S. Ayet

Odd-odd neutron-rich rhodium isotopes studied with the double Penning trap JYFLTRAP

M. Hukkanen [1,2], W. Ryssens [3], P. Ascher [2], M. Bender, T. Eronen [1,2], S. Grévy, A. Kankainen [1], M. Stryjczyk [1], L. Al Ayoubi [1,5], S. Ayet [6], O. Beliuskina [1], C. Delafosse [1], W. Gins [1], M. Gerbaux [2], A. Husson [2], A. Jokinen [1], D. A. Nesterenko, I. Pohjalainen [1], M. Reponen [1], S. Rinta-Antila [1], A. de Roubin [1,7], A. P. Weaver

Abstract

Precision mass measurements of neutron-rich rhodium isotopes have been performed at the JYFLTRAP Penning trap mass spectrometer at the Ion Guide Isotope Separator On-Line (IGISOL) facility. We report results on ground- and isomeric-state masses in $^{110,112,114,116,118}$Rh and the very first mass measurement of $^{120}$Rh. The isomeric states were separated and measured for the first time using the phase-imaging ion-cyclotron-resonance (PI-ICR) technique. For $^{112}$Rh, we also report new half-lives for both the ground state and the isomer. The results are compared to theoretical predictions using the BSkG1 mass model and discussed in terms of triaxial deformation.

Ba$^{2+}$ ion trapping by organic submonolayer: towards an ultra-low background neutrinoless double beta decay detector

P. Herrero-Gómez, J. P. Calupitan, M. Ilyn [1], A. Berdonces-Layunta [1,2], T. Wang [1,2], D. G. de Oteyza [1,2], M. Corso [1,2], R. González-Moreno, I. Rivilla [2,3], B. Aparicio [4,5], A. I. Aranburu, Z. Freixa [5,3], F. Monrabal [2,3,4], F. P. Cossío, J. J. Gómez-Cadenas, C. Rogero [1,2], C. Adams [6,7,8], H. Almazán, V. Alvarez, L. Arazi [9,10], I. J. Arnquist, S. Ayet [11,12], C. D. R. Azevedo, K. Bailey [6], F. Ballester [8,2,13], J. M. Benlloch-Rodríguez, F. I. G. M. Borges, S. Bounasser [7], N. Byrnes [14,15,16], S. Cárcel, J. V. Carrión, S. Cebrián, E. Church [10,13], C. A. N. Conde, T. Contreras [7,17,18,15], A. A. Denisenko, G. Díaz, J. Díaz, T. Dickel [11], J. Escada [13], R. Esteve [8], A. Fahs [7], R. Felkai [9,19], L. M. P. Fernandes, P. Ferrario [2,3,12,17,19], A. L. Ferreira, F. W. Foss, E. D. C. Freitas, J. Generowicz [2], A. Goldschmidt [20,18], D. González-Díaz, R. Guenette [7,21], R. M. Gutiérrez, J. Haefner [7], K. Hafidi [6], J. Hauptman [22,19,18], C. A. O. Henriques, J. A. Hernando Morata, V. Herrero [8], J. Ho [7], Y. Ifergan [9,14], B. J. P. Jones, M. Kekic [18], L. Labarga [23], A. Laing [14], L. Larizgoitia [2], P. Lebrun [24], D. Lopez Gutierrez [7,15], N. López-March, M. Losada [21,19,15,9,2,14,6], R. D. P. Mano, J. Martín-Albo, A. Martínez, G. Martínez-Lema, M. Martínez-Vara, A. D. McDonald, Z. E. Meziani, K. Mistry [14,19,8,15], C. M. B. Monteiro, F. J. Mora, J. Muñoz Vidal, K. Navarro [14], P. Novella [15,14], D. R. Nygren, E. Oblak [2], M. Odriozola-Gimeno [2], B. Palmeiro [18,15], A. Para [24,25], J. Pérez, M. Querol [15], A. Raymond [14,9], A. B. Redwine, J. Renner [18], L. Ripoll [26,21,8], Y. Rodríguez García, J. Rodríguez, L. Rogers [14], B. Romeo [2,25], C. Romo-Luque [15,13,19,9], F. P. Santos, J. M. F. dos Santos, A. Simón, M. Sorel [15], C. Stanford [7,19], J. M. R. Teixeira, P. Thapa [17,8], J. F. Toledo, J. Torrent [2,15,12,17], A. Usón, J. F. C. A. Veloso, T. T. Vuong, R. Webb [27], J. T. White, K. Woodruff [14], N. Yahlali [15]

Abstract

If neutrinos are their own antiparticles, the otherwise-forbidden nuclear reaction known as neutrinoless double beta decay ($ββ0ν$) can occur, with a characteristic lifetime which is expected to be very long, making the suppression of backgrounds a daunting task. It has been shown that detecting (``tagging'') the Ba$^{+2}$ dication produced in the double beta decay ${}^{136}\mathrm{Xe} \rightarrow {}^{136}$Ba$^{+2}+ 2 e + (2 ν)$ in a high pressure gas experiment, could lead to a virtually background free experiment. To identify these \Bapp, chemical sensors are being explored as a key tool by the NEXT collaboration . Although used in many fields, the application of such chemosensors to the field of particle physics is totally novel and requires experimental demonstration of their suitability in the ultra-dry environment of a xenon gas chamber. Here we use a combination of complementary surface science techniques to unambiguously show that Ba$^{+2}$ ions can be trapped (chelated) in vacuum by an organic molecule, the so-called fluorescent bicolour indicator (FBI) (one of the chemosensors developed by NEXT), immobilized on a surface. We unravel the ion capture mechanism once the molecules are immobilised on Au(111) surface and explain the origin of the emission fluorescence shift associated to the trapping of different ions. Moreover, we prove that chelation also takes place on a technologically relevant substrate, as such, demonstrating the feasibility of using FBI indicators as building blocks of a Ba$^{+2}$ detector.