Survivability in IP-over-WDM Networks: WDM Lightpath Protection versus IP LSP Protection

This article compares the performance of WDM lightpath protection and IP LSP protection schemes for IP-over-WDM networks. A mathematical formulation of the maximum throughput problem is presented and analytical expressions for recovery time are derived for both schemes. The throughputs and recovery times are analyzed and compared. Results show that the IP LSP protection scheme presents higher throughputs then WDM lightpath protection. The IP LSP protection scheme, providing individual IP LSP protection has, however, scalability problems. This scheme presents high recovery times when a failure affects many lightpaths and many hops are allowed for the primary routes of IP LSPs.     

Four-wave mixing in semiconductor laser amplifiers: Applications for optical communication systems

Four-wave mixing in semiconductor laser amplifiers enables various applications in photonic switching including wavelength conversion, space and time switching, optical phase conjugation, and demultiplexing. Switching times faster than 1 ps are possible.     

有机光存储材料二芳乙烯化合物研究的发展

本文在介绍光致变色二芳乙烯化合物的发展动向基础上重点叙述了该类化合物的热稳定性、耐疲劳性、吸收光谱、量子产率、响应时间等各种性质.     

采用超连续谱激光的双光束光纤光阱实验

以超连续谱激光器作为捕获光源,首次提出并搭建了超连续谱双光束光纤光阱实验系统,实现了聚苯乙烯微球的捕获和操控。通过改变光纤端面间隔和调整捕获光功率的方式精确控制微球的位置,采用CCD图像分析方法实现了微球位置的精确测量。对微球受限布朗运动下的位置变化进行傅里叶变换,计算得到功率谱,与理论功率谱函数拟合后求出了其光阱刚度。结果表明,捕获光束的功率为28 mW时,光阱刚度达到1.3×10-6N/m,高于相同实验条件下单波长光纤光阱的刚度。与传统采用单色光作为捕获光源的光镊系统不同,超连续谱双光束光阱系统利用其宽谱优势,通过研究被捕获微粒的散射光谱信息可获取其尺寸、折射率等物理特征参数。     

1.5μm波段基于级联二阶非线性的铌酸锂光波导全光波长变换的理论分析

研究了基于级联二阶非线性的铌酸锂波导全光波长变换器的特性.首先从耦合模方程出发,比较了数值分析结果与小信号近似分析的结果.其次在数值分析基础上,分析了铌酸锂晶体的温度变化导致相应基频光波波长与极化反转光栅周期的变化关系.最后分析了在不同相互作用长度下,转换的光波功率与有效基频光波波长带宽、温度调谐带宽、极化反转光栅周期带宽等关系,以对全光波长变换器件进行优化设计 关键词： 级联二阶非线性 波长变换 准位相匹配 铌酸锂光波导     

用数值方法分析微孔激光器出射光的近场特性

微孔激光器作为应用于近场光信息存储系统中的一种新型光源，它的出射光斑的近场特性对于近场光存储是十分重要的。针对纳米孔径运用角谱进行Fox-Li数值迭代，得到不同孔径微孔激光器的基模光强分布，然后运用二维非线性时域有限差分法分析微孔激光器出射端即微孔金属膜的近场光学性质，模拟计算了不同孔径和厚度的微孔金属膜的光强近场分布，从应用于近场光存储的角度，给出反映其近场光学特性的相关数据。发现由于TM模式下金属存在局域表面等离子增强效应，使得其出射强度比TE模式高一个数量级，从而更适于作为实际中近场光存储系统和原理试验的光学头。     

Optical system and lens design for Blu-ray disc optical pick-up

During the design process of Blu-ray disc optical pick-up (BD OPU), the optical system and the collimator lens design is especially important. This paper designs an optical system and some lenses for the BD OPU, including collimator lens, beam shaping lens for laser beam shaping, and cylinder lens for signal detecting. In this OPU, we use a triplet lens to collimate the laser beam. At the same time, we build a series of assembly jigs to make sure that each lens can be put into the OPU basement properly. At last, we get the reading spot image and S-curve photo of OPU, which can be used to read Blu-ray disc (BD).     

Poly(Pyridinium Salt)s Containing 2,7-Diamino-9,9′-Dioctylfluorene Moieties with Various Organic Counterions Exhibiting Both Lyotropic Liquid-Crystalline and Light-Emitting Properties

A series of poly(pyridinium salt)s-fluorene main-chain ionic polymers with various organic counterions were synthesized by using ring-transmutation polymerization and metathesis reactions. Their chemical structures were characterized by Fourier Transform Infrared (FTIR), proton (¹H), and fluorine 19 (¹⁹F) nuclear magnetic resonance (NMR) spectrometers. These polymers showed a number-average molecular weight (M_ns) between 96.5 and 107.8 kg/mol and polydispersity index (PDI) in the range of 1.12–1.88. They exhibited fully-grown lyotropic phases in polar protic and aprotic solvents at different critical concentrations. Small-angle X-ray scattering for one polymer example indicates lyotropic structure formation for 60–80% solvent fraction. A lyotropic smectic phase contains 10 nm polymer platelets connected by tie molecules. The structure also incorporates a square packing motif within platelets. Thermal properties of polymers were affected by the size of counterions as determined by differential scanning calorimetry and thermogravimetric analysis measurements. Their ultraviolet-visible (UV-Vis) absorption spectra in different organic solvents were essentially identical, indicating that the closely spaced π-π* transitions occurred in their conjugated polymer structures. In contrast, the emission spectra of polymers exhibited a positive solvatochromism on changing the polarity of solvents. They emitted green lights in both polar and nonpolar organic solvents and showed blue light in the film-states, but their λ_em peaks were dependent on the size of the counterions. They formed aggregates in polar aprotic and protic solvents with the addition of water (v/v, 0–90%), and their λ_em peaks were blue shifted.