arXiv subjects

Carlos P. Herrero

Publications and source records attributed to Carlos P. Herrero.

At least 37 records · Page 2Linked to original sources

arXiv2017

Path-integral simulation of graphene monolayers under tensile stress

Finite-temperature properties of graphene monolayers under tensile stress have been studied by path-integral molecular dynamics (PIMD) simulations. This method allows one to consider the quantization of vibrational modes in these crystalline membranes and to analyze the influence of anharmonic effects in the membrane properties. Quantum nuclear effects turn out to be appreciable in structural and thermodynamic properties of graphene at low temperature, and they can even be noticeable at room temperature. Such quantum effects become more relevant as the applied stress is increased, mainly for properties related to out-of-plane atomic vibrations. The relevance of quantum dynamics in the out-of-plane motion depends on the system size, and is enhanced by tensile stress. For applied tensile stresses, we analyze the contribution of the elastic energy to the internal energy of graphene. Results of PIMD simulations are compared with calculations based on a harmonic approximation for the vibrational modes of the graphene lattice. This approximation describes rather well the structural properties of graphene, provided that the frequencies of ZA (flexural) acoustic modes in the transverse direction include a pressure-dependent correction.

cond-mat.mtrl-sci↗

arXiv2017

Thermal properties of graphene from path-integral simulations

Thermal properties of graphene monolayers are studied by path-integral molecular dynamics (PIMD) simulations, which take into account the quantization of vibrational modes in the crystalline membrane, and allow one to consider anharmonic effects in these properties. This system was studied at temperatures in the range from 12 to 2000~K and zero external stress, by describing the interatomic interactions through the LCBOPII effective potential. We analyze the internal energy and specific heat and compare the results derived from the simulations with those yielded by a harmonic approximation for the vibrational modes. This approximation turns out to be rather precise up to temperatures of about 400~K. At higher temperatures, we observe an influence of the elastic energy, due to the thermal expansion of the graphene sheet. Zero-point and thermal effects on the in-plane and "real" surface of graphene are discussed. The thermal expansion coefficient $α$ of the real area is found to be positive at all temperatures, in contrast to the expansion coefficient $α_p$ of the in-plane area, which is negative at low temperatures, and becomes positive for $T \gtrsim$ 1000~K.

cond-mat.mtrl-sci↗

arXiv2016

Quantum effects in graphene monolayers: Path-integral simulations

Path-integral molecular dynamics (PIMD) simulations have been carried out to study the influence of quantum dynamics of carbon atoms on the properties of a single graphene layer. Finite-temperature properties were analyzed in the range from 12 to 2000~K, by using the LCBOPII effective potential. To assess the magnitude of quantum effects in structural and thermodynamic properties of graphene, classical molecular dynamics simulations have been also performed. Particular emphasis has been laid on the atomic vibrations along the out-of-plane direction. Even though quantum effects are present in these vibrational modes, we show that at any finite temperature classical-like motion dominates over quantum delocalization, provided that the system size is large enough. Vibrational modes display an appreciable anharmonicity, as derived from a comparison between kinetic and potential energy of the carbon atoms. Nuclear quantum effects are found to be appreciable in the interatomic distance and layer area at finite temperatures. The thermal expansion coefficient resulting from PIMD simulations vanishes in the zero-temperature limit, in agreement with the third law of thermodynamics.

cond-mat.mtrl-sci↗

arXiv2015

Path-integral simulation of ice VII: Pressure and temperature effects

Effects of pressure and temperature on structural and thermodynamic properties of ice VII have been studied by using path-integral molecular dynamics (PIMD) simulations. Temperatures between 25 and 450 K, as well as pressures up to 12 GPa were considered. Interatomic interactions were modeled by using the effective q-TIP4P/F potential for flexible water. We analyze the pressure dependence of the molar volume, bulk modulus, interatomic distances, kinetic energy, and atomic delocalization at various temperatures. Results of PIMD simulations are compared with those derived from a quasi-harmonic approximation (QHA) of vibrational modes, which helps to assess the importance of anharmonic effects, as well as the influence of the different modes on the properties of ice VII. The accuracy of the QHA for describing this high-pressure phase decreases for rising temperature, but this approximation becomes more reliable as pressure grows, since anharmonicity becomes less relevant. Comparisons with low-pressure cubic ice are presented.

physics.chem-ph↗

arXiv2015

Ising model in clustered scale-free networks

The Ising model in clustered scale-free networks has been studied by Monte Carlo simulations. These networks are characterized by a degree distribution of the form P(k) ~ k^(-gamma) for large k. Clustering is introduced in the networks by inserting triangles, i.e., triads of connected nodes. The transition from a ferromagnetic (FM) to a paramagnetic (PM) phase has been studied as a function of the exponent gamma and the triangle density. For gamma > 3 our results are in line with earlier simulations, and a phase transition appears at a temperature T_c(gamma) in the thermodynamic limit (system size N to infinity). For gamma <= 3, a FM-PM crossover appears at a size-dependent temperature T_co, so that the system remains in a FM state at any finite temperature in the limit N to infinity. Thus, for gamma = 3, T_co scales as ln N, whereas for gamma < 3, we find T_co ~ J N^z, where the exponent z decreases for increasing gamma. Adding motifs (triangles in our case) to the networks causes an increase in the transition (or crossover) temperature for exponent gamma > 3 (or <= 3). For gamma > 3, this increase is due to changes in the mean values < k > and < k^2 >, i.e., the transition is controlled by the degree distribution (nearest neighbor connectivities). For gamma <= 3, however, we find that clustered and unclustered networks with the same size and distribution P(k) have different crossover temperature, i.e., clustering favors FM correlations, thus increasing the temperature T_co. The effect of a degree cutoff k_cut on the asymptotic behavior of T_co is discussed.

cond-mat.dis-nn↗

arXiv2014

Configurational entropy of hydrogen-disordered ice polymorphs

The configurational entropy of several H-disordered ice polymorphs is calculated by means of a thermodynamic integration along a path between a totally H-disordered state and one fulfilling the Bernal-Fowler ice rules. A Monte Carlo procedure based on a simple energy model is used, so that the employed thermodynamic path drives the system from high temperatures to the low-temperature limit. This method turns out to be precise enough to give reliable values for the configurational entropy of different ice phases in the thermodynamic limit (number of molecules N --> infinity). The precision of the method is checked for the ice model on a two-dimensional square lattice. Results for the configurational entropy are given for H-disordered arrangements on several polymorphs, including ices Ih, Ic, II, III, IV, V, VI, and XII. The highest and lowest entropy values correspond to ices VI and XII, respectively, with a difference of 3.3\% between them. The dependence of the entropy on the ice structures has been rationalized by comparing it with structural parameters of the various polymorphs, such as the mean ring size. A particularly good correlation has been found between the configurational entropy and the connective constant derived from self-avoiding walks on the ice networks.

physics.chem-ph↗

arXiv2014

Path-integral simulation of solids

The path-integral formulation of the statistical mechanics of quantum many-body systems is described, with the purpose of introducing practicaltechniques for the simulation of solids. Monte Carlo and molecular dynamics methods for distinguishable quantum particles are presented, with particular attention to the isothermal-isobaric ensemble. Applications of these computational techniques to different types of solids are reviewed, including noble-gas solids (helium and heavier elements), group-IV materials (diamond and elemental semiconductors), and molecular solids (with emphasis on hydrogen and ice). Structural, vibrational, and thermodynamic properties of these materials are discussed. Applications also include point defects in solids (structure and diffusion), as well as nuclear quantum effects in solid surfaces and adsorbates. Different phenomena are discussed, as solid-to-solid and orientational phase transitions, rates of quantum processes, classical-to-quantum crossover, and various finite-temperature anharmonic effects (thermal expansion, isotopic effects, electron-phonon interactions). Nuclear quantum effects are most remarkable in the presence of light atoms, so that especial emphasis is laid on solids containing hydrogen as a constituent element or as an impurity.

cond-mat.mtrl-sci↗

arXiv2014

Structural characterization of ice polymorphs from self-avoiding walks

Topological properties of crystalline ice structures are studied by means of self-avoiding walks on their H-bond networks. The number of self-avoiding walks, C_n, for eight ice polymorphs has been obtained by direct enumeration up to walk length n = 27. This has allowed us to determine the `connective constant' or effective coordination number `mu' of these structures as the limit of the ratio C_n/C_{n-1} for large n. This structure-dependent parameter `mu' is related with other topological characteristics of ice polymorphs, such as the mean and minimum ring size, or the topological density of network sites. A correlation between the connective constant and the configurational entropy of hydrogen-disordered ice structures is discussed.

physics.chem-ph↗

arXiv2013

Topological characterization of crystalline ice structures from coordination sequences

Topological properties of crystalline ice structures are studied by considering ring statistics, coordination sequences, and topological density of different ice phases. The coordination sequences (number of sites at topological distance k from a reference site) have been obtained by direct enumeration until at least 40 coordination spheres for different ice polymorphs. This allows us to study the asymptotic behavior of the mean number of sites in the k-th shell, M_k, for high values of k: M_k ~ a k^2, a being a structure-dependent parameter. Small departures from a strict parabolic dependence have been studied by considering first and second differences of the series {M_k} for each structure. The parameter a ranges from 2.00 for ice VI to 4.27 for ice XII, and is used to define a topological density for these solid phases of water. Correlations between such topological density and the actual volume of ice phases are discussed. Ices Ih and Ic are found to depart from the general trend in this correlation due to the large void space in their structures.

physics.chem-ph↗

arXiv2013

Configurational entropy of ice from thermodynamic integration

The configurational entropy of ice is calculated by thermodynamic integration from high to low temperatures. We use Monte Carlo simulations with a simple energy model which reproduces the Bernal-Fowler ice rules. This procedure is found to be precise enough to give reliable values for the residual entropy s_th of different ice phases in the thermodynamic limit. First, we check it for a two-dimensional ice model. Second, we calculate s_th for ice Ih, and compare our result with those previously given in the literature. Third, we obtain s_th for ice VI, for which we find a value clearly higher than for ice Ih.

physics.chem-ph↗

arXiv2012

High-density amorphous ice: A path-integral simulation

Structural and thermodynamic properties of high-density amorphous (HDA) ice have been studied by path-integral molecular dynamics simulations in the isothermal-isobaric ensemble. Interatomic interactions were modeled by using the effective q-TIP4P/F potential for flexible water. Quantum nuclear motion is found to affect several observable properties of the amorphous solid. At low temperature (T = 50 K) the molar volume of HDA ice is found to increase by 6%, and the intramolecular O--H distance rises by 1.4% due to quantum motion. Peaks in the radial distribution function of HDA ice are broadened respect to their classical expectancy. The bulk modulus, B, is found to rise linearly with the pressure, with a slope dB/dP = 7.1. Our results are compared with those derived earlier from classical and path-integral simulations of HDA ice. We discuss similarities and discrepancies with those earlier simulations.

physics.chem-ph↗

arXiv2012

Path-integral simulation of ice Ih: The effect of pressure

The effect of pressure on structural and thermodynamic properties of ice Ih has been studied by means of path-integral molecular dynamics simulations at temperatures between 50 and 300 K. Interatomic interactions were modeled by using the effective q-TIP4P/F potential for flexible water. Positive (compression) and negative (tension) pressures have been considered, which allowed us to approach the limits for the mechanical stability of this solid water phase. We have studied the pressure dependence of the crystal volume, bulk modulus, interatomic distances, atomic delocalization, and kinetic energy. The spinodal point at both negative and positive pressures is derived from the vanishing of the bulk modulus. For P < 0, the spinodal pressure changes from -1.38 to -0.73 GPa in the range from 50 to 300 K. At positive pressure the spinodal is associated to ice amorphization, and at low temperatures is found between 1.1 and 1.3 GPa. Quantum nuclear effects cause a reduction of the metastability region of ice Ih.

cond-mat.mtrl-sci↗

arXiv2011

Diffusion of hydrogen in graphite: A molecular dynamics simulation

Diffusion of atomic and molecular hydrogen in the interstitial space between graphite sheets has been studied by molecular dynamics simulations. Interatomic interactions were modeled by a tight-binding potential fitted to density-functional calculations. Atomic hydrogen is found to be bounded to C atoms, and its diffusion consists in jumping from a C atom to a neighboring one, with an activation energy of about 0.4 eV. Molecular hydrogen is less attached to the host sheets and diffuses faster than isolated H. At temperatures lower than 500 K, H_2 diffuses with an activation energy of 89 meV, whereas at higher T its diffusion is enhanced by longer jumps of the molecule as well as by correlations between successive hops, yielding an effective activation energy of 190 meV.

cond-mat.mtrl-sci↗

arXiv2011

Molecular hydrogen in graphite: A path-integral simulation

Molecular hydrogen in the bulk of graphite has been studied by path-integral molecular dynamics simulations. Finite-temperature properties of H_2 molecules adsorbed between graphite layers were analyzed in the temperature range from 300 to 900 K. The interatomic interactions were modeled by a tight-binding potential fitted to density-functional calculations. In the lowest-energy position, an H_2 molecule is found to be disposed parallel to the sheets plane. At finite temperatures, the molecule explores other orientations, but its rotation is partially hindered by the adjacent graphite layers. Vibrational frequencies were obtained from a linear-response approach, based on correlations of atom displacements. For the stretching vibration of the molecule, we find at 300 K a frequency omega_s = 3916 cm-1, more than 100 cm-1 lower than the frequency corresponding to an isolated H_2 molecule. Isotope effects have been studied by considering also deuterium and tritium molecules. For D_2 in graphite we obtained omega_s = 2816 cm-1}, i.e., an isotopic ratio omega_s(H) / omega_s(D) = 1.39.

cond-mat.mtrl-sci↗

arXiv2011

Isotope effects in ice Ih: A path-integral simulation

Ice Ih has been studied by path-integral molecular dynamics simulations, using the effective q-TIP4P/F potential model for flexible water. This has allowed us to analyze finite-temperature quantum effects in this solid phase from 25 to 300 K at ambient pressure. Among these effects we find a negative thermal expansion of ice at low temperatures, which does not appear in classical molecular dynamics simulations. The compressibility derived from volume fluctuations gives results in line with experimental data. We have analyzed isotope effects in ice Ih by considering normal, heavy, and tritiated water. In particular, we studied the effect of changing the isotopic mass of hydrogen on the kinetic energy and atomic delocalization in the crystal, as well as on structural properties such as interatomic distances and molar volume. For D$_2$O ice Ih at 100 K we obtained a decrease in molar volume and intramolecular O--H distance of 0.6% and 0.4%, respectively, as compared to H$_2$O ice.

cond-mat.mtrl-sci↗

arXiv2009

Zero-temperature Glauber dynamics on small-world networks

The zero-temperature Glauber dynamics of the ferromagnetic Ising model on small-world networks, rewired from a two-dimensional square lattice, has been studied by numerical simulations. For increasing disorder in finite networks, the nonequilibrium dynamics becomes faster, so that the ground state is found more likely. For any finite value of the rewiring probability p, the likelihood of reaching the ground state goes to zero in the thermodynamic limit, similarly to random networks. The spin correlation xi(r) is found to decrease with distance as xi(r) ~ exp(-r/lambda), lambda being a correlation length scaling with p as lambda ~ p^(-0.73). These results are compared with those obtained earlier for addition-type small world networks.

cond-mat.dis-nn↗

arXiv2009

Antiferromagnetic Ising model in scale-free networks

The antiferromagnetic Ising model in uncorrelated scale-free networks has been studied by means of Monte Carlo simulations. These networks are characterized by a connectivity (or degree) distribution P(k) ~ k^(- gamma). The disorder present in these complex networks frustrates the antiferromagnetic spin ordering, giving rise to a spin-glass (SG) phase at low temperature. The paramagnetic-SG transition temperature T_c has been studied as a function of the parameter gamma and the minimum degree present in the networks. T_c is found to increase when the exponent gamma is reduced, in line with a larger frustration caused by the presence of nodes with higher degree.

cond-mat.dis-nn↗

arXiv2009

Molecular hydrogen in silicon: A path-integral simulation

Molecular hydrogen in silicon has been studied by path-integral molecular dynamics simulations in the canonical ensemble. Finite-temperature properties of these point defects were analyzed in the range from 300 to 900 K. Interatomic interactions were modeled by a tight-binding potential fitted to density-functional calculations. The most stable position for these impurities is found at the interstitial T site, with the hydrogen molecule rotating freely in the Si cage. Vibrational frequencies have been obtained from a linear-response approach, based on correlations of atom displacements at finite temperatures. The results show a large anharmonic effect in the stretching vibration, omega_s, which is softened with respect to a harmonic approximation by about 300 cm^{-1}. The coupling between rotation and vibration causes an important decrease in omega_s for rising temperature.

cond-mat.mtrl-sci↗