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Register a new userDipole-Dipole interaction in photonic crystal nanocavity
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Dipole-dipole interaction between two two-level `atoms in photonic crystal nanocavity is investigated based on finite-difference time domain algorithm. This method includes both real and virtual photon effects and can be applied for dipoles with different transition frequencies in both weak and strong coupling regimes. Numerical validations have been made for dipoles in vacuum and in an ideal planar microcavity. For dipoles located in photonic crystal nanocavity, it is found that the cooperative decay parameters and the dipole-dipole interaction potential strongly depend on the following four factors: the atomic position, the atomic transition frequency, the resonance frequency, and the cavity quality factor. Properly arranging the positions of the two atoms, we can acquire equal value of the cooperative decay parameters and the local coupling strength. Large cooperative decay parameters can be achieved when transition frequency is equal to the resonance frequency. For transition frequency varying in a domain of the cavity linewidth around the resonance frequency, dipole-dipole interaction potential changes continuously from attractive to repulsive case. Larger value and sharper change of cooperative parameters and dipole-dipole interaction can be obtained for higher quality factor. Our results provide some manipulative approaches for dipole-dipole interaction with potential application in various fields such as quantum computation and quantum information processing based on solid state nanocavity and quantum dot system.
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The dipole blockade phenomenon is a direct consequence of strong dipole-dipole interaction, where only single atom can be excited because the doubly excited state is shifted out of resonance. The corresponding two-body entanglement with non-zero concurrence induced by the dipole blockade effect is an important resource for quantum information processing. Here, we propose a novel physical mechanism for realizing dipole blockade without the dipole-dipole interaction, where two qubits coupled to a cavity, are driven by a coherent field. By suitably chosen placements of the qubits in the cavity and by adjusting the relative decay strengths of the qubits and cavity field, we kill many unwanted excitation pathways. This leads to dipole blockade. In addition, we show that these two qubits are strongly entangled over a broad regime of the system parameters. We show that a strong signature of this dipole blockade is the bunching property of the cavity photons which thus provides a possible measurement of the dipole blockade. We present dynamical features of the dipole blockade without dipole-dipole interaction. The proposal presented in this work can be realized not only in traditional cavity QED, but also in non-cavity topological photonics involving edge modes.
We compute the interaction energies of a two-atom system placed in the middle of a perfectly reflecting planar cavity, in the perturbative regime. Explicit expressions are provided for the van der Waals potentials of two polarisable atomic dipoles as well as for the electrostatic potential of two induced dipoles. For the van der Waals potentials, several scenarios are considered, namely, a pair of atoms in their ground states, a pair of atoms both excited, and a pair of dissimilar atoms with one of them excited. In addition, the corresponding phase-shift of the two-atom wavefunction is calculated in each case. The effects of the two-dimensional confinement of the electromagnetic field by the cavity are analyzed in each scenario.
We study the two-body bound states of a model Hamiltonian that describes the interaction between two field-oriented dipole moments. This model has been used extensively in many-body physics of ultracold polar molecules and magnetic atoms, but its few-body physics has been explored less fully. With a hard-wall short-range boundary condition, the dipole-dipole bound states are universal and exhibit a complicated pattern of avoided crossings between states of different character. For more realistic Lennard-Jones short-range interactions, we consider parameters representative of magnetic atoms and polar molecules. For magnetic atoms, the bound states are dominated by the Lennard-Jones potential, and the perturbative dipole-dipole interaction is suppressed by the special structure of van der Waals bound states. For polar molecules, we find a dense manifold of dipole-dipole bound states with many avoided crossings as a function of induced dipole or applied field, similar to those for hard-wall boundary conditions. This universal pattern of states may be observable spectroscopically for pairs of ultracold polar molecules.
We have observed resonant energy transfer between cold Rydberg atoms in spatially separated cylinders. Resonant dipole-dipole coupling excites the 49s atoms in one cylinder to the 49p state while the 41d atoms in the second cylinder are transferred down to the 42p state. We have measured the production of the 49p state as a function of separation of the cylinders (0 - 80 um) and the interaction time (0 - 25 us). In addition we measured the width of the electric field resonances. A full many-body quantum calculation reproduces the main features of the experiments.
We study how the radiative properties of a dense ensemble of atoms can be modified when they are placed near or between metallic or dielectric surfaces. If the average separation between the atoms is comparable or smaller than the wavelength of the scattered photons, the coupling to the radiation field induces long-range coherent interactions based on the interatomic exchange of virtual photons. Moreover, the incoherent scattering of photons back to the electromagnetic field is known to be a many-body process, characterized by the appearance of superradiant and subradiant emission modes. By changing the radiation field properties, in this case by considering a layered medium where the atoms are near metallic or dielectric surfaces, these scattering properties can be dramatically modified. We perform a detailed study of these effects, with focus on experimentally relevant parameter regimes. We finish with a specific application in the context of quantum information storage, where the presence of a nearby surface is shown to increase the storage time of an atomic excitation that is transported across a one-dimensional chain.
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