Emission of high-order harmonics from solids provides a new avenue in attosecond science. On the one hand, it allows us to investigate fundamental processes of the nonlinear response of electrons driven by a strong laser pulse in a periodic crystal lattice. On the other hand, it opens new paths toward efficient attosecond pulse generation, novel imaging of electronic wave functions, and enhancement of high-order harmonic-generation (HHG) intensity. A key feature of HHG in a solid (as compared to the well-understood phenomenon of HHG in an atomic gas) is the delocalization of the process, whereby an electron ionized from one site in the periodic lattice may recombine in any other. Here, we develop an analytic model, based on the localized Wannier wave functions in the valence band and delocalized Bloch functions in the conduction band. This Wannier-Bloch approach assesses the contributions of individual lattice sites to the HHG process and hence precisely addresses the question of localization of harmonic emission in solids. We apply this model to investigate HHG in a ZnO crystal for two different orientations, corresponding to wider and narrower valence and conduction bands, respectively. Interestingly, for narrower bands, the HHG process shows significant localization, similar to harmonic generation in atoms. For all cases, the delocalized contributions to HHG emission are highest near the band-gap energy. Our results pave the way to controlling localized contributions to HHG in a solid crystal.

The higher the energy of a particle is above equilibrium, the faster it relaxes because of the growing phase space of available electronic states it can interact with. In the relaxation process, phase coherence is lost, thus limiting high-energy quantum control and manipulation. In one-dimensional systems, high relaxation rates are expected to destabilize electronic quasiparticles. Here, we show that the decoherence induced by relaxation of hot electrons in one-dimensional semiconducting nanowires evolves nonmonotonically with energy such that above a certain threshold hot electrons regain stability with increasing energy. We directly observe this phenomenon by visualizing, for the first time, the interference patterns of the quasi-one-dimensional electrons using scanning tunneling microscopy. We visualize the phase coherence length of the one-dimensional electrons, as well as their phase coherence time, captured by crystallographic Fabry-Pèrot resonators. A remarkable agreement with a theoretical model reveals that the nonmonotonic behavior is driven by the unique manner in which one-dimensional hot electrons interact with the cold electrons occupying the Fermi sea. This newly discovered relaxation profile suggests a high-energy regime for operating quantum applications that necessitate extended coherence or long thermalization times, and may stabilize electronic quasiparticles in one dimension.

In this work, we analyze the dynamical properties of periodically driven band models. Focusing on the case of Bose-Einstein condensates, and using a mean-field approach to treat interparticle collisions, we identify the origin of dynamical instabilities arising from the interplay between the external drive and interactions. We present a widely applicable generic numerical method to extract instability rates and link parametric instabilities to uncontrolled energy absorption at short times. Based on the existence of parametric resonances, we then develop an analytical approach within Bogoliubov theory, which quantitatively captures the instability rates of the system and provides an intuitive picture of the relevant physical processes, including an understanding of how transverse modes affect the formation of parametric instabilities. Importantly, our calculations demonstrate an agreement between the instability rates determined from numerical simulations and those predicted by theory. To determine the validity regime of the mean-field analysis, we compare the latter to the weakly coupled conserving approximation. The tools developed and the results obtained in this work are directly relevant to present-day ultracold-atom experiments based on shaken optical lattices and are expected to provide an insightful guidance in the quest for Floquet engineering.

Organic dye molecules have been used in a great number of scientific and technological applications, but their wider use in quantum optics has been hampered by transitions to short-lived vibrational levels, which limit their coherence properties. To remedy this, one can take advantage of optical resonators. Here, we present the first results on coherent molecule-resonator coupling, where a single polycyclic aromatic hydrocarbon molecule extinguishes 38% of the light entering a microcavity at liquid helium temperature. We also demonstrate fourfold improvement of single-molecule stimulated emission compared to free-space focusing and take first steps for coherent mechanical manipulation of the molecular transition. Our approach of coupling molecules to an open and tunable microcavity with a very low mode volume and moderately low quality factors of the order of $10^3$ paves the way for the realization of nonlinear and collective quantum optical effects.

The transition from a many-body localized phase to a thermalizing one is a dynamical quantum phase transition that lies outside the framework of equilibrium statistical mechanics. We provide a detailed study of the critical properties of this transition at finite sizes in one dimension. We find that the entanglement entropy of small subsystems looks strongly subthermal in the quantum critical regime, which indicates that it varies discontinuously across the transition as the system size is taken to infinity, even though many other aspects of the transition look continuous. We also study the variance of the half-chain entanglement entropy, which shows a peak near the transition, and find substantial variation in the entropy across eigenstates of the same sample. Furthermore, the sample-to-sample variations in this quantity are strongly growing and are larger than the intrasample variations. We posit that these results are consistent with a picture in which the transition to the thermal phase is driven by an eigenstate-dependent sparse resonant “backbone” of long-range entanglement, which just barely gains enough strength to thermalize the system on the thermal side of the transition as the system size is taken to infinity. This discontinuity in a global quantity—the presence of a fully functional bath—in turn implies a discontinuity even for local properties. We discuss how this picture compares with existing renormalization group treatments of the transition.

The quantum dynamics of interacting many-body systems has become a unique venue for the realization of novel states of matter. Here, we unveil a new class of nonequilibrium states that are eigenstates of an emergent local Hamiltonian. The latter is explicitly time dependent and, even though it does not commute with the physical Hamiltonian, it behaves as a conserved quantity of the time-evolving system. We discuss two examples of integrable systems in which the emergent eigenstate solution can be applied for an extensive (in system size) time: transport in one-dimensional lattices with initial particle (or spin) imbalance and sudden expansion of quantum gases in optical lattices. We focus on noninteracting spinless fermions, hard-core bosons, and the Heisenberg model. We show that current-carrying states can be ground states of emergent local Hamiltonians, and that they can exhibit a quasimomentum distribution function that is peaked at nonzero (and tunable) quasimomentum. We also show that time-evolving states can be highly excited eigenstates of emergent local Hamiltonians, with an entanglement entropy that does not exhibit volume-law scaling.

Frequency analysis of the rf emission of oscillating Josephson supercurrent is a powerful passive way of probing properties of topological Josephson junctions. In particular, measurements of the Josephson emission enable the detection of topological gapless Andreev bound states that give rise to emission at half the Josephson frequency $f_J$ rather than conventional emission at $f_J$. Here, we report direct measurement of rf emission spectra on Josephson junctions made of HgTe-based gate-tunable topological weak links. The emission spectra exhibit a clear signal at half the Josephson frequency $f_J/2$. The linewidths of emission lines indicate a coherence time of 0.3–4 ns for the $f_J/2$ line, much shorter than for the $f_J$ line (3–4 ns). These observations strongly point towards the presence of topological gapless Andreev bound states and pave the way for a future HgTe-based platform for topological quantum computation.

Unconventional metallic states which do not support well-defined single-particle excitations can arise near quantum phase transitions as strong quantum fluctuations of incipient order parameters prevent electrons from forming coherent quasiparticles. Although antiferromagnetic phase transitions occur commonly in correlated metals, understanding the nature of the strange metal realized at the critical point in layered systems has been hampered by a lack of reliable theoretical methods that take into account strong quantum fluctuations. We present a nonperturbative solution to the low-energy theory for the antiferromagnetic quantum critical metal in two spatial dimensions. Being a strongly coupled theory, it can still be solved reliably in the low-energy limit as quantum fluctuations are organized by a new control parameter that emerges dynamically. We predict the exact critical exponents that govern the universal scaling of physical observables at low temperatures.

Optical tools are promising for spin-wave generation because of the possibilities of ultrafast manipulation and local excitation. However, a single laser pulse can inject spin waves (SWs) only with a broad frequency spectrum, resulting in short propagation distances and low wave amplitudes. Here, we excite a magnetic garnet film by a train of fs-laser pulses with a 1-GHz repetition rate so that the pulse separation is shorter than the decay time of magnetic modes, which allows us to achieve a collective impact on the magnetization and establish a quasistationary source of spin waves, namely, a coherent accumulation of magnons (“magnon cloud”). This approach has several appealing features: (i) The magnon source is tunable, (ii) the SW amplitude can be significantly enhanced, (iii) the SW spectrum is quite narrow, providing long-distance propagation, (iv) the periodic pumping results in an almost constant-in-time SW amplitude for the distances larger than $20\mu \mathrm{m}$ away from the source, and (v) the SW emission shows pronounced directionality. These results expand the capabilities of ultrafast coherent optical control of magnetization and pave the way for applications in data processing, including the quantum regime. The quasistationary magnon accumulation might also be of interest for applications in magnon Bose-Einstein condensates.

Interferometers enable ultrasensitive measurement in a wide array of applications from gravitational wave searches to force microscopes. The role of quantum mechanics in the metrological limits of interferometers has a rich history, and a large number of techniques to surpass conventional limits have been proposed. In a typical measurement configuration, the trade-off between the probe’s shot noise (imprecision) and its quantum backaction results in what is known as the standard quantum limit (SQL). In this work, we investigate how quantum correlations accessed by modifying the readout of the interferometer can access physics beyond the SQL and improve displacement sensitivity. Specifically, we use an optical cavity to probe the motion of a silicon nitride membrane off mechanical resonance, as one would do in a broadband displacement or force measurement, and observe sensitivity better than the SQL dictates for our quantum efficiency. Our measurement illustrates the core idea behind a technique known as variational readout, in which the optical readout quadrature is changed as a function of frequency to improve broadband displacement detection. And, more generally, our result is a salient example of how correlations can aid sensing in the presence of backaction.

Active-matter systems operate far from equilibrium because of the continuous energy injection at the scale of constituent particles. At larger scales, described by coarse-grained models, the global entropy production rate $\mathcal{S}$ quantifies the probability ratio of forward and reversed dynamics and hence the importance of irreversibility at such scales: It vanishes whenever the coarse-grained dynamics of the active system reduces to that of an effective equilibrium model. We evaluate $\mathcal{S}$ for a class of scalar stochastic field theories describing the coarse-grained density of self-propelled particles without alignment interactions, capturing such key phenomena as motility-induced phase separation. We show how the entropy production can be decomposed locally (in real space) or spectrally (in Fourier space), allowing detailed examination of the spatial structure and correlations that underly departures from equilibrium. For phase-separated systems, the local entropy production is concentrated mainly on interfaces, with a bulk contribution that tends to zero in the weak-noise limit. In homogeneous states, we find a generalized Harada-Sasa relation that directly expresses the entropy production in terms of the wave-vector-dependent deviation from the fluctuation-dissipation relation between response functions and correlators. We discuss extensions to the case where the particle density is coupled to a momentum-conserving solvent and to situations where the particle current, rather than the density, should be chosen as the dynamical field. We expect the new conceptual tools developed here to be broadly useful in the context of active matter, allowing one to distinguish when and where activity plays an essential role in the dynamics.

Quantum randomness is an essential key to understanding the dynamics of complex many-body systems and also a powerful tool for quantum engineering. However, exact realizations of quantum randomness take an extremely long time and are infeasible in many-body systems, leading to the notion of quantum pseudorandomness, also known as unitary designs. Here, to explore microscopic dynamics of generating quantum pseudorandomness in many-body systems, we provide new efficient constructions of unitary designs and propose a design Hamiltonian, a random Hamiltonian of which dynamics always forms a unitary design after a threshold time. The new constructions are based on the alternate applications of random potentials in the generalized position and momentum spaces, and we provide explicit quantum circuits generating quantum pseudorandomness significantly more efficient than previous ones. We then provide a design Hamiltonian in disordered systems with periodically changing spin-glass-type interactions. The design Hamiltonian generates quantum pseudorandomness in a constant time even in the system composed of a large number of spins. We also point out the close relationship between the design Hamiltonian and quantum chaos.

We present a method to show that low-energy states of quantum many-body interacting systems in one spatial dimension are nonlocal. We assign a Bell inequality to the Hamiltonian of the system in a natural way and we efficiently find its classical bound using dynamic programing. The Bell inequality is such that its quantum value for a given state, and for appropriate observables, corresponds to the energy of the state. Thus, the presence of nonlocal correlations can be certified for states of low enough energy. The method can also be used to optimize certain Bell inequalities: in the translationally invariant (TI) case, we provide an exponentially faster computation of the classical bound and analytically closed expressions of the quantum value for appropriate observables and Hamiltonians. The power and generality of our method is illustrated through four representative examples: a tight TI inequality for eight parties, a quasi-TI uniparametric inequality for any even number of parties, ground states of spin-glass systems, and a nonintegrable interacting $XXZ$-like Hamiltonian. Our work opens the possibility for the use of low-energy states of commonly studied Hamiltonians as multipartite resources for quantum information protocols that require nonlocality.

Living cells use readout molecules to record the state of receptor proteins, similar to measurements or copies in typical computational devices. But is this analogy rigorous? Can cells be optimally efficient, and if not, why? We show that, as in computation, a canonical biochemical readout network generates correlations; extracting no work from these correlations sets a lower bound on dissipation. For general input, the biochemical network cannot reach this bound, even with arbitrarily slow reactions or weak thermodynamic driving. It faces an accuracy-dissipation trade-off that is qualitatively distinct from and worse than implied by the bound, and more complex steady-state copy processes cannot perform better. Nonetheless, the cost remains close to the thermodynamic bound unless accuracy is extremely high. Additionally, we show that biomolecular reactions could be used in thermodynamically optimal devices under exogenous manipulation of chemical fuels, suggesting an experimental system for testing computational thermodynamics.

We expand the standard thermodynamic framework of a system coupled to a thermal reservoir by considering a stream of independently prepared units repeatedly put into contact with the system. These units can be in any nonequilibrium state and interact with the system with an arbitrary strength and duration. We show that this stream constitutes an effective resource of nonequilibrium free energy, and we identify the conditions under which it behaves as a heat, work, or information reservoir. We also show that this setup provides a natural framework to analyze information erasure (“Landauer’s principle”) and feedback-controlled systems (“Maxwell’s demon”). In the limit of a short system-unit interaction time, we further demonstrate that this setup can be used to provide a thermodynamically sound interpretation to many effective master equations. We discuss how nonautonomously driven systems, micromasers, lasing without inversion and the electronic Maxwell demon can be thermodynamically analyzed within our framework. While the present framework accounts for quantum features (e.g., squeezing, entanglement, coherence), we also show that quantum resources do not offer any advantage compared to classical ones in terms of the maximum extractable work.

A growing number of biological, soft, and active matter systems are observed to exhibit normal diffusive dynamics with a linear growth of the mean-squared displacement, yet with a non-Gaussian distribution of increments. Based on the Chubinsky-Slater idea of a diffusing diffusivity, we here establish and analyze a minimal model framework of diffusion processes with fluctuating diffusivity. In particular, we demonstrate the equivalence of the diffusing diffusivity process with a superstatistical approach with a distribution of diffusivities, at times shorter than the diffusivity correlation time. At longer times, a crossover to a Gaussian distribution with an effective diffusivity emerges. Specifically, we establish a subordination picture of Brownian but non-Gaussian diffusion processes, which can be used for a wide class of diffusivity fluctuation statistics. Our results are shown to be in excellent agreement with simulations and numerical evaluations.

The melting transition of two-dimensional systems is a fundamental problem in condensed matter and statistical physics that has advanced significantly through the application of computational resources and algorithms. Two-dimensional systems present the opportunity for novel phases and phase transition scenarios not observed in 3D systems, but these phases depend sensitively on the system and, thus, predicting how any given 2D system will behave remains a challenge. Here, we report a comprehensive simulation study of the phase behavior near the melting transition of all hard regular polygons with $3\le n\le 14$ vertices using massively parallel Monte Carlo simulations of up to $1\times {10}^6$ particles. By investigating this family of shapes, we show that the melting transition depends upon both particle shape and symmetry considerations, which together can predict which of three different melting scenarios will occur for a given $n$. We show that systems of polygons with as few as seven edges behave like hard disks; they melt continuously from a solid to a hexatic fluid and then undergo a first-order transition from the hexatic phase to the isotropic fluid phase. We show that this behavior, which holds for all $7\le n\le 14$, arises from weak entropic forces among the particles. Strong directional entropic forces align polygons with fewer than seven edges and impose local order in the fluid. These forces can enhance or suppress the discontinuous character of the transition depending on whether the local order in the fluid is compatible with the local order in the solid. As a result, systems of triangles, squares, and hexagons exhibit a Kosterlitz-Thouless-Halperin-Nelson-Young (KTHNY) predicted continuous transition between isotropic fluid and triatic, tetratic, and hexatic phases, respectively, and a continuous transition from the appropriate $x$-atic to the solid. In particular, we find that systems of hexagons display continuous two-step KTHNY melting. In contrast, due to symmetry incompatibility between the ordered fluid and solid, systems of pentagons and plane-filling fourfold pentilles display a one-step first-order melting of the solid to the isotropic fluid with no intermediate phase.