arXiv subjects

A. G. Volosniev

Publications and source records attributed to A. G. Volosniev.

43 records · Page 3Linked to original sources

arXiv2013

Bound states of Dipolar Bosons in One-dimensional Systems

We consider one-dimensional tubes containing bosonic polar molecules. The long-range dipole-dipole interactions act both within a single tube and between different tubes. We consider arbitrary values of the externally aligned dipole moments with respect to the symmetry axis of the tubes. The few-body structures in this geometry are determined as function of polarization angles and dipole strength by using both essentially exact stochastic variational methods and the harmonic approximation. The main focus is on the three, four, and five-body problems in two or more tubes. Our results indicate that in the weakly-coupled limit the inter-tube interaction is similar to a zero-range term with a suitable rescaled strength. This allows us to address the corresponding many-body physics of the system by constructing a model where bound chains with one molecule in each tube are the effective degrees of freedom. This model can be mapped onto one-dimensional Hamiltonians for which exact solutions are known.

cond-mat.quant-gas↗

arXiv2012

Field-induced long-lived supermolecules

We demonstrate that the long-lived bound states (super-molecules) can exist in the dilute limit when we tune the shape of effective potential between polar molecules by an external microwave field. Binding energies, average sizes, and phase diagrams for both s-orbital (bosons) and p-orbital (fermions) dimers are studied, together with bosonic trimer states. We explicitly show that the non- adiabatic transition rate can be easily tuned small for such ground state super-molecules, so that the system can be stable from collapse even near the associated potential resonance. Our results, therefore, suggest a feasible cold molecule system to investigate both novel few-body and many-body physics (for example, the p-wave BCS-BEC crossover for fermions and the paired condensate for bosons) that can not be easily accessed in single species atomic gases.

cond-mat.quant-gas↗

arXiv2012

Bound Chains of Tilted Dipoles in Layered Systems

Ultracold polar molecules in multilayered systems have been experimentally realized very recently. While experiments study these systems almost exclusively through their chemical reactivity, the outlook for creating and manipulating exotic few- and many-body physics in dipolar systems is fascinating. Here we concentrate on few-body states in a multilayered setup. We exploit the geometry of the interlayer potential to calculate the two- and three-body chains with one molecule in each layer. The focus is on dipoles that are aligned at some angle with respect to the layer planes by means of an external eletric field. The binding energy and the spatial structure of the bound states are studied in several different ways using analytical approaches. The results are compared to stochastic variational calculations and very good agreement is found. We conclude that approximations based on harmonic oscillator potentials are accurate even for tilted dipoles when the geometry of the potential landscape is taken into account.

quant-ph↗

arXiv2012

Few-body bound state stability of dipolar molecules in two dimensions

Bound structures among dipolar molecules in multilayers are a topic of great interest in the light of recent experiments that have demonstrated the feasibility of the setup. While it is known that two molecules in two adjacent layers will always bind, larger complexes have only been scarcely addressed thus far. Here we prove rigorously that three- and four-body states will never be bound when the dipoles are oriented perpendicular to the layers. The technique employed is general and can be used for more molecules/layers and other geometries. Our analytical findings are supported by numerical calculations for both fermionic and bosonic molecules. Furthermore, we calculate the reduction in intralayer repulsion necessary to bind large complexes and estimate the influence of bound complexes in systems with many layers.

cond-mat.quant-gas↗

arXiv2012

Dimers, Effective Interactions, and Pauli Blocking Effects in a Bilayer of Cold Fermionic Polar Molecules

We consider a bilayer setup with two parallel planes of cold fermionic polar molecules when the dipole moments are oriented perpendicular to the planes. The binding energy of two-body states with one polar molecule in each layer is determined and compared to various analytic approximation schemes in both coordinate- and momentum-space. The effective interaction of two bound dimers is obtained by integrating out the internal dimer bound state wave function and its robustness under analytical approximations is studied. Furthermore, we consider the effect of the background of other fermions on the dimer state through Pauli blocking, and discuss implications for the zero-temperature many-body phase diagram of this experimentally realizable system.

cond-mat.quant-gas↗

arXiv2011

Bound Dimers in Bilayers of Cold Polar Molecules

The exploration of cold polar molecules in different geometries is a rapidly developing experimental and theoretical pursuit. Recently, the implementation of optical lattices has enabled confinement in stacks of planes, the number of which is also controllable. Here we consider the bound state structure of two polar molecules confined in two adjacent planes as function of the polarization angle of the dipole moment of the molecules. We prove analytically and present numerical evidence for the existence of bound states for arbitrary dipole moments and polarization directions in this two-dimensional geometry. The spatial structure of the bound states is dominated by two-dimensional s- and p-waves, where the latter exceeds 40 percent over a large range of polarization angles for intermediate or strong dipole strength. Finally, we consider the influence of the dimer bound states on the potential many-body ground-state of the system.

cond-mat.quant-gas↗

arXiv2011

Model independence in two dimensions and polarized cold dipolar molecules

We calculate the energy and wave functions of two particles confined to two spatial dimensions interacting via arbitrary anisotropic potentials with negative or zero net volume. The general rigorous analytic expressions are given in the weak coupling limit where universality or model independence are approached. The monopole part of anisotropic potentials is crucial in the universal limit. We illustrate the universality with a system of two arbitrarily polarized cold dipolar molecules in a bilayer. We discuss the transition to universality as function of polarization and binding energy, and compare analytic and numerical results obtained by the stochastic variational method. The universal limit is essentially reached for experimentally accessible strengths.

quant-ph↗