The science case of the FRS Ion Catcher for FAIR Phase-0

The FRS Ion Catcher at GSI enables precision experiments with thermalized projectile and fission fragments. At the same time it serves as a test facility for the Low-Energy Branch of the Super-FRS at FAIR. The FRS Ion Catcher has been commissioned and its performance has been characterized in five experiments with 238U and 124Xe projectile and fission fragments produced at energies in the range from 300 to 1000 MeV/u. High and almost element-independent efficiencies for the thermalization of short-lived nuclides produced at relativistic energies have been obtained. High-accuracy mass measurements of more than 30 projectile and fission fragments have been performed with a multiple-reflection time-of-flight mass spectrometer (MR-TOF-MS) at mass resolving powers of up to 410,000, with production cross sections down to the microbarn-level, and at rates down to a few ions per hour. The versatility of the MR-TOF-MS for isomer research has been demonstrated by the measurement of various isomers, determination of excitation energies and the production of a pure isomeric beam. Recently, several instrumental upgrades have been implemented at the FRS Ion Catcher. New experiments will be carried out during FAIR Phase-0 at GSI, including direct mass measurements of neutron-deficient nuclides below 100Sn and neutron-rich nuclides below 208Pb, measurement of β-delayed neutron emission probabilities and reaction studies with multi-nucleon transfer.Peer reviewe

Removal of molecular contamination in low-energy RIBs by the isolation-dissociation-isolation method

Experiments with low-energy rare ion beams often suffer from a large amount of molecular contaminant ions. We present the simple isolation-dissociation-isolation method to suppress this kind of contamination. The method can be applied to almost all types of low-energy beamlines. In a first step, a coarse isolation of the massto-charge ratio of interest is performed, e.g. by a dipole magnet. In a second step, the ions are dissociated. The last step is again a coarse isolation of the mass-to-charge ratio around the ion of interest. The method was tested at the FRS Ion Catcher at GSI with a radioactive ion source installed inside the cryogenic stopping cell as well as with relativistic ions delivered by the synchrotron SIS-18 and stopped in the cryogenic stopping cell. The isolation and dissociation, here collision-induced dissociation, have been implemented in a gas-filled RFQ beamline. A reduction of molecular contamination by more than 4 orders of magnitude was achieved.peerReviewe

Determining spontaneous fission properties by direct mass measurements with the FRS Ion Catcher

We present a direct method to measure fission product yield distributions (FPY) and isomeric yield ratios (IYR) for spontaneous fission (SF) fragments. These physical properties are of utmost importance to the understanding of basic nuclear physics, the astrophysical rapid neutron capture process ('r process') of nucle-osynthesis, neutron star composition, and nuclear reactor safety. With this method, fission fragments are produced by spontaneous fission from a source that is mounted in a cryogenic stopping cell (CSC), thermalized and stopped within it, and then extracted and transported to a multiple-reflection time-of-flight mass-spectrometer (MR-TOF-MS). We will implement the method at the FRS Ion Catcher (FRS-IC) at GSI (Germany), whose MR-TOF-MS relative mass accuracy (similar to 10(-7)) and resolving power (similar to 600,000 FWHM) are sufficient to separate all isobars and numerous isomers in the fission fragment realm. The system's essential element independence and its fast simultaneous mass measurement provide a new direct way to measure isotopic FPY distributions, which is complementary to existing methods. It will enable nuclide FPY measurements in the high fission peak, which is hardly accessible by current techniques. The extraction time of the CSC, tens of milliseconds, enables a direct measurement of independent fission yields, and a first study of the temporal dependence of FPY distributions in this duration range. The ability to resolve isomers will further enable direct extraction of numerous IYRs while performing the FPY measurements. The method has been recently demonstrated at the FRS-ICr for SF with a 37 kBq Cf-252 fission source, where about 70 different fission fragments have been identified and counted. In the near future, it will be used for systematic studies of SF with a higher-activity Cf-252 source and a Cm-248 source. The method can be implemented also for neutron induced fission at appropriate facilities

Mass tagging:Verification and calibration of particle identification by high-resolution mass measurements

The access to exotic nuclei at radioactive ion beam facilities is crucial for the state of the art research across several fields of physics such as in nuclear structure, the understanding of fundamental interactions and nuclear astrophysics. The particle identification is of high importance, besides the challenging production of these rare and short-lived nuclei. At in-flight facilities, the particle identification is based on measuring the time-of-flight, energy-deposition and magnetic rigidity. These quantities are calibrated to convert them into A/Q and Z of the ions. To ensure a correct calibration, the unambiguous identification, also called tagging, of one species is necessary. Here, we present a novel tagging method by high-resolution mass measurements using an MR-TOF-MS after thermalization of the ions in a cryogenic stopping cell. The method was successfully established and tested at the fragment separator FRS at GSI with the FRS Ion Catcher in experiments using different FRS operation modes.</p

A novel method for the measurement of half-lives and decay branching ratios of exotic nuclei

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 storage of mother and daughter nuclides 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). We utilized our method to record the decay and growth of the 216Po and 212Pb isotopes (alpha decay) and of the 119m2Sb isomer ( t1/2=850±90 ms) and 119gSb isotope (isomer transition), obtaining half-lives consistent with literature values. The amount of non-nuclear-decay losses in the CSC up to ∼10 s is negligible, which exhibits its extraordinary cleanliness. For 119Sb isotopes, we present the first direct measurements of the mass of its ground state, and the excitation energy and decay branching ratios of its second isomeric state (119m2Sb). This resolves discrepancies in previous excitation energy data, and is the first direct evidence that the 119m2Sb isomer decays dominantly via γ emission. These results pave the way for the measurement of branching ratios of exotic nuclei.peerReviewe

Isomer studies in the vicinity of the doubly-magic nucleus Sn-100: Observation of a new low-lying isomeric state in Ag-97

Long-lived isomeric states in Ag-97 and In101-109 were investigated with the FRS Ion Catcher at GSI. In the isotope Ag-97, a long-lived (1/2(-)) isomeric state was discovered, and its excitation energy was determined to be 618(38) keV. This is simultaneously the first discovery of a nuclear isomeric state by multiple-reflection time-of-flight mass spectrometry. The measured excitation energies were compared to large-scale shell-model calculations, which indicated the importance of core excitation around Sn-100. Furthermore, advanced mean-field calculations for the Ag-97 nucleus and relevant neighboring nuclei were performed, which have contributed to a better understanding of the repetitive appearance of certain isomeric structures in neighboring nuclei, and which have supported the discovery of the isomeric state in Ag-97 in a global shell-evolution scheme. (C) 2020 The Author(s). Published by Elsevier B.V