Deposition And Characterization Of Silicon And Carbon Nitride

1995 ◽  
Vol 410 ◽  
Author(s):  
A. F. Myers ◽  
D. A. Tucker ◽  
S. P. Bozeman ◽  
S. M. Camphausen ◽  
M. J. Powers ◽  
...  

ABSTRACTWe attempted to deposit carbon nitride films on flat Si (111) substrates and on sharp <111>-oriented silicon needles in a radio frequency (rf) inductively coupled plasma system utilizing a graphite source and a nitrogen plasma. The resultant polycrystalline films were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), Auger electron spectroscopy (AES), and electron energy loss spectroscopy (EELS). Both selected area electron diffraction (SAED) and lattice imaging were used to identify and characterize the particles, which grew as faceted crystals up to 1 Rm in size. From SAED, high resolution TEM, and EELS, it was found that the particles on the Si needles were α-Si3N4 and that those on the Si wafer were mostly β-Si3N4 and β-C3N4, with some β-C3N4 possible. Auger quantitative analysis suggests that β-C3N4 could be stabilized by the presence of silicon, resulting in a material with compositions CxSiyNz.

2010 ◽  
Vol 152-153 ◽  
pp. 1222-1226
Author(s):  
Yong Gang Wang ◽  
Lin Lin Yang ◽  
Yu Jiang Wang ◽  
Xiao Feng Wang ◽  
Gao Rong Han

Single-crystal PbTiO3 nanoflakes have been synthesized successfully by a hydrothermal method. The as-prepared powders were characterized by X-ray powder diffraction (XRD), transmission electron microscopy (TEM), high-resolution TEM (HRTEM), and selected area electron diffraction (SAED). It was found that KOH concentration played a key role in the growth of single-crystal tetragonal perovskite PbTiO3 nanoflakes, and the morphology of PbTiO3 crystallites can be controlled by adjusting the KOH concentration.


2013 ◽  
Vol 680 ◽  
pp. 49-53
Author(s):  
Chang Yu ◽  
Xu Zhang ◽  
Kan He ◽  
Yue Liu ◽  
Jie Shan Qiu

A novel biocompatible Fe2+-chitosan (CTS)/citric acid modified carbon nanotube (CA-CNTs) composite (Fe2+-CTS/CA-CNTs) has been successfully synthesized by covalent bonding and crosslinking chemistry, followed by the reduction. The samples were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV-Vis spectrum, X-ray diffraction (XRD), inductively coupled plasma (ICP), thermal gravimetric analysis (TGA), and vibrating sample magnetometer (VSM) techniques. The results show that the CTS has been successfully grafted to the CA-CNTs carrier and Fe2+ ions are absorbed on the CTS by coordination bond mode. It was found that the Fe2+-CTS/CA-CNTs composite shows good magnetic properties with a low ratio of remanence to saturation magnetization and is in a superparamagnetic state at room temperature. It is believed that the Fe2+-CTS/CA-CNTs composite will be potential for application in MRI.


Author(s):  
M. M. Tsai ◽  
J. M. Howe

Precipitation of γ-TiH in α-Ti-H alloys involves a hcp → fct lattice transformation with hydrogen as an interstitial diffusing element Results obtained from a previous TEM study have shown that the lengthening rate of γ-TiH is diffusionally controlled at 25°C, and possibly interfacially controlled at temperatures of 50°C and higher. Therefore, it is essential to ascertain the presence or absence of hydrogen atoms at the interface. TEM foils from a 800 ppm wt.% Ti-H alloy were analyzed using high-resolution TEM and image simulations in order to determine the effects of hydrogen on high-resolution images of the α-Ti/γ-TiH interface, and EELS was used to determine the whether the hydnde structure was fully formed up to the interface.


2011 ◽  
Vol 121-126 ◽  
pp. 1500-1503
Author(s):  
Hui Juan Ren ◽  
Hua Yang ◽  
De Hui Sun ◽  
Zhen Feng Cui ◽  
Guang Yan Hong

Rare earth europium (Eu(III))-pyromellitic acid (H4L)-1,10-phenanthroline (phen) ternary luminescent complex has been synthesized in polyvinylpyrrolidone (PVP) matrix by precipitation method. The chemical constitution of the complex has been demonstrated as PVP/EuL4/3L(phen)•2H2O by a combination of elemental analysis, inductively coupled plasma-atomic emission spectroscopy (ICP-AES) and Fourier-transform infrared spectroscopy (FT-IR). X-ray diffraction analysis (XRD) has shown that the complex is a new kind of crystal whose structure is totally different from two ligands. The morphology of the complex has been investigated by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The results have shown that the complex has a rodlike crystal structure and the diameter of the rod is about 400 nm. Thermogravimetric analysis (TG) has indicated that the luminescent complex is thermally stable below 300 °C. Photoluminescence spectra (PL) have revealed that the complex can emit Eu3+ characteristic red fluorescence under ultraviolet excitation.


2006 ◽  
Vol 21 (11) ◽  
pp. 2941-2947 ◽  
Author(s):  
Hongjun Zhou ◽  
Tae-Jin Park ◽  
Stanislaus S. Wong

Bismuth titanate (Bi2Ti2O7) nanotubes were successfully synthesized with an alumina template-based sol-gel technique. As-synthesized nanotubes are smooth and uniform with diameters ranging from 180 to 330 nm and lengths varying from 7 to 12 μm. Extensive characterization of as-prepared samples has been performed using x-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution TEM (HRTEM), energy-dispersive x-ray spectroscopy (EDS), and selected-area electron diffraction (SAED). Photocatalytic studies indicate that as-prepared nanotubes possess higher photocatalytic activity than the corresponding bulk sample prepared without the use of an alumina template.


2021 ◽  
Author(s):  
Ayat Nuri ◽  
Abolfazl Bezaatpour ◽  
Mandana Amiri ◽  
Nemanja Vucetic ◽  
Jyri-Pekka Mikkola ◽  
...  

AbstractMesoporous SBA-15 silicate with a high surface area was prepared by a hydrothermal method, successively modified by organic melamine ligands and then used for deposition of Pd nanoparticles onto it. The synthesized materials were characterized with infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), nitrogen physisorption, scanning electron microscopy (SEM) coupled with energy dispersive X-ray analysis (EDX), transmission electron microscopy (TEM), nuclear magnetic resonance (NMR) and inductively coupled plasma (ICP-OES). The catalyst was effectively used in the Mizoroki–Heck coupling reaction of various reactants in the presence of an organic base giving the desired products in a short reaction time and with small catalysts loadings. The reaction parameters such as the base type, amounts of catalyst, solvents, and the temperature were optimized. The catalyst was easily recovered and reused at least seven times without significant activity losses. Graphic Abstract


2010 ◽  
Vol 43 (5) ◽  
pp. 990-997 ◽  
Author(s):  
Jie Ma ◽  
Qingsheng Wu

A facile oxides–hydrothermal (O–HT) method is demonstrated to prepare high-purity monazite-type LaPO4nanomaterials. In this approach, La2O3and P2O5powder are first directly used as precursors under additive-free hydrothermal conditions. The as-prepared samples are characterized with X-ray diffraction, Fourier transform IR spectroscopy, thermogravimetry, scanning electron microscopy, transmission electron microscopy (high-resolution TEM, energy dispersive spectroscopy) and selected-area electron diffraction. The typical sample obtained at 433 K in 24 h comprises uniform single-crystal nanofibres with a diameter of ∼15–28 nm and an aspect ratio of 30–50. The influences of treatment time, synthesis temperature and P/La molar ratio are investigated. The phase transition from hexagonal hydrate to monoclinic anhydrous lanthanum phosphate and the growth process of nanofibres are revealed by the experimental results. The formation mechanism of the monoclinic LaPO4is discussed. The result indicates that the P/La ratio does not influence the composition and crystal phase but changes the morphology of the product in the O–HT system.


2005 ◽  
Vol 61 (1) ◽  
pp. 11-16 ◽  
Author(s):  
E. A. Juarez-Arellano ◽  
J. M. Ochoa ◽  
L. Bucio ◽  
J. Reyes-Gasga ◽  
E. Orozco

Single microcrystals of the new compound samarium dimanganese germanium oxide, SmMn2GeO7, were grown using the flux method in a double spherical mirror furnace (DSMF). The micrometric crystals were observed and chemically analysed with scanning electron microscopy (SEM) and X-ray energy dispersive spectroscopy (EDX). The structural characterization and chemical analysis of these crystals were also carried out using transmission electron microscopy (TEM) and high-resolution transmission electron microscopy (HRTEM), together with electron-energy-loss spectroscopy (EELS). We found that the new quaternary compound crystallizes in the orthorhombic system with the point group mmm (D 2h ), space group Immm (No. 71) and cell parameters a = 8.30 (10), b = 8.18 (10), c = 8.22 (10) Å and V = 558.76 Å3.


2003 ◽  
Vol 776 ◽  
Author(s):  
Xicheng Ma ◽  
Yuanhua Cai ◽  
Xia Li ◽  
Ning Lun ◽  
Shulin Wen

AbstractHigh-quality cobalt-filled carbon nanotubes (CNTs) were prepared in situ in the decomposition of benzene over Co/silica-gel nano-scale catalysts. Unlike the previous reports, the catalysts needn't be pre-reduced prior to the forming of Co-filled CNTs, thus the advantage of this method is that Co-filled CNTs can be produced in one step, at a relatively low cost. Transmission electron microscopy (TEM) investigation showed that the products contained abundance of CNTs and most of them were filled with metallic nanoparticles or nanorods. High-resolution TEM (HRTEM), selected area electron diffraction (SAED) patterns and energy dispersive X-ray spectroscopy (EDS) confirmed the presence of Co inside the nanotubes. The encapsulated Co was further identified always as high temperature alpha-Co phase with fcc structure, which frequently consists of twinned boundaries and stacking faults. Based on the experimental results, a possible growth mechanism of the Co-filled CNTs was proposed.


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