Makar Simonov

Interplay between Nuclear Shell Structure and Pairing around Doubly Magic $^{132}$Sn

Rane Simpson, Georgios Palkanoglou, Ellen Brisley, Jaime Cardona, Annabelle Czihaly, Sakshi Kakkar, Makar Simonov, Ethan Taylor, Coulter Walls, Pavithra Weligampola, Chris Chambers, Fernando Maldonado Millan, Ali Mollaebrahimi, Dwaipayan Ray, Andrew Weaver, Jiajun Yu, Iris Dillman, Alexandros Gezerlis, Gerald Gwinner, Augusto Machiavelli, Stephan Malbrunot-Ettenauer, Moritz Pascal Reiter, Anna A. Kwiatkowski

Abstract

Shell structure in finite quantum systems gives rise to sudden changes in observable properties, while pairing correlations often compete against such discontinuities. The region near the doubly magic nucleus $^{132}$Sn provides a fertile ground for testing the combined effect of shell structure and pairing. Here, we provide a novel phenomenological interpretation of existing mass data in the vicinity of the $Z=50$ and $N=82$ shell closures, which we further investigate by performing original Hartree-Fock-Bogolyubov (HFB) mean-field calculations for even-$Z$ nuclei: we find that the proton shell structure enhances an asymmetry of the neutron odd-even staggering in binding energies. We also report mass measurements of $^{137,138}$Sb, including the first experimental mass determination of $^{138}$Sb, performed using TRIUMF's Ion Trap for Atomic and Nuclear Science (TITAN). Together with existing experimental data, our results reveal an interplay between shell structure and pairing in odd-$Z$ nuclei which is more challenging to interpret phenomenologically or using HFB, thereby motivating future experimental and theoretical pairing studies in heavy neutron-rich nuclides.

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.