通过重氮盐分子表面修饰金纳米帽子探究其对等离子体共振吸收的影响

以玻璃基底作为聚苯乙烯纳米球的载体，首先将聚苯乙烯纳米球旋涂在玻璃基底上，然后通过热沉积的方法将金熔融沉积在聚苯乙烯纳米粒子的表面, 再通过超声的方式将负载有金纳米帽子的聚苯乙烯微球从玻璃基底上分离下来，最后用二氯甲烷将聚苯乙烯微球溶解掉，成功制备了空心的金纳米帽子材料。通过共价键链接的方式在这些空心的金纳米帽子的表面成功修饰上苯的衍生物，通过测试分析发现，修饰带有不同电性的基团，金纳米帽子的等离子体共振吸收会发生不同的红移或蓝移现象，推测这是由于金纳米帽子表面结构电子密度的变化所导致。     

中空Ag纳米球壳的制备及性能表征

 以改性聚苯乙烯微球为模板,采用化学镀法在聚苯乙烯微球表面包覆一层银,在四氢呋喃溶液中将聚苯乙烯微球溶解,得到中空Ag纳米球壳。采用扫描电镜、透射电镜和X射线衍射仪对样品进行了表征及分析,并用紫外可见分光光度计研究了粒子的光学性质。实验结果表明：运用此法成功地制备出中空Ag纳米球壳的内径为250 nm,壁厚约为15 nm,并且成功地使纳米粒子的紫外吸收光谱由600 nm红移至900 nm左右,实现了在可见光至近红外光区调节Ag纳米结构的吸收峰。     

球壳结构金阴极及其X射线光电发射特性

以聚苯乙烯微球为模板, 采用种子-生长法在聚苯乙烯微球表面镀覆金球壳层, 以不同浓度旋涂分散在阴极衬底上, 热处理去除聚苯乙烯模板, 初步制备出表面具有金球壳结构的反射式金阴极样品, 通过金相显微镜和扫描电镜研究其表面形貌, 结果表明: 阴极表面球壳的直径约为10 μm, 高温去除聚苯乙烯微球模板后金沉积层具有良好的自支撑性, 球壳厚度约70-90 nm, 球壳表面主要由30-60 nm的晶粒突起组成. X射线光电发射测试表明, 反射式球壳结构阴极在200-1500 eV波段光电效率相对于平面薄膜阴极有明显提升, 其量子效率可达到平面阴极的3倍以上, 理论分析表明: 球壳结构阴极特殊的表面结构引起光电发射面积的增大和表面势垒的降低, 是阴极光电发射效率提高的主要原因.     

微米级锥形光纤的近场光镊

分别从理论和实验上分析了光纤表面倏逝场强度的分布(z=10 nm, 100 nm, 500 nm,1 000 nm),研究了微米级光纤光镊对微球的操纵。实验中把直径为125 m的普通单模光纤拉制成锥腰直径为2 m的锥形光纤。当光纤通光时,在光纤锥区倏逝场的作用下,直径3 m的聚苯乙烯微球保持平衡状态,并且光纤附近的微球被吸引到光纤表面,以5.3 m /s的速度沿着光束的传播方向运动。这个实验不仅实现了对微球的成功捕获,而且验证了光纤光镊的力学作用。光纤光镊对微球的无接触、无损伤操纵,将在生物传感领域有潜在的应用。     

金纳米粒子的图案化组装及表面增强拉曼光谱研究

利用聚苯乙烯纳米粒子有序组装结构为模板,进行了金纳米粒子的图案化组装。金纳米粒子在聚苯乙烯纳米粒子底部自组装聚集,形成规则的“面包圈”结构。表面增强拉曼光谱表明,相对于随机分布的金纳米粒子而言,金纳米粒子组装结构具有聚焦电磁场作用,从而使吸附的对巯基苯甲酸的拉曼散射得以进一步增强。     

空心微球结构Au/Ag合金泡沫块体的制备

将平均晶粒尺寸为4.6 nm的金粒子通过静电作用粘附于聚苯乙烯（PS）微球表面用于化学镀,化学镀金后PS表面的金沉积层几乎达到完全包覆,厚度70~90 nm;在Au/PS表面进行化学镀银,沉积的银颗粒堆积紧密,颗粒大小较先前沉积的金颗粒大,镀覆层厚度增厚至200~400 nm;模板去除后,获得了完全自支撑的Au40Ag60空心微球结构的圆柱状泡沫材料。制备的金银合金泡沫由直径约10 m的空心球壳组成,圆柱体直径约5 mm,密度约1.2 g/cm3。     

亚微米聚苯乙烯微球在气-液界面组装的机理研究

系统地研究了亚微米聚苯乙烯微球在气-液界面的组装机理.聚苯乙烯微球在介质对流的带动下会到达悬浮液的表面并在气-液界面组装，气-液界面处聚苯乙烯微球间由弯液面产生的毛细管力是组装的推动力.界面处聚苯乙烯微球在干燥过程中其润湿性发生了转变，由完全润湿到部分润湿并最终变成不润湿，相应的聚苯乙烯微球与分散介质间接触角也逐渐增大.研究表明，只有接触角达到或超过某数值θ′_critical时，才能够出现气-液界面组装现象.考虑到PS胶粒晶体的表面是“规则”粗糙的表面，由Wenzel公式知θ′_critical大于测量值θ＝22°.聚苯乙烯微球润湿性的转变是界面组装发生和持续进行的关键性因素. 关键词： 自组装 胶粒晶体 聚苯乙烯微球 润湿性     

亚微米聚苯乙烯微球在气-液界面组装的机理研究

系统地研究了亚微米聚苯乙烯微球在气-液界面的组装机理.聚苯乙烯微球在介质对流的带动下会到达悬浮液的表面并在气-液界面组装，气-液界面处聚苯乙烯微球间由弯液面产生的毛细管力是组装的推动力.界面处聚苯乙烯微球在干燥过程中其润湿性发生了转变，由完全润湿到部分润湿并最终变成不润湿，相应的聚苯乙烯微球与分散介质间接触角也逐渐增大.研究表明，只有接触角达到或超过某数值θ′_critical时，才能够出现气-液界面组装现象.考虑到PS胶粒晶体的表面是“规则”粗糙的表面，由Wenzel公式知θ′_critical大于测量值θ＝22°.聚苯乙烯微球润湿性的转变是界面组装发生和持续进行的关键性因素. 关键词： 自组装 胶粒晶体 聚苯乙烯微球 润湿性     

表面镀金SU-8微柱的低频电动旋转特征

依据传统Maxwell-Wagner界面极化理论, 金属微纳米粒子由于具有极高电导率, 在旋转电场作用下无明显电旋转运动. 然而, 本文针对镀金SU-8微柱开展实验研究, 发现镀金微柱在低频条件下的快速旋转运动现象. 据此, 通过考虑镀金微柱表面双电层效应, 理论分析并实验验证镀金微柱的低频电旋转特征. 首先, 建立电场中微柱的近似椭球模型, 分析固-液接触面双电层作用下的金属粒子极化机理, 推导旋转电场作用下镀金微柱的转矩公式及电旋转角速度公式. 其次, 搭建实验平台, 分别对镀金微柱在三种不同电导率溶液、100 Hz–30 MHz频率范围内的电旋转特征进行对比实验研究. 最后, 对实验结果进行分析和讨论, 并通过考虑镀金微柱与基底之间摩擦作用等因素, 验证实验研究与理论研究的一致性. 关键词： 表面镀金微柱 电旋转 双电层 微流控     

桑色素修饰金纳米粒子自组装膜的制备及其性能研究

采用水相硅烷化方法,将γ-氨基丙基三乙氧基硅烷[H₂N(CH₂)₃Si(OC₂H₅)₃](APES)组装在石英表面,在基底表面修饰上氨基为末端的单层膜,并进一步在这种功能化的单层膜基底上组装金纳米粒子得到金纳米粒子/APES/石英的纳米复合结构。以制备的金纳米粒子自组装膜修饰石英为基底及DL-半胱胺酸为中介,利用桑色素(Morin)和DL-半胱胺酸的化学吸附作用,将桑色素间接组装在金纳米粒子自组装膜修饰石英基底表面,所构建的桑色素修饰金纳米粒子自组装膜对三苯基锡有灵敏的荧光识别作用。文章着重研究了桑色素修饰金纳米粒子自组装膜的制备以及组装条件对其荧光行为的影响,探讨了膜的响应特性及响应机理。     

Microwire formation based on dielectrophoresis of electroless gold plated polystyrene microspheres

Microspheres coated with a perfectly conductive surface have many advantages in the applications of biosensors and micro-electromechanical systems.Polystyrene microspheres with the diameter of 10 μm were coated with a 50 nmthick gold layer using an electroless gold plating approach.Dielectrophoresis(DEP) for bare microspheres and shelled microspheres was theoretically analysed and the real part of the Clausius-Mossotti factor was calculated for the two kinds of microspheres.The experiments on the dielectrophoretic characterisation of the uncoated polystyrene microspheres and gold coated polystyrene microspheres(GCPMs) were carried out.Experimental results showed that the gold coated polystyrene microspheres were only acted by a positive dielectrophoretic force when the frequency was below 40M Hz,while the uncoated polystyrene microspheres were governed by a negative dielectrophoretic force in this frequency range.The gold coated polystyrene microspheres were exploited to form the microwire automatically according to their stable dielectrophoretic and electric characterisations.     

Ordered macroporous gold thin film with encaptured polymer spheres

A two-dimensional colloidal crystal fabricated from core-shell polystyrene spheres was employed as a template for the electrochemical deposition of gold. By partially embedding the colloidal spheres into the gold film and selectively removing the shells of the colloidal spheres, highly ordered macroporous gold thin films with captured polystyrene spheres were obtained.     

Large-scale protein/antibody patterning with limiting unspecific adsorption

A simple synthetic route based on nanosphere lithography has been developed in order to design a large-scale nanoarray for specific control of protein anchoring. This technique based on two-dimensional (2D) colloidal crystals composed of polystyrene spheres allows the easy and inexpensive fabrication of large arrays (up to several centimeters) by reducing the cost. A silicon wafer coated with a thin adhesion layer of chromium (15 nm) and a layer of gold (50 nm) is used as a substrate. PS spheres are deposited on the gold surface using the floating-transferring technique. The PS spheres were then functionalized with PEG-biotin and the defects by self-assembly monolayer (SAM) PEG to prevent unspecific adsorption. Using epifluorescence microscopy, we show that after immersion of sample on target protein (avidin and anti-avidin) solution, the latter are specifically located on polystyrene spheres. Thus, these results are meaningful for exploration of devices based on a large-scale nanoarray of PS spheres and can be used for detection of target proteins or simply to pattern a surface with specific proteins.     

Absorption spectrum of surface-bound cap-shaped gold particles

A surface-adsorbed monolayer of cap-shaped gold particles upon submicrometer-sized polystyrene spheres exhibits pronounced absorption in the visible region. When the surrounding refractive index was altered by immersion in a fluid, the direction of the shift in the absorption spectrum was dependent on the incidence angle of the irradiation. When a thiol molecule, known to adsorb selectively on gold upon polystyrene, was added, the resultant shift in the absorption spectrum's peak was consistently toward longer wavelengths. Consequently, at certain incidence angles, a change in the refractive index of the surrounding fluid produces no shift, whereas thiol adsorption results in a clear shift, apparently reflecting the different spatial regions in which the refractive index is altered by these two procedures.     

Gold nanostructures on chemically reinforced PDMS microwell arrays

This paper describes a facile strategy for fabricating arrays of two- and three-dimensional gold nanostructures using PDMS-infiltrated polystyrene (PS) colloidal crystals. PDMS molding of colloidal crystal, gold vapor deposition, and subsequent calcination of PS produced gold thin layers over hexagonal PDMS microwell arrays with hemispherical air-voids of approximately 140 nm on glass substrates. Vapor deposition of perfluoroalkylsilane thin layers improved the thermal stability of the colloidal template over 100 °C, providing a route to preparation of hollow architectures with gold thin layers supported by PDMS nanostructures. Surface modification of the PDMS using poly(allylamine hydrochloride) induced two-dimensional colloidal crystals of PS and PMMA spheres through electrostatic interactions. Particle aggregation of 13 nm gold nanoparticles in the PDMS microwells demonstrated a surface plasmon resonance band red-shifted to 810 nm, in comparison with that on the flat surface at 720 nm.     

Optical trapping of nanoparticles and microparticles by a Gaussian standing wave

The optical trapping of nanoparticles and microparticles by a Gaussian standing wave is experimentally demonstrated for the first time to the authors' knowledge. The standing wave is obtained under a microscope objective as a result of the interference of an incoming laser beam and a beam reflected on a microscope slide that has been coated with a system of reflective dielectric layers. Experimental results show that three-dimensional trapping of nanoparticles (100-nm polystyrene spheres) and one or more vertically aligned micro-objects (5-mum polystyrene spheres, yeast cells) can easily be achieved by use of even highly aberrated beams or objectives with low numerical apertures.     

Hematite/Polystyrene Raspberry-Like Microcomposites as Stable Support for Silver Nanoparticle Immobilization

Among the methods utilized for the preparation of raspberry-like microcomposites, due to its simplicity and universality, the electrostatically-driven deposition of nanoparticles at the surface of microparticles is especially attractive. This process, leading to the formation of a single nanoparticle monolayer, is widely reported. On the other hand, no data concerning the electrostatically-driven formation of nanoparticle bilayers at the surface of microparticles are reported. To fill this gap, the detailed investigation of the formation of silver/hematite nanoparticle bilayers at the surface of polystyrene microparticles is reported. First, the hematite/polystyrene raspberry-like microcomposites are obtained by immobilization of hematite nanoparticles under an electrostatically-driven process. The stability of hematite/polystyrene microcomposites at elevated temperatures up to 323 K is monitored using microelectrophoresis. No significant changes in the hematite nanoparticle layer coverage are observed after prolonged time of incubation. This proves the irreversible character of nanoparticle immobilization. Next, the hematite/polystyrene microcomposites are utilized as the interfaces for immobilization of negatively charged silver nanoparticles. This process is quantitatively described using electrokinetic measurements. The changes in the hydrodynamic diameter of microcomposites are also determined. Finally, the validity of the electrokinetic model used in this work for predicting the zeta potential of the silver/hematite/polystyrene microcomposites is confirmed.     

磁性液体中非磁性小球与磁性纳米颗粒的相互作用及磁组装

利用磁性液体与聚苯乙烯小球溶液混合得到的复合磁性液体, 研究了聚苯乙烯小球和磁性纳米颗粒在外加磁场作用下的动力学过程. 实验结果表明, 当外加磁场的方向平行于样品平面时, 聚苯乙烯小球在沿着磁场的方向上表现出相互吸引而形成链状结构, 其动力学过程可分为聚苯乙烯小球被反磁化产生相互吸引而形成短链的快过程以及短链间相互吸引形成长链的慢过程; 当外加磁场的方向垂直于样品平面时, 相邻聚苯乙烯小球表现出排斥的相互作用而形成短程有序的二维结构, 当磁场强度增加到一定的阈值时, 聚苯乙烯小球和磁性纳米颗粒形成的团簇会产生相互吸引而组装成复合式的花瓣结构. 关键词： 磁性液体 磁组装 非磁性颗粒