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Query: UMLS:C0276640 (TEM)
 20,729 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Ultralong cadmium oxide nanowires were synthesized in high yield on gold-coated silicon substrates by using a vapor transport process. Cadmium vapor generated by the carbothermal reduction of CdO powder in a tube furnace heated to 500 degrees C was carried to the substrate zone by an argon flow with a trace amount of oxygen. The CdO nanowires grew via a vapor-liquid-solid growth mechanism. The diameters of the nanowires are approximately 40-80 nm, and can reach lengths of 30-50 mum. Because the nanowire formation was gold particle catalyzed, patterned nanowire growth on substrates can be achieved. These nanowires grew along the [111] direction and have slightly rough surfaces due to the presence of crystalline CdO shells formed via a physical vapor deposition process. Interesting CdO nanowires with a necklace-like morphology were also observed in a small region of the substrate, where the oxygen supply may be ample to facilitate the lateral growth of rhombohedron-shaped crystals over the straight wires. Electron diffraction and high-resolution TEM results suggest that these side crystals should grow epitaxially on the wire surfaces. The band gap of the CdO nanowires with smoother surfaces was determined to be approximately 2.53 eV. These nanowires exhibit a relatively weak emission band centered at approximately 550 nm.
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PMID:Gold-catalyzed low-temperature growth of cadmium oxide nanowires by vapor transport. 1683 15

Gold micropatterns are deposited from aqueous solutions of NaAuCl(4) on boron-doped Si(100) surfaces (rho = 1.5 x 10(-4) Omega m) using a focused Ar(+) laser beam (TEM(00), lambda = 488 nm, w(0) = 1.5 mum, P = 20-80 mW). The finite-element method employed for computing the surface temperature profiles reveals that the maximum temperature at the precursor/silicon interface increases only to the range 316-372 K, which is not high enough for chemical reactions with formaldehyde in the precursor. This suggests a different mechanism to be responsible for the reduction of gold ions, namely, changes in the surface potential of Si caused by the Dember and Seebeck effects.
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PMID:Laser-induced gold deposition on p+-Si from liquid precursors: a study on the reduction of gold ions through competing Dember and Seebeck effects. 1685 81

A novel nanostructure, cubic silicon carbide (3C-SiC) nanoparticles encapsulated in branched wavelike carbon nanotubes have been prepared by a reaction of 1,2-dimenthoxyethane (CH3OCH2CH2OCH3), SiCl4, and Mg in an autoclave at 600 degrees C. According to X-ray powder diffraction, the products are composed of 3C-SiC and carbon. TEM and HRTEM images show that the as-synthesized products are composed of 3C-SiC nanoparticles encapsulated in branched carbon nanotubes with wavelike walls. The diameter of the 3C-SiC cores is approximately 20-40 nm and the thickness of the carbon shells is about 3-5 nm. In Raman scattering spectroscopy, both the TO (Gamma) phonon line and the LO (Gamma) phonon line have red shifts about 6 cm(-1) relative to that for the bulk 3C-SiC. The photoluminescence (PL) spectrum shows that there are two emission peaks: blue light emission (431 nm) and violet light emission (414 nm). A sequential deposition growth process (with cores as the templates for the shells) for the nanostructure was proposed.
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PMID:Crystalline silicon carbide nanoparticles encapsulated in branched wavelike carbon nanotubes: synthesis and optical properties. 1685 45

Mesoporous molecular sieves Si-MCM-41 (purely siliceous) and Ti-MCM-41 (partly covered with a surface layer of TiO2) were functionalized with phosphate groups by treatment with POCl3 (denoted -MCM-41(P)and Ti-MCM-41(P), respectively). With the use of TEM, X-ray diffraction, and N2 adsorption, it was shown that the initial hexagonal structure, the high specific surface area, and porosity are retained in the functionalized materials but are not as good as in the starting materials. 1H MAS NMR and 31P MAS NMR revealed that the surface of Si-MCM-41(P) consists of silicon phosphate and pyrophosphate species. That of Ti-MCM-41(P) additionally contains titanium dihydro-, hydro-, and pyrophosphate species, the latter being predominant. TPD of adsorbed ammonia for Si-MCM-41(P) and Ti-MCM-41(P) showed that functionalization leads to the creation of moderate and strong acid sites. A combination of mesoporous structure with acidic properties makes the MCM-41 functionalized with phosphate groups promising for use as solid acid catalysts.
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PMID:Synthesis, structure, and acidic properties of MCM-41 functionalized with phosphate and titanium phosphate groups. 1685 50

It is analytically shown that the presence of submicrometer-sized air gaps between the dielectric and metal contact surfaces in a dielectric-filled metallic parallel-plate waveguide can have a dramatic effect on the guided-wave propagation of subpicosecond terahertz pulses. Through the use of metal-evaporated dielectric surfaces to overcome the imperfect contact problem, and a special air-dielectric-air cascaded waveguide geometry to avoid multimode excitation, undistorted subpicosecond terahertz pulse propagation via the single-TEM mode is demonstrated, for what is believed to be the first time, in a silicon-filled PPWG.
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PMID:Nature of subpicosecond terahertz pulse propagation in practical dielectric-filled parallel-plate waveguides. 1690 46

The effects of alkaline treatment on the mesoporosity development and iron speciation in Fe-MFI zeolites have been investigated. To this end, a variety of samples derived from different synthetic routes and having distinct Si/Al ratios and Fe content were treated in NaOH solutions and characterized by N2 adsorption, SEM, TEM, UV/vis spectroscopy, and EPR. The alkaline treatment induces a significant intracrystalline mesoporosity development by framework silicon extraction and promotes disintegration of oligomeric iron species. Iron in framework positions has shown to provoke mesopore formation, whereas nonframework iron species suppresses silicon leaching and lowers the extent of extra porosity.
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PMID:Alkaline treatment of iron-containing MFI zeolites. Influence on mesoporosity development and iron speciation. 1703 20

Ordered mesoporous zirconium phosphate films were prepared on a silicon substrate by spin coating using a mixture of zirconium isopropoxide, triethyl phosphate, Pluronic P123 triblock copolymer, nitric acid, ethanol, and water. The spin-on film was consecutively treated with vapors of phosphoric acid and ammonia. The post-vapor treatments effectively enhanced the thermal stability of an ordered mesostructure when heated to 500 degrees C. XRD and TEM analyses show that the calcined zirconium phosphate film has a hexagonal structure with straight channels parallel to the film surface. The zirconium phosphate film exhibited high proton conductivity of 0.02 S/cm parallel to the film surface at 80% RH and 25 degrees C.
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PMID:Synthesis of ordered mesoporous zirconium phosphate films by spin coating and vapor treatments. 1707 63

We demonstrate the temperature-dependent growth of germanium oxide and silicon oxide based composite nanostructures (multiple nanojunctions of Ge nanowires and SiO(x) nanowires, Ge-filled SiO(2) nanotubes, Ge/SiO(2) coaxial nanocables, and a variety of interesting micrometer-sized structures), aligned SiO(x) nanowire assemblies, and SiO(x) microtubes. The structures were characterized by SEM, TEM, energy-dispersive X-ray spectroscopy, and electron diffraction. The combination of laser ablation of a germanium target and thermal evaoporation of silicon monoxide powders resulted in the formation of Ge and SiO(x) species in a carrier gas; the nano/micro-sized structures grow by either a Ge-catalyzed vapor-liquid-solid or a Ge-nanowire-templated vapor-solid process.
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PMID:Temperature-dependent growth of germanium oxide and silicon oxide based nanostructures, aligned silicon oxide nanowire assemblies, and silicon oxide microtubes. 1719 68

ZnO can be regarded as one of the most important metal oxide semiconductors for future applications. Similar to silicon in microelectronics, it is not only important to obtain nanoscale building blocks of ZnO, but also extraordinary purity has to be ensured. A new gas-phase approach to obtain size-selected, nanocrystalline ZnO particles is presented. The tetrameric alkyl-alkoxy zinc compound [CH(3)ZnOCH(CH(3))(2)](4) is chemically transformed into ZnO, and the mechanism of gas-phase transformation is studied in detail. Furthermore, the morphological genesis of particles via gas-phase sintering is investigated, and for the first time a detailed model of the gas-phase sintering processes of ZnO is presented. Various analytical techniques (powder XRD, TEM/energy-dispersive X-ray spectroscopy, magic-angle spinning NMR spectroscopy, FTIR spectroscopy, etc.) are used to investigate the structure and purity of the samples. In particular, the defect structure of the ZnO was studied by photoluminescence spectroscopy.
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PMID:Chemical vapor synthesis of size-selected zinc oxide nanoparticles. 1719 84

Understanding the mechanisms of biomineralization continues to be an important area of research in physics, chemistry, materials science, medicine, and dentistry due to its importance in the formation of bones, teeth, cartilage, etc. Stimulated by these fascinating natural examples, as well as by certain others such as shells and corals, attempts are being made to develop synthetic, biomimetic nanocomposites by simulating the basic principles of biomineralization. We have grown bio-like hydroxyapatite layers in vitro on substrates of stainless steel, silicon, and silica glass by using a biomimetic approach (i.e., immersion in a supersaturated simulated body fluid). Hydroxyapatite is one of the most common natural biomaterials and an important structural component of bones and teeth. Metal substrates are of interest for hard tissue implants, while semiconductors and glasses are under investigation for their use as biosensors. Using classical techniques such as stylus profiling, atomic force microscopy (AFM), and scanning and transmission electron microscopy (SEM and TEM), it was found difficult, ambiguous, destructive, or time-consuming to measure the topography, thickness, and profile of the grown heterogeneous, thick, and rough hydroxyapatite layers. On the other hand, coherence probe microscopy based on white light scanning interferometry and image processing provides rapid, contactless measurements of surface roughness and does not need any sample preparation. The results obtained have shown a typical layer thickness of up to 20 microm and an average root-mean-square (rms) roughness of about 4 mum. The hydroxyapatite investigated in this work presents nonetheless a challenge for this technique because of its semi-translucency, high surface roughness, and the presence of cavities formed throughout its volume. This results in a variable quality of fringe pattern, ranging from classical fringes (on a smooth surface) to complex fringes displaying properties of white light speckle (on a rough surface), together with multiple fringe signals along the optical axis in the presence of buried layer interfaces, which in certain configurations affect the axial and lateral precision of the measurement. In this paper we present the latest results for optimizing the measurement conditions in order to reduce such errors and to provide additional useful information concerning the layer.
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PMID:White light scanning interferometry adapted for large-area optical analysis of thick and rough hydroxyapatite layers. 1729 21


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