Molecular dynamics simulations of shear band development over 1000% strain in simple shear are used to test whether the local plastic strain rate is proportional to exp(-1/chi), where chi is a dimensionless quantity related to the disorder temperature or free volume that characterizes the structural state of the glass. Scaling is observed under the assumption that chi is linearly related to the local potential energy per atom. We calculate the potential energy per atom corresponding to absolute zero disorder temperature and the energy needed to create a shear transformation zone.
Aberration-corrected transmission electron microscopy was used to study atomic-scale processes in Pd-LaFeO(3) catalysts. Clear evidence for diffusion of Pd into LaFeO(3) and out of LaFe(0.95)Pd(0.05)O(3-δ) under high-temperature oxidizing and reducing conditions, respectively, was found, but the extent to which these processes occurred was quite limited. These observations cast doubt that such phenomena play a significant role in a postulated mechanism of self-regeneration of this system as an automotive exhaust-gas catalyst.
AbstractIn prior research, specimen holders that employ a novel MEMS-based heating technology (AduroTM) provided by Protochips Inc. (Raleigh, NC, USA) have been shown to permit sub-Ångström imaging at elevated temperatures up to 1,000°C duringin situheating experiments in modern aberration-corrected electron microscopes. The Aduro heating devices permit precise control of temperature and have the unique feature of providing both heating and cooling rates of 106°C/s. In the present work, we describe the recent development of a new specimen holder that incorporates the Aduro heating device into a “closed-cell” configuration, designed to function within the narrow (2 mm) objective lens pole piece gap of an aberration-corrected JEOL 2200FS STEM/TEM, and capable of exposing specimens to gases at pressures up to 1 atm. We show the early results of tests of this specimen holder demonstrating imaging at elevated temperatures and at pressures up to a full atmosphere, while retaining the atomic resolution performance of the microscope in high-angle annular dark-field and bright-field imaging modes.
The microstructural evolution of laser powder-bed additively manufactured Inconel 625 during a post-build stress-relief anneal of 1 hour at 1143 K (870°C) is investigated. It is found that this industry-recommended heat treatment promotes the formation of a significant fraction of the orthorhombic D0 a Ni 3 Nb d-phase. This phase is known to have a deleterious influence on fracture toughness, ductility, and other mechanical properties in conventional, wrought Inconel 625; and is generally considered detrimental to materials' performance in service. The d-phase platelets are found to precipitate within the inter-dendritic regions of the as-built solidification microstructure. These regions are enriched in solute elements, particularly Nb and Mo, due to the micro-segregation that occurs during solidification. The precipitation of d-phase at 1073 K (800°C) is found to require up to 4 hours. This indicates a potential alternative stress-relief processing window that mitigates d-phase formation in this alloy. Ultimately, a homogenization heat treatment is recommended for additively manufactured Inconel 625 because the increased susceptibility to d-phase precipitation increases the possibility for significant degradation of materials' properties in service.
Ferroelectric domain structures of epitaxial BiFeO 3 thin films on miscut ͑001͒ SrTiO 3 substrates have been studied by transmission electron microscopy. BiFeO 3 on 0.8°miscut substrates are composed of both 109°and 71°domains; in contrast, only 71°stripe domains are observed in BiFeO 3 on 4°miscut ͑001͒ SrTiO 3 substrates. The domain width in BiFeO 3 on 4°miscut substrates increases as film thickness increases due to a reduction in domain wall energy. The domain configurations of BiFeO 3 thin films affect their ferroelectric switching behavior due to the pinning at the junctions between 109°and 71°domain walls.
Surface
phonon polaritons (SPhPs), the surface-bound electromagnetic
modes of a polar material resulting from the coupling of light with
optic phonons, offer immense technological opportunities for nanophotonics
in the infrared (IR) spectral region. However, once a particular material
is chosen, the SPhP characteristics are fixed by the spectral positions
of the optic phonon frequencies. Here, we provide a demonstration
of how the frequency of these optic phonons can be altered by employing
atomic-scale superlattices (SLs) of polar semiconductors using AlN/GaN
SLs as an example. Using second harmonic generation (SHG) spectroscopy,
we show that the optic phonon frequencies of the SLs exhibit a strong
dependence on the layer thicknesses of the constituent materials.
Furthermore, new vibrational modes emerge that are confined to the
layers, while others are centered at the AlN/GaN interfaces. As the
IR dielectric function is governed by the optic phonon behavior in
polar materials, controlling the optic phonons provides a means to
induce and potentially design a dielectric function distinct from
the constituent materials and from the effective-medium approximation
of the SL. We show that atomic-scale AlN/GaN SLs instead have multiple
Reststrahlen bands featuring spectral regions that exhibit either
normal or extreme hyperbolic dispersion with both positive and negative
permittivities dispersing rapidly with frequency. Apart from the ability
to engineer the SPhP properties, SL structures may also lead to multifunctional
devices that combine the mechanical, electrical, thermal, or optoelectronic
functionality of the constituent layers. We propose that this effort
is another step toward realizing user-defined, actively tunable IR
optics and sources.
Using pulsed laser deposition, TiO2 (-) B and its recently discovered variant Ca:TiO2 (-) B (CaTi5O11) are synthesized as highly crystalline thin films for the first time by a completely water-free process. Significant enhancement in the Li-ion battery performance is achieved by manipulating the crystal orientation of the films, used as anodes, with a demonstration of extraordinary structural stability under extreme conditions.
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