Optical properties of semiconducting iron disilicide thin films

The iron silicides samples were prepared by annealing of iron films evaporated onto silicon wafers and capped with amorphous silicon thin overlayers. Semiconducting FeSi₂ phase is formed by annealing at the temperatures from 550°C to 850°C. The optical properties of the FeSi₂ layers have been deduced from reflectance and transmittance measurements carried out in the temperature range of (77–380) K. The spectral dependence of the absorption coefficient favours direct allowed transitions with forbidden energy gap of 0.87eV at the room temperature. The application of a simple three-parameter semiempirical formula to the temperature dependence of the direct energy gaps leads to the following best fit parameters: the band gap at zero temperature E _g (0) = (0.895 ± 0.004)eV, the dimensionless coupling parameter S = 2.0 ± 0.3, and the average phonon energy <hw> = (46 ± 8)meV. By examining all the reported triplets of parameters for -FeSi₂ fabricated by different techniques and thermal processes, an obvious discrepancy can be found for the lattice coupling parameter and average phonon energy, although the bandgaps at 0 K are very similar. Unlike the theoretical prediction and the earlier reported result, our results do not show any evidence of a particularly strong electron-phonon interaction, which would give the lower carrier mobilities. -FeSi₂ seems to be an intriguing material where states with energies near the band edges permit ambiguous interpretation of the character of transitions. From optical model for the thin film-substrate system we found the index of refraction to be (5–5.9) in the photon energy interval from 0.65 to 1.15eV. There is also indication of an additional higher-energy absorption edge at l.05eV.     

The RATIO method for time‐resolved Laue crystallography

A RATIO method for analysis of intensity changes in time‐resolved pump–probe Laue diffraction experiments is described. The method eliminates the need for scaling the data with a wavelength curve representing the spectral distribution of the source and removes the effect of possible anisotropic absorption. It does not require relative scaling of series of frames and removes errors due to all but very short term fluctuations in the synchrotron beam.     

Bifurcation of periodic solutions to variational inequalities in R κ based on Alexander-Yorke theorem

Variational inequalities are studied, where K is a closed convex cone in , 3, B is a × matrix, G is a small perturbation, a real parameter. The assumptions guaranteeing a Hopf bifurcation at some ₀ for the corresponding equation are considered and it is proved that then, in some situations, also a bifurcation of periodic solutions to our inequality occurs at some _{I 0}. Bifurcating solutions are obtained by the limiting process along branches of solutions to penalty problems starting at ₀ constructed on the basis of the Alexander-Yorke theorem as global bifurcation branches of a certain enlarged system.     

新疆广播电视大学网络教学平台课程个性化学习系统的设计与安全机制研究

新疆广播电视大学的网络教学平台是新疆发展远程教育的骨干力量,提供双语教学,能够满足绝大部分教学需求,但是在教学内容与平台智能方面还未实现精细化教学的目标,难以实现因材施教.本文针对上述问题,引入了个性化学习理论,在现有网络教学平台上设计网上课程个性化学习系统架构,并对系统中的资源建设与管理、个性化设计以及安全性机制进行了探讨.网上课程个性化学习系统可以在确保教学平台安全可信的前提下提高教学质量,有利于学生的个人发展.     

On Possible Singular Solutions to the Navier — Stokes Equations

In this paper, we exclude the possibility of existence of a singular solution of the selfsimilar type proposed by Jean Leray More precisely, using a slightly stronger hypothesis we give a simpler proof to the analogous result established by J. Ne?as, M. Rú?i?ka and V. ?verák. We also discuss the possible existence of a singular solution of pseudo-selfsimilar type.     

Quantifying the lateral lipid domain properties in erythrocyte ghost membranes using EPR-spectra decomposition

Using EPR spectroscopy a typical lateral domain structure was detected in the membranes of spin-labeled bovine erythrocyte ghosts. The spectral parameters were determined by decomposing the EPR spectrum into three spectral components and tuned by a hybrid-evolutionary-optimization method. In our experiments the lateral domain structure and its properties were influenced by the variation in the temperature and by the addition of n-butanol. The specific responses of the particular domain types were detected. For the most-ordered domain type a break was seen in the temperature dependence of its order parameter, while the order parameters of the two less-ordered domain types exhibited a continuous decrease. Below the break-point temperature the alcohol-induced membrane fluidity variation is mainly a consequence of the change in the proportions of the least- and the most-ordered domain type and not the change of the domain-type ordering or dynamics (with n-butanol concentration). On the other hand, the fluidity variation above the break-point temperature arises from both types of changes. Interestingly, the proportion of the domain type that has its order parameter between that of the least- and the most-ordered domain type remains almost constant with concentration as well as with temperature, which implies its stability. Such characterization of the lateral membrane domain structure could be beneficial when considering the lipid-protein interactions, because it can be assumed that the activity of the membrane-bound enzyme depends on the properties of the particular domain type.     

Next nearest neighbor effect in chromite

In this paper the Mossbauer spectra of a chromite at 140K 200K and 298K were measured. Next nearest neighbor effects were used to explain the spectra of the chromite, and multiple doublets of Fe²⁺ ions on the A sites were caused by the different cation combinations on 12 next nearest neighbor B sites. The quandrupole splitting of each of mult iple Fe²⁺ doublets decreases with increasing temperature.     

Ion exchangers containing phosphorus in their functional group

Summary Uranium or thorium separations from a number of various ions were studied by means of cation exchangers containing phosphorus in their functional group. These ion exchangers adsorb selectively only UO₂ ²⁺ or Th⁴⁺ ions from the mixture studied in a medium of >0.4 N nitric or hydrochloric acid. Several di- and trivalent cations are not sorbed under these conditions. In the absence of UO₂ ²⁺ and Th⁴⁺ ions, Me²⁺ may be more easily separated quantitatively from Me³⁺ in 0.2 N nitric or hydrochloric acid than with cation exchangers containing the -SO₃H group.

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Zusammenfassung Die quantitative Trennung von UO₂ ²⁺ oder Th⁴⁺ von einer Reihe anderer Ionen wurde mit Hilfe phosphorhaltiger Kationenaustauscher untersucht. Diese Ionenaustauscher sorbieren selektiv nur UO₂ ²⁺ oder Th⁴⁺-Ionen aus einem Medium von >0,4 N HNO₃ oder HCl. Eine Reihe verschiedener zwei- und dreiwertiger Kationen wird unter diesen Bedingungen nicht sortiert. Bei Abwesenheit von UO₂ ²⁺- und Th⁴⁺-Ionen kann man Me²⁺ in 0,2 N HNO₃- oder HCl-Lösung quantitativ von Me³⁺ trennen, und zwar leichter als mit -SO₃H-haltigen Austauschern.