Total electron scattering cross sections for carbon dioxide at low electron energies

Absolute total electron scattering cross sections for carbon dioxide have been measured at low electron energies using a photoelectron source. The measurements have been carried out at 27 electron energies varying from 0.91–9.14 eV with an accuracy of ±3%. The cross sections obtained in the present experiment have been compared with other measurements and theoretical computations.     

Comparison of Thermodynamic Characteristics of a Potential Well under Quantum and Classical Approaches

The conjecture according to which the mean energy of an equilibrium system in quantum theory exceeds the mean energy of the corresponding classical system is considered. It is rigorously proved that the conjecture holds for the potential well. The estimates for the mean energy of the potential well at high and low temperatures are of special interest.     

透镜空间L~1(p)上向量丛的示性类

本文讨论了透镜空间 L1( p)的上同调环中生成元的运算性质 ,进而利用 L1( p)的 KO -结构得到了L1( p)上任一向量丛的全 Stiefel-Whitney类     

Halin-图的点强全染色

图G(V,E)的一个k-正常全染色f叫做一个k-点强全染色当且仅当对任意v∈V(G), N[v]中的元素被染不同色,其中N[v]={u|uv∈V(G)}∪{v}．χTvs(G)=min{k|存在图G的k- 点强全染色}叫做图G的点强全色数．对3-连通平面图G(V,E),如果删去面fo边界上的所有点后的图为一个树图,则G(V,E)叫做一个Halin-图．本文确定了最大度不小于6的Halin- 图和一些特殊图的的点强全色数XTvs(G),并提出了如下猜想:设G(V,E)为每一连通分支的阶不小于6的图,则χTvs(G)≤△(G) 2,其中△(G)为图G(V,E)的最大度．     

物质纯重力场部分的能量-动量张量研究

认为物质的质量(能量)存在形式可分为两部分，一部分是以纯物质形式存在的，另一部分是以纯重力场形式存在的.物质质量(能量)这两种形式各自对应着相应的能量 动量张量，物质总的能量-动量张量可表示为Tμν=T(Ⅰ)μν+T(Ⅱ)μν,这里，T(Ⅰ)μν，T（Ⅱ）μν分别代表物质纯物质部分和纯重力场部分的能量-动量张量.通过类比电磁理论，定义：ωμ≡-c2gμ0/g00,并引入一个反对称张量Dμν=ωμ/xν-ων/xμ，则物质纯重力场部分的能量-动量张量为T(Ⅱ)μν=(DμρDρν-gμνDαβDαβ/4 关键词： 能量-动量张量 纯重力场 重力场方程 标量重力势 矢量重力势     

A virtual instrumentation based protocol for the automated implementation of the inner field compensation method

One influential parameter which mediates interactions between many types of molecules and biological membranes stems from the lumped contributions of the transmembrane potential, dipole potential and the difference in the surface potentials on both sides of a membrane. With relevance to cell physiology, such electrical features of a biomembrane are prone to undergoing changes as a result of interactions with the aqueous surrounding. Among the most useful tools devoted to exploring changes of electrical parameters of a lipid membrane induced by certain extracellular ions, lipid composition, and embedded membrane peptides and proteins, are spectroscopic imaging and the inner field compensation (IFC) method. In this work we layout the principles of a fully computerized version of the IFC method, which makes it more readily available to users. As a direct application, we deployed this improved version of the IFC method to time-resolve changes induced by alamethicin monomers upon membrane dipole potential, following their aggregation within an artificial lipid membrane. Intriguingly, even prior crossing the membrane core, the membrane-bound alamethicin monomers are shown to significantly increase the dipole potential of the monolayer they reside in. Such data further emphasize the yet less-explored interplay between membrane-based protein and peptides, and the membrane dipole potential.     

Inverse Scattering for a Schroedinger Operator with a Repulsive Potential

We consider a pair of Hamiltonians （H, H0） on L2（R^n）, where H0=p^2 -x^2 is a SchrSdinger operator with a repulsive potential, and H = H0＋V（x）. We show that, under suitable assumptions on the decay of the electric potential, V is uniquely determined by the high energy limit of the scattering operator.     

Classical, phenomenological analysis of the kinetics of reactions at the gas-exposed surface of mixed ionic electronic conductors

The kinetics of reactions occurring at the gas-exposed surfaces of charged mixed ionic electronic conductors (MIECs) are examined from theoretical first principles. Analysis based on the classical electrochemical potential-transition state theory model reveals that the nature of the reactions is electrochemical in general. However, the influence of the surface potential on the reaction rate is opposite for adsorption and incorporation reactions. Two-dimensional finite volume models of an MIEC as working electrode in a half-cell configuration are presented. The results for a simple, two-step reduction process show that the effect of the surface potential on the rate of reactions is minimal for incorporation-limited reactions but more influential for adsorption-limited reactions. An erratum to this article is available at .     

江汉平原上空QTEC变化特征的统计分析

提出了一种观测台网用多接收机性能一致性的标定方法，并利用江汉平原GPS接收台网的观测数据，分析了该地区上空QTEC的日变化、季节变化、年变化和逐年变化的统计特征．标定结果表明，不同接收机之间的仪器偏差是从双频GPS卫星信标推算QTEC的主要误差来源之一，必须校正．统计分析证实，江汉平原上空QTEC的日变化特征同时受电离层和等离子层控制，其年变化以半年周期为主，峰值和谷值分别出现在两分点和两至点附近，QTEC值的逐年变化从太阳活动峰年到低年逐年下降，与以太阳黑子数为代表的太阳活动密切相关．     

Effect of external Gaussian random field on phonon spectrum of linear atomic chains

We present the theoretical study of the effect of external random field characterized by a Gaussian probability distribution function on the continuous phonon spectrum of one-dimensional (1D) chain, based on the Jacobian matrix method. The cumulative effect of the random field and simple isotopic defect is studied analytically and numerically. The Gaussian random field removes a square-root divergence appearing in the phonon spectrum of ideal 1D chain. The impurity phonon DOS shows strong dependence on the variance and the mean of the random field and exhibits very different behavior from the non-random case: the continuous spectrum is expanded and the δ-peak, describing discrete impurity vibrations in the non-random chain with the impurity, falls into a continuous zone.