The “Average” Work Function and Emission Area in the Fowler-Nordheim Equation

Derivation of the elementary Fowler-Nordheim equation is based on several strong physical assumptions (e.g. smooth flat surface and uniform work function across emitting surface, constant emission area and a uniform distribution of the applied field over it). A real emitter, however, definitely does not fulfill these assumptions. In spite of it the total emission current follows the FN equation and is frequently used for an estimation of the "average" work-function. The physical basis of this procedure and of the terms "average" work function and "emission area" are analyzed from the experimentalist's point of view. Thus some of the older - more or less intuitive - conclusions are substantiated.     

Unusual Behavior of Nanocrystalline Strontium Oxide Toward Hydrogen Sulfide

The thermodynamically favored reaction of solid strontium oxide with gaseous hydrogen sulfide is kinetically enhanced to a large degree by the use of higher surface area nanocrystalline SrO in the form of brush-like collections of metal oxide fibers. An unusual feature is that the reaction SrO + H₂S SrS + H₂O proceeds stoichiometrically at room temperature, but at higher temperatures the reaction efficiency goes down, apparently due to rapid temperature induced crystal growth of the nanocrystalline SrO. The samples studied vary in crystallite size from 20 to 27nm, while average particle size (nanocrystal aggregates) varies in the following order; aerogel prepared SrO (100nm) 相似文献   

Burst detection in turbulent channel flows based on large eddy simulation databases

As one of the important coherent structures in the near-wall region, turbulent burst is responsible for the production and transport of major turbulent kinetic energy and Rey- nolds stress[1]. Nearly half of turbulent kinetic energy or Reynolds stress is produced in the near-wall region, and 80% flows in outer region only contribute 20% of them. Both ejection and sweeping events contribute 60―70% of the turbulent shear stress respec- tively[2]. Recently, turbulent burst process has been foun…     

Evaluation of the protein solvent-accessible surface using reduced representations in terms of critical points of the electron density

The aim of our study is the development of a method for calculating the interface of dimerization of protein-protein complexes based on simplified medium-resolution structures. In particular, we wished to evaluate if the existing concepts for the computation of the Solvent-Accessible Surface Area (SASA) of macromolecules could be applied to medium-resolution models. Therefore, we selected a set of 140 protein chains and computed their reduced representations by topological analysis of their electron density maps at 2.85 A crystallographic resolution. This procedure leads to a limited number of critical points (CPs) that can be identified and associated to backbone and side-chain parts. To evaluate the SASA and interfaces of dimerization of the reduced representations, we chose and modified two existing programs that calculate the SASA of atomic representations, and tested (1) several radii tables of amino acids, (2) the influence of the backbone and side-chain points, and (3) the radius of the solvent molecule, which rolls over the surface. The results are shown in terms of relative error compared to the values calculated on the corresponding atomic representations of the proteins.     

Estimates in surfaces with positive constant Gauss curvature

We give optimal bounds of the height, curvature, area and volume of -surfaces in bounding a planar curve. The spherical caps are characterized as the unique -surfaces achieving these bounds.

     

Sectional bodies associated with a convex body

We define the sectional bodies associated to a convex body in and two related measures of symmetry. These definitions extend those of Grünbaum (1963). As Grünbaum conjectured, we prove that the simplices are the most dissymmetrical convex bodies with respect to these measures. In the case when the convex body has a sufficiently smooth boundary, we investigate some limit behaviours of the volume of the sectional bodies.

     

激光金属汽化汽离混合区状态参量的稳定性及其影响因素分析

在汽离混合区激光强度时空修正的基础上,近似求解了流体力学模型下的状态参数,找出了稳定状态参数的共同自洽参量,分析了自洽参量的取值方法,研究了相关参数对自洽参量的影响机制,结果发现:(1)汽离混合区内,状态参量的稳定性可用自洽参量的稳定性来表征;(2)当入射激光强度小于108W.cm-2时,自洽参量随入射激光强度变化相对较快,稳定性差;当激光强度大于108W.cm-2时,自洽参量随入射激光强度变化相对较慢,稳定性高;(3)汽离混合区各处的约化自洽参量随辐照激光的波长成变周期增加的变化,波长越长,约化自洽参量越大;(4)要使自洽参量稳定,纹波较小,宜采取短波激光辐照;(5)当蒸汽压强小于2.7×106Pa时,自洽参量随蒸汽压强成指数递减规律变化;当蒸汽压大于2.7×106Pa时,自洽参量与蒸汽压强之间没有对应关系.     

Performance limits of pico-cell systems using radio-over-fiber techniques with an electroabsorption modulator

We investigate the performance limits of a pico-cell system using the radio- over-fiber technique with an electroabsorption modulator (EAM) in a 2.4 GHz wireless local area network (WLAN) environment. To understand the performance limits of the system using an EAM as the optical transceiver, we vary the optical modulation index (OMI) of the transmitter for different bias voltages to the EAM. Power margins in the links are found to estimate a possible service range, and packet loss rates (PLRs) in the pico-cell system are measured to evaluate the transmission performance. The total service range can be extended up to 3 m by adjusting the OMI of the transmitter for different applied bias voltages to the EAM.     

用于脉冲γ强度测量的Ф60,1000μmPIN探测器

采用电阻率为10000—20000Ω.cm的高阻单晶硅材料,研制成功灵敏区尺寸为60mm,耗尽层厚度~1000μm的大面积厚PIN半导体探测器.设计了该类探测器厚度测量专用的反冲质子测量系统,对探测器的时间响应、γ灵敏度、漏电流、γ/n分辨等物理参数进行了测量和分析,结果表明,这类探测器可满足低强度裂变n/γ混合场中脉冲γ强度测量的需要.     

Dispersion and Confinement Loss Control in Modified Hexagonal Photonic Crystal Fibers

This paper presents a novel technique for the control of chromatic dispersion and confinement loss in hexagonal photonic crystal fibers (H-PCFs). It is demonstrated that it is possible to obtain very low chromatic dispersion of 0 ± 0:38 ps/(nm·km) in the wavelength range of 1.41 to 1.66 μm and confinement loss of less than 0.0001 dB/km from a six ring modified H-PCF (MH-PCF). The higher order dispersion at 1.55 μm is about −0.001 ps/(nm²-km).