106 research outputs found
Sample Preparation Methodologies for In Situ Liquid and Gaseous Cell Analytical Transmission Electron Microscopy of Electropolished Specimens
AbstractIn recent years, an increasing number of studies utilizingin situliquid and/or gaseous cell scanning/transmission electron microscopy (S/TEM) have been reported. Because of the difficulty in the preparation of suitable specimens, these environmental S/TEM studies have been generally limited to studies of nanoscale structured materials such as nanoparticles, nanowires, or sputtered thin films. In this paper, we present two methodologies which have been developed to facilitate the preparation of electron-transparent samples from conventional bulk metals and alloys forin situliquid/gaseous cell S/TEM experiments. These methods take advantage of combining sequential electrochemical jet polishing followed by focused ion beam extraction techniques to create large electron-transparent areas for site-specific observation. As an example, we illustrate the application of this methodology for the preparation ofin situspecimens from a cold-rolled Type 304 austenitic stainless steel sample, which was subsequently examined in both 1 atm of air as well as fully immersed in a H2O environment in the S/TEM followed by hyperspectral imaging. These preparation techniques can be successfully applied as a general procedure for a wide range of metals and alloys, and are suitable for a variety ofin situanalytical S/TEM studies in both aqueous and gaseous environments.</jats:p
Nanometer-scale sharpness in corner-overgrown heterostructures
A corner-overgrown GaAs/AlGaAs heterostructure is investigated with
transmission and scanning transmission electron microscopy, demonstrating
self-limiting growth of an extremely sharp corner profile of 3.5 nm width. In
the AlGaAs layers we observe self-ordered diagonal stripes, precipitating
exactly at the corner, which are regions of increased Al content measured by an
XEDS analysis. A quantitative model for self-limited growth is adapted to the
present case of faceted MBE growth, and the corner sharpness is discussed in
relation to quantum confined structures. We note that MBE corner overgrowth
maintains nm-sharpness even after microns of growth, allowing the realization
of corner-shaped nanostructures.Comment: 4 pages, 3 figure
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Precise determination of atom configuration in partially disordered spinel compounds by HARECSX.
Electron channeling enhanced x-ray spectroscopy has been being widely used to determine ordered arrangement of component atoms in multinary inorganic or metallic crystals. Recent theoretical advancements in the modeling of characteristic x-ray emission by inelastic scattering of incident electrons under dynamical diffraction conditions has achieved remarkable progress, and it has enabled scientists to analyze the experimental intensity of x-ray emission in precise detail. In this study, the ion configuration in magnesium aluminate spinel (MgO{center_dot}nAl{sub 2}O{sub 3}) has been examined by measurements of characteristic x-ray emission as a function of incident electron beam direction at high angular resolution, a technique which we have termed HARECXS (high angular resolution electron channeling x-ray spectroscopy). This paper reports the results and emphasizes the applicability of HARECXS to partially disordered materials
Temperature Dependence of Ion Irradiation Induced Amorphization of Zirconolite
Zirconolite is one of the major host phases for actinides in various wasteforms for immobilizing high level radioactive waste (HLW). Over time, zirconolite's crystalline matrix is damaged by {alpha}-particles and energetic recoil nuclei recoil resulting from {alpha}-decay events. The cumulative damage caused by these particles results in amorphization. Data from natural zirconolites suggest that radiation damage anneals over geologic time and is dependant on the thermal history of the material. Proposed HLW containment strategies rely on both a suitable wasteform and geologic isolation. Depending on the waste loading, depth of burial, and the repository-specific geothermal gradient, burial could result in a wasteform being exposed to temperatures of between 100--450 C. Consequently, it is important to assess the effect of temperature on radiation damage in synthetic zirconolite. Zirconolite containing wasteforms are likely to be hot pressed at or below 1,473 K (1,200 C) and/or sintered at or below 1,623 K (1,350 C). Zirconolite fabricated at temperatures below 1,523 K (1,250 C) contains many stacking faults. As there have been various attempts to link radiation resistance to structure, the authors decided it was also pertinent to assess the role of stacking faults in radiation resistance. In this study, they simulate {alpha}-decay damage in two zirconolite samples by irradiating them with 1.5 MeV Kr{sup +} ions using the High Voltage Electron Microscope-Tandem User Facility (HTUF) at Argonne National Laboratory (ANL) and measure the critical dose for amorphization (D{sub c}) at several temperatures between 20 and 773 K. One of the samples has a high degree of crystallographic perfection, the other contains many stacking faults on the unit cell scale. Previous authors proposed a model for estimating the activation energy of self annealing in zirconolite and for predicting the critical dose for amorphization at any temperature. The authors discuss their results and earlier published data in relation to that model
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Temperature dependence of ion irradiation induced amorphization of zirconolite
Zirconolite is one of the major host phases for actinides in various wasteforms for immobilizing high level radioactive waste (HLW). Over time, zirconolite's crystalline matrix is damaged by {alpha}-particles and energetic recoil nuclei recoil resulting from {alpha}-decay events. The cumulative damage caused by these particles results in amorphization. Data from natural zirconolites suggest that radiation damage anneals over geologic time and is dependant on the thermal history of the material. Proposed HLW containment strategies rely on both a suitable wasteform and geologic isolation. Depending on the waste loading, depth of burial, and the repository-specific geothermal gradient, burial could result in a wasteform being exposed to temperatures of between 100--450 C. Consequently, it is important to assess the effect of temperature on radiation damage in synthetic zirconolite. Zirconolite containing wasteforms are likely to be hot pressed at or below 1,473 K (1,200 C) and/or sintered at or below 1,623 K (1,350 C). Zirconolite fabricated at temperatures below 1,523 K (1,250 C) contains many stacking faults. As there have been various attempts to link radiation resistance to structure, the authors decided it was also pertinent to assess the role of stacking faults in radiation resistance. In this study, they simulate {alpha}-decay damage in two zirconolite samples by irradiating them with 1.5 MeV Kr{sup +} ions using the High Voltage Electron Microscope-Tandem User Facility (HTUF) at Argonne National Laboratory (ANL) and measure the critical dose for amorphization (D{sub c}) at several temperatures between 20 and 773 K. One of the samples has a high degree of crystallographic perfection, the other contains many stacking faults on the unit cell scale. Previous authors proposed a model for estimating the activation energy of self annealing in zirconolite and for predicting the critical dose for amorphization at any temperature. The authors discuss their results and earlier published data in relation to that model
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Future Science Needs and Opportunities for Electron Scattering: Next-Generation Instrumentation and Beyond. Report of the Basic Energy Sciences Workshop on Electron Scattering for Materials Characterization, March 1-2, 2007
To identify emerging basic science and engineering research needs and opportunities that will require major advances in electron-scattering theory, technology, and instrumentation
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Irradiation-assisted stress corrosion cracking of austenitic stainless steels: Recent progress and new approaches
Irradiation-assisted stress corrosion cracking (IASCC) of several types of BWR field components fabricated from solution-annealed austenitic stainless steels (SSs), including a core internal weld, were investigated by means of slow-strain-rate test (SSRT), scanning electron microscopy (SEM), Auger electron spectroscopy (AES), and field-emission-gun advanced analytical electron microscopy (FEG-AAEM). Based on the results of the tests and analyses, separate effects of neutron fluence, tensile properties, alloying elements and major impurities identified in the American Society for Testing and Materials (ASTM) specifications, minor impurities, water chemistry, and fabrication-related variables were determined. The results indicate strongly that minor impurities not specified by the ASTM-specifications play important roles, probably through a complex synergism with grain-boundary Cr depletion. These impurities, typically associated with steelmaking and component fabrication processes, are very low or negligible in solubility in steels and are the same impurities that have been known to promote intergranular SCC significantly when they are present in water as ions or soluble compounds. It seems obvious that IASCC is a complex integral problem which involves many variables that are influenced strongly by not only irradiation conditions, water chemistry, and stress but also iron and steelmaking processes, fabrication of the component, and joining and welding. Therefore, for high-stress components in particular, it would be difficult to mitigate IASCC problems at high fluence based on the consideration of water chemistry alone, and other considerations based on material composition and fabrication procedure would be necessary as well
Quantitation of synthetic polymers using an internal standard by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry
In-source H/D exchange and ion-molecule reactions using matrix assisted laser desorption/ionization Fourier transform ion cyclotron resonance mass spectrometry with pulsed collision and reaction gases
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