Morphology studies of a W/Cu alloy synthesized by hydrogen reduction

2006 ◽  
Vol 21 (6) ◽  
pp. 1467-1475 ◽  
Author(s):  
U. Tilliander ◽  
H. Bergqvist ◽  
S. Seetharaman
Keyword(s):  
Electron Microscopy ◽  
Composite Materials ◽  
Hydrogen Reduction ◽  
Xrd Analysis ◽  
Grain Structure ◽  
Nanocrystalline State ◽  
Tem Analysis ◽  
Cu Alloy ◽  
Morphological Studies ◽  
Pure Cu

Because of the applications for W/Cu composite materials in high technology, the advantages of synthesizing this alloy by the hydrogen reduction route were investigated, with special attention to the properties of the product that was formed. Kinetic studies of reduction indicated that the mechanism changes significantly at 923 K, and the product had unusual properties. In the present work, morphological studies of the W/Cu alloy with 20 wt% Cu, produced at 923 K, were carried out by x-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM) analyses. The structural studies performed by XRD indicated that, at 923 K, Cu dissolved in W, forming a metastable solid solution in the nanocrystalline state. The samples produced at higher as well as lower temperatures, on the other hand, showed the presence of two phases, pure W and pure Cu. The SEM results were in agreement with the XRD analysis and confirmed the formation of W/Cu alloy. TEM analysis results confirmed the above observations and showed that the particle sizes were about 20 nm. The structure of the W/Cu alloy produced in the present work was compared with those for pure Cu, produced from Cu2O produced by hydrogen reduction under similar conditions. This indicated that the presence of W hinders the coalescence of Cu particles, and the alloy retains its nano-grain structure. The present results open up an interesting process route toward the production of intermetallic phases and composite materials under optimized conditions.

scholarly journals Influence of Ce Doping on the Electrical and Optical Properties of TiO2and Its Photocatalytic Activity for the Degradation of Remazol Brilliant Blue R

2013 ◽  
Vol 2013 ◽  
pp. 1-9 ◽  
Author(s):  
Aisha Malik ◽  
S. Hameed ◽  
M. J. Siddiqui ◽  
M. M. Haque ◽  
M. Muneer
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Dopant Concentration ◽  
Atmospheric Oxygen ◽  
Sol Gel ◽  
Analytical Techniques ◽  
Xrd Analysis ◽  
Brilliant Blue ◽  
Tem Analysis ◽  
Remazol Brilliant Blue R

Nanocrystalline TiO2particles doped with different concentrations of Cerium (Ce, 1–10%) have been synthesized using sol-gel method. The prepared particles were characterized by standard analytical techniques such as X-ray diffraction (XRD), FTIR and Scanning Electron Microscopy (SEM), and Transmission Electron Microscopy (TEM). The XRD analysis shows no change in crystal structure of TiO2after doping with different concentrations of Ce, which indicates the single-phase polycrystalline material. The SEM analysis shows the partial crystalline nature of undoped, and doped TiO2and TEM analysis shows the particle sizes were in the range of 9–14 nm in size. The a.c. analysis shows that the dielectric constantεand dielectric loss tanδdecrease with the increase in frequency. The dielectric property decreases with the increase in dopant concentration. It is also observed that the impedance increases with an increase in dopant concentration. The photocatalytic activity of the synthesized particles (Ce-doped TiO2) with dopant concentration of 9% (Ce) showed the highest photocatalytic activity for the degradation of the dye derivative Remazol Brilliant Blue R in an immersion well photochemical reactor with 500 W halogen linear lamp in the presence of atmospheric oxygen.

Scanning Electron Microscopy (Sem), Transmission Electron Microscopy (Tem) and Secondary Ion Mass Spectroscopy (Sims) Characterization of the Morphology of Aluminum Bond Pads for Surface Reflectivity Applications.

1995 ◽  
Vol 406 ◽  
Author(s):  
M. Schade ◽  
R. Ai ◽  
Y. Stein ◽  
T. Anderson
Keyword(s):  
Electron Microscopy ◽  
Film Growth ◽  
Three Dimensional ◽  
Depth Profiling ◽  
Sem Analysis ◽  
Grain Structure ◽  
Island Growth ◽  
Tem Analysis ◽  
Surface Development ◽  
Surface Reflectivity

AbstractExtreme variations in surface reflectivity/topography have been observed on silicon wafers with evaporated aluminum metallization following thermal annealing processes. Such topographic variations negatively impacted the performance of wire bonder pattern recognition systems. It was proposed that this variation was attributed to differences in deposition rates during evaporation of the aluminum front metallization. SEM analysis revealed that the topographically rough sites, deemed as normal for this processing sequence, had large numbers of hillocks, while the smooth sites exhibited limited numbers of hillocks after heat treatment. SIMS depth profiling analyses did not indicate that any elemental difference existed between the smooth and the rough sites, although interfacial differences were detected. Specifically, the Al-Si interface for the rough surface was more graded in nature while the Al-Si interface for the smooth surface was more abrupt. TEM analysis of the rough sites revealed that a three-dimensional island growth mechanism prevailed during film growth, resulting in uneven surface development, whereas analysis of the smooth sites showed a columnar grain structure.

scholarly journals Bacterial Mediated Rapid and Facile Synthesis of Silver Nanoparticles and Their Antimicrobial Efficacy against Pathogenic Microorganisms

Materials ◽  
2021 ◽  
Vol 14 (10) ◽  
pp. 2615
Author(s):  
Md. Amdadul Huq ◽  
Shahina Akter
Keyword(s):  
Electron Microscopy ◽  
Antimicrobial Activity ◽  
Silver Nanoparticles ◽  
Field Emission ◽  
Spherical Shape ◽  
Xrd Analysis ◽  
Gram Positive ◽  
Tem Analysis ◽  
Gram Negative ◽  
X Ray

In the present study, silver nanoparticles (AgNPs), biosynthesized using culture supernatant of bacterial strain Paenarthrobacter nicotinovorans MAHUQ-43, were characterized and their antimicrobial activity was investigated against both Gram-positive Bacillus cereus and Gram-negative bacteria Pseudomonas aeruginosa. Bacterial-mediated synthesized AgNPs were characterized by UV-Visible (UV-Vis) spectrophotometer, field emission-transmission electron microscopy (FE-TEM), energy dispersive X-ray (EDX), X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, and dynamic light scattering (DLS) analysis. The UV-Vis spectral analysis showed the absorption maxima at 466 nm which assured the synthesis of AgNPs. The FE-TEM analysis revealed the spherical shape of nanoparticles with the size range from 13 to 27 nm. The EDX and XRD analysis ensured the crystalline nature of biosynthesized AgNPs. The FTIR analysis revealed the involvement of different biomolecules for the synthesis of AgNPs as reducing and capping agents. The bacterial-mediated synthesized AgNPs inhibited the growth of pathogenic strains B. cereus and P. aeruginosa and developed a clear zone of inhibition (ZOI). The MIC and MBC for both pathogens were 12.5 µg/mL and 25 µg/mL, respectively. Moreover, field emission scanning electron microscopy analysis revealed that the synthesized AgNPs can destroy the outer membrane and alter the cell morphology of treated pathogens, leading to the death of cells. This study concludes the eco-friendly, facile and rapid synthesis of AgNPs using P. nicotinovorans MAHUQ-43 and synthesized AgNPs showed excellent antimicrobial activity against both Gram-positive and Gram-negative pathogens.

scholarly journals Solvents effect of quantum sized SnO2 nanoparticles via solvothermal process and optical properties

2010 ◽  
Vol 7 (2) ◽  
pp. 389-397 ◽  
Author(s):  
K. Anandan ◽  
V. Rajendran
Keyword(s):  
Electron Microscopy ◽  
Sno2 Nanoparticles ◽  
Nano Particles ◽  
Solvothermal Process ◽  
Tem Analysis ◽  
Quantum Size ◽  
Morphological Studies ◽  
Transmission Electron ◽  
Direct Band ◽  
Oxide Nanoparticle

Well-dispersed quantum sized SnO2 nanoparticles have been successfully synthesized by simple solvothermal process using ethylenediamine as both a coordination and an alkali reagent. The size of the prepared tin oxide nanoparticle has been characterized by X-ray powder diffraction (XRD) and transmission electron microscopy (TEM) analysis. The TEM images show nano-particles as clusters with size in the range of 2.27–3.35 nm. Morphological studies were obtained by scanning electron microscopy (SEM). The optical direct band gap values of SnO2 nanoparticles were calculated to be about 3.75–4.27eV, which were confirmed the quantum size effect. The photoluminescence (PL) properties and the possible mechanisms were also discussed.

scholarly journals Effect of Time on a Hierarchical Corn Skeleton-Like Composite of CoO@ZnO as Capacitive Electrode Material for High Specific Performance Supercapacitors

Energies ◽  
2018 ◽  
Vol 11 (12) ◽  
pp. 3285 ◽  
Author(s):  
Yedluri Kumar ◽  
Hee-Je Kim
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
High Performance ◽  
Xrd Analysis ◽  
Cycling Performance ◽  
Energy Storage Devices ◽  
Tem Analysis ◽  
X Ray ◽  
Potential Applications ◽  
Oxygen Groups

CoO–ZnO-based composites have attracted considerable attention for the development of energy storage devices because of their multifunctional characterization and ease of integration with existing components. This paper reports the synthesis of CoO@ZnO (CZ) nanostructures on Ni foam by the chemical bath deposition (CBD) method for facile and eco-friendly supercapacitor applications. The formation of a CoO@ZnO electrode functioned with cobalt, zinc, nickel and oxygen groups was confirmed by X-ray diffraction (XRD) analysis, X-ray photoelectron spectroscopy (XPS), low and high-resolution scanning electron microscopy (SEM), and transmission electron microscopy (TEM) analysis. The as-synthesized hierarchical nanocorn skeleton-like structure of a CoO@ZnO-3h (CZ3h) electrode delivered a higher specific capacitance (Cs) of 1136 F/g at 3 A/g with outstanding cycling performance, showing 98.3% capacitance retention over 3000 cycles in an aqueous 2 M KOH electrolyte solution. This retention was significantly better than that of other prepared electrodes, such as CoO, ZnO, CoO@ZnO-1h (CZ1h), and CoO@ZnO-7h (CZ7h) (274 F/g, 383 F/g, 240 F/g and 537 F/g). This outstanding performance was attributed to the excellent surface morphology of CZ3h, which is responsible for the rapid electron/ion transfer between the electrolyte and the electrode surface area. The enhanced features of the CZ3h electrode highlight potential applications in high performance supercapacitors, solar cells, photocatalysis, and electrocatalysis.

Comparative Microstructures of Ion Milled and Electrochemically Thinned Composite Materials

1974 ◽  
Vol 32 ◽  
pp. 546-547
Author(s):  
R.R. Russell
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Composite Materials ◽  
Great Difficulty ◽  
Ion Milling ◽  
Transmission Electron ◽  
Ion Damage ◽  
Intermetallic Composite

Transmission electron microscopy of metallic/intermetallic composite materials is most challenging since the microscopist typically has great difficulty preparing specimens with uniform electron thin areas in adjacent phases. The application of ion milling for thinning foils from such materials has been quite effective. Although composite specimens prepared by ion milling have yielded much microstructural information, this technique has some inherent drawbacks such as the possible generation of ion damage near sample surfaces.

High-resolution EM study of submicrometer-grained Al-Mg solid solution alloys

1995 ◽  
Vol 53 ◽  
pp. 524-525
Author(s):  
Z. Horita ◽  
D. J. Smith ◽  
M. Furukawa ◽  
M. Nemoto ◽  
R. Z. Valiev ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Solid Solution ◽  
High Resolution ◽  
Grain Boundaries ◽  
Energy State ◽  
High Energy ◽  
Grain Structure ◽  
Boundary Structure ◽  
Solid Solution Alloy ◽  
Average Grain Size

It is possible to produce metallic materials with submicrometer-grained (SMG) structures by imposing an intense plastic strain under quasi-hydrostatic pressure. Studies using conventional transmission electron microscopy (CTEM) showed that many grain boundaries in the SMG structures appeared diffuse in nature with poorly defined transition zones between individual grains. The implication of the CTEM observations is that the grain boundaries of the SMG structures are in a high energy state, having non-equilibrium character. It is anticipated that high-resolution electron microscopy (HREM) will serve to reveal a precise nature of the grain boundary structure in SMG materials. A recent study on nanocrystalline Ni and Ni3Al showed lattice distortion and dilatations in the vicinity of the grain boundaries. In this study, HREM observations are undertaken to examine the atomic structure of grain boundaries in an SMG Al-based Al-Mg alloy.An Al-3%Mg solid solution alloy was subjected to torsion straining to produce an equiaxed grain structure with an average grain size of ~0.09 μm.

Transmission Electron Microscopy of an Aluminum-Silver-Stainless Steel Solid State Bond

1985 ◽  
Vol 43 ◽  
pp. 172-173
Author(s):  
M. J. Carr ◽  
J. F. Shewbridge ◽  
T. O. Wilford
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Solid State ◽  
Specimen Preparation ◽  
Dimensional Control ◽  
Tem Analysis ◽  
Metal Parts ◽  
Dissimilar Metal ◽  
Transmission Electron ◽  
Short Time

Strong solid state bonds are routinely produced between physical vapor deposited (PVD) silver coatings deposited on sputter cleaned surfaces of two dissimilar metal parts. The low temperature (200°C) and short time (10 min) used in the bonding cycle are advantageous from the standpoint of productivity and dimensional control. These conditions unfortunately produce no microstructural changes at or near the interface that are detectable by optical, SEM, or microprobe examination. Microstructural problems arising at these interfaces could therefore easily go undetected by these techniques. TEM analysis has not been previously applied to this problem because of the difficulty in specimen preparation. The purpose of this paper is to describe our technique for preparing specimens from solid state bonds and to present our initial observations of the microstructural details of such bonds.

Morphological studies of linear (AB)n multiblock copolymers and their blends

1992 ◽  
Vol 50 (1) ◽  
pp. 384-385
Author(s):  
Richard J. Spontak ◽  
Steven D. Smith ◽  
Arman Ashraf
Keyword(s):  
Electron Microscopy ◽  
Microphase Separation ◽  
Multiblock Copolymers ◽  
First Order ◽  
Morphological Studies ◽  
Transmission Electron ◽  
First Order Phase Transition ◽  
Covalently Bonded ◽  
Total Molecular Weight ◽  
First Order Phase

Block copolymers are composed of sequences of dissimilar chemical moieties covalently bonded together. If the block lengths of each component are sufficiently long and the blocks are thermodynamically incompatible, these materials are capable of undergoing microphase separation, a weak first-order phase transition which results in the formation of an ordered microstructural network. Most efforts designed to elucidate the phase and configurational behavior in these copolymers have focused on the simple AB and ABA designs. Few studies have thus far targeted the perfectly-alternating multiblock (AB)n architecture. In this work, two series of neat (AB)n copolymers have been synthesized from styrene and isoprene monomers at a composition of 50 wt% polystyrene (PS). In Set I, the total molecular weight is held constant while the number of AB block pairs (n) is increased from one to four (which results in shorter blocks). Set II consists of materials in which the block lengths are held constant and n is varied again from one to four (which results in longer chains). Transmission electron microscopy (TEM) has been employed here to investigate the morphologies and phase behavior of these materials and their blends.

Using crystallographic symmetry in diffraction and contrast analysis

1989 ◽  
Vol 47 ◽  
pp. 504-505
Author(s):  
U. Dahmen ◽  
K.H. Westmacott
Keyword(s):  
Electron Microscopy ◽  
High Symmetry ◽  
Two Phase ◽  
Tem Analysis ◽  
Crystallographic Symmetry ◽  
The Matrix ◽  
Contrast Analysis ◽  
Practical Tool ◽  
Convergent Beam ◽  
Beam Diffraction

Despite the increased use of convergent beam diffraction, symmetry concepts in their more general form are not commonly applied as a practical tool in electron microscopy. Crystal symmetry provides an abundance of information that can be used to facilitate and improve the TEM analysis of crystalline solids. This paper draws attention to some aspects of symmetry that can be put to practical use in the analysis of structures and morphologies of two-phase materials.It has been shown that the symmetry of the matrix that relates different variants of a precipitate can be used to determine the axis of needle- or lath-shaped precipitates or the habit plane of plate-shaped precipitates. By tilting to a special high symmetry orientation of the matrix and by measuring angles between symmetry-related variants of the precipitate it is possible to find their habit from a single micrograph.

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