We report an unconventional quantum spin Hall phase in the monolayer ${\text{WTe}}_2$, which exhibits hitherto unknown features in other topological materials. The low symmetry of the structure induces a canted spin texture in the $yz$ plane, which dictates the spin polarization of topologically protected boundary states. Additionally, the spin Hall conductivity gets quantized ($2e^2/h$) with a spin quantization axis parallel to the canting direction. These findings are based on large-scale quantum simulations of the spin Hall conductivity tensor and nonlocal resistances in multiprobe geometries using a realistic tight-binding model elaborated from first-principle methods. The observation of this canted quantum spin Hall effect, related to the formation of topological edge states with nontrivial spin polarization, demands for specific experimental design and suggests interesting alternatives for manipulating spin information in topological materials.

The interplay of interactions and disorder in two-dimensional (2D) electron systems has actively been studied for decades. The paradigmatic approach involves starting with a clean Fermi liquid and perturbing the system with both disorder and interactions. Instead, we start with a clean non-Fermi liquid near a 2D ferromagnetic quantum critical point and consider the effects of disorder. In contrast with the disordered Fermi liquid, we find that our model does not suffer from runaway flows to strong coupling and the system has a marginally stable fixed point with perfect conduction.

We introduce a method to design topological mechanical metamaterials that are not constrained by Newtonian dynamics. The unit cells in a mechanical lattice are subjected to active feedback forces that are processed through autonomous controllers preprogrammed to generate the desired local response in real time. As an example, we focus on the quantum Haldane model, which is a two-band system with nonreciprocal coupling terms, the implementation of which in mechanical systems requires violating Newton’s third law. We demonstrate that the required topological phase characterized by chiral edge modes can be achieved in an analogous mechanical system only with closed-loop control. We then show that our approach enables us to realize, a modified version of the Haldane model in a mechanical metamaterial. Here, the complex-valued couplings are polarized in a way that modes on opposite edges of a lattice propagate in the same direction, and are balanced by counterpropagating bulk modes. The proposed method is general and flexible, and could be used to realize arbitrary lattice parameters, such as nonlocal or nonlinear couplings, time-dependent potentials, non-Hermitian dynamics, and more, on a single platform.

Studies of energy flow in quantum systems complement the information provided by common conductance measurements. The quantum limit of heat flow in one-dimensional ballistic modes was predicted, and experimentally demonstrated, to have a universal value for bosons, fermions, and fractionally charged anyons. A fraction of this value is expected in non-Abelian states; harboring counterpropagating edge modes. In such exotic states, thermal-energy relaxation along the edge is expected, and can shed light on their topological nature. Here, we introduce a novel experimental setup that enables a direct observation of thermal-energy relaxation in chiral 1D edge modes in the quantum Hall effect. Edge modes, emanating from a heated reservoir, are partitioned by a quantum point contact (QPC) constriction, which is located at some distance along their path. The resulting low frequency noise, measured downstream, allows determination of the “effective temperature” of the edge mode at the location of the QPC. An expected, prominent energy relaxation was found in hole-conjugate states. However, relaxation was also observed in particlelike states, where heat is expected to be conserved. We developed a model, consisting of distance-dependent energy loss, which agrees with the observations; however, we cannot exclude energy redistribution mechanisms, which are not accompanied with energy loss.

We discuss plasmons of biased twisted bilayer graphene when the Fermi level lies inside the gap. The collective excitations are a network of chiral edge plasmons (CEP) entirely composed of excitations in the topological electronic edge states that appear at the AB-BA interfaces. The CEP form a hexagonal network with a unique energy scale ${\epsilon }_p=(e^2)/({\epsilon }_0\epsilon t_0)$ with $t_0$ the moiré lattice constant and $\epsilon$ the dielectric constant. From the dielectric matrix we obtain the plasmon spectra that has two main characteristics: (i) a diverging density of states at zero energy, and (ii) the presence of a plasmonic Dirac cone at $\hslash \omega \sim {\epsilon }_p/2$ with sound velocity $v_D=0.0075c$, which is formed by zigzag and armchair current oscillations. A network model reveals that the antisymmetry of the plasmon bands implies that CEP scatter at the hexagon vertices maximally in the deflected chiral outgoing directions, with a current ratio of $4/9$ into each of the deflected directions and $1/9$ into the forward one. We show that scanning near-field microscopy should be able to observe the predicted plasmonic Dirac cone and its broken symmetry phases.

Magnetic adsorbates on superconductors induce a Kondo resonance outside and Yu-Shiba-Rusinov (YSR) bound states inside the superconducting energy gap. When probed by scanning tunneling spectroscopy, the associated differential-conductance spectra frequently exhibit characteristic bias-voltage asymmetries. Here, we observe correlated variations of Kondo and YSR asymmetries across an Fe-porphyrin molecule adsorbed on Pb(111). We show that both asymmetries originate in interfering tunneling paths via a spin-carrying orbital and the highest occupied molecular orbital (HOMO). Strong evidence for this model comes from nodal planes of the HOMO, where tunneling reveals symmetric Kondo and YSR resonances. Our results establish an important mechanism for the asymmetries of Kondo and YSR line shapes.

The nonlinear optical response of an excitonic insulator coupled to lattice degrees of freedom is shown to depend in strong and characteristic ways on whether the insulating behavior originates primarily from electron-electron or electron-lattice interactions. Linear response optical signatures of the massive phase mode and the amplitude (Higgs) mode are identified. Upon nonlinear excitation resonant to the phase mode, a new in-gap mode at twice the phase mode frequency is induced, leading to a huge second harmonic response. Excitation of in-gap phonon modes leads to different and much smaller effects. A Landau-Ginzburg theory analysis explains these different behaviors and reveals that a parametric resonance of the strongly excited phase mode is the origin of the photoinduced mode in the electron-dominant case. The difference in the nonlinear optical response serves as a measure of the dominant mechanism of the ordered phase.

We develop a two stage renormalization group which connects the continuum Hamiltonian for twisted bilayer graphene at length scales shorter than the moire superlattice period to the Hamiltonian for the active narrow bands only which is valid at distances much longer than the moire period. In the first stage, the Coulomb interaction renormalizes the Fermi velocity and the interlayer tunnelings in such a way as to suppress the ratio of the same sublattice to opposite sublatice tunneling, hence approaching the so-called chiral limit. In the second stage, the interlayer tunneling is treated nonperturbatively. Via a progressive numerical elimination of remote bands the relative strength of the one-particle-like dispersion and the interactions within the active narrow band Hamiltonian is determined, thus quantifying the residual correlations and justifying the strong coupling approach in the final step. We also calculate exactly the exciton energy spectrum from the Coloumb interactions projected onto the renormalized narrow bands. The resulting softening of the collective modes marks the propinquity of the enlarged (“hidden”) $U(4)\times U(4)$ symmetry in the magic angle twisted bilayer graphene.

Hafnia (${\mathrm{HfO}}_2$)-based thin films have promising applications in nanoscale electronic devices due to their robust ferroelectricity and integration with silicon. Identifying and stabilizing the ferroelectric phases of ${\mathrm{HfO}}_2$ have attracted intensive research interest in recent years. In this work, first-principles calculations on (111)-oriented ${\mathrm{HfO}}_2$ are used to discover that imposing an in-plane shear strain on the metastable tetragonal phase drives it to a polar phase. This in-plane-shear-induced polar phase is shown to be an epitaxial-strain-induced distortion of a previously proposed metastable ferroelectric $Pnm{2}_1$ phase of ${\mathrm{HfO}}_2$. This ferroelectric $Pnm{2}_1$ phase can account for the recently observed ferroelectricity in (111)-oriented ${\mathrm{HfO}}_2$-based thin films on a ${\mathrm{SrTiO}}_3$ (STO) (001) substrate [Nat. Mater. 17, 1095 (2018)]. Further investigation of this alternative ferroelectric phase of ${\mathrm{HfO}}_2$ could potentially improve the performances of ${\mathrm{HfO}}_2$-based films in logic and memory devices.

We derive a general criterion for determining the onset of superradiant phase transition in electronic bands coupled to a cavity field, with possibly electron-electron interactions. For longitudinal superradiance in 2D or genuine 1D systems, we prove that it is always prevented, thereby extending existing no-go theorems. Instead, a superradiant phase transition can occur to a nonuniform transverse cavity field and we give specific examples in noninteracting models, either through Fermi surface nesting or parabolic band touching. Investigating the resulting time-reversal symmetry breaking superradiant states, we find in the former case Fermi surface lifting down to four Dirac points on a square lattice model, with topologically protected zero modes, and in the latter case topological bands with nonzero Chern number on an hexagonal lattice.

Spontaneous growth of long-wavelength deformations is a defining feature of active liquid crystals. We investigate the effect of confinement on the instability of 3D active liquid crystals in the isotropic phase composed of extensile microtubule bundles and kinesin molecular motors. When shear aligned, such fluids exhibit finite-wavelength self-amplifying bend deformations. By systematically changing the channel size we elucidate how the instability wavelength and its growth rate depend on the channel dimensions. Experimental findings are qualitatively consistent with a minimal hydrodynamic model, where the fastest growing deformation is set by a balance of active driving and elastic relaxation. Our results demonstrate that confinement determines the structure and dynamics of active fluids on all experimentally accessible length scales.

Recent experiments show a strong rotational diffusion enhancement for self-propelled microrheological probes in colloidal glasses. Here, we provide microscopic understanding using simulations with a frictional probe-medium coupling that converts active translation into rotation. Diffusive enhancement emerges from the medium’s disordered structure and peaks at a second-order transition in the number of contacts. Our results reproduce the salient features of the colloidal glass experiment and support an effective description that is applicable to a broader class of viscoelastic suspensions.

Many experiments over the past half century have shown that, for a range of protocols, granular materials compact under pressure and repeated small disturbances. A recent experiment on cyclically sheared spherical grains showed significant compaction via homogeneous crystallization (Rietz et al., 2018). Here we present numerical simulations of frictionless, purely repulsive spheres undergoing cyclic simple shear via Newtonian dynamics with linear viscous drag at fixed vertical load. We show that for sufficiently small strain amplitudes, cyclic shear gives rise to homogeneous crystallization at a volume fraction $\varphi =0.646\pm 0.001$. This result indicates that neither friction nor gravity is essential for homogeneous crystallization in driven granular media. Understanding how crystal formation is initiated within a homogeneous disordered state gives key insights into the old open problem of glass formation in fluids.

We use the swap Monte Carlo algorithm to analyze the glassy behavior of sticky spheres in equilibrium conditions at densities where conventional simulations and experiments fail to reach equilibrium, beyond predicted phase transitions and dynamic singularities. We demonstrate the existence of a unique ergodic region comprising all the distinct phases previously reported, except for a phase-separated region at strong adhesion. All structural and dynamic observables evolve gradually within this ergodic region, the physics evolving smoothly from well-known hard sphere glassy behavior at small adhesions and large densities, to a more complex glassy regime characterized by unusually broad distributions of relaxation timescales and length scales at large adhesions.

Spontaneous contractions of cardiomyocytes are driven by calcium oscillations due to the activity of ionic calcium channels and pumps. The beating phase is related to the time-dependent deviation of the oscillations from their average frequency, due to noise and the resulting cellular response. Here, we demonstrate experimentally that, in addition to the short-time (1–2 Hz), beat-to-beat variability, there are long-time correlations (tens of minutes) in the beating phase dynamics of isolated cardiomyocytes. Our theoretical model relates these long-time correlations to cellular regulation that restores the frequency to its average, homeostatic value in response to stochastic perturbations.

Demonstrating a quantum computational speed-up is a crucial milestone for near-term quantum technology. Recently, sampling protocols for quantum simulators have been proposed that have the potential to show such a quantum advantage, based on commonly made assumptions. The key challenge in the theoretical analysis of this scheme—as of other comparable schemes such as boson sampling—is to lessen the assumptions and close the theoretical loopholes, replacing them by rigorous arguments. In this work, we prove two open conjectures for a simple sampling protocol that is based on the continuous time evolution of a translation-invariant Ising Hamiltonian: anticoncentration of the generated probability distributions and average-case hardness of exactly evaluating those probabilities. The latter is proven building upon recently developed techniques for random circuit sampling. For the former, we exploit the insight that approximate 2-designs for the unitary group admit anticoncentration. We then develop new techniques to prove that the 2D time evolution of the protocol gives rise to approximate 2-designs. Our work provides the strongest theoretical evidence to date that Hamiltonian quantum simulators are classically intractable.

Though the celebrated spin echoes have been widely used to reverse quantum dynamics, they are not applicable to systems whose constituents are beyond the control of the $su(2)$ algebra. Here, we design echoes to reverse quantum dynamics of breathers in three-dimensional unitary fermions and two-dimensional bosons and fermions with contact interactions, which are governed by an underlying $su(1,1)$ algebra. Geometrically, $SU(1,1)$ echoes produce closed trajectories on a single or multiple Poincaré disks and thus could recover any initial states without changing the sign of the Hamiltonian. In particular, the initial shape of a breather determines the superposition of trajectories on multiple Poincaré disks and whether the revival time has period multiplication. Our work provides physicists with a recipe to tailor collective excitations of interacting many-body systems.

An analytical model for the potential between two rare gas atoms at distances between $R=0$ to $R\to \infty$ is assumed to be conformal with the previously published potential for ${\mathrm{He}}_2$ [J. Chem. Phys. 142, 131102 (2015)]. The potential curves of the rare gas dimers all have the same shape and only depend on the well parameters $D_e$ and $R_e$. The potentials and the vibrational levels for the 11 homonuclear and heteronuclear dimers for which recent ab initio calculations are available agree, within several percent, with the ab initio results. For the other rare gas dimers, the new potential provides the first realistic estimates for the potentials.