scholarly journals Amorphous nano-structured coatings prepared from CVD-composites

2021 ◽  
Vol 12 (4) ◽  
pp. 301-305
Author(s):  
V. F. Zinchenko ◽  
◽  
I. R. Magunov ◽  
O. V. Mozkova ◽  
O. V. Sviridova ◽  
...  
Keyword(s):  
Main Idea ◽  
Chemical Vapor ◽  
Easy Method ◽  
X Ray ◽  
Thin Film Coatings ◽  
Evaporation And Condensation ◽  
System A ◽  
Transmission Electron ◽  
Nanostructured Systems ◽  
Diffraction Patterns

The main idea of the work is the development of a cheap and easy method for the manufacture of nanostructured systems based on the Chemical Vapor Deposition (CVD). Beginning with a new class of materials for interference optics in the infrared (IR) range of the spectrum, the evaporation of composites of systems germanium-metal chalcogenide (oxide), in particular, of the Ge-ZnS and Ge-Sb2Se3 systems was studied. They evaporate in vacuum congruently, and upon condensation on substrates form nano-structured thin-film coatings. In the first of these systems, the coating has an X-ray amorphous nature: the formation of a nano-dispersed composite in a Ge-ZnS film is confirmed by the absence of characteristic peaks of Ge and ZnS in X-ray diffraction patterns, but the formation of a characteristic halo takes place. At the same time, upon evaporation and condensation of a sample of the Ge-Sb2Se3 system, a glassy structure is formed; this is confirmed by high-resolution transmission electron microscopy (TEM), where no crystalline regions were found. The energy-dispersive X-ray (EDX) spectroscopy measurements of the coating (about 10 at.% of Ge, 40 at.% of Sb and Se, respectively) indicate a certain deviation from the stoichiometry compared to the initial sample of the system. This may indicate a slightly lower volatility of germanium selenides compared to antimony selenides. The EDX line scans along the cross-section of the coating exhibited strong fluctuations in the concentration of elements, and, consequently, the heterogeneity of the coating in terms of composition. Both coatings have high mechanical strength (group 0). At the same time, their optical properties differ significantly: the refractive indices are 3.00 and 3.66 for the Ge-ZnS and Ge-Sb2Se3 systems, respectively. It is believed that nano-structuring in the above systems is due to the high capability of germanium to amorphize upon condensation on a glass substrate.

The Microstructure of Fe7C3 Formed at 300°C by Plasma Enhanced Chemical Vapor Deposition (PECVD)

1993 ◽  
Vol 313 ◽  
Author(s):  
H. Siriwardane ◽  
P. Fraundorf ◽  
J.W. Newkirk ◽  
O.A. Pringle ◽  
W.J. James
Keyword(s):  
Oxidation Process ◽  
Iron Carbide ◽  
Chemical Vapor ◽  
Carbon Films ◽  
Corrosion And Wear ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Iron Phase ◽  
Diffraction Patterns

Thin iron carbide films were prepared by introducing iron penta carbonyl (FeCO5) and hydrogen (H2) into a glow discharge. The films are of potential interest in corrosion and wear resistant applications. X-ray diffraction data of films (≈ 7000 Å thick) deposited on glass at 300°C evidenced only Fe7C3. Thinner films were required for examination by analytical and high resolution transmission electron Microscopy. Therefore, two sets of films (“thin” < 200 Å and “thick” ≈ 800 Å) were plasma-deposited on carbon or holey carbon films supported on copper grids. The thin TEM specimens exhibited a fine texture and gave rise to ring diffraction patterns, whereas the thick TEM specimens evidenced two types of structure: (i) half-Micron sized grains separated from one another by 1–2 Microns on the support, although sometimes interconnected by single crystal platelets and (ii) 300 Å grapelike clumps of 100–200 Å crystals, each individually surrounded by a 50 Å non-crystalline coating. The latter structure may result from a post-formation oxidation process which expels carbon from the iron phase into grain boundaries.

Synthesis of Si-O-C Nanoballs by CVD of Polydimethylsiloxane

2012 ◽  
Vol 454 ◽  
pp. 114-117
Author(s):  
Xia Yuan ◽  
Yu Liang An ◽  
Hong Chao Sui ◽  
Chen Zhang
Keyword(s):  
Chemical Vapor ◽  
X Ray Diffraction ◽  
X Ray ◽  
Cvd Method ◽  
Silicon Carbon ◽  
Transmission Electron ◽  
Diffraction Patterns ◽  
Two Populations ◽  
Scan Electronic Microscope ◽  
Electronic Microscope

Here we reported that the Si-O-C nanoballs (SCONBs) were yielded from polyorganosiloxane, polydimethylsiloxane, by chemical vapor deposition (CVD) method. The composite nanoballs with a range of diameters from 50 to 200nm were composed of silicon, carbon and oxygen based on analysis of EDX. At the transmission electron microscope(TEM) and scan electronic microscope(SEM), two populations of nanoballs were found: around 200nm and 500nm. X-ray diffraction patterns demonstrated that the nanoballs were dominatingly amorphous. Temperature played an key role in size distribution of Si-O-C nanoballs, and the 850–900°C temperature range was typical for nanoparticles growth via CVD.

A Novel TEM Technique for Characterizing As-Grown CVD Diamond Films

1991 ◽  
Vol 49 ◽  
pp. 956-957 ◽  
Author(s):  
Z.L. Wang ◽  
J. Bentley ◽  
R.E. Clausing ◽  
L. Heatherly ◽  
L.L. Horton
Keyword(s):  
Diamond Films ◽  
Chemical Vapor ◽  
Growth Direction ◽  
Dark Field ◽  
Growth Surface ◽  
Specimen Preparation ◽  
Transmission Electron ◽  
Diffraction Patterns ◽  
First Time ◽  
Microstructural Studies

Microstructural studies by transmission electron microscopy (TEM) of diamond films grown by chemical vapor deposition (CVD) usually involve tedious specimen preparation. This process has been avoided with a technique that is described in this paper. For the first time, thick as-grown diamond films have been examined directly in a conventional TEM without thinning. With this technique, the important microstructures near the growth surface have been characterized. An as-grown diamond film was fractured on a plane containing the growth direction. It took about 5 min to prepare a sample. For TEM examination, the film was tilted about 30-45° (see Fig. 1). Microstructures of the diamond grains on the top edge of the growth face can be characterized directly by transmitted electron bright-field (BF) and dark-field (DF) images and diffraction patterns.

Cetyltrimethylammonium bromide- and ethylene glycol-assisted preparation of mono-dispersed indium oxide nanoparticles using hydrothermal method

2014 ◽  
Vol 68 (8) ◽  
Author(s):  
Selvakumar Dhanasingh ◽  
Dharmaraj Nallasamy ◽  
Saravanan Padmanapan ◽  
Vinod Padaki
Keyword(s):  
Ethylene Glycol ◽  
Hydrothermal Method ◽  
Indium Oxide ◽  
Cetyltrimethylammonium Bromide ◽  
Oxide Nanoparticles ◽  
X Ray Diffraction ◽  
Hydrothermal Conditions ◽  
X Ray ◽  
Transmission Electron ◽  
Diffraction Patterns

AbstractThe influence of cetyltrimethylammonium bromide and ethylene glycol on the size and dispersion of indium oxide nanoparticles prepared under hydrothermal conditions was investigated. The precursor compound, indium hydroxide, obtained by the hydrothermal method in the absence as well as the presence of cetyltrimethylammonium bromide, was converted to indium oxide by sintering at 400°C. The formation of nanoscale indium oxide upon sintering was ascertained by the characteristic infrared adsorption bands and X-ray diffraction patterns of indium oxide. Transmission electron microscopy and band gap values confirmed that the cetyltrimethylammonium bromide facilitated the formation of indium oxide nanoparticles smaller in size and narrower in distribution than those prepared without the assistance of cetyltrimethylammonium bromide.

Structure And Morphology Of Carbon Nanofibers Synthesized On Cu Nanopowders

2016 ◽  
Vol 11 (3) ◽  
pp. 62-71
Author(s):  
Gulmira Partizan ◽  
Batyr Mansurov ◽  
Botagoz Medyanova ◽  
Аizhan Koshanova ◽  
Madina Mansurova ◽  
...  
Keyword(s):  
Carbon Nanofibers ◽  
Chemical Vapor ◽  
Temperature Growth ◽  
Copper Clusters ◽  
Transmission Electron ◽  
Amorphous Nature ◽  
Diffraction Patterns ◽  
Stable Growth ◽  
Different Diameters ◽  
Copper Nanopowders

This article presents the results of experiments on the synthesis of carbon nanofibers by thermal chemical vapor deposition using copper nanopowders obtained by electric explosion of wire as catalysts. Stable growth of carbon nanofibers was carried out at temperatures significantly lower than normally used. The process parameters that are optimal for low-temperature growth of carbon nanofibers have been identified during the performed experiments. The synthesized samples have different diameters and morphology (from spiral to direct). Copper clusters are both at the ends and inside the fibers. The results of IR spectroscopy indicate that the structure of the obtained carbon nanofibers is polymeric. X-ray analysis revealed the presence of a halo on the diffraction patterns at small values of the angle 2θ, which proves that the grown structures have an amorphous nature. There are no groups that are responsible for long-range order in all Raman spectra. Studies by transmission electron microscopy showed that nanostructures do not have an internal channel and nanofibers are solid.

AlxGa1-xN-Based Materials and Heterostructures

1996 ◽  
Vol 449 ◽  
Author(s):  
P. Kung ◽  
A. Saxler ◽  
D. Walker ◽  
X. Zhang ◽  
R. Lavado ◽  
...  
Keyword(s):  
Chemical Vapor ◽  
Bragg Reflectors ◽  
X Ray Diffraction ◽  
Chemical Vapor Deposition Growth ◽  
X Ray ◽  
Sapphire Substrates ◽  
Transmission Electron ◽  
Dimensional Electron Gas ◽  
P Type

ABSTRACTWe present the metalorganic chemical vapor deposition growth, n-type and p-type doping and characterization of AlxGa1-xN alloys on sapphire substrates. We report the fabrication of Bragg reflectors and the demonstration of two dimensional electron gas structures using AlxGa1-xN high quality films. We report the structural characterization of the AlxGa1-xN / GaN multilayer structures and superlattices through X-ray diffraction and transmission electron microscopy. A density of screw and mixed threading dislocations as low as 107 cm-2 was estimated in AlxGa1-xN / GaN structures. The realization of AlxGa1-xN based UV photodetectors with tailored cut-off wavelengths from 365 to 200 nm are presented.

Facile Refluxing Synthesis of Hydroxyapatite Nanoparticles

2015 ◽  
Vol 68 (8) ◽  
pp. 1293 ◽  
Author(s):  
Pakvipar Chaopanich ◽  
Punnama Siriphannon
Keyword(s):  
Crystallite Size ◽  
Reaction Times ◽  
Single Step ◽  
Hydroxyapatite Nanoparticles ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Aqueous Mixture ◽  
Diffraction Patterns ◽  
Microscopy Images

Hydroxyapatite (HAp) nanoparticles were successfully synthesized from an aqueous mixture of Ca(NO3)2·4H2O and (NH4)2HPO4 by a facile single-step refluxing method using polystyrene sulfonate (PSS) as a template. The effects of reaction times, pH, and PSS concentration on the HAp formation were investigated. It was found that the crystalline HAp was obtained under all conditions after refluxing the precursors for 3 and 6 h. The longer refluxing time, the greater the crystallinity and the larger the crystallite size of the HAp nanoparticles. The HAp with poor crystallinity was obtained at pH 8.5; however, the well-crystallized HAp was obtained when reaction pH was increased to 9.5 and 10.5. In addition, the X-ray diffraction patterns revealed that the presence of PSS template caused the reduction of HAp crystallite size along the (002) plane from 52.6 nm of non-template HAp to 43.4 nm and 41.4 nm of HAp with 0.05 and 0.2 wt-% PSS template, respectively. Transmission electron microscopy images of the synthesized HAp revealed the rod-shaped crystals of all samples. The synthesized HAp nanoparticles were modified by l-aspartic acid (Asp) and l-arginine (Arg), having negative and positive charges, respectively. It was found that the zeta potential of HAp was significantly changed from +5.46 to –24.70 mV after modification with Asp, whereas it was +4.72 mV in the Arg-modified HAp. These results suggested that the negatively charged amino acid was preferentially adsorbed onto the synthesized HAp surface.

A Chemical Solution Route to Rapid Synthesis of Homogeneous Bi100−xSbx Alloys Nanoparticles at Room Temperature

2007 ◽  
Vol 7 (2) ◽  
pp. 525-529 ◽  
Author(s):  
Bo Zhou ◽  
Jun-Jie Zhu
Keyword(s):  
Room Temperature ◽  
Raw Materials ◽  
X Ray Diffraction ◽  
X Ray ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Solution Route ◽  
Diffraction Patterns ◽  
Co Reduction ◽  
Chemical Solution Route

A chemical co-reduction route in aqueous solution was developed to synthesize Bi100−xSbx alloys at room temperature. The hydrolyses of Bi(III) and Sb(III) were effectively avoided by selecting proper raw materials and coordinator. X-ray diffraction analysis indicated that the as-prepared Bi100−xSbx alloys were homogeneous and phase-pure, and the Bi/Sb ratios in the alloys were very close to those in the aqueous solutions. The transmission electron microscope observation showed that the as-prepared Bi100−xSbx (x = 0∼100) alloys were particles with a size of tens of nanometers. The selected area electron diffraction patterns confirmed the high crystallinity, the homogeneousness, and the composition controllability of as-prepared alloys. All these characters and the nanometer-scaled size of the alloys are believed to be beneficial to the thermoelectric property of the Bi100−xSbx alloys.

scholarly journals Deposition Mechanism and Thickness Control of CVD SiC Coatings on NextelTM440 Fibers

Coatings ◽  
2020 ◽  
Vol 10 (4) ◽  
pp. 408
Author(s):  
Yi Wang ◽  
Jian Sun ◽  
Bing Sheng ◽  
Haifeng Cheng
Keyword(s):  
Coating Thickness ◽  
Photoelectron Spectroscopy ◽  
Deposition Time ◽  
Chemical Vapor ◽  
X Ray Diffraction ◽  
Deposition Mechanism ◽  
Thickness Control ◽  
X Ray ◽  
Transmission Electron ◽  
Sic Coatings

SiC coatings were successfully synthesized on NextelTM440 fibers by chemical vapor deposition (CVD) using methyltrichlorosilane as the original SiC source at 1373 K. After deposited, the fibers were fully surrounded by uniform coatings with some bulges. The X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and high-resolution transmission electron microscopy (HR-TEM) results indicated that the coatings were composed of β-SiC and free carbon. Moreover, thickness control of the coatings could be carried out by adjusting the deposition time. The coating thickness rose exponentially, and the exterior of the coatings became looser as the deposition time increased. The thickness of about 1.5 µm was obtained after depositing for 4 h. The coating thickness was also theoretically calculated, and the result agreed well with the measured thickness. Finally, the related deposition mechanism is discussed and a deposition model is built.

Millable Polyurethane/Organoclay Nanocomposites: Preparation, Characterization, and Properties

2007 ◽  
Vol 7 (2) ◽  
pp. 634-640 ◽  
Author(s):  
M. Siliani ◽  
M. A. López-Manchado ◽  
J. L. Valentín ◽  
M. Arroyo ◽  
A. Marcos ◽  
...  
Keyword(s):  
Barrier Properties ◽  
Substantial Improvement ◽  
Nanometer Scale ◽  
X Ray Diffraction ◽  
Transformation Techniques ◽  
Covalent Bonds ◽  
X Ray ◽  
Transmission Electron ◽  
Organically Modified ◽  
Diffraction Patterns

Novel millable polyurethane (PU)/organoclay nanocomposites have been successfully prepared by conventional transformation techniques. One natural (C6A) and two organically modified (C15A and C30B) montmorillonites have been used as clays for preparing PU nanocomposites. The optimum dispersion of nanofiller at a nanometer scale in PU matrix was confirmed by X-ray diffraction patterns and transmission electron microscopy. A substantial improvement of the PU properties by addition of only a small amount of organoclay was observed. It is worthy to note that the organoclays show a different interfacial interaction with the PU matrix, which was reflected in different macroscopic properties. Thus, C30B organoclay seems to react with PU chains to form covalent bonds, while C15Aonly interacts physically with PU chains. Mechanical and barrier properties are analyzed.

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