Search results for "Computation"

showing 10 items of 7362 documents

Nanoscale ear drum: graphene based nanoscale sensors.

2012

The difficulty in determining the mass of a sample increases as its size diminishes. At the nanoscale, there are no direct methods for resolving the mass of single molecules or nanoparticles and so more sophisticated approaches based on electromechanical phenomena are required. More importantly, one demands that such nanoelectromechanical techniques could provide not only information about the mass of the target molecules but also about their geometrical properties. In this sense, we report a theoretical study that illustrates in detail how graphene membranes can operate as nanoelectromechanical mass-sensor devices. Wide graphene sheets were exposed to different types and amounts of molecul…

Chemical Physics (physics.chem-ph)FOS: Computer and information sciencesCondensed Matter - Materials ScienceMaterials scienceDopantGrapheneDopingDetectorNanoparticleMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesNanotechnologylaw.inventionComputational Engineering Finance and Science (cs.CE)Molecular dynamicslawDirect methodsPhysics - Chemical PhysicsGeneral Materials ScienceComputer Science - Computational Engineering Finance and ScienceNanoscopic scaleNanoscale
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Optimal calculation of the pair correlation function for an orthorhombic system

2012

We present a new computational method to calculate arbitrary pair correlation functions of an orthorombic system in the most efficient way. The algorithm is demonstrated by the calculation of the radial distribution function of shock compressed liquid hydrogen.

Chemical Physics (physics.chem-ph)HydrogenCompressed fluidMathematical analysisFOS: Physical scienceschemistry.chemical_elementGeometryComputational Physics (physics.comp-ph)Radial distribution functionShock (mechanics)chemistryPhysics - Chemical PhysicsPair correlationOrthorhombic crystal systemPhysics - Computational PhysicsMathematicsPhysical Review E
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Eliminating Artificial Boundary Conditions in Time-Dependent Density Functional Theory Using Fourier Contour Deformation

2023

We present an efficient method for propagating the time-dependent Kohn-Sham equations in free space, based on the recently introduced Fourier contour deformation (FCD) approach. For potentials which are constant outside a bounded domain, FCD yields a high-order accurate numerical solution of the time-dependent Schrödinger equation directly in free space, without the need for artificial boundary conditions. Of the many existing artificial boundary condition schemes, FCD is most similar to an exact nonlocal transparent boundary condition, but it works directly on Cartesian grids in any dimension, and runs on top of the fast Fourier transform rather than fast algorithms for the application of …

Chemical Physics (physics.chem-ph)Physics - Chemical PhysicsFOS: MathematicsFOS: Physical sciencesTDDFT Open boundariesMathematics - Numerical AnalysisNumerical Analysis (math.NA)Computational Physics (physics.comp-ph)Physical and Theoretical ChemistryPhysics - Computational PhysicsSettore FIS/03 - Fisica Della MateriaComputer Science Applications
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Virtual Orbital Many-Body Expansions: A Possible Route towards the Full Configuration Interaction Limit

2017

In the present letter, it is demonstrated how full configuration interaction (FCI) results in extended basis sets may be obtained to within sub-kJ/mol accuracy by decomposing the energy in terms of many-body expansions in the virtual orbitals of the molecular system at hand. This extension of the FCI application range lends itself to two unique features of the current approach, namely that the total energy calculation can be performed entirely within considerably reduced orbital subspaces and may be so by means of embarrassingly parallel programming. Facilitated by a rigorous and methodical screening protocol and further aided by expansion points different from the Hartree-Fock solution, al…

Chemical Physics (physics.chem-ph)Physics010304 chemical physicsBasis (linear algebra)Embarrassingly parallelFOS: Physical sciences010402 general chemistry01 natural sciencesFull configuration interactionLinear subspace0104 chemical sciencesRange (mathematics)Atomic orbitalComputational chemistryPhysics - Chemical Physics0103 physical sciencesGeneral Materials ScienceLimit (mathematics)Statistical physicsPhysical and Theoretical ChemistryEnergy (signal processing)
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On fermionic shadow wave functions for strongly correlated multi-reference systems based on a single Slater determinant

2015

We demonstrate that extending the Shadow Wave Function to fermionic systems facilitates to accurately calculate strongly-correlated multi-reference systems such as the stretched H2 molecule. This development considerably extends the scope of electronic structure calculations and enables to efficiently recover the static correlation energy using just a single Slater determinant.

Chemical Physics (physics.chem-ph)PhysicsQuantum PhysicsNuclear TheoryStrongly Correlated Electrons (cond-mat.str-el)FOS: Physical sciencesGeneral Physics and AstronomyComputational Physics (physics.comp-ph)Nuclear Theory (nucl-th)Condensed Matter - Strongly Correlated ElectronsPhysics - Chemical PhysicsShadowSlater determinantDevelopment (differential geometry)Statistical physicsQuantum Physics (quant-ph)Wave functionPhysics - Computational PhysicsNuclear theoryEnergy (signal processing)EPL (Europhysics Letters)
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Resonating valence bond quantum Monte Carlo: Application to the ozone molecule

2015

We study the potential energy surface of the ozone molecule by means of Quantum Monte Carlo simulations based on the resonating valence bond concept. The trial wave function consists of an antisymmetrized geminal power arranged in a single-determinant that is multiplied by a Jastrow correlation factor. Whereas the determinantal part incorporates static correlation effects, the augmented real-space correlation factor accounts for the dynamics electron correlation. The accuracy of this approach is demonstrated by computing the potential energy surface for the ozone molecule in three vibrational states: symmetric, asymmetric and scissoring. We find that the employed wave function provides a de…

Chemical Physics (physics.chem-ph)PhysicsQuantum PhysicsStrongly Correlated Electrons (cond-mat.str-el)Electronic correlationGeminalQuantum Monte CarloFOS: Physical sciencesComputational Physics (physics.comp-ph)Condensed Matter PhysicsBond-dissociation energyMolecular physicsAtomic and Molecular Physics and OpticsCondensed Matter - Strongly Correlated ElectronsPhysics - Chemical PhysicsScissoringPotential energy surfaceValence bond theoryPhysics::Chemical PhysicsPhysical and Theoretical ChemistryQuantum Physics (quant-ph)Wave functionPhysics - Computational PhysicsInternational Journal of Quantum Chemistry
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Nuclear quantum effects in liquid water from path-integral simulations using anab initioforce-matching approach

2014

We have applied path integral simulations, in combination with new ab initio based water potentials, to investigate nuclear quantum effects in liquid water. Because direct ab initio path integral simulations are computationally expensive, a flexible water model is parameterized by force-matching to density functional theory-based molecular dynamics simulations. The resulting effective potentials provide an inexpensive replacement for direct ab inito molecular dynamics simulations and allow efficient simulation of nuclear quantum effects. Static and dynamic properties of liquid water at ambient conditions are presented and the role of nuclear quantum effects, exchange-correlation functionals…

Chemical Physics (physics.chem-ph)PhysicsStatistical Mechanics (cond-mat.stat-mech)Liquid waterBiophysicsAb initioFOS: Physical sciencesComputational Physics (physics.comp-ph)Condensed Matter - Soft Condensed MatterCondensed Matter PhysicsMolecular dynamicsForce matchingPhysics - Chemical PhysicsQuantum mechanicsDispersion (optics)Path integral formulationWater modelSoft Condensed Matter (cond-mat.soft)Density functional theoryPhysical and Theoretical ChemistryPhysics - Computational PhysicsMolecular BiologyCondensed Matter - Statistical MechanicsMolecular Physics
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Recent achievements in ab initio modelling of liquid water

2013

The application of newly developed first-principle modeling techniques to liquid water deepens our understanding of the microscopic origins of its unusual macroscopic properties and behaviour. Here, we review two novel ab initio computational methods: second-generation Car-Parrinello molecular dynamics and decomposition analysis based on absolutely localized molecular orbitals. We show that these two methods in combination not only enable ab initio molecular dynamics simulations on previously inaccessible time and length scales, but also provide unprecedented insights into the nature of hydrogen bonding between water molecules. We discuss recent applications of these methods to water cluste…

Chemical Physics (physics.chem-ph)Statistical Mechanics (cond-mat.stat-mech)Biological Physics (physics.bio-ph)Physics - Chemical PhysicsSoft Condensed Matter (cond-mat.soft)FOS: Physical sciencesPhysics - Biological PhysicsComputational Physics (physics.comp-ph)Condensed Matter - Soft Condensed MatterPhysics - Computational PhysicsCondensed Matter - Statistical Mechanics
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Adversarial reverse mapping of equilibrated condensed-phase molecular structures

2020

A tight and consistent link between resolutions is crucial to further expand the impact of multiscale modeling for complex materials. We herein tackle the generation of condensed molecular structures as a refinement -- backmapping -- of a coarse-grained structure. Traditional schemes start from a rough coarse-to-fine mapping and perform further energy minimization and molecular dynamics simulations to equilibrate the system. In this study we introduce DeepBackmap: A deep neural network based approach to directly predict equilibrated molecular structures for condensed-phase systems. We use generative adversarial networks to learn the Boltzmann distribution from training data and realize reve…

Chemical Physics (physics.chem-ph)Structure (mathematical logic)Artificial neural networkComputer sciencePhase (waves)FOS: Physical sciencesLink (geometry)Condensed Matter - Soft Condensed MatterComputational Physics (physics.comp-ph)Energy minimizationMultiscale modelingBoltzmann distributionHuman-Computer InteractionMolecular dynamicsArtificial IntelligencePhysics - Chemical PhysicsSoft Condensed Matter (cond-mat.soft)Physics - Computational PhysicsAlgorithmSoftwareMachine Learning: Science and Technology
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Incremental Treatments of the Full Configuration Interaction Problem

2020

The recent many-body expanded full configuration interaction (MBE-FCI) method is reviewed by critically assessing its advantages and drawbacks in the context of contemporary near-exact electronic structure theory. Besides providing a succinct summary of the history of MBE-FCI to date within a generalized and unified theoretical setting, its finer algorithmic details are discussed alongside our optimized computational implementation of the theory. A selected few of the most recent applications of MBE-FCI are revisited, before we close by outlining its future research directions as well as its place among modern near-exact wave function-based methods.

Chemical Physics (physics.chem-ph)Theoretical computer science010304 chemical physicsComputer scienceFOS: Physical sciencesContext (language use)010402 general chemistry01 natural sciencesBiochemistryFull configuration interaction0104 chemical sciencesComputer Science ApplicationsComputational MathematicsPhysics - Chemical Physics0103 physical sciencesMaterials ChemistryPhysical and Theoretical Chemistry
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