Spacer-controlled aggregation and surface morphology of a selenacarbocyanine dye on gemini monolayers

The adsorption and aggregation of a selenacarbocyanine dye (3,3-disulfopropyl-9-methyl-selenacarbocyanine, SeCy) onto Langmuir monolayers of a series of gemini amphiphiles with different methylene spacers were investigated. When the monolayers of the gemini amphiphiles were spread on the dye-containing subphase, the dye could be easily adsorbed and aggregated onto the monolayers through the electrostatic and pi-pi interaction. The dye formed complexes with gemini amphiphiles and stacked as J-aggregates in all the transferred multilayers, regardless of the structure of gemini amphiphiles. However, the surface morphologies of the complex monolayers showed a significant dependence on the spacer length of the gemini amphiphiles and the temperature of the subphase. Nanorods were observed for the complex films with spacer lengths ranged from 4 to 10 methylenes. With the temperature of the subphases increased from 20 degrees C to 30 degrees C, aligned longer nanofibers were formed instead. Although both the gemini amphiphiles and the dye were achiral, strong circular dichroism (CD) signals were observed for the transferred complex films. However, the CD signals could be just opposite in different places of the transferred films, suggesting that a resolved enantiomeric micro/nanostructure coexisted in the films. On the other hand, for the complex film of the dye with the gemini amphiphile of two methylenes spacer, neither CD signal nor ordered surface morphologies were detected in any place of the film although the dye itself stilled formed J-aggregate in the film. It was suggested that regular nanoarchitectures and resolved chiral domains could be observed only when the spacer of gemini amphiphiles is comparative to the distance between the two SO3- groups in the dye.     

Fabrication and photoluminescence of hybrid organized molecular films of a series of gemini amphiphiles and europium(III)-containing polyoxometalate

Organic/inorganic hybrid monolayers, consisting of an oval decatungstoeuropate (EuW10) with photoluminescence and a series of gemini-type amphiphiles with various lengths of the flexible hydrophobic spacers, were formed through electrostatic interaction at the air/water interface. The ultrathin hybrid multilayer films could be fabricated through the horizontal transfer of the monolayers onto the solid substrates. The characteristic absorption band of EuW10 in the UV spectra of the hybrid films showed a slight red shift in comparison with that in solution, indicating the ordered arrangement of EuW10 in the hybrid films. FT-IR spectra of the hybrid films presented characteristic bands of EuW10, indicating that the structure of the cluster was kept in the films. X-ray diffraction measurements of the films revealed that the well-defined layer structures were formed in these multilayer films and the EuW10 cluster ions were orientated with their short axis parallel to the film surface. Typical photoluminescence of the 5D0 --> 7F2 and 5D0 --> 7F1 transitions of EuW10 was observed in the hybrid films. Interestingly, the relative intensity of the two emission bands varied with the spacer length of the gemini amphiphiles in the films. A size matching between EuW10 and the gemini amphiphile with a hexamethylene spacer was observed, which showed the lowest ratio of the emission intensity of 5D0 --> 7F2 to that of 5D0 --> 7F1. Circular nanoparticles were observed in the AFM images for all these hybrid films. In addition, the size of the formed nanoparticles showed a dependence on the spacer length.     

Design and interfacial assembly of a new series of gemini amphiphiles with hydrophilic poly(ethyleneamine) spacers

A new series of gemini amphiphiles containing two Schiff base moieties linked by the poly(ethyleneamine) with different lengths were designed, and their interfacial assemblies were investigated. Condensed monolayers were obtained on nearly neutral subphase where the hydrophilic spacers were found to immerse into the subphase. On strong alkaline and acidic subphase, the headgroup and the spacer of the gemini amphiphiles underwent dissociation and protonation, respectively, resulting in the enlargement of the molecular areas. Flat and uniform domains were obtained for the monolayers from nearly neutral subphase; flower-like or dendritic domains were observed for the films transferred from strong acidic subphase. On the other hand, when an anionic tetrakis(4-sulfonatonphenyl)porphine (TPPS) was added into an acidic subphase, an in situ complex formation between the gemini amphiphiles and TPPS occurred. The complex monolayers were transferred onto solid substrate and TPPS existed predominantly as J-aggregate in the complex films. Due to the multisited positive charges in the spacer on acidic subphase, the complex films of gemini amphiphiles with TPPS appeared as short fiber or nanorod structures and formed two-dimensional (2D) conglomerate chiral domains.     

Ag-PVA和Ag-PVA/TiO2复合超薄膜的制备及性能研究

用3种方法制备了银纳米粒子-聚乙烯醇复合体系,其中用加热还原法所得体系中Ag纳米粒子的尺寸较大(15nm),其表面等离子体共振吸收峰较宽,最大吸收波长位于420nm;用室温硼氢化钠还原法得到的复合体系的吸收峰蓝移至409nm,且峰形较窄,Ag纳米粒子的平均粒径为8.7nm;低温NaBH4还原法所得体系吸收峰进一步蓝移至397nm,此时Ag纳米粒子粒径最小(3.5nm).将室温还原法所得Ag-PVA复合体系旋涂成膜,所得薄膜光滑、透明、均匀性好,该法适用于制备多层薄膜,以调控薄膜的厚度和光谱性质.将Ag-PVA复合体系与钛酸四丁酯(Ti(O_nBu)₄)的乙醇溶液交替旋涂得到Ag-PVA/TiO₂有机/无机复合薄膜.紫外-可见吸收光谱研究表明,随着Ag-PVA层数的增加,薄膜的表面等离子体共振吸收强度呈线性增加,但是TiO₂层数的增加对吸收光谱没有明显影响.Ag-PVA/TiO₂有机/无机复合薄膜将金属纳米粒子、有机高分子与无机半导体材料结合在一起,这种多层纳米结构在光电、催化功能薄膜等方面具有潜在的应用前景.     

Regulation of aggregation and morphology of cyanine dyes on monolayers via gemini amphiphiles

The aggregation of dyes is of considerable importance in relating to their functions and applications. In this paper, we have investigated the regulation on the aggregation and morphology of two cyanine dyes, 3,3'-disulfopropyl-4,5,4',5'-dibenzo-9-methylthiacarbocyanine triethylammonium salt (MTC) and 3,3'-disulfopropyl-4,5,4',5'-dibenzo-9-phenylthiacarbocyanine triethylammonium salt (PTC), using a series of gemini amphiphiles (bis(2'-heptadecyl-3'-ethylimidazolium)-1,n-alkane dibromide, abbreviated as Gn, n=2, 4, 6, 8, 10). It has been found that both of the dyes could be adsorbed onto the monolayers of the gemini amphiphiles through the electrostatic and pi-pi interaction and stacked into H- or J-aggregate. The spacer of the gemini amphiphile showed good control over the aggregation of MTC: H-aggregate was favored when gemini amphiphiles with short spacer were applied, while J-aggregation was preferred in the case of longer spacer. Only J-aggregate was observed for PTC on gemini monolayer, regardless of the structure of the gemini amphiphiles. Interesting morphologies were observed for all the gemini/dye complex monolayers. Network structure and nanofibers were formed for the gemini/MTC films transferred below the plateau surface pressure and close to the collapse pressure, respectively. The ability of the complex monolayers to form nanofibers strongly depended on the component amphiphiles, G2>G4>G6, and no nanofibers were observed for G8/MTC and G10/MTC after the collapse. Only squared domains were observed for gemini/PTC monolayers. When both G2 and G10 were mixed, an individual control of the gemini amphiphiles over the aggregation of MTC in the complex monolayers was observed. The relationship among the spacer, dye structure, and aggregation was revealed.     

Supramolecular assemblies of a new series of gemini-type schiff base amphiphiles at the air/water interface: in situ coordination, interfacial nanoarchitectures, and spacer effect

Great interest has been devoted to the gemini amphiphiles because of their unique properties. In this article, we report some interesting properties of the interfacial films formed by a series of newly designed gemini amphiphiles containing the Schiff base moiety. This novel series of gemini amphiphiles with their Schiff base headgroups linked by a hydrophobic alkyl spacer (BisSBC18Cn, n = 2, 4, 6, 8, 10) could be spread to form stable monolayers and coordinated with Cu(Ac)(2) in situ in the monolayer. The alkyl spacer in the amphiphiles has a great effect on the regulation of the properties of the Langmuir monolayers. A maximum limiting molecular area was observed for the monolayers of the gemini amphiphile with the spacer length of hexa- or octamethylene groups. Both the monolayers on water and on the aqueous Cu(Ac)(2) subphase were transferred onto solid substrates, and different morphologies were observed for films with different spacers. Nanonail and tapelike morphologies were observed for amphiphile films with shorter spacers (n = 2 and 4) on the water surface. Wormlike morphologies were observed for gemini films with longer spacers of C(8) and C(10) when coordinated with Cu(Ac)(2). An interdigitated layer structure was supposed to form in the multilayer films transferred from water or the aqueous Cu(Ac)(2) subphase.     

Aggregation of photolytic gold nanoparticles at the surface of chitosan films

Formation and aggregation of photolytic gold nanoparticles at the surface of chitosan (CTO) films have been investigated. When thin films of chloroauric acid salt of CTO were irradiated with UV light in wet air at room temperature for 10 min, gold nanoparticles of approximately 10 nm size are formed at the film surface. Detailed X-ray photoelectron spectroscopy (XPS) study and field emission type scanning electron microscopy (FE-SEM) observation have been carried out to characterize gold nanoparticles at the film surface. The shift of Au(4f) peak to the higher energy side and broadening of full width at half-maximum in the XPS spectrum are the direct evidence of the existence of gold atoms and small clusters in the early stage of photolysis. According to FE-SEM observation, growth in the particle diameter and aggregation of nanoparticles were observed after prolonged irradiation, and, finally, the film surface was densely covered with gold particles of 20-100-nm size. Gold atoms and clusters could move in the film and precipitate to the irradiated surface. Chemical composition analysis further suggests that gold particles at the surface are covered with an ultrathin CTO layer, which is partly oxidized by oxygen and chlorinated by chlorine during photochemical reactions.     

Interfacial assemblies of cyanine dyes and gemini amphiphiles with rigid spacers: regulation and interconversion of the aggregates

A series of gemini amphiphiles with a pyridinium headgroup and rigid spacers were designed, and their interfacial assemblies with cyanine dyes, 3,3-disulfopropyl-9-methyl-selenacarbocyanine (SeCy) and 3,3-disulfopropyl-4,5,4',5'-dibenzo-9-methyl-thiocarbocyanine (MTC), through the air/water interface were investigated. Although the dyes have intrinsic tendencies to form J- or H-aggregates in aqueous solutions, their aggregation could be regulated in the complex films. Depending on the spacer, both J- and H-aggregates were formed for SeCy, whereas an H-aggregate with different absorption bands was obtained for MTC. Furthermore, the formed aggregates in the films could be reversibly switched by treating the complex films with HCl, NH3 gas, or water vapor. The J-aggregates of SeCy could be changed into H-aggregates and recovered through an alternative HCl/NH3 exposure in the films. The H-aggregate of the MTC film could be changed into J-aggregate upon exposure to HCl gas and subsequently put into air or NH 3 gas, and the thus-formed J-aggregate could be changed into H-aggregate under hot water vapor. In addition, such a reversible switch between different aggregates of MTC was only observed when the gemini amphiphiles with rigid spacers were applied. A possible explanation related to the protonation of the dye and the reorganizations in the film during the interconversion between different aggregates was proposed.     

Design and interfacial behavior of two series of gemini amphiphiles with different charge positions based on imidazole moiety

Two series of gemini amphiphiles based on 2-heptadecylimidazole were designed. One is exo-BisImC17Cn (n=2, 4, 6, 8, 10), in which the positive charges are positioned on the outsides of the headgroups. The other is endo-BisImC17Cn (n = 2, 4, 6, 8, 10), whose positive charges are localized on the insides of the headgroups. The interfacial behavior at the air/water interface of these gemini amphiphiles was investigated in relation to the effect of the charge position and the spacer length. Monolayers of exo-BisImC17Cn show small differences in interfacial behavior when spread on water and aqueous Na2SO4 subphases. In contrast, significant distinctions were observed for molecules of endo-BisImC17Cn. The limiting areas of endo-BisImC17Cn monolayers on water are obviously larger than those on the aqueous Na2SO4 solution. While the limiting areas of the exo-BisImC17Cn monolayers increased monotonically with the spacer length, those of the endo-BisImC17C10 monolayer on Na2SO4 solution is obviously smaller than those of endo-BisImC17C6 and endo-BisImC17C8 monolayers, suggesting the wicket conformation of the alkyl chain in endo-BisImC17C10. On the other hand, both of the gemini amphiphiles could form complex monolayers with negatively charged TPPS at the air/water interface. The transferred complex multilayer films of the gemini amphiphiles/TPPS showed supramolecular chirality, although both of the gemini amphiphiles and TPPS are achiral. The exciton couplet was observed for the endo-BisImC17Cn/TPPS films, while no couplet was detected for the exo-BisImC17Cn/TPPS films. A reasonable comparison between the two series of geminis in relation to the effect of charge positions and the spacer lengths on the interfacial behavior and the supramolecular chirality was performed.     

Gold nanoparticle embedded, self-sustained chitosan films as substrates for surface-enhanced Raman scattering

In this work, self-sustained, biocompatible, biodegradable films containing gold nanostructures have been fabricated for potential application in nanobioscience and ultrasensitive chemical and biochemical analysis. We report a novel synthesis of gold nanoparticles mediated by the biopolymer chitosan. Self-supporting thin films are formed from the resultant gold-chitosan nanocomposite solutions and characterized by UV-visible surface plasmon absorption, transmission electron microscopy, atomic force microscopy, infrared absorption, and Raman scattering measurements. Results demonstrate control over the size and distribution of the nanoparticles produced, which is promising for several applications, including the development of biosensors. As a proof of principle, we demonstrate that gold-chitosan films can be employed in trace analysis using surface-enhanced Raman scattering.     

Preparation and Characterization of CdTe Nanoparticles in Zirconia Films Prepared by the Sol Gel Method

Two methods for the synthesis of CdTe nanoparticles in zirconia sol-gel films are demonstrated. The nanoparticles were obtained by chemical reduction of Te(IV) using reducing agent (hydrazine) or tin chloride. Particle sizes ranging from 6 to 20 nm in diameter could be prepared by varying the experimetal parameters. The size and crystalline structure of the particles were characterized by optical absorption, X-ray diffraction, transmission electron microscopy and X-ray photoelectron spectroscopy. The film morphology was characterized by scanning force microscopy.The film obtained by SnCl₂ method is smooth and homogeneous. The dense structure of CdTe nanoparticles of a few nm in diameter is revealed. The films prepared with hydrazine are porous as a result of evolution of the decomposition gaseous products during the reduction.Advantages and disadvantages of the two methods are discussed.     

金＠壳聚糖复合材料的合成、表征及其葡萄糖选择氧化性能

采用硼氢化钠化学还原氯金酸的碱性溶液制备了纳米金溶胶, 利用紫外-可见吸收光谱研究了金与壳聚糖的相互作用. 结果表明, 壳聚糖能够捕获金纳米粒子并易于形成金@壳聚糖复合材料. 利用X-光粉末衍射(XRD)、紫外-可见漫反射光谱(UV-vis DRS)、透射电镜(TEM)、红外光谱(IR)、微分热重及差热分析(DTG-DTA)等对这种复合材料进行了表征, 发现该材料具有较小的金纳米粒子, 壳聚糖的存在改变了金纳米粒子的等离子共振吸收, 二者之间存在一定的键合作用. 以分子氧为氧化剂, 在温和条件下, 该材料对葡萄糖选择氧化制葡萄糖酸反应具有良好的催化性能.     

在线性壳聚糖膜内原位还原制备银纳米粒子及银单晶体

采用光还原方法，在线性壳聚糖膜内原位还原获得球形银粒子(粒径10～30 nm)和外观呈三角形、六边形的银单晶体(边长200～2000 nm)；采用电化学方法，在壳聚糖膜内制备了球形银纳米粒子，粒径为5～8 nm.用透射电子显微镜(TEM)、扫描电子显微镜(SEM)、红外光谱(IR)和X射线衍射(XRD)等测试技术对壳聚糖/银复合物进行了表征，对光还原过程中银晶体结构由多晶到单晶的转变原因进行了初步的分析和探讨.     

Selective dissolution of the silver component in colloidal Au and Ag multilayers: a facile way to prepare nanoporous gold film materials

Colloidal Au/Ag multilayer films were prepared by alternate assembly of Au nanoparticles with a size of 5 +/- 1.2 nm and Ag nanoparticles with a size of 10 +/- 2.4 nm by using 1,5-pentanedithiol as cross-linker. Nanoporous gold films with a ligament size of 26.7 +/- 4.6 nm were then prepared by selective dissolution of sacrificial templates of silver particles in colloidal Au/Ag multilayers. The complete dissolution of Ag particles in colloidal Au/Ag multilayers in a mixture solution of 3.0 mM HAuCl(4) and 3 M NaCl took place at room temperature without damage of the colloidal Au film. This method to prepare nanoporous gold films was further extended to the preparation of nanoporous gold nanotubes by depositing colloidal Au/Ag film on the inner wall of anodic aluminum oxides (AAO) followed by dissolution of colloidal Ag and removal of AAO templates.     

Aerosol assisted chemical vapor deposition using nanoparticle precursors: a route to nanocomposite thin films

Gold nanoparticle and gold/semiconductor nanocomposite thin films have been deposited using aerosol assisted chemical vapor deposition (CVD). A preformed gold colloid in toluene was used as a precursor to deposit gold films onto silica glass. These nanoparticle films showed the characteristic plasmon absorption of Au nanoparticles at 537 nm, and scanning electron microscopic (SEM) imaging confirmed the presence of individual gold particles. Nanocomposite films were deposited from the colloid concurrently with conventional CVD precursors. A film of gold particles in a host tungsten oxide matrix resulted from co-deposition with [W(OPh)(6)], while gold particles in a host titania matrix resulted from co-deposition with [Ti(O(i)Pr)(4)]. The density of Au nanoparticles within the film could be varied by changing the Au colloid concentration in the original precursor solution. Titania/gold composite films were intensely colored and showed dichromism: blue in transmitted light and red in reflected light. They showed metal-like reflection spectra and plasmon absorption. X-ray photoelectron spectroscopy and energy-dispersive X-ray analysis confirmed the presence of metallic gold, and SEM imaging showed individual Au nanoparticles embedded in the films. X-ray diffraction detected crystalline gold in the composite films. This CVD technique can be readily extended to produce other nanocomposite films by varying the colloids and precursors used, and it offers a rapid, convenient route to nanoparticle and nanocomposite thin films.     

Supramolecular layer-by-layer assembly: alternating adsorptions of guest- and host-functionalized molecules and particles using multivalent supramolecular interactions

The stepwise construction of a novel kind of self-assembled organic/inorganic multilayers based on multivalent supramolecular interactions between guest-functionalized dendrimers and host-modified gold nanoparticles has been developed, yielding supramolecular layer-by-layer assembly. The deposition process was monitored by surface plasmon resonance spectroscopy. Further characterization of the multilayer films was performed by means of UV/vis absorption spectroscopy, which showed a linear increase in absorption with the number of bilayers. The growth of the gold nanoparticle plasmon absorption band corresponded to approximately a dense monolayer of gold nanoparticles per bilayer. Ellipsometry and atomic force microscopy (AFM) scratching experiments were used to measure the development of the film thickness with the number of bilayers, confirming linear growth and a thickness increase of approximately 2 nm/bilayer.     

基于AFM纳米氧化技术的金纳米粒子定点组装

二维纳米粒子矩阵列在纳米电子器件^[1,2]、表面增强喇曼活性基底^[3,4]、刻蚀掩模^[5]等领域具有广泛的应用前景。在这些纳米粒子阵列为内部,纳米粒子的排布是随机、无序的。这一缺点已经妨碍了纳米粒子阵列在上述领域中的进一步应用。基于此,人们开始关注纳米粒子的可控组装。传统的光刻技术^[6]、微接触印刷技术^[7]以及生物分子模板技术^[8]都被用来实现纳米粒子在固体表面上的可控组装,本实验室在纳米粒子的合成及可控组装方面也进行了研究^[7,9,11]。本文力图精确控制单个纳米粒子在基底表面上的组装位置。利用AFM纳米氧化技术。在硅表面构建了纳米级的化学图形化表面,通过不同的化学官能团,如甲基、氨基对金纳米粒子亲和性质的差异,实现了纳米粒子在固体表面的定点组装。     

Stability and Morphology of Gold Nanoisland Arrays Generated from Layer-by-Layer Assembled Nanoparticle Multilayer Films: Effects of Heating Temperature and Particle Size

This article reports the effects of heating temperature and composition of nanoparticle multilayer films on the morphology, stability, and optical property of gold nanoisland films prepared by nanoparticle self-assembly/heating method. First, nanoparticle-polymer multilayer films are prepared by the layer-by-layer assembly. Nanoparticle multilayer films are then heated at temperature ranging from 500 °C to 625 °C in air to induce an evaporation of organic matters from the films. During the heating process, the nanoparticles on the solid surface undergo coalescence, resulting in the formation of nanostructured gold island arrays. Characterization of nanoisland films using atomic force microscopy and UV-vis spectroscopy suggests that the morphology and stability of gold island films change when different heating temperatures are applied. Stable gold nanoisland thin film arrays can only be obtained after heat treatments at or above 575 °C. In addition, the results show that the use of nanoparticles with different sizes produces nanoisland films with different morphologies. Multilayer films containing smaller gold nanoparticles tend to produce more monodisperse and smaller island nanostructures. Other variables such as capping ligands around nanoparticles and molecular weight of polymer linkers are found to have only minimal effects on the structure of island films. The adsorption of streptavidin on the biotin-functionalized nanoisland films is studied for examining the biosensing capability of nanoisland arrays.     

Surface-grafted hybrid material consisting of gold nanoparticles and dextran exhibits mobility and reversible aggregation on a surface

Gold nanoparticles linked to linear carboxylated dextran chains were attached to 3-aminopropyltriethoxysilane-functionalized glass surfaces. This method provides novel hybrid nanostructures on a surface with the unique optical properties of gold nanoparticles. The particles attached to the surface retain the capability to aggregate and disaggregate in response to their environment. This procedure presents an alternative method to the immobilization of gold nanoparticles onto planar substrates. Compared to gold nanoparticle monolayers, larger particle surface densities were obtained. Exposure to hydrophobic environments changes the conformation of the hydrophilic dextran chains, causing the gold nanoparticles to aggregate and inducing changes in the absorption spectrum such as red-shifting and broadening of the plasmon absorption peaks. These changes, characteristic of particle aggregation, are reversible. When the substrates are dried and then immersed in an aqueous environment, these changes can be visually observed in a reversible fashion and the sample changes color from the red color of colloidal gold to a bluish-purple color of aggregated nanoparticles. Surface-bound nanoparticles that retain their mobility when attached to a surface by means of a flexible polymer chain could expand the use of aggregation-based assays to solid substrates.     

油基-金纳米流体的制备及热稳定性

分别采用N-十六烷基-N-(羟乙基)-N,N-二甲基溴化铵(CHDAB)和丁烷-1,4-二(N-十六烷基-N,N-二甲基溴化铵)(G16-4-16)2种阳离子表面活性剂作为金属表面修饰剂, 在石油醚/正丁醇/水混合体系中用KBH₄ 还原HAuCl₄制备出亲油性纳米金. 其中, 双子表面活性剂G16-4-16显示出更好的包裹分散作用, 其包裹的纳米金粒径分布范围较窄, 平均粒径为5.2 nm. 将该纳米金颗粒分散在液态烷烃、 甲苯和长链烷基醇等溶剂中可制成稳定的油基纳米流体. 采用紫外-可见光谱法跟踪热稳定性随时间的变化, 结果表明, 该纳米流体显示了较好的热稳定性, 在130 ℃稳定时间达20 h. 采用点热源法测定了该纳米流体的导热系数, 结果表明, 50 ℃时添加质量分数1.5%的纳米金可以使其导热系数增大约17%.