It has long been recognized that the diffusion of adsorbed molecules and clusters is the key controlling factor in most dynamical processes occurring on surfaces and in nanoscale-confined spaces. The ability to manipulate diffusion is essential for achieving efficient transport in nano- and microstructures and for many other applications. Through simulations and experiments, we found that under the influence of mechanical oscillations, the diffusion coefficient in nanoscale-confined regions can be greatly enhanced. This effect occurs due to bifurcations of particle trajectories caused by the reconstruction of the energy landscape during oscillations. We derive a parameter-free analytical model for the enhanced diffusion that is in excellent agreement with results of our numerical simulations. The oscillation-induced enhancement of diffusion may have interesting and promising applications in such areas as directed molecular transport, sorting of particles, and tribology. Here, our findings have been applied to studies of mechanical cleaning of surfaces from contamination. Through both experiments and simulations, we have shown that using an oscillating slider, one can significantly reduce the concentration of contaminants in a confined region, which is crucial for achieving superlow friction.

We present an experimental and theoretical study of resonant inelastic x-ray scattering (RIXS) in the carbon disulphide ${\mathrm{CS}}_2$ molecule near the sulfur K-absorption edge. We observe a strong evolution of the RIXS spectral profile with the excitation energy tuned below the lowest unoccupied molecular orbital (LUMO) absorption resonance. The reason for this is twofold. Reducing the photon energy in the vicinity of the LUMO absorption resonance leads to a relative suppression of the LUMO contribution with respect to the emission signal from the higher unoccupied molecular orbitals, which results in the modulation of the total RIXS profile. At even larger negative photon-energy detuning from the resonance, the excitation-energy dependence of the RIXS profile is dominated by the onset of electron dynamics triggered by a coherent excitation of multiple electronic states. Furthermore, our study demonstrates that in the hard x-ray regime, localization of the S 1s core hole occurs in ${\mathrm{CS}}_2$ during the RIXS process because of the orientational dephasing of interference between the waves scattering on the two sulfur atoms. Core-hole localization leads to violation of the symmetry selection rules for the electron transitions observed in the spectra.

We introduce a general framework for analyzing the thermodynamics of small systems that are driven by both a periodic temperature variation and some external parameter modulating their energy. This setup covers, in particular, periodic micro- and nano-heat engines. In a first step, we show how to express total entropy production by properly identified time-independent affinities and currents without making a linear response assumption. In linear response, kinetic coefficients akin to Onsager coefficients can be identified. Specializing to a Fokker-Planck-type dynamics, we show that these coefficients can be expressed as a sum of an adiabatic contribution and one reminiscent of a Green-Kubo expression that contains deviations from adiabaticity. Furthermore, we show that the generalized kinetic coefficients fulfill an Onsager-Casimir-type symmetry tracing back to microscopic reversibility. This symmetry allows for nonidentical off-diagonal coefficients if the driving protocols are not symmetric under time reversal. We then derive a novel constraint on the kinetic coefficients that is sharper than the second law and provides an efficiency-dependent bound on power. As one consequence, we can prove that the power vanishes at least linearly when approaching Carnot efficiency. We illustrate our general framework by explicitly working out the paradigmatic case of a Brownian heat engine realized by a colloidal particle in a time-dependent harmonic trap subject to a periodic temperature profile. This case study reveals inter alia that our new general bound on power is asymptotically tight.

We propose quantum versions of the Bell-Ziv-Zakai lower bounds for the error in multiparameter estimation. As an application, we consider measurement of a time-varying optical phase signal with stationary Gaussian prior statistics and a power-law spectrum $\sim 1/|\omega {|}^p$, with $p>1$. With no other assumptions, we show that the mean-square error has a lower bound scaling as $1/{\mathcal{N}}^{2(p-1)/(p+1)}$, where $\mathcal{N}$ is the time-averaged mean photon flux. Moreover, we show that this scaling is achievable by sampling and interpolation, for any $p>1$. This bound is thus a rigorous generalization of the Heisenberg limit, for measurement of a single unknown optical phase, to a stochastically varying optical phase.

We present the theory of the $k$-core pruning process (progressive removal of nodes with degree less than $k$) in uncorrelated random networks. We derive exact equations describing this process and the evolution of the network structure and solve them numerically and, in the critical regime of the process, analytically. We show that the pruning process exhibits three different behaviors depending on whether the mean degree $⟨q⟩$ of the initial network is above, equal to, or below the threshold $⟨q{⟩}_c$ corresponding to the emergence of the giant $k$-core. We find that above the threshold the network relaxes exponentially to the $k$-core. The system manifests the phenomenon known as “critical slowing-down,” as the relaxation time diverges when $⟨q⟩$ tends to $⟨q{⟩}_c$. At the threshold, the dynamics become critical, characterized by a power-law relaxation ($\propto 1/t^2$). Below the threshold, a long-lasting transient process (a “plateau” stage) occurs. This transient process ends with a collapse in which the entire network disappears completely. The duration of the process diverges when $⟨q⟩\to ⟨q{⟩}_c$. We show that the critical dynamics of the pruning are determined by branching processes of spreading damage. Clusters of nodes of degree exactly $k$ are the evolving substrate for these branching processes. Our theory completely describes this branching cascade of damage in uncorrelated networks by providing the time-dependent distribution function of branching. These theoretical results are supported by our simulations of the $k$-core pruning in Erdős-Rényi graphs.

In recent years, ultracold atoms in optical lattices have proven their great value as quantum simulators for studying strongly correlated phases and complex phenomena in solid-state systems. Here, we reveal their potential as quantum simulators for molecular physics and propose a technique to image the three-dimensional molecular orbitals with high resolution. The outstanding tunability of ultracold atoms in terms of potential and interaction offer fully adjustable model systems for gaining deep insight into the electronic structure of molecules. We study the orbitals of an artificial benzene molecule and discuss the effect of tunable interactions in its conjugated $\pi$ electron system with special regard to localization and spin order. The dynamical time scales of ultracold atom simulators are on the order of milliseconds, which allows for the time-resolved monitoring of a broad range of dynamical processes. As an example, we compute the hole dynamics in the conjugated $\pi$ system of the artificial benzene molecule.

Strong interactions can amplify quantum effects such that they become important on macroscopic scales. Controlling these coherently on a single-particle level is essential for the tailored preparation of strongly correlated quantum systems and opens up new prospects for quantum technologies. Rydberg atoms offer such strong interactions, which lead to extreme nonlinearities in laser-coupled atomic ensembles. As a result, multiple excitation of a micrometer-sized cloud can be blocked while the light-matter coupling becomes collectively enhanced. The resulting two-level system, often called a “superatom,” is a valuable resource for quantum information, providing a collective qubit. Here, we report on the preparation of 2 orders of magnitude scalable superatoms utilizing the large interaction strength provided by Rydberg atoms combined with precise control of an ensemble of ultracold atoms in an optical lattice. The latter is achieved with sub-shot-noise precision by local manipulation of a two-dimensional Mott insulator. We microscopically confirm the superatom picture by in situ detection of the Rydberg excitations and observe the characteristic square-root scaling of the optical coupling with the number of atoms. Enabled by the full control over the atomic sample, including the motional degrees of freedom, we infer the overlap of the produced many-body state with a $W$ state from the observed Rabi oscillations and deduce the presence of entanglement. Finally, we investigate the breakdown of the superatom picture when two Rydberg excitations are present in the system, which leads to dephasing and a loss of coherence.

For quantitative understanding of probabilistic behaviors of living cells, it is essential to construct a correct mathematical description of intracellular networks interacting with complex cell environments, which has been a formidable task. Here, we present a novel model and stochastic kinetics for an intracellular network interacting with hidden cell environments, employing a complete description of cell state dynamics and its coupling to the system network. Our analysis reveals that various environmental effects on the product number fluctuation of intracellular reaction networks can be collectively characterized by Laplace transform of the time-correlation function of the product creation rate fluctuation with the Laplace variable being the product decay rate. On the basis of the latter result, we propose an efficient method for quantitative analysis of the chemical fluctuation produced by intracellular networks coupled to hidden cell environments. By applying the present approach to the gene expression network, we obtain simple analytic results for the gene expression variability and the environment-induced correlations between the expression levels of mutually noninteracting genes. The theoretical results compose a unified framework for quantitative understanding of various gene expression statistics observed across a number of different systems with a small number of adjustable parameters with clear physical meanings.

Weyl semimetals are a class of materials that can be regarded as three-dimensional analogs of graphene upon breaking time-reversal or inversion symmetry. Electrons in a Weyl semimetal behave as Weyl fermions, which have many exotic properties, such as chiral anomaly and magnetic monopoles in the crystal momentum space. The surface state of a Weyl semimetal displays pairs of entangled Fermi arcs at two opposite surfaces. However, the existence of Weyl semimetals has not yet been proved experimentally. Here, we report the experimental realization of a Weyl semimetal in TaAs by observing Fermi arcs formed by its surface states using angle-resolved photoemission spectroscopy. Our first-principles calculations, which match remarkably well with the experimental results, further confirm that TaAs is a Weyl semimetal.

A high-repetition rate electron source is generated by tightly focusing kHz, few-mJ laser pulses into an underdense plasma. This high-intensity laser-plasma interaction leads to stable electron beams over several hours but with strikingly complex transverse distributions even for good quality laser focal spots. We find that the electron beam distribution is sensitive to the laser wave front via the laser midfield distribution rather than the laser focal spot itself. We are able to measure the laser wave front around the focus and include it in realistic particle-in-cell simulations demonstrating the role of the laser wave front on the acceleration of electrons. Distortions of the laser wave front cause spatial inhomogeneities in the midfield laser intensity and, consequently, the laser pulse drives an inhomogeneous transverse wakefield whose focusing and defocusing properties affect the electron distribution. These findings explain the experimental results and suggest the possibility of controlling the electron spatial distribution in laser-plasma accelerators by tailoring the laser wave front.

Topological states of matter are particularly robust, since they exploit global features of a material’s band structure. Topological states have already been observed for electrons, atoms, and photons. It is an outstanding challenge to create a Chern insulator of sound waves in the solid state. In this work, we propose an implementation based on cavity optomechanics in a photonic crystal. The topological properties of the sound waves can be wholly tuned in situ by adjusting the amplitude and frequency of a driving laser that controls the optomechanical interaction between light and sound. The resulting chiral, topologically protected phonon transport can be probed completely optically. Moreover, we identify a regime of strong mixing between photon and phonon excitations, which gives rise to a large set of different topological phases and offers an example of a Chern insulator produced from the interaction between two physically distinct particle species, photons and phonons.

Under ideal conditions, quantum metrology promises a precision gain over classical techniques scaling quadratically with the number of probe particles. At the same time, no-go results have shown that generic, uncorrelated noise limits the quantum advantage to a constant factor. In frequency estimation scenarios, however, there are exceptions to this rule and, in particular, it has been found that transversal dephasing does allow for a scaling quantum advantage. Yet, it has remained unclear whether such exemptions can be exploited in practical scenarios. Here, we argue that the transversal-noise model applies to the setting of recent magnetometry experiments and show that a scaling advantage can be maintained with one-axis-twisted spin-squeezed states and Ramsey-interferometry-like measurements. This is achieved by exploiting the geometry of the setup that, as we demonstrate, has a strong influence on the achievable quantum enhancement for experimentally feasible parameter settings. When, in addition to the dominant transversal noise, other sources of decoherence are present, the quantum advantage is asymptotically bounded by a constant, but this constant may be significantly improved by exploring the geometry.

We demonstrate a photonic circuit with integrated long-lived quantum memories. Precharacterized quantum nodes—diamond microwaveguides containing single, stable, negatively charged nitrogen-vacancy centers—are deterministically integrated into low-loss silicon nitride waveguides. These quantum nodes efficiently couple into the single-mode waveguides with $>1\mathrm{Mcps}$ collected into the waveguide, have narrow single-scan linewidths below 400 MHz, and exhibit long electron spin coherence times up to $120\mu \mathrm{s}$. Our system facilitates the assembly of multiple quantum nodes with preselected properties into a photonic integrated circuit with near unity yield, paving the way towards the scalable fabrication of quantum information processors.

Spontaneous breaking of translational symmetry, known as density-wave order, is common in nature. However, such states are strongly sensitive to impurities or other forms of frozen disorder leading to fascinating glassy phenomena. We analyze impurity effects on a particularly ubiquitous form of broken translation symmetry in solids: a spin-density wave (SDW) with spatially modulated magnetic order. Related phenomena occur in pair-density-wave (PDW) superconductors where the superconducting order is spatially modulated. For weak disorder, we find that the SDW or PDW order can generically give way to a SDW or PDW glass—new phases of matter with a number of striking properties, which we introduce and characterize here. In particular, they exhibit an interesting combination of conventional (symmetry-breaking) and spin-glass (Edwards-Anderson) order. This is reflected in the dynamic response of such a system, which—as expected for a glass—is extremely slow in certain variables, but, surprisingly, is fast in others. Our results apply to all uniaxial metallic SDW systems where the ordering vector is incommensurate with the crystalline lattice. In addition, the possibility of a PDW glass has important consequences for some recent theoretical and experimental work on ${\text{La}}_{2-x}{\text{Ba}}_x{\text{Cu}}_2{\mathrm{O}}_4$.

We investigate the influence of exciton-phonon coupling on the dynamics of a strongly coupled quantum dot-photonic crystal cavity system and explore the effects of this interaction on different schemes for nonclassical light generation. By performing time-resolved measurements, we map out the detuning-dependent polariton lifetime and extract the spectrum of the polariton-to-phonon coupling with unprecedented precision. Photon-blockade experiments for different pulse-length and detuning conditions (supported by quantum optical simulations) reveal that achieving high-fidelity photon blockade requires an intricate understanding of the phonons’ influence on the system dynamics. Finally, we achieve direct coherent control of the polariton states of a strongly coupled system and demonstrate that their efficient coupling to phonons can be exploited for novel concepts in high-fidelity single-photon generation.

The fidelity susceptibility is a general purpose probe of phase transitions. With its origin in quantum information and in the differential geometry perspective of quantum states, the fidelity susceptibility can indicate the presence of a phase transition without prior knowledge of the local order parameter, as well as reveal the universal properties of a critical point. The wide applicability of the fidelity susceptibility to quantum many-body systems is, however, hindered by the limited computational tools to evaluate it. We present a generic, efficient, and elegant approach to compute the fidelity susceptibility of correlated fermions, bosons, and quantum spin systems in a broad range of quantum Monte Carlo methods. It can be applied to both the ground-state and nonzero-temperature cases. The Monte Carlo estimator has a simple yet universal form, which can be efficiently evaluated in simulations. We demonstrate the power of this approach with applications to the Bose-Hubbard model, the spin-$1/2$ $XXZ$ model, and use it to examine the hypothetical intermediate spin-liquid phase in the Hubbard model on the honeycomb lattice.

Energy of propagating electromagnetic waves can be fully absorbed in a thin lossy layer, but only in a narrow frequency band, as follows from the causality principle. On the other hand, it appears that there are no fundamental limitations on broadband matching of thin resonant absorbing layers. However, known thin absorbers produce significant reflections outside of the resonant absorption band. In this paper, we explore possibilities to realize a thin absorbing layer that produces no reflected waves in a very wide frequency range, while the transmission coefficient has a narrow peak of full absorption. Here we show, both theoretically and experimentally, that a thin resonant absorber, invisible in reflection in a very wide frequency range, can be realized if one and the same resonant mode of the absorbing array unit cells is utilized to create both electric and magnetic responses. We test this concept using chiral particles in each unit cell, arranged in a periodic planar racemic array, utilizing chirality coupling in each unit cell but compensating the field coupling at the macroscopic level. We prove that the concept and the proposed realization approach also can be used to create nonreflecting layers for full control of transmitted fields. Our results can have a broad range of potential applications over the entire electromagnetic spectrum including, for example, perfect ultracompact wave filters and selective multifrequency sensors.

Quantum states of light can improve imaging whenever the image quality and resolution are limited by the quantum noise of the illumination. In the case of a bright illumination, quantum enhancement is obtained for a light field composed of many squeezed transverse modes. A possible realization of such a multi-spatial-mode squeezed state is a field which contains a transverse plane in which the local electric field displays reduced quantum fluctuations at all locations, on any one quadrature. Using a traveling-wave amplifier, we have generated a multi-spatial-mode squeezed state and showed that it exhibits localized quadrature squeezing at any point of its transverse profile, in regions much smaller than its size. We observe 75 independently squeezed regions. The amplification relies on nondegenerate four-wave mixing in a hot vapor and produces a bichromatic squeezed state. The result confirms the potential of this technique for producing illumination suitable for practical quantum imaging.

The problem of low Reynolds number turbulence in active nematic fluids is theoretically addressed. Using numerical simulations, I demonstrate that an incompressible turbulent flow, in two-dimensional active nematics, consists of an ensemble of vortices whose areas are exponentially distributed within a range of scales. Building on this evidence, I construct a mean-field theory of active turbulence by which several measurable quantities, including the spectral densities and the correlation functions, can be analytically calculated. Because of the profound connection between the flow geometry and the topological properties of the nematic director, the theory sheds light on the mechanisms leading to the proliferation of topological defects in active nematics and provides a number of testable predictions. A hypothesis, inspired by Onsager’s statistical hydrodynamics, is finally introduced to account for the equilibrium probability distribution of the vortex sizes.

We observe a spontaneous parity breaking bifurcation to a ferromagnetic state in a spatially trapped exciton-polariton condensate. At a critical bifurcation density under nonresonant excitation, the whole condensate spontaneously magnetizes and randomly adopts one of two elliptically polarized (up to 95% circularly polarized) states with opposite handedness of polarization. The magnetized condensate remains stable for many seconds at 5 K, but at higher temperatures, it can flip from one magnetic orientation to another. We optically address these states and demonstrate the inversion of the magnetic state by resonantly injecting 100-fold weaker pulses of opposite spin. Theoretically, these phenomena can be well described as spontaneous symmetry breaking of the spin degree of freedom induced by different loss rates of the linear polarizations.