光学元件群延迟的直接测量

提出了一种测量群延迟的新方法,利用白光干涉仪产生的光谱干涉,通过时间频率联合分析直接得出群延迟,减小了传统相位差分方法产生的误差,并通过测量结果减去系统背景,进一步提高了光学元件色散测量的准确度. 该方法适合于具有复杂色散光学元件群延迟和色散的准确测量,也适合于慢光器件群速度延迟的测量. 关键词： 色散测量 白光干涉 时间频率分析 超快激光     

原子非序列双电离的多次返回碰撞电离机理分析

本文采用三维半经典再散射模型研究了He原子在高光强(1.5×10¹⁵ W/cm²)、少周波激光脉冲作用下的非序列双电离问题,重点分析了沿激光电场极化方向的动量关联谱.发现两个电子沿相反方向发射的比例明显比中等光强区(7×10¹⁴ W/cm²)和低光强区(2.5×10¹⁴ W/cm²),以及同等光强的长脉冲情形都偏高, 同时V形结构也更加明显.通过轨道"回溯"分析, 进一步深入 关键词： 强场 非序列双电离 再散射     

霍尔推进器中磁化二次电子对鞘层特性的影响

为进一步研究霍尔推进器壁面二次电子发射对推进器性能的影响,采用流体模型数值模拟了二次电子磁化效应的等离子体鞘层特性.得到二次电子磁化鞘层的玻姆判据.讨论了不同的磁场强度和方向、二次电子发射系数以及不同种类等离子体推进器的鞘层结构.结果表明:随器壁二次电子发射系数的增大,鞘层中粒子密度增加,器壁电势升高,鞘层厚度减小;鞘层电势及粒子密度随着磁场强度和方位角的增加而增加;而对于不同种类的等离子体,壁面电势和鞘层厚度也不同.这为霍尔推进器的磁安特性实验提供了理论解释. 关键词： 霍尔推进器 磁鞘 二次电子     

白光有机发光器件的研究进展

白光有机发光器件(OLED)能够产生高效饱和的白光,且具有驱动电压低、材料柔性好、可实现大面积显示等特点,在信息显示与固态照明等领域有巨大的应用潜力.目前白光OLED主要分为单发光层、多发光层、下转换、叠层等结构,不同的结构具有各自的优势,都受到了很大关注.首先介绍了白光OLED的性能指标.接着,结合所开展的研究工作综述了白光OLED在结构和性能方面的研究进展,总结了实现高效白光OLED的各种方法,重点探讨了提高白光OLED性能的途径及所面临的挑战. 最后,展望了白光OLED的发展趋势. 关键词： 白光有机发光器件 固态照明 电致磷光 光取出     

含有本征SiGe层的SiGe异质结双极晶体管集电结耗尽层宽度模型

本文分别建立了含有本征SiGe层的SiGe HBT(异质结双极晶体管)集电结耗尽层各区域的电势、电场分布模型,并在此基础上,建立了集电结耗尽层宽度和延迟时间模型,对该模型进行了模拟仿真,定量地分析了SiGe HBT物理、电学参数对集电结耗尽层宽度和延迟时间的影响,随着基区掺杂浓度和集电结反偏电压的提高,集电结耗尽层延迟时间也随之增大,而随着集电区掺杂浓度的提高和基区Ge组分增加,集电结耗尽层延迟时间随之减小. 关键词： SiGe HBT 集电结耗尽层 延迟时间     

多光子偏振态与单光子高维空间态之间的相互变换及其应用

基于一种特殊的控制非门,实现多光子偏振态与单光子空间高维态之间的相互变换,使得对多光子偏振态的操作可以通过对单光子的操作来完成,由此可以实现任意多光子正定算符值测量和多光子任意幺正操作.这种实现方式是以一定概率完成的,但其效率要优于此前的方案,在目前的实验条件下是可行的. 关键词： 单光子空间态 特殊控制非门 线性光学多端口干涉仪     

氦在材料中基于扩散机理的热释放特征

以随机扩散理论为基础,研究该机理下材料中氦的热释放可能呈现的特征,考察了氦的初始深度分布和扩散系数等因素对氦的热释放率的影响;阐明了随机扩散模型下和脱附模型下的氦释放特征之异同;指出对实验观察到的热解析谱的分析应和基底中氦的深度分布的分析以及氦的聚集状态的分析相结合,才能对氦的热释放机理给出正确的理解和判断. 关键词： 随机扩散 热释放 氦     

Thermal activation and reaction of allyl alcohol on Ni(100)

The thermal chemistry of allyl alcohol (CH₂CHCH₂OH) on a Ni(100) single-crystal surface was studied by the temperature programmed desorption (TPD) and the X-ray photoelectron spectroscopy (XPS). The allyl alcohol adsorbs molecularly on the metal surface at 100 K. Intact molecular desorption from the surface occurs at temperatures around 180 K, but some molecules exhibit chemical reactivity on the surface: activation of the OH, CC, and CO bonds produces η¹(O)-allyloxy CH₂CHCH₂O_(a), η²(C, C) allyl alcohol (C_(a)H₂C_(a)HCH₂OH), and η³(C, C, O)-alkoxide (C_(a)H₂C_(a)CH₂ O_(a)) intermediates. Further thermal activation of allyl alcohol on the surface yields propylene (CH₂CHCH₃), 1-propanol (CH₃CH₂CH₂OH), propanal (CH₃CH₂CHO), and combustion and dehydrogenation products (H₂O, H₂, and CO). Propylene desorbs from the surface at temperatures of around 270 K. Hydrogenation to the η³(C, C, O)-alkoxide intermediate leads to the production of propanal which desorbs from the surface around 320 K, while hydrogenation of the η²(C, C) allyl alcohol intermediate produces 1-propanol, which desorbs at around 310 K. The co-adsorption of hydrogen atoms on the surface enhances the formation of the saturated alcohol, while co-adsorption of oxygen enhances the formation of both the saturated alcohol and the saturated aldehydes.     

2D planar field emission devices based on individual ZnO nanowires

2D planar field emission devices based on individual ZnO nanowires were achieved on Si/SiO₂ substrate via a standard e-beam lithography method. The anode, cathode and ZnO nanowires were on the same substrate; so the electron field emission is changed to 2D. Using e-beam lithography, the emitter (cathode) to anode distance could be precisely controlled. Real time, in situ observation of the planar field emission was realized in a scanning electron microscope. For individual ZnO nanowires, an onset voltage of 200 V was obtained at 1 nA. This innovative approach provides a viable and practical methodology to directly implement into the integrated field emission electrical devices for achieving “on-chip” fabrication.     

Control the revisit time of the electron wave packet

Ionization of molecules by strong laser fields launches an electron wave packet. This electron wave packet, which can be driven back by the field to recollide with the parent ion, has been widely explored to probe the ultrafast nuclear dynamics. We numerically demonstrate the precise control of the temporal characteristic of the recolliding electron wave packet (REWP) by orthogonally polarized two-color fields. Through changing the relative phase of the two fields, the revisit time of REWP can be manipulated with a resolution of less than 200 attos, thus significantly improving the resolution of the well known molecular clock. This provides an efficient method for real-time observation of the ultrafast molecular dynamics with attosecond resolution.