Study of the reaction238U (α, α′f) atE α=480 MeV

The excitation function of the fission probability P _E E _x) for²³⁸U has been measured in the reaction²³⁸U(α, α′ f) at 480 MeV bombarding energy. The reaction mechanism of this reaction is discussed for excitation energies belowB _nf , the threshold for second chance fission, and aboveB _nf up toE _x =37 MeV. In comparing with results from fission induced by photons and by particle transfer reactions the (α, α′f) reaction gives too low values for the fission probabilityP _f at excitation energies well aboveB _nE . The role of the quasi-elastic knock-out process in this reaction is discussed.     

Systematic study of the product((E(2_2~+)/E(2_1~+)) * B(E2)↑) through the asymmetric rotor model

A systematic study of the product((E(2_2~+)/E(2_1~+))*B(E2)↑) is carried out in the major shell space Z=50-82,N=82-126 within the framework of the asymmetric rotor model where the asymmetry parameter γ0reflects change in the nuclear structure.A systematic study of the product((E(2+)/E(2+))*B(E2)↑) with neutron number N is also discussed.The product((E(2_2~+)/E(2_1~+))*B(E2)↑) provides a direct correlation with the asymmetry parameter γ0.The effect of subshells is visible in Ba-Gd nuclei with N 82,but not in Hf-Pt nuclei with N 104.We study,for the first time,the dependency of the product((E(2_2~+)/E(2_1~+))*B(E2)↑) on the asymmetry parameterγ0.     

Intersubband resonance polarons in Al/δ-GaAs tunneling junctions

Tunneling spectra of the A1/δ-GaAs junctions fabricated by molecular-beam epitaxy in the regime of “intimate” contact of A1 with GaAs (100) were studied at 1.6 K in a magnetic field B parallel to the two-dimensional electron-gas layer. The concentration of 2D electrons in the δ-layer grown at a distance of 20 nm from the A1/GaAs interface was 1.1 × 10¹² cm^?2 and corresponded to a partial filling of only the lowest subband E ₀. The tunneling spectra exhibited many-particle features, viz., a zero-bias anomaly, lines of longitudinal optical (LO) phonons, and characteristic “dips” corresponding to the energies E _i of the 2D subbands. In the B fields below the critical value B _c ?11 T, the levels of 2D subbands underwent the usual diamagnetic shifts. At B≥B _c , the E ₁ (B) term pinning and the anticrossing of the E ₁(B) and E ₀(B)+2?ω_LO terms were observed, where ?ω_LO is the LO-phonon energy in GaAs. The observed effects are interpreted as manifestations of resonance intersubband polarons arising in the δ-layer upon reaching the E ₁(B _c )?E ₀(B _c )=2?ω_LO resonance.     

Effects of pressure on maghemite nanoparticles with a core/shell structure

The magnetic property and intraparticle structure of the γ phase of Fe₂O₃ (maghemite) nanoparticles with a diameter (D) of 5.1±0.5 nm were investigated through AC and DC magnetic measurements and powder X-ray diffraction (XRD) measurements at pressures (P) up to 27.7 kbar. Maghemite originally exhibits ferrimagnetic ordering below 918 K, and has an inverse-spinel structure with vacancies. Maghemite nanoparticles studied here consist of a core with structural periodicity and a disordered shell without the periodicity, and core shows superparamagnetism. The DC and AC susceptibilities reveal that the anisotropy energy barrier (ΔE/k_B) and the effective value of the core moment decrease against the initial pressure (P≤3.8 kbar), recovering at P≥3.8 kbar. The change of ΔE/k_B with P is qualitatively identical with that of the core moment, suggesting a down-and-up fluctuation of the number of Fe³⁺ ions constituting the core at the pressure threshold of about 4 kbar. This phenomenon was confirmed by the analysis of the XRD measurement using Scherrer’s formula. The core volume decreased for P≤2.5 kbar, whereas at higher pressure the core was restructured. For 2.5≤P≤10.7 kbar, the volume shrinkage of particle hardly occurs. There, ΔE/k_B is approximately proportional to the volume associated to the ordered fraction of the nanoparticles as seen from XRD, V_core. From this dependence it is possible to separate the core/shell contribution to ΔE/k_B and estimate core and surface anisotropy constants. As for the structural experiments, similar experimental data have been obtained for D=12.8±3.2 nm as well.     

Valence inhomogeneities in intermediate-valent Eu compounds

In each of the intermediate valent compounds EuNi₂P₂, EuPd₂Si₂, and EuPd₆B₄, the line width of the ¹⁵¹Eu-Mössbauer resonance attains a maximum when its isomer shift varies most strongly with temperature. We associate this anomalous line broadening with a distribution of the local Eu valence, which may be described by an inhomogeneous width, Δ, of the interconfigurational excitation energy, E_exc, in addition to the homogeneous fluctuation width, k_BT_f. Applying this model to the analysis of isomer shift, line width, and magnetic susceptibility, the model parameters Δ, E_exc, and k_BT_f are obtained. Δ is found to attain maximal values at temperatures where E_exc varies most steeply with temperature.     

Calculations of vacancy formation energies and divacancy binding energies for noble metals using pseudopotential formalism

Vacancy formation energies (E^f_1v) and divacancy binding energies (E^B_2v) for noble metals have been calculated using the Moriarty's pseudopotential. While the calculated E^f_1v are coincident with the experimental values except Cu, E^B_2v agree with them for all the metals tolerably.     

On the separation of initial and final state effects in photoelectron spectroscopy using an extension of the auger-parameter concept

First, we show that the quantity Δβ(i) = ΔE_A(kii) + 2ΔE_B(i) — ΔE_B(k) is directly related to the final state relaxation contribution ΔE_R(i) of the binding energy shift ΔE_B(i). ΔE_A(kii) is the kinetic energy shift of the Auger transition which corresponds to the decay of a hole state with a hole in level k into a final state with two holes in level i. The shift parameter Δβ(i), which is based on information on two binding energies, is conceptually similar to Wagner's Auger parameter. To establish the relation between Δβ(i) and ΔR(i) one needs, however, less drastic approximations than in the case of Auger parameter shifts. The only approximation necessary is the assumption that ΔR(i) is determined by coulomb contributions.Secondly, we use Δβ (i) to analyse the experimental data of eighteen gaseous phosphorus-containing compounds obtained by Sodhi and Cavell¹. It is shown that ΔR(P_2p) is strongly related to changes in the polarizability of the ligands. The initial state effects derived from our study deviate from those expected on the basis of simple electronegativity considerations.     

The Mössbauer effect and magnetic phase transitions

The Mössbauer effect provides a direct method for identifying the spin axis in magnetic crystals and observing magnetic phase transitions. The order of the transition may be inferred from the Mössbauer spectrum. Phase changes can occur as a function of temperature (e.g. when the anisotropy fieldB _A changes sign) or as a function of applied magnetic field. In an antiferromagnet a field ?(2B _E B _A)^1/2 along the spin axis whereB _E is the exchange field causes the spin-flop transition which is normally first order (sharp) whereas the transition to the paramagnetic phase which occurs at higher fields?2B _E is second order (continuous). In quasi-one-dimensional crystals Mössbauer spectra show that the spin-flop transition is first order locally but occurs over a range of fields throughout the crystal, so that the first order character is masked in a conventional magnetization measurement. In fields applied at a finite angle>B _A/2B _E to the spin axis the transition becomes second order, i.e. a continuous rotation of the spins occurs. In canted antiferromagnets (or weak ferromagnets) the spin-flop transition is also continuous; in addition a “screw” re-orientation may be induced by fields applied perpendicular to the spin axis and arises from antisymmetric exchange. For crystals with lowT _N the hyperfine field changes when a magnetic field is applied and has a minimum at a phase transition; this may be used to map out the magnetic phase diagram.     

Excited quark-quark interactions in a bag model

We calculate the colour magnetic and electric fields,B ^a andE ^a , in the static cavity approximation of the MIT bag model. This is done rigorously for all direct and exchange four-currents of quarks in theS _1/2,P _1/2 andP _3/2 bag states. We then find the quark-quark colour interaction for direct and exchange diagrams. The one-pion exchange diagrams due to chiral symmetry are also calculated.     

Camel's back induced stabilization of electron-hole liquids : GaP

A camel's back-like nonparabolicity of the longitudinal electron mass enhances the density of states and strongly stabilized an electron-hole-liquid. In GaP therefore the EHL density is doubled to 8.6 × 18¹⁸cm^?3 and the Fermi energy ratio E_F^h/E_F^e changes from 1.9 to 4.9. The theoretical binding energy agrees with the experimental E_B=17.5±3meV interpreting the luminescence at 2.30 eV as a superposition of liquid and plasma recombination radiation.     

Testing QCD: Direct photons ine + e − collisions

We discuss QCD predictions for the production of direct photons ine ⁺ e ^? collisions,e ⁺ e ^?→ γ^*→γ+ hadrons (C=+). A simple derivation of the QCD results for the structure functions is presented. These turn out to be exactly predicted by the theory, in contrast to hadron production where only the change withQ ² is predictable. We also take up the phenomenology of this process. A dramatic rise of the γ/π⁰ ratio withz=E _γ/E _B (E _π/E _B ) and withQ ² is predicted.     

Non-spherical magnetic moment in MnAlGe

The magnetic structure factors of MnAlGe (space groupP4/nmm) measured with polarised neutrons have been expressed in terms of the magnetic moment of the Mn atom (site symmetry tetrahedral with tetragonal distortion), the Bessel transforms 〈j _n〉 of the Mn radial functions and the fractional occupancies of the moment density in the various crystal field orbitals. The measured structure factors were least-squares fitted with the theoretical expression involving 〈j _n〉 appropriate to the Mn⁰, Mn⁺ and Mn²⁺ atoms. The best fit was got using Mn⁰ transforms, yielding 1·45µ _B as the Mn magnetic moment. The fractional occupancies of the moment density in the crystal field orbitalsA _1g,B _1g E _g andB _2g were obtained. This analysis shows the magnetic moment to be highly non-spherical with a large fractional occupancy (38%) in theA _1g orbital directed along the tetragonal axis while the fractional occupancies ofB _1g andB _2g are found to be 31% and 30% respectively. The fractional occupancy of the moment in theE _g orbital directed towards the Ge and Al atoms is very low (1%). The spatially averaged moment density of Mn in MnAlGe is more diffuse than that of Mn I and Mn II in isostructural Mn₂Sb.     

Reorientation effect measurements and multiple coulomb excitation in102Ru

The quadrupole moment of the first 2⁺ state in¹⁰²Ru and fourB(E2) values have been measured by means of Coulomb excitation. The results are:Q ₂₊=?0.68(8)eb;B(E2, 01/+→21/+)=0.617(5)e ² b ²;B(E2, 01+→22/+)=0.013 (2)e ² b ²;B(E2, 21/+→22/+)= 0.07(1)e ² b ²;B(E2, 2 ₁ ⁺ →4 ₁ ⁺ )=0.30(6)e ² b ². The results are discussed within the frame of the Interacting Boson Approximation.     

Decay properties of very-high-spin states in transitional Er nuclei aroundA=154

Theγ ray continuum structures of the transitional Er isotopes withA～154 are studied using the reaction⁷⁴Ge(⁸⁴Kr,xn)^158?xEr atE _lab=340 MeV. The measurements include energy spectra, total energies, multiplicities, angular distributions and lifetimes using the DSAM method. The analysis of data confirms the previously observed two-bump structure of the continuum radiation. A meticulous subtraction of discrete contributions proves the persistence of the low-energy bump even at high spins, i.e.I>40?. The angular-distribution measurements assign predominant dipole structure to the bump atE _γ=0.65 MeV, whereas the bump atE _γ=1.3 MeV is of almost pure quadrupole character at high spins. The lifetime measurements give evidence for a strong enhancement of theB(E2) values of the upper bump,B(E2)/B _sp>130. Spin-selection studies reveal, in the spin rangeI=30?50? an almost constant energy for the 1.3 MeV bump,ΔE<60 keV.     

An investigation of the adsorption of oxygen and oxygen containing species on platinum by photoelectron spectroscopy

It is shown that XPS can detect 0.01 monolayers of adsorbed carbon or oxygen and can identify the chemical state of the adsorbed atom(s). Two states of adsorbed oxygen were resolved by thermal desorption spectroscopy and by XPS. The O 1s binding energies (^FE_B) were 530.2 and 533 eV below the platinum Fermi level for the strongly and weakly adsorbed states respectively. (^FE_B) did not vary with coverage. The resulting apparent variation of (^VE_B), the vacuum level referenced value, is discussed in terms of a simple model for the work function Φ which was measured in situ. UPS indicated that the weakly adsorbed state is probably molecular, with levels at 6.1, 9.3, 10.4 and l2.4 eV below the Fermi level. The main change in the UPS spectra produced by the strongly adsorbed state was a reduction of a peak close to the Fermi level.     

Determination of nuclear parameters by inelastic electron scattering at low-momentum transfer

The second-order Born-approximation treatment of Cutler and Schucan was applied to inelastic electron scattering data on ⁶Li, ⁶⁰Ni, and ¹¹⁴Cd acquired at low momentum transfers. The form factors as a function of momentum transfer q in the range of 0.25–0.57 fm^?1 were obtained by angular distribution measurements performed at incident energies of 30 to 60 MeV. The correlation between two parameters deduced from the measurements, the reduced transition probability B(E2↑) and the transition radius R⁽²⁾_tr, is discussed. It is suggested that inelastic electron scattering data at low-q is best used either in conjunction with an accurate value of B(EL↑) (available from the model-independent analysis of “photon” experiments at zero momentum transfer) to allow accurate determination of R⁽²⁾_tr, or in conjunction with high-q inelastic electron scattering data to allow accurate determination of B(EL↑) as well as R⁽²⁾_tr.     

Spectral properties of chlorines and electron transfer with their participation in the photosynthetic reaction center of photosystem II

Structural factors that provide localization of excited states and determine the properties of primary donor and acceptor of electron in the reaction center of photosystem II (PSII RC) are studied. The results of calculations using stationary and time-dependent density functional theory indicate an important role of protein environments of chlorophylls P_A, P_B, B_A, and B_B and pheophytins H_A and H_B in the area with a radius of no greater than ≤10 Å in the formation of excitonic states of PSII RC. When the neighboring elements are taken into account, the wavelength of long-wavelength Q _y transition of chlorophyll molecules is varied by about 10 nm. The effect is less developed for pheophytin molecules (Δλ ? 2 nm). The following elements strongly affect energy of the transition: His^A198 and His^D197 amino-acid residues that serve as ligands of magnesium atoms affect P_A and P_B, respectively; Met^A183 affects P_A; Met^A172 and Met^D198 affect B_A; water molecules that are located above the planes of the B_A and B_B macrocycles form H bonds with carbonyl groups; and phytol chains of P_A and P_B affect B_A, B_B, H_A, and H_B. The analysis of excitonic states, mutual positions of molecular orbitals of electron donors and acceptors, and matrix elements of electron transfer reaction shows that (i) charge separation between B_A and H_A and P_B and B_A is possible in the active A branch of cofactors of PSII RC and (ii) electron transfer is blocked at the B_B - H_B fragment in inactive B branch of PSII RC.     

Mechanism by which a single water molecule affects primary charge separation kinetics in a bacterial photosynthetic reaction center of Rhodobacter sphaeroides

Using quantum-chemical methods, we have studied the role played by water molecules W-A and W-B that are bound by hydrogen bonds to accessory bacteriochlorophyll molecules B _A and B _B in the process of primary charge separation in the reaction center of Rhodobacter Sphaeroides. We have found that the occurrence of a rotational mode of the W-A molecule at 32 cm^?1 and/or its harmonics in stimulated emission of an electron donor P* and the dynamics of population of the states P⁺B _A ^? and P⁺H _A ^? may be related to the structural heterogeneity of the reaction center and the existence of a conformation in which the W-A molecule is predominantly involved in one hydrogen bond (with BA). Based on the calculated redox potentials B _A and P, it has been shown that the appearance of the W-A molecule in the reaction center reduces the energy of the P⁺B _A ^? state by ??600 cm^?1. This is somewhat smaller than the influence of the amino-acid residue Tyr^M210 (??870 cm^?1) and correlates well with a substantial decrease in the electron transfer rate in mutant forms of reaction centers GM203L (which do not contain W-A molecules) and YM210F (in which Tyr^M210 is replaced with Phe). The data obtained allow us to suggest that rotation of the water molecule with a fixed position of its H atom that is involved in a hydrogen bond with the keto carbonyl group of B _A is initiated due to the charge separation between the halves of special pair P and the formation of the state P _A ⁺ P _B ^? . The large effect of this rotation on the kinetics of population of the states P⁺B _A ^? and P⁺H _A ^? after the excitation of P is quite consistent with its influence on the energy of the state P⁺B _A ^? .     

Low-temperature specific heat study of Ni85.5PxB18.5−x (0 ⩽ x ⩽ 18.5) metallic glasses

The low-temperature specific heat (LTSH) of the melt-quenched Ni_81.5P_x^- B_18.5?x amorphous alloy system, with 0 ? x ? 18.5, is presented. The decomposition of the LTSH into magnetic, lattice and electronic contributions shows that both Debye temperature θ_D and electronic specific heat coefficient decrease when the concentration of P increases.The electronic density of states N(E_F), deduced from γ for various Ni-metalloid alloys, is plotted as a function of the average electronic concentration xZ^M, where x is the metalloid concentration and Z^M is the chemical valence of M. Following Malozemoff et al.'s work, this plot is considered as a representation of the band structure and yields the change of the Fermi level with alloying.     

Untersuchungen von (d,p)- und (d, α)-Reaktionen an B10 und B11

Investigating reaction mechanisms, angular distributions and cross sections of the reaction B¹⁰(d, p) B¹¹ have been measured in the energy interval from 1,4 to 3,3 MeV of deuteron energy. More detailed measurements than until known have shown, that besides the well known stripping mechanism withl _n =1 contributions of compound nucleus formation are not neglectable. Especially atE _d =2,3 MeV,E _X (C¹²)=27,1 MeV, the effect of a single resonance contributes a great deal to the cross section of the groupsp ₁ andp ₃ . Further angular distributions and yield curves between 1,4 and 3,3 MeV have been measured in the (d, α)-reactions on B¹⁰ and B¹¹, showing quite different behaviour for both target nuclei.