{"title":"Electric dipole polarizability of low-lying excited states in atomic nuclei","authors":"José Nicolás Orce and Cebo Ngwetsheni","doi":"10.1088/1361-6471/ad4faa","DOIUrl":null,"url":null,"abstract":"New equations for the electric dipole polarizability αE1 of low-lying excited states in atomic nuclei—and the related (−2) moment of the total photo-absorption cross section, σ−2—are inferred in terms of electric dipole and quadrupole matrix elements. These equations are valid for arbitrary angular momenta of the initial/ground and final/excited states and have been exploited in fully converged 1ℏω shell-model (SM) calculations of selected p- and sd-shell nuclei that consider configuration mixing; advancing previous knowledge from 17O to 36Ar, where thousands of electric dipole matrix elements are computed from isovector excitations which include the giant dipole resonance (GDR) region. Our results are in reasonable agreement with previous SM calculations and follow—except for 6,7Li and 17,18O—Migdal’s global trend provided by the combination of the hydrodynamic model and second-order non-degenerate perturbation theory. Discrepancies in 6,7Li and 17O arise as a result of the presence of α-cluster configurations in odd-mass nuclei, whereas the disagreement in 18O comes from the mixing of intruder states, which is lacking in the SM interactions. More advanced ab initio calculations of the dipole polarizability for low-lying excited states covering all the isovector states within the GDR region are missing and could be very valuable to benchmark the results presented here and shed further light on how atomic nuclei polarize away from the ground state","PeriodicalId":16766,"journal":{"name":"Journal of Physics G: Nuclear and Particle Physics","volume":"31 1","pages":""},"PeriodicalIF":3.4000,"publicationDate":"2024-06-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Physics G: Nuclear and Particle Physics","FirstCategoryId":"101","ListUrlMain":"https://doi.org/10.1088/1361-6471/ad4faa","RegionNum":3,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHYSICS, NUCLEAR","Score":null,"Total":0}
引用次数: 0
Abstract
New equations for the electric dipole polarizability αE1 of low-lying excited states in atomic nuclei—and the related (−2) moment of the total photo-absorption cross section, σ−2—are inferred in terms of electric dipole and quadrupole matrix elements. These equations are valid for arbitrary angular momenta of the initial/ground and final/excited states and have been exploited in fully converged 1ℏω shell-model (SM) calculations of selected p- and sd-shell nuclei that consider configuration mixing; advancing previous knowledge from 17O to 36Ar, where thousands of electric dipole matrix elements are computed from isovector excitations which include the giant dipole resonance (GDR) region. Our results are in reasonable agreement with previous SM calculations and follow—except for 6,7Li and 17,18O—Migdal’s global trend provided by the combination of the hydrodynamic model and second-order non-degenerate perturbation theory. Discrepancies in 6,7Li and 17O arise as a result of the presence of α-cluster configurations in odd-mass nuclei, whereas the disagreement in 18O comes from the mixing of intruder states, which is lacking in the SM interactions. More advanced ab initio calculations of the dipole polarizability for low-lying excited states covering all the isovector states within the GDR region are missing and could be very valuable to benchmark the results presented here and shed further light on how atomic nuclei polarize away from the ground state
期刊介绍:
Journal of Physics G: Nuclear and Particle Physics (JPhysG) publishes articles on theoretical and experimental topics in all areas of nuclear and particle physics, including nuclear and particle astrophysics. The journal welcomes submissions from any interface area between these fields.
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