factor of²⁰⁷Po was derived as $$g(^{207} Po) = + 0.31(22).$$ Using this value the magnetic hyperfine fields of Po in Fe and Ni were obtained as $$\begin{gathered} B_{hf} (Po\underline {Fe} ) = + 238(16)T \hfill \\ B_{hf} (Po\underline {Ni} ) = 66.3(4.6)T. \hfill \\ \end{gathered}$$ Theg-factor of²⁰⁵Po follows as $$g(^{205} Po) = + 0.304(22).$$ From the temperature dependence of the anisotropies ofγ-lines in the decay of^205,207Po the multipole mixing of several transitions was derived. The electric interaction frequenciesv _Q=eQV_zz/h in the hosts Zn and Be were measured as $$\begin{gathered} v_Q (^{207} Po\underline {Zn} ) = + 42(3)MHz \hfill \\ v_Q (^{207} Po\underline {Be} ) = - 70(20)MHz \hfill \\ v_Q (^{205} Po\underline {Be} ) = - 42(17)MHz. \hfill \\ \end{gathered}$$      

Hyperfine structure,g j factors and lifetimes of excited2 P 1/2 states of Rb

The hyperfine structure of the 6² P _1/2 and 7² P _1/2 state of⁸⁵Rb and⁸⁷Rb and of the 6² P _3/2 state of⁸⁷Rb has been investigated with optical double resonance at intermediate magnetic fields. The magnetic interaction constants,g _j factors and lifetimes are: $$\begin{gathered} 6^2 P_{1/2} state: A\left( {^{85} Rb} \right) = 39.11\left( 3 \right) MHz,A\left( {^{87} Rb} \right) = 132.56 \left( 3 \right)MHz, \hfill \\ g_j = 0.6659\left( 3 \right), \tau = 1.14\left( {13} \right) \cdot 10^{ - 7} \sec , \hfill \\ 7^2 P_{1/2} state: A\left( {^{85} Rb} \right) = 17.68\left( 8 \right)MHz,A\left( {^{87} Rb} \right) = 59.92\left( 9 \right)MHz, \hfill \\ g_j = 0.6655\left( 5 \right), \hfill \\ 6^2 P_{3/2} state: g_j = 1.3337\left( {10} \right), \tau = 1.12\left( 8 \right) \cdot 10^{ - 7} \sec for ^{87} Rb. \hfill \\ \end{gathered} $$ From the hfs coupling constants of then ² P multiplets a 11.5% core polarization contribution to the magnetic hfs of then ² P _3/2 states is obtained, which is found to be independent from the main quantum numbern. The expectation values <r ^?3> _j for thenp valence electrons corrected for core polarization are compared with those derived from the² P fine structure separation. Good agreement is achieved for allnp levels with the choice ofZ _i =Z?3=34 for the effective nuclear charge number. The nuclear quadrupole moments of⁸⁵Rb and⁸⁷Rb are rederived on the basis of this more improved treatment for thep-electron-nucleus interaction yielding $$\begin{gathered} Q_N \left( {^{85} Rb} \right) = + 0.274\left( 2 \right) \cdot 10^{ - 24} cm^2 \hfill \\ Q_N \left( {^{85} Rb} \right) = + 0.132\left( 1 \right) \cdot 10^{ - 24} cm^2 \hfill \\ \end{gathered} $$ where the error does not include the remaining theoretical uncertainty of about 10%.     

Gleichzeitige Messung von Hyperfeinstruktur,Starkeffekt und Zeemaneffekt des23Na19F mit einer Molekülstrahl-Resonanzapparatur

An electric molecular beam resonance spectrometer has been used to measure simultaneously the Zeeman- and Stark-effect splitting of the hyperfine structure of²³Na¹⁹F. Electric four pole lenses served as focusing and refocusing fields of the spectrometer. A homogenous magnetic field (Zeeman field) was superimposed to the electric field (Stark field) in the transition region of the apparatus. The observed (Δm _J=±1)-transitions were induced electrically. Completely resolved spectra of NaF in theJ=1 rotational state have been measured in several vibrational states. The obtained quantities are: The electric dipolmomentμ _el of the molecule forv=0, 1 and 2, the rotational magnetic dipolmomentμ _J forv=0, 1, the difference of the magnetic shielding (σ _⊥-σ _‖) by the electrons of both nuclei as well as the difference of the molecular susceptibility (ξ _⊥-ξ _‖), the spin rotational constantsc _F andc _Na, the scalar and the tensor part of the molecular spin-spin interaction, the quadrupol interactione q Q forv=0, 1 and 2. The numerical values are

$$\begin{gathered} \mu _{\mathfrak{e}1} = 8,152(6) deb \hfill \\ \frac{{\mu _{\mathfrak{e}1} (v = 1)}}{{\mu _{\mathfrak{e}1} (v = 0)}} = 1,007985 (7) \hfill \\ \frac{{\mu _{\mathfrak{e}1} (v = 2)}}{{\mu _{\mathfrak{e}1} (v = 1)}} = 1,00798 (5) \hfill \\ \mu _J = - 2,89(3)10^{ - 6} \mu _B \hfill \\ \frac{{\mu _J (v = 0)}}{{\mu _J (v = 1)}} = 1,020 (13) \hfill \\ (\sigma _ \bot - \sigma _\parallel )_{Na} = - 51(12) \cdot 10^{ - 5} \hfill \\ (\sigma _ \bot - \sigma _\parallel )_F = - 51(12) \cdot 10^{ - 6} \hfill \\ (\xi _ \bot - \xi _\parallel ) = - 1,59(120)10^{ - 30} erg/Gau\beta ^2 \hfill \\ {}^CNa/^h = 1,7 (2)kHz \hfill \\ {}^CF/^h = 2,2 (2)kHz \hfill \\ {}^dT/^h = 3,7 (2)kHz \hfill \\ {}^dS/^h = 0,2 (2)kHz \hfill \\ eq Q/h = - 8,4393 (19)MHz \hfill \\ \frac{{eq Q(v = 0)}}{{eq Q(v = 1)}} = 1,0134 (2) \hfill \\ \frac{{eq Q(v = 1)}}{{eq Q(v = 2)}} = 1,0135 (2) \hfill \\ \end{gathered} $$     

An expansion of Hartree-Fock and correlation energies,relativistic corrections and the dipole matrix element in the powers of of 1/Z

Feynman diagrammatic technique was used for the calculation of Hartree-Fock and correlation energies, relativistic corrections, dipole matrix element. The whole energy of atomic system was defined as a polen-electron Green function. Breit operator was used for the calculation of relativistic corrections. The Feynman diagrammatic technique was developed for 〈H_B>. Analytical expressions for the contributions from diagrams were received. The calculations were carried out for the terms of such configurations as 1s² 2sⁿ¹ 2pⁿ² (2 ≧n₁≧ 0, 6≧ n₂ ≧ 0). Numerical results are presented for the energies of the terms in the form $$E = E_0 Z^2 + \Delta {\rm E}_2 + \frac{1}{Z}\Delta {\rm E}_3 + \frac{{\alpha ^2 }}{4}(E_0^r + \Delta {\rm E}_1^r Z^3 )$$ and for fine structure of the terms in the form $$\begin{gathered} \left\langle {1s^2 2s^{n_1 } 2p^{n_2 } LSJ|H_B |1s^2 2s^{n_1 \prime } 2p^{n_2 \prime } L\prime S\prime J} \right\rangle = \hfill \\ = ( - 1)^{\alpha + S\prime + J} \left\{ {\begin{array}{*{20}c} {L S J} \\ {S\prime L\prime 1} \\ \end{array} } \right\}\frac{{\alpha ^2 }}{4}(Z - A)^3 [E^{(0)} (Z - B) + \varepsilon _{co} ] + \hfill \\ + ( - 1)^{L + S\prime + J} \left\{ {\begin{array}{*{20}c} {L S J} \\ {S\prime L\prime 2} \\ \end{array} } \right\}\frac{{\alpha ^2 }}{4}(Z - A)^3 \varepsilon _{cc} . \hfill \\ \end{gathered} $$ Dipole matrix elements are necessary for calculations of oscillator strengths and transition probabilities. For dipole matrix elements two members of expansion by 1/Z have been obtained. Numerical results were presented in the form P(a,a′) = a/Z(1+τ/Z).     

Ground state hyperfine structure and nuclear magnetic dipole moments of177Hf and179Hf

Using the atomic beam magnetic resonance method the experimental hyperfine structure data of the 5d ²6s ^{2 3} F ₂ ground state of¹⁷⁷Hf and¹⁷⁹Hf described in a previous paper [1] have been completed. After applying corrections due to perturbations by other fine structure levels of the configuration 5d ²6s ² we got the following multipole interaction constants: $$\begin{gathered} ^{177} Hf:A = 113.43314 (7) MHz B = 624.3293 (13) MHz \hfill \\ C = 0.27 (18) KHz D = 0.045 (40) KHz \hfill \\ ^{179} Hf: A = - 71.42891 (9) MHz B = 705.5181 (24) MHz \hfill \\ C = - 0.43 (20) MHz D = 0.07 (6) KHz. \hfill \\ \end{gathered} $$ By measuring rf transitions at magnetic fields between 1100 and 1550 Gauss the nuclear ground state magnetic dipole moments were determined. The results are: $$\mu _I (^{177} Hf) = 0.7836 (6) \mu _N , \mu _I (^{179} Hf) = - 0.6329 (13) \mu _N $$ (uncorrected for diamagnetic shielding).     

Gyromagnetic ratios of collective states of166Er

The static hyperfine field ofB _hf ^4.2k (ErHo) = 739(18)T of a ferromagnetic holmium single crystal polarized in an external magnetic field of ± 0.48T at ～4.2K was used for integral perturbed γ-γ angular correlation (IPAQ measurements of the g-factors of collective states of¹⁶⁶Er. The 1,200y ^166m Ho activity was used which populates the ground state band and the γ vibrational band up to high spins. The results: $$\begin{gathered} g(4_g^ + ) = + 0.315(16) \hfill \\ g(6_g^ + ) = + 0.258(11) \hfill \\ g(8_g^ + ) = + 0.262(47)and \hfill \\ g(6_\gamma ^ + ) = + 0.254(32) \hfill \\ \end{gathered}$$ exhibit a significant reduction of the g-factors with increasing rotational angular momentum. The followingE2/M1 mixing ratios of interband transitions were derived from the angular correlation coefficients: $$\begin{gathered} 5_\gamma ^ + \Rightarrow 4_g^ + :\delta (810keV) = - (36_{ - 7}^{ + 11} ) \hfill \\ 7_\gamma ^ + \Rightarrow 6_g^ + :\delta (831keV) = - (18_{ - 2}^{ + 3} )and \hfill \\ 7_\gamma ^ + \Rightarrow 8_g^ + :\delta (465keV) = - (63_{ - 12}^{ + 19} ). \hfill \\ \end{gathered}$$ The results are discussed and compared with theoretical predictions.     

Gleichzeitige Messung von Hyperfeinstruktur,Starkeffekt und Zeemaneffekt des133Cs19F mit einer Molekülstrahl-Resonanzapparatur

An electric molecular beam resonance spectrometer has been used to measure simultaneously the Zeeman- and Stark-effect splitting of the hyperfine structure of¹³³Cs¹⁹F. Electric four pole lenses served as focusing and refocusing fields of the spectrometer. A homogenous magnetic field (Zeeman field) was superimposed to the electric field (Stark field) in the transition region of the apparatus. Electrically induced (Δ m _J =±1)-transitions have been measured in theJ=1 rotational state, υ=0, 1 vibrational state. The obtained quantities are: The electric dipolmomentμ _el of the molecule for υ=0, 1; the rotational magnetic dipolmomentμ _J for υ=0, 1; the anisotropy of the magnetic shielding (σ _⊥-σ‖) by the electrons of both nuclei as well as the anisotropy of the molecular susceptibility (ξ _⊥-ξ‖), the spin rotational interaction constantsc _Cs andc _F, the scalar and the tensor part of the nuclear dipol-dipol interaction, the quadrupol interactioneqQ for υ=0, 1. The numerical values are:

$$\begin{gathered} \mu _{el} \left( {\upsilon = 0} \right) = 73878\left( 3 \right)deb \hfill \\ \mu _{el} \left( {\upsilon = 1} \right) - \mu _{el} \left( {\upsilon = 0} \right) = 0.07229\left( {12} \right)deb \hfill \\ \mu _J /J\left( {\upsilon = 0} \right) = - 34.966\left( {13} \right) \cdot 10^{ - 6} \mu _B \hfill \\ \mu _J /J\left( {\upsilon = 1} \right) = - 34.823\left( {26} \right) \cdot 10^{ - 6} \mu _B \hfill \\ \left( {\sigma _ \bot - \sigma _\parallel } \right)_{Cs} = - 1.71\left( {21} \right) \cdot 10^{ - 4} \hfill \\ \left( {\sigma _ \bot - \sigma _\parallel } \right)_F = - 5.016\left( {15} \right) \cdot 10^{ - 4} \hfill \\ \left( {\xi _ \bot - \xi _\parallel } \right) = 14.7\left( {60} \right) \cdot 10^{ - 30} erg/Gau\beta ^2 \hfill \\ c_{cs} /h = 0.638\left( {20} \right)kHz \hfill \\ c_F /h = 14.94\left( 6 \right)kHz \hfill \\ d_T /h = 0.94\left( 4 \right)kHz \hfill \\ \left| {d_s /h} \right|< 5kHz \hfill \\ eqQ/h\left( {\upsilon = 0} \right) = 1238.3\left( 6 \right) kHz \hfill \\ eqQ/h\left( {\upsilon = 1} \right) = 1224\left( 5 \right) kHz \hfill \\ \end{gathered} $$     

Polarization-optical and X-ray diffraction investigations on the symmetry of distorted phases of ammonium cryolite (NH4)3 ScF6

Single-crystal plates of different sections of the (NH₄)₃ScF₆ crystal have been investigated by polarization-optical microscopy and X-ray diffraction over a wide temperature range, including the temperatures of two known phase transitions and the third transition found recently. It is established that the symmetry of 5 phases changes in the following sequence: $\begin{gathered} O_h^5 - Fm3m(Z = 4) \leftrightarrow C_{2h}^5 - {{P12_1 } \mathord{\left/ {\vphantom {{P12_1 } {n1}}} \right. \kern-0em} {n1}}(Z = 2) \leftrightarrow C_{2h}^3 - {{I12} \mathord{\left/ {\vphantom {{I12} {m1}}} \right. \kern-0em} {m1}} \\ (Z = 16) \leftrightarrow C_i^1 - I\bar 1(Z = 16) \\ \end{gathered} $ .     

The band spectrum of SbO: A new doublet system

The band spectrum of SbO was excited in a heavy current discharge from a 2000 volt D. C. generator. A new doublet system of bands occurring in the region λ 2800 toλ 3600 arising from a transition of the type²Δ_r?² Π _r was identified. The lower² Π _r state is found to be common to those of the three band systems reported earlier, which is in all probability the ground state of the SbO molecule. The band heads of the high frequency and low frequency components could be represented by the following quantum formulae:

$$\begin{gathered} ^2 \Delta _{\tfrac{3}{2}} - ^2 \Pi _{\tfrac{1}{2}} : \hfill \\ v = 29754 \cdot 6 + 570 \cdot 6 (v' + \tfrac{1}{2}) - 3 \cdot 52 (v' + \tfrac{1}{2})^2 - 820 \cdot 5 (v'' + \tfrac{1}{2}) + 4 \cdot 62 (v'' + \tfrac{1}{2})^2 \hfill \\ ^2 \Delta _{\tfrac{5}{2}} - ^2 \Pi _{\tfrac{3}{2}} : \hfill \\ v = 28044 \cdot 8 + 568 \cdot 1 (v' + \tfrac{1}{2}) - 3 \cdot 28 (v' + \tfrac{1}{2})^2 - 819 \cdot 2 (v'' + \tfrac{1}{2}) + 4 \cdot 62 (v'' + \tfrac{1}{2})^2 . \hfill \\ \end{gathered} $$     

Alpha decay of neutron-deficient rhenium and osmium isotopes

Neutron-deficient osmium and rhenium isotopes were produced by bombarding an enriched¹⁴⁴Sm target with beams of²⁷Al and²⁸Si. Previously reported decay data concerning^168,169,170Os were confirmed. Three newα groups, observed in the¹⁴⁴Sm+²⁷Al reaction, were assigned to the decay of^166,167,168Re based on excitation functions,α-energy systematics and theoretical half-life predictions. Their decay properties are: $$\begin{gathered} {}^{166}\operatorname{Re} , E_\alpha = 5,372 (10) keV, T_{1/2} = 2.8 (3) s; \hfill \\ {}^{167}\operatorname{Re} , E_\alpha = 5,136 (8) keV, T_{1/2} = 6.1 (2) s and \hfill \\ {}^{168}\operatorname{Re} , E_\alpha = 4,894 (10) keV, T_{1/2} = 6.9 (8) s. \hfill \\ \end{gathered}$$ It is proposed that twoα groups, observed in the¹⁴⁴Sm+²⁸Si reaction, originate from isomeric states in^168,169Re. Our measured data for the isomeric states are: $$\begin{gathered} {}^{168m}\operatorname{Re} , E_\alpha = 5,250 (10) keV, T_{1/2} = 6.6 (15) s and \hfill \\ {}^{169m}\operatorname{Re} , E_\alpha = 5,050 (10) keV, T_{1/2} = 12.9 (11) s. \hfill \\ \end{gathered} $$      

Nuclear quadrupole moments of radioactive83Rb,84Rb and86Rb

Excited atomic² P _3/2-states of radioactive Rb isotopes have been investigated by level crossing and optical double resonance spectroscopy. The measured hyperfine structure constants yielded the nuclear moments $$\begin{gathered} \mu _I (^{84} Rb) = - 1.296(11)\mu _K Q(^{83} Rb) = + 0.27(5) \cdot 10^{ - 24} cm^2 \hfill \\ Q(^{84} Rb) = + 0.005(13) \cdot 10^{ - 24} cm^2 \hfill \\ Q(^{86} Rb) = + 0.20(3) \cdot 10^{ - 24} cm^2 \hfill \\ \end{gathered} $$ and the hyperfine anomaly₈₄Δ₈₅=+1.7(1.0) · 10^?2. The quadrupole moments of⁸³Rb to⁸⁷Rb can be explained with the unified model of vibrations.     

Detection of a hexadecapole interaction in the atomic ground state3 H 6 of167Er

Using the atomic beam magnetic resonance method, precision measurements of the hyperfine structure and Zeeman interactions have been performed in the ground state 4f ¹²6s ^{2 3} H ₆ of¹⁶⁷Er. The experimental data were analyzed using an effective operator parametrized in the space of states of the ground state multiplet. It yielded eight effective hyperfine structure and Zeeman interaction constants which served to calculate the seven hyperfine separations of the ground state. The results are: $$\begin{gathered} 2F 2F' v_{FF'} (MHz) \hfill \\ 5 7 - 354.371 9409 (27) \hfill \\ 7 9 - 2{\text{78}}{\text{.231}} {\text{8263(14)}} \hfill \\ {\text{9}} 11 - 69.050 7785 (4) \hfill \\ 11 13 + 302.735 3731(12) \hfill \\ 13 15 + 866.691 3871(10) \hfill \\ 15 17 + 1,652.383 5154 (6) \hfill \\ 17 19 + 2,689.380 8050(10) \hfill \\ \end{gathered}$$ From the effective Zeeman interaction constants it was possible to determine an improvedg _I -value, uncorrected for atomic diamagnetism: $$ g_I = + 0.086 775 (19) \cdot 10^{ - 3}$$ Furthermore a hexadecapole interaction corresponding to a diagonal hexadecapole interaction constant $$A_4 = - 16 (10) Hz$$ could be established which is of the order of magnitude expected from Coulomb excitation experiments as well as theoretical calculations.     

Search for rare radiative decays ofΦ-meson at VEPP-2M

Results of the search for rare radiative decay modes of the ?-meson performed with the Neutral Detector at the VEPP-2M collider are presented. For the first time upper limits for the branching ratios of the following decay modes have been placed at 90% confidence level: $$\begin{gathered} B(\phi \to \eta '\gamma )< 4 \cdot 10^{ - 4} , \hfill \\ B(\phi \to \pi ^0 \pi ^0 \gamma )< 10^{ - 3} , \hfill \\ B(\phi \to f_0 (975)\gamma )< 2 \cdot 10^{ - 3} , \hfill \\ B(\phi \to H\gamma )< 3 \cdot 10^{ - 4} , \hfill \\ \end{gathered} $$ whereH is a scalar (Higgs) boson with a mass 600 MeV<m _H <1000 MeV, the real measurement isB(φ→H γ)·B(H→2π⁰)<0.8·10^-4, the quoted result is model dependent, as explained in the text, $$\begin{gathered} B(\phi \to a\gamma ) \cdot B(a \to e^ + e^ - )< 5 \cdot 10^{ - 5} , \hfill \\ B(\phi \to a\gamma ) \cdot B(a \to \gamma \gamma )< 2 \cdot 10^{ - 3} , \hfill \\ \end{gathered} $$ wherea is a particle with a low mass and a short lifetime, $$B(\phi \to a\gamma )< 0.7 \cdot 10^{ - 5} ,$$ wherea is a particle with a low mass not observed in the detector.     

Determination of hyperfine interactions from partly resolved moessbauer spectra

Moessbauer spectra with different sets of parameters were calculated. A fit with a superposition of Lorentzians to these theoretical spectra showed, that systematic errors must be expected if the hyperfine structure of the spectrum is only partly resolved. Correction factors for some simple cases are given. Experiments to test the calculations were performed with¹³³Cs (81 keV transition),¹⁶⁵Ho (94.7 keV transition) and¹⁷⁸Hf (93 keV transition). In all cases fits using the transmission integral and superpositions of Lorentzians showed the expected trends. We get the following results: $$\begin{gathered} ^{133} Cs:\frac{{g_{ex} }}{{g_{gr} }} = 1.90\left( 4 \right) \hfill \\ ^{165} Ho:\tau \left( {94.7keVlevel} \right) = 32\left( 1 \right)ps \hfill \\ \frac{{g_{ex} }}{{g_{gr} }} = 0.77\left( 3 \right) \hfill \\ ^{178} Hf:|H_{eff} \left( {4K,in iron} \right)| = 633\left( {40} \right)KG \hfill \\ |H_{eff} \left( {77K,in iron} \right)| = 630\left( {41} \right)KG. \hfill \\ \end{gathered}$$      

Mössbauer study of197Au in Zn and Cd single crystals

The 77.3 keV Mössbauer transition of¹⁹⁷Au was used to study the hyperfine interactions and recoilfree fractions of dilute Au impurities in Zn and Cd single crystals at 4 K. Mössbauer sources were prepared by ion implantation of^197mHg/¹⁹⁷Hg at ambient temperature. From the quadrupole splittings the electric field gradients $$\begin{gathered} eq(Au\underline {Cd} ) = + 11.7(6) \times 10^{17} v/cm^2 and \hfill \\ eq(Au\underline {Zn} ) = ( + )15.0(2.5) \times 10^{17} v/cm \hfill \\ \end{gathered} $$ were determined. The electric field gradients as well as the isomer shifts are in good agreement with the systematics of other impurity host systems. The recoilfree fractions agree with estimates using the mass corrected Debye temperatures of the host lattice.     

Lifetimes andg J factors of 6s7p and 5d6p levels of Ba I

Excited states of Ba have been investigated with optical double resonance and Hanle effect. The followingg _J factors and natural lifetimes (in 10^?9 sec) have been measured $$\begin{gathered} 6s7p\left\{ {\begin{array}{*{20}c} {^1 P_1 :g_J = 1.003(2)\tau = 13.5(6)} \\ {^3 P_1 :g_J = 1.4971(8)\tau = 85.0(8.0)} \\ \end{array} } \right. \hfill \\ 5d6p\left\{ {\begin{array}{*{20}c} {^1 P_1 :g_J = 1.004(2)\tau = 12.4(9)} \\ {^3 P_1 :g_J = 1.4847(15)\tau = 11.7(9)} \\ {^3 D_1 :g_J = 0.5064(3)\tau = 17.0(5).} \\ \end{array} } \right. \hfill \\ \end{gathered}$$ g _J is utilized to test the mixing coefficients of the wave functions in the intermediate coupling model. The lifetimes are converted into absolute transition probabilities for all the decays originating from the states investigated under the assumption that their branching ratios obtained elsewhere are correct. This assumption is not unquestionable, however.     

Internal magnetic hyperfine fields at Hf nuclei in iron,cobalt and nickel hosts

Integral perturbed angular correlation technique has been used to measure the internal hyperfine magnetic fields at Hf nuclei in Fe, Co and Ni matrices. These represent a consistent set of measurements with diffused sources. The 9+/2 (208 keV) 9?/2 (113 keV) 7?/2 cascade in the decay of¹⁷⁷Lu→¹⁷⁷Hf was used for measurements. The results obtained are: $$\begin{gathered} H_{Fe}^{Hf} = - 266 \pm 47 kG, \hfill \\ H_{Co}^{Hf} = - 116 \pm 18 kG, \hfill \\ H_{Ni}^{Hf} = - 118 \pm 26 kG. \hfill \\ \end{gathered} $$ These measurements are compared with previous results and discussed in terms of methods of source preparation.     

Covariant differential calculus on the quantum exterior vector space

We formulate a differential calculus on the quantum exterior vector space spanned by the generators of a non-anticommutative algebra satisfying

Three-loop on-shell charge renormalization without integration:\Lambda _{QED}^{\overline {MS} } to four loops

Using algebraic methods, we find the three-loop relation between the bare and physical couplings of one-flavourD-dimensional QED, in terms of Γ functions and a singleF ₃₂ series, whose expansion nearD=4 is obtained, by wreath-product transformations, to the order required for five-loop calculations. Taking the limitD→4, we find that the \(\overline {MS} \) coupling \(\bar \alpha (\mu )\) satisfies the boundary condition $$\begin{gathered} \frac{{\bar \alpha (m)}}{\pi } = \frac{\alpha }{\pi } + \frac{{15}}{{16}}\frac{{\alpha ^3 }}{{\pi ^3 }} + \left\{ {\frac{{11}}{{96}}\zeta (3) - \frac{1}{3}\pi ^2 \log 2} \right. \hfill \\ \left. { + \frac{{23}}{{72}}\pi ^2 - \frac{{4867}}{{5184}}} \right\}\frac{{\alpha ^4 }}{{\pi ^4 }} + \mathcal{O}(\alpha ^5 ), \hfill \\ \end{gathered} $$ wherem is the physical lepton mass and α is the physical fine structure constant. Combining this new result for the finite part of three-loop on-shell charge renormalization with the recently revised four-loop term in the \(\overline {MS} \) β-function, we obtain $$\begin{gathered} \Lambda _{QED}^{\overline {MS} } \approx \frac{{me^{3\pi /2\alpha } }}{{(3\pi /\alpha )^{9/8} }}\left( {1 - \frac{{175}}{{64}}\frac{\alpha }{\pi } + \left\{ { - \frac{{63}}{{64}}\zeta (3)} \right.} \right. \hfill \\ \left. { + \frac{1}{2}\pi ^2 \log 2 - \frac{{23}}{{48}}\pi ^2 + \frac{{492473}}{{73728}}} \right\}\left. {\frac{{\alpha ^2 }}{{\pi ^2 }}} \right), \hfill \\ \end{gathered} $$ at the four-loop level of one-flavour QED.