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We report on the masses and hyperfine structure of ground and isomeric states in $^{114,116,118,120}$Ag isotopes, measured with the phase-imaging ion-cyclotron-resonance technique (PI-ICR) with the JYFLTRAP mass spectrometer and the collinear laser spectroscopy beamline at the Ion Guide Isotope Separator On-Line (IGISOL) facility, Jyv\"askyl\"a, Finland. We measured the masses and excitation energies, electromagnetic moments, and charge radii, and firmly established the nuclear spins of the long-lived states. A new isomer was discovered in $^{118}$Ag and the half-lives of $^{118}$Ag long-lived states were reevaluated. We unambiguously pinned down the level ordering of all long-lived states, placing the inversion of the $I = 0^-$ and $I = 4^+$ states at $A = 118$ $(N = 71)$. Lastly, we compared the electromagnetic moments of each state to empirical single-particle moments to identify the dominant configuration where possible., Comment: 11 pages paper (excl. references) + 3 pages of supplementary material

The radiative lifetime of the $A$ $^2 \Pi_{1/2}$ (v=0) state in radium monofluoride (RaF) is measured to be 35(1) ns. The lifetime of this state and the related decay rate $\Gamma = 2.86(8) \times 10^7$ $s^{-1}$ are of relevance to the laser cooling of RaF via the optically closed $A$ $^2 \Pi_{1/2} \leftarrow X$ $^2\Sigma_{1/2}$ transition, which makes the molecule a promising probe to search for new physics. RaF is found to have a comparable photon-scattering rate to homoelectronic laser-coolable molecules. Thanks to its highly diagonal Franck-Condon matrix, it is expected to scatter an order of magnitude more photons than other molecules when using just 3 cooling lasers, before it decays to a dark state. The lifetime measurement in RaF is benchmarked by measuring the lifetime of the $8P_{3/2}$ state in Fr to be 83(3) ns, in agreement with literature., Comment: Accepted as a Letter in Physical Review A; 8 pages of main text, 5 pages of supplemental material

The masses of $^{84}$Br, $^{105}$Mo, $^{115,119,121}$Pd, $^{122}$Ag, $^{127,129}$In, $^{132}$Sb and their respective isomeric states have been measured with the JYFLTRAP Penning trap mass spectrometer using the phase-imaging ion-cyclotron-resonance technique. The excitation energies of the isomeric states in $^{132}$Sb and $^{119}$Pd were experimentally determined for the first time, while for $^{84}$Br, $^{115}$Pd and $^{127,129}$In, the precision of the mass values was substantially improved. In $^{105}$Mo and $^{121}$Pd there were no signs of a long-lived isomeric state. The ground-state measurements of $^{119}$Pd and $^{122}$Ag indicated that both are significantly more bound than the literature values. For $^{122}$Ag, there was no indication of a proposed third long-lived state. The results for the $N=49$ nucleus $^{84}$Br and isomers close to doubly magic $^{132}$Sn have been compared to the shell-model and the microscopic quasiparticle-phonon model calculations., Comment: 14 pages, 10 figures

Collinear laser spectroscopy has been performed on He-like C$^{4+}$ ions extracted from an electron beam ion source (EBIS). In order to determine the transition frequency with the highest-possible accuracy, the lineshape of the fluorescence response function was studied for pulsed and continuous ion extraction modes of the EBIS in order to optimize its symmetry and linewidth. We found that the best signal-to-noise ratio is obtained using the continuous beam mode for ion extraction. Applying frequency-comb-referenced collinear and anticollinear laser spectroscopy, we achieved a measurement accuracy of better than 2\,MHz including statistical and systematic uncertainties. The origin and size of systematic uncertainties, as well as further applications for other isotopes and elements are discussed.

Transition frequencies and fine-structure splittings of the $2\,{}^3\!S_1 \rightarrow 2\,{}^3\!P_{\!J}$ transitions in helium-like $^{12}\mathrm{C}^{4+}$ were measured by collinear laser spectroscopy on a 1-ppb level. Accuracy is increased by more than three orders of magnitude with respect to previous measurements, enabling tests of recent non-relativistic QED calculations including terms up to $m\alpha^7$. Deviations between the theoretical and experimental values are within theoretical uncertainties and are ascribed to $m\alpha^8$ and higher-order contributions in the series expansion of the NR-QED calculations. Finally, prospects for an all-optical charge radius determination of light isotopes are evaluated.

Nuclear moments of the antimony isotopes $^{113-133}$Sb are measured by collinear laser spectroscopy and used to benchmark phenomenological shell-model and \textit{ab initio} calculations in the valence-space in-medium similarity renormalization group (VS-IMSRG). The shell-model calculations reproduce the electromagnetic moments over all Sb isotopes when suitable effective $g$-factors and charges are employed. Good agreement is achieved by VS-IMSRG for magnetic moments on the neutron-deficient side for both odd-even and odd-odd Sb isotopes while its results deviate from experiment on the neutron-rich side. When the same effective $g$-factors are used, VS-IMSRG agrees with experiment nearly as well as the shell model. Hence, the wave functions are very similar in both approaches and missing contributions to the M1 operator are identified as the cause of the discrepancy of VS-IMSRG with experiment. Electric quadrupole moments remain more challenging for VS-IMSRG.

Collinear laser spectroscopy was performed on the isomer of the aluminium isotope $^{26m}$Al. The measured isotope shift to $^{27}$Al in the $3s^{2}3p\;^{2}\!P^\circ_{3/2} \rightarrow 3s^{2}4s\;^{2}\!S_{1/2}$ atomic transition enabled the first experimental determination of the nuclear charge radius of $^{26m}$Al, resulting in $R_c$=\qty{3.130\pm.015}{\femto\meter}. This differs by 4.5 standard deviations from the extrapolated value used to calculate the isospin-symmetry breaking corrections in the superallowed $\beta$ decay of $^{26m}$Al. Its corrected $\mathcal{F}t$ value, important for the estimation of $V_{ud}$ in the CKM matrix, is thus shifted by one standard deviation to \qty{3071.4\pm1.0}{\second}., Comment: 5 pages, 2 figures, submitted to Phys. Rev. Lett

We report the spectroscopy of the 14 lowest excited electronic states in the radioactive molecule radium monofluoride (RaF). The observed excitation energies are compared with fully relativistic state-of-the-art Fock-space coupled cluster (FS-RCC) calculations, which achieve an agreement of >=99.64% (within ~12 meV) with experiment for all states. Guided by theory, a firm assignment of the angular momentum and term symbol is made for 10 states and a tentative assignment for 4 states. The role of high-order electron correlation and quantum electrodynamics effects in the excitation energy of excited states is studied, found to be important for all states. Establishing the simultaneous accuracy and precision of calculations is an important step for research at the intersection of particle, nuclear, and chemical physics, including searches of physics beyond the Standard Model, for which RaF is a promising probe., Comment: Significant changes compared to previous version with additional experimental data. Accepted for publication under a different title

Nuclear charge radii of $^{55,56}$Ni were measured by collinear laser spectroscopy. The obtained information completes the behavior of the charge radii at the shell closure of the doubly magic nucleus $^{56}$Ni. The trend of charge radii across the shell closures in calcium and nickel is surprisingly similar despite the fact that the $^{56}$Ni core is supposed to be much softer than the $^{48}$Ca core. The very low magnetic moment $\mu(^{55}\mathrm{Ni})=-1.108(20)\,\mu_N$ indicates the impact of M1 excitations between spin-orbit partners across the $N,Z=28$ shell gaps. Our charge-radii results are compared to \textit{ab initio} and nuclear density functional theory calculations, showing good agreement within theoretical uncertainties.