arXiv subjects

Stefan Scheel

Publications and source records attributed to Stefan Scheel.

At least 55 records · Page 3Linked to original sources

arXiv2018

Charge-Parity violating effects in Casimir-Polder potentials

We demonstrate under which conditions a violation of the charge-parity (CP) symmetry in molecules will manifest itself in the Casimir-Polder interaction of these with a magnetodielectric surface. Charge-parity violation induces a specific electric-magnetic cross-polarisability in a molecule that is not chiral, but time-reversal (T) symmetry violating. As we show, a detection of such an effect via the Casimir-Polder potential requires a material medium that is also sensitive to time-reversal, i.e., it must exhibit a non-reciprocal electromagnetic response. As simple examples of such media we consider a perfectly reflecting non-reciprocal mirror that is a special case of a perfect electromagnetic conductor as well as a Chern-Simons medium. In addition, we show that Chern-Simons and related media can induce unusual atom-surface interactions for anisotropic molecules with and without a chiral response.

quant-ph↗

arXiv2017

A Green's function approach to giant-dipole systems

In this work we perform a Green's function analysis of giant-dipole systems. First we derive the Green's functions of different magnetically field-dressed systems, in particular of electronically highly excited atomic species in crossed electric and magnetic fields, so-called giant-dipole states. We determine the dynamical polarizability of atomic giant-dipole states as well as the adiabatic potential energy surfaces of giant-dipole molecules in the framework of the Green's function approach. Furthermore, we perform an comparative analysis of the latter to and exact diagonalization scheme and show the general divergence behavior of the widely applied Fermi-pseudopotential approach. Finally, we derive the giant-dipole's regularized Green's function representation.

physics.atom-ph↗

arXiv2017

Van der Waals interaction potential between Rydberg atoms near surfaces

Van der Waals interactions, as a result of the exchange of photons between particles, can be altered by modifying the environment through which these photons propagate. As a consequence, phenomena such as the Rydberg blockade mechanism between highly excited atoms or excitons, can be controlled by adding reflecting surfaces. We provide the quantum electrodynamic framework for the van der Waals interaction in the nonretarded limit that is relevant for long-wavelength transitions such as those between Rydberg systems, and show its intimate connection with common static dipole-dipole interactions, thereby providing a generalization to include macroscopic bodies.

physics.atom-ph↗

arXiv2017

Angular-Momentum Couplings in Ultra-Long-Range Giant Dipole Molecules

In this article we extend the theory of ultra-long-range giant dipole molecules, formed by an atom in a giant dipole state and a ground-state alkali atom, by angular-momentum couplings known from recent works on Rydberg molecules. In addition to $s$-wave scattering, the next higher order of $p$-wave scattering in the Fermi-pseudopotential describing the binding mechanism is considered. Furthermore, the singlet and triplet channels of the scattering interaction as well as angular-momentum couplings such as hyperfine interaction and Zeeman interactions are included. Within the framework of Born--Oppenheimer theory, potential energy surfaces are calculated in both first-order perturbation theory and exact diagonalization. Besides the known pure triplet states, mixed-spin character states are obtained, opening up a whole new landscape of molecular potentials. We determine exact binding energies and wave functions of the nuclear rotational and vibrational motion numerically from the various potential energy surfaces.

physics.atom-ph↗

arXiv2017

Radiative heat transfer between spatially nonlocally responding dielectric objects

We calculate numerically the heat transfer rate between a spatially dispersive sphere and a half-space. By utilising Huygens' principle and the extinction theorem, we derive the necessary reflection coefficients at the sphere and the plate without the need to resort to additional boundary conditions. We find for small distances $d\sim 1$nm a significant modification of the spectral heat transfer rate due to spatial dispersion. As a consequence, the spurious divergencies that occur in spatially local approach are absent.

physics.optics↗

arXiv2017

Excitonic giant-dipole potentials in cuprous oxide

In this work we predict the existence of a novel species of Wannier excitons when exposed to crossed electric and magnetic fields. In particular, we present a theory of giant-dipole excitons in $\textrm{Cu}_2\rm O$ in crossed fields. Within our theoretical approach we perform a pseudoseparation of the center-of-mass motion for the field-dressed excitonic species, thereby obtaining an effective single-particle Hamiltonian for the relative motion. For arbitrary gauge fields we exactly separate the gauge-dependent kinetic energy terms from the effective single-particle interaction potential. Depending on the applied field strengths and the specific field orientation, the potential for the relative motion of electron and hole exhibits an outer well at spatial separations up to several micrometers and depths up to $380\, μ\rm eV$, leading to possible permanent excitonic electric dipole moments of around three million Debye.

cond-mat.mes-hall↗

arXiv2016

Deviations of the exciton level spectrum in cuprous oxide from the hydrogen series

Recent high-resolution absorption spectroscopy on excited excitons in cuprous oxide [Nature (London) 514, 343 (2014)] has revealed significant deviations of their spectrum from that of the ideal hydrogen-like series. Here we show that the complex band dispersion of the crystal, which determines the kinetic energy of electrons and holes, strongly affects the exciton binding energy. Specifically, we show that the nonparabolicity of the band dispersion is the main cause of the deviation from the hydrogen series. Experimental data collected from high-resolution absorption spectroscopy in electric fields validate the assignment of the deviation to the nonparabolicity of the band dispersion.

cond-mat.mes-hall↗

arXiv2015

Impact of anisotropy on the interaction of an atom with a one-dimensional nano-grating

We study the interaction of an atom with a one-dimensional nano-grating within the framework of macroscopic QED, with special emphasis on possible anisotropic contributions. To this end, we first derive the scattering Green's tensor of the grating by means of a Rayleigh expansion and discuss its symmetry properties and asymptotes. We then determine the Casimir--Polder potential of an atom with the grating. In particular, we find that strong anisotropy can lead to a repulsive Casimir--Polder potential in the normal direction.

quant-ph↗

arXiv2015

Casimir-Polder interaction from exact diagonalization and state mixing near surfaces

Dispersion forces have a sizeable effect on the energy levels of highly excited Rydberg atoms when brought close to material surfaces. Rydberg atoms experience energy shifts in the GHz range at micrometer distances, suggestive of considerable state admixture. We show that despite the non-applicability of perturbation theory for Rydberg atoms near a surface, the energy shift due to the dispersion interaction can be obtained from an exact diagonalization of the interaction Hamiltonian by finding the zeros of the Pick function. Moreover, we show that contrary to intuition from single-mode approaches, surface-induced state mixing is generally suppressed even for large interaction energies. We give a tailored example where mixing is observable despite this effect.

quant-ph↗

arXiv2015

Directional spontaneous emission and lateral Casimir-Polder force on an atom close to a nanofiber

We study the spontaneous emission of an excited atom close to an optical nanofiber and the resulting scattering forces. For a suitably chosen orientation of the atomic dipole, the spontaneous emission pattern becomes asymmetric and a resonant Casimir--Polder force parallel to the fiber axis arises. For a simple model case, we show that the such a lateral force is due to the interaction of the circularly oscillating atomic dipole moment with its image inside the material. With the Casimir--Polder energy being constant in the lateral direction, the predicted lateral force does not derive from a potential in the usual way. Our results have implications for optical force measurements on a substrate as well as for laser cooling of atoms in nanophotonic traps.

quant-ph↗

arXiv2015

Modified and controllable dispersion interaction in a 1D waveguide geometry

Dispersion interactions such as the van der Waals interaction between atoms or molecules derive from quantum fluctuations of the electromagnetic field and can be understood as the exchange of virtual photons between the interacting partners. Any modification of the environment in which those photons propagate will thus invariably lead to an alteration of the van der Waals interaction. Here we show how the two-body dispersion interaction inside a cylindrical waveguide can be made to decay asymptotically exponentially, and how this effect sensitively depends on the material properties and the length scales of the problem, eventually leading to the possibility of controllable interactions. Further, we discuss the possibility to detect the retarded van der Waals interaction by resonant enhancement of the interaction between Rydberg atoms in the light of long-range potentials due to guided modes.

quant-ph↗

arXiv2015

Casimir-Polder repulsion: Three-body effects

In this paper we study an archetypical scenario in which repulsive Casimir-Polder forces between an atom or molecule and two macroscopic bodies can be achieved. This is an extension of previous studies of the interaction between a polarizable atom and a wedge, in which repulsion occurs if the atom is sufficiently anisotropic and close enough to the symmetry plane of the wedge. A similar repulsion occurs if such an atom passes a thin cylinder or a wire. An obvious extension is to compute the interaction between such an atom and two facing wedges, which includes as a special case the interaction of an atom with a conducting screen possessing a slit, or between two parallel wires. To this end we further extend the electromagnetic multiple-scattering formalism for three-body interactions. To test this machinery we reinvestigate the interaction of a polarizable atom between two parallel conducting plates. In that case, three-body effects are shown to be small, and are dominated by three- and four-scattering terms. The atom-wedge calculation is illustrated by an analogous scalar situation, described in the Appendix. The wedge-wedge-atom geometry is difficult to analyze because this is a scale-free problem. But it is not so hard to investigate the three-body corrections to the interaction between an anisotropic atom or nanoparticle and a pair of parallel conducting cylinders, and show that the three-body effects are very small and do not affect the Casimir-Polder repulsion at large distances between the cylinders. Finally, we consider whether such highly anisotropic atoms needed for repulsion are practically realizable. Since this appears rather difficult to accomplish, it may be more feasible to observe such effects with highly anisotropic nano particles.

quant-ph↗

arXiv2015

Friction forces on atoms after acceleration

The aim of this paper is to revisit the calculation of atom-surface quantum friction in the quantum field theory formulation put forward by Barton [New J. Phys. 12 (2010) 113045]. We show that the power dissipated into field excitations and the associated friction force depend on how the atom is boosted from being initially at rest to a configuration in which it is moving at constant velocity (v) parallel to the planar interface. In addition, we point out that there is a subtle cancellation between the one-photon and part of the two-photon dissipating power, resulting in a leading order contribution to the frictional power which goes as v^4. These results are also confirmed by an alternative calculation of the average radiation force, which scales as v^3.

quant-ph↗

arXiv2014

Giant Rydberg Excitons in Cuprous Oxide

Highly excited atoms with an electron moved into a level with large principal quantum number are fascinating hydrogen-like objects. The giant extension of these Rydberg atoms leads to huge interaction effects. Monitoring these interactions has provided novel insights into molecular and condensed matter physics problems on a single quantum level. Excitons, the fundamental optical excitations in semiconductors consisting of a negatively charged electron and a positively charged hole, are the condensed matter analogues of hydrogen. Highly excited excitons with extensions similar to Rydberg atoms are attractive because they may be placed and moved in a crystal with high precision using microscopic potential landscapes. Their interaction may allow formation of ordered exciton phases or sensing of elementary excitations in the surrounding, also on a quantum level. Here we demonstrate the existence of Rydberg excitons in cuprous oxide, Cu2O, with principal quantum numbers as large as n=25 . These states have giant wave function extensions of more than 2 micrometers, compared to about a nanometer for the ground state. The strong dipole-dipole interaction is evidenced by a blockade effect, where the presence of an exciton prevents excitation of a further exciton in its vicinity.

cond-mat.mes-hall↗

arXiv2014

Shielding vacuum fluctuations with graphene

The Casimir-Polder interaction of ground-state and excited atoms with graphene is investigated with the aim to establish whether graphene systems can be used as a shield for vacuum fluctuations of an underlying substrate. We calculate the zero-temperature Casimir-Polder potential from the reflection coefficients of graphene within the framework of the Dirac model. For both doped and undoped graphene we show limits at which graphene could be used effectively as a shield. Additional results are given for AB-stacked bilayer graphene.

quant-ph↗

arXiv2013

Controlled ripple texturing of suspended graphene membrane due to coupling with ultracold atoms

We discuss the possibility to create hybrid quantum systems that combine ultracold atoms with graphene membranes. We investigate a setup in which a cold atom cloud is placed close to a free-standing sheet of graphene at distances on the order of a few hundred nanometers. The atoms then couple to the graphene membrane via Casimir-Polder forces. Temporal changes in the atomic state of the atomic cloud changes the Casimir-Polder interaction, thereby leading to the creation of a backaction force in the graphene sheet. This setup provides a controllable way to engineer ripples in a graphene sheet.

quant-ph↗

arXiv2013

Probing atom-surface interactions by diffraction of Bose-Einstein condensates

In this article we analyze the Casimir-Polder interaction of atoms with a solid grating and an additional repulsive interaction between the atoms and the grating in the presence of an external laser source. The combined potential landscape above the solid body is probed locally by diffraction of Bose-Einstein condensates. Measured diffraction efficiencies reveal information about the shape of the Casimir-Polder interaction and allow us to discern between models based on a pairwise-summation (Hamaker) approach and Lifshitz theory.

physics.atom-ph↗

arXiv2012

Second order coupling between excited atoms and surface polaritons

Casimir-Polder interactions between an atom and a macroscopic body are typically regarded as due to the exchange of virtual photons. This is strictly true only at zero temperature. At finite temperature, real-photon exchange can provide a significant contribution to the overall dispersion interaction. Here we describe a new resonant two-photon process between an atom and a planar interface. We derive a second order effective Hamiltonian to explain how atoms can couple resonantly to the surface polariton modes of the dielectric medium. This leads to second-order energy exchanges which we compare with the standard nonresonant Casimir-Polder energy.

quant-ph↗