Ground-State Formula Presented Factor of Highly Charged Formula Presented Ions: An Access to the M1 Transition Probability between the Isomeric and Ground Nuclear States

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Vladimir M. Shabaev - , St. Petersburg State University (Author)
  • Dmitry A. Glazov - , St. Petersburg State University (Author)
  • A. Ryzhkov - , St. Petersburg State University (Author)
  • C. Brandau - , Justus Liebig University Giessen, GSI Helmholtz Centre for Heavy Ion Research (Author)
  • G. Plunien - , Chair of Theoretical Quantum Optics, TUD Dresden University of Technology (Author)
  • W. Quint - , GSI Helmholtz Centre for Heavy Ion Research (Author)
  • A. Volchkova - , St. Petersburg State University (Author)
  • D. Zinenko - , St. Petersburg State University (Author)

Abstract

A method is proposed to determine the Formula Presented nuclear transition amplitude and hence the lifetime of the “nuclear clock transition” between the low-lying (Formula Presented) first isomeric state and the ground state of Formula Presented from a measurement of the ground-state Formula Presented factor of few-electron Formula Presented ions. As a tool, the effect of nuclear hyperfine mixing in highly charged Formula Presented ions such as Formula Presented or Formula Presented is used. The ground-state-only Formula Presented-factor measurement would also provide first experimental evidence of nuclear hyperfine mixing in atomic ions. Combining the measurements for H-, Li-, and B-like Formula Presented ions has a potential to improve the initial result for a single charge state and to determine the nuclear magnetic moment to a higher accuracy than that of the currently accepted value. The calculations include relativistic, interelectronic-interaction, QED, and nuclear effects.

Details

Original languageEnglish
Article number043001
JournalPhysical review letters
Volume128
Issue number4
Publication statusPublished - 28 Jan 2022
Peer-reviewedYes

External IDs

PubMed 35148134

Keywords

ASJC Scopus subject areas