We propose a thermodynamic refrigeration cycle which uses indefinite causal orders to achieve nonclassical cooling. The cycle cools a cold reservoir while consuming purity in a control qubit. We first show that the application to an input state of two identical thermalizing channels of temperature $T$ in an indefinite causal order can result in an output state with a temperature not equal to $T$. We investigate the properties of the refrigeration cycle and show that thermodynamically, the result is compatible with unitary quantum mechanics in the circuit model but could not be achieved classically. We believe that this cycle could be implemented experimentally using tabletop photonics. Our result suggests the development of a new class of thermodynamic resource theories in which operations are allowed to be performed in an indefinite causal order.

Lateral optical forces in a direction perpendicular to light propagation have attracted increasing interest in recent years. Up to now, all lateral forces can be attributed to the symmetry breaking in the lateral directions caused by either the morphology of the scatterer geometry or the optical fields impinging on the scatterer. Here we demonstrate, both numerically and analytically, that when an isotropic scatterer breaks the electric-magnetic symmetry, a new type of anomalous lateral force can be induced along the direction of translational invariance where the illumination striking the scatterer has no propagation, field gradient, or spin density vortex (Belinfante’s spin momentum). Our analytical results are rigorous for an arbitrary size scatterer, ensuring the universality of our conclusion. Furthermore, the electric-magnetic symmetry-breaking-induced lateral force is comparable in magnitude to other components of the optical force and reversible in direction for different polarizations of the illuminating light, rendering it capable of practical optical manipulation as well as enriching the understanding of light-matter interaction.

We use computationally simple neutral pseudoatom (“average atom”) density functional theory (DFT) and standard DFT to elucidate liquid-liquid phase transitions (LPTs) in liquid silicon. An ionization-driven transition and three LPTs including the known LPT near $2.5\mathrm{g}/{\mathrm{cm}}^3$ are found. They are robust even to 1 eV. The pair distributions functions, pair potentials, electrical conductivities, and compressibilites are reported. The LPTs are elucidated within a Fermi liquid picture of electron scattering at the Fermi energy that complements the transient covalent bonding picture.

The charging of electrical double layers inside a cylindrical pore has applications to supercapacitors, batteries, desalination and biosensors. The charging dynamics in the limit of thin double layers, i.e., when the double layer thickness is much smaller than the pore radius, is commonly described using an effective RC transmission line circuit. Here, we perform direct numerical simulations (DNS) of the Poisson-Nernst-Planck equations to study the double layer charging for the scenario of overlapping double layers, i.e., when the double layer thickness is comparable to the pore radius. We develop an analytical model that accurately predicts the results of DNS. Also, we construct a modified effective circuit for the overlapping double layer limit, and find that the modified circuit is identical to the RC transmission line but with different values and physical interpretation of the capacitive and resistive elements. In particular, the effective surface potential is reduced, the capacitor represents a volumetric current source, and the charging timescale is weakly dependent on the ratio of the pore radius and the double layer thickness.

We study the structural dynamics of liquid water by time-resolved anisotropic x-ray scattering under the optical Kerr effect condition. In this way, we can separate the anisotropic scattering decay of 160 fs from the delayed temperature increase of $\sim 0.1\mathrm{K}$ occurring at 1 ps and quantify transient changes in the O-O pair distribution function. Polarizable molecular dynamics simulations reproduce well the experiment, indicating transient alignment of molecules along the electric field, which shortens the nearest-neighbor distances. In addition, analysis of the simulated water local structure provides evidence that two hypothesized fluctuating water configurations exhibit different polarizability.

We study the viscous properties of a system of weakly interacting spin-$\frac{1}{2}$ fermions in one dimension. Accounting for the effect of interactions on the quasiparticle energy spectrum, we obtain the bulk viscosity of this system at low temperatures. Our result is valid for frequencies that are small compared with the rate of fermion backscattering. For frequencies larger than this exponentially small rate, the excitations of the system become decoupled from the center of mass motion, and the fluid is described by two-fluid hydrodynamics. We calculate the three transport coefficients required to describe viscous dissipation in this regime.

A particle beam may undergo an anomalous spatial shift when it is reflected at an interface. The shift forms a vector field defined in the two-dimensional interface momentum space. We show that, although the shift vector at individual momentum is typically sensitive to the system details, its integral along a close loop, i.e., its circulation, could yield a robust quantized number under certain conditions of interest. Particularly, this is the case when the beam is incident from a trivial medium, then the quantized circulation of anomalous shift (CAS) directly manifests the topological character of the other medium. We demonstrate that the topological charge of a Weyl medium as well as the unconventional pair potentials of a superconductor can be captured and distinguished by CAS. Our work unveils a hidden quantized feature in a ubiquitous physical process, which may also offer a new approach for probing topological media.

van der Waals heterostructures of atomically thin layers with rotational misalignments, such as twisted bilayer graphene, feature interesting structural moiré superlattices. Because of the quantum coupling between the twisted atomic layers, light-matter interaction is inherently chiral; as such, they provide a promising platform for chiral plasmons in the extreme nanoscale. However, while the interlayer quantum coupling can be significant, its influence on chiral plasmons still remains elusive. Here we present the general solutions from full Maxwell equations of chiral plasmons in twisted atomic bilayers, with the consideration of interlayer quantum coupling. We find twisted atomic bilayers have a direct correspondence to the chiral metasurface, which simultaneously possesses chiral and magnetic surface conductivities, besides the common electric surface conductivity. In other words, the interlayer quantum coupling in twisted van der Waals heterostructures may facilitate the construction of various (e.g., bi-anisotropic) atomically-thin metasurfaces. Moreover, the chiral surface conductivity, determined by the interlayer quantum coupling, determines the existence of chiral plasmons and leads to a unique phase relationship (i.e., $\pm \mathit{\pi }/2$ phase difference) between their transverse-electric (TE) and transverse-magnetic (TM) wave components. Importantly, such a unique phase relationship for chiral plasmons can be exploited to construct the missing longitudinal spin of plasmons, besides the common transverse spin of plasmons.

We experimentally and numerically show that chirality can play a major role in the nonlinear optical response of soft birefringent materials, by studying the nonlinear propagation of laser beams in frustrated cholesteric liquid crystal samples. Such beams exhibit a periodic nonlinear response associated with a bouncing pattern for the optical fields, as well as a self-focusing effect enhanced by the chirality of the birefringent material. Our results open new possible designs of nonlinear optical devices with low power consumption and tunable interactions with localized topological solitons.

Maximally entangled bipartite unitary operators or gates find various applications from quantum information to many-body physics wherein they are building blocks of minimal models of quantum chaos. In the latter case, they are referred to as “dual unitaries.” Dual unitary operators that can create the maximum average entanglement when acting on product states have to satisfy additional constraints. These have been called “2-unitaries” and are examples of perfect tensors that can be used to construct absolutely maximally entangled states of four parties. Hitherto, no systematic method exists in any local dimension, which results in the formation of such special classes of unitary operators. We outline an iterative protocol, a nonlinear map on the space of unitary operators, that creates ensembles whose members are arbitrarily close to being dual unitaries. For qutrits and ququads we find that a slightly modified protocol yields a plethora of 2-unitaries.

Two lowest-energy odd-parity atomic levels of actinium, $7s^{2}7p{{}^{2}P}_{1/2}^o$, $7s^{2}7p{{}^{2}P}_{3/2}^o$, were observed via two-step resonant laser-ionization spectroscopy and their respective energies were measured to be 7477.36(4) and $12276.59(2){\mathrm{cm}}^{-1}$. The lifetimes of these states were determined as 668(11) and 255(7) ns, respectively. In addition, we observed the effect of the hyperfine structure on the line for the transition to ${{}^{2}P}_{3/2}^o$. These properties were calculated using a hybrid approach that combines configuration interaction and coupled-cluster methods, in good agreement with the experiment. The data are of relevance for understanding the complex atomic spectra of actinides and for developing efficient laser cooling and ionization schemes for actinium, with possible applications for high-purity medical-isotope production and future fundamental physics experiments.

Nitric oxide (NO) molecules initially traveling at $795\mathrm{m}/\mathrm{s}$ in pulsed supersonic beams have been photoexcited to long-lived hydrogenic Rydberg-Stark states, decelerated and electrostatically trapped in a cryogenically cooled, chip-based transmission-line Rydberg-Stark decelerator. The decelerated and trapped molecules were detected in situ by pulsed electric field ionization. The operation of the decelerator was validated by comparison of the experimental data with the results of numerical calculations of particle trajectories. Studies of the decay of the trapped molecules on timescales up to 1 ms provide new insights into the lifetimes of, and effects of blackbody radiation on, Rydberg states of NO.

Interaction of a strong laser pulse with matter transfers not only energy but also linear momentum of the photons. Recent experimental advances have made it possible to detect the small amount of linear momentum delivered to the photoelectrons in strong-field ionization of atoms. We present numerical simulations as well as an analytical description of the subcycle phase (or time) resolved momentum transfer to an atom accessible by an attoclock protocol. We show that the light-field-induced momentum transfer is remarkably sensitive to properties of the ultrashort laser pulse such as its carrier-envelope phase and ellipticity. Moreover, we show that the subcycle-resolved linear momentum transfer can provide novel insights into the interplay between nonadiabatic and nondipole effects in strong-field ionization. This work paves the way towards the investigation of the so-far unexplored time-resolved nondipole nonadiabatic tunneling dynamics.

We theoretically assess two mechanisms thought to be responsible for the enhanced performance observed in plasma discharges of the Wendelstein 7-X stellarator experiment fueled by pellet injection. The effects of the ambipolar radial electric field and the electron density peaking on the turbulent ion heat transport are separately evaluated using large-scale gyrokinetic simulations. The essential role of the stellarator magnetic geometry is demonstrated, by comparison with a tokamak.

We investigate the hypothesis of dynamic tetragonal domains occurring in cubic ${\mathrm{CH}}_3{\mathrm{NH}}_3{\mathrm{PbI}}_3$ using high-resolution neutron spectroscopy to study a fully deuterated single crystal. The $R$-point scattering above the 327.5 K cubic-tetragonal phase transition is always resolution limited in energy and therefore inconsistent with dynamic-domain predictions. This behavior is instead consistent with the central peak phenomenon observed in other perovskites. The scattering may originate from small, static, tetragonal-phase domains nucleating about crystal defects, and the temperature dependence demonstrates the transition is first order.

We achieve current-induced switching in collinear insulating antiferromagnetic $\mathrm{CoO}/\mathrm{Pt}$, with fourfold in-plane magnetic anisotropy. This is measured electrically by spin Hall magnetoresistance and confirmed by the magnetic field-induced spin-flop transition of the CoO layer. By applying current pulses and magnetic fields, we quantify the efficiency of the acting current-induced torques and estimate a current-field equivalence ratio of $4\times {10}^{-11}\mathrm{T}{\mathrm{A}}^{-1}{\mathrm{m}}^2$. The Néel vector final state $(\mathit{n}\perp \mathit{j})$ is in line with a thermomagnetoelastic switching mechanism for a negative magnetoelastic constant of the CoO.

We present a microscopic theory of the neutral collective modes supported by the non-Abelian fractional quantum Hall states at filling factor $5/2$. The theory is formulated in terms of the trial states describing the Girvin–MacDonald–Platzman mode and its fermionic counterpart. These modes are superpartners of each other in a concrete sense, which we elucidate.

Spectral properties of a quantum circuit are efficiently read out by monitoring the resonance frequency shift it induces in a microwave resonator coupled to it. When the two systems are strongly detuned, theory attributes the shift to an effective resonator capacitance or inductance that depends on the quantum circuit state. At small detuning, the shift arises from the exchange of virtual photons, as described by the Jaynes-Cummings model. Here we present a theory bridging these two limits and illustrate, with several examples, its necessity for a general description of quantum circuits readout.