Complex rotation method for the Dirac Hamiltoniain

dc.contributor.authorIvanov, Igor
dc.contributor.authorHo, Y K
dc.date.accessioned2015-12-08T22:17:58Z
dc.date.issued2004
dc.date.updated2015-12-08T08:11:35Z
dc.description.abstractA modification of the complex rotation method applied to the Dirac Hamiltonian was proposed. The positions and widths of resonance levels of hydrogenlike ions in the presence of the uniform dc electric field was computed. The external dc electric field was less than the critical value for which the multiparticle processes, such as electron-positron pair creation, become significant. The convergence of the results with respect to the maximum value of the angular momentum was examined. The results show that with increasing field strength, the accuracy of the perturbation expansion deteriorates rapidly.
dc.identifier.issn1050-2947
dc.identifier.urihttp://hdl.handle.net/1885/31129
dc.publisherAmerican Physical Society
dc.sourcePhysical Review A: Atomic, Molecular and Optical Physics
dc.subjectKeywords: Complex rotation method; Multiparticle process; Convergence of numerical methods; Data reduction; Electric fields; Electric potential; Ground state; Hamiltonians; Ions; Perturbation techniques; Quantum theory; Resonance; Wave equations; Atomic physics
dc.titleComplex rotation method for the Dirac Hamiltoniain
dc.typeJournal article
local.bibliographicCitation.startpage023407-1-5
local.contributor.affiliationIvanov, Igor, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationHo, Y K, Academia Sinica
local.contributor.authoremailu4156396@anu.edu.au
local.contributor.authoruidIvanov, Igor, u4156396
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor020201 - Atomic and Molecular Physics
local.identifier.ariespublicationu4169254xPUB80
local.identifier.citationvolume69
local.identifier.doi10.1103/PhysRevA.69.023407
local.identifier.scopusID2-s2.0-1942475392
local.identifier.uidSubmittedByu4169254
local.type.statusPublished Version

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