scholarly journals Characterization of Dark-Colored Nanoporous Anodic Films on Zinc

Coatings ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. 1014
Author(s):  
Ryoya Masuda ◽  
Damian Kowalski ◽  
Sho Kitano ◽  
Yoshitaka Aoki ◽  
Taisuke Nozawa ◽  
...  
Keyword(s):  
Electron Micrographs ◽  
Metal Film ◽  
Metal Nanoparticle ◽  
Scanning Electron Micrographs ◽  
X Ray Diffraction ◽  
Anodic Films ◽  
X Ray ◽  
Transmission Electron ◽  
Film Interface

In this study, zinc is anodized at different voltages in 0.1 mol·dm−3 KOH electrolyte to form nanoporous anodic films. Dark-colored anodic films are formed at anodizing voltages ≤6 V, whereas colorless anodic films are developed at voltages ≥7 V. The anodic films formed at all voltages consist of crystalline ZnO, which was identified by X-ray diffraction and Raman spectroscopy. The Raman spectra of the dark-colored anodic films show the enhanced intensity of the LO phonon mode due to electric-field-induced Raman scattering, which may be associated with the presence of metallic Zn nanoparticles in the anodic films. Scanning electron micrographs and transmission electron micrographs of the cross-section of the dark-colored anodized zinc reveal the formation of two-layer porous anodic films with a highly rough metal/film interface. In contrast, nanoporous anodic films of uniform thickness with a relatively flat metal/film interface are formed for the colorless anodized zinc. The transmission electron microscopy (TEM)/energy dispersive X-ray spectroscopy (EDS) analysis suggested the presence of zinc nanoparticles in the dark-colored anodic films. The non-uniform anodizing and the formation of metal-nanoparticle-dispersed porous anodic films cause the formation of dark-colored anodic films on zinc.

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.

Preparation and Characterization of Pt/Superfine Mesocarbon Microbead Powers Electrocatalysts

2005 ◽  
Vol 3 (3) ◽  
pp. 358-360 ◽  
Author(s):  
Jia Rong-Li ◽  
Wang Cheng-Yang ◽  
Zhu Bin
Keyword(s):  
Reduction Method ◽  
Direct Methanol Fuel Cells ◽  
Electrochemical Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Platinum Particles ◽  
Platinum Electrocatalyst ◽  
Direct Methanol

Superfine mesocarbon microbead powders (SFMCMBs) as the new supports for platinum electrocatalysts were first investigated. The Pt∕SFMCMB electrocatalysts were prepared by an impregnation-reduction method, with hexachloroplatinic acid as the platinum precursor and formaldehyde as the reducing agent. The catalysts were characterized with x-ray diffraction (XRD), field emission gun transmission electron microscope (TEM), and electrochemical analysis. TEM photos showed the platinum particles were dispersed uniformly on the surface of SFMCMBs and there existed a little aggregation of platinum particles in the Pt∕SFMCMB catalysts. The TEM photos showed the existence of the platinum on the supports where the average platinum particle size were 4-6nm. The electrochemical analysis proved that SFMCMBs are excellent candidates to be used as the support of platinum electrocatalyst for methanol electrochemical oxidation as the potential catalyst candidate for direct methanol fuel cells (DMFCs).

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.

scholarly journals Synthesis and Characterization of K-Ta Mixed Oxides for Hydrogen Generation in Photocatalysis

2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
Beata Zielińska ◽  
Ewa Mijowska ◽  
Ryszard J. Kalenczuk
Keyword(s):  
Diffuse Reflectance ◽  
Hydrogen Generation ◽  
Mixed Oxides ◽  
X Ray Diffraction ◽  
X Ray ◽  
Raman Spectroscopic ◽  
Photocatalytic Hydrogen Generation ◽  
Irregular Structure ◽  
Transmission Electron

K-Ta mixed oxides photocatalysts have been prepared by impregnation followed by calcination. The influence of the reaction temperature (450°C–900°C) on the phase formation, crystal morphology, and photocatalytic activity in hydrogen generation of the produced materials was investigated. The detailed analysis has revealed that all products exhibit high crystallinity and irregular structure. Moreover, two different crystal structures of potassium tantalates such as KTaO3and K2Ta4O11were obtained. It was also found that the sample composed of KTaO3and traces of unreacted Ta2O5(annealed at 600°C) exhibits the highest activity in the reaction of photocatalytic hydrogen generation. The crystallographic phases, optical and vibronic properties were examined by X-ray diffraction (XRD) and diffuse reflectance (DR) UV-vis and resonance Raman spectroscopic methods, respectively. Morphology and chemical composition of the produced samples were studied using a high-resolution transmission electron microscope (HR-TEM) and an energy dispersive X-ray spectrometer (EDX) as its mode.

Preparation and Characterization of γ-Fe2O3-ZnFe2O4 Composite Nanoparticles

2013 ◽  
Vol 873 ◽  
pp. 152-157
Author(s):  
Long Long Chen ◽  
Jun Ming Li ◽  
Xiao Min Gong ◽  
Jian Li
Keyword(s):  
Photoelectron Spectroscopy ◽  
Chemical Species ◽  
Composite Nanoparticles ◽  
X Ray Diffraction ◽  
Ferrite Core ◽  
Phase Synthesis ◽  
X Ray ◽  
Transmission Electron ◽  
Chemically Induced

Using a chemically induced transition in an FeCl2 solution, γ-Fe2O3 nanoparticles can be prepared from an amorphous precursor composed of FeOOH and Mg (OH)2. Surface modification by adding ZnCl2 during liquid-phase synthesis was attempted. The magnetization, morphology, crystal structure, and chemical species of as-prepared samples were characterized by vibrating sample magnetometer (VSM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray energy-dispersive spectroscopy (EDX), and X-ray photoelectron spectroscopy (XPS). The experimental results showed that the surface of the γ-Fe2O3 nanoparticles can be modified by adding ZnCl2 to form composite nanoparticles with a γ-Fe2O3/ZnFe2O4 ferrite core coated with Zn (OH)2 and absorbed FeCl36H2O; this modification can be enhanced by additional NaOH.

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