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141.
We show that an electron confined to a single finite parabolic quantum well in crossed electric and magnetic fields can behave as a double quantum well system. The magnetic field is parallel to the heterostructure layers and the electric field is perpendicular to those. For a suitable choice of both fields and quantum well width, the electron can be confined to a double quantum well effective potential that is very similar to the electronic potential model for diatomic molecules. The double quantum well spectrum is calculated using a numerical algorithm based on semiclassical methods. A physical interpretation of this quantum system is given based on the analogy to the electrons bound to diatomic molecules. 相似文献
142.
Hans-Rudolf Buser Michael Oehme Walter Vetter Bernd Luckas 《Fresenius' Journal of Analytical Chemistry》1993,347(12):502-512
Summary Conventional electron ionization (EI) mass spectrometry (MS) and MS/MS techniques were applied to the analysis of two abundant octa and nonachlorobornanes isolated from seals of the Baltic sea and originating from technical toxaphene. The exact sterical structures of the two compounds were previously determined using nuclear magnetic resonance (NMR) spectroscopy by two independent research groups. The MS and MS/MS data generated in this study allowed partial structure elucidation of these polychlorobornanes, in particular revealing the distribution of the Cl substituents between the six-membered carbon ring, the bridge and the bridgehead in the parent bornane structure. Fragmentation of the six-membered carbon ring and the bridge by retro-Diels-Alder (RDA) and related mechanisms was discovered by studying specific parent/daughter ion transitions. The detailed fragmentation pathways formulated may be applicable to the structure elucidation of other toxaphene congeners and the monitoring of strategic transitions is highly selective for the detection of these compounds in technical toxaphene and in environmental samples. 相似文献
143.
1IntroductionThebrainofmankindhasmanycognitivefunctionssuchaslearning,asociationandoptimizationetc..Theneuronisthemostfoundam... 相似文献
144.
SINGULARBOUNDARYPROPERTIESOFHARMONICFUNCTIONSANDFRACTALANALYSISWENZHIYINGZHANGYIPINGManuscriptreceivedJanuary11,1995.Revi... 相似文献
145.
146.
Lizeng Wang Chengsong Ma Xiaoli Zhang Yibing Ren Yong Yu 《Fresenius' Journal of Analytical Chemistry》1995,351(7):689-691
The electrochemical behavior of the copper-tyrosine complex has been studied by linear-sweep adsorption voltammetry. In 0.02 mol/L Na2HPO4 buffer solution (pH=9.6), the complex can be adsorped on a hanging mercury drop electrode and reduced at a peak potential of about –0.42 V (vs. SCE). The secondary derivative peak height is linear proportional to the concentration of tyrosine in the range 1.0×10–7–5.0×10–5 mol/L. The detection limit is 5×10–8 mol/L.Project supported by the Provincial Science Foundation of Shandong Province 相似文献
147.
Modified Stern-Volmer equation is obeyed by bovine serum albumin (BSA)-iodide system showing selective quenching of tryptophanyl
fluorescence of BSA. The fraction of accessible protein fluorescence is 0.56 and the effective Stern-Volmer constant is 290
M-1 at pH 7.4 in 0.005 M phosphate buffer at 25°C. Collisional quenching is operative both in the BSA -I−1 system and the model system, tryptophan-I−1. It is supported by the observed relationship between the ratio of quenching rate constants (k
q
) and diffusion coefficients and alsok
q
with bulk viscosity. 相似文献
148.
The microwave subsidiary absorption threshold in tangentially magnetized yttrium-iron-garnet (YIG) films was measured as a function of the static magnetic field, film thickness and decrease in the 0.3–3 μm range is observed. The effect is explained quantitatively by using modified Damon-Eshbach dispersion relations which take into account exchange interactions.
The effect of temperature on hcrit, the smallest threshold field amplitude, in the 250<T< 450 K temperature range can be expressed by an empirical relationship hcrit Ms(T)-1.6 where Ms is the saturation magnetization. This hcrit vs Ms relationship is similar to that obtained for the magnetization dependence of parallel pump thresholds in Li-Ti ferrite compounds. 相似文献
149.
H. Grübmeier A. Naoumidis G. Stochniol A. Tsoga 《Fresenius' Journal of Analytical Chemistry》1995,353(3-4):393-398
Chemical interactions at the phase boundaries of materials applied for the solid oxide fuel cell (SOFC) have been studied by EPMA. The chemical reactivity at the interface of Lay-xSrxMnO3/ZrO2-Y2O3 is dependent on the stoichiometry (y) and the Sr content (x) of the perovskite. Typical reaction products (zirconates) and a diffusion zone in the ZrO2–Y2O3 have been observed. The extension of cation release (Mn) is related to the increasing chemical activity of Mn oxide in the perovskite by the Sr substitution for La. The wettability of the metal/oxide interface in the anode cermet (Ni/ZrO2–Y2O3) has been found to be influenced by chemical reactions resulting from the applied reducing atmosphere with high carbon activity. The disintegration of ZrO2–Y2O3 in contact with molten Ni or Ni-Ti and Ni-Cr alloys leads to the redeposition of Y2O3-enriched oxides and also to Zr-rich intermetallic compounds and eutectics. 相似文献
150.
ALEPH Collaboration D. Buskulic D. Casper I. De Bonis D. Decamp P. Ghez C. Goy J. -P. Lees A. Lucotte M. -N. Minard et al. 《Zeitschrift fur Physik C Particles and Fields》1995,69(1):379-392
A data sample of about 3.0 million hadronicZ decays collected by the ALEPH experiment at LEP in the years 1991 through 1994 is used to make an inclusive selection of
B hadron events. In this event sample 4227±140±252B* mesons in the decayB*→Bγ and 1944±108±161B**
u,d
mesons decaying into a B meson and a charged pion are reconstructed. Here and in the followingB**
u,d
denotes the eightL=1(bū) and (bd) states and their charge conjugate.
For the well establishedB* meson the following quantities are obtained:ΔM=M
B*−MB=(45.30±0.35±0.87) MeV/c2 andN
B*/(N
B+N
B*)=(77.1±2.6±7.0)%. The angular distribution of the photons in theB* rest frame is used to measure the relative contribution of longitudinalB* polarization states to beσ
L/(σ
L+σ
T)=(33±6±5)%. 相似文献