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arXiv:1710.08965 · Physical Review A

van der Waals interaction potential between Rydberg atoms near surfaces

Johannes Block, Stefan Scheel

Published Dec 29, 2017• 10 citations
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Abstract

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.

DOI
10.1103/physreva.96.062509

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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.
van der Waals interactions between atoms and dielectric surfaces are reinvestigated. To describe the nonretarded interaction potential between a dispersive dielectric surface and an atom in an arbitrary internal energy state, we derive a general expression in terms of an integral, over real frequency, of the combined atom and surface polarizabilities. It is shown that, for excited atoms, the expression is equivalent to the one obtained by Wylie and Sipe [Phys. Rev. A 32, 2030 (1985)]. We thus demonstrate how to extend this approach to excited atoms interacting with birefringent dielectrics. For isotropic dielectrics, a method of integration in closed form allows us to derive an approximate formula for the van der Waals interaction constant in terms of resonance frequencies and oscillator strengths of both the atom and the dielectric. Frequency-dependent ``dielectric reflection'' coefficients are introduced for virtual atomic dipole couplings either in absorption or in emission. In absorption, the reflection coefficient is always positive and smaller than unity. In emission, it may take arbitrary values, positive or negative (corresponding to van der Waals repulsion). Such a behavior is shown to be related to resonant excitation exchange between the atomic system and the dielectric medium, when an atomic transition frequency gets in resonance with a dielectric absorption band. Numerical calculations performed for the cesium-sapphire system are shown to be in good agreement with data obtained by selective-reflection spectroscopy. Finally, experimental tests of the birefringent character of the sapphire response are discussed.
Abstract Coherently manipulating Rydberg atoms in mesoscopic systems has proven challenging due to the unwanted population of nearby Rydberg levels by black-body radiation. Recently, there have been some efforts towards understanding these effects using states with a low principal quantum number that only have resonant dipole–dipole interactions. We perform experiments that exhibit black-body-induced dipole–dipole interactions for a state that also has a significant van der Waals interaction. Using an enhanced rate-equation model that captures some of the long-range properties of the dipolar interaction, we show that the initial degree of Rydberg excitation is dominated by the van der Waals interaction, while the observed linewidth at later times is dominated by the dipole–dipole interaction. We also point out some prospects for quantum simulation.
Assemblies of Rydberg atoms subject to resonant dipole-dipole interactions exhibit Frenkel excitons. We show that van der Waals shifts can significantly modify the exciton wave function, whenever atoms approach each other closely. As a result, attractive dipole-dipole potentials and repulsive van der Waals interactions can be combined to form stable one-dimensional atom chains, akin to bound aggregates. Here the van der Waals shifts ensure a stronger homogeneous delocalization of a single excitation over the whole chain, enabling it to bind several atoms. When brought into unstable configurations, such Rydberg aggregates allow the direct monitoring of their dissociation dynamics.
Resonant laser excitation of multiple Rydberg atoms are prohibited, leading to Rydberg blockade, when the long-range van der Waals interactions are stronger than the laser-atom coupling. Rydberg blockade can be violated, i.e., simultaneous excitation of more than one Rydberg atom, by off-resonant laser excitation, causing an excitation antiblockade. Rydberg antiblockade gives rise to strongly correlated many-body dynamics and spin-orbit coupling and also finds quantum computation applications. Instead of commonly used van der Waals interactions, we investigate antiblockade dynamics of two Rydberg atoms interacting via dipole-dipole exchange interactions. We study typical situations in current Rydberg atom experiments, where different types of dipole-dipole interactions can be achieved by varying Rydberg state couplings. An effective Hamiltonian governing underlying antiblockade dynamics is derived. We illustrate that geometric gates can be realized with the Rydberg antiblockade which is robust against the decay of Rydberg states. Our study may stimulate new experimental and theoretical exploration of quantum optics and strongly interacting many-body dynamics with Rydberg antiblockade driven by dipole-dipole interactions.
The London-van der Waals potential experienced by an atom under reflection from an atomic mirror is modeled as a quantum dipole-dipole interaction between the atomic dipole induced by the evanescent wave and its image dipole in the dielectric mirror. The quantum dipole-dipole interaction arises from the combined effect of the evanescent field and spontaneous emission. It depends on the electronic structure of the atom and is described by an effective non-Hermitian Hamiltonian that yields dissipative effects under reflection. The analytical expression obtained here preserves the power-law dependence of the static van der Waals interaction at distances close to the wall, but its long-distance behavior reflects that of the evanescent wave.
We analyze the effects of Zeeman degeneracies on the long-range interactions between like Rydberg atoms, with particular emphasis on applications to quantum-information processing using the van der Waals blockade. We present a general analysis of how degeneracies affect the primary error sources in blockade experiments, emphasizing that blockade errors are sensitive primarily to the weakest possible atom-atom interactions between the degenerate states, not the mean interaction strength. We present explicit calculations of the van der Waals potentials in the limit where the fine-structure interaction is large compared to the atom-atom interactions. The results are presented for all potential angular momentum channels involving s\mathit{s}s, p\mathit{p}p, and d\mathit{d}d states. For most channels there are one or more combinations of Zeeman levels that have extremely small dipole-dipole interactions and are therefore poor candidates for effective blockade experiments. Channels with promising properties are identified and discussed. We also present numerical calculations of Rb and Cs dipole matrix elements and relevant energy levels using quantum defect theory, allowing for convenient quantitative estimates of the van der Waals interactions to be made for principal quantum numbers up to 100. Finally, we combine the blockade and van der Waals results to quantitatively analyze the angular distribution of the blockade shift and its consequence for angular momentum channels and geometries of particular interest for blockade experiments with Rb.