Fluorescence Spectral Properties of Rhodamine 6G at the Silica/Water Interface

In this work, total internal reflection synchronous fluorescence spectroscopy (TIRSF) is applied successfully to investigate rhodamine 6G (R6G) at the silica/water interface. In comparison with the bulk spectra, 5 nm red shift is observed in the interface spectra, which is mainly due to the limitation of freedom of rotational movement of R6G molecules at the interface. The increase of R6G concentration induces the self-quenching of adsorbate at the interface. The dependence of interfacial fluorescence on the acidity and ionic strength was studied. Both the acidity and ionic strength affect the adsorptive behaviors of R6G at the silica/water interface.     

考虑信号灯影响的交通流模型与数值模拟

基于信号灯交通系统中跟车行为的特点,改进了现有跟车方程,提出一个考虑信号影响的交通流模型.数值计算结果表明,该模型可以很好地再现车流的聚集与消散、停车波和启动波的演化规律及传播特性,证明模型是合理有效的. 关键词： 交通流模型 信号灯 停车波 启动波     

基于互注入半导体激光器的混沌输出产生17.5 Gbit/s随机码

采用两个借助光纤连接的相互注入半导体激光器,实验获取了10 GHz超宽带混沌种子信号.通过8-bit模数转换器将混沌信号转换为二进制数据流,并进行进一步的逻辑异或处理和舍弃最高有效位操作,最终获得了能顺利通过美国国家标准与技术研究院(National Institute of Standard and Technology,简记为NIST)800-22标准测试以及Diehard测试,速率达17.5 Gbit/s的高速随机码. 关键词： 随机码 混沌激光 互注入半导体激光器     

转捩边界层中流向条纹的新特性

基于边界层转捩后阶段的高精度直接数值模拟结果,发现流向条纹结构的低速条纹的演化过程中存在不连续现象,以及随高速条纹的发展会出现称之为"高速斑"的新特性. 通过详细剖析边界层转捩过程中的复杂涡系结构以及上喷下扫流动现象,证实流向高低速条纹新特性与流场涡系结构的演化过程紧密相关. 关键词： 流向条纹 边界层 转捩 直接数值模拟     

超高速碰撞产生磁场的1维模型

 为研究超高速弹丸碰撞靶板产生等离子体诱生的磁场,引用已有关于激光产生等离子体的磁场理论,结合麦克斯韦方程和法拉第电磁感应定律得到了超高速碰撞产生等离子体诱生磁场的1维理论模型。基于已有关于超高速正碰撞产生半球状等离子体云诱生磁场的偏微分方程,建立了柱坐标系下超高速斜碰撞产生部分椭球状等离子体云的偏微分方程。通过感应线圈进行了磁感应强度的实验测量,实验结果与模型预言表明,该模型可近似地描述超高速斜碰撞产生等离子体诱生的磁感应强度。     

Effective Polytropic Indices of Anisotropic Planetary Magnetosheath Plasmas with Magnetoacoustic Waves

Magnetosheath models for the planets Earth, Jupiter and Saturn are developed within the frame of the double‐adiabatic Chew‐Goldberger‐Low approximation. It is shown that in all three magnetosheaths slow and fast magnetoacoustic waves are generated, the dispersions of which considerably differ from that of isotropic systems. If slow magnetoacoustic waves exist in the magnetosheaths, then the effective polytropic coefficient of the plasma may be smaller than unity ‐ that means compression of the plasma is accompanied, in the average, by cooling. Such polytropic coefficients are not obtained when fast magnetoacoustic waves are excited (© 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Nanoscale retention‐loss dynamics of polycrystalline PbTiO3 nanotubes

We observed the nanoscale retention dynamics of polycrystalline PbTiO₃ nanotubes using piezoresponse force microscopy. We found that the retention loss of the nanodot domains on the nanotubes showed the stretched exponential relaxation behaviors with stretched exponential factor n being less than 1 (0.523 and 0.692), which are similar to the thin films. In addition, the nanodot domains showed a diverse relaxation time constant τ due to different remnant polarization of each dot domains. (© 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Hydrolysis and retro‐aldol cleavage of ethyl threo‐2‐(1‐adamantyl)‐3‐hydroxybutyrate: competing reactions

The hydrolysis of ethyl threo‐2‐(1‐adamantyl)‐3‐hydroxybutyrate ( 1 ) and the parent ester ethyl 3‐hydroxybutyrate ( 4 ) has been studied experimentally and computationally. In the hydrolysis of threo‐ester 1 with 2 M NaOH, predominantly retro‐aldol product was observed, whereas the hydrolyzed product was present in a minor amount. When the reaction is carried out under the same conditions with the parent ester ethyl 3‐hydroxybutyrate ( 4 ), hydrolyzed product is exclusively observed. The competitive pathways, namely hydrolysis and the retro‐aldol reaction for 1 and 4 were investigated using DFT calculations in the both gas and solvent phase. The calculated results in the solvent phase at B3LYP/6–31 + G* level revealed that the formation of retro‐aldol products is kinetically preferred over the hydrolysis of threo‐ester 1 in the presence of a base. However, the parent ester 4 showed that the retro‐aldol process is less favored than the hydrolysis process under similar conditions. The steric effect imposed by the bulky adamantyl group to enhance the activation barriers for the hydrolysis of the ethyl threo‐2‐(1‐adamantyl)‐3‐hydroxybutyrate ( 1 ) was further supported by the calculations performed with tert‐butyl group at the α‐carbon atom of ethyl 3‐hydroxybutyrate ( 7 ). Copyright © 2010 John Wiley & Sons, Ltd.