571 research outputs found
Density functional simulation of small Fe nanoparticles
We calculate from first principles the electronic structure, relaxation and
magnetic moments in small Fe particles, applying the numerical local orbitals
method in combination with norm-conserving pseudopotentials. The accuracy of
the method in describing elastic properties and magnetic phase diagrams is
tested by comparing benchmark results for different phases of crystalline iron
to those obtained by an all-electron method. Our calculations for the
bipyramidal Fe_5 cluster qualitatively and quantitatively confirm previous
plane-wave results that predicted a non-collinear magnetic structure. For
larger bcc-related (Fe_35) and fcc-related (Fe_38, Fe_43, Fe_62) particles, a
larger inward relaxation of outer shells has been found in all cases,
accompanied by an increase of local magnetic moments on the surface to beyond 3
mu_B.Comment: 15 pages with 6 embedded postscript figures, updated version,
submitted to Eur.Phys.J.
Dislocation formation from a surface step in semiconductors: an ab initio study
The role of a simple surface defect, such as a step, for relaxing the stress
applied to a semiconductor, has been investigated by means of large scale first
principles calculations. Our results indicate that the step is the privileged
site for initiating plasticity, with the formation and glide of 60
dislocations for both tensile and compressive deformations. We have also
examined the effect of surface and step termination on the plastic mechanisms
Anomalous electron-phonon interaction in doped LaOFeAs: a First Principles calculation
We present first principles calculations of the atomic and electronic
structure of electron-doped LaOFeAs. We find that whereas the undoped compound
has an antiferromagnetic arrangement of magnetic moments at the Fe atoms, the
doped system becomes non magnetic at a critical electron concentration. We have
studied the electron-phonon interaction in the doped paramagnetic phase. For
the phonon, the separation between the As and Fe planes induces a
non-collinear arrangement of the Fe magnetic moments. This arrangement is anti
parallel for interactions mediated by As, and perpendicular for Fe-Fe direct
interactions, thus avoiding frustration. This coupling of magnetism with
vibrations induces anharmonicities and an electron-phonon interaction much
larger than in the pure paramagnetic case. We propose that such enhanced
interactions play an essential role in superconducting compounds close to an
atiferromagnetic phase transition.Comment: 4 pages, 5 figure
Density, structure and dynamics of water: the effect of Van der Waals interactions
It is known that ab initio molecular dynamics (AIMD) simulations of liquid
water, based on the generalized gradient approximation (GGA) to density
functional theory (DFT), yield structural and diffusive properties in
reasonable agreement with experiment only if artificially high temperatures are
used in the simulations. The equilibrium density, at normal conditions, of DFT
water has been recently shown by Schmidt et al. [J. Phys. chem. B, 113, 11959
(2009)] to be underestimated by different GGA functionals for exchange and
correlation, and corrected by the addition of interatomic pair potentials to
describe van derWaals (vdW) interactions. In this contribution we present a
DFTAIMD study of liquid water using several GGA functionals as well as the van
der Waals density functional (vdW-DF) of Dion et al. [Phys. Rev. Lett. 92,
246401(2004)]. As expected, we find that the density of water is grossly
underestimated by GGA functionals. When a vdW-DF is used, the density improves
drastically and the experimental diffusivity is reproduced without the need of
thermal corrections. We analyze the origin of the density differences between
all the functionals. We show that the vdW-DF increases the population of
non-H-bonded interstitial sites, at distances between the first and second
coordination shells. However, it excessively weakens the H-bond network,
collapsing the second coordination shell. This structural problem is partially
associated to the choice of GGA exchange in the vdW-DF. We show that a
different choice for the exchange functional is enough to achieve an overall
improvement both in structure and diffusivity.Comment: 11 pages, 9 figures, submitted. Revised versio
Stability, Adsorption and Diffusion of CH4, CO2 and H2 in Clathrate Hydrates
We present a study of the adsorption and diffusion of CH4, CO2 and H2
molecules in clathrate hydrates using ab initio van der Waals density
functional formalism [Dion et al. Phys. Rev. Lett. 92, 246401 (2004)]. We find
that the adsorption energy is dominated by van der Waals interactions and that,
without them, gas hydrates would not be stable. We calculate the maximum
adsorption capacity as well as the maximum hydrocarbon size that can be
adsorbed.The relaxation of the host lattice is essential for a good description
of the diffusion activation energies, which are estimated to be of the order of
0.2, 0.4, and 1.0 eV for H2, CO2, and CH4, respectively.Comment: 4 pages, 4 figures, 3 table
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