TMB·TCNQ和硬脂酸混合LB膜的制备及表征

将没有双亲性的电荷转移配合物TMB·TCNQ (TMB：3, 3′,5,5′-Tetramethylbenzidine;TCNQ：7,7,8,8-tetracyanoquinodimethane)通过与硬脂酸混合组装制备了混合LB膜。TMB·TCNQ和硬脂酸的摩尔比例在1∶1, 1∶2和1∶3的情况下都可以成功进行组装。利用紫外-可见-近红外光谱、透射和掠角反射红外光谱、X射线衍射以及原子力显微镜研究了混合LB膜中各组分的结构、分子取向和表面形貌等。研究结果表明,混合LB膜中的TMB·TCNQ是混合堆积排列的,电荷转移度ρ约为0.35。配合物中的电子给体TMB和电子受体TCNQ分子的苯环平面都垂直于基底表面。硬脂酸的碳氢长链以一定角度倾斜于基底表面。混合LB膜的小角X射线衍射图中出现了两组衍射峰。混合比例为1∶1的单层和多层LB膜中出现纳米棒和微粒,而且,纳米棒和粒子的数量随着LB膜层数的增加而增多。     

十八胺LB膜吸附组装金纳米颗粒研究

制备了十八胺单层、多层LB膜及粒径为几个纳米的金纳米粒子。pH值小于10.3时十八胺带正电荷,将其置于金纳米溶胶(pH值10.3)中,带负电荷的金纳米粒子与带正电荷的十八胺之间通过静电作用,金纳米颗粒被成功地吸附组装到十八胺LB膜中,形成纳米薄膜。紫外-可见光谱、红外光谱及扫描电镜显示:金纳米颗粒通过这种方法能够很好的组装在十八胺LB膜上,且其组装层整齐有序,同时也受十八胺LB膜层数及组装时间的影响。     

银纳米粒子自组装复合LB膜的结构与性质

纳米粒子的自组装和有序组装膜的结构与性质近年来受到了人们的广泛关注,纳米粒子的表面结构与性质对由其组装成的有序膜的结构与性质有直接的影响。文章报道了利用自组装技术制备的银纳米粒子与双亲有机分子的单层和多层复合LB膜,通过吸收光谱和表面增强拉曼光谱研究了银纳米粒子与吸附分子间的相互作用,探讨了复合膜的成膜特性及银纳米粒子的拉曼增强特性。十八胺/银粒子复合LB膜的吸收光谱及拉曼光谱显示,十八胺分子与银纳米粒子表面的活位通过NH₂中的氮原子以复合体的形式结合;同时,在激发光的作用下复合体可能存在光催化过程。根据银粒子复合LB膜的实验结果,十八胺和十八酸之间的反应产物在复合膜中起空间位阻作用,与银粒子表面的相互作用较弱。     

铁纳米粒子的结晶形态与表面氧化膜分析

铁纳米粒子样品系采用气体蒸发法制备,用透射电子显微镜观察其结晶形态和粒径大小,采用X射线衍射、电子衍射、X射线光电子能谱和俄歇电子能谱等多种分析手段详细分析了粒子表面氧化膜的组成、结构和厚度及其稳定性,提出了铁纳米粒子组成和结构模型。结果发现铁纳米粒子本身的晶体结构与普通α-Fe是一致的,为体心立方结构,粒子表面存在约3nm厚的双层氧化膜,外面一层为γ-Fe₂O₃,厚度约为1nm。里面一层为Fe₃O₄,厚度约为2nm, 关键词：     

由组分可控的LB膜前驱物法制备Y2O3稳定立方相ZrO2的超薄陶瓷膜

由有机LB膜技术发展了一种制备组分、厚度可控的无机超薄陶瓷膜的方法 .以Zr、Y的 β 二酮络合物的作为“表面离子”代替传统的亚相离子 ,沉积它们与花生酸的混合LB膜 .并将它作为前驱物 ,经臭氧处理和热处理 ,成功制得了Y2 O3 稳定的立方相ZrO2 超薄膜 (YSZ) .用X射线衍射 (XRD)、X射线光电子能谱 (XPS)等手段研究了YSZ薄膜的相结构和其组成 .结果表明 ,超薄陶瓷膜中Zr与Y的含量比率控制得很好 ,且形成Y2 O3 稳定的立方相ZrO2 .说明这种方法可以成功地用来制备组分和膜厚均可控的纳米陶瓷膜 .     

酞菁铜衍生物在酞菁酮—氧化铁纳米粒子交替LB膜中的分子取向

通过Langmuir-Blodett技术制备了酞菁酮－氧化铁纳米粒子交替LB膜,利用偏振紫外－可见光谱对酞菁铜衍生物在不同制膜条件下所制得的交替膜中的分子取向进行了研究。结果表明,在同一氧化铁溶胶亚相中,随着表面压的增大,或在相同的表面压下,随着亚相中氧化铁浓度的减小,酞菁铜分子在其复合LB膜中倾斜程度变大。     

酞菁铜衍生物在酞菁铜氧化铁纳米粒子交替LB膜中的分子取向

通过Langmuir Blodgett技术制备了酞菁铜 氧化铁纳米粒子交替LB膜 ,利用偏振紫外 可见光谱对酞菁铜衍生物在不同制膜条件下所制得的交替膜中的分子取向进行了研究。结果表明 ,在同一氧化铁溶胶亚相中 ,随着表面压的增大 ,或在相同的表面压下 ,随着亚相中氧化铁浓度的减小 ,酞菁铜分子在其复合LB膜中倾斜程度变大。     

表面活性剂包埋的硫化锌纳米粒子LB膜的研究

采用ＬＢ膜技术制备了表面活性剂包埋的硫化锌纳米粒子多层膜,并利用小角Ｘ射线衍射、光电子能谱、原子力显微镜和透射电镜春结构进行了表征。结果表明制成的ＺｎＬ纳米粒子ＬＢ膜为一维准超晶格。     

微波辅助法制备纤维状NaFeS2纳米粒子及其XPS研究

常温下用微波辅助法制得了直径小于10nm的纤维状NaFeS2 三元化合物纳米粒子,并用X射线粉末衍射、透射电子显微镜、选区电子衍射和X射线光电子能谱对纳米微粒进行了表征。XPS能谱分析表明:产物中含有Na ,Fe,S三种元素,其比值为Na∶Fe∶S =1∶1 1∶1 9。探讨了纤维状NaFeS2 纳米粒子的形成机理。     

3-巯基丙酸包裹的金纳米粒子自组装膜的制备及其层状周期性结构分析

制备了 3-巯基丙酸包裹的金钠米粒子水溶胶。在胺丙基三甲氧基硅烷覆盖的 Si或Si O2 基底上组装了上述金纳米粒子的单层膜和由 1 ,6-二巯基己烷联接的金纳米粒子多层膜。紫外 -可见吸收光谱和 X-射线衍射实验分析了多层膜的层状周期性结构     

CdS/ZnS core–shell nanoparticles in arachidic acid LB films

Core–shell CdS/ZnS nanoparticles in arachidic acid film were prepared through a novel Langmuir–Blodgett (LB) approach. Post-deposition treatment of the precursor LB multilayers of cadmium arachidate with H₂S gas followed by intercalation of Zn²⁺ ions and further sulfidation result in the formation of CdS/ZnS nanoparticles in the LB film. The formation of these nanoparticles and resulting changes in layered structures were studied by FTIR and X-ray reflection measurements. The optical properties were studied using UV–vis absorption and photoluminescence spectroscopy. A red-shift in the absorption spectrum and enhancement of CdS excitonic emission together with reduction of surface states emission suggest that after the intercalation step, a thin layer of ZnS surrounds the CdS nanoparticles, thus forming a core–shell structure. Subsequent to the second sulfidation, a further red-shift in absorption suggests the formation of a thicker ZnS coating on CdS. Electron diffraction of CdS nanoparticles coated with thicker ZnS showed the diffraction patterns of only ZnS, as expected for core–shell structures.     

微波合成银包覆金纳米粒子膜的拉曼散射活性研究

采用微波加热加压法和静电吸附自组装法在石英玻璃表面制备了银包覆金纳米粒子薄膜,利用原子力显微镜分析了薄膜的表面形态和结构,测定结晶紫分子在薄膜表面的拉曼光谱。结果表明,银包覆金纳米粒子薄膜具有很强的表面增强拉曼散射效应(SERS)活性和稳定性。     

Optical investigation of CdS quantum dots in Langmuir–Blodgett films

Structures with CdS quantum dots produced by the Langmuir–Blodgett (LB) technique were investigated by Raman, IR, and UV spectroscopies. The confinement effect of longitudinal optical (LO) phonons in CdS quantum dots was investigated by Raman spectroscopy. Surface vibrational modes of CdS quantum dots were observed in IR spectra. It was shown experimentally that the frequency of the surface vibrational modes depends on the properties of the surrounding media. An average size of CdS quantum dots of about 3–6.4 nm was obtained from the analysis of UV measurements. Received: 1 February 1999 / Accepted: 1 April 1999 / Published online: 19 May 1999     

The comparison between CdS thin films grown on Si(111) substrate and quartz substrate by femtosecond pulsed laser deposition

Two kinds of cadmium sulfate (CdS) thin films have been grown at 600 °C onto Si(111) and quartz substrates using femtosecond pulsed laser deposition (PLD). The influence of substrates on the structural and optical properties of the CdS thin films grown by femtosecond pulsed laser deposition have been studied. The CdS thin films were characterized by X-ray diffraction (XRD), atomic force microscopy (AFM), scanning electron microscopy (SEM), photoluminescence (PL) and Raman spectroscopy. Although CdS thin films deposited both on Si(111) and quartz substrates were polycrystalline and hexagonal as shown by the XRD , SEM and AFM results, the crystalline quality and optical properties were found to be different. The size of the grains for the CdS thin film grown on Si(111) substrate were observed to be larger than that of the CdS thin film grown on quartz substrate, and there is more microcrystalline perpendicularity of c-axis for the film deposited on the quartz substrate than that for the films deposited on the Si substrate. In addition, in the PL spectra, the excitonic peak is more intense and resolved for CdS film deposited on quartz than that for the CdS film deposited on Si(111) substrate. The LO and TO Raman peaks in the CdS films grown on Si(111) substrate and quartz substrate are different, which is due to higher stress and bigger grain size in the CdS film grown on Si(111) substrate, than that of the CdS film grown on the amorphous quartz substrate. All this suggests that the substrates have a significant effect on the structural and optical properties of thin CdS films. PACS 81.15.Fg; 81.05.Ea; 78.20.-e; 78.67.-n; 42.62.-b     

金属纳米粒子薄膜对辐射散热的影响的研究

通过分析不同螺旋线慢波组件的散热性能,研究了金属纳米粒子薄膜的采用对辐射散热性能的改善作用.利用实验测试和模拟仿真的方法,分析比较了采用普通金属管壳,沉积普通金属铱膜管壳和沉积纳米铱膜管壳的慢波组件的导热能力.结合实验数据,准确地推算出几种研究材料的热辐射发射率,并利用模拟仿真给予了验证.实验结果和模拟结果具有很好的一致性.研究表明,与普通金属材料相比,金属纳米粒子薄膜具有较强的热辐射能力,能够改善器件的散热性能.     

Synthesis and photoelectrochemical behavior of CdS quantum dots-sensitized indium-tin-oxide mesoporous film

In this paper, we reported an investigation on a new photoelectrode of quantum dots-sensitized solar cell (QDSC) combining indium-tin-oxide (ITO) mesoporous film and CdS quantum dots (QDs). The ITO mesoporous film was prepared by doctor-blade technique and CdS QDs attached on ITO mesoporous film were synthesized by successive ionic layer adsorption and reaction method. X-ray diffraction, field emission scanning electron microscopy, transmission electron microscope, X-ray spectroscopy and UV-vis spectroscopy were used to characterize the samples. The results indicated that the ITO mesoporous film was uniform, crack-free and highly porous. And absorbance in visible region was enhanced after the deposition of CdS QDs on ITO mesoporous film. The photoelectrochemical property of the CdS QDs-sensitized ITO mesoporous film photoelectrode was investigated by forming a photoelectrochemical cell. Photocurrent-voltage measurement showed that the photoelectrode was efficient in the cell as working electrode.     

Visualization of the langmuir-blodgett film structure in liquid-crystal cells

The use of liquid-crystal (LC) cells for the visualization of the Langmuir-Blodgett (LB) film structure is described. Images appearing in LC cells upon LB film application are presented. The images are analyzed in relation to the LB film structure (application conditions) and to the relief formed by indium tin oxide (ITO) electrodes.     

Fabrication and characterization of photocatalytic activity of Fe3O4-doped CdS hollow spheres

A new hollow sphere photocatalyst has been fabricated by combining Fe₃O₄ with nanoparticulate CdS. Their microstructures and photocatalytic behavior were examined by X-ray powder diffraction, transmission electron microscope, scanning electron microscope and ultraviolet and visible spectroscopy. These hollow nanostructures displayed superparamagnetism at room temperature. It showed higher activity on hollow sphere than solid particle as the catalysis result.     

Langmuir Blodgett multilayers and related nanostructures

Langmuir Blodgett (LB) process is an important route to the development of organized molecular layered structures of a variety of organic molecules with suitably designed architecture and functionality. LB multilayers have also been used as templates and precursors to develop nano-structured thin films. In this article, studies on the molecular packing and three-dimensional structure of prototypic cadmium arachidate (CdA), zinc arachidate (ZnA) and mixed CdA-ZnA LB multilayers are presented. The formation of semiconducting nano-clusters of CdS, ZnS and Cd_xZn_1−xS alloys within the organic multilayer matrix, using arachidate LB multilayers as precursors is also discussed.     

PbTiO3超微粒-硬脂酸复合LB膜的光谱特性

ＰｂＴｉＯ３超微粒－硬脂酸复合超薄膜用ＬＢ膜技术制备,用π－Ａ曲线和原子力显微镜进行膜性能的表征。紫外－可见光吸收光谱、荧光光谱和拉曼光谱表明：ＰｂＴｉＯ３超微粒及其复ＬＢ膜具有量子尺寸效应和介电限域效应。