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Published on: May 3, 2019
Direct observation of long-lived isomers in 212Bi
L Chen1, P M Walker2, H Geissel3
1GSI Helmholtzzentrum für Schwerionenforschung, Planckstraße 1, 64291 Darmstadt, Germany and II Physikalisches Institut, Justus-Liebig-Universität Gießen, 35392 Gießen, Germany and Cyclotron Institute, Texas A & M University, Texas 77843, USA.
Researchers studied long-lived isomers in Bismuth-212 (212Bi) using projectile fragmentation. A new, lower energy and significantly longer half-life for a 212Bi isomer were observed, attributed to an internal decay branch.
Area of Science:
- Nuclear Physics
- Atomic Physics
Background:
- Long-lived isomers in Bismuth-212 (212Bi) are nuclear states with significant implications for nuclear structure and decay studies.
- Previous measurements of the second isomer's energy and half-life in 212Bi were limited, necessitating further investigation.
Purpose of the Study:
- To investigate the properties of long-lived isomers in 212Bi.
- To accurately determine the excitation energy and half-life of the second isomer in 212Bi.
- To understand the discrepancies observed in previous measurements.
Main Methods:
- Studying 212Bi isomers produced via Uranium-238 (238U) projectile fragmentation at 670 MeV per nucleon.
- Injecting highly charged ions into a storage ring to measure masses and half-lives.
- Comparing experimental data with shell-model calculations.
Main Results:
- Confirmed the excitation energy of the first isomer of 212Bi.
- Observed the second isomer at 1478(30) keV, differing from the previous >1910 keV value.
- Measured an extended Lorentz-corrected in-ring half-life of >30 min for the second isomer, significantly longer than the 7.0(3) min for the neutral atom.
- Identified a substantial internal decay branch for neutral atoms as the cause for energy and half-life differences.
Conclusions:
- The observed energy and half-life differences are explained by an unrecognized internal decay branch in neutral 212Bi atoms.
- Shell-model calculations show good agreement with the determined isomer excitation energy.
- New calculations predict states that could aid future isomer deexcitation studies.
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