2,515 research outputs found
Development of an Advanced Force Field for Water using Variational Energy Decomposition Analysis
Given the piecewise approach to modeling intermolecular interactions for
force fields, they can be difficult to parameterize since they are fit to data
like total energies that only indirectly connect to their separable functional
forms. Furthermore, by neglecting certain types of molecular interactions such
as charge penetration and charge transfer, most classical force fields must
rely on, but do not always demonstrate, how cancellation of errors occurs among
the remaining molecular interactions accounted for such as exchange repulsion,
electrostatics, and polarization. In this work we present the first generation
of the (many-body) MB-UCB force field that explicitly accounts for the
decomposed molecular interactions commensurate with a variational energy
decomposition analysis, including charge transfer, with force field design
choices that reduce the computational expense of the MB-UCB potential while
remaining accurate. We optimize parameters using only single water molecule and
water cluster data up through pentamers, with no fitting to condensed phase
data, and we demonstrate that high accuracy is maintained when the force field
is subsequently validated against conformational energies of larger water
cluster data sets, radial distribution functions of the liquid phase, and the
temperature dependence of thermodynamic and transport water properties. We
conclude that MB-UCB is comparable in performance to MB-Pol, but is less
expensive and more transferable by eliminating the need to represent
short-ranged interactions through large parameter fits to high order
polynomials
Understanding brønsted-acid catalyzed monomolecular reactions of Alkanes in Zeolite Pores by combining insights from experiment and theory
Acidic zeolites are effective catalysts for the cracking of large hydrocarbon molecules into lower molecular weight products required for transportation fuels. However, the ways in which the zeolite structure affects the catalytic activity at BrOnsted protons are not fully understood. One way to characterize the influence of the zeolite structure on the catalysis is to study alkane cracking and dehydrogenation at very low conversion, conditions for which the kinetics are well defined. To understand the effects of zeolite structure on the measured rate coefficient (k(app)), it is necessary to identify the equilibrium constant for adsorption into the reactant state (Kads-H+) and the intrinsic rate coefficient of the reaction (k(int)) at reaction temperatures, since k(app) is proportional to the product of Kads-H+ and k(int). We show that Kads-H+ cannot be calculated from experimental adsorption data collected near ambient temperature, but can, however, be estimated accurately from configurational-bias Monte Carlo (CBMC) simulations. Using monomolecular cracking and dehydrogenation of C-3-C-6 alkanes as an example, we review recent efforts aimed at elucidating the influence of the acid site location and the zeolite framework structure on the observed values of k(app) and its components, Kads-H+ and k(int)
Inelastic transport theory from first-principles: methodology and applications for nanoscale devices
We describe a first-principles method for calculating electronic structure,
vibrational modes and frequencies, electron-phonon couplings, and inelastic
electron transport properties of an atomic-scale device bridging two metallic
contacts under nonequilibrium conditions. The method extends the
density-functional codes SIESTA and TranSIESTA that use atomic basis sets. The
inelastic conductance characteristics are calculated using the nonequilibrium
Green's function formalism, and the electron-phonon interaction is addressed
with perturbation theory up to the level of the self-consistent Born
approximation. While these calculations often are computationally demanding, we
show how they can be approximated by a simple and efficient lowest order
expansion. Our method also addresses effects of energy dissipation and local
heating of the junction via detailed calculations of the power flow. We
demonstrate the developed procedures by considering inelastic transport through
atomic gold wires of various lengths, thereby extending the results presented
in [Frederiksen et al., Phys. Rev. Lett. 93, 256601 (2004)]. To illustrate that
the method applies more generally to molecular devices, we also calculate the
inelastic current through different hydrocarbon molecules between gold
electrodes. Both for the wires and the molecules our theory is in quantitative
agreement with experiments, and characterizes the system-specific mode
selectivity and local heating.Comment: 24 pages, 17 figure
Introduction to protein folding for physicists
The prediction of the three-dimensional native structure of proteins from the
knowledge of their amino acid sequence, known as the protein folding problem,
is one of the most important yet unsolved issues of modern science. Since the
conformational behaviour of flexible molecules is nothing more than a complex
physical problem, increasingly more physicists are moving into the study of
protein systems, bringing with them powerful mathematical and computational
tools, as well as the sharp intuition and deep images inherent to the physics
discipline. This work attempts to facilitate the first steps of such a
transition. In order to achieve this goal, we provide an exhaustive account of
the reasons underlying the protein folding problem enormous relevance and
summarize the present-day status of the methods aimed to solving it. We also
provide an introduction to the particular structure of these biological
heteropolymers, and we physically define the problem stating the assumptions
behind this (commonly implicit) definition. Finally, we review the 'special
flavor' of statistical mechanics that is typically used to study the
astronomically large phase spaces of macromolecules. Throughout the whole work,
much material that is found scattered in the literature has been put together
here to improve comprehension and to serve as a handy reference.Comment: 53 pages, 18 figures, the figures are at a low resolution due to
arXiv restrictions, for high-res figures, go to http://www.pabloechenique.co
Structure optimization in an off-lattice protein model
We study an off-lattice protein toy model with two species of monomers
interacting through modified Lennard-Jones interactions. Low energy
configurations are optimized using the pruned-enriched-Rosenbluth method
(PERM), hitherto employed to native state searches only for off lattice models.
For 2 dimensions we found states with lower energy than previously proposed
putative ground states, for all chain lengths . This indicates that
PERM has the potential to produce native states also for more realistic protein
models. For , where no published ground states exist, we present some
putative lowest energy states for future comparison with other methods.Comment: 4 pages, 2 figure
Entanglement Measures for Single- and Multi-Reference Correlation Effects
Electron correlation effects are essential for an accurate ab initio
description of molecules. A quantitative a priori knowledge of the single- or
multi-reference nature of electronic structures as well as of the dominant
contributions to the correlation energy can facilitate the decision regarding
the optimum quantum chemical method of choice. We propose concepts from quantum
information theory as orbital entanglement measures that allow us to evaluate
the single- and multi-reference character of any molecular structure in a given
orbital basis set. By studying these measures we can detect possible artifacts
of small active spaces.Comment: 14 pages, 4 figure
Liquid State Anomalies for the Stell-Hemmer Core-Softened Potential
We study the Stell-Hemmer potential using both analytic (exact and
approximate ) solutions and numerical simulations. We observe in the
liquid phase an anomalous decrease in specific volume and isothermal
compressibility upon heating, and an anomalous increase in the diffusion
coefficient with pressure. We relate the anomalies to the existence of two
different local structures in the liquid phase. Our results are consistent with
the possibility of a low temperature/high pressure liquid-liquid phase
transition.Comment: 4 pages in one gzipped ps file including 11 figures; One RevTex and
11 gzipped eps figure
Ab initio coupled-cluster and configuration interaction calculations for 16-O using V_UCOM
Using the ground-state energy of 16-O obtained with the realistic V_UCOM
interaction as a test case, we present a comprehensive comparison of different
configuration interaction (CI) and coupled-cluster (CC) methods, analyzing the
intrinsic advantages and limitations of each of the approaches. In particular,
we use the importance-truncated (IT) CI and no-core shell model (NCSM) schemes
with up to 4-particle-4-hole (4p4h) excitations as well as the size extensive
CC methods with a complete treatment of one- and two-body clusters (CCSD) and a
non-iterative treatment of connected three-body clusters via the completely
renormalized correction to the CCSD energy defining the CR-CC(2,3) approach. We
discuss the impact of the center-of-mass contaminations, the choice of the
single-particle basis, and size-extensivity on the resulting energies. When the
IT-CI and IT-NCSM methods include the 4p4h excitations and when the CC
calculations include the 1p1h, 2p2h, and 3p3h clusters, as in the CR-CC(2,3)
approach, we observe an excellent agreement among the different methodologies.
This shows that despite their individual limitations, the IT-CI, IT-NCSM, and
CC methods can provide precise and consistent ab initio nuclear structure
predictions. Furthermore, the IT-CI, IT-NCSM, and CC ground-state energy values
obtained with 16-O are in good agreement with the experimental value, proving
that the V_UCOM two-body interaction allows for a realistic description of
binding energies for heavier nuclei and that all of the methods used in this
study account for most of the relevant particle correlation effects.Comment: 20 pages, 4 figures, 1 table (v2: extended version in response to
referees' comments
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