掺杂无机纳米超微粒的有机聚合物体系听光折变效应

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复合超微粒为光敏度，ＰＶＫ为载流子输运剂，电光分子为ＥＰＮＡＣ。     

GaAs／GaAlAs多量子阱反射型光调制器及自电光效应器件

采用分子束外延技术生长含有大周期数的ＧａＡｓ／ＧａＡｌＡｓ多量子阶（ＭＱＷ）及分布布喇格反射器（ＤＢＲ）的ＰＩＮ结构器件。研究了量子限制斯塔克效应（ＱＣＳＥ），分布布喇格反射及非对称腔模（ＡＳＦＰ）效应对光的反射调制作用及这三种效应的兼容性对光调制及逻辑器件的重要影响。给出我们研制的反射型光调制器及自电光效应器件的实验结果。对于常通型及常闭型调制器，其两态衬比度可达１０ｄＢ。所研制的ＳＥＥＤ器件，其导通光能耗低于１０ｆＪ／（μｍ）￣２，实现其光学双稳态及Ｒ－Ｓ光触发器工作。     

掺杂Cu^2＋的ZnS纳米超微粒的PVA复合膜的制备和时间分辨光谱的研究

报导了ＺｎＳＣｕ水溶液和ＺｎＳＣｕ／ＰＶＡ复合膜的制备过程，分析了分散剂所起的作用．研究了室温下复合膜的激发光谱和发射光谱，以及室温和液氮温度下的分时光谱．初步探讨了ＺｎＳＣｕ纳米超微粒的发光过程．     

有机高分子光折变材料的研究进展

基于有机高分子材料独特的化学和物理性质，阐明了发展有机高分子光折变材料的重要意义。通过对有机高分子材料的光电导和电光效应的分析，讨论了有机高分子材料成为高性能光折变材料的可能性。着重介绍了有机高分子光折变材料的化学结构和光折变性能。同时，简单分析了有机高分子光折变材料的研究现状以及当前存在的一些问题。     

有机超微粒的制备及其尺寸效应的研究

有机超微粒是国际上刚刚起步的研究领域，是纳米科技领域和有机光电子领域的重要前沿课题，文章从有机功能小分子出发，在制备粒径和形状可控的，高度单分散的纳米超微粒的基础上，首次系统地研究了有机超微粒的电子态随尺寸大小的变化过程，发现有机超微粒和无机超微粒一样具有显著的尺寸效应，而且更具多样性，该项研究工作为探索和比较无机和有机材料介观尺寸效应的异同点这一科学问题奠定了坚实的基础，对于理解有机分子晶体这类传统材料中的基本过程和现象以及开发新型光电材料和器件也极具意义。     

掺杂CdS纳米粒子聚合物的光折变效应研究

研究了掺杂CdS纳米粒子的有机聚合物体系的光折变效应,体系中以CdS纳米粒子为光敏剂,聚乙烯咔唑(PVK)为载流子输运剂,4-(4-硝基苯偶氮)苯胺染料(DO3)为非线性生色团,9-乙基咔唑(ECZ)为增塑剂。反胶束法合成的CdS胶束颗粒采用紫外可见吸收光谱和透射电子显微镜(TEM)表征,结果表明,具有纳米尺寸和量子限制效应。研究了PVK-CdS薄膜的光电导特性,实验结果表明,CdS纳米粒子与PVK之间的电荷转移可以有效的提高PVK的光电导率。双光束耦合实验证明了该体系的光折变特性,在无外加电场下,获得二波耦合增益系数78.4 cm-1,分析表明聚合物薄膜具有强的光致取向增强效应;样品在两相干光束作用下,可建立折射率光栅,其衍射效率达到4.4%。     

线性和二次电光效应共同主导的非相干耦合空间孤子族

基于加偏压的单光子光折变晶体,理论推导了线性和二次电光效应共同主导下的亮孤子族和暗孤子族的解,数值研究了亮孤子族和暗孤子族的强度包络和稳定特性,讨论了线性和二次电光效应在孤子族形成中的不同作用.结果表明:线性和二次电光效应的相互作用能够增强亮孤子族的光折变非线性,而减弱暗孤子族的光折变非线性.此外,在传输过程中,亮孤子族的各个分量能够稳定传输;暗孤子族各个分量在较长传输距离时表现出不稳定性.     

线性和二次电光效应共同主导的非相干耦合空间孤子族（英文）

基于加偏压的单光子光折变晶体,理论推导了线性和二次电光效应共同主导下的亮孤子族和暗孤子族的解,数值研究了亮孤子族和暗孤子族的强度包络和稳定特性,讨论了线性和二次电光效应在孤子族形成中的不同作用.结果表明:线性和二次电光效应的相互作用能够增强亮孤子族的光折变非线性,而减弱暗孤子族的光折变非线性.此外,在传输过程中,亮孤子族的各个分量能够稳定传输;暗孤子族各个分量在较长传输距离时表现出不稳定性.     

液晶显示用取向材料聚甲基丙烯酸肉桂酰氧基乙酯的光控取向研究

通过实验研究了光聚合物材料聚甲基丙烯酸肉桂酰氧基乙酯（ＣＥＭＣ）的光化学反应过程, 以及对液晶材料ＬＣ－６７１０Ａ 的取向能力． 通过原子力显微镜（ＡＦＭ）观察了取向层表面在光化学反应前后的变化, 测量了光控取向膜液晶盒中液晶分子的预倾角及单面光控取向扭曲向列液晶显示器（ＴＮＬＣＤ）的电光特性和时间响应特性曲线, 研究了液晶分子排列取向的机理．     

全功能型有机光折变材料的研究进展

本文综述了全功能型光折变聚合物和小分子材料的研究进展 ,并详细汇总了这种材料的热特性 ,光电和电光特性 ,及光折变特性参数。基于对材料从分子水平上的设计思想 ,阐述了这种光折变材料的发展思路     

Encapsulation of Photosensitizers and Upconversion Nanocrystals in Lipid Micelles for Photodynamic Therapy

Photodynamic therapy (PDT) is a promising method for cancer therapy. However, it is constrained by limited penetration depth of visible light, hydrophobicity of photosensitizers, and lack of tumor targeting. In this work, the photosensitizer zinc phthalocyanine (ZnPc) and upconversion nanocrystals (UCNs) are encapsulated into OQPGA‐PEG/RGD/TAT lipid micelles. The UCNs acting as a nanotransducer convert deep‐penetrating near‐infrared (NIR) light to visible light for activating the photosensitizer. OQPGA‐PEG/RGD/TAT lipid micelles are used as a carrier for the photosensitizer, with improved biocompatibility and cancer‐targeting ability. The results show that the photosensitizer ZnPc‐ and UCNs‐loaded OQPGA‐PEG/RGD/TAT lipid micelles are nanoparticles with an average size of 25 nm. The lipid micelle nanoparticles are stable in water with low leakage of photosensitizer. The absorption peak of the photosensitizer overlaps with the emission peak of UCNs, so the visible fluorescence emitted from the UCNs upon excitation by the NIR laser at 980 nm can activate the photosensitizer to produce singlet oxygen for PDT. The targeting RGD peptide and cell‐penetrating TAT peptide on the surface help the nanoparticles getting into cancer cells. The OQPGA‐PEG/RGD/TAT lipid micelles encapsulated with both the photosensitizer ZnPc and UCNs could be used for targeted PDT by using deep‐penetrating NIR light as the light source.     

Polydopamine Nanoparticle as a Multifunctional Nanocarrier for Combined Radiophotodynamic Therapy of Cancer

Combination of different therapeutic strategies to treat cancer has attracted tremendous attention in recent years. Herein, the authors develop polydopamine (PDA) nanoparticles with polyethylene glycol (PEG) modification as a multifunctional nanocarrier for coloading photosensitizer chlorine6 (Ce6) and curcumin (Cur) for combined photodynamic therapy (PDT) and radiotherapy (RT) of cancer. PEGylated PDA nanoparticles (PDA‐PEG) exhibit well water soluble and biocompatible in different physiological solutions and cause no obvious toxicity to cancer cells. In this nanoparticle, the loaded Ce6 can trigger the generation of single oxygen under near‐infrared laser irradiation for PDT, while the loaded Cur can act as an excellent radiosensitizer under X‐ray irradiation for enhanced external RT. As demonstrated by in vitro and in vivo therapeutic efficiency, combined PDT and RT based on PDA‐PEG/Cur/Ce6 nanoparticles exhibits significant inhibition the growth of cancer cells, revealing perfect performance in cancer treatment. Therefore, the study not only presents a polymer‐based theranostic platform for cancer treatment but also demonstrates the potential applications of combined RT and PDT for the future clinic cancer therapy.     

溶胶-凝胶法制备Polyme/MS/SiO2(M=Pb,Cd)复合纳米材料

采用溶胶－凝胶结合水热结晶技术,可成功把高聚物引入MS－SiO2网络结构。合成一种新型的有机－无机硫化物即Polymer/MS/SiO2(M=Pb,Cd)复合纳米材料,其中聚甲基丙烯酸甲酯或聚丙烯酰胺等高聚物的引入将有效地防止无机粒子团聚,控制粒子尺寸,前者还能形成核－壳结构复合粒子。作者还详细讨论了该复合纳米材料的热分析,结果表明,聚合物的存在提高了原有MS－SiO2(M=Pb,Cd)材料的热稳定性。     

The transition from spark to arc discharge and its implications with respect to nanoparticle production

Indium (III) phthalocyanine (InPc) was encapsulated into nanoparticles of PEGylated poly(d,l-lactide-co-glycolide) (PLGA-PEG) to improve the photobiological activity of the photosensitizer. The efficacy of nanoparticles loaded with InPc and their cellular uptake was investigated with MCF-7 breast tumor cells, and compared with the free InPc. The influence of photosensitizer (PS) concentration (1.8–7.5 μmol/L), incubation time (1–2 h), and laser power (10–100 mW) were studied on the photodynamic effect caused by the encapsulated and the free InPc. Nanoparticles with a size distribution ranging from 61 to 243 nm and with InPc entrapment efficiency of 72 ± 6 % were used in the experiments. Only the photodynamic effect of encapsulated InPc was dependent on PS concentration and laser power. The InPc-loaded nanoparticles were more efficient in reducing MCF-7 cell viability than the free PS. For a light dose of 7.5 J/cm² and laser power of 100 mW, the effectiveness of encapsulated InPc to reduce the viability was 34 ± 3 % while for free InPc was 60 ± 7 %. Confocal microscopy showed that InPc-loaded nanoparticles, as well as free InPc, were found throughout the cytosol. However, the nanoparticle aggregates and the aggregates of free PS were found in the cell periphery and outside of the cell. The nanoparticles aggregates were generated due to the particles concentration used in the experiment because of the small loading of the InPc while the low solubility of InPc caused the formation of aggregates of free PS in the culture medium. The participation of singlet oxygen in the photocytotoxic effect of InPc-loaded nanoparticles was corroborated by electron paramagnetic resonance experiments, and the encapsulation of photosensitizers reduced the photobleaching of InPc.     

Preparation, characterization and surface morphology of novel optically active poly(ester-amide)/functionalized ZnO bionanocomposites via ultrasonication assisted process

Novel bionanocompoites (BNCs) were prepared using zinc oxide (ZnO) nanoparticles which functionalized by γ-methacryloxypropyltrimethoxysilane (KH570) as a coupling agent. Poly(ester-amide) (PEA) based on tyrosine natural amino acid was synthesized and used as a polymer matrix. PEA/ZnO BNCs were characterized by fourier transform infrared spectra (FT-IR), X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), atomic force microscopy (AFM) and transmission electron microscopy (TEM). All the results confirmed that the surface of ZnO particle has sufficient compatibility with PEA through the link of the coupling agent between ZnO and polymer and also proved that the presence of ZnO nanoparticles appeared to be dispersed in nanosize in polymer composite matrix. In addition, thermogravimetric analysis (TGA) data indicated an enhancement of thermal stability of new BNC materials compared with the pure polymer.     

基于多形貌银纳米颗粒的多波长相干随机激光研究

采用溶剂热法分别制备了球形银纳米颗粒和多形貌银纳米颗粒,其中球形银纳米颗粒具有400 nm的窄带等离激元共振峰,而多形貌银纳米颗粒的共振区间在400～700 nm之间,将它们分别掺入R6G与PVP的混合溶液中,利用旋涂法在玻璃基板上制备银纳米颗粒嵌入染料掺杂聚合物薄膜随机激光器。采用纳秒脉冲激光进行随机激光泵浦实验,实验结果表明球形银纳米颗粒染料掺杂聚合物薄膜只有自发辐射峰,而多形貌银纳米颗粒染料掺杂聚合物薄膜具有线宽<0.8 nm的相干随机激光发射光谱,其阈值为1.9 mJ·cm-2, 这可能是由于银纳米颗粒的等离激元共振区间与R6G的发射光谱重叠,支持局域等离激元效应的形成,明显的局域场增强有效地改善了与附近分子的相互作用,从而激发了更多的辐射光子,促进了高增益的形成。进一步,利用多形貌银纳米颗粒在银纳米颗粒染料掺杂聚合物薄膜中随机分布的特性,通过改变泵浦位置,实现了20 nm范围内的随机激光输出波长的调控,具体输出范围为590.1～610.4 nm。认为这是由于多形貌银纳米颗粒在不同位置的组成和分布不同,改变了表面等离激元的相互作用和光子的散射能力,从而形成不同的增益效应和不同的封闭光振荡路径。此外,考虑到多形貌银纳米颗粒的共振波长较宽,探究了其用于输出其他颜色光的可能性。以与上述银纳米颗粒R6G染料掺杂聚合物薄膜相似的制备方法,制备了多形貌银纳米颗粒掺杂DCJTB染料聚合物薄膜,并且进行随机激光泵浦实验。结果表明,可以有效的产生波长为675 nm,半高宽<0.8 nm的相干红光随机激光,并且阈值仅为0.98 mJ·cm-2。研究结果在宽带可调谐随机激光器研究以及多色随机激光器研究领域具有重要的参考价值。     

Controlled oxidation of iron nanoparticles in chemical vapour synthesis

Enteric-coated formulations can delay the release of drugs until they have passed through the stomach. However, high concentration of drugs caused by rapidly released in the small intestine leads to the intestinal damage, and frequent administration would increase the probability of missing medication and reduce the patient compliance. To solve the above-mentioned problems, aspirin-loaded enteric-coated sustained-release nanoparticles with core–shell structure were prepared via one-step method using coaxial electrospray in this study. Eudragit L100-55 as pH-sensitive polymer and Eudragit RS as sustained-release polymer were used for the outer coating and inner core of the nanoparticles, respectively. The maximum loading capacity of nanoparticles was 23.66 % by changing the flow rate ratio of outer/inner solutions, and the entrapment efficiency was nearly 100 %. Nanoparticles with core–shell structure were observed via fluorescence microscope and transmission electron microscope. And pH-sensitive and sustained drug release profiles were observed in the media with different pH values (1.2 and 6.8). In addition, mild cytotoxicity in vitro was detected, and the nanoparticles could be taken up by Caco-2 cells within 1.0 h in cellular uptake study. These results indicate that prepared enteric-coated sustained-release nanoparticles would be a more safety and effective carrier for oral drug delivery.     

New nanocomposites containing metal nanoparticles, carbon nanotube and polymer

Metal-carbon nanotube-graft-polymer (MCNT-g-P) nanocomposites were synthesized and characterized successfully. In this work, multiwall carbon nanotubes (MWCNT) were opened using HNO₃/H₂SO₄ mixture and filled by metal nanoparticles such as silver nanoparticles through wet chemistry method. Then MWCNT containing metal nanoparticles were used as macroinitiator for ring opening polymerization of ε-caprolactone and MCNT-g-P nanocomposites were obtained. Length of grafted polymer arms onto the MWCNT was controlled using MWCNT/ε-caprolactone ratio. Structure and properties of nanocomposites were evaluated by TEM, DSC, TGA, and spectroscopy methods.     

新型光动力学疗法光敏剂5-ALA-GNPs的制备及其光谱分析

通过聚二烯丙基二甲基胺盐酸盐和氯金酸制备阳离子纳米金,将纳米金和5-氨基乙酰丙酸(5-aminolevulinic acid, 5-ALA)通过静电吸附作用有效结合得到新型光敏剂。应用共振瑞利散射光谱, 紫外-可见吸收光谱, 透射电镜和激光散射等方法对其进行了表征。结果表明通过这种方法纳米金与5-ALA可以有效结合。这种新型光敏剂对提高光动力学疗法临床疗效具有重要指导意义。     

Optical properties of nanocomposites based on polymers and metal nanoparticles

The optical properties of nanocomposites of metal nanoparticles and polymers of two types have been studied. Gold and silver nanoparticles were obtained by laser ablation of corresponding metal targets in acetone and chloroform. The thus formed colloidal solutions were used to prepare nanocomposites of these nanoparticles in polymer matrices of polymethylmethacrylate (PMMA) and fluorine-containing polymer LF-32. The polymer matrix is found to promote aggregation of the metal nanoparticles under study into elongated chains. In turn, metal nanoparticles affect the polymer matrix. In the case of PMMA, suppression of the vibrational peaks of polymer in the low-frequency region of its Raman spectrum occurs. In the case of LF-32, gold and silver nanoparticles amplify the Raman signal of the polymer matrix. In addition, the Raman spectra of nanocomposites indicate aggregation of disordered carbon around the nanoparticles obtained by laser ablation in organic solvents. The possibilities of studying the ultrafast (about 1 ps) optical response of the nanocomposites obtained in order to use it in photonics elements are discussed.