Non-line-of-sight (NLOS) imaging enables monitoring around corners and is promising for diverse applications. The resolution of transient NLOS imaging is limited to a centimeter scale, mainly by the temporal resolution of the detectors. Here, we construct an up-conversion single-photon detector with a high temporal resolution of $\sim 1.4\mathrm{ps}$ and a low noise count rate of 5 counts per second (cps). Notably, the detector operates at room temperature, near-infrared wavelength. Using this detector, we demonstrate high-resolution and low-noise NLOS imaging. Our system can provide a $180\mu \mathrm{m}$ axial resolution and a 2 mm lateral resolution, which is more than 1 order of magnitude better than that in previous experiments. These results open avenues for high-resolution NLOS imaging techniques in relevant applications.

We observed electronic $K$ x rays emitted from muonic iron atoms using superconducting transition-edge sensor microcalorimeters. The energy resolution of 5.2 eV in FWHM allowed us to observe the asymmetric broad profile of the electronic characteristic $K\alpha$ and $K\beta$ x rays together with the hypersatellite $K^h\alpha$ x rays around 6 keV. This signature reflects the time-dependent screening of the nuclear charge by the negative muon and the $L$-shell electrons, accompanied by electron side feeding. Assisted by a simulation, these data clearly reveal the electronic $K$- and $L$-shell hole production and their temporal evolution on the 10–20 fs scale during the muon cascade process.

Metasurfaces have recently entered the realm of quantum photonics, enabling manipulation of quantum light using a compact nanophotonic platform. Realizing the full potential of metasurfaces at the deepest quantum level requires the ability to tune coherent light-matter interactions continuously in space and time. Here, we introduce the concept of space-time quantum metasurfaces for arbitrary control of the spectral, spatial, and spin properties of nonclassical light using a compact photonic platform. We show that space-time quantum metasurfaces allow on-demand tailoring of entanglement among all degrees of freedom of a single photon. We also show that spatiotemporal modulation induces asymmetry at the fundamental level of quantum fluctuations, resulting in the generation of steered and vortex photon pairs out of vacuum. Space-time quantum metasurfaces have the potential to enable novel photonic functionalities, such as encoding quantum information into high-dimensional color qudits using designer modulation protocols, sculpting multispectral and multispatial modes in spontaneous emission, and generating reconfigurable hyperentanglement for high-capacity quantum communications.

We present the first experimental realization of a time crystal stabilized by dissipation. The central signature in our implementation in a driven open atom-cavity system is a period doubled switching between distinct checkerboard density wave patterns, induced by the interplay between controlled cavity dissipation, cavity-mediated interactions, and external driving. We demonstrate the robustness of this dynamical phase against system parameter changes and temporal perturbations of the driving.

We report an intense broadband midinfrared absorption band in the ${{\mathrm{Au}}_{10}}^{+}$ cluster in a region in which only molecular vibrations would normally be expected. Observed in the infrared multiple photon dissociation spectra of ${\mathrm{Au}}_{10}{\mathrm{Ar}}^{+}$, ${\mathrm{Au}}_{10}{({\mathrm{N}}_2\mathrm{O})}^{+}$, and ${\mathrm{Au}}_{10}{(\mathrm{OCS})}^{+}$, the smooth feature stretches $700–3400{\mathrm{cm}}^{-1}$ ($\lambda =14–2.9\mu \mathrm{m}$). Calculations confirm unusually low-energy allowed electronic excitations consistent with the observed spectra. In ${\mathrm{Au}}_{10}{(\mathrm{OCS})}^{+}$, IR absorption throughout the band drives OCS decomposition resulting in CO loss, providing an alternative method of bond activation or breaking.

We investigate the problem of an infinitely heavy impurity interacting with a dilute Bose gas at zero temperature. When the impurity-boson interactions are short-ranged, we show that boson-boson interactions induce a quantum blockade effect, where a single boson can effectively block or screen the impurity potential. Since this behavior depends on the quantum granular nature of the Bose gas, it cannot be captured within a standard classical-field description. Using a combination of exact quantum Monte Carlo methods and a truncated basis approach, we show how the quantum correlations between bosons lead to universal few-body bound states and a logarithmically slow dependence of the polaron ground-state energy on the boson-boson scattering length. Moreover, we expose the link between the polaron energy and the spatial structure of the quantum correlations, spanning the infrared to ultraviolet physics.

Isotope shifts of ${}^{223–226,228}\mathrm{Ra}{}^{19}\mathrm{F}$ were measured for different vibrational levels in the electronic transition $A^2{\mathrm{\Pi }}_{1/2}\leftarrow X^2{\mathrm{\Sigma }}^{+}$. The observed isotope shifts demonstrate the particularly high sensitivity of radium monofluoride to nuclear size effects, offering a stringent test of models describing the electronic density within the radium nucleus. Ab initio quantum chemical calculations are in excellent agreement with experimental observations. These results highlight some of the unique opportunities that short-lived molecules could offer in nuclear structure and in fundamental symmetry studies.

Spin-polarized samples and spin mixtures of quantum degenerate fermionic atoms are prepared in selected excited Bloch bands of an optical checkerboard square lattice. For the spin-polarized case, extreme band lifetimes above 10 s are observed, reflecting the suppression of collisions by Pauli’s exclusion principle. For spin mixtures, lifetimes are reduced by an order of magnitude by two-body collisions between different spin components, but still remarkably large values of about 1 s are found. By analyzing momentum spectra, we can directly observe the orbital character of the optical lattice. The observations demonstrated here form the basis for exploring the physics of Fermi gases with two paired spin components in orbital optical lattices, including the regime of unitarity.

Dynamical fermionization refers to the phenomenon in Tonks-Girardeau gases where, upon release from harmonic confinement, the gases’ momentum density profile evolves asymptotically to that of an ideal Fermi gas in the initial trap. This phenomenon has been demonstrated theoretically in hardcore and anyonic Tonks-Girardeau gases and was recently experimentally observed in a strongly interacting Bose gas. We extend this study to a one-dimensional spinor gas of arbitrary spin in the strongly interacting regime and analytically prove that the total momentum distribution after the harmonic trap is turned off approaches that of a spinless ideal Fermi gas, while the asymptotic momentum distribution of each spin component takes the same shape of the initial real space density profile of that spin component. Our work demonstrates the rich physics arising from the interplay between the spin and the charge degrees of freedom in a spinor system.

Nondestructive quantum measurements are central for quantum physics applications ranging from quantum sensing to quantum computing and quantum communication. Employing the toolbox of cavity quantum electrodynamics, we here concatenate two identical nondestructive photon detectors to repeatedly detect and track a single photon propagating through a 60 m long optical fiber. By demonstrating that the combined signal-to-noise ratio of the two detectors surpasses each single one by about 2 orders of magnitude, we experimentally verify a key practical benefit of cascaded nondemolition detectors compared to conventional absorbing devices.

In the short time since the first observation of supersolid states of ultracold dipolar atoms, substantial progress has been made in understanding the zero-temperature phase diagram and low-energy excitations of these systems. Less is known, however, about their finite-temperature properties, particularly relevant for supersolids formed by cooling through direct evaporation. Here, we explore this realm by characterizing the evaporative formation and subsequent decay of a dipolar supersolid by combining high-resolution in-trap imaging with time-of-flight observables. As our atomic system cools toward quantum degeneracy, it first undergoes a transition from thermal gas to a crystalline state with the appearance of periodic density modulation. This is followed by a transition to a supersolid state with the emergence of long-range phase coherence. Further, we explore the role of temperature in the development of the modulated state.

The new physics of magic-angle twisted bilayer graphene (TBG) motivated extensive studies of flat bands hosted by moiré superlattices in van der Waals structures, inspiring the investigations into their photonic counterparts with potential applications including Bose-Einstein condensation. However, correlation between photonic flat bands and bilayer photonic moiré systems remains unexplored, impeding further development of moiré photonics. In this work, we formulate a coupled-mode theory for low-angle twisted bilayer honeycomb photonic crystals as a close analogy of TBG, discovering magic-angle photonic flat bands with a non-Anderson-type localization. Moreover, the interlayer separation constitutes a convenient degree of freedom in tuning photonic moiré bands without high pressure. A phase diagram is constructed to correlate the twist angle and separation dependencies to the photonic magic angles. Our findings reveal a salient correspondence between fermionic and bosonic moiré systems and pave the avenue toward novel applications through advanced photonic band or state engineering.

We observe signatures of radial and angular roton excitations around a droplet crystallization transition in dipolar Bose-Einstein condensates. In situ measurements are used to characterize the density fluctuations near this transition. The static structure factor is extracted and used to identify the radial and angular roton excitations by their characteristic symmetries. These fluctuations peak as a function of the interaction strength indicating the crystallization transition of the system. We compare our observations to a theoretically calculated excitation spectrum allowing us to connect the crystallization mechanism with the softening of the angular roton modes.

We prepare mixtures of ultracold CaF molecules and Rb atoms in a magnetic trap and study their inelastic collisions. When the atoms are prepared in the spin-stretched state and the molecules in the spin-stretched component of the first rotationally excited state, they collide inelastically with a rate coefficient $k_2=(6.6\pm 1.5)\times {10}^{-11}{\mathrm{cm}}^3/\mathrm{s}$ at temperatures near $100\mu \mathrm{K}$. We attribute this to rotation-changing collisions. When the molecules are in the ground rotational state we see no inelastic loss and set an upper bound on the spin-relaxation rate coefficient of $k_2<5.8\times {10}^{-12}{\mathrm{cm}}^3/\mathrm{s}$ with 95% confidence. We compare these measurements to the results of a single-channel loss model based on quantum defect theory. The comparison suggests a short-range loss parameter close to unity for rotationally excited molecules, but below 0.04 for molecules in the rotational ground state.

Overcoming the detrimental effect of disorder at the nanoscale is very hard since disorder induces localization and an exponential suppression of transport efficiency. Here we unveil novel and robust quantum transport regimes achievable in nanosystems by exploiting long-range hopping. We demonstrate that in a 1D disordered nanostructure in the presence of long-range hopping, transport efficiency, after decreasing exponentially with disorder at first, is then enhanced by disorder [disorder-enhanced transport (DET) regime] until, counterintuitively, it reaches a disorder-independent transport (DIT) regime, persisting over several orders of disorder magnitude in realistic systems. To enlighten the relevance of our results, we demonstrate that an ensemble of emitters in a cavity can be described by an effective long-range Hamiltonian. The specific case of a disordered molecular wire placed in an optical cavity is discussed, showing that the DIT and DET regimes can be reached with state-of-the-art experimental setups.

We demonstrate the coherent creation of a single NaCs molecule in its rotational, vibrational, and electronic (rovibronic) ground state in an optical tweezer. Starting with a weakly bound Feshbach molecule, we locate a two-photon transition via the $|c^3{\mathrm{\Sigma }}_1,v^{\prime }=26⟩$ excited state and drive coherent Rabi oscillations between the Feshbach state and a single hyperfine level of the NaCs rovibronic ground state $|X^1\mathrm{\Sigma },v^{\prime \prime }=0,N^{\prime \prime }=0⟩$ with a binding energy of $D_0=h\times 147044.63(11)\mathrm{GHz}$. We measure a lifetime of $3.4\pm 1.6\mathrm{s}$ for the rovibronic ground state molecule, which possesses a large molecule-frame dipole moment of 4.6D and occupies predominantly the motional ground state. These long-lived, fully quantum-state-controlled individual dipolar molecules provide a key resource for molecule-based quantum simulation and information processing.

We study the properties of an impurity immersed in a weakly interacting Bose gas, i.e., of a Bose polaron. In the perturbatively tractable limit of weak impurity-boson interactions many of its properties are known to depend only on the scattering length. Here we demonstrate that for strong (unitary) impurity-boson interactions all quasiparticle properties of a heavy Bose polaron, such as its energy, its residue, its Tan’s contact, and the number of bosons trapped nearby the impurity, depend on the impurity-boson potential via a single parameter characterizing its range.

We demonstrate a source for correlated pairs of atoms characterized by two opposite momenta and two spatial modes forming a Bell state only involving external degrees of freedom. We characterize the state of the emitted atom beams by observing strong number squeezing up to $-10\mathrm{dB}$ in the correlated two-particle modes of emission. We furthermore demonstrate genuine two-particle interference in the normalized second-order correlation function $g^{(2)}$ relative to the emitted atoms.

We investigate transport dynamics of a single low-energy ionic impurity in a Bose-Einstein condensate. The impurity is implanted into the condensate starting from a single Rydberg excitation, which is ionized by a sequence of fast electric field pulses aiming to minimize the ion’s initial kinetic energy. Using a small electric bias field, we study the subsequent collisional dynamics of the impurity subject to an external force. The fast ion-atom collision rate, stemming from the dense degenerate host gas and the large ion-atom scattering cross section, allow us to study a regime of frequent collisions of the impurity within only tens of microseconds. Comparison of our measurements with stochastic trajectory simulations based on sequential Langevin collisions indicate diffusive transport properties of the impurity and allows us to measure its mobility. Our results open a novel path to study dynamics of charged quantum impurities in ultracold matter.

We present an all-optical mass spectrometry technique to identify trapped ions. The new method uses laser-cooled ions to determine the mass of a cotrapped dark ion with a sub-dalton resolution within a few seconds. We apply the method to identify the first controlled synthesis of cold, trapped ${\mathrm{RaOH}}^{+}$ and ${{\mathrm{RaOCH}}_3}^{+}$. These molecules are promising for their sensitivity to time and parity violations that could constrain sources of new physics beyond the standard model. The nondestructive nature of the mass spectrometry technique may help identify molecular ions or highly charged ions prior to optical spectroscopy. Unlike previous mass spectrometry techniques for small ion crystals that rely on scanning, the method uses a Fourier transform that is inherently broadband and comparatively fast. The technique’s speed provides new opportunities for studying state-resolved chemical reactions in ion traps.