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The multinucleon transfer (MNT) reaction approach was successfully employed for the first time to measure the isomeric ratios (IRs) of $^{211}$Po (25/2$^+$) isomer and its (9/2$^+$) ground state at the IGISOL facility using a 945 MeV $^{136}$Xe beam impinged on $^{209}$Bi and $^{\rm nat}$Pb targets. The dominant production of isomers compared to the corresponding ground states was consistently revealed in the $\alpha$-decay spectra. Deduced IR of $^{211}$Po populated through the $^{136}$Xe+$^{\rm nat}$Pb reaction was found to enhance $\approx$1.8-times than observed for $^{136}$Xe+$^{209}$Bi. State-of-the-art Langevin-type model calculations have been utilized to estimate the spin distribution of an MNT residue. The computations qualitatively corroborate with the considerable increase in IRs of $^{211}$Po produced from $^{136}$Xe+$^{\rm nat}$Pb compared to $^{136}$Xe+$^{209}$Bi. Theoretical investigations indicate a weak influence of target spin on IRs. The enhancement of the $^{211}$Po isomer in the $^{136}$Xe+$^{\rm nat}$Pb over $^{136}$Xe+$^{209}$Bi can be attributed to the different proton ($p$)-transfer production routes. Estimations demonstrate an increment in the angular momentum transfer, favorable for isomer production, with increasing projectile energy. Comparative analysis indicates the two entrance channel parameters, projectile mass and $p$-transfer channels, strongly influencing the population of the high-spin isomer of $^{211}$Po (25/2$^+$). This is the first experimental and theoretical investigation on the IRs of nuclei produced via different channels of MNT reactions, with the latter quantitatively underestimating the former by a factor of two., Comment: 5 figures

At the FRS Ion Catcher (FRS-IC), projectile and fission fragments are produced at relativistic energies, separated in-flight, energy-bunched, slowed down, and thermalized in the ultra-pure helium gas-filled cryogenic stopping cell (CSC). Thermalized nuclei are extracted from the CSC using a combination of DC and RF electric fields and gas flow. This CSC also serves as the prototype CSC for the Super-FRS, where exotic nuclei will be produced at unprecedented rates making it possible to go towards the extremes of the nuclear chart. Therefore, it is essential to efficiently extract thermalized exotic nuclei from the CSC under high beam rate conditions, in order to use the rare exotic nuclei which come as cocktail beams. The extraction efficiency dependence on the intensity of the impinging beam into the CSC was studied with a primary beam of 238U and its fragments. Tests were done with two different versions of the DC electrode structure inside the cryogenic chamber, the standard 1 m long and a short 0.5 m long DC electrode. In contrast to the rate capability of 10^4 ions/s with the long DC electrode, results show no extraction efficiency loss up to the rate of 2x10^5 ions/s with the new short DC electrode. This order of magnitude increase of the rate capability paves the way for new experiments at the FRS-IC, including exotic nuclei studies with in-cell multi-nucleon transfer reactions. The results further validate the design concept of the CSC for the Super-FRS, which was developed to effectively manage beams of even higher intensities.

Low-energy investigations on rare ion beams are often limited by the available intensity and purity of the ion species in focus. Here, we present the first application of a technique that combines in-flight production at relativistic energies with subsequent secondary beam storage, accumulation and finally deceleration to the energy of interest. Using the FRS and ESR facilities at GSI, this scheme was pioneered to provide a secondary beam of $^{118}$Te$^{52+}$ for the measurement of nuclear proton-capture at energies of 6 and 7 MeV/u. The technique provided stored beam intensities of about $10^6$ ions at high purity and brilliance, representing a major step towards low-energy nuclear physics studies using rare ion beams.

Mass measurements of the $^{69}$As, $^{70,71}$Se and $^{71}$Br isotopes, produced via fragmentation of a $^{124}$Xe primary beam at the FRS at GSI, have been performed with the multiple-reflection time-of-flight mass spectrometer (MR-TOF-MS) of the FRS Ion Catcher with an unprecedented mass resolving power of almost 1,000,000. For the $^{69}$As isotope, this is the first direct mass measurement. A mass uncertainty of 22 keV was achieved with only 10 events. For the $^{70}$Se isotope, a mass uncertainty of 2.6 keV was obtained, corresponding to a relative accuracy of $\delta$m/m = 4.0$\times 10^{-8}$, with less than 500 events. The masses of the $^{71}$Se and $^{71}$Br isotopes were measured with an uncertainty of 23 and 16 keV, respectively. Our results for the $^{70,71}$Se and $^{71}$Br isotopes agree with the 2016 Atomic Mass Evaluation, and our result for the $^{69}$As isotope resolves the discrepancy between previous indirect measurements. We measured also the mass of $^{14}$N$^{15}$N$^{40}$Ar (A=69) with a relative accuracy of $\delta$m/m = 1.7$\times 10^{-8}$, the highest yet achieved with a MR-TOF-MS. Our results show that the measured restrengthening of the proton-neutron interaction ($\delta$V$_{pn}$) for odd-odd nuclei at the N=Z line above Z=29 (recently extended to Z=37) is hardly evident at N-Z=2, and not evident at N-Z=4. Nevertheless, detailed structure of $\delta$V$_{pn}$ along the N-Z=2 and N-Z=4 lines, confirmed by our mass measurements, may provide a hint regarding the ongoing $\approx$500 keV discrepancy in the mass value of the $^{70}$Br isotope, which prevents including it in the world average of ${Ft}$-value for superallowed 0$^+\rightarrow$ 0$^+$ $\beta$ decays. The reported work sets the stage for mass measurements with the FRS Ion Catcher of nuclei at and beyond the N=Z line in the same region of the nuclear chart, including the $^{70}$Br isotope., Comment: 11 pages, 4 figures, accepted for publication at Physical Review C

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 FRS Ion Catcher with a mass resolving powers (FWHM) up to 410,000 and an uncertainty of $6\cdot 10^{-8}$. 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, characterized only by a broader common peak shape. With this procedure, the resolution of low-lying isomers is increased by a factor of up to three compared to standard data analysis. The ground-state masses of 31 short-lived nuclides of 15 different elements with half-lives 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-ground state ratios of six isomeric states with excitation energies down to about 280~keV were measured. For nuclides with known mass values, the average relative deviation from the literature values is $(2.9 \pm 6.2) \cdot 10^{-8}$. 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.

In-situ purification of the gas used as stopping medium in a noble gas ion catcher by operating the device at low temperatures of 60 to 150 K was investigated. Alpha-decay recoil ions from a 223Ra source served as energetic probes. The combined ion survival and transport efficiencies for 219Rn ions saturated below about 90 K, reaching 28.7(17) % in helium, 22.1(13) % in neon, and 17.0(10) % in argon. These values may well reflect the charge exchange and stripping cross sections during the slowing down of the ions, and thus represent a fundamental upper limit for the efficiency of noble gas ion catcher devices. We suggest the cryogenic noble gas ion catcher as a technically simpler alternative to the ultra-high purity noble gas ion catcher operating at room temperature., Comment: Submitted to Nucl. Instrum. Meth. Phys. Res. A