Effects of anisotropy on the equilibrium shape of nanoscale pores at grain boundaries

Molecular dynamics simulations have been performed to study the interaction between a faceted pore and an anisotropic grain boundary (GB). Nickel was chosen as a convenient model system. In order to establish the equilibrium crystal shape (ECS) of the pore, studies were also conducted on isolated pores. Isolated pores were found to be subject to the nucleation inhibition of equilibration that has been predicted by Rohrer et al. (J Am Ceram Soc 2000;83:214, 2001;84: 2099). This work shows that configurations close to the ECS can be obtained if supersaturation within a pore is artificially increased by adding mobile adatoms to the internal surfaces of the pores. In the case of pores located at GBs, the nucleation energy barriers to facet displacement are not present for facets in contact with the GB at the triple line, but may still persist for facets that have no contact with the GB. This problem can be overcome by approaching the equilibrium shape from different initial configurations. The configuration of the GB in the vicinity of the pore has been found to be essentially planar, indicating that GB puckering in the vicinity of anisotropic pores is not generally necessary. The present calculations show that incompatibilities between misoriented pore facets that meet at the triple line with the GB are easily accommodated by local atomic rearrangements at the disordered region of intersection with the GB

Prewetting transition on a weakly disordered substrate : evidence for a creeping film dynamics

We present the first microscopic images of the prewetting transition of a liquid film on a solid surface. Pictures of the local coverage map of a helium film on a cesium metal surface are taken while the temperature is raised through the transition. The film edge is found to advance at constant temperature by successive avalanches in a creep motion with a macroscopic correlation length. The creep velocity varies strongly in a narrow temperature range. The retreat motion is obtained only at much lower temperature, conforming to the strong hysteresis observed for prewetting transition on a disordered surface. Prewetting transition on such disordered surfaces appears to give rise to dynamical phenomena similar to what is observed for domain wall motions in 2D magnets.Comment: 7 pages, 3 figures, to be published in Euro.Phys.Let

Динамическая устойчивость работы ветроэлектростанций в составе электроэнергетических систем

Объектом исследования являются: модели энергосистем, тепловая электростанция мощностью 556 МВт. Цель работы – исследование динамической устойчивости крупных ветроферм, работающих в энергосистеме, оценка влияния внедрения ветроэлектростанций на динамическую устойчивость синхронных генераторов энергосистемы. Выпускная квалификационная работа выполнена с помощью программ MS Excel, MS Visio, PSS/E, EnergyPRO Software в текстовом редакторе MS Word.Objects of the research: power system models, thermal power station with total capacity 556 MW. Object of the work – investigation of dynamic stability of large wind farms, working in power system, evaluation of wind farms implementation influence on large synchronous generators of power system. Master thesis work was performed in MS Word, MS Excel, MS Visio, PSS/E, EnergyPRO Software

Normal scaling in globally conserved interface-controlled coarsening of fractal clusters

Globally conserved interface-controlled coarsening of fractal clusters exhibits dynamic scale invariance and normal scaling. This is demonstrated by a numerical solution of the Ginzburg-Landau equation with a global conservation law. The sharp-interface limit of this equation is volume preserving motion by mean curvature. The scaled form of the correlation function has a power-law tail accommodating the fractal initial condition. The coarsening length exhibits normal scaling with time. Finally, shrinking of the fractal clusters with time is observed. The difference between global and local conservation is discussed.Comment: 4 pages, 3 eps figure

Decay of isolated surface features driven by the Gibbs-Thomson effect in analytic model and simulation

A theory based on the thermodynamic Gibbs-Thomson relation is presented which provides the framework for understanding the time evolution of isolated nanoscale features (i.e., islands and pits) on surfaces. Two limiting cases are predicted, in which either diffusion or interface transfer is the limiting process. These cases correspond to similar regimes considered in previous works addressing the Ostwald ripening of ensembles of features. A third possible limiting case is noted for the special geometry of "stacked" islands. In these limiting cases, isolated features are predicted to decay in size with a power law scaling in time: A is proportional to (t0-t)^n, where A is the area of the feature, t0 is the time at which the feature disappears, and n=2/3 or 1. The constant of proportionality is related to parameters describing both the kinetic and equilibrium properties of the surface. A continuous time Monte Carlo simulation is used to test the application of this theory to generic surfaces with atomic scale features. A new method is described to obtain macroscopic kinetic parameters describing interfaces in such simulations. Simulation and analytic theory are compared directly, using measurements of the simulation to determine the constants of the analytic theory. Agreement between the two is very good over a range of surface parameters, suggesting that the analytic theory properly captures the necessary physics. It is anticipated that the simulation will be useful in modeling complex surface geometries often seen in experiments on physical surfaces, for which application of the analytic model is not straightforward.Comment: RevTeX (with .bbl file), 25 pages, 7 figures from 9 Postscript files embedded using epsf. Submitted to Phys. Rev. B A few minor changes made on 9/24/9

Microscopic View on Short-Range Wetting at the Free Surface of the Binary Metallic Liquid Gallium-Bismuth: An X-ray Reflectivity and Square Gradient Theory Study

We present an x-ray reflectivity study of wetting at the free surface of the binary liquid metal gallium-bismuth (Ga-Bi) in the region where the bulk phase separates into Bi-rich and Ga-rich liquid phases. The measurements reveal the evolution of the microscopic structure of wetting films of the Bi-rich, low-surface-tension phase along different paths in the bulk phase diagram. A balance between the surface potential preferring the Bi-rich phase and the gravitational potential which favors the Ga-rich phase at the surface pins the interface of the two demixed liquid metallic phases close to the free surface. This enables us to resolve it on an Angstrom level and to apply a mean-field, square gradient model extended by thermally activated capillary waves as dominant thermal fluctuations. The sole free parameter of the gradient model, i.e. the so-called influence parameter, $\kappa$, is determined from our measurements. Relying on a calculation of the liquid/liquid interfacial tension that makes it possible to distinguish between intrinsic and capillary wave contributions to the interfacial structure we estimate that fluctuations affect the observed short-range, complete wetting phenomena only marginally. A critical wetting transition that should be sensitive to thermal fluctuations seems to be absent in this binary metallic alloy.Comment: RevTex4, twocolumn, 15 pages, 10 figure

Measuring the surface stress polar dependence

While measurements of the polar dependence of the surface free energy are easily available, measurements of the whole polar dependence of the surface stress of a crystal do not exist. In this paper is presented a new procedure that allows, for the first time, the experimental determination of the surface stress polar dependence of a crystal. For this purpose (1) electromigration is used to control the kinetic faceting of surface orientations that belong to the equilibrium shape of the crystal and (2) for each destabilised surface, the period of faceting as well as the crystallographic angles of the appearing facets are measured by AFM. The so-obtained data lead to a set of equations whose mathematical solution, compatible with physical constraints, gives access to the surface stress polar dependence of the whole crystal and thus to a better understanding of surface stress properties.Comment: 8 pages, 6 Figure

Microstructure and thermal stability of Fe, Ti and Ag implanted Yttria-stabilized zirconia

Yttria-stabilized zirconia (YSZ) was implanted with 15 keV Fe or Ti ions up to a dose of 8×1016 at cm−2. The resulting “dopant” concentrations exceeded the concentrations corresponding to the equilibrium solid solubility of Fe2O3 or TiO2 in YSZ. During oxidation in air at 400° C, the Fe and Ti concentration in the outermost surface layer increased even further until a surface layer was formed of mainly Fe2O3 and TiO2, as shown by XPS and ISS measurements. From the time dependence of the Fe and Ti depth profiles during anneal treatments, diffusion coefficients were calculated. From those values it was estimated that the maximum temperature at which the Fe- and Ti-implanted layers can be operated without changes in the dopant concentration profiles was 700 and 800° C, respectively. The high-dose implanted layer was completely amorphous even after annealing up to 1100° C, as shown by scanning transmission electron microscopy. Preliminary measurements on 50 keV Ag implanted YSZ indicate that in this case the amorphous layer recrystallizes into fine grained cubic YSZ at a temperature of about 1000° C. The average grain diameter was estimated at 20 nm, whereas the original grain size of YSZ before implantation was 400 nm. This result implies that the grain size in the surface of a ceramic material can be decreased by ion beam amorphisation and subsequent recrystallisation at elevated temperatures

Anomalous coarsening driven by reversible charge transfer at metal–organic interfaces

The unique electronic properties and functional tunability of polycyclic aromatic hydrocarbons have recently fostered high hopes for their use in flexible, green, portable, and cheap technologies. Most applications require the deposition of thin molecular films onto conductive electrodes. The growth of the first few molecular layers represents a crucial step in the device fabrication since it determines the structure of the molecular film and the energy level alignment of the metal–organic interface. Here, we explore the formation of this interface by analyzing the interplay between reversible molecule–substrate charge transfer, yielding intermolecular repulsion, and van der Waals attractions in driving the molecular assembly. Using a series of ad hoc designed molecules to balance the two effects, we combine scanning tunnelling microscopy with atomistic simulations to study the self-assembly behavior. Our systematic analysis identifies a growth mode characterized by anomalous coarsening that we anticipate to occur in a wide class of metal–organic interfaces and which should thus be considered as integral part of the self-assembly process when depositing a molecule on a conducting surface

Direct Observations of Oxygen-induced Platinum Nanoparticle Ripening Studied by In Situ TEM

This study addresses the sintering mechanism of Pt nanoparticles dispersed on a planar, amorphous Al2O3 support as a model system for a catalyst for automotive exhaust abatement. By means of in situ transmission electron microscopy (TEM), the model catalyst was monitored during the exposure to 10 mbar air at 650 degrees C. Time-resolved image series unequivocally reveal that the sintering of Pt nanoparticles was mediated by an Ostwald ripening process. A statistical analysis of an ensemble of Pt nanoparticles shows that the particle size distributions change shape from an initial Gaussian distribution via a log-normal distribution to a Lifshitz-Slyozov-Wagner (LSW) distribution. Furthermore, the time-dependency of the ensemble-averaged particle size and particle density is determined. A mean field kinetic description captures the main trends in the observed behavior. However, at the individual nanoparticle level, deviations from the model are observed suggesting in part that the local environment influences the atom exchange process