Metallurgical Study of Contacts to Gallium Nitride

1995 ◽  
Vol 395 ◽  
Author(s):  
S.E. Mohney ◽  
B.P. Luther ◽  
T.N. Jackson ◽  
M.A. Khan
Keyword(s):  
Phase Equilibria ◽  
Photoelectron Spectroscopy ◽  
Thermally Stable ◽  
X Ray Diffraction ◽  
X Ray ◽  
Potential Contact ◽  
Metallurgical Study ◽  
Metallurgical Reactions ◽  
Further Development

ABSTRACTThermally stable contacts to GaN that also have desirable electrical characteristics are required for the further development of optoelectronic and high temperature devices based on GaN. To make improvements on existing contacts or to develop new ones, information on the metallurgy of potential contact systems is needed. In this work, the Metal-Ga-N ternary phase equilibria and the contact metallurgy are examined for Ti, Re, and Ni. Annealed contacts of these metals have been examined with x-ray diffraction and/or x-ray photoelectron spectroscopy, and the observed metallurgical reactions are discussed in light of estimated or experimentally determined Metal-Ga-N phase diagrams. Particular attention is paid to the gas phase equilibria and the role of the annealing environment on the metallurgical reactions. Finally, the consequences of this work for the design of thermally stable contacts are considered.

scholarly journals Patterning Luminescent Nanocrystalline  : Eu and  : Tb Particles Embedded in Hybrid Organosilica with Soft-Lithographic Techniques

2012 ◽  
Vol 2012 ◽  
pp. 1-11 ◽  
Author(s):  
Sajid U. Khan ◽  
Johan E. ten Elshof
Keyword(s):  
Photoelectron Spectroscopy ◽  
Substrate Surface ◽  
Solution Chemistry ◽  
Ion Scattering ◽  
X Ray Diffraction ◽  
X Ray ◽  
Low Energy Ion Scattering ◽  
Pattern Shape ◽  
Secondary Ion

Eu3+-doped LaPO4and Tb3+-doped CePO4luminescent nanoparticles embedded in hybrid organosilica were patterned by two soft lithographic techniques. The role of various parameters such as solution chemistry, thermal protocols, and modification of the mold-substrate surface energies related to pattern shape formation and adhesion to the substrates have been studied. The shrinkage of the oxide patterns and shape evolution during the process was also examined. The patterns were characterized with optical and photoluminescence (PL) microscopy, X-ray diffraction (XRD), and scanning electron microscopy (SEM). Compositional analyses were carried out with X-ray photoelectron spectroscopy (XPS), low-energy ion scattering (LEIS), and secondary ion mass spectroscopy (SIMS). The results indicated that the final patterns obtained with these two techniques for the same material have different shapes and adherence to the substrates.

scholarly journals Structural Characterizations of Palladium Clusters Prepared by Polyol Reduction of [PdCl4]2−Ions

2016 ◽  
Vol 2016 ◽  
pp. 1-6 ◽  
Author(s):  
Loredana Schiavo ◽  
Lucrezia Aversa ◽  
Roberta Tatti ◽  
Roberto Verucchi ◽  
Gianfranco Carotenuto
Keyword(s):  
Photoelectron Spectroscopy ◽  
Chemical Properties ◽  
Nucleating Agent ◽  
X Ray Diffraction ◽  
Palladium Clusters ◽  
X Ray ◽  
Transmission Electron ◽  
Hydrogen Technology ◽  
Physical And Chemical

Palladium nanoparticles are of great interest in many industrial fields, ranging from catalysis and hydrogen technology to microelectronics, thanks to their unique physical and chemical properties. In this work, palladium clusters have been prepared by reduction of [PdCl4]2−ions with ethylene glycol, in the presence of poly(N-vinyl-2-pyrrolidone) (PVP) as stabilizer. The stabilizer performs the important role of nucleating agent for the Pd atoms with a fast phase separation, since palladium atoms coordinated to the polymer side-groups are forced at short distances during nucleation. Quasispherical palladium clusters with a diameter of ca. 2.6 nm were obtained by reaction in air at 90°C for 2 hours. An extensive materials characterization by transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and other characterizations (TGA, SEM, EDS-SEM, and UV-Vis) has been performed in order to evaluate the structure and oxidation state of nanopalladium.

Characterization of carbides in iron Fischer-Tropsch catalysts

1995 ◽  
Vol 53 ◽  
pp. 434-435
Author(s):  
Mehul D. Shroff ◽  
Dinesh S. Kalakkad ◽  
Nancy B. Jackson ◽  
Mark S. Harrington ◽  
Allen G. Sault ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Carbide Phase ◽  
Low Cost ◽  
High Water ◽  
X Ray Diffraction ◽  
Fischer Tropsch ◽  
X Ray ◽  
Water Gas

The Fischer - Tropsch synthesis (FTS) for the production of synthetic hydrocarbons from the indirect liquefaction of coal has tremendous potential as an alternative to petroleum - based fuels. The use of iron catalysts is desirable due to their low cost, easy availability, good FTS activity and high water - gas shift activity thus enabling use with low H2 / CO ratios. However, problems relating to attrition and deactivation need to be addressed. In addition, there has been a controversy in the literature regarding the role of the carbide phase and the identity of the active catalytic phase. The main reason for the existence of this debate has been the use of different characterization techniques. Our results with a commercial, precipitated and spray-dried, Fe2O3 - CuO - K2O Fischer-Tropsch catalyst point to the fact that conventional techniques like X - ray Diffraction (XRD), X - ray Photoelectron Spectroscopy (XPS) and Auger Electron Spectroscopy (AES) which have been traditionally used to characterize these catalysts (1,2) are not very successful in detecting the existence of the carbide phase, which generally forms as 20 - 30 nm crystallites on the surface of the micron - sized magnetite crystals.

scholarly journals Effect of Ti on dibenzothiophene hydrodesulfurization performance over bulk Ni2P

2019 ◽  
Vol 44 (1) ◽  
pp. 45-54
Author(s):  
Chunbao Han ◽  
Hua Song ◽  
Nan Jiang ◽  
Yanguang Chen ◽  
Feng Li ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Molar Fraction ◽  
P System ◽  
Temperature Programmed Reduction ◽  
X Ray Diffraction ◽  
X Ray ◽  
Highly Dispersed ◽  
Temperature Programmed ◽  
Hydrodesulfurization Activity

A series of Ti-incorporated bulk Ni2P catalysts was prepared by means of temperature-programmed reduction, and the role of metallic Ti on the structure and catalytic activity of the Ni2P catalysts was studied. For this purpose, bulk Ni2P catalysts with metal Ti contents of 0.005 wt%, 0.01 wt%, and 0.02 wt% were synthesized. X-ray diffraction, CO uptake, Brunauer–Emmett–Teller measurements, and X-ray photoelectron spectroscopy were utilized to characterize the catalysts. Addition of titanium could increase the surface area and promote the formation of small, highly dispersed Ni2P particles. The Ti0.02-Ni2P system with a Ti molar fraction of 0.02 showed the highest hydrodesulfurization activity of 99.6%, which was an increase of 44% compared with that found for the bulk Ni2P.

scholarly journals Reexamining the Role of Ammonium Ions in the Sulfidization, Xanthate-Flotation of Malachite

Minerals ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 537 ◽  
Author(s):  
Ruizeng Liu ◽  
Zhicheng Liu ◽  
Jianmin Li ◽  
Shunfu Ao ◽  
Bin Pei ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Coating Layer ◽  
Ammonium Nitrogen ◽  
X Ray Diffraction ◽  
Ammonium Ions ◽  
X Ray ◽  
Positive Effects ◽  
Before And After ◽  
Underlying Mechanisms

Ammonium ions have positive effects on the sulfidization flotation of malachite; however, the underlying mechanisms remain poorly understood. In the present work, micro-flotation tests, field emission scanning electron microscopy (FESEM), energy dispersive spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD) and solution analysis for ammonium nitrogen were carried out. The flotation results showed positive effects of ammonium on the sulfidization flotation of malachite. Macroscopically, the sulfidized malachite produced with ammonium exhibited a darker color than that without ammonium, whereas the opposite appeared to be true for their corresponding residual liquids. FESEM images highlighted the larger particle size and higher converge density of the sulfidization product when the presence of ammonium. Furthermore, XPS results indicated a higher sulfur concentration on malachite surfaces when the presence of ammonium. XRD results showed that Cu31S16 (djurleite) and Cu7S4 (anilite) comprised the sulfidization products, regardless of the presence or absence of ammonium. However, neither EDS nor XPS analysis showed nitrogen on malachite surfaces; moreover, the residual-ratio results for ammonium nitrogen clearly demonstrated that most ammonium continued to be held in solution before and after malachite sulfidization. Based on these findings, we inferred that ammonium ions may mediate the nucleation and growth of sulfidization product during malachite sulfidization, rendering larger sulfidization product particles. The larger size of sulfidization products may result in a darker, stabler and denser sulfidization product coating layer, and then may reduce the generation of colloidal copper sulfide in the residual liquids. Ultimately, ammonium facilitates better performance of sulfidization flotation of malachite.

The Role of Sputter Pressure in Influencing Electrical and Optical Properties of ITO on Glass

2010 ◽  
Vol 1256 ◽  
Author(s):  
Shereen Elhalawaty ◽  
Karthik Sivaramakrishnan ◽  
Theodore David ◽  
Terry L Alford
Keyword(s):  
Indium Tin Oxide ◽  
Photoelectron Spectroscopy ◽  
Visible Spectrum ◽  
Rf Magnetron Sputtering ◽  
Thin Layers ◽  
X Ray Diffraction ◽  
X Ray ◽  
Glass Substrates ◽  
Hall Effect Measurements

AbstractThin layers of indium tin oxide (ITO) were deposited onto glass substrates by RF magnetron sputtering with the pressure varying from 6 mTorr to 15 mTorr. The films were annealed in a reducing atmosphere at 500 °C for 30 minutes. Sheet resistance was determined by four-point-probe measurement. Resistivity, mobility, and carrier concentration were obtained by Hall effect measurements. Transmission of the films in the visible spectrum was determined by photospectrometry. The structure of the films was characterized by X-ray diffraction. X-ray photoelectron spectroscopy was used to determine the oxidation state of Sn, which was used to determine the fraction of active tin clusters. The effect of additional anneals was investigated. The results reveal that the lowest resistivity obtained was 1.69×10-4 -cm at 9 mTorr and the highest transmittance of 90% was obtained after a second anneal. However, the second anneal decreased the mobility and conductivity for high sputter pressures.

Investigation of the Effect of Uv-Assisted Oxidation and Nitridation of Hafnium Metal Films

2003 ◽  
Vol 780 ◽  
Author(s):  
C. Essary ◽  
V. Craciun ◽  
J. M. Howard ◽  
R. K. Singh
Keyword(s):  
Uv Radiation ◽  
Photoelectron Spectroscopy ◽  
Grazing Angle ◽  
X Ray Diffraction ◽  
Metal Thin Films ◽  
X Ray ◽  
Force Microscopy ◽  
Si Substrates ◽  
Atomic Force ◽  
Silicon Interface

AbstractHf metal thin films were deposited on Si substrates using a pulsed laser deposition technique in vacuum and in ammonia ambients. The films were then oxidized at 400 °C in 300 Torr of O2. Half the samples were oxidized in the presence of ultraviolet (UV) radiation from a Hg lamp array. X-ray photoelectron spectroscopy, atomic force microscopy, and grazing angle X-ray diffraction were used to compare the crystallinity, roughness, and composition of the films. It has been found that UV radiation causes roughening of the films and also promotes crystallization at lower temperatures.Furthermore, increased silicon oxidation at the interface was noted with the UVirradiated samples and was shown to be in the form of a mixed layer using angle-resolved X-ray photoelectron spectroscopy. Incorporation of nitrogen into the film reduces the oxidation of the silicon interface.

Role of the Structure and Electronic Properties of Fe2O3-MoO3 Catalyst on the Dehydration of Isopropyl Alcohol

1993 ◽  
Vol 58 (7) ◽  
pp. 1591-1599 ◽  
Author(s):  
Abd El-Aziz A. Said
Keyword(s):  
Active Sites ◽  
Isopropyl Alcohol ◽  
Oxide Catalyst ◽  
Flow System ◽  
Charge Carriers ◽  
X Ray Diffraction ◽  
X Ray ◽  
Catalyst Composition ◽  
Surface Active

Molybdenum oxide catalyst doped or mixed with (1 - 50) mole % Fe3+ ions were prepared. The structure of the original samples and the samples calcined at 400 °C were characterized using DTA, X-ray diffraction and IR spectra. Measurements of the electrical conductivity of calcined samples with and without isopropyl alcohol revealed that the conductance increases on increasing the content of Fe3+ ions up to 50 mole %. The activation energies of charge carriers were determined in presence and absence of the alcohol. The catalytic dehydration of isopropyl alcohol was carried out at 250 °C using a flow system. The results obtained showed that the doped or mixed catalysts are active and selective towards propene formation. However, the catalyst containing 40 mole % Fe3+ ions exhibited the highest activity and selectivity. Correlations were attempted to the catalyst composition with their electronic and catalytic properties. Probable mechanism for the dehydration process is proposed in terms of surface active sites.

scholarly journals α-Cellulose Fibers of Paper-Waste Origin Surface-Modified with Fe3O4 and Thiolated-Chitosan for Efficacious Immobilization of Laccase

Polymers ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 581
Author(s):  
Gajanan S. Ghodake ◽  
Surendra K. Shinde ◽  
Ganesh D. Saratale ◽  
Rijuta G. Saratale ◽  
Min Kim ◽  
...  
Keyword(s):  
Enzyme Immobilization ◽  
Photoelectron Spectroscopy ◽  
Cellulose Fibers ◽  
Relative Activity ◽  
Significant Activity ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Laccase Immobilization ◽  
Surface Modified

The utilization of waste-paper-biomass for extraction of important α-cellulose biopolymer, and modification of extracted α-cellulose for application in enzyme immobilization can be extremely vital for green circular bio-economy. Thus, in this study, α-cellulose fibers were super-magnetized (Fe3O4), grafted with chitosan (CTNs), and thiol (-SH) modified for laccase immobilization. The developed material was characterized by high-resolution transmission electron microscopy (HR-TEM), HR-TEM energy dispersive X-ray spectroscopy (HR-TEM-EDS), X-ray diffraction (XRD), vibrating sample magnetometer (VSM), X-ray photoelectron spectroscopy (XPS), and Fourier transform infrared spectroscopy (FT-IR) analyses. Laccase immobilized on α-Cellulose-Fe3O4-CTNs (α-Cellulose-Fe3O4-CTNs-Laccase) gave significant activity recovery (99.16%) and laccase loading potential (169.36 mg/g). The α-Cellulose-Fe3O4-CTNs-Laccase displayed excellent stabilities for temperature, pH, and storage time. The α-Cellulose-Fe3O4-CTNs-Laccase applied in repeated cycles shown remarkable consistency of activity retention for 10 cycles. After the 10th cycle, α-Cellulose-Fe3O4-CTNs possessed 80.65% relative activity. Furthermore, α-Cellulose-Fe3O4-CTNs-Laccase shown excellent degradation of pharmaceutical contaminant sulfamethoxazole (SMX). The SMX degradation by α-Cellulose-Fe3O4-CTNs-Laccase was found optimum at incubation time (20 h), pH (3), temperatures (30 °C), and shaking conditions (200 rpm). Finally, α-Cellulose-Fe3O4-CTNs-Laccase gave repeated degradation of SMX. Thus, this study presents a novel, waste-derived, highly capable, and super-magnetic nanocomposite for enzyme immobilization applications.

scholarly journals Stable and Metastable Phase Equilibria Involving the Cu6Sn5 Intermetallic

2021 ◽  
Author(s):  
A. Leineweber ◽  
M. Löffler ◽  
S. Martin
Keyword(s):  
Phase Equilibria ◽  
Electron Backscatter Diffraction ◽  
Metastable Phase ◽  
Stable Phase ◽  
X Ray Diffraction ◽  
X Ray ◽  
Heat Treated ◽  
Ordered Phases ◽  
Backscatter Diffraction ◽  
Kinetics Of

Abstract Cu6Sn5 intermetallic occurs in the form of differently ordered phases η, η′ and η′′. In solder joints, this intermetallic can undergo changes in composition and the state of order without or while interacting with excess Cu and excess Sn in the system, potentially giving rise to detrimental changes in the mechanical properties of the solder. In order to study such processes in fundamental detail and to get more detailed information about the metastable and stable phase equilibria, model alloys consisting of Cu3Sn + Cu6Sn5 as well as Cu6Sn5 + Sn-rich melt were heat treated. Powder x-ray diffraction and scanning electron microscopy supplemented by electron backscatter diffraction were used to investigate the structural and microstructural changes. It was shown that Sn-poor η can increase its Sn content by Cu3Sn precipitation at grain boundaries or by uptake of Sn from the Sn-rich melt. From the kinetics of the former process at 513 K and the grain size of the η phase, we obtained an interdiffusion coefficient in η of (3 ± 1) × 10−16 m2 s−1. Comparison of this value with literature data implies that this value reflects pure volume (inter)diffusion, while Cu6Sn5 growth at low temperature is typically strongly influenced by grain-boundary diffusion. These investigations also confirm that η′′ forming below a composition-dependent transus temperature gradually enriches in Sn content, confirming that Sn-poor η′′ is metastable against decomposition into Cu3Sn and more Sn-rich η or (at lower temperatures) η′. Graphic Abstract

Sign in / Sign up

Export Citation Format

Share Document