基于石墨烯振幅可调的宽带类电磁诱导透明超材料设计

基于石墨烯的电控特性提出了一种由金属线谐振器和"H"型谐振器组成的宽带可调的类电磁诱导透明(类EIT)超材料结构.首先,利用CST Microwave Studio软件对该超材料结构的透射特性进行了仿真.该结构在1.05—1.46 THz内的透射窗由金属线谐振器的等离子谐振和"H"型谐振器的电感-电容谐振干涉相消引起,且暗模式谐振器的数量增多导致了透射窗带宽的增加.其次,仿真模拟了该结构在不同石墨烯费米能级下的透射特性.当石墨烯费米能级由0 eV逐渐增加到1.5 eV时,该结构透射窗在1.05—1.46 THz内的平均透射振幅由87%逐渐减少到25%,实现了宽带可调.同时,通过仿真模拟该结构在1.26 THz下的电场分布对其透射机理进行了分析,并实验制备了类EIT超材料结构样品,且利用太赫兹时域光谱对样品进行了透射性能测试,测试结果与仿真分析的趋势基本一致.     

基于渐进添边的准循环压缩感知时延估计算法

针对时延估计问题中压缩感知类算法现有测量矩阵需要大量数据存储量的问题,提出了一种基于渐进添边的准循环压缩感知时延估计算法,实现了稀疏测量矩阵条件下接收信号时延的准确估计.该算法首先建立压缩感知与最大似然译码之间的理论桥梁,然后推导基于低密度奇偶校验码的测量矩阵的设计准则,引入渐进添边的思想构造具有准循环结构的稀疏测量矩阵,最后利用正交匹配追踪算法正确估计出时延.对本文算法的计算复杂度与测量矩阵的数据存储量进行理论分析.仿真结果表明,所提算法在测量矩阵维数相同的条件下正确重构概率高于高斯随机矩阵和随机奇偶校验测量矩阵,相比于随机奇偶校验矩阵,在数据存储量相等的条件下,以较少的计算复杂度代价得到了重构概率的较大提高.     

顺式羰基铑碘络合物催化甲醇制乙酸反应的动力学研究

本文运用密度泛函理论DFT-B3LYP方法,对铑、碘元素采用相对论校正赝势基组SDD,对C、O、H采用6-311+G(2d,p)基组,计算研究了顺式羰基铑碘络合物催化甲醇羰基化制乙酸反应的微观机理,优化了各反应物、中间体和过渡态的构型特征,用频率分析方法和内禀反应坐标方法对过渡态进行了验证,运用Kozuch撰写的能量跨度模型获得循环反应的动力学信息,确定了决定循环反应速率的决速过渡态和决速中间体,并利用转化频率评估了催化性能与温度的变化关系.     

定性检验牛奶中的营养素

利用常用仪器、微型实验和相应物质的特征反应,对牛奶中所含营养素进行定性检验,结果表明：牛奶中含有蛋白质、维生素、钙、镁、磷、钾、铁元素。该实验具有微型化、绿色化、简约化和生活化的特质。     

有限时间Lyapunov指数的高精度计算新方法

针对目前有限时间Lyapunov指数(FTLE)计算方法准确度不高和无法获得边界值的问题,基于对偶数理论提出了一种新的高精度计算方法.首先描述了基于有限空间差分方法计算FTLE的缺点和问题:其次介绍了基于对偶数理论的高精度导数计算方法及其显著优点,并将动力系统的柯西一格林形变张量计算问题转化为对偶数空间中非线性微分方程数值求解问题;最后对单摆和非线性Duffing振子两个典型物理动力系统进行了数值实验.结果表明:基于对偶数理论的新方法能有效、方便和高精度地计算出有限时间Lyapunov指数场,并成功识别出所包含的拉格朗日相关结构.     

基于Chua电路的四维超混沌忆阻电路

近年来,忆阻混沌电路受到国内外学者的广泛关注,然而目前四维忆阻系统往往只存在普通混沌(仅有一个正Lyapunov指数),本文通过用忆阻替换Chua电路中电阻的新途径,得出一个简单的四维忆阻电路,与仅含有限个孤立不稳定平衡点的大多已知系统不同,本系统存在无穷多个稳定和不稳定平衡点,研究发现该系统存在着极限环、混沌、超混沌等丰富的复杂行为,通过进一步数值分析和电路仿真实验,证实了超混沌吸引子的存在,从而解决了关于四维忆阻电路是否存在超混沌的疑问。     

基于FPGA的储存环束流轨道联锁系统设计

上海光源储存环束流轨道联锁系统是加速器机器联锁保护系统(MPS)的重要组成部分,针对日常供光和机器研究的需求,需要对束流位置测量系统前各Libera电子学输出的联锁信号进行标记,以区分联锁信号的先后顺序和误报的联锁信号,同时触发所有Libera电子学前锁存逐圈(TBT)数据。新的联锁系统将所有联锁信号通过光纤传输汇总至FPGA数据采集板卡进行甄别,并将该系统集成储存环EPICS控制系统中。实验室测试显示该系统能够能够分辨数十ns范围内模拟的联锁信号,同时输出特定的触发信号至对应的Libera电子学,表明该系统达到设计要求。     

Distribution Algorithm for Torque Control of New Energy Four-Wheel Hub Motor

Russian Physics Journal - Due to the nonlinear, strong coupling and uncertain parameters of the new energy four-wheel hub motor, it is more difficult to control the torque of the motor. In order to...     

Hydrophobic drying and hysteresis at different length scales by molecular dynamics simulations

We performed molecular dynamics simulations to investigate hydrophobic interactions between two parallel hydrophobic plates immersed in water. The two plates are separated by a distance D ranging from contact to a few nanometers. To mimic the attractive hydrophobic force measurement in a surface force experiment, a driving spring is used to measure the hydrophobic force between two hydrophobic plates. The force-distance curves, in particular the force variations from spontaneous drying to hydrophobic collapse are obtained. These details are usually not accessible in the surface force measurement due to the unstable jump into contact. The length-scale effect on the hydrophobic drying during normal approach and the hydrophobic hysteresis during retraction has been studied. We find that the critical distance at which a spontaneous drying occurs is determined by the shorter characteristic dimension of the plate, whereas the hydrophobic hysteresis is determined by the longer characteristic dimension of the plate. The variations of the potential of mean force versus separation during approach and retraction are also calculated. The results show that water confined between two parallel hydrophobic plates is in a thermodynamic metastable state. This comparably high energy state leads to the spontaneous drying at some critical distance.     

Hydration force between mica surfaces in aqueous KCl electrolyte solution

Liquid-vapor molecular dynamics simulations are performed to study the interaction forces between two mica surfaces in an aqueous KCl electrolyte solution. Strong repulsive hydration force is obtained within a distance of ~2 nm between the two mica surfaces, which cannot be explained by the continuum theory of double-layer repulsion. We find that this short-range repulsive hydration force is much stronger than the double-layer force between mica surfaces. Whereas the simulation system is much smaller than the surface force measurement system, fundamental mechanisms of repulsive hydration force are revealed. In particular, important features of the step-like force oscillatory behavior during normal compression and force hysteresis during retraction are observed. Detailed analysis of the ionic density distributions shows that the "forced adsorption" of diffusive K(+) ions onto mica surfaces during compression and the subsequent "slow desorption" of the absorbed K(+) ions from mica surfaces upon retraction are responsible for the hysteresis phenomenon. From a mechanics point of view, we attribute the load bearing capacity of the dense electrolyte to the very hard hydration shells of K(+) metal ions under confinement. We find that the hydrated K(+) ions and Cl(-) co-ions remain very diffusive in the aqueous film. Water molecules in the hydration layer are also very fluidic, in the sense that the diffusion constant of water molecules is less than its bulk value by at most 3 orders of magnitude under the extreme confinement.