arXiv subjects

Alan B. de Oliveira

Publications and source records attributed to Alan B. de Oliveira.

17 recordsLinked to original sources

arXiv2024

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↗

arXiv2023

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↗

arXiv2023

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↗

arXiv2020

Water diffusion in carbon nanotubes under directional electric fields: Coupling between mobility and hydrogen bonding

We have investigated the diffusion and structure of TIP4P/2005 water confined in carbon nanotubes subjected to external electric fields. A wide range of diameters has been used to show a highly size-dependent behavior of the water diffusion. We also found that the diffusion is extremely affected by the intensity of the applied field. However, is the relative direction between the field and the tube axis that causes the most intriguing behavior. Electric fields forming angles of $0^{\circ}$ and $45^{\circ}$ with the tube axis were found to slow down the water dynamics by increasing organization, while fields perpendicular to the tube axis can enhance water diffusion in some cases by decreasing the hydrogen bond formation. Remarkably, for the 1.2 nm diameter long (9,9) nanotube, the field along the tube axis melts the water structure increasing the water mobility. These results points out that the structure and dynamics of confined water are extremely sensitive to external fields and suggest the use of electric fields as a facilitator for filtration processes.

cond-mat.soft↗

arXiv2020

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↗

arXiv2020

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↗

arXiv2019

Evidence for a pressure-induced phase transition of few-layer graphene to 2D diamond

We unveil the diamondization mechanism of few-layer graphene compressed in the presence of water, providing robust evidence for the pressure-induced formation of 2D diamond. High-pressure Raman spectroscopy provides evidence of a phase transition occurring in the range of 4-7 GPa for 5-layer graphene and graphite. The pressure-induced phase is partially transparent and indents the silicon substrate. Our combined theoretical and experimental results indicate a gradual top-bottom diamondization mechanism, consistent with the formation of diamondene, a 2D ferromagnetic semiconductor. High-pressure x-ray diffraction on graphene indicates the formation of hexagonal diamond, consistent with the bulk limit of eclipsed-conformed diamondene.

cond-mat.mtrl-sci↗

arXiv2018

Diffusion behavior of water confined in deformed carbon nanotubes

We use molecular dynamics simulations to study the diffusion of water inside deformed carbon nanotubes, with different degrees of eccentricity at 300K. We found a water structural transition between tubular-like to single-file for the (7,7) nanotubes associated with a change from a high to low mobility regimes. The water which in the undeformed (9,9) nanotubes is frozen, becomes liquid for the distortion above a certain threshold. These water diffusion enhancement (suppresion) is related to a reduction (increase) in the number of hydrogen bonds. This suggests that the shape of the nanotube is a particularly important ingredient when considering the dynamical and structural properties of confined water.

cond-mat.soft↗

arXiv2015

Insights into the flux of water in a water desalination through nanopores process

Water desalination through nanopores has been shown to be a promising alternative to the currently water purification processes. In spite the results in this direction obtained by means of computational simulations were animating there are still pending issues to be resolved. For example, water desalination involves macro numbers (in size and time) but in such a scale it is literally impossible to attack this problem using all-atoms simulations. It is common to extrapolate results from nano to macro sizes in order to estimate quantities of interest, which must be taken with care. Here we present a simple model which mimics the separation of salt from water, which may help to attack bigger problems on water desalination subjects. Besides, we show that the investigation of a restrict space of parameters imposed by expensive models may hidden interesting, important features involved in the water desalination problem. Finally, we present an analytical calculation which explains the rich behaviour of the water flux through nanopores in a water-salt separation scenario.

cond-mat.soft↗

arXiv2012

Tunable Band Gap of Boron Nitride Interfaces under Uniaxial Pressure

In this work we show, by means of a density functional theory formalism, that the simple physical contact between hydrogen terminated boron nitride surfaces gives rise to a metallic interface with free carries of opposite sign at each surface. A band gap can be induced by applying uniaxial pressure. The size of the band gap changes continuously from zero up to 4.4 eV with increasing pressure, which is understood in terms of the interaction between surface states. Due to the high thermal conductivity of cubic boron nitride and the coupling between band gap and applied pressure, such tunable band gap interfaces may be used in high stable electronic and electromechanical devices. In addition, the spacial separation of charge carries at the interface may lead to photovoltaic applications.

cond-mat.mtrl-sci↗

arXiv2012

Diffusion Enhancement in Core-softened fluid confined in nanotubes

We study the effect of confinement in the dynamical behavior of a core-softened fluid. The fluid is modeled as a two length scales potential. This potential in the bulk reproduces the anomalous behavior observed in the density and in the diffusion of liquid water. A series of $NpT$ Molecular Dynamics simulations for this two length scales fluid confined in a nanotube were performed. We obtain that the diffusion coefficient increases with the increase of the nanotube radius for wide channels as expected for normal fluids. However, for narrow channels, the confinement shows an enhancement in the diffusion coefficient when the nanotube radius decreases. This behavior, observed for water, is explained in the framework of the two length scales potential.

cond-mat.soft↗

arXiv2011

Boron Nitride Nanotubes as Templates for Half-Metal Nanowires

We investigate by means of DFT/GGA+U calculations the electronic and structural properties of magnetic nanotubes composed of an iron oxide monolayer and (n,0) Boron Nitride (BN) nanotubes, with n ranging from 6 up to 14. The formation energy per FeO molecule of FeO covered tubes is smaller than the formation energy of small FeO nanoparticles which suggest that the FeO molecules may cover the BN nanotubes rather than to aggregate to form the FeO bulk. We propose a continuous model for the FeO covered BN nanotubes formation energy which predicts that BN tubes with diameter of roughly 13 Åare the most stable. Unlike carbon nanotubes, the band structure of FeO covered BN nanotubes can not be obtained by slicing the band structure of a FeO layer, the curvature and the interaction with the BN tube is determinant for the electronic behavior of FeO covered tubes. As a result the tubes are semiconductors, intrinsic half-metals or semi-half-metals that can become half-metals charged with either electrons and holes. Such a result may be important in the spintronics context.

cond-mat.mes-hall↗

arXiv2011

Core-softened Fluids, Water-like Anomalies and the Liquid-Liquid Critical Points

Molecular dynamics simulations are used to examine the relationship between water-like anomalies and the liquid-liquid critical point in a family of model fluids with multi-Gaussian, core-softened pair interactions. The core-softened pair interactions have two length scales, such that the longer length scale associated with a shallow, attractive well is kept constant while the shorter length scale associated with the repulsive shoulder is varied from an inflexion point to a minimum of progressively increasing depth. As the shoulder well depth increases, the pressure required to form the high density liquid decreases and the temperature up to which the high-density liquid is stable increases, resulting in the shift of the liquid-liquid critical point to much lower pressures and higher temperatures. The pair correlation entropy is computed to show that the excess entropy anomaly diminishes when the shoulder well depth increases. Excess entropy scaling of diffusivity in this class of fluids is demonstrated, showing that decreasing strength of the excess entropy anomaly with increasing shoulder depth results in the progressive loss of water-like thermodynamic, structural and transport anomalies. Instantaneous normal mode analysis was used to index the overall curvature distribution of the fluid and the fraction of imaginary frequency modes was shown to correlate well with the anomalous behaviour of the diffusivity and the pair correlation entropy. The results suggest in the case of core-softened potentials, in addition to the presence of two length scales, energetic and entropic effects associated with local minima and curvatures of the pair interaction play an important role in determining the presence of water-like anomalies and the liquid-liquid phase transition.

cond-mat.soft↗

arXiv2010

Iron oxide doped boron nitride nanotubes: structural and magnetic properties

A first-principles formalism is employed to investigate the interaction of iron oxide (FeO) with a boron nitride (BN) nanotube. The stable structure of the FeO-nanotube has Fe atoms binding N atoms, with bond length of roughly $\sim$2.1 Å, and binding between O and B atoms, with bond length of 1.55 Å. In case of small FeO concentrations, the total magnetic moment is (4$μ_{Bohr}$) times the number of Fe atoms in the unit cell and it is energetically favorable to FeO units to aggregate rather than randomly bind to the tube. As a larger FeO concentration case, we study a BN nanotube fully covered by a single layer of FeO. We found that such a structure has square FeO lattice with Fe-O bond length of 2.11 Å, similar to that of FeO bulk, and total magnetic moment of 3.94$μ_{Bohr}$ per Fe atom. Consistently with experimental results, the FeO covered nanotube is a semi-half-metal which can become a half-metal if a small change in the Fermi level is induced. Such a structure may be important in the spintronics context.

cond-mat.mes-hall↗

arXiv2006

Structural anomalies for a three dimensional isotropic core-softened potential

Using molecular dynamics simulations we investigate the structure of a system of particles interacting through a continuous core-softened interparticle potential. We found for the translational order parameter, t, a local maximum at a density $ρ_{t-max}$ and a local minimum at $ρ_{t-min} > ρ_{t-max}$. Between $ρ_{t-max}$ and $ρ_{t-min}$, the $t$ parameter anomalously decreases upon pressure. For the orientational order parameter, $Q_6$, was observed a maximum at a density $ρ_{t-max}< ρ_{Qmax} < ρ_{t-min}$. For densities between $ρ_{Qmax}$ and $ρ_{t-min}$, both the translational (t) and orientational ($Q_6$) order parameters have anomalous behavior. We know that this system also exhibits density and diffusion anomaly. We found that the region in the pressure-temperature phase-diagram of the structural anomaly englobes the region of the diffusion anomaly that is larger than the region limited by the temperature of maximum density. This cascade of anomalies (structural, dynamic and thermodynamic) for our model has the same hierarchy of that one observed for the SPC/E water.

cond-mat.soft↗

arXiv2005

Thermodynamic and dynamic anomalies for a three dimensional isotropic core-softened potential

Using molecular dynamics simulations and integral equations (Rogers-Young, Percus-Yevick and hypernetted chain closures) we investigate the thermodynamic of particles interacting with continuous core-softened intermolecular potential. Dynamic properties are also analyzed by the simulations. We show that, for a chosen shape of the potential, the density, at constant pressure, has a maximum for a certain temperature. The line of temperatures of maximum density (TMD) was determined in the pressure-temperature phase diagram. Similarly the diffusion constant at a constant temperature, $D$, has a maximum at a density $ρ_{max}$ and a minimum at a density $ρ_{min}<ρ_{max}$. In the pressure-temperature phase-diagram the line of extrema in diffusivity is outside of TMD line. Although in this interparticle potential lacks directionality, this is the same behavior observed in SPC/E water.

cond-mat.soft↗

arXiv2004

Density anomaly in a competing interactions lattice gas model

We study a very simple model of a short-range attraction and an outer shell repulsion as a test system for demixing phase transition and density anomaly. The phase-diagram is obtained by applying mean field analysis and Monte Carlo simulations to a two dimensional lattice gas with nearest-neighbors attraction and next-nearest-neighbors repulsion (the outer shell). Two liquid phases and density anomaly are found. The coexistence line between these two liquid phases meets a critical line between the fluid and the low density liquid at a tricritical point. The line of maximum density emerges in the vicinity of the tricritical point, close to the demixing transition.

cond-mat.stat-mech↗