No Arabic abstract
We investigate the possibility of trapping quasi-particles possessing spin degree of freedom in hybrid structures. The hybrid system we are considering here is composed of a semi-magnetic quantum well placed a few nanometers below a ferromagnetic micromagnet. We are interested in two different micromagnet shapes: cylindrical (micro-disk) and rectangular geometry. We show that in the case of a micro-disk, the spin object is localized in all three directions and therefore zero-dimensional states are created, and in the case of an elongated rectangular micromagnet, the quasi-particles can move freely in one direction, hence one-dimensional states are formed. After calculating profiles of the magnetic field produced by the micromagnets, we analyze in detail the possible light absorption spectrum for different micromagnet thicknesses, and different distances between the micromagnet and the semimagnetic quantum well. We find that the discrete spectrum of the localized states can be detected via spatially-resolved low temperature optical measurement.
The length scale separation in dilute quantum gases in quasi-one- or quasi-two-dimensional traps has spatially divided the system into two different regimes. Whereas universal relations defined in strictly one or two dimensions apply in a scale that is much larger than the characteristic length of the transverse confinements, physical observables in the short distances are inevitably governed by three-dimensional contacts. Here, we show that $p$-wave contacts defined in different length scales are intrinsically connected by a universal relation, which depends on a simple geometric factor of the transverse confinements. While this universal relation is derived for one of the $p$-wave contacts, it establishes a concrete example of how dimensional crossover interplays with contacts and universal relations for arbitrary partial wave scatterings.
Strongly interacting particles in one dimension subject to external confinement have become a topic of considerable interest due to recent experimental advances and the development of new theoretical methods to attack such systems. In the case of equal mass fermions or bosons with two or more internal degrees of freedom, one can map the problem onto the well-known Heisenberg spin models. However, many interesting physical systems contain mixtures of particles with different masses. Therefore, a generalization of the recent strong-coupling techniques would be highly desirable. This is particularly important since such problems are generally considered non-integrable and thus the hugely successful Bethe ansatz approach cannot be applied. Here we discuss some initial steps towards this goal by investigating small ensembles of one-dimensional harmonically trapped particles where pairwise interactions are either vanishing or infinitely strong with focus on the mass-imbalanced case. We discuss a (semi)-analytical approach to describe systems using hyperspherical coordinates where the interaction is effectively decoupled from the trapping potential. As an illustrative example we analyze mass-imbalanced four-particle two-species mixtures with strong interactions between the two species. For such systems we calculate the energies, densities and pair-correlation functions.
A series of oxytetrahalides WO$X_4$ ($X$: a halogen element) that form quasi-one-dimensional chains is investigated using first-principles calculations. The crystal structures, electronic structures, as well as ferroelectric and piezoelectric properties are discussed in detail. Group theory analysis shows that the ferroelectricity in this family originates from an unstable polar phonon mode $Gamma_1^-$ induced by the Ws $d^0$ orbital configuration. Their polarization magnitudes are found to be comparable to widely used ferroelectric perovskites. Because of its quasi-one-dimensional characteristics, the inter-chain domain wall energy density is low, leading to loosely-coupled ferroelectric chains. This is potentially beneficial for high density ferroelectric memories: we estimate that the upper-limit of memory density in these compounds could reach hundreds of terabytes per square inch.
The formation of a Ag stabilized regular step lattice on vicinal Si(111) miscut towards [11-2] is reported. The step bunching characteristic of the clean surface is prevented by a single-domain Si(111)-(3x1)-Ag reconstruction. The nanostructured surface is used as a template for growing one-dimensional arrays of 1 nm sized Ag quantum dots with a preferential spacing of 1.5 nm along the rows.
Anisotropic photonic materials with linear dichroism are crucial components in many sensing, imaging and communication applications. Such materials play an important role as polarizers, filters and wave-plates in photonic devices and circuits. Conventional crystalline materials with optical anisotropy typically show unidirectional linear dichroism over a broad wavelength range. The linear dichroism conversion phenomenon has not been observed in crystalline materials. Here, we report the investigation of the unique linear dichroism conversion phenomenon in quasi-one-dimensional (quasi-1D) hexagonal perovskite chalcogenide BaTiS3. The material shows record level of optical anisotropy within the visible wavelength range. In contrast to conventional anisotropic optical materials, the linear dichroism polarity in BaTiS3 makes an orthogonal change at an optical wavelength corresponding to the photon energy of 1.78 eV. First principle calculations reveal that this anomalous linear dichroism conversion behavior originates from different selection rules of the optical transitions from the parallel bands in the BaTiS3 material. Wavelength dependent polarized Raman spectroscopy further confirms this phenomenon. Such material with linear dichroism conversion property can facilitate new ability to control and sense the energy and polarization of light, and lead to novel photonic devices such as polarization-wavelength selective detectors and lasers for multispectral imaging, sensing and optical communication applications.