光栅周期包含的Bragg层数对Bragg型凹面衍射光栅的影响

单个衍射光栅周期所包含的Bragg周期层数是连续Bragg齿型凹面衍射光栅的主要参数之一,该参数可改变光栅齿结构,对凹面衍射光栅的分辨力.自由光谱范围及衍射效率有重要影响.本文通过理论分析与仿真模拟,对比了4种不同层数的Bragg型凹面衍射光栅的特性参数.研究结果表明:在衍射光栅尺寸不变的情况下,改变单个光栅周期包含的Bragg周期层数不会显著提高器件主衍射级次的分辨力;单个光栅周期包含的Bragg周期层数与光栅可衍射的级次数成正相关.单周期层数的Bragg凹面衍射光栅的主衍射级次效率最高,其可衍射的级次数最少,且其他衍射级次分散的能量最少;增加单个光栅周期所包含的Bragg周期层数会降低主衍射级次的自由光谱范围.该研究对于设计低插损、高分辨率、宽工作波段的波分复用器或光栅光谱仪具有重要的指导意义.     

The way to high-performance single nanowire photodetectors: problems and prospects

<正>As potential building blocks for micro-nano devices,one-dimensional semiconductor nanowires(NWs)have been widely studied in recent decades.Due to limited dimension and large surface-to-volume ratio,devices based on NWs are more likely to exhibit unique properties.NW photodetectors adopting different materials have been fabricated.However,the performance is greatly affected by several issues such as lattice quality,surface homogeneity,contact electrodes and     

三种胺羧配合物的113Cd NMR研究

该文对Cd-HEDTA(N-(2-羟基乙基)乙二胺-N',N',N'-三乙酸),Cd-PDTA(1,2丙二胺四乙酸)和Cd-DTPA(二乙三胺五乙酸)的¹¹³Cd NMR谱和自旋晶格弛豫时间T₁,及NOE因子进行了研究.结果表明,Cd-HEDTA和Cd-PDTA结构与Cd-EDTA类似,Cd-PDTA双线归因于其可能的两种异构体.Cd-DTPA大的化学位移表明其具有七配位的五角双锥结构.在这种结构中DTPA可用三个氮原子参加配位.对¹¹³Cd自旋晶格弛豫时间分析表明,Cd-DTPA配合物中质子偶极作用机理的贡献较大,这归因于Cd DTPA有更多的乙酸根亚甲基质子参与偶极作用.     

兰州重离子加速器控制系统DSP组件设计

针对重离子加速器部分电源的控制要求,进行了分析研究,提出并实现了一种实时、高效、多功能的控制系统。该系统基于数字信号处理器（DSP）和两片现场可编程门阵列（FPGA）芯片相结合的核心处理构架,在系统后端利用PXI总线接口配合FPGA来与工控机箱中的系统控制器和其他控制组件进行大批量数据交互;系统前端利用直接数字频率合成器、模数转换器和数模转换器等器件结合DSP和FPGA中的控制算法及相应控制机制来实现对不同电源控制参数的处理和功率的输出;平台中两组光纤模块也与FPGA相配合实现对同步触发事例等实时数据的收发和调试。     

Novel miniature high power ring filter

The power handling capability of high temperature superconducting (HTS) filters is limited due to current concentration at the edges of the superconducting films. This problem can be overcome by using ring resonator, which employs the edge current free and reduces the current concentration. However, this kind of filter has large size. In order to reduce the cost and size and increase the power handling capability, in this paper a HTS photonic bandgap (PBG) structure filter is developed. The proposed pass band filter with PBG structure exhibits center frequency 12.23 GHz, steepness (about 35 dB/GHz), bandwidth (−3 dB bandwidth is 0.045 GHz), and low insertion loss (about −0.5 dB), and can handle input power up to 1 W (this value was limited by the measurement instrument used in the experiment). The size is reduced by 25%, insertion loss reduced by 37.5%, and steeper roll-off of the filter is also obtained compared with that in published literature.     

乙醇在TiO2(110)表面光催化解离的动力学和超快电子动态学 (cited: 2)

采用实时双光子光电子能谱和时间分辨双光子光电子能谱技术分别研究了乙醇在该表面光催化解离的动力学和超快电子动态学过程. 通过测量与乙醇光催化解离相关的电子激发态随时间的演化,发现这个反应满足分型动力学. 乙醇在还原性TiO₂(110)上的光催化解离比在氧化性表面快,这归结于缺陷的存在降低了反应能垒. 这样一个反应的加速过程很可能是与缺陷电子相关的. 通过干涉双脉冲相关的测量,得到了乙醇-TiO₂界面电子激发态的超快动态学. 与甲醇的情况类似,这个电子激发态的寿命为24 fs. 激发态的出现为TiO₂和它周围环境的电子转移提供了一个通道.     

离子速度成像技术研究2-溴戊烷的光解离动力学

运用离子速度成像技术研究了2-溴戊烷分子在～234 nm处的光解离动力学. 通过分析光解产物Br(²P_3/2)(简称Br)和Br(²P_1/2) (简称Br*)的速度影像,分别得到其速度分布和角度分布. Br和Br*的速度分布可以用两个高斯分布拟合,分别对应于2-溴戊烷在～234 nm处两个独立的光解离反应通道. 高能的高斯分量对应于C-Br伸缩振动模式的直接解离,低能的高斯分量对应于弯曲振动和C-Br伸缩振动耦合所导致的解离. 确定出光解离产物Br的相对量子产率为0.892,结合Br和Br*碎片的各项异性参数和溴原子的相对量子产率,讨论了³Q₀、³Q₁和¹Q₁激发态分别对产物Br和Br*的贡献. 通过对比溴代戊烷4种同分异构体光解离过程的差异,讨论了分子烷基分支化对光解机理的影响.     

基于动态地场和元胞自动机的自行车流建模

针对现有自行车流模型对车辆间作用考虑不足的问题,在原多车道元胞自动机模型的基础上引入动态地场,在模型中纳入了排斥力,并充分考虑了前车速度对后车行驶的影响,体现了自行车的灵活性等特征,提出了换道成本的概念并建立了新的基于比较交通环境的换道规则. 数值仿真结果表明：1）该模型能更准确地描述自行车流,反映自行车流的特征,得到的数据符合实际;2）单位车道宽度的通行能力随着车道数的增加有小幅下降;3）激进的驾驶风格使得换道次数大幅增加,通行能力下降. 关键词： 自行车流 元胞自动机 动态地场 仿真     

A Mössbauer spectroscopic study of an industrial catalyst for dehydrogenation of etylbenzene to styrene

Iron oxide catalyst with spinel structure used for dehydrogenation of ethylbenzene is one kind of important catalyst in petrochemical industry. In this work several series of industrial catalyst were prepared with different components and different manufacturing processes. Mössbauer Spectroscopy has been used to determine the optimal components and the better manufacturing process for spinel structure formation. The results may prove useful for producing the industrial dehydrogenation catalyst with better catalytic property.