Mass measurements of fission and projectile fragments, produced via 238 U and 124 Xe primary beams, have been performed with the multiple-reflection time-of-flight mass spectrometer (MR-TOF-MS) of the Fragment Separator (FRS) Ion Catcher with a mass resolving power (FWHM) of up to 410 000 and an uncertainty of down to 6 × 10 −8. The nuclides were produced and separated in flight with the fragment separator FRS at 300 to 1000 MeV/u and thermalized in a cryogenic stopping cell. The data-analysis procedure was developed to determine with highest accuracy the mass values and the corresponding uncertainties for the most challenging conditions: down to a few events in a spectrum and overlapping distributions, which can be distinguished from a single peak only by a broader peak shape. With this procedure, the resolution of low-lying isomers is increased by a factor of up to 3 compared to standard data analysis. The ground-state masses of 31 short-lived nuclides of 15 different elements with half-lives of down to 17.9 ms and count rates as low as 11 events per nuclide were determined. This is the first direct mass measurement for seven nuclides. The excitation energies and the isomer-to-groundstate ratios of six isomeric states with excitation energies of as little as 280 keV were measured. For nuclides with known mass values, the average relative deviation from the literature values is (4.5 ± 5.3) × 10 −8. The measured two-neutron separation energies and their slopes near and at the N = 126 and Z = 82 shell closures indicate a strong element-dependent binding energy of the first neutron above the closed proton shell Z = 82. The experimental results deviate strongly from the theoretical predictions, especially for N = 126 and N = 127.

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A cryogenic stopping cell (CSC) has been commissioned with 238 U projectile fragments produced at 1000 MeV/u. The spatial isotopic separation in flight was performed with the FRS applying a monoenergetic degrader. For the first time, a stopping cell was operated with exotic nuclei at cryogenic temperatures (70 to 100 K). A helium stopping gas density of up to 0.05 mg/cm 3 was used, about two times higher than reached before for a stopping cell with RF ion repelling structures. An overall efficiency of up to 15%, a combined ion survival and extraction efficiency of about 50%, and extraction times of 24 ms were achieved for heavy α-decaying uranium fragments. Mass spectrometry with a multiple-reflection time-of-flight mass spectrometer has demonstrated the excellent cleanliness of the CSC. This setup has opened a new field for the spectroscopy of short-lived nuclei.

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Masses of uranium fission fragments have been measured with the FRS-ESR facility at GSI.A 410-415 MeV/u 238 U projectile beam was fast extracted from the synchrotron SIS-18 with an average intensity of 10 9 /spill. The projectiles were focused on a 1 g/cm 2 beryllium target at the entrance of the in-flight separator FRS to create neutron-rich isotopes via abrasion-fission. The fission fragments were spatially separated with the FRS and injected into the isochronous storage ring ESR for fast mass measurements without applying cooling. The Isochronous Mass Spectrometry (IMS) was performed under two different experimental conditions, with and without Bρ-tagging at the high-resolution dispersive central focal plane of the FRS. A new method of data analysis has provided experimental mass values for 25 different neutron-rich isotopes for the first time and 6 masses with improved uncertainties. The results were obtained by the use of a correlation matrix for the combined data set from both experiments. The new masses were obtained for nuclides in the element range from Ge to Ce. The applied analysis has given access even to rare isotopes detected with an intensity of a few atoms per week. The novel data analysis and systematic error determination are described and the results are compared with extrapolations of experimental values and theoretical models.