Total cross sections for electrons scattering from simple molecules containing the larger atom sulfur at 30-5000eV

A complex optical model potential modified by the concept of bonded atom, which takes into consideration the overlapping effect of electron clouds, is employed to calculate the total cross sections for electrons scattering from simple molecules （SO2, H2S, OCS, CS2 and SO3） containing the larger atom, sulfur, at 30-5000eV by using the additivity rule model at Hartree-Fock level. The quantitative molecular total cross section results are compared with those obtained in experiments and other calculations wherever available, and good agreement is obtained. It is shown that the additivity rule model together with the complex optical model potential modified by the concept of bonded atom can give the results closer to the experiments than the one unmodified by it. So, the introduction of bonded-atom concept in complex optical model potential betters the accuracy of the total cross section calculations of electrons from the molecules containing the larger atom, sulfur.     

GaAs基GaAsSb/GaInAs双层量子阱的发光

嵌入GaAs中的GaAsSb／GaInAs量子阱因其在1．3～1．5μm光通信波段发光的潜力而受到关注,我们研究了一系列MBE生长的GaAsSb／GaInAs量子阱样品的光致发光,发现所有样品在室温下都出现了一个较强的、波长在1．3μm附近的低能峰和一个较弱的高能峰。变温及变激发功率的荧光谱测量研究发现,高能峰只有在150K以上的测试条件下才能观测到,并且其相对强度随着温度的升高而增加,其调制光谱显示出第一类跃迁的特征。他们建立了理论模型,计算的结果支持将这一发光峰指派为GaInAs层内电子的基态与重空穴激发态间的跃迁,并与实验数据吻合得很好。同时初步讨论了改善1．3μm的低能峰发光的方法。     

Photocatalytic degradation of methyl orange by nano-TiO_2 thin films prepared by RF magnetron sputtering

Nano-TiO2 thin films are deposited by radio frequency （RF） magnetron sputtering using TiO2 ceramic target and characterized by X-ray diffractometer, atomic force microscope, and ultraviolet-visible spectrophotometer. The photocatalytic activity is evaluated by light-induced degradation of methyl orange solutions （5, 10, and 20 ppm） using a high pressure mercury lamp as the light source. The film is amorphous, and its energy gap is 3.02 eV. The photocatalytic degradation of methyl orange solution is the first-order reaction and the apparent reaction rate constants are 0.00369, 0.0024, and 0.00151 for the methyl orange solution concentrations of 5, 10, and 20 ppm, respectively.     

Effect of Temperature on Polaron Stability in a One-Dimensional Organic Lattice

Effect of temperature on the polaron stability in a one-dimensional organic lattice is investigated within the Su-Schrieffer-Heeger model. The temperature effect is simulated by introducing random forces to the equation of the lattice motion. It is found that the localized polaron state becomes delocalized even at low temperatures. The time of polaron keeping localized depends on the magnitude of temperatures. By taking into account the thermal effect, we find that the dissociation field is weaker as compared with earlier works.     

Research on performance of multicasting in optical packet switched networks

Different multicasting schemes in optical packet switched networks are discussed, including the parallel mode, serial mode, and hybrid mode multicasting schemes. Simulated modeling technique is applied to compare the network-level performance of the three multicasting schemes. A conclusion can be drawn from the results that since the hybrid-mode multicasting scheme can increase the multicast success ratio and reduce the packet retransmission times compared with the other two schemes, it is the best choice for delivering multicasting sessions in the optical packet switched networks.     

激光感生色散光学滤波理论

利用半经典理论，建立了激光感生色散光学滤波的理论模型.通过求解密度矩阵方程，得到 感生极化率.并利用该理论计算出钾694 nm激光感生色散光学滤波器的透射谱，与发表的实 验结果基本符合. 关键词： 激光感生色散光学滤波 透射谱 极化率     

Branching fractions for psi(2S)-to-J/psi transitions

We describe new measurements of the inclusive and exclusive branching fractions for psi(2S) transitions to J/psi using e(+)e(-) collision data collected with the CLEO detector operating at CESR. All branching fractions and ratios of branching fractions reported here represent either the most precise measurements to date or the first direct measurements. Indirectly and in combination with other CLEO measurements, we determine B(chi(cJ) --> gamma(J/psi)) and B[psi(2S) --> light hadrons].     

Experimental observation of classical subwavelength interference with a pseudothermal light source

We report the experimental observation of classical subwavelength double slit interference with a pseudothermal light source. The experimental results are in good agreement with the theoretical simulation using the second order correlation function for the thermal light.     

Two universal equations of state for solids satisfying the limiting condition at high pressure

In this paper it is shown that the relationship of bulk modulus with pressure, B=f(P), should be linear both at low and high-pressure limiting conditions. Because most of present equations of state (EOS) for solids cannot satisfy such linear relationship at high pressure, a new function f(P) is proposed to satisfy the linearity. By integrating the bulk modulus, an EOS with three parameters and satisfying the quantum-statistics limitation is derived. It is shown that the EOS can be reduced to two-parameter EOS approximately satisfying the limiting condition. By applying the two EOSs and other three typical EOSs to 50 materials, it is concluded that for materials at low and middle-pressure regimes, the limiting condition does not operate, the Baonza EOS gives the best results, but it cannot provide analytic expression for cohesive energy. The Vinet and our second EOSs are slightly inferior, both EOSs can provide analytic expression for cohesive energy, and for materials at high-pressure regimes our second EOS gives the best results. The Holzapfel and our first EOSs give the worst results, although they strictly satisfy the limiting condition. For practical applications, the limiting condition is not important because it only operates as V→0.     

The SN3–SN2 spectrum. Rate constants and product selectivities for solvolyses of benzenesulfonyl chlorides in aqueous alcohols

Rate constants for a wide range of binary aqueous mixtures and product selectivities (S) in ethanol–water (EW) and methanol–water (MW) mixtures, are reported at 25 °C for solvolyses of benzenesulfonyl chloride and the 4‐chloro‐derivative. S is defined as follows using molar concentrations: S = ([ester product]/[acid product]) × ([water solvent]/[alcohol solvent]). Additional selectivity data are reported for solvolyses of 4‐Z‐substituted sulfonyl chlorides (Z = OMe, Me, H, Cl and NO₂) in 2,2,2‐trifluoroethanol–water. To explain these results and previously published data on kinetic solvent isotope effects (KSIEs) and on other solvolyses of 4‐nitro and 4‐methoxybenzenesulfonyl chloride, a mechanistic spectrum involving a change from third order to second order is proposed. The molecularity of these reactions is discussed, along with new term ‘S_N3–S_N2 spectrum’ and its connection with the better established term ‘S_N2–S_N1 spectrum’. Copyright © 2009 John Wiley & Sons, Ltd.