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dc.date.accessioned2024-03-08T16:35:46Z
dc.date.available2024-03-08T16:35:46Z
dc.date.created2023-05-31T17:50:47Z
dc.date.issued2023
dc.identifier.citationLedum, Morten Sen, Samiran Bore, Sigbjørn Løland Cascella, Michele . On the equivalence of the hybrid particle-field and Gaussian core models. Journal of Chemical Physics. 2023, 158(19)
dc.identifier.urihttp://hdl.handle.net/10852/109303
dc.description.abstractHybrid particle–field molecular dynamics is a molecular simulation strategy, wherein particles couple to a density field instead of through ordinary pair potentials. Traditionally considered a mean-field theory, a momentum and energy-conserving hybrid particle–field formalism has recently been introduced, which was demonstrated to approach the Gaussian Core model potential in the grid-converged limit. Here, we expand on and generalize the correspondence between the Hamiltonian hybrid particle–field method and particle–particle pair potentials. Using the spectral procedure suggested by Bore and Cascella, we establish compatibility to any local soft pair potential in the limit of infinitesimal grid spacing. Furthermore, we document how the mean-field regime often observed in hybrid particle–field simulations is due to the systems under consideration, and not an inherent property of the model. Considering the Gaussian filter form, in particular, we demonstrate the ability of the Hamiltonian hybrid particle–field model to recover all structural and dynamical properties of the Gaussian Core model, including solid phases, a first-order phase transition, and anomalous transport properties. We quantify the impact of the grid spacing on the correspondence, as well as the effect of the particle–field filtering length scale on the emergent particle–particle correlations.
dc.languageEN
dc.titleOn the equivalence of the hybrid particle-field and Gaussian core models
dc.title.alternativeENEngelskEnglishOn the equivalence of the hybrid particle-field and Gaussian core models
dc.typeJournal article
dc.creator.authorLedum, Morten
dc.creator.authorSen, Samiran
dc.creator.authorBore, Sigbjørn Løland
dc.creator.authorCascella, Michele
cristin.unitcode185,15,12,70
cristin.unitnameHylleraas-senteret
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode1
dc.identifier.cristin2150598
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Journal of Chemical Physics&rft.volume=158&rft.spage=&rft.date=2023
dc.identifier.jtitleJournal of Chemical Physics
dc.identifier.volume158
dc.identifier.issue19
dc.identifier.pagecount0
dc.identifier.doihttps://doi.org/10.1063/5.0145142
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn0021-9606
dc.type.versionAcceptedVersion
cristin.articleid194902
dc.relation.projectDFG/233630050
dc.relation.projectNFR/262695
dc.relation.projectNR/NN4654K


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