Compositional and structural studies of amorphous GaN grown by ion-assisted deposition

2001 ◽  
Vol 693 ◽  
Author(s):  
U. D. Lanke ◽  
A. Koo ◽  
B. J. Ruck ◽  
H. K. Lee ◽  
A. Markwitz ◽  
...  
Keyword(s):  
Atomic Ratio ◽  
Nuclear Reaction Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Local Bonding ◽  
Ion Energies ◽  
Nitrogen Ion ◽  
Tetrahedral Bonding ◽  
X Ray Absorption

AbstractAmorphous GaN films have been deposited onto various substrates by ion-assisted deposition. The films were deposited at room temperature using nitrogen ion energies in the range 40-900 eV. Rutherford backscattering spectroscopy and nuclear reaction analysis show that the Ga:N atomic ratio is approximately one for films grown with ion energy near 500 eV; these films have the highest transparency. Films grown with ion energies below 300 eV are Ga rich, and show reduced transparency across the visible. Raman spectroscopy, x-ray diffraction, and transmission electron microscopy confirm the amorphous nature of the films. Annealing studies on a-GaN establish that the films begin to crystallise at a temperature of about 700 C. To investigate the local bonding environment of the Ga or N atoms, we have measured the extended x-ray absorption fine structure (EXAFS) of the transparent GaN films. The EXAFS results indicate that the films are dominated by heteropolar tetrahedral bonding, with a low density of homopolar bonds.

scholarly journals Structural Evolution in Wet Mechanically Alloyed Co-Fe-(Ta,W)-B Alloys

Metals ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 800
Author(s):  
Vladimír Girman ◽  
Maksym Lisnichuk ◽  
Daria Yudina ◽  
Miloš Matvija ◽  
Pavol Sovák ◽  
...  
Keyword(s):  
Structural Changes ◽  
Magnetic Measurements ◽  
Structural Evolution ◽  
High Energy ◽  
Control Agent ◽  
X Ray Diffraction ◽  
Mechanically Alloyed ◽  
X Ray ◽  
Transmission Electron ◽  
X Ray Absorption

In the present study, the effect of wet mechanical alloying (MA) on the glass-forming ability (GFA) of Co43Fe20X5.5B31.5 (X = Ta, W) alloys was studied. The structural evolution during MA was investigated using high-energy X-ray diffraction, X-ray absorption spectroscopy, high-resolution transmission electron microscopy and magnetic measurements. Pair distribution function and extended X-ray absorption fine structure spectroscopy were used to characterize local atomic structure at various stages of MA. Besides structural changes, the magnetic properties of both compositions were investigated employing a vibrating sample magnetometer and thermomagnetic measurements. It was shown that using hexane as a process control agent during wet MA resulted in the formation of fully amorphous Co-Fe-Ta-B powder material at a shorter milling time (100 h) as compared to dry MA. It has also been shown that substituting Ta with W effectively suppresses GFA. After 100 h of MA of Co-Fe-W-B mixture, a nanocomposite material consisting of amorphous and nanocrystalline bcc-W phase was synthesized.

Size dependent behavior of Fe3O4crystals during electrochemical (de)lithiation: an in situ X-ray diffraction, ex situ X-ray absorption spectroscopy, transmission electron microscopy and theoretical investigation

2017 ◽  
Vol 19 (31) ◽  
pp. 20867-20880 ◽  
Author(s):  
David C. Bock ◽  
Christopher J. Pelliccione ◽  
Wei Zhang ◽  
Janis Timoshenko ◽  
K. W. Knehr ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Structural Changes ◽  
Ex Situ ◽  
X Ray Diffraction ◽  
X Ray ◽  
Size Dependent ◽  
Transmission Electron ◽  
Dependent Behavior ◽  
X Ray Absorption

Crystal and atomic structural changes of Fe3O4upon electrochemical (de)lithiation were determined.

CeO2/TiO2 Nanotubes Composites: Synthesis, Characterization, and Photocatalytic Properties

2012 ◽  
Vol 583 ◽  
pp. 86-90 ◽  
Author(s):  
Hai Bin Li ◽  
Xin Yong Li ◽  
Yan De Song ◽  
Shu Guang Chen ◽  
Ying Wang ◽  
...  
Keyword(s):  
Diffuse Reflectance Spectroscopy ◽  
Atomic Ratio ◽  
X Ray Diffraction ◽  
Hydrothermal Route ◽  
Electron Hole ◽  
Calcination Process ◽  
X Ray ◽  
Transmission Electron ◽  
Hole Recombination

TiO2nanotubes were prepared via a hydrothermal route. CeO2nanoparticles with diameters around 5nm were loaded onto the surface of TiO2nanotubes via a deposition approach followed by a calcination process. Transmission electron microscopy (TEM), X-ray diffraction (XRD), and UV-vis diffuse reflectance spectroscopy (UV-vis) were applied for the characterization of the as-prepared CeO2/TiO2nanotubes composites. The results show that CeO2particles are highly dispersed on the surface of TiO2nanotubes. The TiO2 nanotubes are modified to response to the visible light due to the combination with CeO2. The CeO2/TiO2nanotubes composites with a CeO2/TiO2atomic ratio of 2.5% show a further improvement on the photocatalytic activity for degradation of Rhodamine B in water. The presence of CeO2improves the light absorption of TiO2nanotubes and inhibits the electron-hole recombination.

EFFECT OF ION-ENERGY ON THE PROPERTIES OF AMORPHOUS GaN FILMS PRODUCED BY ION-ASSISTED DEPOSITION

2001 ◽  
Vol 15 (28n29) ◽  
pp. 1355-1360 ◽  
Author(s):  
UDAY LANKE ◽  
ANNETTE KOO ◽  
SIMON GRANVILLE ◽  
JOE TRODAHL ◽  
ANDREAS MARKWITZ ◽  
...  
Keyword(s):  
Room Temperature ◽  
Single Phase ◽  
Thermal Evaporation ◽  
Ion Beam ◽  
Atomic Ratio ◽  
Nuclear Reaction Analysis ◽  
Ion Energy ◽  
X Ray ◽  
Nitrogen Ions ◽  
Nitrogen Ion

Amorphous GaN films were deposited on various substrates viz. Si (100), quartz, glass, Al, stainless steel and glassy carbon by thermal evaporation of gallium in the presence of energetic nitrogen ions from a Kaufman source. The films were deposited at room temperature and 5 × 10-4 mbar nitrogen partial pressure. The effect of a low energy nitrogen ion beam during the synthesis of films was investigated for energies 40 eV and 90 eV. The N:Ga atomic ratio, bonding state, microstructure, surface morphology, and electrical properties of the deposited a-GaN films were studied by different characterisation techniques. The films are found to be X-ray amorphous in nature, which is confirmed by Raman spectroscopy. Rutherford Backscattering Spectroscopy (RBS) and Nuclear Reaction Analysis (NRA) indicate the N:Ga atomic ratio in the films. The 400-750 eV energy range is thought to be optimal for the production of single-phase amorphous GaN . The effect of ion-energy on optical, Raman, and electrical conductivity measurements of the films is also presented.

scholarly journals Observation and Characterization of Fragile Organometallic Molecules Encapsulated in Single-Wall Carbon Nanotubes

2014 ◽  
Vol 2014 ◽  
pp. 1-5
Author(s):  
Daisuke Ogawa ◽  
Ryo Kitaura ◽  
Takeshi Saito ◽  
Shinobu Aoyagi ◽  
Eiji Nishibori ◽  
...  
Keyword(s):  
Carbon Nanotubes ◽  
High Yield ◽  
Single Wall Carbon Nanotubes ◽  
X Ray Diffraction ◽  
Single Wall Carbon ◽  
X Ray ◽  
Transmission Electron ◽  
Organometallic Molecules ◽  
X Ray Absorption

Thermally fragile tris(η5-cyclopentadienyl)erbium (ErCp3) molecules are encapsulated in single-wall carbon nanotubes (SWCNTs) with high yield. We realized the encapsulation of ErCp3with high filling ratio by using high quality SWCNTs at an optimized temperature under higher vacuum. Structure determination based on high-resolution transmission electron microscope observations together with the image simulations reveals the presence of almost free rotation of each ErCp3molecule in SWCNTs. The encapsulation is also confirmed by X-ray diffraction. Trivalent character of Er ions (i.e., Er3+) is confirmed by X-ray absorption spectrum.

Thiol-Capped CdSe and CdTe Nanoclusters: Synthesis by a Wet Chemical Route, Structural and Optical Properties

1998 ◽  
Vol 536 ◽  
Author(s):  
A. L. Rogach ◽  
A Eychmüller ◽  
J. Rockenberger ◽  
A. Kornowski ◽  
H. Weller ◽  
...  
Keyword(s):  
Particle Size ◽  
X Ray Diffraction ◽  
Structural And Optical Properties ◽  
Chemical Route ◽  
X Ray ◽  
Stabilizing Agents ◽  
Transmission Electron ◽  
Wet Chemical ◽  
Wet Chemical Route ◽  
X Ray Absorption

AbstractCdSe and CdTe nanoclusters were formed in aqueous solutions at moderate temperatures by a wet chemical route in the presence of thiols as effective stabilizing agents. The nature of the stabilizing agent (thioalcohols or thioacids) had an important influence on the particle size and largely determined the photoluminescence properties. The nanoclusters were characterized by means of UV-vis absorption and photoluminescence spectroscopy, powder X-ray diffraction, high resolution transmission electron microscopy, and extended X-ray absorption fine structure measurements. CdSe and CdTe nanoclusters were crystalline, in the cubic zincblende phase, with mean sizes in the range of 2 to 5 nm depending on the preparative conditions and the postpreparative size-selective fractionation, and showed pronounced electronic transitions in the absorption spectra. Thioglycerol-stabilized CdTe nanoclusters possessed sharp band-egde photoluminescence being tunable with particle size.

Structural, morphological, and magnetic study of nanocrystalline cobalt-copper powders synthesized by the polyol process

1995 ◽  
Vol 10 (6) ◽  
pp. 1546-1554 ◽  
Author(s):  
G.M. Chow ◽  
L.K. Kurihara ◽  
K.M. Kemner ◽  
P.E. Schoen ◽  
W.T. Elam ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Face Centered Cubic ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Copper Powders ◽  
Face Centered ◽  
Increasing Temperature ◽  
X Ray Absorption

Nanocrystalline CoxCu100−x (4 ⋚ x ⋚ 49 at. %) powders were prepared by the reduction of metal acetates in a polyol. The structure of powders was characterized by x-ray diffraction (XRD), transmission electron microscopy (TEM), high resolution transmission electron microscopy (HRTEM), extended x-ray absorption fine structure (EXAFS) spectroscopy, solid-state nuclear magnetic resonance (NMR) spectroscopy, and vibrating sample magnetometry (VSM). As-synthesized powders were composites consisting of nanoscale crystallites of face-centered cubic (fcc) Cu and metastable face-centered cubic (fcc) Co. Complementary results of XRD, HRTEM, EXAFS, NMR, and VSM confirmed that there was no metastable alloying between Co and Cu. The NMR data also revealed that there was some hexagonal-closed-packed (hcp) Co in the samples. The powders were agglomerated, and consisted of aggregates of nanoscale crystallites of Co and Cu. Upon annealing, the powders with low Co contents showed an increase in both saturation magnetization and coercivity with increasing temperature. The results suggested that during preparation the nucleation of Cu occurred first, and the Cu crystallites served as nuclei for the formation of Co.

Doping and Characterisation of Nanocrystalline Materials

2007 ◽  
Vol 128 ◽  
pp. 61-72
Author(s):  
Th. Wichert ◽  
Z. Guan
Keyword(s):  
Nanocrystalline Materials ◽  
Local Information ◽  
Atomic Scale ◽  
Radioactive Isotopes ◽  
Correlation Technique ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Significant Process ◽  
X Ray Absorption

The synthesis behaviour and characterisation of nanocrystalline materials is presented. The materials synthesised are ZnO and InP doped with shallow donors and acceptors, respectively. Characterisation was performed with radioactive isotopes using the perturbed γγ angular correlation technique (PAC), thereby yielding local information on an atomic scale. The characterisation was supplemented by X-ray diffraction, transmission electron microscopy, UV/VIS absorption spectroscopy, photoluminescence spectroscopy, and extended X-ray absorption fine structure spectroscopy. It was shown that the successful incorporation of dopants in nanocrystalline ZnO and InP requires annealing at temperatures at which the growth of the nanocrystals in the sample becomes a significant process.

scholarly journals The Influences of Magnesium upon Calcium Phosphate Mineral Formation and Structure as Monitored by X-ray and Vibrational Spectroscopy

Soil Systems ◽  
2020 ◽  
Vol 4 (1) ◽  
pp. 8
Author(s):  
David M. Hilger ◽  
Jordan G. Hamilton ◽  
Derek Peak
Keyword(s):  
Calcium Phosphate ◽  
Calcareous Soils ◽  
X Ray Diffraction ◽  
Edge Structure ◽  
X Ray ◽  
Transmission Electron ◽  
Phosphate Mineral ◽  
Local Bonding ◽  
Wide Range ◽  
High Concentrations

Calcium phosphate minerals are typically the solubility-limiting phase for phosphate in calcareous soils. Magnesium (Mg), despite being present in high concentrations in calcareous soils, has been largely neglected in the study of formation and stabilization of soil phosphate minerals due to the high solubility of pure Mg phosphate phases. In this study, a series of four common calcium and magnesium phosphate minerals, hydroxyapatite/bobierrite and brushite/newberyite were synthesized in the presence of widely varying Mg concentrations to examine the effects of Mg substitution upon the local bonding environment and overall structure of the precipitates. Phosphorus K-edge X-Ray absorption near edge structure (XANES) and attenuated total reflectance Fourier transform infrared (ATR-FTIR) provide insight into the local coordination environment, whereas synchrotron powder X-Ray diffraction (SP-XRD) and transmission electron microscopy (TEM) were used for structural analysis. In acidic to neutral pH, Mg-bearing brushite phases formed over a wide range of Ca:Mg ratios. In neutral to high pH systems, a short-range order amorphous calcium phosphate (ACP) with a local structure analogous with hydroxyapatite precipitated for a wide range of Ca to Mg ratios. It can be inferred that the presence of Mg in soils leads to stabilization of metastable phases: via cation substitution in brushite and via poisoning of crystal growth propagation for hydroxyapatite.

Engineering Disorder at a Nanoscale: A Combined TEM and XAS Investigation of Amorphous versus Nanocrystalline Sodium Birnessite

2015 ◽  
Vol 68 (11) ◽  
pp. 1715 ◽  
Author(s):  
Rosalie K. Hocking ◽  
Hannah J. King ◽  
Aimee Hesson ◽  
Shannon A. Bonke ◽  
Bernt Johannessen ◽  
...  
Keyword(s):  
Water Oxidation ◽  
Nanocrystalline Material ◽  
Oxidation Catalysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Water Oxidation Catalysis ◽  
Catalytically Active ◽  
Amorphous Metal Oxide ◽  
X Ray Absorption

The term amorphous metal oxide is becoming widely used in the catalysis community. The term is generally used when there are no apparent peaks in an X-ray diffraction pattern. However, the absence of such features in X-ray diffraction can mean that the material is either truly amorphous or that it is better described as nanocrystalline. By coprecipitating a sodium birnessite-like phase with and without phosphate (1.5 %), we are able to engineer two very similar but distinct materials – one that is nanocrystalline and the other that is amorphous. The two closely related phases were characterized with both Mn K-edge X-ray absorption spectroscopy and high-resolution transmission electron microscopy. These structural results were then correlated with catalytic and electrocatalytic activities for water oxidation catalysis. In this case, the amorphous phosphate-doped material was less catalytically active than the nanocrystalline material.

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