聚酰亚胺LB膜上液晶表面锚定的研究

通过测试光延迟研究了聚酰亚胺ＬＢ膜的光学各向异性,分析了在ＬＢ膜成膜过程中成膜分子的流动取向特性,并研究了液晶的表面锚定能,分析了ＬＢ膜上液晶的取向机制．聚酰亚胺ＬＢ膜的链段的取向程度较强摩擦情形的聚酰亚胺表面的链段取向要差．强摩擦的聚酰亚胺会比聚酰亚胺ＬＢ膜具有更好的排列液晶分子的能力．ＬＢ膜的流动取向模式使得聚酰亚胺成膜分子沿拉伸方向形成一定的有序排列,并诱导液晶分子定向排列,液晶和聚合物分子相互作用是液晶表面排列的主要动力关键词：     

萘酞菁LB膜取向液晶研究

利用二(3-叔丁基硅氧基)萘酞菁硅 (SiNc) Langmuir-Blodgett (LB) 膜对丝状液晶的定向进行了研究,发现在不同膜压下沉积的SiNc LB膜具有不同的定向效果.在15mN/m低膜压下沉积的LB膜上丝状液晶主要呈沿膜面水平排列,而30mN/m高膜压下沉积的LB膜则取垂直膜面取向.原子力显微镜(AFM)对相应的LB单层膜和多层膜进行的分子尺度上的形貌研究发现,高膜压条件下SiNc分子以分离的单体或聚集体形式非连续地在基片上呈线性堆积排列,形成一定的分子“纳米线”,并且大环平面垂直于基片关键词：     

表面稳定模式铁电液晶分子定向和电光特性研究

通过倾斜蒸镀ＳｉＯ，获得对铁电液晶分子的均匀定向。液晶单池的对比度达１５０１，响应速度达６０μｓ，并具有良好的双稳性能。利用该定向方法制成的６４×６４电寻址铁电液晶空间光调制器，对比度高于８０１，帧数高于３９／ｓ。     

聚酰亚胺LB膜的研究：Ⅰ聚酰胺酸N,N—二甲基十八胺前聚物的LB膜

聚酰胺酸Ｎ,Ｎ－二甲基十八胺是制备本身不具备两亲性的聚酰亚胺ＬＢ膜的前聚物。合成制备了均苯四酸二酐－４,４’－二胺基二苯酸Ｎ,Ｎ－二甲基十八胺,研究了它单分子膜的各异性,比较了伯胺和叔胺膜的不同,并用低角Ｘ射线衍射研究这前聚物ＬＢ膜分子的详细排列。     

聚合物网络稳定铁电液晶中的条纹织构的研究

对聚合物网络稳定的铁电液晶体系进行了研究.实验表明,在聚合物网络单体聚合过程中施加低频交变电场,在偏光显微镜下观察到均匀的液晶分子排列出现一新的条纹织构.从体系自由能的角度对条纹织构给出合理的解释.关键词：     

单体浓度对聚合物稳定铁电液晶稳定性的影响

制备了不同单体浓度的聚合物稳定铁电液晶器件,测试了震动实验和热稳定实验前后样品的排列织构、电光特性和对比度.用原子力显微镜研究了各样品的聚合物形貌,表明在器件内部形成了沿摩擦方向延伸的聚合物网络,并且随着单体含量的增加聚合物网络更加致密.由于聚合物网络体锚定的引入,使得铁电液晶分子在外力和温度场下的运动受到限制,聚合物体锚定的增强使聚合物稳定铁电液晶的稳定性也逐渐提高.实验结果表明,单体含量为4％时,聚合物稳定铁电液晶的抗震性和热稳定性良好,电光曲线为无阈值“V”字型,对比度达150∶1.     

LB膜技术在液晶取向中的应用

本文以ＬＢ膜技术研究了向列相液晶的取向机理。选择了四种不同金属的可溶性酞菁化合物ＭＰｃ－Ｒ４作为取向材料，拉制成ＬＢ膜，诱导向列相正性液晶Ｅ－７。通过对菁酞ＬＢ膜的表征和液晶取向及电光性能的研究，认为液晶的取向是由分子间的相互作用力决定的。     

铁电超微粒/硬脂酸LB膜的制备和光谱特性研究

用LB膜技术组装铁电超微粒,实验结果显示：LB膜中的铁电超微粒比较稳定,覆盖度也比较高,并且存在介电限域效应,在室温下具有光致发光现象;荧光光谱具有宽的发光带,激发光谱存在上转换现象.关键词：     

典型控制参量对铁电液晶光电响应速度的影响

利用Pspice等效电路模型,模拟了入射光波长、温度以及激励电压频率等典型参量对铁电液晶光电响应速度的控制作用.模拟结果表明,在可见光范围内,响应速度随波长的增加而减慢;温度参量则存在一个拐点,响应速度在该点达到极小值;同时,激励电压存在一个上界频率,当频率参量取值超过界值时会对响应速度产生较大影响.     

True atomic resolution imaging of surface structure and surface charge on the GaAs(110)

We demonstrated a novel method to detect the van der Waals and the electrostatic force interactions simultaneously on an atomic scale, which is based on frequency modulation detection method. For the first time, the surface structure and the surface charge at atomic-scale point defects on the GaAs(110) surface have been simultaneously resolved with true atomic resolution under ultra-high vacuum condition. From the bias voltage dependence of the image contrast, we can verify that the sign of the atomically resolved surface charge at the point defect was positive.     

MeV-ion axial surface-channeling from an electron irradiated KCl(0 0 1) surface

Surface-channeling of protons incident with 5 mrad on an electron-irradiated surface is investigated using a 0.55 MeV beam of protons. The target surface is KCl(0 0 1), which is damaged by electron-stimulated desorption with 5 keV electron irradiation. The direction of the incident beam is adjusted along the 〈1 0 0〉 and 〈1 1 0〉 channeling conditions and the channeling-dips of the scattering yields are observed. The irradiation dose-dependence of the minimum yields and widths of the dips is measured. Two dips are compared, i.e., for the 〈1 0 0〉 and 〈1 1 0〉 channelings. By increasing the irradiation dose up to 2 × 10¹⁶ cm⁻², the dip around the 〈1 0 0〉 axis becomes opened, but that of the 〈1 1 0〉 axis becomes shallow. The irradiated surfaces are observed to have many overlapped terraces of sub-micron with monolayer steps. The surface morphology deformed by the irradiation effects to truncate trajectories of the 〈1 0 0〉 channeling protons. This roughness of the surface is more effective for the trajectories of the 〈1 1 0〉 channeling protons. The protons incident on the rough surface along the 〈1 1 0〉 axis are not reflected from the atomic row but reflected by a potential of the surface with steps. Results by a simple computer simulation of the trajectories of protons at stepped surfaces also indicate the scattering processes.     

Atomic force microscopic studies of thin oriented films of ferroelectric liquid crystalline elastomers with varying network architecture

Cross-linked ferroelectric liquid crystalline (FLC) polymers were studied by atomic force microscopy (AFM). Polysiloxane copolymers were synthesized with mesogenic and photo-cross-linkable side groups, the latter connected either directly to the backbone via a short spacer or as a terminal group on a part of the mesogens. These elastomers were prepared as thin, freely suspended films in homeotropic orientation. Topographic measurements depict plateaus separated by steps of characteristic height corresponding to the surfaces and edges of smectic layers. From the temperature behavior, as well as from the reaction to mechanical deformation, a model for the network architectures is proposed. In the first case (“intralayer cross-linking”), a predominantly two-dimensional network is formed within the backbone layers separating the smectic layers; in the second case (“interlayer cross-linking”), a three-dimensional network is established that is dependent on the mesophase present during cross-linking.     

Ferroelectric domain structure of the BiFeO3 film grown on different substrates

Domain structure of BiFeO₃ (BFO) films grown on different substrates, with a conductive La_0.7Sr_0.3MnO₃ underlayer, has been experimentally studied. Two oppositely orientated polarizations, along the long body diagonal to the perovskite unit cell of BFO, are detected in the BFO films on the (0 0 1)-oriented NdGaO₃. Electric pulses applied in the [0 0 1] direction produce a polarization switching, resulting in the domain structure characterized by the 109° domain walls. Contrary to the BFO films on NdGaO₃, the BFO films on SrTiO₃ (0 0 1) exhibit a much complex domain structure. Both 71° and 109° domain walls are possible with a uniform polarization component pointing to the bottom electrode.     

Comparison of organic thin films deposited by supersonic molecular-beam epitaxy and organic molecular-beam epitaxy: The case of titanyl phthalocyanine

Recently, supersonic molecular-beam epitaxy (SuMBE) was invented as an alternative method for the deposition of organic material, using higher kinetic energies for deposition than conventional organic molecular-beam epitaxy (OMBE). Using titanyl phthalocyanine (TiOPc) as a model substance, we show that the SuMBE deposition results in increased crystal quality of the deposited material. This is induced by the high kinetic energy of the molecular-beam in SuMBE, which leads to increased molecular mobility on the surface, resulting in larger crystal sizes and higher crystal quality. Alternatively, similar films as made by OMBE can be deposited by SuMBE at lower substrate temperatures. This temperature reduction may be of interest for the deposition of stacked organic devices on underlying heat sensitive layers, as they are quite common in organic electronic devices.     

Differentiation between tracks and damages in SSNTD under the atomic force microscope

We have observed three-dimensional sponge-like structures as well as strips of connecting pits on the surface of the LR 115 detector after etching, which can be confused with the small tracks formed after short etching time. We have employed an atomic force microscope (AFM) to study these “damages” as well as genuine alpha tracks for short etching time. It was found that while the track and damage openings could be similar in size and shape, the depths for the damages were consistently smaller. Therefore, the depth of the pits will serve as a clear criterion to differentiate between tracks and other damages. The ability to discriminate between genuine tracks from other damages is most important for etching for short time intervals.     

Determination of backbone chain direction of PDA using FFM

The effect of backbone chains on friction force was investigated on both Langmuir-Blodgett (LB) films of 10,12-heptacosadiynoic acid and the (0 1 0) surfaces of single crystals of 2,4-hexadiene-1,6-diol using friction force microscopy (FFM). It was observed that friction force decreased when the scanning direction was parallel to the [0 0 1] direction in both samples. Moreover, friction force decreased when the scanning direction was parallel to the crystallographic [1 0 2], [1 0 1], [1 0 0] and directions in only the single crystals. For the LB films, the [0 0 1] direction corresponds to the backbone chain direction of 10,12-heptacosadiynoic acid. For the single crystals, both the [0 0 1] and [1 0 1] directions correspond to the backbone chain direction, and the [1 0 2], [1 0 0] and directions correspond to the low-index crystallographic direction. In both the LB films and single crystals, the friction force was minimized when the directions of scanning and the backbone chain were parallel.     

铁电液晶MBOPDOB相变的光散射研究

我们对铁电液晶 MBOPDOB 进行了温度有关的拉曼散射研究。在低频范围记录了三条拉曼谱线(15,49,93cm~(-1))。其中15和49cm~(-1)谱线消失于 C-Sm C相变温度,没有检测到任何频移现象。93cm~(-1)拉曼线产生部分频移,消失于各向同性相,联系着偶极-偶极互作用。高频范围四个振动模(1178和1116cm~(-1),1710和1738cm~(-1))之间能量转移归于由电子转移引起的 C=0键硬化和 C-0健的弱化。同时也讨论了该液晶 Sm C-Sm A 相变的二级连续型特征。     

One-dimensional dynamics of nano-scale oxidation

A continuum model is proposed to describe the process of scanned probe oxidation in the presence of a thin water layer on the surface of a substrate. The model describes the electric field and ion transport in both the liquid and the oxide layers and incorporates the reaction mechanism at the substrate/oxide interface. Further, the influence of the space charge due to ions trapped near the substrate/oxide interface is taken into account.Separation of time scales for the chemical reactions and ion transport as well as the asymptotic limit in terms of a small aspect ratio of the oxide layer are used to reduce the complex system of partial differential equations to a one-dimensional system of ordinary differential equations. The analytical solution of the reduced system results in the evolution equation for the oxide thickness. Numerical simulations of the evolution equation predict features of oxide growth that qualitatively agree with the experimental observations. A parametric study is conducted to determine the influence of the key operating and material parameters on the thickness of the oxide, the electric field, and ion concentration in the system.     

原子力显微镜观察脂胞囊形貌结构及稳定性

用原子力显微镜(AFM)观察了液晶态脂胞囊形貌结构和稳定性.实验结果显示,对于1,2-二油酸甘油-3-磷脂酰乙醇胺(DOPE)超分子聚集体,在扫描区域内,可观察到一些大小不同球形颗粒;对于1,2-二油酸甘油-3-磷脂酸乙醇胺(DOPE)和1,2-二油酸甘油-3-磷脂酰胆碱(DOPC)混合的超分子聚集体,则不仅观察到类似脂胞囊的球形颗粒,而且也观察到了双层膜结构,其厚度约为5～6 nm.