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dc.date.accessioned2020-01-24T13:08:11Z
dc.date.created2019-04-14T15:52:04Z
dc.date.issued2019
dc.identifier.citationPedersen, Thomas Bondo Kvaal, Simen . Symplectic integration and physical interpretation of time-dependent coupled-cluster theory. Journal of Chemical Physics. 2019, 150
dc.identifier.urihttp://hdl.handle.net/10852/72497
dc.description.abstractThe formulation of the time-dependent Schrödinger equation in terms of coupled-cluster theory is outlined, with emphasis on the bivariational framework and its classical Hamiltonian structure. An indefinite inner product is introduced, inducing physical interpretation of coupled-cluster states in the form of transition probabilities, autocorrelation functions, and explicitly real values for observables, solving interpretation issues which are present in time-dependent coupled-cluster theory and in ground-state calculations of molecular systems under the influence of external magnetic fields. The problem of the numerical integration of the equations of motion is considered, and a critical evaluation of the standard fourth-order Runge–Kutta scheme and the symplectic Gauss integrator of variable order are given, including several illustrative numerical experiments. While the Gauss integrator is stable even for laser pulses well above the perturbation limit, our experiments indicate that a system-dependent upper limit exists for the external field strengths. Above this limit, time-dependent coupled-cluster calculations become very challenging numerically, even in the full configuration interaction limit. The source of these numerical instabilities is shown to be rapid increases of the amplitudes as ultrashort high-intensity laser pulses pump the system out of the ground state into states that are virtually orthogonal to the static Hartree-Fock reference determinant.
dc.languageEN
dc.publisherAmerican Institute of Physics (AIP)
dc.titleSymplectic integration and physical interpretation of time-dependent coupled-cluster theoryen_US
dc.typeJournal articleen_US
dc.creator.authorPedersen, Thomas Bondo
dc.creator.authorKvaal, Simen
cristin.unitcode185,15,12,59
cristin.unitnameTeoretisk kjemi
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode1
dc.identifier.cristin1692446
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=150&rft.spage=&rft.date=2019
dc.identifier.jtitleJournal of Chemical Physics
dc.identifier.volume150
dc.identifier.doihttp://dx.doi.org/10.1063/1.5085390
dc.identifier.urnURN:NBN:no-75596
dc.type.documentTidsskriftartikkelen_US
dc.type.peerreviewedPeer reviewed
dc.source.issn0021-9606
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/72497/6/paper.pdf
dc.type.versionAcceptedVersion
cristin.articleid144106
dc.relation.projectNFR/240698
dc.relation.projectNFR/262695
dc.relation.projectEC/H2020/ERC-STG-2014-639508


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