arXiv subjects

F. J. Dominguez-Gutierrez

Publications and source records attributed to F. J. Dominguez-Gutierrez.

At least 19 recordsLinked to original sources

arXiv2026

High-Temperature Deformation Behavior of Co-Free Non-Equiatomic CrMnFeNi Alloy

Cobalt-free high-entropy alloys (HEAs) have garnered interest for nuclear structural applications due to their good mechanical performance, thermal stability, and resistance to radiation-induced degradation, while avoiding long-lived Co radioisotopes. This study presents an experimental and computational investigation of the plastic deformation behavior of a non-equatomic CrMnFeNi alloy, designed to maintain a stability of fcc phase in a large domain of temperatures and to balance stacking fault (SF) energies for enhanced strain hardening and ductility. Tensile tests reveal a temperature-dependent reduction in mechanical strength, attributed to thermally activated deformation mechanisms and microstructural evolution. Molecular dynamics simulations of single- and polycrystals capture dislocation activity, SF formation, and twin nucleation as a function of strain and temperature. Electron backscatter diffraction (EBSD) confirms twin formation and grain boundary activity. The Schmid factor mapping is drawn to interpret local slip activity and anisotropic deformation behavior. The absence of Co leads to enhanced high-temperature strength compared to the Cantor alloy.

cond-mat.mtrl-sci↗

arXiv2026

A literature-grounded scientific reasoning framework for defect-engineered TiO$_{2}$ photocatalysts

Defect-engineered TiO$_2$ photocatalysts are extensively investigated for photocatalytic hydrogen evolution; however, the highly heterogeneous nature of the literature, including inconsistent descriptors, diverse synthesis protocols, non-uniform activity metrics, and incomplete mechanistic reporting, limits the applicability of conventional machine-learning approaches based solely on statistical regression. Here, we present a literature-grounded large language model (LLM)-assisted scientific reasoning framework for defect-engineered TiO$_2$ photocatalysts integrating curated literature data, mechanistic rule extraction, and retrieval-augmented reasoning. A harmonized database was constructed from experimentally relevant publications specifically selected for hydrogen-evolution-related defect engineering in TiO$_2$, covering polymorph-dependent behavior, hydrogenation conditions, Ti$^{3+}$ defect states, oxygen vacancies, illumination conditions, and photocatalytic activity descriptors. In parallel, mechanistic evidence sentences and publications-defined scientific rules were encoded into a structured reasoning layer enabling explainable inference beyond black-box prediction. The resulting framework combines structured experimental descriptors, semantic literature retrieval, and mechanistic interpretation to generate confidence-aware recommendations for optimal defect-engineering conditions. For example, the AI agent identified a consistent optimal anatase hydrogenation window centered at ~500 $°$C under H$_2$-containing atmospheres for approximately 1 h, supported by mechanistic evidence linking balanced Ti$^{3+}$/oxygen-vacancy populations with enhanced photocatalytic hydrogen evolution.

cond-mat.mtrl-sci↗

arXiv2026

Influence of Manganese Content on Plastic Deformation Mechanisms in Polycrystalline α-Ti-Mn Alloys

Titanium alloys are widely used in aerospace, biomedical, and energy applications owing to their high specific strength, corrosion resistance, and biocompatibility. Among them, $α$-titanium alloys with a hexagonal close-packed (hcp) crystal structure exhibit characteristic deformation mechanisms governed by crystallographic slip and defect evolution. In this study, the influence of manganese content on the plastic deformation mechanisms of polycrystalline $α$-Ti-2Mn and $α$-Ti-4Mn (at.%) alloys is investigated using molecular dynamics simulations. Atomistic models were subjected to uniaxial loading at room temperature at a strain rate of 10$^9$ s$^{-1}$. The mechanical response was evaluated through stress-strain behavior, structural evolution, dislocation nucleation and interaction, and analysis of the local deformation field. Plastic deformation in these $α$-Ti-Mn alloys is dominated by dislocation nucleation and their subsequent evolution within the hcp lattice. Increasing Mn content leads to higher stress levels and enhanced resistance to plastic deformation, accompanied by changes in dislocation activity and defect evolution.

cond-mat.mtrl-sci↗

arXiv2026

Nanoindentation induced plasticity in equiatomic MoTaW alloys by experimentally guided machine learning molecular dynamics simulations

Refractory complex concentrated alloys (RCCA) exhibit exceptional strength and thermal stability, yet their plastic deformation mechanisms under complex contact loading remain insufficiently understood. Here, the nanoindentation response of an equiatomic MoTaW alloy is investigated through a combined experimental and atomistically resolved modeling approach. Spherical nanoindentation experiments are coupled with large scale molecular dynamics simulations employing a tabulated low dimensional Gaussian Approximation Potential (tabGAP), enabling near DFT accuracy. A physics based similarity criterion, implemented via PCA of load-displacement curves, is used to identify mechanically representative experimental responses for quantitative comparison with simulations. Indentation stress-strain curves are constructed yielding excellent agreement in the elastic regime between experiment and simulation, with reduced Young's moduli of approximately 270 GPa. Generalized stacking fault energy calculations reveal elevated unstable stacking- and twinning-fault energies in MoTaW relative to pure refractory elements, indicating suppressed localized shear and a preference for dislocation-mediated plasticity. Atomistic analyses demonstrate a strong crystallographic dependence of plastic deformation, with symmetric {110}<111> slip activation and four-fold rosette pile-ups for the [001] orientation, and anisotropic slip, strain localization, and enhanced junction formation for [011]. Local entropy and polyhedral template matching analyses further elucidate dislocation network evolution and deformation-induced local structural transformations. Overall, this study establishes a direct mechanistic link between fault energetics, orientation-dependent dislocation activity, and experimentally observed nanoindentation behavior in RCCA.

cond-mat.mtrl-sci↗

arXiv2025

Dissociative Mechanism from NH3 and CH4 on Ni-Doped Graphene: Tuning Electronic and Optical Properties

In this study, we employ a multi-scale computational modeling approach, combining density functional theory (DFT) and self-consistent charge density functional tight binding (SCC-DFTB), to investigate hydrogen (H2) production and dissociation mechanisms from ammonia (NH3) and methane (CH4) on pristine and nickel-doped graphene. These two-dimensional materials hold significant potential for applications in advanced gas sensing and catalysis. Our analysis reveals that Ni-doped graphene, validated through work function calculations, is a promising material for gas separation and hydrogen production. The samples with adsorbed molecules are characterized by calculating chemical potential, chemical hardness, electronegativity, electrophilicity, vibrational frequencies, adsorbtion and Gibbs energies by DFT calculations. Methane molecules preferentially adsorb at the hexagonal ring centers of graphene, while ammonia inter-acts more strongly with carbon atoms, highlighting distinct molecular doping mechanisms for CH4 and NH3. Dynamic simulations show that CH4 splits into CH3+H, with Ni-doped graphene facilitating enhanced hydrogen transmission, while NH3 dissociates into NH2+H, which may lead to N2H4 formation. Our non-equilibrium Green's function (NEGF) simulations demonstrate increased H-atom transmission on Ni-doped graphene during gas interactions. These findings suggest that Ni-doped graphene is superior to pristine graphene for applications in gas separation, hydrogen production, and high-sensitivity sensors.

cond-mat.mtrl-sci↗

arXiv2025

Synergistic modulation of band structure and phonon transport for higher thermoelectric performance of WSe2

Tungsten diselenide (WSe2) emerges as a promising thermoelectric (TE) candidate due to its high thermopower (S), cost-effectiveness, and environmentally friendly characteristics. However, pristine WSe2 exhibits limited electrical conductivity (sigma), a low power factor (PF), and high lattice thermal conductivity (k_L), which restrict its overall TE performance. Here, we show that through co-doping of Nb for W and Te for Se in WSe2, its power factor increases 17-fold, reaching 8.91 microW cm^-1 K^-2 at 850 K. Simultaneously, its lattice thermal conductivity (k_L) decreases from 1.70 W m^-1 K^-1 to 0.48 W m^-1 K^-1. Experiments and density functional theory (DFT) analysis demonstrate that the enhancement of PF is linked to an increased density of states, higher effective mass (md*), improved mobility (mu), and elevated electrical conductivity (sigma) owing to the replacement of Se2- with Te2-; while the observed 72% reduction in k_L results primarily from phonon scattering at Te-Se and Nb-W defects. As a result, a remarkable ZT_max ~ 1 is obtained at 850 K for the sample W0.95Nb0.05Se2-yTey with y = 0.3, which is about a 30-fold increase compared to WSe2, proving that Nb and Te co-doping in WSe2 can significantly boost its TE performance.

cond-mat.mtrl-sci↗

arXiv2025

Thermally Activated Plasticity in Single-Crystal Titanium: A Molecular Dynamics Study of Nanoscale Deformation

Hexagonal close-packed (hcp) titanium exhibits a complex temperature-dependent mechanical response that is central to its use in structural applications. We employ large-scale molecular dynamics simulations to investigate the nanoindentation behavior of single-crystalline a-Ti along the [0001], [10-10], and [2-110] orientations at 10, 300, and 600 K. The simulations reveal how temperature modifies the onset of plasticity and the subsequent evolution of dislocation activity, including nucleation, glide, and the competition between basal and pyramidal slip. Schmid factor mapping establishes a direct correlation between the orientation-dependent activation of slip systems and the resolved shear stress fields beneath the indenter. The results demonstrate a pronounced increase in thermally assisted dislocation motion with temperature, which manifests as diffuse slip traces and less localized pile-up patterns. Surface morphologies obtained at 300 K are consistent with atomic force microscopy observations, validating the atomistic modeling approach. At elevated temperatures, enhanced dislocation recovery and redistribution of slip pathways dominate the indentation response, highlighting the role of thermal activation in controlling plasticity in hcp titanium.

cond-mat.mtrl-sci↗

arXiv2025

Atomistic Study of Radiation-Induced Ductile-to-Brittle Transition in Austenitic Steel

Neutron irradiation in structural alloys promotes defect clustering, which suppresses plasticity and triggers a ductile-to-brittle transition (DBT), a key degradation mechanism limiting fracture resistance in nuclear materials. This study investigates the fracture mechanisms underlying this transition in irradiated Fe-Ni-Cr alloys. Using Molecular Dynamics simulations, we examine how different defect types influence crack propagation and energy dissipation mechanisms. The results reveal distinct roles of these defects: voids facilitate crack growth by reducing local cohesive energy, while dislocation loops act as barriers that impede crack advancement and redirect crack paths, significantly altering crack morphology. Building on the classical approach of separating fracture energy into brittle cleavage and plastic components, this study adapts the decomposition to irradiated materials. This framework quantifies the evolving contributions of surface energy and plastic work across increasing radiation damage levels, providing critical insight into how irradiation-induced defects govern fracture dynamics

cond-mat.mtrl-sci↗

arXiv2025

Evaluating Compression and Nanoindentation in FCC Nickel: A Methodology for Interatomic Potential Selection

We performed molecular dynamics simulations to investigate the mechanical response of face-centered cubic (FCC) nickel under uniaxial compression and nanoindentation using traditional interatomic potentials, including the Embedded Atom Method (EAM) and Modified Embedded Atom Method (MEAM). By calculating the generalized stacking fault energy (GSFE), we analyzed the dissociated slip paths responsible for stacking fault formation and partial Shockley dislocations during mechanical loading. Our findings highlight the critical importance of selecting appropriate interatomic potentials to model compression and nanoindentation tests accurately, aligning simulations with experimental observations. We propose a practical methodology for identifying empirical interatomic potentials suitable for mechanical testing of single-element materials. This approach establishes a benchmark for FCC nickel simulations and provides a basis for extending these methods to more complex Ni-based alloys, facilitating comparisons with experimental results such as those from electron microscopy.

cond-mat.mtrl-sci↗

arXiv2025

Self-ion irradiation effects on nanoindentation-induced plasticity of crystalline iron: A joint experimental and computational study

In this paper, experimental work is supported by multi-scale numerical modeling to investigate nanomechanical response of pristine and ion irradiated with Fe2+ ions with energy 5 MeV high purity iron specimens by nanoindentation and Electron Backscatter Diffraction. The appearance of a sudden displacement burst that is observed during the loading process in the load-displacement curves is connected with increased shear stress in a small subsurface volume due to dislocation slip activation and mobilization of pre-existing dislocations by irradiation. The molecular dynamics (MD) and 3D-discrete dislocation dynamics (3D-DDD) simulations are applied to model geometrically necessary dislocations (GNDs) nucleation mechanisms at early stages of nanoindentation test; providing an insight to the mechanical response of the material and its plastic instability and are in a qualitative agreement with GNDs density mapping images. Finally, we noted that dislocations and defects nucleated are responsible the material hardness increase, as observed in recorded load-displacement curves and pop-ins analysis.

cond-mat.mtrl-sci↗

arXiv2025

CH$_4$ and CO$_2$ Adsorption Mechanisms on Monolayer Graphenylene and their Effects on Optical and Electronic Properties

In this study, we employ a computational chemistry-based modeling approach to investigate the adsorption mechanisms of CH$_4$ and CO$_2$ on monolayer GPNL, with a specific focus on their effects on optical adsorption and electrical transport properties at room temperature. To simulate the adsorption dynamics as closely as possible to experimental conditions, we utilize the self-consistent charge tight-binding density functional theory (SCC-DFTB). Through semi-classical molecular dynamics (MD) simulations, we observe the formation of H$_2$ molecules from the dissociation of CH$_4$ and the formation of CO+O species from carbon dioxide molecules. This provides insights into the adsorption and dispersion mechanisms of CH$_4$ and CO$_2$ on GPNL. Furthermore, we explore the impact of molecular adsorption on optical absorption properties. Our results demonstrate that CH$_4$ and CH$_2$ affects drastically the optical adsorption of GPNL, while CO$_2$ does not significantly affect the optical properties of the two-dimensional material. To analyze electron transport, we employ the open-boundary non-equilibrium Green's function method. By studying the conductivity of GPNL and graphene under voltage bias up to 300 mV, we gain valuable insights into the electrical transport properties of GPNL under optical absorption conditions. The findings from our computational modeling approach might contribute to a deeper understanding of the potential applications of GPNL in hydrogen production and advanced electronic devices.

physics.comp-ph↗

arXiv2025

Dynamical pathways for the interaction of O2, H2O, CH4, and CO2 with a-alumina surfaces: Density functional tight-binding calculations

In this study, we investigated the physisorption mechanisms of O2, H2O, CH4, and CO2 molecules on alumina and their effect on electronic properties. We employed quantum-classical molecular dynamics simulations and the self-consistent-charge density-functional tight-binding (SCC-DFTB) approach to dynamically model these mechanisms. Our results revealed the binding pathways of O, H, and C atoms in the various molecules to Al and O atoms at the top atomic layers of the alpha-alumina surface. We examined several adsorption sites and molecular orientations relative to Al-terminated and Ox-terminated alumina surfaces and found that the most stable physisorbed state on the Al-terminated surface is located above the Al atom, while the Ox-terminated state is found above the oxygen, resulting in enhanced optical adsorbance. The dissociation of CH4 into CH2+H2 after interaction with the surface resulted in hydrogen production, but with low adsorbate rates. While, O2 molecules primarily bond to the Al atoms, leading to the highest adsorbance rate among the other molecules. Our findings provide important insights into the physisorption mechanisms of molecules on alumina and their impact on electronic properties

cond-mat.mtrl-sci↗

arXiv2025

Multiscale nanoindentation modeling of concentrated solid solutions: A continuum plasticity model

Recently developed single-phase concentrated solid-solution alloys (CSAs) contain multiple elemental species in high concentrations with different elements randomly arranged on a crystalline lattice. These chemically disordered materials present excellent physical properties, including high-temperature thermal stability and hardness, with promising applications to industries at extreme operating environments. The aim of this paper is to present a continuum plasticity model accounting for the first time for the behaviour of a equiatomic five-element CSA, that forms a face-centered cubic lattice. The inherent disorder associated with the lattice distortions caused by an almost equiatomic distribution of atoms, is captured by a single parameter α that quantifies the relative importance of an isotropic plastic contribution to the model. This results in multiple plasticity mechanisms that go beyond crystallographic symmetry-based ones, common in the case of conventional single element metals. We perform molecular dynamics simulations of equiatomic CSAs: NiFe, NiFeCr, NiFeCrCo, and Cantor alloys to validate the proposed continuum model which is implemented in the finite element method and applied to model nanoindentation tests for three different crystallographic orientations. We obtain the representative volume element model by tracking the combined model yield surface.

physics.comp-ph↗

arXiv2024

Collision Cascade-Driven Evolution of Vacancy Defects in Ni-Based Concentrated Solid-Solution Alloys

Concentrated solid--solution alloys (CSAs) in single--phase form have recently garnered considerable attention owing to their potential for exceptional irradiation resistance. This computational study delves into the intricate interplay of alloying elements on the generation, recombination, and evolution of irradiation-induced defects. Molecular dynamics simulations were conducted for collision cascades at room temperature, spanning a range of primary knock-on atom energies from 1 to 10 keV. The investigation encompasses a series of model crystals, progressing from pure Ni to binary CSAs such as NiFe$_{20}$, NiFe, NiCr$_{20}$, and culminating in the more intricate NiFeCr$_{20}$ CSA. We observe that materials rich in chromium actively facilitate dislocation emissions and induce the nucleation of stacking fault tetrahedra in the proximity of nanovoids, owing to Shockley partial interactions. This result is validated by molecular static simulations, which calculate the surface, vacancy, and defect formation energies. Among various shapes considered, the spherical void proves to be the most stable, followed by the truncated octahedron and octahedron shapes. On the other hand, the tetrahedron cubic shape is identified as the most unstable, and stacking fault tetrahedra exhibit the highest formation energy. Notably, among the materials studied, NiCr$_{20}$ and NiFeCr$_{20}$ CSAs stood out as the sole alloys capable of manifesting this mechanism, mainly observed at high impact energies.

cond-mat.mtrl-sci↗

arXiv2024

Atomistic-Level Analysis of Nanoindentation-Induced Plasticity in Arc--Melted NiFeCrCo Alloys: The role of stacking faults

Concentrated solid solution alloys (CSAs) have attracted attention for their promising properties; however, current manufacturing methods face challenges in complexity, high costs, and limited scalability, raising concerns about industrial viability. The prevalent technique, arc melting, yields high-purity samples with complex shapes. In this study, we explore nanoindentation tests at room temperature where arc-melted samples exhibit larger grain sizes, diminishing the effects of grain boundaries on the results. Motivated by these findings, our investigation focuses on the atomistic-level exploration of plasticity mechanisms, specifically dislocation nucleation and propagation during nanoindentation tests. The intricate chemistry of NiFeCrCo CSA influences pile-ups and slip traces, aiming to elucidate plastic deformation by considering both pristine and pre-existing stacking fault tetrahedra. Our analysis scrutinizes dynamic deformation processes, defect nucleation, and evolution, complemented by stress-strain and dislocation densities-strain curves illustrating the hardening mechanism of defective materials. Additionally, we examine surface morphology and plastic deformation through atomic shear strain and displacement mappings. This integrated approach provides insights into the complex interplay between material structure and mechanical behavior, paving the way for an enhanced understanding and potential advancements in CSA applications.

cond-mat.mtrl-sci↗

arXiv2023

Plastic deformation mechanisms during nanoindentation of W, Mo, V body-centered cubic single crystals and their corresponding W-Mo, W-V equiatomic random solid solutions

Deformation plasticity mechanisms in alloys and compounds may unveil the material capacity towards optimal mechanical properties. We conduct a series of molecular dynamics (MD) simulations to investigate plasticity mechanisms due to nanoindentation in pure tungsten, molybdenum and vanadium body-centered cubic single crystals, as well as the also body-centered cubic, equiatomic, random solid solutions (RSS) of tungsten--molybdenum and tungsten--vanadium alloys. Our analysis focuses on a thorough, side-by-side comparison of dynamic deformation processes, defect nucleation, and evolution, along with corresponding stress--strain curves. We also check the surface morphology of indented samples through atomic shear strain mapping. As expected, the presence of Mo and V atoms in W matrices introduces lattice strain and distortion, increasing material resistance to deformation and slowing down dislocation mobility of dislocation loops with a Burgers vector of 1/2 $\langle 111 \rangle$. Our side-by-side comparison displays a remarkable suppression of the plastic zone size in equiatomic W--V RSS, but not in equiatomic W--Mo RSS alloys, displaying a clear prediction for optimal hardening response equiatomic W--V RSS alloys. If the small-depth nanoindentation plastic response is indicative of overall mechanical performance, it is possible to conceive a novel MD-based pathway towards material design for mechanical applications in complex, multi-component alloys.

cond-mat.mtrl-sci↗

arXiv2022

Atomistic simulations of nanoindentation in single crystalline tungsten: The role of interatomic potentials

Computational modeling is usually applied to aid experimental exploration of advanced materials to better understand the fundamental plasticity mechanisms during mechanical testing. In this work, we perform Molecular dynamics (MD) simulations to emulate experimental room temperature spherical-nanoindentation of crystalline W matrices by different interatomic potentials: EAM, modified EAM, and a recently developed machine learned based tabulated Gaussian approximation potential (tabGAP) for describing the interaction of W-W. Results show similarities between load displacements and stress-strain curves, regardless of the numerical model. However, a discrepancy is observed at early stages of the elastic to plastic deformation transition showing different mechanisms for dislocation nucleation and evolution, that is attributed to the difference of Burgers vector magnitudes, stacking fault and dislocation glide energies. Besides, contact pressure is investigated by considering large indenters sizes that provides a detailed analysis of screw and edge dislocations during loading process. Furthermore, the glide barrier of this kind of dislocations are reported for all the interatomic potentials showing that tabGAP model presents the most accurate results with respect to density functional theory calculations and a good qualitative agreement with reported experimental data

physics.comp-ph↗

arXiv2022

Dynamic nanoindentation and short-range order in equiatomic NiCoCr medium entropy alloy lead to novel density wave ordering

Chemical short-range order (CSRO) is believed to be a key contributor to the exceptional properties of multicomponent alloys. However, direct validation and confirmation of CSRO has been highly elusive in most compounds. Recent studies for equiatomic NiCoCr alloys have shown that thermal treatments (i.e., annealing/aging) may facilitate and manipulate CSRO. In this work, by using molecular simulations, we show that nanomechanical probes, such as nanoindentation, may be utilized towards further manipulation of CSRO, providing explicit validation pathways. By using well established interatomic potentials, we perform hybrid Molecular-Dynamics/Monte-Carlo (MD/MC) at room temperature to demonstrate that particular dwell nanoindentation protocols can lead, through thermal MC equilibration, to the reorganization of CSRO under the indenter tip, to a density-wave stripe pattern (DWO). We characterize the novel DWO structures, that are directly correlated to incipient SRO but are highly anisotropic and dependent on local, nanoindentation-induced stress concentrations, and we show how they deeply originate from the peculiarities of the interatomic potentials. Furthermore, we show that the DWO patterns consistently scale up with the incipient plastic zone under the indenter tip, justifying the observation of the DWO patterning at any experimentally feasible nanoindentation depth.

cond-mat.mtrl-sci↗