scholarly journals Preparation and Characterization of Ni(OH)2and NiO Mesoporous Nanosheets

2012 ◽  
Vol 2012 ◽  
pp. 1-6 ◽  
Author(s):  
Changyu Li ◽  
Shouxin Liu
Keyword(s):  
Decomposition Method ◽  
Mixed Solution ◽  
X Ray Diffraction ◽  
Facile Hydrothermal Method ◽  
Sodium Dodecylbenzenesulfonate ◽  
Single Crystalline ◽  
X Ray ◽  
Thermal Decomposition Method ◽  
Transmission Electron

Mesoporous nanosheets of single-crystallineβ-nickel hydroxide (β-Ni(OH)2) were successfully synthesized via a facile hydrothermal method using Ni(NO3)2 · 6H2O as precursor in a mixed solution of sodium hydroxide (NaOH) and sodium dodecylbenzenesulfonate (SDBS). Single-crystalline nickel oxide (NiO) mesoporous nanosheets can be obtained through a thermal decomposition method usingβ-Ni(OH)2mesoporous nanosheets as precursor. The influences of SDBS and hydrothermal treatment were carefully investigated; the results showed that they played important roles in the formation ofβ-Ni(OH)2mesoporous nanosheets. The as-obtainedβ-Ni(OH)2and NiO were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), thermal gravity-differential thermal analysis (TG-DTA), and specific surface area, and pore size test.

scholarly journals A novel technique to synthesis of tenorite (CuO) nanoparticles from low concentration CuSO4 solution

2011 ◽  
Vol 47 (1) ◽  
pp. 73-78 ◽  
Author(s):  
E. Darezereshki ◽  
F. Bakhtiari
Keyword(s):  
Electron Microscopy ◽  
Decomposition Method ◽  
Raw Materials ◽  
Spherical Shape ◽  
Cuo Nanoparticles ◽  
X Ray Diffraction ◽  
X Ray ◽  
Thermal Decomposition Method ◽  
Novel Technique ◽  
Transmission Electron

In this study CuO nanoparticles were prepared via direct thermal decomposition method using basic copper sulphates as wet chemically synthesized precursor which was calcined in air at 750?C for 2h. Samples were characterized by thermogravimetric (TG-DSC), X-ray diffraction (XRD), energy dispersive spectroscopy (EDS), infrared spectrum (IR), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The XRD, EDS, and IR results indicated that the synthesized CuO particles were pure. The SEM and TEM results showed that the CuO nanoparticles were of approximate spherical shape, and 170?5 nm in size. Using this method, Cuo nanoparticles could be produced without using organic solvent, expensive raw materials, and complicated equipment.

Synthesis and Characterization of Topological Insulator Bi2Te3 Nanowires

2015 ◽  
Vol 645-646 ◽  
pp. 32-39
Author(s):  
Zhen Guo ◽  
Lan Lu ◽  
Jing Yun Wang ◽  
Ying Jie Xing
Keyword(s):  
Low Cost ◽  
Diffraction Field ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
Facile Hydrothermal Method ◽  
Experimental Conditions ◽  
X Ray ◽  
Structure And Morphology ◽  
Transmission Electron

Bi2Te3 nanowires are prepared by a low-cost and facile hydrothermal method without any surfactant. The structure and morphology of the nanowires are characterized by X-ray diffraction, field emission scanning electron microscopy, and transmission electron microscope. The influences of experimental conditions on the products are investigated. The growth mechanism is proposed based on the experimental results. This work is promising for the synthesis of Bi2Te3 nanowires with less impurity.

scholarly journals ZnO Nanocrystals as Anode Electrodes for Lithium-Ion Batteries

2016 ◽  
Vol 2016 ◽  
pp. 1-7 ◽  
Author(s):  
Wenhui Zhang ◽  
Lijuan Du ◽  
Zongren Chen ◽  
Juan Hong ◽  
Lu Yue
Keyword(s):  
Electron Microscopy ◽  
Decomposition Method ◽  
Storage Capacity ◽  
Lithium Ion ◽  
X Ray Diffraction ◽  
Lithium Storage ◽  
X Ray ◽  
Thermal Decomposition Method ◽  
Zno Nanocrystals ◽  
Transmission Electron

ZnO nanocrystals were synthesized via a thermal decomposition method. X-ray diffraction, transmission electron microscopy, and photoluminescence were used to investigate the composition and nanostructure of the material. Compared with commercial ZnO nanoparticles, ZnO nanocrystals showed higher lithium storage capacity and better cycling characteristics and exhibited a reversible discharge capacity of 500 mAh g−1after 100 cycles at 200 mA g−1.

Preparation and Characterization of a Magnetic Binary System Comprise of γ-Fe2O3 and α-FeO(OH) Nanoparticles

2016 ◽  
Vol 852 ◽  
pp. 264-271
Author(s):  
Xiao Min Gong ◽  
Jian Li ◽  
Jun Ming Li ◽  
Hong Mao
Keyword(s):  
Volume Ratio ◽  
Transformation Method ◽  
Mixed Solution ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Chemically Induced ◽  
Naoh Solution ◽  
Low Crystalline

Magnetic nanoparticles were prepared from a low crystalline ferrihydrite (Fe5O7(OH)·4H2O) precursor by a chemically-induced transformation method using mixed FeCl2/NaOH solution. The products obtained were characterized using a vibrating sample magnetometer, X-ray diffraction, transmission electron microscopy, and energy dispersive X-ray spectroscopy. Experimental results show that while the concentration of NaOH was 0.17 mol/L, and the FeCl2 concentration was increased from 0.09 mol/L to 0.42 mol/L in the mixed solution, the as-prepared products were binary nanoparticle systems comprised of ferrimagnetic γ-Fe2O3 sphere-type particles and antiferromagnetic α-FeO(OH) rod-type particles. The resulting particles were highly crystalline. The volume ratio of γ-Fe2O3 and α-FeO(OH) particles was estimated from magnetization data, which showed that the volume of γ-Fe2O3 particles decreased and α-FeO(OH) particles increased with increasing FeCl2 concentration. Such nanoparticle systems could be suitable for synthesis of binary ferrofluids, which have different behavior to conventional ferrofluids.

The Use of Advanced Analytical Techniques for Characterization of the Chemical, Physical, and Crystallographic Nature of a Surface

1973 ◽  
Vol 31 ◽  
pp. 132-133 ◽  
Author(s):  
R. E. Herfert
Keyword(s):  
Surface Characterization ◽  
Analytical Techniques ◽  
X Ray Diffraction ◽  
Depth Of Penetration ◽  
X Ray ◽  
The Past ◽  
Transmission Electron ◽  
Scanning Electron

Studies of the nature of a surface, either metallic or nonmetallic, in the past, have been limited to the instrumentation available for these measurements. In the past, optical microscopy, replica transmission electron microscopy, electron or X-ray diffraction and optical or X-ray spectroscopy have provided the means of surface characterization. Actually, some of these techniques are not purely surface; the depth of penetration may be a few thousands of an inch. Within the last five years, instrumentation has been made available which now makes it practical for use to study the outer few 100A of layers and characterize it completely from a chemical, physical, and crystallographic standpoint. The scanning electron microscope (SEM) provides a means of viewing the surface of a material in situ to magnifications as high as 250,000X.

Detonation Synthesis of Nano-Size Materials

1995 ◽  
Vol 418 ◽  
Author(s):  
J. Forbes ◽  
J. Davis ◽  
C. Wong
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Nucleation And Growth ◽  
Detonation Synthesis ◽  
X Ray Diffraction ◽  
Crystalline Materials ◽  
X Ray ◽  
Transmission Electron ◽  
Nano Size

AbstractThe detonation of explosives typically creates 100's of kbar pressures and 1000's K temperatures. These pressures and temperatures last for only a fraction of a microsecond as the products expand. Nucleation and growth of crystalline materials can occur under these conditions. Recovery of these materials is difficult but can occur in some circumstances. This paper describes the detonation synthesis facility, recovery of nano-size diamond, and plans to synthesize other nano-size materials by modifying the chemical composition of explosive compounds. The characterization of nano-size diamonds by transmission electron microscopy and electron diffraction, X-ray diffraction and Raman spectroscopy will also be reported.

One Step Synthesis and Characterization of Zirconia-Graphene Composites

2012 ◽  
Vol 600 ◽  
pp. 174-177 ◽  
Author(s):  
Jian Fei Xia ◽  
Zong Hua Wang ◽  
Yan Zhi Xia ◽  
Fei Fei Zhang ◽  
Fu Qiang Zhu ◽  
...  
Keyword(s):  
Synthesis And Characterization ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
X Ray ◽  
Graphene Composite ◽  
Transmission Electron ◽  
One Step ◽  
Ft Ir ◽  
Xrd Techniques

Zirconia-graphene composite (ZrO2-G) has been successfully synthesized via decomposition of ZrOCl2•6H2O in a water-isopropanol system with dispersed graphene oxide (GO) utilizing Na2S as a precursor could enable the occurrence of the deposition of Zr4+ and the deoxygenation of GO at the same time. Transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction (XRD) techniques were used to characterize the samples. It was found that graphene were fully coated with ZrO2, and the ZrO2 existing in tetragonal phase, which resulted in the formation of two-dimensional composite.

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.

scholarly journals Characterization of ferrite nanoparticles for preparation of biocomposites

2017 ◽  
Vol 8 ◽  
pp. 1257-1265 ◽  
Author(s):  
Urszula Klekotka ◽  
Magdalena Rogowska ◽  
Dariusz Satuła ◽  
Beata Kalska-Szostko
Keyword(s):  
Chemical Method ◽  
Ferrite Nanoparticles ◽  
Chemical Activity ◽  
Nominal Composition ◽  
X Ray Diffraction ◽  
Wet Chemical Method ◽  
X Ray ◽  
Transmission Electron ◽  
Wet Chemical

Ferrite nanoparticles with nominal composition Me0.5Fe2.5O4 (Me = Co, Fe, Ni or Mn) have been successfully prepared by the wet chemical method. The obtained particles have a mean diameter of 11–16 ± 2 nm and were modified to improve their magnetic properties and chemical activity. The surface of the pristine nanoparticles was functionalized afterwards with –COOH and –NH2 groups to obtain a bioactive layer. To achieve our goal, two different modification approaches were realized. In the first one, glutaraldehyde was attached to the nanoparticles as a linker. In the second one, direct bonding of such nanoparticles with a bioparticle was studied. In subsequent steps, the nanoparticles were immobilized with enzymes such as albumin, glucose oxidase, lipase and trypsin as a test bioparticles. The characterization of the nanoparticles was acheived by transmission electron microscopy, X-ray diffraction, energy dispersive X-ray and Mössbauer spectroscopy. The effect of the obtained biocomposites was monitored by Fourier transform infrared spectroscopy. The obtained results show that in some cases the use of glutaraldehyde was crucial (albumin).

Solvothermal synthesis and characterization of well-dispersed cerium-doped Y2SiO5 phosphor particles

2021 ◽  
Vol 112 (10) ◽  
pp. 812-816
Author(s):  
Xianxue Li
Keyword(s):  
Solvothermal Method ◽  
Luminescence Decay ◽  
X Ray Diffraction ◽  
X Ray ◽  
Fluorescence Spectrophotometry ◽  
Decay Properties ◽  
Transmission Electron ◽  
Water As Solvent ◽  
Pure Phase

Abstract Well-dispersed cerium-doped Y2SiO5 (Ce:YSO) phosphor particles with spherical morphology and good luminescence intensity have been achieved by a solvothermal method with ethanol and water as solvent media. X-ray diffraction, Fourier transform infrared spectroscopy, fluorescence spectrophotometry and transmission electron microscopy were employed to characterize the as-synthesized Ce:YSO precursor and powders. The results showed that pure-phase Ce:YSO powders with a mean particle size of about 162 nm were accurately available at 310°C and above. The fluorescence ability and persistent luminescence decay properties of the Ce:YSO powders were also studied, and the excellent fluorescence properties could be attributed to the homogeneous Ce:YSO particles obtained through the solvothermal method.

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