SiO2-GeO2薄膜二次谐波产生的稳定性研究

利用溶胶－凝胶（ｓｏｌ－ｇｅｌ）方法制备了ＳｉＯ２－ＧｅＯ２薄膜,并测量了薄样品电场极化后光学二次谐波信号的相对大小和时间弛以豫特性,通过对汪同衬底材料及不同温度下电场极化薄膜样品二次谐波信号的时间弛豫特性比较,表明薄膜与衬底之间界面电荷的稳定性受衬底材料体电导率的影响,从而影响了薄薄膜样品二次谐波信号的稳定性。     

偶氮聚合物薄膜的全光极化研究

报告了分散红共聚物膜HMMM-DR1,HMMM-DR19和偶氮侧链聚合物膜PCN6和PCN2的合成和制备, 并以HMMM-DR1和PCN6为代表比较研究了这两种具有不同吸收性质材料的全光极化特性,研究了他们的实时极化和弛豫过程,对他们的全光极化性质作了最基本的表征.研究了倍频光吸收对薄膜光极化效率的影响,讨论了偶氮聚合物材料光诱导二阶非线性极化率的效率和倍频光透射率之间的折衷关系,这对实用化的全光器件的研制是至关重要的.实验确证了在PCN6薄膜中实现了准相位匹配.对厚膜中光诱导二阶非线性极化率的弛豫抑制效应作出解释.     

非线性光学聚合物的电晕极化与弛豫特性研究

本文研究了非线性光学聚合物薄膜的极化过程,对影响电晕极化的因素进行了细致分析;利用紫外-可见吸收光谱研究了极化薄膜的弛豫特性。比较了三种聚合物体系的极化与弛豫特性。     

分散橙25掺杂的聚合物PMMA薄膜全光极化的研究

制备了以分散橙25为客体的掺杂型有机聚合物PMMA薄膜样品，对之进行了全光极化研究，极化使薄膜产生诱导二阶非线性光学效应，种子光的强度越大，其二阶非线性极化率达到的饱和值越大;种子光的位相差、相对强度比、光场强度等因素影响薄膜的二阶非线性的优劣.     

掺半花菁二氧化硅薄膜二阶光学非线性与薄膜结构的动态变化关系

用溶胶－凝胶技术制备的掺入半花菁染料的二氧化硅薄膜在不加电场极化条件下，由半花菁分子的自取向导致光学二次谐波产生，定量测得厚度为５０ｎｍ薄膜的二阶非线性系数ｘ（２）为６．６ｐｍ／Ｖ，着重研究了薄膜稳定前的溶剂挥发过程中，膜结构的变化以及相应二阶光学非线性的变化，在成膜后的四个小时中，质子化半花菁逐步转化为单体和聚集体态，同时，光学二次谐波信号也不断增大，还观察到在这一过程中出现了单体和聚集态半花菁     

键合型DANS聚合物光波导电晕极化及其二阶非线性衰减

对键合型DANS聚合物薄膜光波导的电晕极化过程及其二阶非线性衰减特性进行了研究.采用本文给出的电晕极化参数,制成了具有较长极化寿命的极化聚合物薄膜光波导,为进一步研究其二阶非线性光学性质奠定了基础.     

两种偶氮化合物主客体掺杂薄膜的全光极化特性研究

利用旋涂法制备了两种PMMA-偶氮化合物主客体掺杂型薄膜,并对其进行全光极化,采用紫外-可见吸收谱和二次谐波产生的方法研究了薄膜的二阶非线性光学特性.实验结果表明,4′-Nitro-4-dimethylaminoazobenzene的二阶非线性光学系数d33＝6.89×10-1 pm/V,4′-Iodo-4-dimethylaminoazobenzene的d33＝7.77×10-2 pm/V;这两种薄膜在全光极化过程中二次谐波产生(SHG)强度随膜厚的变化规律以及极化饱和后的弛豫情况不相同.这些现象可从理论上解释为偶氮化合物的取代基不同而导致偶氮分子的偶极性和偶氮分子与基质间相互作用不同所产生的影响.     

硅材料场致等效二阶极化率张量的研究

具有反演对称中心的硅单晶在电场作用下体内的反演对称中心消失,因而理论上应产生偶数阶非线性极化率。从理论上根据矢量与张量的作用,利用(eχf2f)=χ(3).E这一关系和张量变换理论系统地阐述了硅材料在内建电场或外加电场的作用下,具体在方向分别沿[111][、110]和[001]的电场作用下,得到的等效二阶极化率张量(eχf2f)分别与C3v、C2v和C4v点群的二阶极化率张量具有相同的形式,说明在物理性质方面,硅的对称性由Oh群在相应方向电场作用下分别被降低为C3v、C2v和C4v群,因此应该具有相应对称性晶体的二阶非线性光学性质;提出了电场E沿任意方向时硅的等效二阶极化率张量e(χf2f)的计算方法,对研究硅材料和其他具有反演对称中心材料的场致二阶非线性光学性质实验具有指导意义。     

聚集效应对银纳米粒子的二阶非线性光学特性的影响研究

运用超瑞利散射(HRS)技术,对由KNO3诱导聚集的银纳米粒子的二阶光学非线性特性进行了实验研究.通过粒子尺寸测量和透射电镜观察，表明银纳米粒子的聚集方式为链状聚集.当聚集体平均尺寸为120nm时，银纳米粒子聚集体的HRS信号强度比聚集前增大了约15倍.分析表明，聚集导致银纳米粒子表面电场极化强度的增强和极化分布的改变，并通过表面和体贡献机理对二阶非线性极化过程产生影响. 关键词： 银纳米粒子 超瑞利散射 二阶光学非线性 聚集     

掺半花菁二氧化硅薄膜光学二次谐波产生

报道了用溶胶 凝胶技术制备掺入半花菁染料的二氧化硅薄膜．在不加电场极化条件下，由半花菁分子的自取向导致光学二次谐波产生，定量测得厚度为50nm薄膜的二阶非线性系数χ^（2）为6.6pm/V，并初步研究了半花菁分子自取向的机理 关键词：     

Threshold Conditions for Bulk Second-Order Nonlinearity and Near-Surf ace Second-Order Nonlinearity in Thermally Poled Infrasil Silica

Generation of bulk second-order nonlinearity in silica glass requires higher poling temperature or longer poling time than that of near-surface second-order nonlinearity. The threshold conditions for initiating the bulk second-order nonlinearity are studied on Infrasil fused silica glass. The threshold poling time is strongly dependent on the poling temperature. The near-surface second-order nonlinearity is also studied, especially the dependence of thickness of the nonlinear layer on the poling temperature, poling voltage and poling time. Secondary-ion mass-spectroscopy measurement showed depletion of Na⁺ ions at the anodic surface. We assume there is an ionic wave during poling traveling from the anodic surface to generate the dipolar electric field that induces the near-surface second-order nonlinearity.     

硼酸铅玻璃的光学二次谐波产生

对硼酸铅玻璃体材料样品进行热辅助的平板电场极化(简称热极化)后,通过观察其光学二次谐波(SHG)信号的强弱,得到了不同组分的样品的最佳极化温度,发现其最佳极化温度与玻璃化温度满足一定的关系;同时得到了不同组分的样品在各自的最佳极化温度条件下极化后的二次谐波信号强度与组分的关系;经过对一种组分的样品进行细致研究,发现样品的二次谐波信号强度随着极化电压的增大而增大,并满足幂函数关系.利用有效偶极子释放模型解释了样品的二次谐波信号强度与极化电压之间的超平方关系 关键词： SHG 玻璃 极化     

Large optical second-order nonlinearity of poled WO3-TeO2 glass

Second-harmonic generation, one of the second-order nonlinear optical properties of thermally and electrically poled WO>(3)-TeO>(2) glasses, has been examined. We poled glass samples with two thicknesses (0.60 and 0.86 mm) at various temperatures to explore the effects of external electric field strength and poling temperature on second-order nonlinearity. The dependence of second-harmonic intensity on the poling temperature is maximum at a specific poling temperature. A second-order nonlinear susceptibility of 2.1 pm/V was attained for the 0.60-mm-thick glass poled at 250 degrees C. This value is fairly large compared with those for poled silica and tellurite glasses reported thus far. We speculate that the large third-order nonlinear susceptibility of WO>(3)- TeO>(2) glasses gives rise to the large second-order nonlinearity by means of a X((2)) = 3X((3)) E(dc) process.     

Second-order optical nonlinearity in thermally poled Pyrex borosilicate glass

The thermal poling method was utilized to create second-order optical nonlinearity in Pyrex borosilicate glass. The distribution and amplitude of the induced nonlinearity were characterized with second harmonic microscopy. The induced optical nonlinearity was found in a thin layer around 1.9 μm under the anode surface with a magnitude as high as 0.24 pm/V, comparable to that observed in fused silica samples. SEM observation of the cross-section of the poled glass region, after it had been etched in diluted hydrofluoric acid for several minutes, revealed an etched trench, ∼1.8 μm under the anode edge and ∼0.3 μm in width; while in post-annealed samples, no such etched trench could be observed. The effect of poling voltage on the magnitude of the induced nonlinearity was also studied, where the results showed that higher poling voltage resulted in higher nonlinearity with a threshold of ∼0.9 kV.     

Photoinduced stable second-harmonic generation in chalcogenide glasses

We report on photoinduced second-harmonic generation (SHG) in chalcogenide glasses. Fundamental and second-harmonic waves from a nanosecond pulsed Nd:YAG laser were used to induce second-order nonlinearity in chalcogenide glasses. The magnitude of SHG in 20G?20A?60S glass was 10(4) larger than that of tellurite glass with a composition of 15Nb(2)O (5) 85TeO(2) (mol.%). Moreover, no apparent decay of photoinduced SHG in 20G?20A?60S glass was observed after optical poling at room temperature. We suggest that the large and stable value of chi((2)) is due to the induced defect structures and large chi((3)) of the chalcogenide glasses.     

SiO2-GeO2薄膜电场极化后倍频效率与极化电压的超平方关系

采用溶胶-凝胶方法制备了SiO₂-GeO₂薄膜.通过对薄膜样品平板电极极化和电晕极化后二次谐波产生信号的研究,发现样品中有效偶极子数目随平板电极极化电压的增加而逐渐增大.提出了有效偶极子释放模型,解释了样品倍频效率与极化电压之间的超平方关系. 关键词：     

Creating second-order nonlinearity in pure synthetic silica optical fibers by thermal poling

A twin-hole optical fiber with pure synthetic silicate glass between the two electrode holes was thermally poled. The induced second-order nonlinearity (SON) was located at the core-cladding interface sections that were nearly parallel to the poling electric field. The polarization dependence of the induced SON suggests that nonlinearity was due to the presence of a space-charge field, which was probably formed by electron migration among the defects located at the core-cladding interface. The magnitude of the induced SON was measured to be approximately 0.06 pm /V.     

Influence of electrode composition on the second-order nonlinearity profile in thermally poled silica glass

Silica glass plates (Infrasil from Heraeus) have been thermally poled with different types of electrodes (evaporated or pressed-on) having different chemical compositions (Au, Al, n-doped Si or p-doped Si). We show for the first time to our best knowledge that the profile of the induced second-order nonlinearity strongly depends on the composition of electrodes used for the thermal poling process.     

Static and dynamic profile of the electric field within the bulk of fused silica glass during and after thermal poling

We use the electric-field-induced second-harmonic (EFISH) technique to characterize, for the first time to our knowledge, the profile of the electric field induced within the bulk of fused silica glass samples both during and after thermal-poling treatment. During thermal poling, the initially homogeneous electric field decays exponentially from the anodic to the cathodic surface. After the poling treatment, a permanent electric field is induced within the bulk of the sample. It also decays exponentially from a positive value on the anodic surface to a negative value on the cathodic surface. The exponential decay constant depends on the thickness of the sample, the poling time, and the temperature. The temperature evolution of this constant makes it possible to retrieve the activation energy of the rapidly moving ionic species. This ensemble of observations indicates that modifications to models previously proposed are necessary.