Azimuthal orientational correlations due to excluded volume epitaxy in growing anisotropic grains

The microstructure of anisotropically shaped grains can strongly influence a range of material properties, including transport, mechanical and electro-optical. A grain-structure-related phenomenon, known as excluded volume epitaxy (EVE), is reported in this study. EVE is a local, inter-grain orientational correlations effect, which results from a combination of continuous nucleation of anisotropic grains and impingement of growing grains. Due to EVE, anisotropically shaped grains have a tendency to be similarly aligned in a local neighbourhood, despite the absence of any forced global orientation in the sample. The effect has been repeatedly observed by the authors in block copolymers, as illustrated by a representative TEM image. Optical microscopy of anisotropically shaped non-polymeric crystals revealed the generality of this effect. The simulation study revealed a tendency for azimuthal, inter-grain orientational correlation and re-confirmed the experimental observation of EVE.     

Microstructures of InN film on 4H-SiC (0001) substrate grown by RF-MBE

InN film was grown on 4H-SiC (0001) substrate by RF plasma-assisted molecular beam epitaxy (RF-MBE). Prior to the growth of InN film, an InN buffer layer with a thickness of ~ 5.5 nm was grown on the substrate. Surface morphology, microstructure and structural quality of InN film were investigated. Micro-structural defects, such as stacking faults and anti-phase domain in InN film were carefully investigated using transmission electron microscopy (TEM). The results show that a high density of line contrasts, parallel to the growth direction (c-axis), was clearly observed in the grown InN film. Dark field TEM images recorded with diffraction vectors g = 1120 and g = 0002 revealed that such line contrasts evolved from a coalescence of the adjacent misoriented islands during the initial stage of the InN nucleation on the substrate surface. This InN nucleation also led to a generation of anti-phase domains.     

电子束辐照在POSS／环氧树脂二元体系TEM观察中的作用

本文以POSS／环氧树脂的二元体系为主体,研究了电子束辐照对该二元体系在透射电镜观察中的作用。研究表明,随着电子束辐照强度和辐照时间的增加,二元体系中POSS分散相的衬度越来越明显,得到的TEM图像也更加清晰。本文采用TEM图像的相对灰度值定量研究了电子束辐照时间对图像清晰度的影响,探索了电子束辐照对该二元体系TEM像衬度提高的原理。     

TEM原位光电双功能样品杆改造及电源系统优化设计

为了研制用于透射电子显微镜(TEM)的光学和电学双功能原位测试样品杆,在理解国外进口电学原位样品杆电路和电极结构的基础上,引入微型LED芯片作为发光源对其进行光电双功能升级改造,并通过优化光电双功能基片供电电源系统以保障TEM清晰成像。测试结果表明,利用自制的基片供电电源,改造后的电学测试样品杆能同时测试样品的光学和电学特性,且透射电子显微镜成像清晰稳定。     

一种考虑互耦的脉冲天线阵列快速计算方法

基于有源单元方向图思想,提出了一种可用于计算脉冲天线阵列时域辐射场的快速方法.该方法在考虑单元间互耦的情况下,将大型阵列的时域辐射场计算问题转化为一个小型阵列的计算问题,大大地减少了计算量.采用文中的阵列综合方法,结合有限积分法软件,仅对一个5×5元阵列进行模拟,即可推算出大型阵列的远场方向图,其计算时间不超过全波模拟时的十分之一.计算结果与仿真软件的仿真结果吻合较好,验证了方法的正确性.     

Preparation and Characterization of Poly Vinyl Alcohol/Poly Vinyl Pyrrolidone/Clay Based Nanocomposite by Gamma Irradiation

A series of PVA/PVP/clay nanocomposite were prepared by gamma irradiation with different clay contents of (0.15, 0.3, 1, 1.5, 3 and 5 wt%). The gelation content and swelling behavior were investigated. The morphology and structure of PVA/PVP/clay nanocomposite and dispersion of the clay nanoparticles in the polymeric matrix were examined by infrared spectroscopy (FT-IR) and scanning electron microscopy (SEM). The introduction of clay into polymeric matrix was investigated by X-ray diffraction pattern (XRD) and Transmission electron microscope (TEM). It is observed that, the increase of the clay content causes a decrease in the swelling percent. The thermal stability studies confirmed that the introduction of clay lead to an increase in the thermal stability. The TEM results showed that the clay nanoparticles are interchelated or exfoliated in the polymeric matrix. Some desirable characteristics such as relatively good swelling and excellent barrier capability against microbe penetration suggested that PVA/PVP/clay nanocomposite can be a good candidate as a wound dressing.     

Thermal stability,morphology and electronic band gap of Zn(NCN)

The thermal behavior of zinc carbodiimide Zn(NCN) was examined in the temperature range between 200 and 1100 °C in Ar atmosphere. The material starts to partially decompose at about 800 °C. Heat treatment at temperatures beyond 800 °C results in the formation of the byproducts nitrogen-containing bamboo-like multiwall carbon-nanotubes of 20–50 nm in diameter due to a partial decomposition of Zn(NCN) into dicyan (CN)₂, zinc and nitrogen gas followed by the polymerization of the former product to paracyanogen (CN)_n. At 1100 °C, the yield of the residual carbodiimide depends on the dwelling time and the initial amount of powder used for pyrolysis. One hour dwelling at 1100 °C yields ∼50% of the Zn(NCN) separated as pure material. Temperature-induced change in the band structure, namely indirect-to-direct band gap transition, is registered when compared the Zn(NCN) at room temperature with the residual material annealed at 1100 °C. The transition from indirect (E_g = 4.32 eV) to direct band gap (E_g = 4.93 eV) is due to the thermal annealing process which results in healing of crystal defects.     

Salinity Controlled Vesicle Formation and Growth in Aqueous Mixture of Aerosol OT/Triton X‐100

Mixed vesicles can be formed spontaneously from aqueous mixture of the double‐tailed anionic surfactant sodium bis(2‐ethylhexyl) sulfosuccinate (AOT) and the nonionic surfactant octylphenoxypolyethoxyethanol (Triton X‐100) under the inducement of salt, the formation mechanism of which should be attributed to the compression of salt on the electric bilayers of the head groups. The stability and the polydispersity of the vesicles are superior to single‐component AOT vesicles, which can be proved by the TEM image and visual observation. The vesicle region was presented in a pseudo‐ternary diagram of AOT/TX‐100/brine. The size of the vesicle was measured using dynamic light scattering. It is found that the vesicle size increases with the salinity but decreases with the content of TX‐100 in the mixture at the same salinity. Especially, the vesicle size is independent of the surfactant concentration at fixed salinity.     

Spectrophotometric and physicochemical investigations of Congo,alizarin red dyes and BSA interactions with Au,Ag and Au/Ag mix nanoparticles,and their antimicrobial activities

Individual and mix metal nanoparticles of Ag and Au have been prepared by the reducing method where citrate was used as reducing/stabilizing agent. The prepared NPs were characterized with UV/Visible and transmission electron microscopic (TEM) tools. The characteristic peak in UV/Visible at 525, 444 and 531 nm for Au, Ag and Ag/Au mix NPs respectively, gave primary confirmation of prepared NPs. TEM analysis showed the size of nanoparticles as 44.04, 19.78 and 30.93 nm for Ag, Au and Ag/Au mix NPs respectively. Congo and alizarin red dye interactions studies have been performed with prepared NPs to see the removal of the pollutants from water. Congo dye has shown weaker interaction as compared to alizarin due to structural symmetry. Amongst all, the AgNPs have shown maximum 67% and 75% interactions with Congo red and alizarin respectively due to high negative charges on the surface. The Au, Ag and Au/Ag mix NPs have shown stronger interaction with bovine serum albumin (BSA) protein up to 51, 59, 55% respectively, estimated through UV/Vis and physicochemical analysis. The biological evaluations of the prepared NPs have shown their antibacterial activity against Gram + ve and –ve species showing up to 9 cm zone of inhibition. The BSA interaction and antibacterial activity of NPs reveal the importance of NPs in medicinal field.