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Microscopy Reveal (microscopy + reveal)
Kinds of Microscopy Reveal Selected AbstractsMorphological, structural and optical study of quasi-1D SnO2 nanowires and nanobeltsCRYSTAL RESEARCH AND TECHNOLOGY, Issue 10-11 2005D. Calestani Abstract 0.1,0.3 mm thick entanglements of quasi-one-dimensional semiconducting Tin dioxide nanocrystals, in form of nanowires and nanobelts, are successfully grown by low cost Chemical Vapour Deposition directly on large area (100 mm2) Al2O3, SiO2 and Si substrates. Their lateral size ranges from 50 to 700 nm and their length can achieve several hundreds of micrometers. Transmission Electron Microscopy reveals either the nanowires and the nanobelts grow in the tetragonal Rutile structure. Diffraction contrast analyses and selected area diffraction investigations show the nanowires are single crystals without defects while the nanobelts sometimes present twins inside. An almost cylindrical shape and an average diameter of about 30,50 nm for the smallest nanowires is reported. X-ray diffraction investigations exclude the presence of spurious phases. A broad band structured in two emissions peaked at about 450 nm and 560 nm is revealed by large area Cathotoluminescence, while single nanocrystal spectroscopy shows that the reduction of the lateral dimension of the nanobelts from 1000 nm to 50 nm blue-shifts the main emission band at 560 nm of about 40 nm (at room temperature). These preliminary results suggest a possible role of oxygen vacancies and of the surface/volume ratio on the origin and the blue shift of Cathodoluminescence spectra. The near band edge emission, typical of bulk tin dioxide (,320 nm), is not found in nanobelts narrower than 1000 nm. (© 2005 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Biomimetic Composites: Protein Localization in Silica Nanospheres Derived via Biomimetic Mineralization (Adv. Funct.ADVANCED FUNCTIONAL MATERIALS, Issue 18 2010Mater. Abstract Lysozyme-templated precipitation of silica synthesized by sol-gel chemistry produces a composite material with antimicrobial properties. This study investigates the structural properties of the composite material that allow for retention of the antimicrobial activity of lysozyme. Scanning (SEM) and transmission (TEM) electron microscopy reveal that the composite has a hierarchical structure composed of quasi-spherical structures (,450 nm diameter), which are in turn composed of closely packed spherical structures of ,8,10 nm in diameter. Using small-angle neutron scattering (SANS) with contrast variation, the scattering signatures of the lysozyme and silica within the composite were separated. It was determined that the lysozyme molecules are spatially correlated in the material and form clusters with colloidal silica particles. The size of the clusters determined by SANS agrees well with the structural architecture observed by TEM. BET analysis revealed that the surface area of the composite is relatively low (4.73 m2/g). However, after removal of the protein by heating to 200 °C, the surface area is increased by ,20%. In addition to demonstrating a well organized sol-gel synthesis which generates a functional material with antimicrobial applications, the analysis and modeling approaches described herein can be used for characterizing a wide range of mesoporous and ultrastructural materials. [source] Protein Localization in Silica Nanospheres Derived via Biomimetic MineralizationADVANCED FUNCTIONAL MATERIALS, Issue 18 2010Mateus B. Cardoso Abstract Lysozyme-templated precipitation of silica synthesized by sol-gel chemistry produces a composite material with antimicrobial properties. This study investigates the structural properties of the composite material that allow for retention of the antimicrobial activity of lysozyme. Scanning (SEM) and transmission (TEM) electron microscopy reveal that the composite has a hierarchical structure composed of quasi-spherical structures (,450 nm diameter), which are in turn composed of closely packed spherical structures of ,8,10 nm in diameter. Using small-angle neutron scattering (SANS) with contrast variation, the scattering signatures of the lysozyme and silica within the composite were separated. It was determined that the lysozyme molecules are spatially correlated in the material and form clusters with colloidal silica particles. The size of the clusters determined by SANS agrees well with the structural architecture observed by TEM. BET analysis revealed that the surface area of the composite is relatively low (4.73 m2/g). However, after removal of the protein by heating to 200 °C, the surface area is increased by ,20%. In addition to demonstrating a well organized sol-gel synthesis which generates a functional material with antimicrobial applications, the analysis and modeling approaches described herein can be used for characterizing a wide range of mesoporous and ultrastructural materials. [source] Novel Magnetic Hydroxyapatite Nanoparticles as Non-Viral Vectors for the Glial Cell Line-Derived Neurotrophic Factor GeneADVANCED FUNCTIONAL MATERIALS, Issue 1 2010Hsi-Chin Wu Abstract Nanoparticles (NPs) of synthetic hydroxyapatite (Hap) and natural bone mineral (NBM) are rendered magnetic by treatment with iron ions using a wet-chemical process. The magnetic NPs (mNPs), which are about 300,nm in diameter, display superparamagnetic properties in a superconducting quantum interference device, with a saturation magnetization of about 30,emu g,1. X-ray diffraction and transmission electron microscopy reveal that the magnetic properties of the NPs are the result of the hetero-epitaxial growth of magnetite on the Hap and NBM crystallites. The mNPs display a high binding affinity for plasmid DNA in contrast to magnetite NPs which do not bind the plasmid well. The mHap and mNBM NPs result in substantial increases in the transfection of rat marrow-derived mesenchymal stem cells with the gene for glial cell line-derived neurotrophic factor (GDNF), with magnetofection compared to transfection in the absence of a magnet. The amount of GDNF recovered in the medium approaches therapeutic levels despite the small amount of plasmid delivered by the NPs. [source] Improved surface-enhanced Raman scattering of polypyrrole electrodeposited on roughened substrates composed of Au,Ag bimetallic nanoparticlesJOURNAL OF RAMAN SPECTROSCOPY, Issue 6-7 2005Thomas C. Chuang Abstract We report here the first electrochemical method to prepare a roughened gold substrate with bimetallic silver and gold nanoparticles. First, a silver substrate was roughened by a triangular-wave oxidation,reduction cycle in 0.1 N HCl aqueous solutions. Silver-containing complexes were found in the solution after the ORC treatment. Then a gold substrate was subsequently roughened by a similar oxidation,reduction treatment in this solution. Scanning electron microscopy and atomic force microscopy reveal that the surface of the roughened gold was intrinsically modified with silver nanoparticles, which demonstrates two different kinds of deposition domains. Encouragingly, surface-enhanced Raman scattering of polypyrrole electrodeposited on the roughened gold substrate, modified with finer silver nanoparticles, exhibits an eightfold higher intensity. Copyright © 2005 John Wiley & Sons, Ltd. [source] Reproducible Solvent,Thermal Synthesis, Controlled Microstructure, and Photoluminescence of REPO4:Eu3+, Tb3+ (RE=Y, La, and Gd) NanophosphorsJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 8 2010Xiuzhen Xiao By altering the temperature and solvents, we have synthesized hydrated and dehydrated Eu3+/Tb3+ -doped REPO4 (RE=Y, La, and Gd) nanophosphors via a solvo-thermal technology. X-ray powder diffraction and scanning electronic microscopy reveal that they have different structures and different morphologies. REPO4 prepared under subsequent heating at 80°, 120°, and 160°C for 1 day, respectively, present larger particle size than that formed by heating at 160°C for 3 days. Moreover, at the same temperature of 160°C and pH 3, three different solvents (ethanol, N,N -dimethylformamide (DMF), and water) were used, whose influence on the microstructure of LaPO4 has been examined. As a result, LaPO4 samples from anhydrous ethanol solvent show a pure hexagonal phase and nanowire morphology, just like that prepared from the water solvent. On the other hand, the microstructure of LaPO4 samples from DMF,H2O-mixed solvents have been changed: with the increasing volume ratio of DMF to H2O, the crystal phase of LaPO4 has been changed from hexagonal phase to monoclinic phase and the morphology from nanowires to nanoparticles. Finally, the photoluminescence properties of these Eu3+ (Tb3+)-activated rare earth phosphates have been investigated, indicating that the photoluminescent behavior are related to their crystal phases and microstructures. [source] Magnetic and Electrical Properties of (Mn, La)-Codoped SrTiO3 Thin FilmsJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 10 2008Song-Yin Zhang Mn-doped SrTiO3 -based thin films have been prepared by a simple sol,gel spin-coating method on silicon substrate. X-ray diffraction and high-resolution transmission electron microscopy reveal that these thin films are composed of amorphous and crystalline SrTiO3 phases. Optical and electrical measurements indicate that La codoping can make the band gap of SrTiO3 narrow and cause the leakage current to increase. Ferromagnetic behavior can be observed in these Mn- and/or La-codoped SrTiO3 -based thin films at room temperature, which should be ascribed to the magnetic coupling between the induced free electrons and Mn 3d spins. [source] Mineralogy and petrology of melt rocks from the Popigai impact structure, SiberiaMETEORITICS & PLANETARY SCIENCE, Issue 5 2002J. Whitehead The fine-grained to cryptocrystalline texture of the more melt-rich rocks, despite their occurrence in bodies locally in excess of 800 m thick and 28 km long, suggests that the melt crystallized in response to (1) cooling by the clast load, and/or; (2) rapid nucleation on finely brecciated clasts, which have since been assimilated and/or; (3) crystallization enhanced by the relatively low water contents of the melts. Rapid crystallisation of the melt is indicated by the lack of zoning in minerals, the presence of glass, the lack of strain recovery features in clasts and the lack of evidence for fractionation in the major and trace elements, including the rare earth elements. Optical and analytical electron microscopy reveal that the previously reported division of the melt rocks into high- and low-temperature variants based on hand sample appearance, or glass content, is not warranted. Clasts within the melt-rich rocks exhibit a wide range of shock metamorphic features, though they are not distributed in the impact melts in a systematic manner. This indicates that the melt-rich rocks were well mixed during their formation, thus juxtaposing unshocked with shocked material. Injection of mesostasis melt into partially melted checkerboard plagioclase and orthopyroxene clasts also occurred during this mixing stage. [source] Competition of Epitaxy and Ion Beam Irradiation-Determined Texture during Ion Beam-Assisted Deposition of Gallium Nitride Films on r-Plane SapphirePHYSICA STATUS SOLIDI (C) - CURRENT TOPICS IN SOLID STATE PHYSICS, Issue 1 2003J.W. Gerlach Abstract The nitrogen ion beam-assisted growth of wurtzitic gallium nitride thin films on the r -plane of sapphire is investigated. X-ray diffraction and electron microscopy reveal that the crystallographic texture of the films is very sensitive to the ion beam parameters. By carefully choosing these parameters it is possible to direct intentionally the orientation of the GaN films. [source] Rapid crystal growth without inherent supersaturation induced by nanoscale fluid flows?CRYSTAL RESEARCH AND TECHNOLOGY, Issue 1 2006M. J. Jones Abstract Crystal growth is a process that only takes place under non-equilibrium conditions and a necessary prerequisite is that the crystal is exposed to a phase that is supersaturated in the material the crystal is composed of, be it a solution, a vapour or a supercooled melt. In industrial mass crystallization the growth rate for a population of crystals (in suspension growth processes [1]) rarely exceeds mean linear velocities of 10 -7 ms -1. Here we present a mass crystallization process which is accompanied by rapid crystal growth several orders of magnitude faster and into a region of solution that is without inherent supersaturation. The material investigated is a solid hydrate that exhibits a solution mediated phase transition to its anhydrous form in the presence of methanol [2]. The phase transition is initiated simply by placing an amount of hydrate crystals into the solvent and is characterized by the rapid emergence of needle-shaped crystals. The needles emanate from the crystal faces of the hydrate crystals and grow into the solution, which is nominally free of the substance to be crystallized. The high growth rate of the crystals, which of the order of up to 10 -4 ms -1 is surprising. Although rapid needle growth has been observed before [3-9], to date a satisfactory explanation for needles growing under the abovementioned conditions is still outstanding. Based upon the topology of the crystals we propose a tentative mechanism for this phenomenon capable of explaining the unusually rapid growth and highlight those questions that need addressing in order to verify this mechanism. X-ray powder diffraction is used to characterize the crystal phase of the needles; confocal fluorescence microscopy reveals that the needles are hollow. The width of these needles is between 0.5 and 5 ,m, their length appears to be limited only by the amount of hydrate available for their formation. (© 2005 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Planar Alignment of Columnar Discotic Liquid Crystals by Isotropic Phase Dewetting on Chemically Patterned SurfacesADVANCED FUNCTIONAL MATERIALS, Issue 6 2010Jonathan P. Bramble Abstract A novel method of creating planar aligned columnar discotic liquid crystals (cDLCs) on surfaces, which also gives control over the azimuthal angle, is presented. Surfaces are chemically patterned with stripes via microcontact printing of organothiol self-assembled monolayers (SAMs) on gold, or via deep UV patterning of organosilane SAMs on silicon. These are then used to isolate long droplets of cDLCs by dewetting in the isotropic phase. Upon cooling from the isotropic into the hexagonal columnar phase, polarizing microscopy reveals that the cDLC aligns in a planar orientation. Results for three triphenylene derivatives (HAT-6, HHTT, H7T) and for a phthalocyanine derivative (8H2Pc) are presented. H7T and HAT-6 are found to align with the director perpendicular to the stripe direction, but HHTT and 8H2Pc align parallel to the stripe direction. This relatively simple new method for creating planar aligned columnar phases of DLCs gives control over the azimuthal angle: a condition required for organic field-effect transistor applications of cDLCs. [source] CAST2: identification and characterization of a protein structurally related to the presynaptic cytomatrix protein CASTGENES TO CELLS, Issue 1 2004Maki Deguchi-Tawarada The cytomatrix at the active zone (CAZ) is thought to define the site of Ca2+ -dependent exocytosis of neurotransmitters. We have recently identified a novel CAZ protein from rat brain which we have named CAST (CAZ-associated structural protein). CAST forms a large molecular complex with other CAZ proteins such as Bassoon, RIM1 and Munc13-1, at least through direct binding to RIM1. Here, we have identified a rat protein that is structurally related to CAST and named it CAST2. Subcellular fractionation analysis of rat brain shows that CAST2 is also tightly associated with the postsynaptic density fraction. Like CAST, CAST2 directly binds RIM1 and forms a hetero-oligomer with CAST. In primary cultured rat hippocampal neurones, CAST2 co-localizes with Bassoon at synapses. Furthermore, immunoelectron microscopy reveals that CAST2 localizes to the vicinity of the presynaptic membrane of synapses in mouse brain. Sequence analysis reveals that CAST2 is a rat orthologue of the human protein ELKS. ELKS has also recently been identified as Rab6IP2 and ERC1. Accordingly, the original CAST is tentatively re-named CAST1. These results indicate that CAST2 is a new component of the CAZ and, together with CAST1, may be involved in the formation of the CAZ structure. [source] Nucleation-Governed Reversible Self-Assembly of an Organic Semiconductor at Surfaces: Long-Range Mass Transport Forming Giant Functional Fibers,ADVANCED FUNCTIONAL MATERIALS, Issue 18 2007G. De, Luca Abstract The use of solvent-vapor annealing (SVA) to form millimeter-long crystalline fibers, having a sub-micrometer cross section, on various solid substrates is described. Thin films of a perylene-bis(dicarboximide) (PDI) derivative, with branched alkyl chains, prepared from solution exhibit hundreds of nanometer-sized PDI needles. Upon exposure to the vapors of a chosen solvent, tetrahydrofuran (THF), the needles re-organize into long fibers that have a remarkably high aspect ratio, exceeding 103. Time- and space-resolved mapping with optical microscopy allows the self-assembly mechanism to be unravelled; the mechanism is found to be a nucleation-governed growth, which complies with an Avrami-type of mechanism. SVA is found to lead to self-assembly featuring i),long-range order (up to the millimeter scale), ii),reversible characteristics, as demonstrated through a series of assembly and disassembly steps, obtained by cycling between THF and CHCl3 as solvents, iii),remarkably high mass transport because the PDI molecular motion is found to occur at least over hundreds of micrometers. Such a detailed understanding of the growth process is fundamental to control the formation of self-assembled architectures with pre-programmed structures and physical properties. The versatility of the SVA approach is proved by its successful application using different substrates and solvents. Kelvin probe force microscopy reveals that the highly regular and thermodynamically stable fibers of PDI obtained by SVA exhibit a greater electron-accepting character than the smaller needles of the drop-cast films. The giant fibers can be grown in,situ in the gap between microscopic electrodes supported on SiOx, paving the way towards the application of SVA in micro- and nanoelectronics. [source] Nitridation of Silica to an ,-Silicon Nitride Nanorod Using NaNH2 in the Autoclave at 700°CJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 4 2007Lingling Zhu ,-silicon nitride nanorods have been synthesized through solid-state reduction,nitridation of silica using NaNH2 as both a reductant and a nitriding reagent. X-ray powder diffraction patterns show that the products have a hexagonal phase with lattice parameters a=7.767 Å and c=5.630 Å. Transmission electron microscopy reveals that the as-synthesized products are pure nanorods with an average size about 30 nm in diameter and 400 nm in length. X-ray photoelectron spectra indicate that the molar ratio of Si/N is 2.988:4. Fourier-transform infrared spectrum yields a strong Si,N absorption at 926 cm,1 that may be a red shift due to size effect. [source] Synaptic structure, distribution, and circuitry in the central nervous system of the locust and related insectsMICROSCOPY RESEARCH AND TECHNIQUE, Issue 3 2002Alan Hugh David Watson Abstract The Orthopteran central nervous system has proved a fertile substrate for combined morphological and physiological studies of identified neurons. Electron microscopy reveals two major types of synaptic contacts between nerve fibres: chemical synapses (which predominate) and electrotonic (gap) junctions. The chemical synapses are characterized by a structural asymmetry between the pre- and postsynaptic electron dense paramembranous structures. The postsynaptic paramembranous density defines the extent of a synaptic contact that varies according to synaptic type and location in single identified neurons. Synaptic bars are the most prominent presynaptic element at both monadic and dyadic (divergent) synapses. These are associated with small electron lucent synaptic vesicles in neurons that are cholinergic or glutamatergic (round vesicles) or GABAergic (pleomorphic vesicles). Dense core vesicles of different sizes are indicative of the presence of peptide or amine transmitters. Synapses are mostly found on small-diameter neuropilar branches and the number of synaptic contacts constituting a single physiological synapse ranges from a few tens to several thousand depending on the neurones involved. Some principles of synaptic circuitry can be deduced from the analysis of highly ordered brain neuropiles. With the light microscope, synaptic location can be inferred from the distribution of the presynaptic protein synapsin I. In the ventral nerve cord, identified neurons that are components of circuits subserving known behaviours, have been studied using electrophysiology in combination with light and electron microscopy and immunocytochemistry of neuroactive compounds. This has allowed the synaptic distribution of the major classes of neurone in the ventral nerve cord to be analysed within a functional context. Microsc. Res. Tech. 56:210,226, 2002. © 2002 Wiley-Liss, Inc. [source] Comparison of Structural and Chemical Properties of Black and Red Human Hair Melanosomes,PHOTOCHEMISTRY & PHOTOBIOLOGY, Issue 1 2005Yan Liu ABSTRACT Melanosomes in black and red human hair are isolated and characterized by various chemical and physical techniques. Different yields of 4-amino-hydroxyphenolanaline by HI hydrolysis (a marker for pheomelanin) and pyrrole-2,3,5-tricarboxylic acid by KMnO4/H+ oxidation (a marker for eumelanin) indicate that the melanosomes in black hair are eumelanosomes, whereas those in red hair are mainly pheomelanosomes. Atomic force microscopy reveals that eumelanosomes and pheomelanosomes have ellipsoidal and spherical shapes, respectively. Eumelanosomes maintain structural integrity upon extraction from the keratin matrix, whereas pheomelanosomes tend to fall apart. The black-hair eumelanosomes have an average of 14.6 ± 0.5% amino acids content, which is attributed to the internal proteins entrapped in the melanosomes granules. The red-hair melanosomes contain more than 44% of amino acid content even after extensive proteolytic digestion. This high content of amino acids and the poorly reserved integrity of red-hair melanosomes suggest that some proteins are possibly covalently bonded with the melanin constituents in addition to those that are entrapped inside the melanin species. Soluene solubilization assay indicates the absorbance of melanin per gram of sample, adjusted for the amino acid content, is a factor of 2.9 greater for the black-hair melanosomes than the red-hair melanosomes. Metal analysis reveals significant amounts of diverse heavy metal ions bound to the two types of melanosomes. The amount of Cu(II) and Zn(II) are similar but Fe(III) content is four times higher in the red-hair melanosomes. 13C solid-state nuclear magnetic resonance spectra and infrared spectra are presented and are shown to be powerful techniques for discerning differences in the amino acid contents, the 5,6-dihydroxyindole-2-carboxylic acid:5,6-dihydroxyindole ratio, and the degree of cross-linking in the pigment. Excellent agreement is observed between these spectral results and the chemical degradation data. [source] | ||||||||||||||||