203 research outputs found
Structure and binding in crystals of cage-like molecules: hexamine and platonic hydrocarbons
In this paper, we show that first-principle calculations using a van der
Waals density functional (vdW-DF), [Phys. Rev. Lett. , 246401
(2004)] permits determination of molecular crystal structure. We study the
crystal structures of hexamine and the platonic hydrocarbons (cubane and
dodecahedrane). The calculated lattice parameters and cohesion energy agree
well with experiments. Further, we examine the asymptotic accounts of the van
der Waals forces by comparing full vdW-DF with asymptotic atom-based pair
potentials extracted from vdW-DF. The character of the binding differ in the
two cases, with vdW-DF giving a significant enhancement at intermediate and
relevant binding separations. We analyze consequences of this result for
methods such as DFT-D, and question DFT-D's transferability over the full range
of separations
Ab initio structure modeling of complex thin-film oxides: thermodynamical stability of TiC/thin-film alumina
We present an efficient and general method to identify promising candidate
configurations for thin-film oxides and to determine structural characteristics
of (metastable) thin-film structures using ab initio calculations. At the heart
of this method is the complexity of the oxide bulk structure, from which a
large number of thin films with structural building blocks, that is motifs,
from metastable bulk oxide systems can be extracted. These span a coarse but
well-defined network of initial configurations for which density functional
theory (DFT) calculations predict and implement dramatic atomic relaxations in
the corresponding, resulting thin-film candidates. The network of thin-film
candidates (for various film thicknesses and stoichiometries) can be ordered
according to their variation in ab initio total energy or in ab initio
equilibrium Gibbs free energy. Analysis of the relaxed atomic structures for
the most favored structures gives insight into the nature of stable and
metastable thin-film oxides. We investigate ultrathin alumina nucleated on TiC
as a model system to illustrate this method.Comment: Submitted to PRB; 16 pages, 11 figure
Nonequilibrium thermodynamics of interacting tunneling transport: variational grand potential, density-functional formulation, and nature of steady-state forces
The standard formulation of tunneling transport rests on an open-boundary
modeling. There, conserving approximations to nonequilibrium Green function or
quantum-statistical mechanics provide consistent but computational costly
approaches; alternatively, use of density-dependent ballistic-transport
calculations [e.g., Phys. Rev. B 52, 5335 (1995)], here denoted `DBT', provide
computationally efficient (approximate) atomistic characterizations of the
electron behavior but has until now lacked a formal justification. This paper
presents an exact, variational nonequilibrium thermodynamic theory for fully
interacting tunneling and provides a rigorous foundation for frozen-nuclei DBT
calculations as a lowest order approximation to an exact nonequilibrium
thermodynamics density functional evaluation. The theory starts from the
complete electron nonequilibrium quantum statistical mechanics and I identify
the operator for the nonequilibrium Gibbs free energy. I demonstrate a minimal
property of a functional for the nonequilibrium thermodynamic grand potential
which thus uniquely identifies the solution as the exact nonequilibrium density
matrix. I also show that a uniqueness-of-density proof from a closely related
study [Phys. Rev. B 78, 165109 (2008)] makes it possible to provide a
single-particle formulation based on universal electron-density functionals. I
illustrate a formal evaluation of the thermodynamics grand potential value
which is closely related to the variation in scattering phase shifts and hence
to Friedel density oscillations. This paper also discusses the difference
between the here-presented exact thermodynamics forces and the often-used
electrostatic forces. Finally the paper documents an inherent adiabatic nature
of the thermodynamics forces and observes that these are suited for a
nonequilibrium implementation of the Born-Oppenheimer approximation.Comment: 37 pages, 3 Figure
Understanding adhesion at as-deposited interfaces from ab initio thermodynamics of deposition growth: thin-film alumina on titanium carbide
We investigate the chemical composition and adhesion of chemical vapour
deposited thin-film alumina on TiC using and extending a recently proposed
nonequilibrium method of ab initio thermodynamics of deposition growth (AIT-DG)
[Rohrer J and Hyldgaard P 2010 Phys. Rev. B 82 045415]. A previous study of
this system [Rohrer J, Ruberto C and Hyldgaard P 2010 J. Phys.: Condens. Matter
22 015004] found that use of equilibrium thermodynamics leads to predictions of
a non-binding TiC/alumina interface, despite the industrial use as a
wear-resistant coating. This discrepancy between equilibrium theory and
experiment is resolved by the AIT-DG method which predicts interfaces with
strong adhesion. The AIT-DG method combines density functional theory
calculations, rate-equation modelling of the pressure evolution of the
deposition environment and thermochemical data. The AIT-DG method was
previously used to predict prevalent terminations of growing or as-deposited
surfaces of binary materials. Here we extent the method to predict surface and
interface compositions of growing or as-deposited thin films on a substrate and
find that inclusion of the nonequilibrium deposition environment has important
implications for the nature of buried interfaces.Comment: 8 pages, 6 figures, submitted to J. Phys.: Condens. Matte
Van der Waals density functional: Self-consistent potential and the nature of the van der Waals bond
We derive the exchange-correlation potential corresponding to the nonlocal
van der Waals density functional [M. Dion, H. Rydberg, E. Schroder, D. C.
Langreth, and B. I. Lundqvist, Phys. Rev. Lett. 92, 246401 (2004)]. We use this
potential for a self-consistent calculation of the ground state properties of a
number of van der Waals complexes as well as crystalline silicon. For the
latter, where little or no van der Waals interaction is expected, we find that
the results are mostly determined by semilocal exchange and correlation as in
standard generalized gradient approximations (GGA), with the fully nonlocal
term giving little effect. On the other hand, our results for the van der Waals
complexes show that the self-consistency has little effect at equilibrium
separations. This finding validates previous calculations with the same
functional that treated the fully nonlocal term as a post GGA perturbation. A
comparison of our results with wave-function calculations demonstrates the
usefulness of our approach. The exchange-correlation potential also allows us
to calculate Hellmann-Feynman forces, hence providing the means for efficient
geometry relaxations as well as unleashing the potential use of other standard
techniques that depend on the self-consistent charge distribution. The nature
of the van der Waals bond is discussed in terms of the self-consistent bonding
charge.Comment: submitted to Phys. Rev.
Understanding rapid infant weight gain prevention: a systematic review of quantitative and qualitative evidence.
This is the author accepted manuscriptBACKGROUND: Rapid infant weight gain (RIWG) is strongly related to childhood overweight and obesity, and prevention of RIWG is an approach to early years obesity prevention. This systematic review aimed to explore effectiveness, deliverers' and recipients' experiences of involvement, and key intervention components and processes of such prevention activities. METHODS: Key databases and websites were searched systematically for quantitative and qualitative studies covering intervention effectiveness, experiences with intervention involvement or process outcomes. After duplicate screening and quality assessment, papers were analyzed through narrative synthesis, thematic synthesis and intervention component analysis. RESULTS: Seven quantitative and seven qualitative studies were eligible for inclusion. Most intervention studies reported small, but significant results on infant weight gain. More significant results were measured on weight gain during the first compared with the second year of life. A weak evidence base made elaboration of the relationship between intervention effectiveness and content challenging. Home-delivered interventions may be more relevant for parents. Contextual factors, such as social norms, beliefs and professional identity should be considered during intervention development. Stakeholder involvement can be key to increase intervention acceptability and feasibility. CONCLUSIONS: The field of RIWG prevention is new and evolving, but more research is needed before further conclusions about intervention effectiveness and intervention content can be drawn. Future interventions should take parents, health professionals and other contextual needs into account to improve chances of success. More research on long-term effects on overweight and obesity is needed.UK Clinical Research Collaboratio
The effect of inelastic processes on tunneling
We study an electron that interacts with phonons or other linear or nonlinear
excitations as it resonantly tunnels. The method we use is based on mapping a
many-body problem in a large variational space exactly onto a one-body problem.
The method is conceptually simpler than previous Green's function approaches,
and allows the essentially exact numerical solution of much more general
problems. We solve tunneling problems with transverse channels, multiple sites
coupled to phonons, and multiple phonon degrees of freedom and excitations.Comment: 12 pages, REVTex, 4 figures in compressed tar .ps forma
Randomized clinical trial of remote ischaemic preconditioning versus no preconditioning in the prevention of perioperative myocardial infarction during open surgery for ruptured abdominal aortic aneurysm
Influence of adatom interactions on second layer nucleation
We develop a theory for the inclusion of adatom interactions in second layer
nucleation occurring in epitaxial growth. The interactions considered are due
to ring barriers between pairs of adatoms and binding energies of unstable
clusters. The theory is based on a master equation, which describes the time
development of microscopic states that are specified by cluster configurations
on top of an island. The transition rates are derived by scaling arguments and
tested against kinetic Monte-Carlo simulations. As an application we reanalyze
experiments to determine the step edge barrier for Ag/Pt(111).Comment: 4 pages, 4 figure
Benchmarking van der Waals Density Functionals with Experimental Data: Potential Energy Curves for H2 Molecules on Cu(111), (100), and (110) Surfaces
Detailed physisorption data from experiment for the H_2 molecule on low-index
Cu surfaces challenge theory. Recently, density-functional theory (DFT) has
been developed to account for nonlocal correlation effects, including van der
Waals (dispersion) forces. We show that the functional vdW-DF2 gives a
potential-energy curve, potential-well energy levels, and difference in lateral
corrugation promisingly close to the results obtained by resonant elastic
backscattering-diffraction experiments. The backscattering barrier is found
selective for choice of exchange-functional approximation. Further, the DFT-D3
and TS-vdW corrections to traditional DFT formulations are also benchmarked,
and deviations are analyzed.Comment: 15 pages, 9 figure
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