In the Landau levels of a two-dimensional electron system or when flat bands are present, e.g., in twisted van der Waals bilayers, strong electron-electron interaction gives rise to quantum Hall ferromagnetism with spontaneously broken symmetries in the spin and isospin sectors. Quantum Hall ferromagnets support a rich variety of low-energy collective excitations that are instrumental to understand the nature of the magnetic ground states and are also potentially useful as carriers of quantum information. Probing such collective excitations, especially their dispersion $\omega (k)$, is experimentally challenging due to small sample size and measurement constraints. In this work, we demonstrate an all-electrical approach that integrates a Fabry-Pérot cavity with nonequilibrium transport to achieve the excitation, wave vector selection, and detection of spin waves in graphene heterostructures. Our experiments reveal gapless, linearly dispersed spin wave excitations in the $E=0$ Landau level of bilayer graphene, thus providing direct experimental evidence for a predicted canted antiferromagnetic order. We show that the gapless spin wave mode propagates with a high group velocity of several tens of kilometers per second and maintains phase coherence over a distance of many micrometers. Its dependence on the magnetic field and temperature agree well with the hydrodynamic theory of spin waves. These results lay the foundation for the quest of spin superfluidity in this high-quality material. The resonant cavity technique we develop offers a powerful and timely method to explore the collective excitation of many spin- and isospin-ordered many-body ground states in van der Waals heterostructures and opens the possibility of engineering magnonic devices.

Interatomic processes play a crucial role in weakly bound complexes exposed to ionizing radiation; therefore, gaining a thorough understanding of their efficiency is of fundamental importance. Here, we directly measure the timescale of interatomic Coulombic decay (ICD) in resonantly excited helium nanodroplets using a high-resolution, tunable, extreme ultraviolet free-electron laser. Over an extensive range of droplet sizes and laser intensities, we discover the decay to be surprisingly fast, with decay times as short as 400 fs, nearly independent of the density of the excited states. Using a combination of time-dependent density functional theory and ab initio quantum chemistry calculations, we elucidate the mechanisms of this ultrafast decay process, where pairs of excited helium atoms in one droplet strongly attract each other and form merging void bubbles, which drastically accelerates ICD.

The dynamics of quantum information in strongly interacting systems, known as quantum information scrambling, has recently become a common thread in our understanding of black holes, transport in exotic non-Fermi liquids, and many-body analogs of quantum chaos. To date, verified experimental implementations of scrambling have focused on systems composed of two-level qubits. Higher-dimensional quantum systems, however, may exhibit different scrambling modalities and are predicted to saturate conjectured speed limits on the rate of quantum information scrambling. We take the first steps toward accessing such phenomena, by realizing a quantum processor based on superconducting qutrits (three-level quantum systems). We demonstrate the implementation of universal two-qutrit scrambling operations and embed them in a five-qutrit quantum teleportation protocol. Measured teleportation fidelities $F_{\mathrm{avg}}=0.568\pm 0.001$ confirm the presence of scrambling even in the presence of experimental imperfections and decoherence. Our teleportation protocol, which connects to recent proposals for studying traversable wormholes in the laboratory, demonstrates how quantum technology that encodes information in higher-dimensional systems can exploit a larger and more connected state space to achieve the resource efficient encoding of complex quantum circuits.

In canonical optomechanical systems, mechanical vibrations are dynamically encoded on an optical probe field, which reciprocally exerts a backaction force. Because of the weak single-photon coupling strength achieved with macroscopic oscillators, most of the existing experiments were conducted with large photon numbers to achieve sizable effects, thereby hiding the original optomechanical nonlinearity. To increase the optomechanical interaction, we make use of subwavelength-sized ultrasensitive suspended nanowires inserted in the mode volume of a fiber-based microcavity. By scanning the nanowire within the cavity mode volume and measuring its impact on the cavity mode, we obtain a map of the 2D optomechanical interaction. Then, by using the toolbox of nanowire-based force-sensing protocols, we explore the backaction of the optomechanical interaction and map the optical force field experienced by the nanowire. These measurements also allow us to demonstrate the possibility to detect variations of the mean intracavity photon number smaller than unity. This implementation should also allow us to enter the promising regime of cavity optomechanics, where a single intracavity photon can displace the oscillator by more than its zero-point fluctuations, which will open novel perspectives in the field.

We consider a clean quantum system subject to strong periodic driving. The existence of a dominant energy scale, $h_D^x$, can generate considerable structure in an effective description of a system that, in the absence of the drive, is nonintegrable and interacting, and does not host localization. In particular, we uncover points of freezing in the space of drive parameters (frequency and amplitude). At those points, the dynamics is severely constrained due to the emergence of an almost exact, local conserved quantity, which scars the entire Floquet spectrum by preventing the system from heating up ergodically, starting from any generic state, even though it delocalizes over an appropriate subspace. At large drive frequencies, where a naïve Magnus expansion would predict a vanishing effective (average) drive, we devise instead a strong-drive Magnus expansion in a moving frame. There, the emergent conservation law is reflected in the appearance of the “integrability” of an effective Hamiltonian. These results hold for a wide variety of Hamiltonians, including the Ising model in a transverse field in any dimension and for any form of Ising interaction. The phenomenon is also shown to be robust in the presence of two-body Heisenberg interactions with any arbitrary choice of couplings. Furthermore, we construct a real-time perturbation theory that captures resonance phenomena where the conservation breaks down, giving way to unbounded heating. This approach opens a window on the low-frequency regime where the Magnus expansion fails.

Confocal microscopy is an essential imaging tool for biological systems, solid-state physics and nanophotonics. Using confocal microscopes allows performing resonant fluorescence experiments, where the emitted light has the same wavelength as the excitation laser. These challenging experiments are carried out under linear cross-polarization conditions, rejecting laser light from the detector. In this work, we uncover the physical mechanisms that are at the origin of the yet-unexplained high polarization rejection ratio which makes these measurements possible. We show in both experiment and theory that the use of a reflecting surface (i.e., the beam splitter and mirrors) placed between the polarizer and analyzer in combination with a confocal arrangement explains the giant cross-polarization extinction ratio of ${10}^8$ and beyond. We map the modal transformation of the polarized optical Gaussian beam. We find an intensity “hole” in the reflected beam under cross-polarization conditions. We interpret this hole as a manifestation of the Imbert-Fedorov effect, which deviates the beam depending on its polarization helicity. This result implies that this topological effect is amplified here from the usually observed nanometer to the micrometer scale due to our cross-polarization dark-field methods. We confirm these experimental findings for a large variety of commercially available mirrors and polarization components, allowing their practical implementation in many experiments.

The quantitative prediction of electronic properties in correlated materials requires simulations without empirical truncations and parameters. We present a method to achieve this goal through a new ab initio formulation of dynamical mean-field theory (DMFT). Instead of using small impurities defined in a low-energy subspace, which require complicated downfolded interactions which are often approximated, we describe a full cell $GW+\mathrm{DMFT}$ approach, where the impurities comprise all atoms in a unit cell or supercell of the crystal. Our formulation results in large impurity problems, which we treat here with efficient quantum chemistry impurity solvers that work on the real-frequency axis, combined with a one-shot $G_0{W}_0$ treatment of long-range interactions. We apply our full cell approach to bulk Si, two antiferromagnetic correlated insulators NiO and $\alpha \text{−}{\mathrm{Fe}}_2{\mathrm{O}}_3$, and the paramagnetic correlated metal ${\mathrm{SrMoO}}_3$, with impurities containing up to ten atoms and 124 orbitals. We find that spectral properties, magnetic moments, and two-particle spin correlation functions are obtained in good agreement with experiment. In addition, in the metal oxide insulators, the balanced treatment of correlations involving all orbitals in the cell leads to new insights into the orbital character around the insulating gap.

A system with charge conservation and lattice translation symmetry has a well-defined filling $\nu$, which is a real number representing the average charge per unit cell. We show that if $\nu$ is fractional (i.e., not an integer), this imposes very strong constraints on the low-energy theory of the system and give a framework to understand such constraints in great generality, vastly generalizing the Luttinger and Lieb-Schultz-Mattis theorems. The most powerful constraint comes about if $\nu$ is continuously tunable (i.e., the system is charge compressible), in which case, we show that the low-energy theory must have a very large emergent symmetry group—larger than any compact Lie group. An example is the Fermi surface of a Fermi liquid, where the charge at every point on the Fermi surface is conserved. We expect that in many, if not all, cases, even exotic non-Fermi liquids will have the same emergent symmetry group as a Fermi liquid, even though they could have very different dynamics. We call a system with this property an ersatz Fermi liquid. We show that ersatz Fermi liquids share a number of properties in common with Fermi liquids, including Luttinger’s theorem (which is thus extended to a large class of non-Fermi liquids) and periodic “quantum oscillations” in the response to an applied magnetic field. We also establish versions of Luttinger’s theorem for the composite Fermi liquid in quantum Hall systems and for spinon Fermi surfaces in Mott insulators. Our work makes a connection between filling constraints and the theory of symmetry-protected topological phases, in particular through the concept of “’t Hooft anomalies.”

The Green function completely encapsulates a system’s linear response to external sources, and plays a central role in optics, electromagnetism, and acoustics. In electromagnetism, a broad range of phenomena are connected to the Green function, including the local density of optical states, superradiance, and the cooperative Lamb shift. Therefore, knowing the Green function is important for progress in fields as diverse as cavity quantum electrodynamics, plasmonics, metamaterials, and photovoltaics. However, experimentally characterizing the full complex Green function is challenging, as it requires amplitude and phase sensitive measurements with deep-subwavelength spatial resolution. Here, we report a method to characterize the full complex Green function with a resolution of $\lambda /100$ by measuring the mutual impedance between two dipoles at microwave frequencies. We apply it to a resonant planar cavity, with both parallel and nonparallel sides, and also explore the effects of modal resonances in a dielectric cube on dipole-dipole interactions. The ability to characterize the Green function with high spatial resolution provides a unique way to investigate cooperative effects in complex photonic systems.

Community detection methods attempt to divide a network into groups of nodes that share similar properties, thus revealing its large-scale structure. A major challenge when employing such methods is that they are often degenerate, typically yielding a complex landscape of competing answers. As an attempt to extract understanding from a population of alternative solutions, many methods exist to establish a consensus among them in the form of a single partition “point estimate” that summarizes the whole distribution. Here, we show that it is, in general, not possible to obtain a consistent answer from such point estimates when the underlying distribution is too heterogeneous. As an alternative, we provide a comprehensive set of methods designed to characterize and summarize complex populations of partitions in a manner that captures not only the existing consensus but also the dissensus between elements of the population. Our approach is able to model mixed populations of partitions, where multiple consensuses can coexist, representing different competing hypotheses for the network structure. We also show how our methods can be used to compare pairs of partitions, how they can be generalized to hierarchical divisions, and how they can be used to perform statistical model selection between competing hypotheses.

We derive exact nonlocal homogenized constitutive relations for the effective electromagnetic wave properties of disordered two-phase composites and metamaterials from first principles. This exact formalism enables us to extend the long-wavelength limitations of conventional homogenization estimates of the effective dynamic dielectric constant tensor ${\mathit{ϵ}}_e({\mathbf{k}}_I,\omega )$ for arbitrary microstructures so that it can capture spatial dispersion well beyond the quasistatic regime (where $\omega$ and ${\mathbf{k}}_I$ are the frequency and wave vector of the incident radiation). We accomplish this task by deriving nonlocal strong-contrast expansions that exactly account for complete microstructural information (infinite set of $n$-point correlation functions) and hence multiple scattering to all orders for the range of wave numbers for which our extended homogenization theory applies, i.e., $0\le |{\mathbf{k}}_I|\ell \lesssim 1$ (where $\ell$ is a characteristic heterogeneity length scale). Because of the fast-convergence properties of such expansions, their lower-order truncations yield accurate closed-form approximate formulas for ${\mathit{ϵ}}_e({\mathbf{k}}_I,\omega )$ that apply for a wide class of microstructures. These nonlocal formulas are resummed representations of the strong-contrast expansions that still accurately capture multiple scattering to all orders via the microstructural information embodied in the spectral density, which is easy to compute for any composite. The accuracy of these microstructure-dependent approximations is validated by comparison to full-waveform simulation computations for both 2D and 3D ordered and disordered models of composite media. Thus, our closed-form formulas enable one to predict accurately and efficiently the effective wave characteristics well beyond the quasistatic regime for a wide class of composite microstructures without having to perform full-blown simulations. We find that disordered hyperuniform media are generally less lossy than their nonhyperuniform counterparts. We also show that certain disordered hyperuniform particulate composites exhibit novel wave characteristics, including the capacity to act as low-pass filters that transmit waves “isotropically” up to a selected wave number and refractive indices that abruptly change over a narrow range of wave numbers. Our results demonstrate that one can design the effective wave characteristics of a disordered composite by engineering the microstructure to possess tailored spatial correlations at prescribed length scales. Thus, our findings can accelerate the discovery of novel electromagnetic composites.

We numerically investigate the morphology and disclination line dynamics of active nematic droplets in three dimensions. Although our model incorporates only the simplest possible form of achiral active stress, active nematic droplets display an unprecedented range of complex morphologies. For extensile activity, fingerlike protrusions grow at points where disclination lines intersect the droplet surface. For contractile activity, however, the activity field drives cup-shaped droplet invagination, run-and-tumble motion, or the formation of surface wrinkles. This diversity of behavior is explained in terms of an interplay between active anchoring, active flows, and the dynamics of the motile disclination lines. We discuss our findings in the light of biological processes such as morphogenesis, collective cancer invasion, and the shape control of biomembranes, suggesting that some biological systems may share the same underlying mechanisms as active nematic droplets.

In principle, there is no obstacle to gapping fermions preserving any global symmetry that does not suffer a ’t Hooft anomaly. In practice, preserving a symmetry that is realized on fermions in a chiral manner necessitates some dynamics beyond simple quadratic mass terms. We show how this can be achieved using familiar results about the strong coupling dynamics of supersymmetric gauge theories and, in particular, the phenomenon of confinement without chiral symmetry breaking. We present simple models that gap fermions while preserving a symmetry group under which they transform in chiral representations. For example, we show how to gap a collection of 4D fermions that carry the quantum numbers of one generation of the standard model, but without breaking electroweak symmetry. We further show how to gap fermions in groups of 16 while preserving certain discrete symmetries that exhibit a mod 16 anomaly.

Geometrical frustration in thin sheets is ubiquitous across scales in biology and becomes increasingly relevant in technology. Previous research identified the origin of the frustration as the violation of Gauss’s Theorema Egregium. Such “Gauss frustration” exhibits rich phenomenology; it may lead to mechanical instabilities, anomalous mechanics, and shape-morphing abilities that can be harnessed in engineering systems. Here we report a new type of geometrical frustration, one that is as general as Gauss frustration. We show that its origin is the violation of Mainardi-Codazzi-Peterson compatibility equations and that it appears in Euclidean sheets. Combining experiments, simulations, and theory, we study the specific case of a Euclidean ribbon with radial and geodesic curvatures. Experiments, conducted using different materials and techniques, reveal shape transitions, symmetry breaking, and spontaneous stress focusing. These observations are quantitatively rationalized using analytic solutions and geometrical arguments. We expect this frustration to play a significant role in natural and engineering systems, specifically in slender 3D printed sheets.

Quantum catalysis is a fascinating concept that demonstrates how certain transformations can only become possible when given access to a specific resource that has to be returned unaffected. It was first discovered in the context of entanglement theory, and since then, it has been applied in a number of resource-theoretic frameworks, including quantum thermodynamics. Although, in that case, the necessary (and sometimes also sufficient) conditions on the existence of a catalyst are known, almost nothing is known about the precise form of the catalyst state required by the transformation. In particular, it is not clear whether it has to have some special properties or be finely tuned to the desired transformation. In this work, we describe a surprising property of multicopy states: We show that in resource theories governed by majorization, all resourceful states are catalysts for all allowed transformations. In quantum thermodynamics, this means that the so-called “second laws of thermodynamics” do not require a fine-tuned catalyst; rather, any state, given sufficiently many copies, can serve as a useful catalyst. These analytic results are accompanied by several numerical investigations that indicate that neither a multicopy form nor a very-large-dimension catalyst is required to activate most allowed transformations catalytically.

Polarized neutron diffraction (PND) is a powerful technique to distinguish a weak magnetic contribution from the total scattering intensity. It can provide a detailed insight into the microscopic spin ordering at the unit cell level, but also into the mesoscopic magnetic ordering, like different types of domain populations. Here we report on the application of this technique to the long-standing problem of determining the absolute direction of the Dzyaloshinskii-Moriya vector in relation to the crystal structure. The proposed PND method, based on the measurement of one representative reflection, is easy to perform and straightforward to interpret. The absolute sign of the Dzyaloshinskii-Moriya interaction (DMI) in ${\mathrm{MnCO}}_3$ has been independently determined by PND and found to be in agreement with recent results obtained by resonant magnetic synchrotron scattering. This validates the method. In addition, the absolute DMI vector direction in the prototypical room-temperature weak ferromagnet $\alpha \text{−}{\mathrm{Fe}}_2{\mathrm{O}}_3$ (hematite) has been determined for the first time. To demonstrate the generality of our method, further examples with different symmetries are also presented. Ab initio calculations of the resulting weak noncollinear magnetization using the quantum espresso package, considering DMI in addition to the symmetric magnetic exchange interaction, were also conducted and found to be in agreement with the experimental results from PND.

Electron-phonon-driven charge-density waves can in some circumstances allow electronic correlations to become predominant, driving a system into a Mott insulating state. New insight into both the Mott state and preceding charge-density wave may result from observations of the coupled dynamics of their underlying degrees of freedom. Here, tunneling injection of single electrons into the upper Hubbard band of the Mott charge-density-wave material $1T\text{−}{\mathrm{TaS}}_2$ reveals extraordinarily narrow electronic excitations which couple to amplitude mode phonons associated with the charge-density wave’s periodic lattice distortion. This gives a vivid microscopic view of the interplay between excitations of the Mott state and the lattice dynamics of its charge-density wave precursor.

The Hubbard model represents the fundamental model for interacting quantum systems and electronic correlations. Using the two-dimensional half-filled Hubbard model at weak coupling as a testing ground, we perform a comparative study of a comprehensive set of state-of-the-art quantum many-body methods. Upon cooling into its insulating antiferromagnetic ground state, the model hosts a rich sequence of distinct physical regimes with crossovers between a high-temperature incoherent regime, an intermediate-temperature metallic regime, and a low-temperature insulating regime with a pseudogap created by antiferromagnetic fluctuations. We assess the ability of each method to properly address these physical regimes and crossovers through the computation of several observables probing both quasiparticle properties and magnetic correlations, with two numerically exact methods (diagrammatic and determinantal quantum Monte Carlo methods) serving as a benchmark. By combining computational results and analytical insights, we elucidate the nature and role of spin fluctuations in each of these regimes. Based on this analysis, we explain how quasiparticles can coexist with increasingly long-range antiferromagnetic correlations and why dynamical mean-field theory is found to provide a remarkably accurate approximation of local quantities in the metallic regime. We also critically discuss whether imaginary-time methods are able to capture the non-Fermi-liquid singularities of this fully nested system.

The concept of “Floquet engineering” relies on an external periodic drive to realize novel, effectively static Hamiltonians. This technique is being explored in experimental platforms across physics, including ultracold atoms, laser-driven electron systems, nuclear magnetic resonance, and trapped ions. The key challenge in Floquet engineering is to avoid the uncontrolled absorption of photons from the drive, especially in interacting systems in which the excitation spectrum becomes effectively dense. The resulting dissipative coupling to higher-lying modes, such as the excited bands of an optical lattice, has been explored in recent experimental and theoretical works, but the demonstration of a broadly applicable method to mitigate this effect is lacking. Here, we show how two-path quantum interference applied to strongly correlated fermions in a driven optical lattice suppresses dissipative coupling to higher bands and increases the lifetime of double occupancies and spin correlations by 2 to 3 orders of magnitude. Interference is achieved by introducing a weak second modulation at twice the fundamental driving frequency with a definite relative phase. This technique is shown to suppress dissipation in both weakly and strongly interacting regimes of an off-resonantly driven Hubbard system, opening an avenue to realizing low-temperature phases of matter in interacting Floquet systems.