金纳米棒三聚体中的等离激元诱导透明

基于金纳米棒构成的三聚体微元结构模型,详细地研究了等离激元诱导透明(plasmon induced transparency,PIT)现象产生的物理过程.研究发现,三聚体的吸收谱线随着其耦合距离以及尺寸的变化,竖直金纳米棒所对应的偶极明模在平行双长条金纳米棒对应的暗模作用下会产生分裂.依据这一结果提出了一个新的物理解释,PIT现象的产生主要来自于竖直金纳米棒中偶极振荡的模式分裂后的相干叠加.同时,考虑到两个振子之间的耦合会伴随着一定的相位关联性,进而引入了耦合相位因子修正了洛伦兹振子耦合模型,解析地研究了耦合相位因子对吸收谱的调控作用和分裂明模之间的相干叠加效应对PIT效应的影响.这为在纳米尺寸范围设计人造原子、光开关、慢光效应等方面的应用提供了理论参考.     

轴向相干叠加高斯光束的M2传输因子

本文分别用标量叠加和矢量叠加的方法,对由两个束腰位置不同的高斯光束相干叠加而成的光束的传输特性进行了研究,结果表明,这种光束的传输因子M²不再是常数,而是随传输距离变化的.     

COMPLEX FUNDAMENTAL SOLUTIONS FOR SEMI-INFINITE PLANE AND INFINITE PLANE WITH HOLE UNDER VARIOUS BOUNDARY CONDITIONS

I.IntroductionBoundaryelementmethod(BEM)hasbeenwidelyusedforlinearandnonlinearanalysisofengineeringstructures.ThetriditionalboundaryelementdiscretizationforthecouplingproblemoftbullditliollandpipeinFig.IisshowninFig.2.ConlparcdwithFEM,BEMIlasmoreadvantages.Inthispaper,thegeneralmethodoffindingthecomplexfundamentalsolutions(CFSs)I'orsemi-illfiniteplanealldintllliteplanewithholeundervariousboundaryconditions(aCs)hasbeenestablishedbyLlsillgRiemann-Schwarzsymmetricprincipleandsuperpositio…     

四角点支撑纳米板稳态受迫振动解析解

本文基于非局部弹性理论及辛叠加方法,得到放置在黏弹性介质上四角点支撑矩形纳米板稳态受迫振动问题的解析解．将纳米板受迫振动问题导入哈密顿体系,得到哈密顿控制方程,在无需任何预设函数的情况下可直接对哈密顿控制方程进行求解,得到简支纳米板稳态受迫振动问题在辛空间展开形式的解析解．进而通过边界叠加,可求出四角点支撑纳米板稳态受迫振动的解析解．数值算例中验证了本文应用辛叠加方法得到解析解的准确性,并以石墨烯纳米板为例,分析了非局部参数和黏弹性介质参数对四角点支撑石墨烯纳米板稳态受迫振动的影响．结果表明,非局部参数和黏弹性介质参数的变化会影响石墨烯纳米板的共振频率及共振幅值．     

模糊桁架结构在模糊激励下的动力响应分析

研究了模糊参数桁架结构在模糊荷载激励下的动力响应分析问题. 不仅模糊桁架结构的物 理参数、几何尺寸具有模糊性,而且外载荷幅值也具有模糊性时,从Duhamel积分式出发,利用模糊因子法、区间运算和振型叠加法求出了结构动力响应模糊变量的表达式. 最后通过算例考察了结构参数和作用荷载的模糊性对结构动力响应的影响,表明所提出的计算模型和 分析方法是正确与可行的.     

TGSA: A molecular superposition program based on topo‐geometrical considerations

In this article, a new molecular alignment procedure to provide general‐purpose, fast, automatic, and user‐intuitive three‐dimensional molecular alignments is presented. This procedure, called Topo‐Geometrical Superposition Approach (TGSA), is only based on comparisons of atom types and interatomic distances; hence, the procedure can handle large molecular sets within affordable computational costs. The method is able to accurately align 3D structures using the common molecular substructures, as inferred by the bonding pattern (atom correspondences), where present. The algorithm has been implemented into a program named TGSA99, and it has been tested over eight different molecular sets: flavilium salts, amino acids, indole derivatives, AZT, steroids, anilide derivatives, poly‐aromatic‐hydrocarbons, and inhibitors of thrombine. The TGSA algorithm performance is evaluated by means of computational time, number of superposed atoms, and index of fit between the compared structures. © 2000 John Wiley & Sons, Inc. J Comput Chem 22: 255–263, 2001     

相位差与一般相干迭加态压缩特性

研究一般相干态的迭加态|ψ＞=a|β＞ beiψ|mβeiδ＞的k次方压缩特性,结果表明:一般相干态的迭加态和量子涨落的k次方压缩,在m=1时可表为k≠2nπ/δ,此处n是整数;在m≠1时,压缩的次方数可以是偶数也可以是奇数;当δ=π时,无论m[m∈(0.∞)]取何值均存在奇次方压缩,当δ=π/2时,无论m取何值均存在奇次方压缩和偶次方压缩.这说明参数相位差δ对一般相干态的k次方压缩的次方数起关键性的作用.     

Thermorheological analysis of PVC blends

The effect of temperature on dynamic viscoelastic measurements of miscible poly (vinyl chloride) (PVC)/ethylene‐vinyl acetate–carbon monoxide terpolymer (EVA‐CO) and immiscible PVC/high‐density polyethylene (HDPE) and PVC/chlorinated polyethylene (CPE) molten blends is discussed. PVC plasticized with di(2 ethyl hexyl) phthalate (PVC/DOP) and CaCO₃ filled HDPE (HDPE/CaCO₃) are also considered for comparison purposes. Thermorheological complexity is analyzed using two time–temperature superposition methods: double logarithmic plots of storage modulus, G′, vs. loss modulus, G″, and loss tangent, tan δ, vs. complex modulus, G*, plots. Both methods reveal that miscible PVC/EVA‐CO and PVC/DOP systems are thermorheologically complex, which is explained by the capacity of PVC to form microdomains or crystallites during mixing and following cooling of the blends. For immiscible PVC/HDPE and PVC/CPE blends the results of log G′ vs. log G″ show temperature independence. However, when tan δ vs. log G* plots are used, the immiscible blends are shown to be thermorheologically complex, indicating that the morphology observed by microscopy and constitued by a PVC phase dispersed in a HDPE or CPE matrix, is reflected by this rheological technique. © 2000 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 38: 469–477, 2000     

Generation of intense water window X-ray pulses by superposition of an initial state of the helium atom driven by a three-color field

We theoretically study the generation of high-order harmonics and attosecond pulses from the superposition of an initial state in helium atom driven by a three-color laser field. It is shown that when the initial state is chosen to be a single electronic state, due to the rapid depletion of the ground state, the efficiency of the spectral continuum will be decreased as the initial state increases. When the initial state is chosen to be the coherent superposition of the ground state and an arbitrary excited state, the efficiency of the spectral continuum can be enhanced compared to that from the single initial state. Further, with the optimization of the three-color laser beam, not only can the harmonic cutoff be extended to the water window X-ray region but also the spectral continuum is contributed by the single harmonic emission peak with the dominant short quantum path. Consequently, two combinations of the laser parameters can be found to generate the water window spectral continuum. By properly superposing some harmonics on the spectral continuum, a number of intense water window pulses with the duration of sub-35 as can be produced.     

声子晶体中SH波缺陷模的相干叠加理论

利用波的相干叠加原理推导出一维掺杂声子晶体中SH波缺陷模的透射率公式和频率公式,即建立了缺陷模的相干叠加法。将相干叠加法与转移矩阵法和共振理论进行了比较研究,结果表明缺陷模的相干叠加法具备转移矩阵法和共振理论各自的优点,又克服了转移矩阵法和共振理论各自的不足。相干叠加法是研究一维掺杂声子晶体中SH波缺陷模的一种更有效的方法。