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Two-dimensional transition metal dichalcogenides (TMDs) and organic semiconductors (OSCs) have emerged as promising material platforms for next-generation optoelectronic devices. The combination of both is predicted to yield emergent properties while retaining the advantages of their individual components. In OSCs the optoelectronic response is typically dominated by localized Frenkel-type excitons, whereas TMDs host delocalized Wannier-type excitons. However, much less is known about the spatial and electronic characteristics of excitons at hybrid TMD/OSC interfaces, which ultimately determine the possible energy and charge transfer mechanisms across the 2D-organic interface. Here, we use ultrafast momentum microscopy and many-body perturbation theory to elucidate a hybrid exciton at an TMD/OSC interface that forms via the ultrafast resonant F\"orster energy transfer process. We show that this hybrid exciton has both Frenkel- and Wannier-type contributions: Concomitant intra- and interlayer electron-hole transitions within the OSC layer and across the TMD/OSC interface, respectively, give rise to an exciton wavefunction with mixed Frenkel-Wannier character. By combining theory and experiment, our work provides previously inaccessible insights into the nature of hybrid excitons at TMD/OSC interfaces. It thus paves the way to a fundamental understanding of charge and energy transfer processes across 2D-organic heterostructures.

The electric dipole strength distribution in $^{58}$Ni between 6 and 20 MeV has been determined from proton inelastic scattering experiments at very forward angles at RCNP, Osaka. The experimental data are rather well reproduced by quasiparticle random-phase approximation calculations including vibration coupling, despite a mild dependence on the adopted Skyrme interaction. They allow an estimate of the experimentally inaccessible high-energy contribution above 20 MeV, leading to an electric dipole polarizability $\alpha_\mathrm{D}(^{58}{\rm Ni}) = 3.48(31)$ fm$^3$. This serves as a test case for recent extensions of coupled-cluster calculations with chiral effective field theory interactions to nuclei with two nucleons on top of a closed-shell system., Comment: 8 pages, 4 figures

The island of inversion is a region of neutron-rich nuclei that are deformed in their ground states. In this region, less is known about the energy levels of odd-mass nuclei, how they evolve with increasing neutron numbers, and how they can be organized into rotational bands. We perform {\it ab initio} coupled-cluster calculations of spectra in odd-mass Ne, Na, and Mg nuclei based on an interaction of chiral effective field theory. Our results confirm some tentative spin and parity assignments, predict the structure of nuclei near the neutron dripline, and inform us about rotational bands in this region of the nuclear table., Comment: 12 pages, 9 figures

We present coupled-cluster computations of nuclei with neutron number $N=50$ "south" of $^{78}$Ni using nucleon-nucleon and three-nucleon forces from chiral effective field theory. We find an erosion of the magic number $N=50$ toward $^{70}$Ca manifesting itself by an onset of deformation and increased complexity in the ground states. For $^{78}$Ni, we predict a low-lying rotational band consistent with recent data, which up until now has been a challenge for ab initio nuclear models. Ground states are deformed in $^{76}$Fe, $^{74}$Cr, and $^{72}$Ti, although the spherical states are too close in energy to unambiguously identify the shape of the ground state within the uncertainty estimates. In $^{70}$Ca, the potential energy landscape from quadrupole-constrained Hartree-Fock computations flattens, and the deformation becomes less rigid. We also compute the low-lying spectra and $B({\rm E2})$ values for these neutron-rich $N=50$ nuclei., Comment: 10 pages, 6 figures, supplementary material

Atomic nuclei exhibit multiple energy scales ranging from hundreds of MeV in binding energies to fractions of an MeV for low-lying collective excitations. As the limits of nuclear binding is approached near the neutron- and proton driplines, traditional shell-structure starts to melt with an onset of deformation and an emergence of coexisting shapes. It is a long-standing challenge to describe this multiscale physics starting from nuclear forces with roots in quantum chromodynamics. Here we achieve this within a unified and non-perturbative framework that captures both short- and long-range correlations starting from modern nucleon-nucleon and three-nucleon forces from chiral effective field theory. The short-range correlations which accounts for the bulk of the binding energy is included within a symmetry-breaking framework, while long-range correlations (and fine details about the collective structure) are included via symmetry projection. Our calculations accurately reproduce available experimental data for low-lying collective states and the electromagnetic quadrupole transitions in $^{20-30}$Ne. We also reveal coexisting spherical and deformed shapes in $^{30}$Ne, which indicates the breakdown of the magic neutron number $N=20$ as the key nucleus $^{28}$O is approached, and we predict that the dripline nuclei $^{32,34}$Ne are strongly deformed. By developing reduced-order-models for symmetry-projected states, we perform a global sensitivity analysis and find that the subleading singlet S-wave contact and a pion-nucleon coupling strongly impact nuclear deformation in chiral effective-field-theory. The techniques developed in this work clarify how microscopic nuclear forces generate the multiscale physics of nuclei spanning collective phenomena as well as short-range correlations and allow to capture emergent and dynamical phenomena in finite fermion systems., Comment: This work significantly expands upon ideas from arXiv:2305.06955. While it includes some overlap in text to maintain context, substantial new content, methodology, and analysis are presented. 26 pages, 16 figures

Extreme ultraviolet pulses as generated by high harmonic generation (HHG) are a powerful tool for both time-resolved spectroscopy and coherent diffractive imaging. However, the integration of spectroscopy and microscopy to harness the unique broadband spectra provided by HHG is hardly explored due to the challenge to decouple spectroscopic and microscopic information. Here, we present an interferometric approach to this problem that combines Fourier transform spectroscopy (FTS) with Fourier transform holography (FTH). This is made possible by the generation of phase-locked pulses using a pair of HHG sources. Crucially, in our geometry the number of interferometric measurements required is at most equal to the number of high harmonics in the illumination, and can be further reduced by incorporating prior knowledge about the structure of the FTH sample. Compared to conventional FTS, this approach achieves over an order of magnitude increase in acquisition speed for full spectro-microscopic data, and furthermore allows diffraction-limited computational imaging.

Excitons -- two-particle correlated electron-hole pairs -- are the dominant low-energy optical excitation in the broad class of semiconductor materials, which range from classical silicon to perovskites, and from two-dimensional to organic materials. Recently, the study of excitons has been brought on a new level of detail by the application of photoemission momentum microscopy -- a technique that has dramatically extended the experimental capabilities of time- and angle-resolved photoemission spectroscopy (trARPES). Here, we review how the energy- and momentum-resolved photoelectron detection scheme enables direct access to the energy landscape of bright and dark excitons, and, more generally, to the momentum-coordinate of the exciton that is fundamental to its wavefunction. Focusing on two-dimensional materials and organic semiconductors as two tuneable platforms for exciton physics, we first discuss the typical photoemission fingerprint of excitons in momentum microscopy and highlight that is is possible to obtain information not only on the electron- but also hole-component of the former exciton. Second, we focus on the recent application of photoemission orbital tomography to such excitons, and discuss how this provides a unique access to the real-space properties of the exciton wavefunction. Throughout the review, we detail how studies performed on two-dimensional transition metal dichalcogenides and organic semiconductors lead to very similar conclusions, and, in this manner, highlight the strength of time-resolved momentum microscopy for the study of optical excitations in semiconductors., Comment: review-article

Photoemission orbital tomography provides direct access from laboratory measurements to the real-space molecular orbitals of well-ordered organic semiconductor layers. Specifically, the application of phase retrieval algorithms to photon-energy- and angle-resolved photoemission data enables the direct reconstruction of full 3D molecular orbitals without the need for simulations using density functional theory or the like. A major limitation for the direct approach has been the need for densely-sampled, well-calibrated 3D photoemission patterns. Here, we present an iterative projection algorithm that completely eliminates this challenge: for the benchmark case of the pentacene frontier orbitals, we demonstrate the reconstruction of the full orbital based on a dataset containing only four simulated photoemission momentum measurements. We discuss the algorithm performance, sampling requirements with respect to the photon energy, optimal measurement strategies, and the accuracy of orbital images that can be achieved., Comment: 27 pages, 10 figures, 44 references

Gamma decays were observed in $^{56}$Ca and $^{58}$Ca following quasi-free one-proton knockout reactions from $^{57,59}$Sc beams at $\approx 200$ MeV/nucleon. For $^{56}$Ca, a $\gamma$ ray transition was measured to be 1456(12) keV, while for $^{58}$Ca an indication for a transition was observed at 1115(34) keV. Both transitions were tentatively assigned as the $2^+_1 \rightarrow 0^+_{gs}$ decays, and were compared to results from ab initio and conventional shell-model approaches. A shell-model calculation in a wide model space with a marginally modified effective nucleon-nucleon interaction depicts excellent agreement with experiment for $2^+_1$ level energies, two-neutron separation energies, and reaction cross sections, corroborating the formation of a new nuclear shell above the $N$ = 34 shell. Its constituents, the $0f_{5/2}$ and $0g_{9/2}$ orbitals, are almost degenerate. This degeneracy precludes the possibility for a doubly magic $^{60}$Ca and potentially drives the dripline of Ca isotopes to $^{70}$Ca or even beyond., Comment: 8 pages, 3 figures

The optical intersite spin transfer (OISTR) effect was recently verified in Fe$_{50}$Ni$_{50}$ using magneto-optical Kerr measurements in the extreme ultraviolet range. However, one of the main experimental signatures analyzed in this work, namely a magnetic moment increase at a specific energy in Ni, was subsequently found also in pure Ni, where no transfer from one element to another is possible. Hence, it is a much-discussed issue whether OISTR in FeNi alloys is real and whether it can be verified experimentally or not. Here, we present a comparative study of spin transfer in Fe$_{50}$Ni$_{50}$, Fe$_{19}$Ni$_{81}$ and pure Ni. We conclusively show that an increase in the magneto-optical signal is indeed insufficient to verify OISTR. However, we also show how an extended data analysis overcomes this problem and allows to unambiguously identify spin transfer effects. Concomitantly, our work solves the long-standing riddle about the origin of delayed demagnetization behavior of Ni in FeNi alloys.

The magneto-optical Kerr effect (MOKE) in the extreme ultraviolet (EUV) regime has helped to elucidate some of the key processes that lead to the manipulation of magnetism on ultrafast timescales. However, as we show in this paper, the recently introduced spectrally-resolved analysis of such data can lead to surprising experimental observations, which might cause misinterpretations. Therefore, an extended analysis of the EUV magneto-optics is necessary. Via experimental determination of the dielectric tensor, we find here that the non-equilibrium excitation in an ultrafast magnetization experiment can cause a rotation of the off-diagonal element of the dielectric tensor in the complex plane. In direct consequence, the commonly analyzed magneto-optic asymmetry may show time-dependent behaviour that is not directly connected to the magnetic properties of the sample. We showcase such critical observations for the case of ultrafast magnetization dynamics in Ni, and give guidelines for the future analysis of spectrally-resolved magneto-optical data and its comparison with theory.

The role and impact of spatial heterogeneity in two-dimensional quantum materials represents one of the major research quests regarding the future application of these materials in optoelectronics and quantum information science. In the case of transition-metal dichalcogenide heterostructures, in particular, direct access to heterogeneities in the dark-exciton landscape with nanometer spatial and ultrafast time resolution is highly desired, but remains largely elusive. Here, we introduce ultrafast dark field momentum microscopy to spatio-temporally resolve dark exciton formation dynamics in a twisted WSe$_2$/MoS$_2$ heterostructure with 55 femtosecond time- and 500~nm spatial resolution. This allows us to directly map spatial heterogeneity in the electronic and excitonic structure, and to correlate these with the dark exciton formation and relaxation dynamics. The benefits of simultaneous ultrafast nanoscale dark-field momentum microscopy and spectroscopy is groundbreaking for the present study, and opens the door to new types of experiments with unprecedented spectroscopic and spatiotemporal capabilities., Comment: 39 pages, 4 main figures, 8 supplemental figures

We compute the structure of the exotic even nuclei $^{20-34}$Ne and $^{34-40}$Mg using interactions from chiral effective field theory (EFT). Our results for the ground-state rotational bands in $^{20-32}$Ne and $^{36-40}$Mg agree with data. We predict a well-deformed $^{34}$Ne and find that $^{40}$Mg exhibits an oblate deformed band close to the prolate ground-state, indicating the emergence of shape co-existence at the neutron dripline. A global sensitivity analysis shows that the subleading singlet $S$-wave contact and a pion-nucleon coupling strongly impact deformation in chiral EFT., Comment: 13 pages, 8 figures, supplemental material

The energy landscape of optical excitations in mono- and few-layer transition metal dichalcogenides (TMDs) is dominated by optically bright and dark excitons. These excitons can be fully localized within a single TMD layer, or the electron- and the hole-component of the exciton can be charge-separated over multiple TMD layers. Such intra- or interlayer excitons have been characterized in detail using all-optical spectroscopies, and, more recently, photoemission spectroscopy. In addition, there are so-called hybrid excitons whose electron- and/or hole-component are delocalized over two or more TMD layers, and therefore provide a promising pathway to mediate charge-transfer processes across the TMD interface. Hence, an in-situ characterization of their energy landscape and dynamics is of vital interest. In this work, using femtosecond momentum microscopy combined with many-particle modeling, we quantitatively compare the dynamics of momentum-indirect intralayer excitons in monolayer WSe$_2$ with the dynamics of momentum-indirect hybrid excitons in heterobilayer WSe$_2$/MoS$_2$, and draw three key conclusions: First, we find that the energy of hybrid excitons is reduced when compared to excitons with pure intralayer character. Second, we show that the momentum-indirect intralayer and hybrid excitons are formed via exciton-phonon scattering from optically excited bright excitons. And third, we demonstrate that the efficiency for phonon absorption and emission processes in the mono- and the heterobilayer is strongly dependent on the energy alignment of the intralayer and hybrid excitons with respect to the optically excited bright exciton. Overall, our work provides microscopic insights into exciton dynamics in TMD mono- and bilayers., Comment: 27 pages, 5 figures

Excitons are two-particle correlated bound states that are formed due to Coulomb interaction between single-particle holes and electrons. In the solid-state, cooperative interactions with surrounding quasiparticles can strongly tailor the exciton properties and potentially even create new correlated states of matter. It is thus highly desirable to access such cooperative and correlated exciton behavior on a fundamental level. Here, we find that the ultrafast transfer of an exciton's hole across a type-II band-aligned moir\'e heterostructure leads to a surprising sub-200-fs upshift of the single-particle energy of the electron being photoemitted from the two-particle exciton state. While energy relaxation usually leads to an energetic downshift of the spectroscopic signature, we show that this unusual upshift is a clear fingerprint of the correlated interactions of the electron and hole parts of the exciton quasiparticle. In this way, time-resolved photoelectron spectroscopy is straightforwardly established as a powerful method to access exciton correlations and cooperative behavior in two-dimensional quantum materials. Our work highlights this new capability and motivates the future study of optically inaccessible correlated excitonic and electronic states in moir\'e heterostructures., Comment: 32 pages, 4 main figures, 5 supplemental figures

Harnessing the optoelectronic response of organic semiconductors requires a thorough understanding of the fundamental light-matter interaction that is dominated by the excitation of correlated electron-hole pairs, i.e. excitons. The nature of these excitons would be fully captured by knowing the quantum-mechanical wavefunction, which, however, is difficult to access both theoretically and experimentally. Here, we use femtosecond photoemission orbital tomography in combination with many-body perturbation theory to gain access to exciton wavefunctions in organic semiconductors. We find that the coherent sum of multiple electron-hole pair contributions that typically make up a single exciton can be experimentally evidenced by photoelectron spectroscopy. For the prototypical organic semiconductor buckminsterfullerene (C$_{60}$), we show how to disentangle such multiorbital contributions and thereby access key properties of the exciton wavefunctions including localization, charge-transfer character, and ultrafast exciton formation and relaxation dynamics.

Ab initio has been used as a label in nuclear theory for over two decades. Its meaning has evolved and broadened over the years. We present our interpretation, briefly review its historical use, and discuss its present-day relation to theoretical uncertainty quantification., Comment: Contribution to Research Topic "Uncertainty Quantification in Nuclear Physics" of Frontiers in Physics

Single-reference coupled-cluster theory is an accurate and affordable computational method for the nuclear many-body problem. For open-shell nuclei, the reference state typically breaks rotational invariance and angular momentum must be restored as a good quantum number. We perform angular-momentum projection after variation and employ the disentangled coupled-cluster formalism and a Hermitian approach. We compare our results with benchmarks for $^8$Be and $^{20}$Ne using a two-nucleon interaction from chiral effective field theory and for $pf$-shell nuclei within the traditional shell model. We compute the rotational band in the exotic nucleus $^{34}$Mg and find agreement with data., Comment: 23 pages, 12 figures

Moir\'e superlattices in atomically thin van-der-Waals heterostructures hold great promise for an extended control of electronic and valleytronic lifetimes, the confinement of excitons in artificial moir\'e lattices, and the formation of novel exotic quantum phases. Such moir\'e-induced emergent phenomena are particularly strong for interlayer excitons, where the hole and the electron are localized in different layers of the heterostructure. In order to exploit the full potential of correlated moir\'e and exciton physics, a thorough understanding of the ultrafast interlayer exciton formation process and the real-space wavefunction confinement in the moir\'e potential is indispensable. However, direct experimental access to these parameters is limited since most excitonic quasiparticles are optically dark. Here we show that femtosecond photoemission momentum microscopy provides quantitative access to these key properties of the moir\'e interlayer excitons. We find that interlayer excitons are dominantly formed on the sub-50~fs timescale via interlayer tunneling at the K valleys of the Brillouin zones. In addition, we directly measure energy-momentum fingerprints of the moir\'e interlayer excitons by mapping their spectral signatures within the mini Brillouin zone that is built up by the twisted heterostructure. From these momentum-fingerprints, we gain quantitative access to the modulation of the exciton wavefunction within the moir\'e potential in real-space. Our work provides the first direct access to the interlayer moir\'e exciton formation dynamics in space and time and reveals new opportunities to study correlated moir\'e and exciton physics for the future realization of exotic quantum phases of matter., Comment: 7 pages main text, 11 pages SI

Collinear laser spectroscopy is performed on the nickel isotopes $^{58-68,70}$Ni, using a time-resolved photon counting system. From the measured isotope shifts, nuclear charge radii $R_c$ are extracted and compared to theoretical results. Three ab initio approaches all employ, among others, the chiral interaction NNLO$_{\rm sat}$, which allows an assessment of their accuracy. We find agreement with experiment in differential radii $\delta \left\langle r_\mathrm{c}^2 \right\rangle$ for all employed ab initio methods and interactions, while the absolute radii are consistent with data only for NNLO$_{\rm sat}$. Within nuclear density functional theory, the Skyrme functional SV-min matches experiment more closely than the Fayans functional Fy($\Delta r$,HFB).

We construct an effective shell-model interaction for the valence space spanned by single-particle neutron and single-hole proton states in $^{100}$Sn. Starting from chiral nucleon-nucleon and three-nucleon forces and single-reference coupled-cluster theory for $^{100}$Sn we apply a second similarity transformation that decouples the valence space. The particle-particle components of the resulting effective interaction can be used in shell model calculations for neutron deficient tin isotopes. The hole-hole interaction can be used to calculate the $N = 50$ isotones south of $^{100}$Sn, and the full particle-hole interaction describes nuclei in the region southeast of $^{100}$Sn. We compute low-lying excited states in selected nuclei southeast of $^{100}$Sn, and find reasonable agreement with data. The presented techniques can also be applied to construct effective shell-model interactions for other regions of the nuclear chart., Comment: 9 pages, 8 figures, interaction files in supplemental material

Normal-ordering provides an approach to approximate three-body forces as effective two-body operators and it is therefore an important tool in many-body calculations with realistic nuclear interactions. The corresponding neglect of certain three-body terms in the normal-ordered Hamiltonian is known to influence translational invariance, although the magnitude of this effect has not yet been systematically quantified. In this work we study in particular the normal-ordering two-body approximation applied to a single harmonic-oscillator reference state. We explicate the breaking of translational invariance and demonstrate the magnitude of the approximation error as a function of model space parameters for $^4\rm{He}$ and $^{16}\rm{O}$ by performing full no-core shell-model calculations with and without three-nucleon forces. We combine two different diagnostics to better monitor the breaking of translational invariance. While the center-of-mass effect is shown to become potentially very large for $^4\rm{He}$, it is also shown to be much smaller for $^{16}\rm{O}$ although full convergence is not reached. These tools can be easily implemented in studies using other many-body frameworks and bases., Comment: 13 pages, 10 figures

We present a novel setup to measure the transverse magneto-optical Kerr effect in the extreme ultraviolet spectral range at exceptionally high repetition rates based on a fiber laser amplifier system. This affords a very high and stable flux of extreme ultraviolet light, which we use to measure element-resolved demagnetization dynamics with unprecedented depth of information. Furthermore, the setup is equipped with a strong electromagnet and a cryostat, allowing measurements between 10 and 420 K using magnetic fields up to 0.86 T. The performance of our setup is demonstrated by a set of temperature- and time-dependent magnetization measurements showing distinct element-dependent behavior.

Nuclear charge radii are sensitive probes of different aspects of the nucleon-nucleon interaction and the bulk properties of nuclear matter; thus, they provide a stringent test and challenge for nuclear theory. The calcium region has been of particular interest, as experimental evidence has suggested a new magic number at $N = 32$ [1-3], while the unexpectedly large increases in the charge radii [4,5] open new questions about the evolution of nuclear size in neutron-rich systems. By combining the collinear resonance ionization spectroscopy method with $\beta$-decay detection, we were able to extend the charge radii measurement of potassium ($Z =19$) isotopes up to the exotic $^{52}$K ($t_{1/2}$ = 110 ms), produced in minute quantities. Our work provides the first charge radii measurement beyond $N = 32$ in the region, revealing no signature of the magic character at this neutron number. The results are interpreted with two state-of-the-art nuclear theories. For the first time, a long sequence of isotopes could be calculated with coupled-cluster calculations based on newly developed nuclear interactions. The strong increase in the charge radii beyond $N = 28$ is not well captured by these calculations, but is well reproduced by Fayans nuclear density functional theory, which, however, overestimates the odd-even staggering effect. These findings highlight our limited understanding on the nuclear size of neutron-rich systems, and expose pressing problems that are present in some of the best current models of nuclear theory., Comment: submitted version; revision accepted in Nature Physics

Auger scattering channels are of fundamental importance to describe and understand the non-equilibrium charge carrier dynamics in graphene. While impact excitation increases the number of carriers in the conduction band and has been observed experimentally, direct access to its inverse process, Auger recombination, has so far been elusive. Here, we tackle this problem by applying our novel setup for ultrafast time-resolved photoelectron momentum microscopy. Our approach gives simultaneous access to charge carrier dynamics at all energies and in-plane momenta within the linearly dispersive Dirac cones. We thus provide direct evidence for Auger recombination on a sub-10~fs timescale by identifying transient energy- and momentum-dependent populations far above the excitation energy. We compare our results with model calculations of scattering processes in the Dirac cone to support our experimental findings., Comment: 15 pages, paper and SI, 4+3 figures

Light-engineering of quantum materials via electromagnetic dressing is considered an on-demand approach for tailoring electronic band dispersions and even inducing topological phase transitions. For probing such dressed bands, photoemission spectroscopy is an ideal tool, and we employ here a novel experiment based on ultrafast photoemission momentum microscopy. Using this setup, we measure the in-plane momentum-dependent intensity fingerprints of the electromagnetically-dressed sidebands from a Au(111) surface for s- and p-polarized infrared driving. We find that at metal surfaces, due to screening of the driving laser, the contribution from Floquet-Bloch bands is negligible, and the dressed bands are dominated by the laser-assisted photoelectric effect. Also, we find that in contrast to general expectations, s-polarized light can dress free-electron states at large photoelectron momenta. Our results show that the dielectric response of the material must carefully be taken into account when using photoemission for the identification of light-engineered electronic band structures., Comment: 19 pages: 6 pages letter with 4 figures, 13 pages SI with 5 figures

We use coupled-cluster theory and nuclear interactions from chiral effective field theory to compute the nuclear matrix element for the neutrinoless double-beta decay of $^{48}$Ca. Benchmarks with the no-core shell model in several light nuclei inform us about the accuracy of our approach. For $^{48}$Ca we find a relatively small matrix element. We also compute the nuclear matrix element for the two-neutrino double-beta decay of $^{48}$Ca with a quenching factor deduced from two-body currents in recent ab-initio calculation of the Ikeda sum-rule in $^{48}$Ca [Gysbers et al., Nature Physics 15, 428-431 (2019)]., Comment: 14 pages, 13 figures; Version accepted for publication, Supplemental material also updated

We compute the charge radii of even-mass neon and magnesium isotopes from neutron number N = 8 to the dripline. Our calculations are based on nucleon-nucleon and three-nucleon potentials from chiral effective field theory that include delta isobars. These potentials yield an accurate saturation point and symmetry energy of nuclear matter. We use the coupled-cluster method and start from an axially symmetric reference state. Binding energies and two-neutron separation energies largely agree with data and the dripline in neon is accurate. The computed charge radii have an estimated uncertainty of about 2-3% and are accurate for many isotopes where data exist. Finer details such as isotope shifts, however, are not accurately reproduced. Chiral potentials correctly yield the subshell closure at N = 14 and also a decrease in charge radii at N = 8 (observed in neon and predicted for magnesium). They yield a continued increase of charge radii as neutrons are added beyond N = 14 yet underestimate the large increase at N = 20 in magnesium., Comment: 9 pages, 8 figures

We optimize $\Delta$-full nuclear interactions from chiral effective field theory. The low-energy constants of the contact potentials are constrained by two-body scattering phase shifts, and by properties of bound-state of $A=2$ to $4$ nucleon systems and nuclear matter. The pion-nucleon couplings are taken from a Roy-Steiner analysis. The resulting interactions yield accurate binding energies and radii for a range of nuclei from $A=16$ to $A=132$, and provide accurate equations of state for nuclear matter and realistic symmetry energies. Selected excited states are also in agreement with data., Comment: 7 pages, 6 figures

We report the measurement of reaction cross sections ($\sigma_R^{\rm ex}$) of $^{27,29}$F with a carbon target at RIKEN. The unexpectedly large $\sigma_R^{\rm ex}$ and derived matter radius identify $^{29}$F as the heaviest two-neutron Borromean halo to date. The halo is attributed to neutrons occupying the $2p_{3/2}$ orbital, thereby vanishing the shell closure associated with the neutron number $N = 20$. The results are explained by state-of-the-art shell model calculations. Coupled-cluster computations based on effective field theories of the strong nuclear force describe the matter radius of $^{27}$F but are challenged for $^{29}$F., Comment: 8 pages, 4 figures

Recent progress in laser-based high-repetition rate extreme ultraviolet (EUV) lightsources and multidimensional photoelectron spectroscopy enable the build-up of a new generation of time-resolved photoemission experiments. Here, we present a setup for time-resolved momentum microscopy driven by a 1 MHz femtosecond EUV table-top light source optimized for the generation of 26.5 eV photons. The setup provides simultaneous access to the temporal evolution of the photoelectron's kinetic energy and in-plane momentum. We discuss opportunities and limitations of our new experiment based on a series of static and time-resolved measurements on graphene.

We present energy-resolved photoelectron momentum maps for orbital tomography that have been collected with a novel and efficient time-of-flight momentum microscopy setup. This setup is combined with a 0.5 MHz table-top femtosecond extreme-ultraviolet light source, which enables unprecedented speed in data collection and paves the way towards time-resolved orbital imaging experiments in the future. Moreover, we take a significant step forward in the data analysis procedure for orbital imaging, and present a sparsity-driven approach to the required phase retrieval problem, which uses only the number of non-zero pixels in the orbital. Here, no knowledge of the object support is required, and the sparsity number can easily be determined from the measured data. Used in the relaxed averaged alternating reflections algorithm, this sparsity constraint enables fast and reliable phase retrieval for our experimental as well as noise-free and noisy simulated photoelectron momentum map data.

$\beta$-decay, a process that changes a neutron into a proton (and vice versa), is the dominant decay mode of atomic nuclei. This decay offers a unique window to physics beyond the standard model, and is at the heart of microphysical processes in stellar explosions and the synthesis of the elements in the Universe. For 50 years, a central puzzle has been that observed $\beta$-decay rates are systematically smaller than theoretical predictions. This was attributed to an apparent quenching of the fundamental coupling constant $g_A \simeq $ 1.27 in the nucleus by a factor of about 0.75 compared to the $\beta$-decay of a free neutron. The origin of this quenching is controversial and has so far eluded a first-principles theoretical understanding. Here we address this puzzle and show that this quenching arises to a large extent from the coupling of the weak force to two nucleons as well as from strong correlations in the nucleus. We present state-of-the-art computations of $\beta$-decays from light to heavy nuclei. Our results are consistent with experimental data, including the pioneering measurement for $^{100}$Sn. These theoretical advances are enabled by systematic effective field theories of the strong and weak interactions combined with powerful quantum many-body techniques. This work paves the way for systematic theoretical predictions for fundamental physics problems. These include the synthesis of heavy elements in neutron star mergers and the search for neutrino-less double-$\beta$-decay, where an analogous quenching puzzle is a major source of uncertainty in extracting the neutrino mass scale., Comment: 20 pages, 18 figures

The exotic Borromean nucleus $^{20}$Mg with $N$ = 8, located at the proton drip-line provides a unique testing ground for nuclear forces and the evolution of shell structure in the neutron-deficient region. We report on the first observation of proton unbound resonances together with bound states in $^{20}$Mg from the $^{20}$Mg($d$,$d'$) reaction performed at TRIUMF. Phenomenological shell-model calculations offer a reasonable description. However, our experimental results present a challenge for current first-principles nuclear structure approaches and point to the need for improved chiral forces and {\it ab initio} calculations. Furthermore, the differential cross section of the first excited state is compared with distorted-wave Born approximation calculations to deduce a neutron quadrupole deformation parameter of $\beta_n$=0.46$\pm$0.21. This provides the first indication of a possible weakening of the $N$ = 8 shell closure at the proton drip-line., Comment: 6 pages, 4 figures

The first $\gamma$-ray spectroscopy of $^{52}$Ar, with the neutron number N = 34, was measured using the $^{53}$K(p,2p) one-proton removal reaction at $\sim$210 MeV/u at the RIBF facility. The 2$^{+}_{1}$ excitation energy is found at 1656(18) keV, the highest among the Ar isotopes with N $>$ 20. This result is the first experimental signature of the persistence of the N = 34 subshell closure beyond $^{54}$Ca, i.e., below the magic proton number Z = 20. Shell-model calculations with phenomenological and chiral-effective-field-theory interactions both reproduce the measured 2$^{+}_{1}$ systematics of neutron-rich Ar isotopes, and support a N = 34 subshell closure in $^{52}$Ar.

We construct nucleonic microscopic optical potentials by combining the Green's function approach with the coupled-cluster method for $\rm{^{40}Ca}$ and $\rm{^{48}Ca}$. For the computation of the ground-state of $\rm{^{40}Ca}$ and $\rm{^{48}Ca}$, we use the coupled-cluster method in the singles-and-doubles approximation, while for the A = $\pm 1$ nuclei we use particle-attached/removed equation-of-motion method truncated at two-particle-one-hole and one-particle-two-hole excitations, respectively. Our calculations are based on the chiral nucleon-nucleon and three-nucleon interaction $\rm{NNLO_{sat}}$, which reproduces the charge radii of $^{40}$Ca and $^{48}$Ca, and the chiral nucleon-nucleon interaction $\rm{NNLO_{opt}}$. In all cases considered here, we observe that the overall form of the neutron scattering cross section is reproduced for both interactions, but the imaginary part of the potential, which reflects the loss of flux in the elastic channel, is negligible. The latter points to neglected many-body correlations that would appear beyond the coupled-cluster truncation level considered in this work. We show that, by artificially increasing the parameter $\eta$ in the Green's function, practical results can be further improved., Comment: 11 pages, 10 figures, typos corrected, accepted for publication in Phys. Rev. C

We present an approach to derive effective shell-model interactions from microscopic nuclear forces. The similarity-transformed coupled-cluster Hamiltonian decouples the single-reference state of a closed-shell nucleus and provides us with a core for the shell model. We use a second similarity transformation to decouple a shell-model space from the excluded space. We show that the three-body terms induced by both similarity transformations are crucial for an accurate computation of ground and excited states. As a proof of principle we use a nucleon-nucleon interaction from chiral effective field theory, employ a $^4$He core, and compute low-lying states of $^{6-8}$He and $^{6-8}$Li in $p$-shell model spaces. Our results agree with benchmarks from full configuration interaction., Comment: 12 pages, 16 figures

We demonstrate a novel imaging approach and associated reconstruction algorithm for far-field coherent diffractive imaging, based on the measurement of a pair of laterally sheared diffraction patterns. The differential phase profile retrieved from such a measurement leads to improved reconstruction accuracy, increased robustness against noise, and faster convergence compared to traditional coherent diffractive imaging methods. We measure laterally sheared diffraction patterns using Fourier-transform spectroscopy with two phase-locked pulse pairs from a high harmonic source. Using this approach, we demonstrate spectrally resolved imaging at extreme ultraviolet wavelengths between 28 and 35 nm.