Synthesis and Characterization of Novel AlF3 Cubes

NANO ◽  
2015 ◽  
Vol 10 (05) ◽  
pp. 1550071 ◽  
Author(s):  
Maoquan Xue ◽  
Changsheng Li
Keyword(s):  
Electron Microscopy ◽  
Synthesis And Characterization ◽  
Metal Fluoride ◽  
Controlled Synthesis ◽  
X Ray ◽  
Transmission Electron ◽  
Cubic Structure ◽  
Synthesis Approach ◽  
Scanning Electron

In this paper, regularly shaped AlF 3 particles with cubic structure were successfully synthesized via a solvothermal route. The as-prepared products were characterized by X-ray powder diffraction (XRD), energy-dispersive spectroscopy (EDS), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The experimental results indicated that reaction temperature and time have significant effects on the morphology of the as-prepared products. A possible formation process has also been investigated on the basis of a series of XRD and SEM studies of the product obtained at different conditions. This well-controlled synthesis approach may be extended to fabricate other metal fluoride materials.

Hydrothermal Synthesis and Characterization of BiFeO3 Polyhedral Crystallites

2012 ◽  
Vol 174-177 ◽  
pp. 508-511
Author(s):  
Lin Lin Yang ◽  
Yong Gang Wang ◽  
Yu Jiang Wang ◽  
Xiao Feng Wang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
Xrd Pattern ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

BiFeO3 polyhedrons had been successfully synthesized via a hydrothermal method. The as-prepared products were characterized by power X-ray diffraction (XRD) pattern, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The possible mechanisms for the formation of BiFeO3 polyhedrons were discussed. Though comparison experiments, it was found that the kind of precursor played a key role on the morphology control of BiFeO3 crystals.

Synthesis and characterization of homogeneous lead-substituted tin oxide with the (110) face of rutile structure

2000 ◽  
Vol 15 (10) ◽  
pp. 2076-2079
Author(s):  
Chika Nozaki ◽  
Takashi Yamada ◽  
Kenji Tabata ◽  
Eiji Suzuki
Keyword(s):  
Electron Microscopy ◽  
Tin Oxide ◽  
Photoelectron Spectroscopy ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
Rutile Structure ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

Synthesis of a rutile-type lead-substituted tin oxide with (110) face was investigated. The characterization was performed by x-ray diffraction, scanning electron microscopy, transmission electron microscopy, energy dispersive x-ray spectroscopy, infrared spectroscopy, x-ray photoelectron spectroscopy, and Brunauer–Emmett–Teller surface area measurements. The homogeneous rutile-type lead-substituted tin oxide was obtained until 4.1 mol% of tin was substituted with lead. The surface of obtained oxide had a homogeneously lead-substituted (110) face.

Surfactant-Assisted Synthesis and Characterization of SrCrO4 Nanostructures

2006 ◽  
Vol 6 (3) ◽  
pp. 738-742 ◽  
Author(s):  
Di Chen ◽  
Kaibin Tang ◽  
Shuyuan Zhang ◽  
Huagui Zheng ◽  
Yitai Qian
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Synthesis And Characterization ◽  
Reaction Systems ◽  
X Ray ◽  
Transmission Electron ◽  
High Resolution Tem ◽  
Surfactant Assisted ◽  
Scanning Electron

A simple and efficient microemulsion-based technique, which used the new Tx-100/cyclohexanol/H2O system, was developed to synthesize SrCrO4 nanowire based nanostructures, including nanowire bundles and flower-like structures at different temperature. X-ray powder diffraction (XRD), field emission scanning electron microscope (FE-SEM), transmission electron microscopy (TEM) and high-resolution TEM (HRTEM) were used to characterize the products. Studies found that the reaction temperatures and the reaction systems have great influences on the final products. Optical properties studies by UV-Vis spectra and photoluminescence (PL) spectra confirmed that the as-obtained nanowires showed distinct optical activity under UV and visible light irradiation.

Superconductors in confined geometries

2005 ◽  
Vol 887 ◽  
Author(s):  
Zhili Xiao ◽  
Yew-San Hor ◽  
Ulrich Welp ◽  
Yasuo Ito ◽  
Umesh Patel ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
Confined Geometries ◽  
Superconducting Nanowires ◽  
One Dimensional ◽  
X Ray ◽  
Transmission Electron ◽  
Synthesis Approach

ABSTRACTThe synthesis of nanoscale superconductors with controlled geometries is extremely challenging. In this paper we present results on synthesis and characterization of one-dimensional (1D) NbSe2 superconducting nanowires/nanoribbons. Our synthesis approach includes the synthesis of 1D NbSe3 nanostructure precursors followed by nondestructive and controlled adjustment of the Se composition to formulate NbSe2. The morphology, composition and crystallinity of the synthesized 1D NbSe2 nanostructures were analyzed with scanning electron microscopy, x-ray diffraction and transmission electron microscopy. Transport measurements were carried out to explore the electronic properties of these confined superconducting nanostructures.

Synthesis and Characterization of Nanosized Cu/ZnO Catalyst by Polyol Method

2008 ◽  
Vol 8 (2) ◽  
pp. 874-877 ◽  
Author(s):  
Tuba Gürkaynak Altınçekiç ◽  
Ismail Boz ◽  
Selçuk Aktürk
Keyword(s):  
Electron Microscopy ◽  
Metallic Copper ◽  
Average Crystallite Size ◽  
Synthesis And Characterization ◽  
X Ray ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Nanosized Catalysts ◽  
Scanning Electron

Nanosized catalysts composed of metallic copper supported on zinc oxide have been synthesized by the polyol process. Average crystallite size of copper was between 10 and 45 nm. Cu/ZnO catalyst particles were characterized by various techniques, such as X-ray Powder Diffraction (XRD), Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), Selected Area Electron Diffraction (SAED), and dynamic light scattering analysis (DLS).

Microwave Assisted Reflux Synthesis and Characterization of Magnetic Fe3O4 Micro Bubbles Embed in Nano Particles

2013 ◽  
Vol 763 ◽  
pp. 12-16
Author(s):  
Saba Jamil ◽  
Xiao Yan Jing ◽  
Jun Wang ◽  
Song Nan Li ◽  
Jing Yuan Liu
Keyword(s):  
Electron Microscopy ◽  
Nano Particles ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
Microwave Assisted ◽  
Transmission Electron ◽  
Small Nanoparticles ◽  
Scanning Electron

Magnetic Fe3O4 nanobubbles surrounded by nanoparticles are prepared by adopting microwave assisted reflux method. The nanomagnetic particles surrounded by small beads like particles are fabricated by irradiating the prepaperd sample solutions by microwave radiations coupled with reflux method simultaneously at 90°C for 45 mins. The characterization of the prepared Fe3O4 particles are carried out by using x ray diffraction, scanning electron microscopy and transmission electron microscopy. The instrumentations shows the morphology that is thick walled bubble like with approximate diameter of about 300 nm to 400 nm surrounded by small nanoparticles of 5 nm to 30 nm in range. The particles are bubbles like and some broken bubbles showed that these might be hollow from inside.

scholarly journals Synthesis and characterization of Fe, Co, and Ni colloids in 2-mercaptoethanol

2020 ◽  
Vol 10 ◽  
pp. 184798042096688
Author(s):  
Galo Cárdenas-Triviño ◽  
Sergio Triviño-Matus
Keyword(s):  
Electron Microscopy ◽  
Electron Diffraction ◽  
Colloidal Dispersions ◽  
Synthesis And Characterization ◽  
X Ray ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Chemical Liquid Deposition ◽  
Liquid Deposition

Metal colloids in 2-mercaptoethanol using nanoparticles (NPs) of iron (Fe), cobalt (Co), and nickel (Ni) were prepared by chemical liquid deposition method. Transmission electron microscopy, electron diffraction, UV-VIS spectroscopy, and scanning electron microscopy with electron dispersive X-ray spectroscopy characterized the resulting colloidal dispersions. The NPs exhibited sizes with ranges from 9.8 nm for Fe, 3.7 nm for Co, and 7.2 nm for Ni. The electron diffraction shows the presence of the metals in its elemental state Fe (0), Co (0), and Ni (0) and also some compounds FeO (OH), CoCo2S4, and NiNi2S4.

Characterization of Al65.0Cu32.9Co2.1 Alloy Containing Nanofibres

2012 ◽  
Vol 186 ◽  
pp. 212-215
Author(s):  
Jacek Krawczyk ◽  
Włodzimierz Bogdanowicz ◽  
Grzegorz Dercz ◽  
Wojciech Gurdziel
Keyword(s):  
Electron Microscopy ◽  
Average Diameter ◽  
Chemical Compositions ◽  
X Ray ◽  
Transmission Electron ◽  
Orthogonal Set ◽  
T Phase ◽  
Terminal Area ◽  
Scanning Electron

Microstructure of terminal area of Al65Cu32.9Co2.1ingots (numbers indicate at.%), obtained via directional solidification was studied. Scanning Electron Microscopy, Transmission Electron Microscopy and X-ray powder diffraction were applied. Point microanalysis by Scanning Electron Microscope was used for examination of chemical compositions of alloy phases. It was found that tetragonal θ phase of Al2Cu stoichiometric formula was the dominate phase (matrix). Additionally the alloy contained orthogonal set of nanofibres of Al7Cu2Co T phase with the average diameter of 50-500 nm and oval areas of hexagonal Al3(Cu,Co)2H-phase, surrounded by monoclinic AlCu η1phase rim. Inside some areas of H-phase cores of decagonal quasicrystalline D phase were observed.

scholarly journals Synthesis and characterization of apatite silicated powders with wet precipitation method

2021 ◽  
Vol 234 ◽  
pp. 00106
Author(s):  
Houda Labjar ◽  
Hassan Chaair
Keyword(s):  
Electron Microscopy ◽  
Heat Treatment ◽  
Analytical Techniques ◽  
Precipitation Method ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
Wet Precipitation ◽  
Scanning Electron

The synthesis of apatite silicated Ca10(PO4)6-x(SiO4)x(OH)2-x (SiHA) with 0≤x≤2 was investigated using a wet precipitation method followed by heat treatment using calcium carbonate CaCO3 and phosphoric acid H3PO4 and silicon tetraacetate SiC8H20O4 (TEOS) in medium of water ethanol, with three different silicate concentrations. After drying, the samples are ground and then characterized by different analytical techniques like X-ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR) and Scanning electron Microscopy (SEM) and chemical analysis.

scholarly journals Preparation and Characterization of Nanostructured Hollow MgO Spheres

Materials ◽  
2019 ◽  
Vol 12 (3) ◽  
pp. 537
Author(s):  
Jishuo Han ◽  
Guohua Li ◽  
Lin Yuan
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Shell Thickness ◽  
Template Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Carbon Microsphere ◽  
Transmission Electron ◽  
Scanning Electron

Nanostructured hollow MgO microspheres were prepared by the template method. First, D-Anhydrous glucose was polymerized by the hydrothermal method to form a template. Second, a colorless solution was obtained by mixing magnesite with hydrochloric acid in a 1:2 proportion and heating in an 80 °C water bath for 2 h. Finally, the template from the first step was placed in the colorless solution, and the resulting precipitate was calcined at 550 °C for 2 h. The phase composition and microstructure of the calcined samples were characterized by means of X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The XRD results indicated that the main crystal is periclase. The SEM results indicates that the template carbon microsphere surface is smooth, and the its size is uniform and concentrated in the range of 100–200 nm. The diameters of the samples range from 60 to 90 nm, which is smaller than the size of the carbon microsphere. The TEM results indicates that the sample is hollow with a shell thickness of about 6–10 nm. The specific surface area of the calcined hollow sphere is 59.5 m²·g−1.

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