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Izabela Szlufarska

Publications and source records attributed to Izabela Szlufarska.

At least 37 records · Page 2Linked to original sources

Exploration of Characteristic Temperature Contributions to Metallic Glass Forming Ability

Various combinations of characteristic temperatures, such as the glass transition temperature, liquidus temperature, and crystallization temperature, have been proposed as predictions of the glass forming ability of metal alloys. We have used statistical approaches from machine learning to systematically explore a wide range of possible characteristic temperature functions for predicting glass forming ability in the form of critical casting diameter, $D_{max}$. Both linear and non-linear models were used to learn on the largest database of $D_{max}$ values to date consisting of 747 compositions. We find that no combination of temperatures for features offers a better prediction of $D_{max}$ in a machine learning model than the temperatures themselves, and that regression models suffer from poor performance on standard machine learning metrics like root mean square error (minimum value of $3.3 \pm 0.1$ $mm$ for data with a standard deviation of 4.8 $mm$). Examination of the errors vs. database size suggest that a larger database may improve results, although a database significantly larger than that used here would likely be required. Shifting a focus from regression to categorization models learning from characteristic temperatures can be used to weakly distinguish glasses likely to be above vs. below our database's median $D_{max}$ value of 4.0 $mm$, with a mean F1 score of $0.77 \pm 0.02$ for this categorization. The overall weak results on predicting $D_{max}$ suggests that critical cooling rate might be a better target for machine learning model prediction.

cond-mat.mtrl-sci↗

Deciphering water-solid reactions during hydrothermal corrosion of SiC

Water solid interfacial reactions are critical to understanding corrosion. More specifically, it is notoriously difficult to determine how water and solid interact beyond the initial chemisorption to induce the surface dissolution. Here, we report atomic-scale mechanisms of the elementary steps during SiC hydrothermal corrosion, from the initial surface attack to surface dissolution. We find that hydrogen scission reactions play a vital role in breaking Si-C bonds, regardless of the surface orientations. Stable silica layer does not form on the surface, but the newly identified chemical reactions on SiC are analogous to those observed during the dissolution of silica. SiC is dissolved directly into the water as soluble silicic acid. The rate of hydrothermal corrosion determined based on the calculated reaction activation energies is consistent with available experimental data. Our work sheds new light on understanding and interpreting the experimental observations and it provides foundation for design of materials that are resistant to corrosion in water.

physics.chem-ph↗

Effects of point defects on oxidation of 3C-SiC

The influence of implantation-induced point defects (PDs) on SiC oxidation is investigated via molecular dynamics simulations. PDs generally increase the oxidation rate of crystalline grains. Particularly, accelerations caused by Si antisites and vacancies are comparable, and followed by Si interstitials, which are higher than those by C antisites and C interstitials. However, in the grain boundary (GB) region, defect contribution to oxidation is more complex, with C antisites decelerating oxidation. The underlying reason is the formation of a C-rich region along the oxygen diffusion pathway that blocks the access of O to Si and thus reduces the oxidation rate, as compared to the oxidation along a GB without defects.

cond-mat.mtrl-sci↗

An Unexpected Role of H During SiC Corrosion in Water

During aqueous corrosion, atoms in the solid react chemically with oxygen, leading either to the formation of an oxide film or to the dissolution of the host material. Commonly, the first step in corrosion involves an oxygen atom from the dissociated water that reacts with the surface atoms and breaks near surface bonds. In contrast, hydrogen on the surface often functions as a passivating species. Here, we discovered that the roles of O and H are reversed in the early corrosion stages on a Si terminated SiC surface. O forms stable species on the surface, and chemical attack occurs by H that breaks the Si-C bonds. This so-called hydrogen scission reaction is enabled by a newly discovered metastable bridging hydroxyl group that can form during water dissociation. The Si atom that is displaced from the surface during water attack subsequently forms H2SiO3, which is a known precursor to the formation of silica and silicic acid. This study suggests that the roles of H and O in oxidation need to be reconsidered.

cond-mat.mtrl-sci↗

Physical Origin of the Mechanochemical Coupling at Interfaces

We used density functional theory (DFT) calculations to investigate the physical origin of the mechano-chemical response of materials interfaces. Our results show that the mechano-chemical response can be decomposed into the contribution from the interface itself (deformation of interfacial bonds) and a contribution from the underlying solid. The relative contributions depend on the stiffness of these regions and the contact geometry, which affects the stress distribution within the bulk region. We demonstrate that, contrary to what is commonly assumed, the contribution to the activation volume from the elastic deformation of the surrounding bulk is significant and, in some case, may be dominant. We also show that the activation volume and the mechanochemical response of interfaces should be finite due to the effects on the stiffness and stress distribution within the near-surface bulk region. Our results indicate that the large range of activation volumes measured in the previous experiments even for the same material system might originate from the different degrees of contributions probed from the bulk vs. interface.

cond-mat.mtrl-sci↗

Structural Signatures for Thermodynamic Stability in Vitreous Silica: Insight from Machine Learning and Molecular Dynamics Simulations

The structure-thermodynamic stability relationship in vitreous silica is investigated using machine learning and a library of 24,157 inherent structures generated from melt-quenching and replica exchange molecular dynamics simulations. We find the thermodynamic stability, i.e., enthalpy of the inherent structure ($e_{\mathrm{IS}}$), can be accurately predicted by both linear and nonlinear machine learning models from numeric structural descriptors commonly used to characterize disordered structures. We find short-range features become less indicative of thermodynamic stability below the fragile-to-strong transition. On the other hand, medium-range features, especially those between 2.8-~6 $\unicode{x212B}$;, show consistent correlations with $e_{\mathrm{IS}}$ across the liquid and glass regions, and are found to be the most critical to stability prediction among features from different length scales. Based on the machine learning models, a set of five structural features that are the most predictive of the silica glass stability is identified.

cond-mat.dis-nn↗

Defect behavior and radiation tolerance of MAB phases (MoAlB and Fe2AlB2) with comparison to MAX phases

MAB phases are a new class of layered ternary materials that have already shown a number of outstanding properties. Here, we investigate defect evolution and radiation tolerance of two MAB phases, MoAlB and Fe2AlB2, using a combination of experimental characterization and first-principles calculations. We find that Fe2AlB2 is more tolerant to radiation-induced amorphization than MoAlB, both at 150 °C and at 300 °C. The results can be explained by the fact that the Mo Frenkel pair is unstable in MoAlB and as a result, irradiated MoAlB is expected to have a significant concentration of MoAl antisites, which are difficult to anneal even at 300 °C. We find that the tolerance to radiation-induced amorphization of MAB phases is lower than in MAX phases, but it is comparable to that of SiC. However, MAB phases do not show radiation-induced cracking which is observed in MAX phases under the same irradiation conditions. This study suggests that MAB phases might be a promising class of materials for applications that involve radiation.

cond-mat.mtrl-sci↗

Helium effects and bubbles formation in irradiated Ti3SiC2

Ti3SiC2 is a potential structural material for nuclear reactor applications. However, He irradiation effects in this material are not well understood, especially at high temperatures. Here, we compare the effects of He irradiation in Ti3SiC2 at room temperature (RT) and at 750 °C. Irradiation at 750 °C was found to lead to extremely elongated He bubbles that are concentrated in the nano-laminate layers of Ti3SiC2, whereas the overall crystal structure of the material remained intact. In contrast, at RT, the layered structure was significantly damaged and highly disordered after irradiation. Our study reveals that at elevated temperatures, the unique structure of Ti3SiC2 can accommodate large amounts of He atoms in the nano-laminate layer, without compromising the structural stability of the material. The structure and the mechanical tests results show that the irradiation induced swelling and hardening at 750 °C are much smaller than those at RT. These results indicate that Ti3SiC2 has an excellent resistance to accumulation of radiation-induced He impurities and that it has a considerable tolerance to irradiation-induced degradation of mechanical properties at high temperatures.

cond-mat.mtrl-sci↗

Corrosion of Si, C, and SiC in molten salt

Corrosion of Si, C, and SiC in fluoride salt has been studied by ab initio molecular dynamics. The standard dissolution potential for Si is found to be smaller (easier to corrode) than that of C. The dissolved Si attracts F- ions and forms SiF62-, whereas the dissolved C species forms neutral CF4 molecules. A swapping mechanism is identified for the initial corrosion stage, where Si first comes to the surface and then is dissolved, leaving behind chain- and ring-like C structures. A strategy to suppress SiC corrosion is also discussed based on Be doping, including avoiding Be2C formation.

physics.comp-ph↗

Chemical aging of large-scale randomly rough frictional contacts

It has been shown that contact aging due to chemical reactions in single asperity contacts can have a significant effect on friction. However, it is currently unknown how chemically-induced contact aging of friction depends on roughness that is typically encountered in macroscopic rough contacts. Here, we develop an approach that brings together a kinetic Monte Carlo model of chemical aging with a contact mechanics model of rough surfaces based on the boundary element method to determine the magnitude of chemical aging in silica/silica contacts with random roughness. Our multi-scale model predicts that chemical aging for randomly rough contacts has a logarithmic dependence on time. It also shows that friction aging switches from a linear to a non-linear dependence on the applied load as the load increase. We discover that surface roughness affects the aging behavior primarily by modifying the real contact area and the local contact pressure, whereas the effect of contact morphology is relatively small. Our results demonstrate how understanding of chemical aging can be translated from studies of single asperity contacts to macroscopic rough contacts.

cond-mat.mtrl-sci↗

Multiphysics model of chemical aging in frictional contacts

An increase of static friction during stationary contacts of two solids due to interfacial chemical bonding has been reported in multiple experiments. However, the physics underlying such frictional aging is still not fully understood because it involves multiple physical and chemical effects coupled with each other, making direct interpretation of experimental results difficult. Here, we develop a multiphysics chemical aging model that combines contact mechanics, mechanochemistry, and interfacial chemical reaction kinetics. Our model predicts that aging is proportional to normal loads in a low-load regime and becomes nonlinear at higher loads. We also discovered a nonmonotonic temperature dependence of aging with a peak near room temperature. In addition, our simulations provide insights into contributions from specific physical/chemical effects on the overall aging. Our model shows quantitative agreement with available single-asperity experiments on silica-silica interfaces, and it provides a framework for building a chemical aging model for other material systems with arbitrary types of physical and chemical effects involved.

cond-mat.soft↗

Cs diffusion in SiC high-energy grain boundaries

Cesium (Cs) is a radioactive fission product whose release is of concern for Tristructural-Isotropic (TRISO) fuel particles. In this work, Cs diffusion through high energy grain boundaries (HEGBs) of cubic-SiC is studied using an ab-initio based kinetic Monte Carlo (kMC) model. The HEGB environment was modeled as an amorphous SiC (a-SiC), and Cs defect energies were calculated using density functional theory (DFT). From defect energies, it was suggested that the fastest diffusion mechanism as Cs interstitial in an amorphous SiC. The diffusion of Cs interstitial was simulated using a kMC, based on the site and transition state energies sampled from the DFT. The Cs HEGB diffusion exhibited an Arrhenius type diffusion in the range of 1200-1600°C. The comparison between HEGB results and the other studies suggests not only that the GB diffusion dominates the bulk diffusion, but also that the HEGB is one of the fastest grain boundary paths for the Cs diffusion. The diffusion coefficients in HEGB are clearly a few orders of magnitude lower than the reported diffusion coefficients from in- and out-of- pile samples, suggesting that other contributions are responsible, such as a radiation enhanced diffusion.

cond-mat.mtrl-sci↗

Optimization of self-interstitial clusters in 3C-SiC with Genetic Algorithm

Under irradiation, SiC develops damage commonly referred to as black spot defects, which are speculated to be self-interstitial atom clusters. To understand the evolution of these defect clusters and their impacts (e.g., through radiation induced swelling) on the performance of SiC in nuclear applications, it is important to identify the cluster composition, structure, and shape. In this work the genetic algorithm code StructOpt was utilized to identify groundstate cluster structures in 3C-SiC. The genetic algorithm was used to explore clusters of up to ~30 interstitials of C-only, Si-only, and Si-C mixtures embedded in the SiC lattice. We performed the structure search using Hamiltonians from both density functional theory and empirical potentials. The thermodynamic stability of clusters was investigated in terms of their composition (with a focus on Si-only, C-only, and stoichiometric) and shape (spherical vs. planar), as a function of the cluster size (n). Our results suggest that large Si-only clusters are likely unstable, and clusters are predominantly C-only for n <= 10 and stoichiometric for n > 10. The results imply that there is an evolution of the shape of the most stable clusters, where small clusters are stable in more spherical geometries while larger clusters are stable in more planar configurations. We also provide an estimated energy vs. size relationship, E(n), for use in future analysis.

cond-mat.mtrl-sci↗

Continuum model for hydrogen pickup in Zirconium alloys of LWR fuel cladding

A continuum model for calculating the time-dependent hydrogen pickup fractions in various Zirconium alloys under steam and pressured water oxidation has been developed in this study. Using only one fitting parameter, the effective hydrogen gas partial pressure at the oxide surface, a qualitative agreement is obtained between the predicted and previously measured hydrogen pickup fractions. The calculation results therefore demonstrate that H diffusion through the dense oxide layer plays an important role in the hydrogen pickup process. The limitations and possible improvement of the model are also discussed.

cond-mat.mtrl-sci↗

Size Dependence of Nanoscale Wear of Silicon Carbide

Nanoscale, single-asperity wear of single-crystal silicon carbide (sc-SiC) and nanocrystalline silicon carbide (nc-SiC) is investigated using single-crystal diamond nanoindenter tips and nanocrystalline diamond atomic force microscopy (AFM) tips under dry conditions, and the wear behavior is compared to that of single-crystal silicon with both thin and thick native oxide layers. We discovered a transition in the relative wear resistance of the SiC samples compared to that of Si as a function of contact size. With larger nanoindenter tips (tip radius around 370 nm), the wear resistances of both sc-SiC and nc-SiC are higher than that of Si. This result is expected from the Archard's equation because SiC is harder than Si. However, with the smaller AFM tips (tip radius around 20 nm), the wear resistances of sc-SiC and nc-SiC are lower than that of Si, despite the fact that the contact pressures are comparable to those applied with the nanoindenter tips, and the plastic zones are well-developed in both sets of wear experiments. We attribute the decrease in the relative wear resistance of SiC compared to that of Si to a transition from a wear regime dominated by the materials' resistance to plastic deformation (i.e., hardness) to a regime dominated by the materials' resistance to interfacial shear. This conclusion is supported by our AFM studies of wearless friction, which reveal that the interfacial shear strength of SiC is higher than that of Si. The contributions of surface roughness and surface chemistry to differences in interfacial shear strength are also discussed.

cond-mat.mtrl-sci↗

Modeling the Effect of Dissolved Hydrogen Sulfide on Mg2+-water Complex on Dolomite {104} Surfaces

The key kinetic barrier to dolomite formation is related to the surface Mg2+-H2O complex, which hinders binding of surface Mg2+ ions to the CO3 2- ions in solution. It has been proposed that this reaction can be catalyzed by dissolved hydrogen sulfide. To characterize the role of dissolved hydrogen sulfide in the dehydration of surface Mg 2+ ions, ab initio simulations based on density functional theory (DFT) were carried out to study the thermodynamics of competitive adsorption of hydrogen sulfide and water on dolomite (104) surfaces from solution. We find that water is thermodynamically more stable on the surface with the difference in adsorption energy of -13.6 kJ/mol (in vacuum) and -12.8 kJ/mol (in aqueous solution). However, aqueous hydrogen sulfide adsorbed on the surface increases the Mg2+-H2O distances on surrounding surface sites. Two possible mechanisms were proposed for the catalytic effects of adsorbed hydrogen sulfide on the anhydrous Ca-Mg-carbonate crystallization at low temperature.

physics.geo-ph↗

Investigation of the role of polysaccharide in the dolomite growth at low temperature by using atomistic simulations

Dehydration of water from surface Mg2+ is most likely the rate-limiting step in the dolomite growth at low temperature. Here, we investigate the role of polysaccharide in this step using classical molecular dynamics (MD) calculations. Free energy (potential of mean force, PMF) calculations have been performed for water molecules leaving the first two hydration layers above the dolomite (104) surface under the following three conditions: without catalyst, with monosaccharide (mannose) and with oligosaccharide (three units of mannose). MD simulations reveal that there is no obvious effect of monosaccharide in lowering the dehydration barrier for surface Mg2+. However, we found that there are metastable configurations of oligosaccharide, which can decrease the dehydration barrier of surface Mg2+ by about 0.7-1.1 kcal/mol. In these configurations, the molecule lies relatively flat on the surface and forms a bridge shape. The hydrophobic space near the surface created by the non-polar -CH groups of the oligosaccharide in the bridge conformation is the reason for the observed reduction of dehydration barrier.

physics.geo-ph↗

Z-contrast imaging and ab initio study on "d" superstructure in sedimentary dolomite

Nano-precipitates with tripled periodicity along the c-axis are observed in a Ca-rich dolomite sample from Proterozoic carbonate rocks with "molar tooth" structure. This observation is consistent with previous description of d reflections. High-angle annular dark-field STEM imaging (or Z-contrast imaging) that avoids dynamic diffraction as seen in electron diffraction and high-resolution TEM imaging modes, confirms that d reflections correspond to nanoscale precipitates aligned parallel to (001) of the host dolomite. The lamellae precipitates have a cation ordering sequence of Ca-Ca-Mg-Ca-Ca- Mg along the c direction resulting in a chemical composition of Ca0.67Mg0.33CO3. This superstructure is attributed to the extra or d reflections, thus is referred to as the d superstructure in this study. The structure can be simply described as interstratified calcite/dolomite. The crystal structure of the d superstructure calculated from density functional theory (DFT) has a space group of P31c and has a and c unit-cell parameters of 4.879 and 16.260 Å, respectively, values between those of dolomite and calcite. The detailed structural characteristics and parameters obtained from ab initio calculations are also reported in this paper. The method of combining Z-contrast imaging and ab initio calculations can be used for solving structures of other nano-precipitates and nano-phases.

physics.geo-ph↗