Julian Bergmann

A pathway towards decentralized studies of radioactive post-lead elements and their applications in beyond standard model physics

Moritz Pascal Reiter [1], Kriti Mahajan [2,6], Meetika Narang [3,7,4], Carsten Zuelch, Timo Dickel [2,3], Daler Amanbayev [2,3], Robert Berger [4], Julian Bergmann [2], Agnieszka Bukowicka [1], Mariam Fadel [4], Tayemar Fowler-Davies [1,3], Zhuang Ge [3], Simeon Gloeckner [3], Gabriella Kripko-Koncz [1,2], Nasser Kalantar-Nayestanaki [7], Cameron Merron [1], David J. Morrissey [3,5,2], Wolfgang Plass, Christoph Scheidenberger [2,3,6], Makar Simonov [2], Nazarena Tortorelli [3,8], Jiajun Yu [3], Alexandra Zadvornaya [1,2], Jianwai Zhao [3]

Abstract

Molecules have proven to be sensitive tools for studying physics beyond the standard model, with heavy and deformed nuclei offering decisive sensitivity to parity- and time-reversal-violating effects. However, almost all elements beyond lead, occupying the 6p~to~5f atomic orbitals, lack stable isotopes, hence molecules containing them are referred to as radioactive molecules. Among those, radium monofluoride has seen particular interest, but to date, research on radioactive molecules has mainly been limited to large-scale nuclear facilities. Here, we present a scheme that allows efficient and fast harvest of radioactive ions (including short-lived Ra), and show ion gas-phase reaction studies of singly and doubly charged Ra, Po, and Pb ions with SF$_6$ gas inside an ion trap. Our results show that the chemical reaction rate of Ra$^+$ is in line with trends of other alkaline earth elements, further support by quantum chemical computations. The reaction Ra$^{2+}$ + SF$_6$ $\rightarrow$ RaF${^+}$ + SF$_5^{+}$ achieves an almost unity conversion efficiency, making it particularly suitable for the application for studies in physics beyond the standard model. The scheme enables future decentralized research avenues with short-lived radioactive molecules for fundamental physics research at laboratories without the need for local nuclear reactors or accelerators.

A Novel Method for the Measurement of Half-Lives and Decay Branching Ratios of Exotic Nuclei

Ivan Miskun [1], Timo Dickel [1,2], Israel Mardor [3,4], Christine Hornung [1], Daler Amanbayev [1,2], Samuel Ayet San Andrés, Julian Bergmann [1], Jens Ebert [1], Hans Geissel [1,2], Magdalena Górska, Florian Greiner [1], Emma Haettner [2,1], Wolfgang R. Plaß, Sivaji Purushothaman [2], Christoph Scheidenberger [1,2], Ann-Kathrin Rink [1], Helmut Weick [2], Soumya Bagchi [1,2,6], Paul Constantin [5], Satbir Kaur [6], Wayne Lippert [1], Bo Mei [5], Iain Moore [7], Jan-Hendrick Otto [1], Stephane Pietri [2], Ilkka Pohjalainen [7], Andrej Prochazka [2], Christoph Rappold [1,2], Moritz P. Reiter [1,8], Yoshiki K. Tanaka [2], John S. Winfield [2]

Abstract

A novel method for simultaneous measurement of masses, Q-values, isomer excitation energies, half-lives and decay branching ratios of exotic nuclei has been demonstrated. The method includes first use of a stopping cell as an ion trap, combining containment of precursors and decay-recoils for variable durations in a cryogenic stopping cell (CSC), and afterwards the identification and counting of them by a multiple-reflection time-of-flight mass spectrometer (MR-TOF-MS). Feasibility has been established by recording the decay and growth of $^{216}$Po and $^{212}$Pb (alpha decay) and of $^{119m2}$Sb (t$_{1/2}$ = 850$\pm$90 ms) and $^{119g}$Sb (isomer transition), obtaining half-lives and branching ratios consistent with literature values. Hardly any non-nuclear-decay losses have been observed in the CSC for up to $\sim$10 seconds, which exhibits its extraordinary cleanliness. For $^{119}$Sb, this is the first direct measurement of the ground and second isomeric state masses, resolving the discrepancies in previous excitation energy data. These results pave the way for the measurement of branching ratios of exotic nuclei with multiple decay channels.