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.     

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.     

Natural radiative lifetimes in the2S1/2 and2D5/2,3/2 sequences of aluminum

Natural radiative lifetimes have been measured for the 3s ² ns ² S _1/2 (n≦10) and 3s ² nd ² D _5/2,3/2 (n≦11) sequences of aluminum using pulsed laser excitation of an atomic beam. The investigated states were populated from the ground configuration using UV pulses of wavelength down to 210 nm produced by a Nd: YAG- or an excimer-pumped dye-laser system. TheS-state lifetimes increase regularily with increasing principal quantum number but this is not the case for theD sequence.     

Core polarisation effect on the 3p 1/2, 3p 3/2, 2f 5/2, 2f 7/2 and 1i 13/2 proton states of209Bi

The weak fragments of the 3p_1/2, 3p_3/2, 2f_5/2, 2f_7/2 and 1i_13/2 proton states of²⁰⁹Bi as seen in the²⁰⁸Pb (³He,d) reaction can be explained with the coupling of the renormalised proton states and the vibrational states of²⁰⁸Pb. The energies of the zerothorder proton shell-model states as well as the collective admixtures of the weak fragmented proton states of²⁰⁹Bi have been deduced from the core-particle coupling model.     

Velocity dependence of the chemi-ionization of H2O and D2O on impact of 21S and 23S helium atoms

The velocity dependence for the ionization of H₂O and D₂O to form H₂O⁺ and D₂O⁺ in collisions with both 2³S and 2¹S metastable helium atoms has been measured in a crossed molecular beam apparatus using a mechanical velocity-selector on the metastable beam. The cross-sections are found to be proportional to the —n power of the relative collision energy, with n ? 0.4 for both metastable atoms in both gases. The branching ratios H₂O⁺/OH⁺ and D₂O⁺/OD⁺ were both found to be 4.3 for both metastable helium atoms, and to be independent of the relative collision energy.     

Stark-Effekt-Untersuchungen in der Hyperfeinstruktur der 3s 2 3d 2 D 5/2- und2 D 3/2-Terme des Al I-Spektrums

The resonance fluorescence of the transitions 3d ² D _5/2,3/2 3p ² P _3/2,1/2 in the Al I-spectrum was observed as a function of a magnetic field. Adding an electric field parallel to the magnetic field the shifts of level crossing signals caused by the Stark effect of the electric field were used to separate overlapping signals of the 3d ² D _5/2- and 3d ² D _3/2-states. The following values of the Stark parametersβ of both states and the hyperfine structure constantsA andB of the 3d ² D _3/2-states were deduced: 3d ² D _3/2∶ ¦A¦=99(1) Me/sec · g_J/0,8,B/A=?0,22(12), ¦β¦=0.45 (8) Mc/sec/(kV/cm)² · g_J,/0.8, A/β< 0 3d²D_5/2∶ ¦β¦=0.16 (4) Mc/sec/(kV/cm)² · g_J/1.2, A/β>0. Some qualitative aspects of interconfiguration mixing in the 3d²D-states are discussed.     

On the properties of the 1s-forms of TaSe2 and TaS2

The 1s-forms of TaSe₂ and TaS₂ with octahedral coordination of the metal are diamagnetic; 1s-TaS₂ is a semiconductor at low temperature. The diamagnetism is explained by taking account of spin-orbit coupling which leads to a ground state with zero magnetic moment (g = 0). This spin-orbit coupling stabilizes the d¹ configuration of the metal with respect to d² + d⁰. Thus, it can be understood that 1s−TaS₂ is semiconducting, while isostructural VSe₂ is metallic. Similarly, BaTaS₂ and BaTaSe₃ are semiconductors, but BaVS₃ is metallic.     

Fragmented 2d 5/2, 1g 7/2 and 1g 9/2 deep proton-hole states of207TI

The three proton-hole states ?2d_5/2, 1g_7/2 and 1g_9/2 are found to be fragmented as a result of coupling of these states with the 3^?, 5^?, 2⁺, 4⁺ and 6⁺ collective states of²⁰⁸Pb. The excited states in²⁰⁸Pb (t,α) reaction can be quantitatively explained in terms of altered 2d_5/2, 1g_7/2 and 1g_9/2 states with the hole-core coupling model.     

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.     

Electrochemical behavior of Li intercalation processes into a Li[NixLi(1/3−2x/3)Mn(2/3−x/3)]O2 cathode

Li[Ni_xLi_(1/3−2x/3)Mn_(2/3−x/3)]O₂ (X=0.17, 0.25, 0.33, 0.5) compounds are prepared by a simple combustion method. The Rietvelt analysis shows that these compounds could be classified as having the α-NaFeO₂ structure. The initial charge-discharge and irreversible capacity increases with the decrease of x in Li[Ni_xLi_(1/3−2x/3)Mn_(2/3−x/3)]O₂. Indeed, Li[Ni_0.50Mn_0.50]O₂ compound shows relatively low initial discharge capacity of 200 mAh/g and large capacity loss during cycling, with Li[Ni_0.17Li_0.22Mn_0.61]O₂ and Li[Ni_0.25Li_0.17Mn₀.₅₈]O₂ compounds exhibit high initial discharge capacity over 245 mAh/g and stable cycle performance in the voltage range of 4.8 -2.0 V. On the other hand, XANES analysis shows that the oxidation state of Ni ion reversibly changes between Ni²⁺ and about Ni³⁺, while the oxidation state of Mn ion sustains Mn⁴⁺ during charge-discharge process. This result does not agree with the previously reported ‘electrochemistry model’ of Li[Ni_xLi_(1/3−2x/3)Mn_(2/3−x/3)]O₂, in which Ni ion changes between Ni²⁺ and NI⁴⁺. Based on these results, we modified oxidation-state change of Mn and Ni ion during charge-discharge process.     

Emission analysis of Dy and Pr:Bi2O3-ZnF2-B2O3-Li2O-Na2O glasses

In this paper, we present the spectral results of Dy³⁺ and Pr³⁺ (1.0 mol%) ions doped Bi₂O₃-ZnF₂-B₂O₃-Li₂O-Na₂O glasses. Measurements of X-ray diffraction (XRD), differential scanning calorimetry (DSC) profiles of these rare-earth ions doped glasses have been carried out. From the DSC thermograms, glass transition (T_g), crystallization (T_c) and melting (T_m) temperatures have been evaluated. The direct and indirect optical band gaps have been calculated based on the glasses UV absorption spectra. The emission spectrum of Dy³⁺:glass has shown two emission transitions ⁴F_7/2→⁶H_15/2 (482 nm) and ⁴F_7/2→⁶H_13/2 (576 nm) with an excitation at 390 nm wavelength and Pr³⁺:glass has shown a strong emission transition ¹D₂→³H₄ (610 nm) with an excitation at 445 nm. Upon exposure to UV radiation, Dy³⁺ and Pr³⁺ glasses have shown bright yellow and reddish colors, respectively, from their surfaces.     

Antiferromagnetic phase transition in garnet-type AgCa2Co2V3O12 and AgCa2Ni2V3O12

Antiferromagnetic phase transition in two vanadium garnets AgCa₂Co₂V₃O₁₂ and AgCa₂Ni₂V₃O₁₂ has been found and investigated extensively. The heat capacity exhibits sharp peak due to the antiferromagnetic order with the Néel temperature T_N=6.39 K for AgCa₂Co₂V₃O₁₂ and 7.21 K for AgCa₂Ni₂V₃O₁₂, respectively. The magnetic susceptibilities exhibit broad maximum, and these T_N correspond to the inflection points of the magnetic susceptibility χ a little lower than T(χ_max). The magnetic entropy changes from zero to 20 K per mol Co²⁺ and Ni²⁺ ions are 5.31 J K⁻¹ mol-Co²⁺-ion⁻¹ and 6.85 J K⁻¹ mol-Ni²⁺-ion⁻¹, indicating S=1/2 for Co²⁺ ion and S=1 for Ni²⁺ ion. The magnetic susceptibility of AgCa₂Ni₂V₃O₁₂ shows the Curie-Weiss behavior between 20 and 350 K with the effective magnetic moment μ_eff=3.23 μ_B Ni²⁺-ion⁻¹ and the Weiss constant θ=−16.4 K (antiferromagnetic sign). Nevertheless, the simple Curie-Weiss law cannot be applicable for AgCa₂Co₂V₃O₁₂. The complex temperature dependence of magnetic susceptibility has been interpreted within the framework of Tanabe-Sugano energy diagram, which is analyzed on the basis of crystalline electric field. The ground state is the spin doublet state ²E(t₂⁶e) and the first excited state is spin quartet state ⁴T₁(t₂⁵e²) which locates extremely close to the ground state. The low spin state S=1/2 for Co²⁺ ion is verified experimentally at least below 20 K which is in agreement with the result of the heat capacity.     

Solid solution formation in the systems CuMIIIX2-AgMIIIX2 where MIII=Al,Ga, In and X2=S,Se

A study of solid solution formation in the systems CuAlX₂-AgAlX₂, CuGaX₂-AgGaX₂ and CuInX₂-AgInX₂, where X=S, Se, has shown that when M^III=Al and Ga, CuM^IIIX₂ and AgM^IIIX₂ were not completely miscible. The CuInX₂-AgInX₂ system, however, showed complete solid solubility. The limits of solid solubility are explained in terms of the c/a ratio, and the internal atomic coordinate u. The lattice constant a is a linear function of composition, while c bows upwards. This behavior is also discussed in terms of trends in 2-c/a.     

Vibration-rotation spectrum of N2O in the region of the lowest fundamental ν2

The high resolution infrared spectrum of N₂O in the region of ν₂ has been studied with a Fourier transform spectrometer at a resolution of (about) 0.005 cm^?1 and an accuracy of about ±0.00005 cm^?1. In addition to ν₂, “hot” bands associated with this band and the bending fundamental ν₂ of ¹⁵N¹⁴N¹⁶O and ¹⁴N¹⁵N¹⁶O were analyzed.     

Preparation, characterization and magnetic properties of the doped barium hexaferrites BaFe12−2xCox/2Znx/2SnxO19, x=0.0-2.0

A series of powders of M-typed barium hexaferrites doped with Co, Zn and Sn of general formula BaFe_12-2xCo_x/2Zn_x/2Sn_xO₁₉ (x=0-2.0) were prepared by the co-precipitation/molten salt method. The structures, particle morphology and magnetic properties of the products were characterized by X-ray powder diffraction, vibrating sample magnetometer and ESEM/EDX. The results show that the crystallinity of the samples decreases with increase in the doping amount x. When x is less than 0.6, it is possible to obtain perfectly crystallized hexagonal BaFe_12-2xCo_x/2Zn_x/2Sn_xO₁₉, where the diameters of the particles are around 500 nm. The saturation magnetization of pure barium ferrite BaFe₁₂O₁₉ produced with this method is 71.9 A m² kg⁻¹ at room temperature and the intrinsic coercivity (H_c) is 367.8 kA m⁻¹. The doped barium hexaferrite powder obtained when x is between 0.3 and 0.4 exhibits high saturation magnetization and a temperature dependence of coercivity close to zero.     

Loss of alignment gain in the πh 9/2[541 1/2−] ⊗ (νi 13/2)2 band in 167Tm and neighbouring odd-Z N = 98 nuclei

Theπh_9/2[541 1/2^?] band in ¹⁶⁷Tm has been studied through the ¹²⁴Sn(⁴⁸Ca, p4n)¹⁶⁷Tm reaction at E _beam = 210 MeV. The favoured signature of the πh_9/2[541 1/2^?] band is observed to spin 61/2h?. A remarkable small gain in aligned angular momentum at the AB-band crossing has been found. The crossing frequency and the gain in aligned angular momentum for ¹⁶⁷Tm are compared with data for the N = 98 isotones of Lu, Ta and Re, and contrasted with Cranked Shell Model predictions, based on frequency diabatic configurations. Large deviations are found for the gain in aligned angular momentum.     

Decay of the 21/2− isomer in211Bi and structure of thevg 9 2/2 πh 9/2 levels

Gamma rays and conversion electrons have been measured in²¹¹Bi populated by the²⁰⁹Bi(t,p) reaction, and the near yrast levels were observed up to 21/2^?. The 21/2^? state is isomeric withT _1/2=70(5) ns. No alpha decaying isomer was found in²¹¹Bi. ObservedM1 transitions reveal mixing of the²¹⁰Pb parent states in the levels of²¹¹Bi. The levels and transitions are well reproduced by the shell model with experimental matrix elements and pure configurations.     

The infrared spectrum of C2N2 in the region of the bending fundamental ν5

The high resolution infrared spectrum of C₂N₂ in the region 200–270 cm^?1 has been studied with a Fourier transform spectrometer. In addition to ν₅, the “hot” bands 2ν₅⁰ ← ν₅¹, 2ν₅² ← ν₅¹ and 3ν₅³ ← 2ν₅² have been analysed. Polynomial fits have been applied to obtain the vibrational term values and the rotational constants for the levels involved.     

Collisional relaxation of ionic2 P 3/2 excited states in rare gases

Optical pumping with theD ₂ line is used to study the depolarization of the first excited² P _3/2 states of alkaline earth ions and Yb⁺ ions in collisions with rare gas atoms. The deorientation cross sections for the even isotopes of Ba⁺ and Yb⁺ ions are obtained (in units of 10^?16 cm²): rare gas He Ne Ar Kr Xeσ ₁ (Ba⁺ 6p ² P _3/2) 79(11) 89(13) 123(18) 152(22) 204(30)σ ₁ (Yb⁺ 6p ² P _3/2) 60(10) 62(9) 107(18) 133(17) 167(37) The cross sections are discussed in comparison with theoretical calculations and those of isoelectronic atoms. The comparison of the² P _3/2 relaxation of even and odd (I=3/2) isotopes of Ba⁺ allows to draw conclusions on the nature of the depolarization interaction.     

Investigation of spectroscopic properties and thermal stability of Er/Yb-co-doped Bi2O3-B2O3-Ga2O3 glasses

A series of Er³⁺/Yb³⁺-co-doped 60Bi₂O₃-(40−x) B₂O₃ -xGa₂O₃ (BBGA x=0, 4, 8, 12, 16 mol%) glasses have been prepared. The absorption spectra, emission spectra, fluorescence lifetime of Er³⁺:⁴I_13/2 level and thermal stability were measured and investigated. Three Judd-Ofelt intensity parameters Ω_t (t=2,4,6) (Ω₂=(4.67-5.93)×10⁻²⁰ cm², Ω₄=(1.50-1.81)×10⁻²⁰ cm², Ω₆=(0.92-1.17)×10⁻²⁰ cm²) of Er³⁺ ions were calculated by Judd-Ofelt theory. It is found that the Ω₆ first increases with the increase of Ga₂O₃ content from 0 to 8 mol% and then decreases, which is mainly affected by the number of non-bridging oxygen ions of the glass network. The high peak of stimulated emission cross-section () of Er³⁺: ⁴I_13/2→⁴I_15/2 transition were obtained according to McCumber theory and broad full width at half maximum (FWHM=69-76 nm) of the ⁴I_13/2→⁴I_15/2 transition of Er³⁺ ions were measured. The results indicate that these new BBGA glasses can be used as a candidate host material for potential broadband optical amplifiers.