131 resultados para Langmuir Blodgett films


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An octadecanethiol monolayer was formed on an aqueous gold sols subphase, it's LB films were characterized by means of pi-A isotherms, TEM (transmission electron microscopy), XRD (X-ray diffraction) and UV-Vis spectroscopy. (C) 1998 Elsevier Science Limited. All rights reserved.

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Three new amphiphilic rare earth complexes with only two organic long chains Ln (MOP)(2)Cl (MOP=monooctadecyl phthalate, Ln=Eu, Tb, Gd) were synthesized and characterized by elemental analysis. The complexes (Eu, Tb) showed good luminescence property with long fluorescence lifetime, whereas the intensity and lifetime of Tb complex are greater than those of Eu complex, By measuring the triplet energy levels of ligand based on energy transfer mechanism, above phenomena have been well explained. The Langmuir films of the complexes on the air/water interface were also studied and the results show that all of them have good film-forming property.

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The structure information of orientation and packing of molecular chains can be obtained from infrared transmission and reflection-absorbance (RA) spectra. In the present paper, on the basis of Umemura et al., their FORTRAN program of minicomputer was developed and can be run on 486 personal computer. By comparison of infrared transmission and RA intensities, surface enhancement factors and molecular orientation angle were calculated using the above program, and the influence of complex refractive index, angle of incidence, and thickness of LB film were discussed. These results are consistent with that of Umemura et al.

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The deposition of Langmuir-Blodgett film of neodymium bisphthalocyanine derivatives is reported for the first time. Optical absorption data reveal that these films call be deposited in a reproducible manner; results are also presented showing the extreme sensitivity and selectivity of their electrical conductivity to NH3 in room temperature. The Nd bisphthalocyanine LB film is a sensitive, reproducible. rapid and stable gas sensor. Neodymium bisphthalocyanine derivatives will be candidates for thin film gas-sensitive materials. (C) 1998 Elsevier Science S.A. All rights reserved.

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The multilayer Langmuir-Blodgett (LB) films of pr,ly 3-(2-(5-chlorobenzotriazole)ethyl) thiophene (PCBET) blended with amphibious arachidic acid (AA) were prepared and characterized. The photoluminescence intensity of the blend film was enhanced as the AA increased by a certain amount. The PCBET excimers were not formed in the blend LB films.

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A number of synthetic and natural source porphyrins without long alkyl chains have been examined in the form of monolayers and multilayers on solid substrates. These compounds formed stable solid condensed films with measured molecular areas compatible with a vertical or tilted orientation of these molecules on the substrate. Spectral study and fluorescence lifetime measurement, in particular, revealed the formation of aggregates as the main species in these films.

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The monolayer and deposition behaviour of a symmetrically substituted copper tetra-4-(2, 4-di-t-amylphenoxy) phthalocyanine (tapCuPc) and an asymmetrically substituted copper [tri-4-(2, 4-di-t-amylphenoxy)-mono-4-(-2-methoxyethoxy)]phthalocyanine (AsyCuPc) were investigated. The results on monolayer behaviour and spectroscopic characterization of the LB films show that both CuPc molecules in a monolayer at the air-water interface and the LB films are stacked and inclined. The gas-sensitive properties show that the responding speed of AsyCuPc LB film is faster than that of tapCuPc LB film.

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The dependence of morphology and properties on film-forming conditions is described for the symmetrically substituted copper tetra-4-(2, 4-di-t-amylphenoxy) phthalocyanine (tapCuPc) Langmuir-Blodgett (LB) films. The effects of LB film-forming conditions (such as the surface pressure, pH value and the concentrations of spreading solutions) on film quality were studied with the help of a UV-visible spectrophotometer and a transmission electron microscope. Transmission electron microscopy photographs of the surface morphology of tapCuPc LB films show that a smooth and homogeneous surface structure can be obtained under optimum film-forming conditions.

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Langmuir-Blodgett(LB)膜技术由于在电子学、非线性光学以及化学传感器等领域具有潜在的应用前景而引起了人们的研究兴趣,其中它的热稳定性对LB膜的应用领域和范围具有一定的影响。本论文在此领域的主要研究内容如下: 利用LB膜技术分别制备了十八胺及硬脂酸、氘代硬脂酸的多层LB膜,采用变温傅立叶变换红外光谱研究了三种LB膜的相变行为。实验发现:十八胺LB膜在55-75 oC温度区间内发生相变,其CH2对称和反对称伸缩振动频率向高能量区发生明显移动;硬脂酸LB膜在70-80 oC的温度区间内发生了明显的相转变,CH2对称和反对称伸缩振动的强度比在升温过程中也有显著改变;氘代硬脂酸LB膜的相行为发生在65-70 oC的温度区间内。 利用LB膜技术制备了十八铵硬脂酸盐(C18H37NH3+C17H35COO-, ODASA)与十八铵氘代硬脂酸盐(C18H37NH3+C17D35COO-, ODASA-d35) Langmuir-Blodgett (LB)膜,使用变温傅立叶变换红外透射光谱研究了它们的热行为。发现LB膜中十八铵硬脂酸盐分子的两个碳氢链高度有序,然而在十八铵氘代硬脂酸盐LB分子中的来自于十八胺的碳氢链部分无序,即在常温下有一些扭曲构象存在于碳氢链中。而十八铵硬脂酸盐的热稳定性也与十八铵氘代硬脂酸盐的热稳定性有些不同。在十八铵硬脂酸盐LB膜中,碳氢链在85 oC到90 oC的温度区间内发生非常明显的有序-无序变化。而在十八铵氘代硬脂酸盐LB膜中,碳氢链和来自于硬脂酸的氘代的烃链各自呈现出不同的热行为,即:碳氢链在80-90 oC的温度区间发生有序-无序变化,尤其是在80-85 oC的温度范围内这个变化非常显著;而氘代的烃链则在70 oC到85 oC这个较长的温度区间发生缓慢的相变。 分别制备了十八铵十二酸盐 (C18H37NH3+C11H23COO-,ODALA)和十八铵二十四酸盐(C18H37NH3+C23H45COO-,ODATA)LB膜,并用变温傅立叶变换红外透射光谱法研究了十八铵十二酸盐和十八铵二十四酸盐LB膜的热行为,比较了十八铵十二酸盐、十八铵硬脂酸盐和十八铵二十四酸盐这三种双链化合物LB膜的热行为。温度相关的红外光谱显示,这三种物质LB膜的热稳定性取决于碳链的长度。其中,十八铵十二酸盐LB膜在50-65 oC的温度区间内发生相变。对应的,十八铵二十四酸盐LB膜在80-90 oC的温度范围内发生有序-无序变化。令人感兴趣的是,十八铵二十四酸盐LB膜的相变温度与十八铵硬脂酸盐LB膜的相变温度基本一样,都是80-90 oC,也即在十八铵二十四酸盐和十八铵硬脂酸盐两种LB膜中,即使二十四酸取代了硬脂酸对前者的热稳定性的影响非常小。以上结果说明,在双长链化合物中,有效链长度取决于双链中的较短的那个烃链,从而来决定膜的热稳定性。在十八铵二十四酸盐LB膜中,十八胺的全部碳链对膜的热稳定性有贡献,而二十四酸的碳链则只有部分(有效部分)烃链有贡献。 制备了十八胺单层和多层LB膜和粒径为几个纳米的金纳米粒子。由于十八胺在pH值小于10.3的溶液中氨基带正电荷,使其置于金纳米溶胶中,利用带正电荷的十八胺和附着负电荷的金纳米粒子之间的静电作用,使得金纳米颗粒成功地吸附组装到十八胺的有序分子膜中,形成有规律的纳米颗粒层。通过紫外-可见光谱、红外光谱以及扫描电镜观察到,金纳米颗粒通过这种方法能够很好的组装在有机分子膜上,而且由于十八胺LB膜的高度有序性使得金纳米颗粒的组装层有序。而且,不同层数的十八胺LB膜对金纳米粒子呈现出不同的吸附行为。 测量了含微量甲醇(体积分数为0.04%~0.24%)的系列乙醇水溶液的近红外光谱,利用近红外光谱分析建立了预测甲醇含量的定量分析模型。比较了用外部检验法(Test Set-Validation)和交叉检验法(Cross-Validaton)建立的数学模型以及研究了使用外部检验法时校正集和检验集样品数的改变对模型预测结果的影响。结果发现,当校正集样品数为15检验集样品数为6(总样品数为21)时,使用外部检验法建立的数学模型预测结果较好,外部检验与交叉检验的预测均方根误差(分别为RMSEE和RMSEP)都较小(分别为0.0105和0.0115)而且很接近。结果表明,近红外光谱方法简单,准确而且实用。

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Mixed Langmuir-Blodgett films of tri-(2,4-di-t-amylphenoxy)-(8-quinolinolyl) copper phthalocyanine and water-soluble fullerenols are prepared. Their behavior at the air-water interface and the monolayer morphology are studied. (C) 1998 Elsevier Science Limited. All rights reserved.

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近年来,LangmuirBlodgett(LB)薄膜诱导晶体生长的方法引起了人们的极大关注。通过优化LB膜的结构和化学性质可以调控晶体的结构、形貌、取向、晶型。本论文在此领域的主要研究内容如下: (1) 制备了硬脂酸和十八胺两种具有不同结构和官能团的LB膜,然后把这两种膜垂直浸入到中性的甘氨酸溶液中。实验结果表明用不同结构和化学性质的LB膜不仅可以调控晶体的结构、形貌和取向,并且可以在相同的溶液中诱导出不同晶型的晶体。 (2) 制备了Y型硬脂酸LB膜,然后把这种模板以不同的方式浸入到氯化钾溶液中。通过改变LB膜模板在溶液中的放置方式,控制溶液中的诱导成核和自发成核的过程,从而生成不同形貌的氯化钾晶体。 (3)我们研究了不同热力学状态的LB膜诱导五水硫酸铜晶体生长过程。结果表明LB膜即使在液态状态下,仍有诱导晶体生长的能力。且LB膜的热力学状态对晶体的形貌和取向有很大的影响。 另外,我们在以上工作之外,还作了两项其他工作。 (4) 研究了各种羧酸类(甲酸、乙酸、丙酸)、丙酮、醇类(甲醇、乙醇、丙醇、丁醇)对谷氨酸溶液结晶晶型的影响。结果表明:当70°C的谷氨酸饱和溶液快速冷却搅拌到0°C时,有羧酸类物质存在时可以得到β型晶体;而当有酮类、醇类、或无添加剂时在相同条件下得到α型晶体。 (5) 利用LB技术制备了聚苯乙烯和硬脂酸的混合薄膜。实验结果证明PS和SA在混合LB膜中是相分离的。其过程是PS在空气/水界面上首先发生聚集,然后这种聚集的程度随着膜压的增加而增大.并且PS在空气-LB膜界面上在空气/LB膜界面上的聚集程度随着时间仍继续发生改变。

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Langmuir-Blodgett (LB) film of stearic acid was used as template to induce the nucleation and growth of KCl crystals when the KCl solution was cooled from 50 to 25 degrees C. When the LB film template was vertically dipped into the solution, only induced crystals with (1 1 0) orientation were formed. However, if the template was horizontally placed into solutions, both the induced nuclei at the solution/film interface and spontaneous nuclei formed in solution were simultaneously absorbed onto the LB film, and then grew further to form crystals. X-ray diffraction (XRD) patterns and optical microscopy images showed that the orientation and morphology of the crystals were controlled properly by changing the orientation and position of the LB films in the solutions.

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The formation process of monolayer of octa-n-butoxy-2,3-naphthalocyanine copper ( I), [CuNc(OBu)(8)], on water subphase was studied. Its multilayers were successifully deposited on the hydrophilic substrates by Z-type deposition mode using LB technique. Stable solid film with a limiting molecular area of 0.74 nm(2) and a collapse pressure of 55 mN/m were formed. The LB film structure was characterized by IR and electronic absorption spectra. Macrocycle of CuNc (OBu)(8) molecules have a face-to-face arrangement in the multilayers. These films have good sensitivities to vapor of alcohols, with the following sequence of sensitivities: i-PrOH>EtOH>MeOH. The response time and recovery time of the LB films to vapor of MeOH, EtOH and i-PrOH[volume fraction (1-5) X 10(-5)] were within 2 and 5 seconds respectively, while those of the LB films to ammonia(1 X 10(-4)) were 30-60 seconds and 4-5 minutes respectively.

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Terbium(III) stearoylanthranilate has been prepared as a high property Z-type Langmuir-Blodgett (LB) film on various substrates by a vertical transfer process. The UV-visible absorption spectra and the low angle X-ray diffraction peaks have been collected in order to investigate the molecular arrangement and aggregation in the LB films. The average molecular orientation in multilayer stacking was determined by Attenuated Total Reflection Spectroscopy. The influence of the chemical environment of terbium within the LB films on the luminescence properties has been discussed. (C) 1997 Elsevier Science S.A.

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Langmuir-Blodgett (LB) monolayers of three kinds of soluble polyimides were prepared with the direct deposition method, The monolayer structures were characterized with W-vis absorption spectroscopy, the wide angle X-ray scattering method and electrochemical techniques. The polyimide molecules in the LB monolayers lie orderly on the substrate surfaces with the orientation in which the dianhydride group is normal to the substrate surface and two carbonyl oxygen groups close to the surface. Therefore, the thickness of the three kinds of polyimide LB monolayers are the same because it depends on the distance between the two carbonyl oxygen groups in the same ring. The area of monomeric units are dependent on the length of the diamine group. The model of the molecular packing proposed from the quantomechanical calculation is in good agreement with the experimental results. (C) 1997 Elsevier Science S.A.