Unidirectional amplification with acoustic non-Hermitian space−time varying metamaterial

Space−time modulated metamaterials support extraordinary rich applications, such as parametric amplification, frequency conversion, and non-reciprocal transmission. The non-Hermitian space−time varying systems combining non-Hermiticity and space−time varying capability, have been proposed to realize wave control like unidirectional amplification, while its experimental realization still remains a challenge. Here, based on metamaterials with software-defined impulse responses, we experimentally demonstrate non-Hermitian space−time varying metamaterials in which the material gain and loss can be dynamically controlled and balanced in the time domain instead of spatial domain, allowing us to suppress scattering at the incident frequency and to increase the efficiency of frequency conversion at the same time. An additional modulation phase delay between different meta-atoms results in unidirectional amplification in frequency conversion. The realization of non-Hermitian space−time varying metamaterials will offer further opportunities in studying non-Hermitian topological physics in dynamic and nonreciprocal systems.

Prediction of heptagonal bipyramidal nonacoordination in highly viable [OB-M©B7O7-BO]− (M = Fe, Ru, Os) complexes

Non-spherical distributions of ligand atoms in coordination complexes are generally unfavorable due to higher repulsion than for spherical distributions. To the best of our knowledge, non-spherical heptagonal bipyramidal nonacoordination is hitherto unreported, because of extremely high repulsion among seven equatorial ligand atoms. Herein, we report the computational prediction of such nonacoordination, which is constructed by the synergetic coordination of an equatorial hepta-dentate centripetal ligand (B7O7) and two axial mono-dentate ligands (-BO) in the gear-like mono-anionic complexes [OB-M©B7O7-BO]– (M = Fe, Ru, Os). The high repulsion among seven equatorial ligand B atoms has been compensated by the strong B–O bonding. These complexes are the dynamically stable (up to 1500 K) global energy minima with the HOMO-LUMO gaps of 7.15 to 7.42 eV and first vertical detachment energies of 6.14 to 6.66 eV (being very high for anions), suggesting their high probability for experimental realization in both gas-phase and condensed phases. The high stability stems geometrically from the surrounded outer-shell oxygen atoms and electronically from meeting the 18e rule as well as possessing the σ + π + δ triple aromaticity. Remarkably, the ligand-metal interactions are governed not by the familiar donation and backdonation interactions, but by the electrostatic interactions and electron-sharing bonding.

Atom-optically synthetic gauge fields for a noninteracting Bose gas

Synthetic gauge fields in synthetic dimensions are now of great interest. This concept provides a convenient manner for exploring topological phases of matter. Here, we report on the first experimental realization of an atom-optically synthetic gauge field based on the synthetic momentum-state lattice of a Bose gas of 133Cs atoms, where magnetically controlled Feshbach resonance is used to tune the interacting lattice into noninteracting regime. Specifically, we engineer a noninteracting one-dimensional lattice into a two-leg ladder with tunable synthetic gauge fields. We observe the flux-dependent populations of atoms and measure the gauge field-induced chiral currents in the two legs. We also show that an inhomogeneous gauge field could control the atomic transport in the ladder. Our results lay the groundwork for using a clean noninteracting synthetic momentum-state lattice to study the gauge field-induced topological physics.

Physical realization of complex dynamical pattern formation in magnetic active feedback rings

We report the clean experimental realization of cubic-quintic complex Ginzburg-Landau physics in a single driven, damped system. Four numerically predicted categories of complex dynamical behavior and pattern formation are identified for bright and dark solitary waves propagating around an active magnetic thin film-based feedback ring: (1) periodic breathing; (2) complex recurrence; (3) spontaneous spatial shifting; and (4) intermittency. These nontransient, long lifetime behaviors are observed in self-generated microwave spin wave envelopes circulating within a dispersive, nonlinear yttrium iron garnet waveguide. The waveguide is operated in a ring geometry in which the net losses are directly compensated for via linear amplification on each round trip (of the order of 100~ns). These behaviors exhibit periods ranging from tens to thousands of round trip times (of the order of $\mu$s) and are stable for 1000s of periods (of the order of~ms). We present 10 observations of these dynamical behaviors which span the experimentally accessible ranges of attractive cubic nonlinearity, dispersion, and external field strength that support the self-generation of backward volume spin waves in a four-wave-mixing dominant regime. Three-wave splitting is not explicitly forbidden and is treated as an additional source of nonlinear losses. All observed behaviors are robust over wide parameter regimes, making them promising for technological applications. We present ten experimental observations which span all categories of dynamical behavior previously theoretically predicted to be observable. This represents a complete experimental verification of the cubic-quintic complex Ginzburg-Landau equation as a model for the study of fundamental, complex nonlinear dynamics for driven, damped waves evolving in nonlinear, dispersive systems. The reported dynamical pattern formation of self-generated dark solitary waves in attractive nonlinearity without external sources or potentials, however, is entirely novel and is presented for both the periodic breather and complex recurrence behaviors.

Twist-angle two-dimensional superlattices and their application in (opto)electronics

Twist-angle two-dimensional systems, such as twisted bilayer graphene, twisted bilayer transition metal dichalcogenides, twisted bilayer phosphorene and their multilayer van der Waals heterostructures, exhibit novel and tunable properties due to the formation of Moiré superlattice and modulated Moiré bands. The review presents a brief venation on the development of “twistronics” and subsequent applications based on band engineering by twisting. Theoretical predictions followed by experimental realization of magic-angle bilayer graphene ignited the flame of investigation on the new freedom degree, twist-angle, to adjust (opto)electrical behaviors. Then, the merging of Dirac cones and the presence of flat bands gave rise to enhanced light-matter interaction and gate-dependent electrical phases, respectively, leading to applications in photodetectors and superconductor electronic devices. At the same time, the increasing amount of theoretical simulation on extended twisted 2D materials like TMDs and BPs called for further experimental verification. Finally, recently discovered properties in twisted bilayer h-BN evidenced h-BN could be an ideal candidate for dielectric and ferroelectric devices. Hence, both the predictions and confirmed properties imply twist-angle two-dimensional superlattice is a group of promising candidates for next-generation (opto)electronics.

Exact Solutions for Solitary Waves in a Bose-Einstein Condensate under the Action of a Four-Color Optical Lattice

We address dynamics of Bose-Einstein condensates (BECs) loaded into a one-dimensional four-color optical lattice (FOL) potential with commensurate wavelengths and tunable intensities. This configuration lends system-specific symmetry properties. The analysis identifies specific multi-parameter forms of the FOL potential which admits exact solitary-wave solutions. This newly found class of potentials includes more particular species, such as frustrated double-well superlattices, and bichromatic and three-color lattices, which are subject to respective symmetry constraints. Our exact solutions provide options for controllable positioning of density maxima of the localized patterns, and tunable Anderson-like localization in the frustrated potential. A numerical analysis is performed to establish dynamical stability and structural stability of the obtained solutions, which makes them relevant for experimental realization. The newly found solutions offer applications to the design of schemes for quantum simulations and processing quantum information.

Experimental realization of linearly polarized X-ray detected ferromagnetic resonance

We present the first theoretical and experimental evidence of time-resolved dynamic X-ray magnetic linear dichroism (XMLD) measurements of GHz magnetic precessions driven by ferromagnetic resonance in both metallic and insulating thin films. Our findings show a dynamic XMLD in both ferromagnetic Ni80Fe20 and ferrimagnetic Ni0.65Zn0.35Al0.8Fe1.2O4 for different measurement geometries and linear polarizations. A detailed analysis of the observed signals reveals the importance of separating different harmonic components in the dynamic signal in order to identify the XMLD response without the influence of competing contributions. In particular, RF magnetic resonance elicits a large dynamic XMLD response at the fundamental frequency under experimental geometries with oblique x-ray polarization. The geometric range and experimental sensitivity can be improved by isolating the 2ω Fourier component of the dynamic response.These results illustrate the potential of dynamic XMLD and represent a milestone accomplishment towards the study of GHz spin dynamics in systems beyond ferromagnetic order.

Defined core–shell particles as the key to complex interfacial self-assembly

The two-dimensional self-assembly of colloidal particles serves as a model system for fundamental studies of structure formation and as a powerful tool to fabricate functional materials and surfaces. However, the prevalence of hexagonal symmetries in such self-assembling systems limits its structural versatility. More than two decades ago, Jagla demonstrated that core–shell particles with two interaction length scales can form complex, nonhexagonal minimum energy configurations. Based on such Jagla potentials, a wide variety of phases including cluster lattices, chains, and quasicrystals have been theoretically discovered. Despite the elegance of this approach, its experimental realization has remained largely elusive. Here, we capitalize on the distinct interfacial morphology of soft particles to design two-dimensional assemblies with structural complexity. We find that core–shell particles consisting of a silica core surface functionalized with a noncrosslinked polymer shell efficiently spread at a liquid interface to form a two-dimensional polymer corona surrounding the core. We controllably grow such shells by iniferter-type controlled radical polymerization. Upon interfacial compression, the resulting core–shell particles arrange in well-defined dimer, trimer, and tetramer lattices before transitioning into complex chain and cluster phases. The experimental phase behavior is accurately reproduced by Monte Carlo simulations and minimum energy calculations, suggesting that the interfacial assembly interacts via a pairwise-additive Jagla-type potential. By comparing theory, simulation, and experiment, we narrow the Jagla g-parameter of the system to between 0.9 and 2. The possibility to control the interaction potential via the interfacial morphology provides a framework to realize structural features with unprecedented complexity from a simple, one-component system.