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961.
962.
E. S. Moskalenko M. Larsson K. F. Karlsson P. O. Holtz B. Monemar W. V. Schoenfeld P. M. Petroff 《Physics of the Solid State》2007,49(10):1995-1998
We report on low-temperature microphotoluminescence (μ-PL) measurements of InAs/GaAs quantum dots (QDs) exposed to a lateral
external electric field. It is demonstrated that the QDs’ PL signal could be increased severalfold by altering the external
and/or the internal electric field, which could be changed by an additional infrared laser. A model which accounts for a substantially
faster lateral transport of the photoexcited carriers achieved in an external electric field is employed to explain the observed
effects. The results obtained suggest that the lateral electric fields play a major role for the dot luminescence intensity
measured in our experiment—a finding which could be used to tailor the properties of QD-based optoelectronic applications.
The text was submitted by the authors in English. 相似文献
963.
N. B. Voznesensky E. V. Gavrilov A. P. Zhevlakov V. K. Kirillovskiĭ P. V. Orlov 《Technical Physics》2007,52(2):271-275
Methods and schemes to inspect the EUV mirror shape are developed on the basis of a point diffraction interferometer with computer processing of interferograms. A measurement accuracy to within 0.001 of a wavelength in the visual range is achieved. 相似文献
964.
José A. Anquela Teresa Cortés Miguel Gómez-Lozano Mercedes Siles-Molina 《Acta Mathematica Hungarica》2004,103(3):177-196
We investigate the basic properties of the different socles that can be considered in not necessarily semiprime associative
systems. Among other things, we show that the socle defined as the sum of minimal (or minimal and trivial) inner ideals is
always an ideal. When trivial inner ideals are included, this inner socle contains the socles defined in terms of minimal
left or right ideals.
This revised version was published online in June 2006 with corrections to the Cover Date. 相似文献
965.
The variation of the density functions on chaotic spheres in chaotic space-like Minkowski space time
A.E. El-Ahmady 《Chaos, solitons, and fractals》2007,31(5):1272-1278
In this article we introduce types of chaotic spheres in chaotic space-like Minkowski space time Mn+1. The variations of the density functions under the folding of these chaotic spheres are defined. The foldings restriction imposed on the density function are also discussed. The relations between the folding of geometry and pure chaotic manifolds are deduced. Some theorems concerning these relations are presented. 相似文献
966.
967.
Nieves Gonzlez Carlos Elvira Julio San Romn 《Journal of polymer science. Part A, Polymer chemistry》2003,41(3):395-407
This article deals with the synthesis of hydrophilic methacrylic monomers derived from ethyl pyrrolidone [2‐ethyl‐(2‐pyrrolidone) methacrylate (EPM)] and ethyl pyrrolidine [2‐ethyl‐(2‐pyrrolidine) methacrylate (EPyM)] and their respective homopolymers. For the determination of their reactivity in radical copolymerization reactions, both monomers were copolymerized with methyl methacrylate (MMA), the reactivity ratios being calculated by the application of linear and nonlinear mathematical methods. EPM and MMA had ratios of rEPM = 1.11 and rMMA = 0.76, and this indicated that EPM with MMA had a higher reactivity in radical copolymerization processes than vinyl pyrrolidone (VP; rVP = 0.005 and rMMA = 4.7). EPyM and MMA had reactivity ratios of rEPyM = 1.31 and rMMA = 0.92, and this implied, as for the EPM–MMA copolymers, a tendency to form random or Bernoullian copolymers. The glass‐transition temperatures of the prepared copolymers were determined by differential scanning calorimetry (DSC) and were found to adjust to the Fox equation. Total‐conversion copolymers were prepared, and their behavior in aqueous media was found to be dependent on the copolymer composition. The swelling kinetics of the copolymers followed water transport mechanism case II, which is the most desirable kinetic behavior for a swelling controlled‐release material. Finally, the different states of water in the hydrogels—nonfreezing water, freezing bound water, and unbound freezing water—were determined by DSC and found to be dependent on the hydrophilic and hydrophobic units of the copolymers. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 395–407, 2003 相似文献
968.
Mary E. Neubert DAVID G. ABDALLAH Jr Sandra S. Keast Julie M. Kim Soonnam Lee Ryan M. Stayshich Margaret E. Walsh Rolfe G. Petschek Shin-Tson Wu 《Liquid crystals》2003,30(6):711-731
New diphenyldiacetylenes of the type with A, B = H and/or F; m = 0, 1; n = 1-4; and X = C n H 2n + 1 , F, CF 3 or CN were synthesized and their mesomorphic properties determined by hot stage polarizing microscopy and DSC. When m = 0, all of these compounds showed only a nematic phase except when X = CF 3 when both nematic and smectic A phases were seen. Both clearing and melting temperatures were higher than those reported for substitution with the corresponding alkyl chains but the much larger increase in clearing temperatures produced considerably wider nematic phases. Eutectic mixtures of a few of these olefins yielded nematic materials also having much wider temperature ranges and higher clearing temperatures than the eutectic mixtures of the alkyl compounds, while retaining their high birefringence and low viscosities. Such materials are of interest for beam-steering devices.
Four of the diacetylenes with m = 1 ( A, B = H) were also prepared ( X = C 6 H 13 , F, n = 2, 3). When X was C 6 H 13 ( n = 2), the nematic range was smaller in the 2- than in the 1-olefin but wider than in the alkyl series. When X = F, either no nematic phase or a monotropic one was observed, whereas the 1-olefins gave a much wider nematic phase. Both transition temperatures were lower than those for the corresponding 1-olefin and alkyl analogues. The compound with X = C 6 H 13 and n = 2 had a melting temperature below room temperature. 相似文献
Four of the diacetylenes with m = 1 ( A, B = H) were also prepared ( X = C 6 H 13 , F, n = 2, 3). When X was C 6 H 13 ( n = 2), the nematic range was smaller in the 2- than in the 1-olefin but wider than in the alkyl series. When X = F, either no nematic phase or a monotropic one was observed, whereas the 1-olefins gave a much wider nematic phase. Both transition temperatures were lower than those for the corresponding 1-olefin and alkyl analogues. The compound with X = C 6 H 13 and n = 2 had a melting temperature below room temperature. 相似文献
969.
V. G. Lakhtin V. L. Ryabkov A. V. Kisin V. M. Nosova M. V. Polyakova E. A. Chernyshev 《Russian Chemical Bulletin》1995,44(11):2163-2167
Liquid-phase chlorination of a number of chloro(chlorovinyl)methylsilanes was investigated. A number of novelC-chlorosilanes were characterized by IR and1H NMR spectra. Some regularities of these reactions were determined; correlations between the structure of chloro(chlorovinyl)methylsilanes and their reactivities were identified.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 2256–2260, November, 1995. 相似文献
970.
Runge–Kutta based convolution quadrature methods for abstract, well-posed, linear, and homogeneous Volterra equations, non
necessarily of sectorial type, are developed. A general representation of the numerical solution in terms of the continuous
one is given. The error and stability analysis is based on this representation, which, for the particular case of the backward
Euler method, also shows that the numerical solution inherits some interesting qualitative properties, such as positivity,
of the exact solution. Numerical illustrations are provided. 相似文献