PV型HgCdTe光电探测器中的混沌及其诊断

 对激光辐照半导体光电探测器的实验研究，发现当一束不太强的稳定连续波激光照射在PV型HgCdTe光电探测器上时，可以引起探测器出现混沌行为。利用光电探测器的光电压信号随时间变化的实验数据，通过求功率谱、计算Lyapunov指数对混沌进行了诊断。     

Path integrals on half-line

In the framework of path integrals we present a solution to the Schrödinger equation for a free particle confined to the half-linex > 0. A solution in question corresponds to the boundary condition (/x) (0,t)= (0,t) where is a real constant.     

Preparation d'alcools acetyleniques et propargyliques F-alkyles

A number of α-β acetylenic carbinols R_FCCC(OH)RR′, in which the acetylenic proton was substituted by a F-alkyl group, were first prepared, from a classical reaction of (F-alkynyl)- lithium derivatives R_FCCLi upon various carbonyl compounds.On another hand, the reaction of propargyl bromide metallic complexes (organoaluminic, or ultrasonic irradiation activated organozinc) upon some polyfluorinated ketones R_FCOR led to the formation, in convenient yields, of the propargylic carbinols HCCCH₂C(OH)RR_F.The synthesis and properties of these series of new (F-alkyl) substituted acetylenic and propargylic alcohols are described and discussed.     

Preparation of enantiomerically pure (E)-β-sulfinylenones from β-ketoesters

Enantiomerically pure (E)-β-sulfinylenones are smoothly prepared from β-ketoesters in three steps with good overall yield. Since they can be the substrates of many diastereoselective reactions, they represent versatile precursors of a wide range of chiral building blocks. We propose a rationale to explain the formation of (E)-β-sulfinylenones from the corresponding δ-enol-methylethers.     

Two Intercalation Mechanisms of Oxazole Yellow Dimer (YOYO-1) into DNA

The oxazole yellow dye, YOYO-1 (a symmetric homodimer), is a commonly used molecule for staining DNA. We applied the brightness analysis to study the intercalation of YOYO-1 into the DNA. We distinguished two binding modes of the dye to dsDNA: mono-intercalation and bis-intercalation. Bis-intercalation consists of two consecutive mono-intercalation steps, characterised by two distinct equilibrium constants (with the average number of base pair per binding site equals 3.5): <math xmlns:mml="http://www.w3.org/1998/Math/MathML" id="mm1">mathvariant="normal">K1=3.36±0.43×107mathvariant="normal">M−1math> and <math xmlns:mml="http://www.w3.org/1998/Math/MathML" id="mm2">mathvariant="normal">K2=1.90±0.61×105mathvariant="normal">M−1math>, respectively. Mono-intercalation dominates at high concentrations of YOYO-1. Bis-intercalation occurs at low concentrations.     

On path integrals and relativistic quantum mechanics

A proposal for formulation of relativistic quantum mechanics in terms of path integrals is presented.We are deeply indebted to Dr. M.mall>Petrámall> for many stimulating discussions.     

Field and temperature dependence of magnetization of U3P4

Conclusions We conclude that the occurrence of a maximum in the magnetization versus temperature curve observed under certain circumstances on U₃P₄ is not connected with its intrinsic magnetic structure, but substantially depends on the form in which the material is studied (polycrystalline powder, single crystal, single crystal powders with various dimensions of grains). This phenomenon seems to be affected by quenching of the state from the region of low anisotropy at higher temperature in the small particles with a strong tendency to single domain behaviour and thus it may be a consequence of rotation magnetization process in the fields relatively small for U₃P₄. The assertion about transitions between magnetic ordering, sometimes proposed in the literature on the basis of observed anomalies in the temperature course of magnetization without simultaneous confirmation by neutron diffraction, should be accepted with some reservation, especially in the case of simple uranium compounds. However, another situation arises for pseudobinary alloys of ferro- and antiferromagnetic components (e.g. UP_0·75S_0·25) where such transitions were confirmed both by magnetic methods and by neutron diffraction studies [13].The authors would like to express their thanks to Ing. A.mall>Meovskýmall> for careful preparation of samples.     

Impedance Response of a Thin Film on an Electrode: Deciphering the Influence of the Double Layer Capacitance

The different contributions of the interfacial capacitance are identified in the case of passive materials or thin protective coatings deposited on the electrode surface. The method is based on a graphical analysis of the EIS results to determine both the passive-film capacitance in the high-frequency domain and the double-layer capacitance in the low-frequency domain. The proposed analysis is shown to be independent of the physicochemical origins of the frequency dispersion of the interfacial capacitances which results, from an analysis point of view of the experimental results, in the use of a constant-phase element However, for a correct evaluation of the thin-film properties such as its thickness, the high-frequency data must be corrected for the double-layer contribution. In particular, it is shown that if the double-layer capacitance gives a frequency-dispersed response, it is necessary to correct the high-frequency part for the double-layer constant-phase elements. This is first demonstrated on synthetic data and then used for the determination of the thickness of thin oxide film formed on Al in neutral pH solution.     

激光辐照PC型HgCdTe探测器的实验研究

分别用连续波1.319μm激光和10.6μm激光辐照PC型HgCdTe红外探测器时,得到了不同辐照光功率密度下,探测器输出的一系列实验结果。给出了在波长为1.319μm的波段内激光辐照下PC型HgCdTe探测器的饱和阈值;用波长为10.6μm的波段外CO2激光辐照探测器时,发现了一些与波段内激光辐照探测器时大不相同的实验现象;对实验结果进行了分析。简要总结了PC型HgCdTe探测器对于波段内和波段外激光辐照的响应机制。