新型聚偶氮苯取向增强光折变效应及全息存储

合成了新型偶氮分子偶氮二苯胺ADPA(Azo-diphenylamine),将其掺入聚乙烯咔唑Poly(N-Vinylcarba-zole)(PVK)和聚丙烯丁酯(Poly-butylacrylate)(PBA)的聚合物(PVK-PBA)以及三硝基芴酮2,4,7-trinitro-9-flu-orenone(TNF)聚合制成薄膜器件。结果表明掺杂偶氮苯聚合物薄膜在非共振吸收下具有强的光致取向增强光折变效应。光致折射率变化值Δn达到1.3×10-3以上。样品在两相干光束作用下,可建立光折射率光栅,其衍射效率可超过30%,实现了光全息存储。讨论了影响折射率光栅的因素,并对全息存储相关结果形成的机制进行了分析。     

掺杂无机纳米超微粒的有机聚合物体系中的光折变效应

研究了掺杂无机纳米超微粒的有机聚合物体系中的光折变效应．体系中以Ｃｕ２Ｓ／ＣｄＳ／ＺｎＳ复合超微粒为光敏剂,ＰＶＫ为载流子输运剂,电光分子为ＥＰＮＡＣ．给出了光敏剂的制备方法,ＥＰＮＡＣ的分子结构及电光特性,以及该光折变材料中的两波耦合效应的实验结果．结果表明,无机纳米超微粒可用作光折变材料中的光敏剂,这是它的一种新的应用．     

PVK/SiO2纳米粒子复合体系能量传递的研究

通过溶胶反应在乙醇溶液中合成了60nm的SiO2纳米粒子，将其与聚乙烯咔唑（PVK）共混，得到了不同质量分数的PVK／SiO2复合体系，利用荧光光谱，吸收光谱，研究了PVK／SiO2复合体系的荧光效应，光致发光的研究表明在PVK与SiO2纳米粒子之间存在界面能量传递过程，这种能量传递的必要条件是PVK的发射谱与SiO2纳米粒子的吸收谱有重叠，以上研究表明PVK／SiO2复合体系存在较强的界面效应，是研究有机与无机纳米体系界面效应的良好模型。     

低玻璃化转变温度的光折变聚合物中光敏剂作用研究

通过对光敏剂C₆₀含量不同的低玻璃化转变温度的光折变聚合物聚乙烯咔唑掺杂2,5-二甲基-4-(4′-硝基苯偶氮基)苯甲醚、N-乙基咔唑和C₆₀的空间相移角和二波耦合系数的测量,研究了光敏剂在此类光折变聚合物中的作用- 关键词：     

基于有机染料盐掺杂薄膜体系的能量转移及光致发光特性研究

利用稳态和时间分辨瞬态光谱研究了有机盐trans-4-［p-(N-ethyl-N-(hydroxyethyl)amino)phenylstyryl］-N-(hydroxyethyl)pyridinium iodide (ASPI)掺杂聚合物PVK(聚乙烯咔唑)薄膜体系的光致发光和能量转移特性. 在ASPI：PVK掺杂薄膜体系中,PVK的荧光强度与寿命随掺杂浓度的升高而降低,表明两者存在有效的Forster能量转移. 通过在相对低浓度的掺杂体系中加入适量高量子效率的Alq3作为能量转移过渡体,形成能量转移级 关键词： 有机染料盐 荧光光谱 荧光寿命 能量转移     

尺寸相关的CdS纳米颗粒的拉曼散射特性

采用反胶束法,合成了具有不同尺寸的CdS纳米颗粒。利用透射电镜(TEM)和高分辨透射电镜(HR-TEM)以及紫外-可见光吸收谱(UV/vis)对这些纳米颗粒的结构特性进行了表征和分析。利用拉曼光谱仪测量了这些具有不同尺寸的CdS纳米颗粒的拉曼特性。研究结果表明：当纳米颗粒尺寸小于一定值时,拉曼峰出现了蓝移,大于一定值时出现了红移,这些不同的结果是与纳米颗粒的尺寸效应以及纳米颗粒结构中具有各向异性的电子－声子耦合作用有关。     

“反胶团法”合成的CdS半导体纳米粒子的光谱性质研究

反相胶束是指由介于油和水界面的表面活性剂分子, 稳定、且均匀分散于连续油介质中的微液滴。它可以作为“微反应器”合成性能优良的CdS粒子。文章研究了反相胶束的W值(W=[水]/[表面活性剂])、[Cd2+]与[S2-]的比例和Cd2+和S2- 离子的起始浓度对CdS纳米粒子发光特性均有明显影响。回流处理可以对CdS纳米粒子的表面进行修饰,可以使CdS粒子的缺陷发光减弱并消失而显著增强激子发射,同时可增大粒径使激子发射峰位红移,体现了明显的量子限域效应; 所得材料的室温最大荧光量子效率高达11%。     

核-壳结构ZnS∶Tb/CdS纳米晶的电致发光

利用微乳液方法合成出粒径为4 nm的核-壳结构ZnS∶Tb/CdS纳米晶。用XRD、TEM及荧光光谱等手段对合成的纳米晶的结构、形态和光学特性分别进行了表征。将ZnS∶Tb/CdS纳米晶制作成有机-无机杂化结构电致发光器件,其结构为ITO/poly(3,4-ethylene d ioxythiophene)∶poly(styrene sulfonate)(PEDOT-PSS)(70 nm)/poly(vinylcobarzale)(PVK)(100 nm)/ZnS∶Tb/CdS纳米晶(120 nm)/2,9-d im ethyl-4,7-d iphenyl-1,10-phenanthroline(BCP)(30 nm)/L iF(1.0 nm)/A l(100 nm)。当驱动电压为13 V时,可以测到Tb3+离子的两个特征峰。在电致发光光谱中未测到聚合物PVK的发光,说明电子和空穴是在纳米晶层上复合的。当驱动电压为25 V时,得到器件的最大亮度为19 cd/m2。     

掺杂偶氮化合物的PMMA光折变聚合物的拉曼光谱分析

光折变聚合物具有良好的光折变效应,采用以惰性聚合物PMMA为基体,掺杂偶氮化合物染料的光折变聚合物具有较好的光学非线性和稳定性。文章主要介绍使用激光拉曼光谱仪对合成聚合物的各单体和聚合物薄膜进行拉曼光谱扫描,对比分析各个单体成分的特征谱峰与聚合物薄膜特征谱峰,肯定了实验中得到的光折变聚合物薄膜与理论上要求得到的一致性。     

闭路光伏光折变聚合物中非相干耦合亮-暗空间孤子对

为了得到闭路光折变有机聚合物中存在非相干耦合亮-暗光伏空间孤子对,采用数值模拟的方法,对稳态情况下两束互不相干的光束,在闭路光伏光折变有机聚合物中的传播进行了研究。结果表明,具有相同偏振和相同波长的两束互不相干的光束,可在光伏光折变有机聚合物中形成非相干耦合亮-暗光伏孤子对。在给定适当参量或扰动不太大的情况下,孤子对中的亮孤子和暗孤子都能在光伏光折变有机聚合物中稳定传播。研究结果可为光折变有机聚合物空间孤子理论的发展提供理论依据。     

Organic light-emitting diodes based on polyvinylcarbazole films doped with polymer nanoparticles

The optical and electrical properties of light-emitting diode structures with an active layer based on nanocomposite polyvinylcarbazole (PVK) films doped with nanoparticles of another light-emitting polymer, MEH-PPV, have been studied. It has been established that the size of MEH-PPV particles in the PVK matrix is of the order of 100 nm. The spectral range of photoluminescence of such structures can be changed by varying the ratio of PVK to MEH-PPV. The current-voltage characteristics of composite light-emitting diodes based on PVK: MEH-PPV films indicate p-type conductivity. It has been shown that a decrease in the MEH-PPV nanoparticle concentration in the PVK matrix shifts the threshold values of the bias for the onset of electroluminescence toward smaller values and makes the photoluminescence and electroluminescence spectra more similar to the spectrum of the white light-emitting diode. The influence of the form of the polymer and polymer nanoparticles on the mechanisms of injection and transport of charge carriers and the radiative recombination in the studied structures has been discussed.     

光折变聚合物PVK∶5CB∶C_(60)中生色团动态取向的研究

考虑到聚合物基体对生色团的取向的阻尼作用 ,以及外电场对生色团的极化作用 ,在已有的生色团气体取向模型基础上 ,建立了非气体取向模型 .并利用数值计算方法求解了这一非气体取向模型方程 .讨论了外加电场、温度对生色团取向的动态过程和稳态分布的影响 ,比较了两模型的计算结果 .采用椭圆偏振法 ,测量了光折变聚合物PVK∶5CB∶C60 中的生色团 5CB在聚合物基体PVK中动态取向过程 .给出了生色团的稳态和动态取向参量随外加电场和温度的变化关系 .理论与实验的比较 ,进一步证明了非气体取向模型的合理性     

Influence of intensity on the steady and transient state space—charge fields in photorefractive polymers

We have proven theoretically that there are sublinear,linear and superlinear relations between the response rates and total incident intensity for different cases of traps in photorefractive polymer materials.These relations were observed in inorganic photorefractive crystals many years ago.Also,the steady-state space-charge field is a function of the total incident intensity,which has also been found in inorganic photorefractive crystals.We have measured the relations of the steady-state diffraction efficiency and the response rate with respect to the total incident intensity in the photorefractive composite consisting of the polymer (N-vinylcarbazole) (PVK) doped with 4,4‘-n-pentylcyanobiphenyl (5CB) and C60.The results obtained show that the composite belongs to the case of low trap density.     

Higher-order diffraction images in photorefractive materials

We report some photorefractive higher-order diffraction phenomena of a liquid crystal polymer composite. The photorefractive composite consists of the polymer poly[N-vinylcarbazole] (PVK) doped with the chromophore 4,4′-n-entylcyanobiphenyl (5CB) and the sensitizer C₆₀. In two-wave coupling experiments, the signal beam was interfered by a mutually coherent reference beam within composite materials at a small incident angle. Results are given when the composite was placed behind the focal plane, in front of the focal plane, and in the focal plane. Higher-order diffraction images were obtained by amplification and reduction. A theory of the properties of higher-order diffraction images in a photorefractive liquid crystal polymer composite is developed. The theory is in good agreement with the results of experimental work. The experiments demonstrate the feasibility of optical image processing.     

表面修饰的CdS纳米荧光探针的研究

采用溶胶-凝胶法合成硫脲表面修饰的硫化镉纳米粒子[CdS/SC(NH₂)₂],研究硫脲的用量对其粒径的影响,用X射线粉末衍射、透射电子显微镜,红外光谱以及荧光光谱等手段进行了表征。并研究了小牛胸腺DNA的加入对该纳米粒子荧光光谱的影响。实验结果表明,硫脲的用量对该纳米粒子的粒径大小及发光特性有明显影响,随反应物中硫脲与镉离子的物质的量的比值增加,CdS/SC(NH₂)₂纳米粒子粒径变小,其发射波长蓝移,表现出明显的量子尺寸特性;小牛胸腺DNA的加入使CdS/SC(NH₂)₂纳米粒子的发射光谱强度减弱,实验推测该纳米粒子与小牛胸腺DNA存在静电相互作用, 该研究结果可望用于DNA的分析测定。     

Large Third-Order Optical Nonlinearity of Cadmium Sulphide Nanoparticles Embedded in Polymer Thin Films

A simple method for synthesis of well dispersed cadmium sulphide nanoparticles embedded in a polyethylene glycol matrix （PEG 400） in thin film form is presented. The large blue shift of the band gap energy of the CdS nanoparticles compared to the bulk semiconductors is observed via UV-vis absorption spectra. Photoluminescence spectra of CdS nanocomposite films show that the emission peaks shift towards the longer wavelength with the increase of annealing temperature. Transmission electron microscopic images as well as Raman scattering studies confirm the CdS nanometer size particle formation within the polymer matrix. The particle size is about 8 nm. Selected area electron diffraction （SAED） shows the cubic zinc blende polycrystalline rings. Third-order optical nonlinearity of the CdS nanopartieles embedded in polymer thin films is studied with the Z-scan technique under 1064 nm excitation. The results show that the CdS nanocomposite film exhibits negative nonlinear refraction index and positive absorption coefficient. The film shows large optical nonlinearity, and the magnitude of the third-order nonlinear susceptibility of the film is calculated to be 1.73 × 10^-9 esu. The corresponding mechanism is discussed.     

Nonvolatile Memory Devices Based on Gold Nanoparticle and Poly （N-Vinylcarbazole） Composite

A rewritable polymer memory device based on gold nanoparticle doped poly （N-vinylcarbazole） （PVK）, which can be easily fabricated by simple spin coating, has been described. An electrical bistable phenomenon is observed in the current-voltage characteristics of this device, and it is found that the electrical bistability is repeatable by proper writing voltage and erasing voltage. The unique behaviour of the devices provides an interesting approach such that doping nanoparticles in polymer can be used to realize high performance nonvolatile polymer memory devices.     

Synthesis of organic phenothiazine-based molecular glasses and effect of racemic/homochiral aliphatic chain on near-infrared photorefractive property

Organic near-infrared photorefractive molecular glasses with a phenothiazine moiety are designed and synthesized through the introduction of linear, racemic/homochiral asymmetrically branched aliphatic chains into photorefractive chromophore as an auxiliary group. The compounds are characterized with ¹H-NMR, IR, FAB-MS, UV–vis, TG, DSC, etc. The effect of different aliphatic chains on the absorption and thermal properties is investigated in detail. The molar absorption coefficiency at the absorption maximum wavelength showed that the homochiral asymmetrically branched aliphatic chain has a strong hypochromic effect in the dilute solution when it is introduced into photorefractive chromophore. The DSC measurement indicated that the introduction of asymmetrically branched aliphatic chain is the key issue to design organic molecular glasses whether it is racemic or homochiral. The effect of racemic/homochiral asymmetrically branched aliphatic groups on photorefractive property is investigated carefully with poly(N-vinylcarbazole) (PVK) as a photoconductor and with (2,4,7-trinitro-9-fluorenylidene) malononitrile (TNFM) as a photosensitizer. The results suggested that the racemic group is more beneficial to the improvement of photorefractive performance than the homochiral when the homochiral cannot induce rigid photorefractive chromophore to be much more ordered.