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Marcia C. Barbosa

Publications and source records attributed to Marcia C. Barbosa.

At least 19 recordsLinked to original sources

Specific heat and density anomaly in the Hubbard model

Understanding thermal properties of materials is fundamental to technological applications and to discovering new phenomena. In particular, advances in experimental techniques such as cold-atom measurements allow the simulation of paradigmatic Hamiltonians with great control over model parameters, such as the Hubbard model. One aspect of this model which is not much explored is the behavior of the specific heat as a function of density. In this work, we perform Determinant Quantum Monte Carlo simulations of the Hubbard model interpolating between the square and triangular lattices to analyze the specific heat as the filling, interaction, and temperature of the system are changed. We found that, with strong correlations, the specific heat presents a three-maxima structure as a function of filling, with local minima between them. This effect can be explained by a decomposition of kinetic and potential contributions to the specific heat, demonstrating interesting phenomena away from the commonly studied half-filling regime. Moreover, by analyzing the kinetic contribution in momentum space we show that, connected to this specific heat behavior, there is a density anomaly detected through the thermal expansion coefficient. These momentum-space quantities are accessible using cold-atom experiments measurements at multiple temperatures. Finally, we map the location of these phenomena and connect the thermal expansion anomaly with the well-known Seebeck coefficient change of sign. Our results provide a new perspective to analyze this change of sign.

cond-mat.str-el

Condensation effect and transport on Alumina porous membranes

Understanding the adsorption of water and characterizing the water film formed within nanostructures are essential for advancements in fields such as nanofluidics, water purification, and biosensing devices. In our research, we focus on studying the condensation and transport of water through an alumina membrane with nanopores of varying wettabilities. We introduce a method to alter the membrane's wettability and enhance dissociative adsorption by varying the duration of exposure during plasma cleaning. To create different experimental environments, we modify humidity levels by controlling vapor pressure. To investigate water transport within the membrane, we apply a voltage and analyze the resulting current response. Our analysis indicates that transport properties improve with thicker water films. We use the Polanyi theory of adsorption to capture the physics of the problem. Analyzing the conductance inside the nanopores, we find that the first monolayers may stagnate due to interactions with the pore walls. This research significantly enhances our understanding of vapor condensation within nanomaterials, particularly considering the influence of different wettabilities. These findings have broad implications for applications such as water vapor capture and related technologies.

cond-mat.soft

Wetting in Associating Lattice Gas Model Confined by Hydrophilic Walls

Through Monte Carlo simulations and the Associating Lattice Gas Model, the phases of a two-dimensional fluid under hydrophilic confinement are evaluated. The model, in its unconfined version, reproduces the anomalous behavior of water regarding its density, diffusion, and solubility, among other dynamic and thermodynamic properties. Extreme confinements suppress phase transitions since fluctuations suppress ordering. The fluid under hydrophilic confinement forms a single wetting layer that gradually wets the wall. From the wetting layer, the low-density liquid structure is formed. The confined fluid presents a first-order liquid-liquid transition, but always at lower temperatures than that observed in the bulk.

physics.app-ph

Waterlike density anomaly in fermions

In this work we explore the one-dimensional extended Hubbard model as a fluid system modelling liquid phases of different densities. This model naturally displays two length scales of interaction, which are connected with waterlike anomalies. We analyze the density anomaly as a function of the model parameters, namely the hopping, on-site and first neighbor interactions. We show that this anomaly is present for a wide range of model parameters and is connected to a ground-state liquid-liquid critical point.

cond-mat.stat-mech

Flow through deformed carbon nanotubes predicted by rigid and flexible water models

In this study, using non-equilibrium molecular dynamics simulation, the flow of water in deformed carbon nanotubes is studied for two water models TIP4P/2005 and SPC/FH. The results demonstrated a non-uniform dependence of the flow on the tube deformation and the flexibility imposed on the water molecules, leading to an unexpected increase in the flow in some cases. The effects of tube diameter and pressure gradient are investigated to explain the abnormal flow behavior with different degrees of structural deformation.

cond-mat.mtrl-sci

Density anomaly in water-alcohol mixtures: minimum model for structure makers and breakers

We modeled the change in the temperature of maximum density (TMD) of a water-like solvent when small amounts of solute are added to the mixture. The solvent is modeled as a two length scales potential, which is known to exhibit water-like characteristic anomalies, while the solute is chosen to have an attractive interaction with the solvent which is tuned from small to large attractive potential. We show that if the solute exhibits high attraction with the solvent it behaves as a structure maker and the TMD increases with the addition of solute, while if the solute shows a low attraction with the solvent the TMD decreases, with the solute behaving as a structure breaker.

cond-mat.soft

Water diffusion in carbon nanotubes for rigid and flexible models

We compared the diffusion of water confined in armchair and zigzag carbon nanotubes for rigid and flexible water models. Using one rigid model, TIP4P/2005, and two flexible models, SPC/Fw and SPC/FH, we found that the number of the number of hydrogen bonds that water forms depends on the structure of the nanotube, directly affecting the diffusion of water. The simulation results reveal that due to the hydrophobic nature of carbon nanotubes and the degrees of freedom imposed by the water force fields, water molecules tend to avoid the surface of the carbon nanotube. This junction of variables plays a central role in the diffusion of water, mainly in narrow and/or deformed nanotubes, governing the mobility of confined water in a non-trivial way, where the greater the degree of freedom of the water force field, the smaller it will be mobility in confinement, as we limit the competition between area/volume, and it no longer plays the unique role in changing water diffusivity.

cond-mat.soft

Density anomaly in a minimum model of water-alcohol mixtures

We study the change in the temperature of maximum density (TMD) of a water-like solvent when small amounts of solute are added to the mixture. The water is modeled as a two length scales potential, which is known to exhibit water-like characteristic anomalies, while the solute is chosen to have an attractive interaction with the solvent. If the solute is a structure maker the TMD increases with the addition of solute, while if it is a structure breaker the TMD decreases. Both in an exact one dimensional model and using molecular dynamics in three dimensions we show that the necessary ingredient to represent structure makers is a strong solute-solvent attraction.

cond-mat.soft

Water inside charged nanoslits: Structure and Dielectric study with a novel water model FAB/$ε$

In this work, the dielectric behavior of water inside charged nanoslit of graphene is studied to analized the water molecules under electrical confinement; through polarizing the nanoslit of graphene, creating an electric field inside the nanopore. How the water molecules are structured under this type of electrical confinement is studied with two force fields of water, the three-site water models here used are the SCP/$ε$ and the FAB/$ε$, the first is a rigid model that improves the SPC model and the second is a flexible model that improves all the force fields of three sites non-polarizables and flexibles.

cond-mat.soft

Molecular Dynamics Simulations of Water Anchored in Multi-Layered Nanoporous MoS$_2$ Membranes: Implications for Desalination

One of the most promising applications in nanoscience is the design of new materials to improve water permeability and selectivity of nanoporous membranes. Understanding the molecular architecture behind these fascinating structures and how it impacts the water flow is an intricate but necessary task. We studied here, the water flux through multi-layered nanoporous molybdenum disulfide (MLNMoS$_2$) membranes with different nanopore sizes and length. Molecular dynamics simulations show that the permeability do not increase with the inverse of the membrane thickness, violating the classical hydrodynamic behavior. The data also reveals that the water dynamics is slower than that observed in frictionless carbon nanotubes and multi-layer graphene membranes, which we explain in terms of an anchor mechanism observed in between layers. We show that the membrane permeability is critically dependent on the nanopore architecture, bringing important insights into the manufacture of new desalination membranes.

cond-mat.soft

Water permeability in nanopores: when size, shape, and charge matter

Nanoscale materials are a promising desalination technology. While fast water flow in nanotubes is well understood, this is not the case for water permeability in single-layer membranes. The physical-chemical balance between nanopore size, shape, and charge might be the answer.

cond-mat.soft

Double-peak specific heat anomaly and correlations in the Bose-Hubbard model

Considering the thermodynamics of bosons in a lattice described by the Bose-Hubbard Hamiltonian, we report the occurrence of anomalous double peaks in their specific heat dependence on temperature. This feature, usually associated with a high geometrical frustration, can also be a consequence of a purely energetic competition. By employing self-energy functional calculations combined with finite-temperature perturbation theory, we propose a mechanism based on ground-state degeneracies expressed as residual entropies. A general decomposition of the specific heat regarding all possible transitions between the system's eingenvalues provides an insight into the nature of each maximum. Furthermore, we address how the model parameters modify the structure of these peaks based on its spectral properties and atom-atom correlation function.

cond-mat.quant-gas

Molecular Fluid Flow in MoS$_2$ Nanoporous Membranes and Hydrodynamics Interactions

The shift in water security demands improvements in alternative solutions such as saltwater desalination. One of the most efficient technologies in this scope is the reverse osmosis systems, a technology based on a membrane separation process. MoS$_2$ nanoporous membranes are gained attention as a promise for the next-generation high selective and permeable membranes technology. Besides that, one aspect of nanoconfined fluid flow not yet investigated but studied from the fluid mechanics calculations is the impact of induced pressure fields in the water flux in neighboring microfilters, described as hydrodynamic interactions. For this purpose, we studied the water flow through adjacent MoS$_2$ nanopores by running Non-Equilibrium Molecular Dynamics simulations and obtained that in this scale the hydrodynamics interactions are not significant as expected.

cond-mat.soft

Water diffusion in carbon nanotubes: interplay between confinement, surface deformation and temperature

In this article we investigate through molecular dynamics simulations the diffusion behavior of the TIP4P/2005 water when confined in pristine and deformed carbon nanotubes (armchair and zigzag). To analyze different diffusive mechanisms, the water temperature was varied from $210\leq T\leq 380$~K. The results of our simulations reveal that water present a non-Arrhenius to Arrhenius diffusion crossover. The confinement shifts the diffusion transition to higher temperatures when compared with the bulk system. In addition, for narrower nanotubes, water diffuses in a single line which leads to a mobility independent of the activation energy.

cond-mat.soft

Modeling the temperature of maximum density of aqueous tert-butanol solutions

Short-chain alcohols at high dilution are among the very few solutes that enhance the anomalous behavior of water, in particular the value of the temperature of maximum density. This peculiar feature, first discovered experimentally in the early sixties, has remained elusive to a full explanation in terms of atomistic models. In this paper, we first introduce a two-site model of tert-butanol in which the interactions involving hydrogen bonding are represented by a Stillinger-Weber potential, following the ideas first introduced by Molinero and Moore, [J. Phys. Chem. B, 113, 4008, (2009)]. Our model parameters are fit so as to semi-quantitatively reproduce the experimental densities and vaporization enthalpies of previously proposed united atom and all atom OPLS models. Water is represented using the aforementioned potential model introduced by Molinero and Moore, with cross interaction parameters between water and tert-butanol optimized to yield a reasonable description of the experimental excess enthalpies and volumes over the whole composition range of the mixture. We will see that our simple model is able to reproduce the presence of a maximum in the change of the temperature of maximum density for very low alcohol mole fractions, followed by a considerable decrease until the density anomaly itself disappears. We have correlated this behavior with changes in the local structure of water and compared it with the results of all-atom simulations of water/tert-butanol mixtures.

cond-mat.soft

Salt parameterization can drastically affect the results from classical atomistic simulations of water desalination by MoS$_2$ nanopores

Water scarcity is a reality in our world, and scenarios predicted by leading scientists in this area indicate that it will worsen in the next decades. However, new technologies based in low-cost seawater desalination can prevent the worst scenarios, providing fresh water for humanity. With this goal, membranes based in nanoporous materials have been suggested in recent years. One of the materials suggested is MoS$_2$, and classical Molecular Dynamics (MD) simulation is one of the most powerful tools to explore these nanomaterials. However, distinct Force Fields employed in MD simulations are parameterized based on distinct experimental quantities. In this paper, we compare two models of salt that were build based on distinct properties of water-salt mixtures. One model fits the hydration free energy and lattice properties, the second fits the crystal density and the density and the dielectric constant of water and salt mixtures. To compare the models, MD simulations for salty water flow through two nanopores sizes were used -- one pore big enough to accommodate hydrated ions, and one smaller in which the ion has to dehydrate to enter, and two rigid water models from the TIP4P family -- the TIP4P/2005 and TIP4P/$ε$. Our results indicate that the water permeability and salt rejection by the membrane are more influenced by the salt model than by the water model, especially for the narrow pore. In fact, completely distinct mechanisms were observed, and they are related to the characteristics employed in the ion model parameterization. The results show that not only the water model can influence the outcomes, but the ion model plays a crucial role.

cond-mat.soft

Water diffusion in rough carbon nanotubes

We use molecular dynamics simulations to study the diffusion of water inside deformed carbon nanotubes with different degrees of deformation at 300 K. We found that the number of hydrogen bonds that water forms depends on nanotube topology, leading to enhancement or suppression of water diffusion. The simulation results reveal that more realistic nanotubes should be considered to understand the confined water diffusion behavior, at least for the narrowest nanotubes, when the interaction between water molecules and carbon atoms is relevant.

cond-mat.soft

Waterlike anomalies in hard core-soft shell nanoparticles using a effective potential approach: pinned vs adsorbed polymers

In this work, a two dimensional system of polymer grafted nanoparticles is analyzed using large-scale Langevin Dymanics simulations. Effective core-softened potentials were obtained for two cases: one where the polymers are free to rotate around the nanoparticle core and a second where the polymers are fixed, with a $45^\circ$ angle between them. The use of effective core-softened potentials allow us to explore the complete system phase space. In this way, the $PT$, $Tρ$ and $Pρ$ phase diagrams for each potential were obtained, with all fluid and solid phases. The phase boundaries were defined analyzing the specific heat at constant pressure, the system mean square displacement, the radial distribution function and the discontinuities in the density-pressure phase diagram. Also, due the competition in the system we have observed the presence of waterlike anomalies, such as the temperature of maximum density - in addition with a tendency of the TMD to move to lower temperatures (negative slope)- and the diffusion anomaly. It was observed different morphologies (stripes, honeycomb, amorphous) for each nanoparticle. We observed that for the fixed polymers case the waterlike anomalies are originated by the competition between the potential characteristic length scales, while for the free to rotate case the anomalies arises due a smaller region of stability in the phase diagram and no competition between the scales was observed.

cond-mat.soft