Dissociative Excitation of the Even Quartet and Sextet Levels of the Manganese Atom by Collisions of Electrons with Manganese Diiodide Molecules

Dissociative excitation of even quartet and sextet levels of the manganese atom by electron collisions with manganese diiodide molecules was studied experimentally. Twelve excitation cross-sections for transitions from quartet levels and 23 cross-sections for transitions from sextet levels were measured at an incident electron energy of 100 eV. The optical excitation function (OEF) was recorded in the range of electron energies 0?100 eV for transitions originating at the 3d⁵4s4de⁶D_J levels. The potential channels of dissociative excitation in the range of low electron energies (E < 22 eV) were discussed.     

Features of the Emission Spectra of Ni-Like Ions. Application to Calculating the Wavelengths of Self-Photo-Pumped X-Ray Lasers

The energy levels and probabilities of radiative transitions to the ground state of Ni-like ions with Z = 36–51 are calculated. The energies of the upper working level 3d_3/24f_5/2 [J = 1] and the lower working level 3d_3/24d_3/2 [J = 1] of self-photo-pumped X-ray lasers along the sequence of Ni-like ions are studied. It is shown that, at the points of intersection of levels of the same parity, a strong interaction of these levels takes place, which leads to a redistribution of the oscillator strengths of the radiative transitions from these levels. Near the intersection points, the emission spectra change abruptly with variation in the nuclear charge Z.     

Study of absorption spectra of Er<Superscript>3+</Superscript> in KTaO<Subscript>3</Subscript> crystals

The first results of the study of optical absorption spectra of KTaO₃: Er³⁺ crystals are presented. In the 350–660-nm region, lines are observed deriving from intraconfigurational electronic transitions from the ⁴ I _15/2 ground state to levels of the ⁴ F _9/2, ⁴ S _3/2, ² H _11/2, ⁴ F _7/2, ⁴ F _5/2(⁴ F _3/2), ² G _9/2, and ⁴ G _11/2 excited states of the Er³⁺ ions. A comprehensive study of transitions to the ⁴ F _9/2, ⁴ S _3/2, ² H _11/2, and ⁴ F _7/2 levels at 77 K is carried out. The number of lines observed for the above transitions fits the theoretically possible number for ?-? electronic transitions in Er³⁺ ions in the cubic crystal field. In the case of a differently charged substituted ion, this situation occurs only under nonlocal impurity charge compensation. The energies of the excited state levels for the transitions under study are determined.     

Niederenergetische Gammalinien vom Neutroneneinfang in Lu 175 und Lu 176

The low energy gamma-rays from neutron-capture in Lu 175 and Lu 176 have been investigated by means of the bent crystal-spectrometer at the DR-3-reactor at Risø. From the transitions in Lu 177 3 rotational bands have been determined. The levels of the (404)K=7/2⁺ groundstate rotational band are: 121,62 keV (I=9/2), 268,79keV (I=11/2), 440,66 keV (I=13/2), 636,22 keV (I=15/2), 854,34 keV (I=17/2). The level-sequence of the (514)K=9/2^?-band is: 150,39 keV (I=9/2), 288,99 keV (I=11/2), 451,49 keV (I=13/2), 637,05 keV (I=15/2) and 844,88 keV (I=17/2). At 457,92 keV is the basis for the (402)K=5/2⁺-band the higher levels of which are 552,05 keV (I=7/2), 671,89 keV (I=9/2), 816,63 keV (I=11/2), 985,23 keV (I=13/2), 1176,73keV (I=15/2) and probably 1389,5 keV (I=17/2). The energies of the levels apart from the 1389 keV-level have an accuracy of 7×10^?5. The energy differences between the 3 bands agree very well with the values expected from the Bohr-Mottelson-formulaE=A·I(I+1)+B·I ²(I+1)². The calculated branching-ratios within the 3 bands are in fairly good agreement with the experimental values. Theg _K -factors have been determined for 2 bands: It was found that for the (514)-bandg _K =1,16±0,04 and for the (402)-bandg _K =1,33±0,07.     

Monomer counterrotations and tunneling splitting in CO dimer by data of millimeter wave spectroscopy

Analysis of the rotational spectrum of the molecular dimer (CO)₂ measured in the millimeter wave range has been performed and four new rotational states are revealed. Three of these states are characterized by almost free rotations of both monomers in the dimer. These states have approximately the same first term σ in the expansion of the rotational energy in powers of the rotational angular momentum J for various values of the momentum projections on the dimer axis (K=0, 1, 2) and various rotational constants B. The intrinsic rotational angular momenta of CO dimers, j₁=j₂=1, are determined from the σ value. In addition, a state with K=2 is found which corresponds to one of the known shape isomers of (CO)₂. The values of the tunneling splitting for each of the new states are determined. The results indicate that previous data on the suppressed tunneling are determined by the asymmetry of internal rotations in the CO monomers rather than by the _K value.     

Microwave spectroscopy of the weakly bound CO-<Emphasis Type="Italic">ortho</Emphasis>-D<Subscript>2</Subscript> molecular complex

A van der Waals complex that consists of a deuterium molecule in the ortho state and a carbon monoxide molecule, CO-ortho-D₂, was studied in the frequency range 85–130 GHz with the help of an intracavity orotron-based spectrometer. Nine new lines, which correspond to rotational transitions and belong to the R and Q branches, were measured and identified. The positions of the rotational energy levels of CO-ortho-D₂ were refined by comparative analysis of the transition frequencies measured in this work and previously reported microwave and infrared data.     

Neutroneneinfangs-Gammaspektrum und Niveauschema von Erbium 167

The (n, γ)-spectrum of Er 167 was investigated by means of the Risø bent crystal spectrometer. The energies and intensities of 47 transitions were measured. 22 of them were fitted into a level scheme. The rotational bands of theK=7/2⁺[633],K=1/2^?[521], andK=5/2^?[512] states were found up to the spin valuesI=11/2⁺, 9/2^?, and 7/2^?. Gammavibrational states of these Nilsson orbitals were determined or proposed. The energy of theK=5/2^?[523] state was suggested. Branching ratios of gamma transitions were compared with theoretical predictions.     

Two-photon Rydberg resonances in lithium-7 obtained by recording reduction of resonance fluorescence

In a magneto-optical trap (MOT) of ⁷Li, two-photon Rydberg resonances are recorded by using a spectroscopic technique, which based on variation in the resonance fluorescence. The first excitation frequency is detuned by 0.59 GHz from the intermediate 2P _3/2 state. Two counter-propagating laser beams are used. The resonances are studied on two-photon transitions 2S _1/2 ? nl in a range of principal quantum number n from 38 to 120. The widths of the observed resonances are varied from 4.4 to 13 MHz for different MOT parameters.     

Energy levels of ions of silver and rhodium isoelectronic sequences with <Emphasis Type="Italic">Z</Emphasis> < 86

The method of extrapolation of the parameter of a model potential for states of one electron (4f, 5s, 5p, 5d, 5f) above the core 1s ²2s ²2p ⁶3s ²3p ⁶3d ¹⁰4s ²4p ⁶4d ¹⁰ and one vacancy (4d ⁹) in the same core is applied to calculate the energy levels in the silver and rhodium isoelectronic sequences with the maximum nuclear charge Z = 86. The energy levels of Ag-and Rh-like ions were used for the calculation of the energies of resonance transitions to the ground state ¹ S ₀ in Pd-like ions. Good agreement between the theoretical and calculated energies of the resonance transitions in Pd-like ions indicates the reliability of the results obtained.     

Observation of the state of CH2 by optical–optical double resonance

We report the observation of levels in the state of CH₂ via optical–optical double resonance spectroscopy. Direct transitions between the lowest singlet state and the state are allowed by symmetry, but weak because they correspond to a two electron excitation in the single configuration approximation to the electronic wavefunction. The observed transitions involve sequential single photon absorptions at visible and near infrared wavelengths using state intermediate levels. Recent ab initio results (S.N. Yurchenko et al., J. Mol. Spectrosc. 208 (2001), 136) predicted the positions of some of the levels which are confirmed by the present results. The new spectra provide accurate energies for rotational levels in the , l = 0 level of the state.     

Auger- und Coster-Kronig-Übergänge der M-Schale von Krypton

The Auger spectra of theM ₂,M ₃,M ₄,M ₅ subshells of krypton and the Coster-Kronig spectra of theM ₁,M ₂,M ₃ subshells of krypton were measured with an electrostatical spectrometer. The ionization in theM shells was caused by electron impact. The use of a gaseous target made it possible to measure the Auger lines even at energies as low as 25 eV. The absolute energies and relative intensities of a great number of transitions were determined: 22 of theM _{4, 5} spectrum, 14 of theM _{2, 3} spectrum and 2 of theM ₁ spectrum. Only in the case of theM _{2, 3} spectrum a comparison between the relative intensities, determined experimentally, and those calculated byRubenstein forZ=47 was possible. The agreement is only qualitatively. Moreover, from the Auger electron energies measured, the following binding energies were calculated:E(M ₁)=(292,1±1,0) eV,E(M ₂)=(222,1±0,6) eV,E(M ₃)=(214,6±0,6)eV,E(N ₁ N ₁)=(62,81±0,05) eV.     

Ion-pair states of I<Subscript>2</Subscript>, Br<Subscript>2</Subscript>, IBr,and ICl

The experimentally determined energies and rotational constants of the vibrational levels v = 0–20 of the Ion-Pair states Ω = 0⁺, Ω = 1 of the I₂, Br₂, IBr, and ICl molecules are modeled. The model used includes three diabatic states, which correlate to X⁺(3P, 1D) + Y^～(1S₀). These states are coupled by the spin-orbit interaction, which is assumed to be independent of the internuclear distance. For IBr and ICl, as well as for the ungerade states of I₂ and Br₂, satisfactory results are obtained. The model is less applicable to the gerade states of I₂ and Br₂, which is possibly results from the retainment of the asymptotic J _A J _B coupling of the angular momenta at equilibrium internuclear distances.     

Atomic level energies in hafnium

The photo electron method for obtaining electron binding energies is described. The method has been applied to theL _I,L _II, andL _III levels in hafnium. The HfK α₁ and HfK α₂ x-ray emission lines have been measured with a crystal spectrometer. The electron binding energies of theK toO _III shells in hafnium are obtained from photo electron and x-ray emission data. A new type of Moseley diagram is described and is demonstrated for theK andL levels in theZ region 57 to 75. From these diagrams accurate binding energies for the element Pm (Z=61) have been obtained by interpolation.     

Phase states and dielectric properties of sodium-potassium niobate solid solutions

The temperature dependence of dielectric constant ? for single crystals of Na_1?xK_xNbO₃ (0.04?x?0.15) is studied for the first time. From the shape of the ?(T) anomalies corresponding to rotational phase transitions, the type of interaction between the order parameters and the polarization is determined. A phenomenological model is developed which adequately describes the experimentally observed sequence of high-temperature (T>300°C) phase transitions, the dielectric anomalies associated with these transitions, and the changes in the phase states under the action of external factors (pressure, electric field).     

Modeling of the structure and electronic spectra of green fluorescent protein chromophore

The structure and electronic absorption spectra of a model green fluorescent protein chromophore were studied in the neutral, cationic, and anionic forms in the isolated state. The energies of S ₀-S ₁ vertical transitions were calculated using a new method based on a modified multiconfiguration quasi-degenerate perturbation theory (aug-MCQDPT2). This method was used to obtain quantitative estimates of S ₀-S ₁ vertical transition energies for chromophores in the isolated state, 2.54, 3.12, and 3.11 eV (the experimental values were 2.59, 3.05, and 2.99 eV) for the anionic, cationic, and neutral forms, respectively.     

Determination of absoluteK-internal conversion coefficients of some transitions in Ce140 by the internal-external conversion method

The internalK-conversion coefficients of the 331, 431, 815 and 933 keV transitions following the decay of La¹⁴⁰ have been determined absolutely by the method of comparing internal and external conversion lines measured in a double — focusing beta — ray spectrometers. TheK-internal conversion coefficients of the 4+→2+ 487 keV transition in Ce¹⁴⁰ was used to normalize relativeK-electron and gamma-ray intensities for these transitions. The results obtained are:α _K (331)=0.04432±0.00471,α _K (431)=0.28110±0.02913,α _K (815)=0.00396±0.00043,α _K (933)=0.00282±0.00031. Multipolarity assignments based on these values are suggested. The 815 keV transition is found to be pure magnetic dipole character in good agreement with the theoretical values calculated bySliv andBand. The 331 and 933 keV transitions are proved to have magnetic dipole character withE2/M1 equal 0.2852±0.0143 and 0.1750±0.0088 respectively. The 431 keV transition was found to have magnetic octupole character. The results obtained are most consistent with the assignment 2+, 4+, 2+, 3+ and 1+ for the 1597, 2084, 2184, 2410 and 2515 keV levels respectively.     

Computation of the electronic structure and direct-gap absorption spectra in Ge-rich Si<Subscript>1−x</Subscript> Ge<Subscript>x</Subscript>/Ge/Si<Subscript>1−x</Subscript>Ge<Subscript>x</Subscript> type-I quantum wells

This paper presents the results of conduction band discontinuities calculation for strained/relaxed Si_1?x Ge _x /Si_1?y Ge _y heterointerfaces in Γ _15C , Γ _2′C and L upper bands minima, as well as the room-temperature strained (vs. relaxed) band gaps deduced from the classical model-solid theory. Based upon the obtained data, we propose a type-I W-like Si_1?y Ge _y /Si_1?x Ge _x /Ge/Si_1?x Ge _x /Si_1?y Ge _y quantum wells heterostructure optimized in terms of compositions and thicknesses. Electronic states and wave functions are found by solving Schrödinger equation without and under applied bias voltage. An accurate investigation of the optical properties of this heterostructure is done by calculating the energies of the interband transitions and their oscillator strengths. Moreover, a detailed computation of the bias-voltage evolution of the absorption spectra is presented. These calculations prove the existence of type-I band alignment at Γ _2′C point in compressively strained Ge quantum wells grown on relaxed Ge-rich Si_1?y Ge _y buffers. The strong absorption coefficient (> 8 × 10³ cm^-1) and the large Stark effect (0.1 eV @ 2 V) of the Γ _2′C transitions thresholds open up perspectives for application of these heterostructures for near-infrared optical modulators.     

Gammaübergänge und Energieniveaus in Dy 165

220 neutron capture Gamma rays of Dy 165 were measured with the Risø curved crystal spectrometer. The intense transitions permitted the construction of a level scheme for this oddN nucleus. The rotational bandsK=7/2⁺[633],K=1/2^?[521] andK=5/2^?[512] were precisely localized, including the spin 11/2 states. Gammavibrational bands built on these Nilsson orbits were observed with their band heads at 538.6, 573.5 and 570.2 keV. TheI=5/2 term at 533 keV can be considered as the 5/2^?[523] Nilsson state. The branching ratios allowed the determination of (g _K?g^R)²-factors for the [633], [521] and [512] bands and yieldedE 1-hindrance factors.     

Fermi Surface Topology in the Case of Spontaneously Broken Rotational Symmetry

The relation between the broken rotational symmetry of a system and the topology of its Fermi surface is studied for the two-dimensional system with the quasiparticle interaction f(p, p') having a sharp peak at |p ? p'| = q₀. It is shown that, in the case of attraction and q₀ = 2p_F the first instability manifesting itself with the growth of the interaction strength is the Pomeranchuk instability. This instability appearing in the L = 2 channel gives rise to a second order phase transition to a nematic phase. The Monte Carlo calculations demonstrate that this transition is followed by a sequence of the first and second order phase transitions corresponding to the changes in the symmetry and topology of the Fermi surface. In the case of repulsion and small values of q₀, the first transition is a topological transition to a state with the spontaneously broken rotational symmetry, namely, corresponding to the nucleation of L ? π(p_F/q₀ ? 1) small hole pockets at the distance p_F ? q₀ from the center and the deformation of the outer Fermi surface with the characteristic multipole number equal to L. At q₀ → 0, when the model under study transforms to the two-dimensional Nozières model, the multipole number characterizing the spontaneous deformation is L → ∞, whereas the infinitely folded Fermi curve acquires the Hausdorff dimension D = 2 which corresponds to the state with the fermion condensate.     

Ultra-high resolution trap-loss spectroscopy of ultracold <Superscript>133</Superscript>Cs atom long-range states in a magnetooptical trap

We present an ultra-high resolution spectroscopic study of the photoassociation of cesium atoms inside a magnetooptical trap using trap-loss detection with photoassociation laser slow scanning. The photoassociation spectra show vibrational levels of three molecular symmetries below the 6S _1/2 + 6P _3/2 dissociation limit. A dynamic model is derived to extract the photoassociation rate from the trap-loss spectrum. Many observed rotational levels are well resolved, which indicate d-wave and higher partial wave contributions to the photoassociation cross section.