光子晶体光纤带隙及模场的一种综合模拟分析方法

提出直接由MATLAB读入光纤端面图实现复杂结构光子晶体光纤(PCF)模型的快速建立,并综合平面波法(PWM)和频域有限差分(FDFD)法,模拟分析带隙型光子晶体光纤(PBG-PCF)的带隙和模场分布.利用PWM计算得到了在PBG-PCF中传输的光波频率及模式有效折射率范围;基于FDFD法在给定波长及模式有效折射率范围情况下,模拟得到了PBG-PCF中可能存在的模场分布及其他特性.以市售的PBG-PCF为例,验证了数值模拟的正确性,随后系统地分析了结构参数(晶格结构、"原子"占有率、背景材料折射率及"原子     

中心外缺陷对带隙型光子晶体光纤色散特性的影响

利用时域有限差分法(FDTD)模拟仿真了在中心缺陷外出现点缺陷、空气柱位错和内层空气柱发生形变三种缺陷形态对光子带隙型光子晶体光纤(PBG-PCF)色散特性的影响.发现一方面缺陷的出现会使色散曲线趋于平坦,另一方面点缺陷和位错缺陷的出现会使零色散点向长波移动,内层空气柱的形变使零色散点向短波长移动.这对PBG-PCF的实际生产实践会有指导意义.     

光子晶体光纤中孤子内拉曼散射的研究

利用快速分步傅里叶方法数值计算了孤子在光子晶体光纤中的传输。计算结果表明:光子晶体光纤中会产生较强的拉曼散射,非线性越强,孤子分裂得越快,同时分裂出更多孤子。而且,初始啁啾对光子晶体光纤中的拉曼散射有较大的影响,正初始啁啾会增大拉曼孤子的红移速度,而负初始啁啾则会减小拉曼孤子的红移速度。随着光子晶体光纤非线性加强,初始啁啾的作用减弱。     

光子晶体光纤中零色散点处超连续谱演变的研究

从非线性薛定谔方程出发,采用分步傅立叶分析方法数值模拟光子晶体光纤中超连续谱的产生,计算、模拟并分析初始啁啾在光子晶体光纤的零色散点对超连续谱演变和带宽的影响.结果表明,非线性作用使频谱分裂成多峰不对称的结构,初始啁啾C的引入能明显的改善超连续谱的带宽和平坦性.由于二阶色散β2=0,三阶色散猹对超连续光谱的展宽影响较大.当β3>0时,C取正值时,随着C的增大,带宽减小; C取负值时,带宽有所增大,平坦性也有改善;β3<0时,无论C取正取负,频谱带宽增大,且平坦性较好.     

双包层多芯光子晶体光纤自相干合成的数值分析与实验

依据耦合模理论分析了双包层多芯光子晶体光纤的超模模场特性,通过倏逝波对7束光的相位调节,可实现相干合成,激光亮度得到很大提高.利用相干合成原理对双包层多芯光子晶体光纤的出射光相干功率密度进行了分析与测量,对此种结构的光子晶体光纤实现自相干合成提出了理论和实验依据.     

输出近百纳焦耳脉冲能量的光子晶体光纤锁模激光器

设计并搭建了一种支持百纳焦耳量级的单脉冲能量输出的锁模光纤激光器.激光器基于σ型腔结构,采用掺Yb偏振型大模场面积光子晶体光纤作为增益介质,利用半导体可饱和吸收镜实现自启动锁模.激光器内没有色散补偿机理,使其工作在全正色散锁模状态.通过在谐振腔内引入多通长腔使激光器的重复频率降低至11.1 MHz,直接获得了平均功率为1.08 W,单脉冲能量为 97 nJ,脉冲宽度为4.17 ps的稳定锁模脉冲输出,经腔外色散补偿,脉冲宽度压缩至740 fs.     

Archimedes 32,4,3,4结构光子晶体中与偏振无关的自准直分束器

通过等频图分析并结合时域有限差分法法模拟, 在Archimedes 3²,4,3,4结构排列的二维光子晶体中同一频率下同时实现了电磁波两种偏振态的自准直. 研究发现,在该结构光子晶体中引入缺陷,当线缺陷宽度改变时, TE和TM两种偏振态光束的分束效果将会随之变化.由此通过控制缺陷宽度,分别实现了两种偏振态光束的50% ∶50%分束以及90°大角度光折弯,分束和折弯的效率都较为理想,为未来设计基于光子晶体的新型光子学器件提供了一种新的思路.     

二维GaAs 基光子晶体微腔的制作与光谱特性分析

研究了以InAs量子点为有源区的二维GaAs基光子晶体微腔的设计与制作,测试并分析了室温下微腔的光谱特性.观察到了波长约为1137 nm,谱线半高宽度约为1 nm的尖锐低阶谐振模式发光峰.我们比较了不同刻蚀条件下光子晶体微腔的发光谱线,结果表明空气孔洞截面的垂直度是影响光子晶体微腔发光特性的重要因素之一.通过调节干法刻蚀工艺,改变空气孔半径与晶格常数的比率,可以在较大范围内调节谐振模式发光峰位置,达到谐振模式与量子点发光峰调谐的目的.     

各向异性光子晶体中二能级原子和自发辐射场间的纠缠

应用 Von Neumann熵 和 Schmidt number K两种纠缠度量讨论了各向异性光子晶体中二能级原子和自发辐射场间纠缠度的演化性质. 研究发现,原子-光场纠缠度的演化与原子上能级和光子晶体能带带边的相对位置有关,当原子上能级处于光子晶体禁带内,原子-光场纠缠度将保持稳定,当原子上能级处于光子晶体能带中,原子-光场纠缠度先增大后衰减到零. 纠缠度的大小还与原子的初态有关. 可以通过控制原子的初态和原子上能级与带边的相对位置来控制原子-光场纠缠度的演化特性.     

基于机器学习的声子晶体结构声隐身设计

针对声呐导流罩中低频段振动控制以提高其全频段声隐身性能问题,提出了一种基于条件自编码器的声子晶体结构逆向设计方法,在目标频段逆向设计出的具有带隙的声子晶体结构可作为夹芯结构芯层, 为声呐导流罩声振特性治理工作提供新思路。首先随机生成大量声子晶体周期单元,并提出 2 种策略扩充在目标频段内具有带隙的样本数量。针对有限元软件批量计算声子晶体结构带隙效率较低的问题,训练了卷积神经网络用于识别声子晶体是否具有带隙。最后,将声子晶体结构以及带隙分布作为训练集训练条件自编码器。结果显示：卷积神经网络对结构的带隙具有很好的识别效果,识别准确率可以达到 89%;条件自编码器能学习到人工周期结构的轴对称结构,生成的人工周期结构与原结构仅相差几个像素,且生成结构的带隙与原结构带隙误差小于 1%,说明该方法可以应用于声子晶体结构的逆向设计。     

Modification of the spontaneous emission of quantum dots near the surface of a three-dimensional colloidal photonic crystal

This paper demonstrates experimentally and numerically that a significant modification of spontaneous emission rate can be achieved near the surface of a three-dimensional photonic crystal. In experiments, semiconductor core-shell quantum dots are intentionally confined in a thin polymer film on which a three-dimensional colloidal photonic crystal is fabricated. The spontaneous emission rate of quantum dots is characterised by conventional and time-resolved photoluminescence (PL) measurements. The modification of the spontaneous emission rate, which is reflected in the change of spectral shape and PL lifetime, is clearly observed. While an obvious increase in the PL lifetime is found at most wavelengths in the band gap, a significant reduction in the PL lifetime by one order of magnitude is observed at the short-wavelength band edge. Numerical simulation reveals a periodic modulation of spontaneous emission rate with decreasing modulation strength when an emitter is moved away from the surface of the photonic crystal. It is supported by the fact that the modification of spontaneous emission rate is not pronounced for quantum dots distributed in a thick polymer film where both enhancement and suppression are present simultaneously. This finding provides a simple and effective way for improving the performance of light emitting devices.     

Aggregation of riverine colloidal iron in estuaries: A new kinetic study using stopped-flow mixing

The kinetics of aggregation of riverine colloidal iron have been examined using a stopped-flow technique which probes the first few seconds of mixing between river and sea water end members. A significant fraction, up to 80%, of the colloidal iron is aggregated during the first 1–2 s of mixing, indicating that the aggregation process is much faster than previously thought. Most of the aggregation induced by seawater results from the divalent cations Mg²⁺ and Ca²⁺, with the overall ionic strength having little influence. At equal concentrations of 27 mM, the rate of aggregation by alkaline earth cations increased with ionic size Mg²⁺ < Ca²⁺ < Sr²⁺ < Ba²⁺. The aggregation rates were indifferent to the anion (Cl⁻ or SO₄²⁻) present. Very high aggregation rates were also induced by the common water treatment coagulant Al₂(SO₄)₃ at concentrations in the range 20–30 µM Al(III), several orders of magnitude lower that those used for the seawater cations. Our results support the view that specific chemical interactions between the cations and the colloid particle surface, rather than simple electrical effects, control the colloid stability.     

近岸海水中络合态铁的离心超滤粒径分级方法研究

建立了基于离心超滤技术的近岸海水中络合态铁(Fe)粒径分级方法。经0.45μm滤膜过滤的海水样品,分别用不同孔径(3 k Da、10 k Da、30 k Da、100 k Da)的超滤膜离心超滤并脱盐。不同分子量范围的化合物富集于相应孔径的超滤膜上,以酸溶液提取出Fe,用原子吸收光谱法(GFAAS)测定。在优化的条件下,方法检测限为0.10μg·L-1,线性范围0.25~10μg·L-1,4组不同孔径超滤膜测定同一份样品的相对标准偏差(RSD)为6.4%~10.3%。本方法成功应用于福建九龙江口至厦门西海域水样的测定,结果显示各分子量范围内的络合态Fe含量随盐度增高而降低,且呈非保守分布的变化趋势。     

海水中胶体有机碳的测定──高温燃烧法和紫外/过硫酸钾法的比较

利用切向超滤(cross-flow ultrafiltration)技术对海水中胶体有机碳(COC)和真溶解有机碳(UOC)进行了分离,并分别用高温燃烧法和紫外/过硫酸钾法对胶体有机碳和真溶解有机碳进行了测定。测定结果表明,切向超滤能定量分离海水中的胶体有机碳,高温燃烧法和紫外/过硫酸钾法对胶体有机碳和真溶解有机碳的测定结果没有明显的系统误差,表明这两种方法的氧化效率基本相同,胶体粒子的存在,对紫外/过硫酸钾法的氧化效率没有显着影响。     

Relative molar mass distributions of chromophoric colloidal organic matter in coastal seawater determined by Flow Field-Flow Fractionation with UV absorbance and fluorescence detection

A new method for the characterization of chromophoric colloidal organic matter in seawater has been applied to samples from the Baltic Sea, Kattegatt and Skagerrak seas. Size fractionation of the sample by Flow Field-Flow Fractionation and measurement of the fluorescent and UV absorbing properties of the individual size fractions result in a relative molar mass distribution (RMM) of the optical properties. The RMM distributions have been used to estimate number and weight average relative molar masses, and polydispersity indices. At least two sources of coloured organic matter were identified from the ratio of fluorescence to UV: the Baltic surface water and the Skagerrak deep water. The dominating processes were mixing and dilution, but processes such as photo bleaching of fluorescence are also believed to be important. The RMM distribution derived from UV detection (1150–1300 Dalton) increased with increasing salinity while that derived for fluorescence (1500–1250 Dalton) decreased with increasing salinity. The specific UV absorbance taken as a proxy of the aromaticity of the chromophoric organic material showed decreasing trend with both increasing salinity and increasing UV derived weight average relative molar mass. Increasing polydispersity of the colloidal material was also observed as a function of salinity.