Evaluation of performance enhancing proxies in internet over satellite

Performance enhancing proxies (PEPs) are widely used to improve the performance of TCP over high delay‐bandwidth product links and links with high error probability. In this paper we analyse the performance of using TCP connection splitting in combination with web caching via traces obtained from a commercial satellite system. We examine the resulting performance gain under different scenarios, including the effect of caching, congestion, random loss and file sizes. We show, via analysing our measurements, that the performance gain from using splitting is highly sensitive to random losses and the number of simultaneous connections, and that such sensitivity is alleviated by caching. On the other hand, the use of a splitting proxy enhances the value of web caching in that cache hits result in much more significant performance improvement over cache misses when TCP splitting is used. We also compare the performance of using different versions of HTTP in such a system. Copyright © 2003 John Wiley & Sons, Ltd.     

步进扫描时间分辨光谱及其在太阳电池光电导上的应用

建立傅里叶变换步进扫描时间分辨光电导光谱，并研究太阳电池中与转换效率密切相关的少数载流子寿命.实验选取三种典型的硅太阳电池(单晶硅样品1、多晶硅样品2和多晶硅样品3 )，发现其瞬态光电导的上升和衰退曲线可以分别用两个简单的指数函数描述.由于有复合中心的参与，复合过程中少数载流子的寿命比产生过程中的寿命短.为验证实验结果的可靠性，采用了提取样品少数载流子的体寿命和计算其有效扩散长度两种方法.通过与太阳电池暗伏安特性和负载特性研究相结合，进一步分析和讨论了少数载流子寿命与短路电流、开路电压和转换效率的关系.同时探讨了步进扫描时间分辨光谱实验的其他用途. 关键词： 步进扫描 时间分辨 硅太阳电池 瞬态光电导     

立方相GaN的持续光电导

研究了金属有机物化学气相外延 (MOVPE)方法生长的非故意掺杂的立方相 Ga N的持续光电导效应 .在六方相 Ga N中普遍认为持续光电导效应与黄光发射有关 ,而实验则显示在立方 Ga N中 ,持续光电导效应与其中的六方相 Ga N夹杂有关系 ,而与黄光发射没有关系 .文中提出 ,立方相 Ga N与其中的六方相 Ga N夹杂之间的势垒引起的空间载流子分离是导致持续光电导现象的物理原因 .通过建立势垒限制复合模型 ,解释了立方相 Ga N的持续光电导现象的物理过程 ,并对光电导衰减过程的动力学作了分析 .对实验数据拟合的结果证明以上的模型和推导是与实验相符的 .     

GaAs半导体中三光子吸收的非线性光电导测量

采用非线性光电导技术测量2.06μm激光激发的GaAs本征半导体三光子吸收,观察到三光子和单光子吸收的混合光电导,测得了三光子吸收系数.测量结果与理论计算符合较好.     

变温长波碲镉汞光电导现象研究

报道了ｎ型Ｈｇ０．８Ｃｌ０．２Ｔｅ光电导体的变温材料参数与性能参数的对照关系，并讨论了材料的锭条参数与小芯片霍耳参数的差异，得到一组光电导的实验优化数据，实测小芯片载流子浓度ｎ≈１．８×１０＾１５ｃｍ＾－３，这与高性能器件实测值的倒推数值一致，这被解释为长江红外高背景辐射的结果。     

Ohmic contact and transport properties of II–VI Green/Blue laser diodes

The employment of the Zn(Se,Te) pseudo-graded contacting scheme to p-type ZnSe-based alloys contributes directly to the recent demonstration of room temperature continuous-wave operation of II– VI green-blue laser diodes. Contact ohmicity is maintained down to cryogenic temperatures which enabled the investigation of electrical transport properties associated with the p-type nitrogen-doped ZnSe, Zn(S,Se), and (Zn,Mg)(S,Se). The observation of both persistent photoconductivity and a metastable population of holes which are in thermodynamic equilibrium with hydrogenic acceptors having reduced activation energy suggests the presence of a DX-like behavior for holes in p-type (Zn,Mg)(S,Se).     

Synthesis and properties of a poly(diphenylacetylene) containing carbazolyl groups

1-(p-N-Carbazolylphenyl)-2-phenylacetylene (p-CzDPA) was polymerized by TaCl₅–co-catalyst systems (cocatalysts: n-Bu₁Sn, Et₃SiH, and 9BBN) to produce acetone-insoluble polymers in about 60-70% yields. Poly(p-CzDPA) was a yellowish-orange solid, most part of which was soluble in toluene, chloroform, etc., and its weight-average molecular weights were around 4×10⁵. This polymer formed a tough film by solution casting, and was thermally very stable (the onset temperature of weight loss in TGA in air 470°C). The oxygen per-meability coefficient of the polymer at 25°C was lower than two barrers. The present polymer showed photoconductivity and redox activity. © 1995 John Wiley & Sons, Inc.     

Exciton Formation Dynamics and Band-Like Free Charge-Carrier Transport in 2D Metal Halide Perovskite Semiconductors

Metal halide perovskite (MHP) semiconductors have driven a revolution in optoelectronic technologies over the last decade, in particular for high-efficiency photovoltaic applications. Low-dimensional MHPs presenting electronic confinement have promising additional prospects in light emission and quantum technologies. However, the optimisation of such applications requires a comprehensive understanding of the nature of charge carriers and their transport mechanisms. This study employs a combination of ultrafast optical and terahertz spectroscopy to investigate phonon energies, charge-carrier mobilities, and exciton formation in 2D (PEA)₂PbI₄ and (BA)₂PbI₄ (where PEA is phenylethylammonium and BA is butylammonium). Temperature-dependent measurements of free charge-carrier mobilities reveal band transport in these strongly confined semiconductors, with surprisingly high in-plane mobilities. Enhanced charge-phonon coupling is shown to reduce charge-carrier mobilities in (BA)₂PbI₄ with respect to (PEA)₂PbI₄. Exciton and free charge-carrier dynamics are disentangled by simultaneous monitoring of transient absorption and THz photoconductivity. A sustained free charge-carrier population is observed, surpassing the Saha equation predictions even at low temperature. These findings provide new insights into the temperature-dependent interplay of exciton and free-carrier populations in 2D MHPs. Furthermore, such sustained free charge-carrier population and high mobilities demonstrate the potential of these semiconductors for applications such as solar cells, transistors, and electrically driven light sources.     

Highly luminescent diyne (?CC?CC?) containing hybrid polyphenyleneethynylene/poly(p‐phenylenevinylene) polymer: Synthesis and characterization

Luminophoric dialdehyde 1,4‐bis[4‐formylphenylethynyl‐(2,5‐dioctadecyloxyphenyl)‐buta‐1,3‐diyne] ( 4 ) enables the synthesis of diyne‐containing hybrid polyphenyleneethynylene/poly(p‐phenylenevinylene) polymer poly[1,4‐phenylene‐ethynylene‐1,4‐(2,5‐dioctadecyloxy)phenylene‐butadi‐1,3‐ynylene‐1,4‐(2,5‐dioctadecyloxy)phenylene‐ethynylene‐1,4‐phenylene‐ethene‐1,2‐diyl‐1,4‐(2,5‐dioctadecyloxy)phenylene‐ethene‐1,2‐diyl] ( 7 ) with a well‐defined general structure (? Ph? C?C? Ar? C?C? C?C? Ar? C?C? Ph? CH?CH? Ar? CH?CH? )_n, which was confirmed by NMR and infrared spectroscopy. The highly luminescent material is thermostable, soluble in usual organic solvents through the grafting of octadecyloxy side groups, and can be processed into transparent films. With the aim to investigate the effect of ? C?C? C?C? in the photophysical behavior of 7 , a comparison of the photophysics of monomers 3 [1,4‐bis(4‐formylphenylethynyl)‐2,5‐dioctadecyloxybenzene] and 4 and subsequently of their respective polymers 6 and 7 has been carried out. Similar photophysical behaviors for 6 (poly[1,4‐phenylenethynylene‐1,4‐(2,5‐dioctadecyloxyphenylene)ethene‐1,2‐diyl]) and 7 were observed in dilute CHCl₃ solution as a result of an identical chromophore system responsible for the absorption (λ_a = 448 nm) and emission (λ_f = 490 nm) in both compounds. The increased planarization and enhanced rigidity of the conjugated backbone in the solid state at room temperature as well as in frozen dilute tetrahydrofuran solution at 77 K cause the bathochromic shift of the absorption and emission spectra. The large octadecyloxy side chains obviously limit strong π‐π interchain interactions in the solid films, which explains the high fluorescence quantum yields of 35 and 52% obtained for 6 and 7 , respectively. The energetically arduous migration of the π electron through the diyne units not only requires a higher threshold voltage for the detection of photoconductivity in 7 but could possibly limit radiationless deactivation channels of the exciton, which explains the approximate 20% fluorescence quantum yields difference between 6 and 7 in the solid state. The electron‐withdrawing effect of the triple bonds confer both 6 and 7 with a good electron‐accepting property (E^ox = 1.39 V vs Ag/AgCl) if used in light‐emitting diode devices. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 2670–2679, 2002