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arXiv:1806.06546

Polarization-dependent property of dipole-dipole interaction mediated by localized surface plasmon of an Ag nanosphere

Yun-Jin Zhao, Yonggang Y. Huang, Hong Sun Yang, Xiaoyun Wang, Ke Deng, Zheng Zhang, Heping Zhao, Zhengyou Liu

Published Jun 18, 2018• 0 citations
arXivHTMLPDF

Abstract

The effect of the dipole polarization on the quantum dipole dipole interaction near an Ag nanosphere (ANS) is investigated. A theoretical formalism in terms of classical Green function is developed for the transfer rate and the potential energy of the dipole dipole interaction (DDI) between two polarized dipoles. It is found that a linear transition dipole can couple to a left circularly polarized transition dipole much stronger than to a right circularly polarized transition dipole. This polarization selectivity exists over a wide frequency range and is robust against the variation of the dipoles' position or the radius of the ANS. In contrast, a right circularly polarized transition dipole, can change sharply from coupling strongly to another right circularly polarized dipole to coupling strongly to a left circularly polarized dipole with varying frequency. However, if the two dipoles are placed in the same radial direction of the sphere, the right circularly polarized transition dipole can only couple to the dipole with the same polarization while not to the left circularly polarized transition dipole. These findings may be used in solid-state quantum-information processing based on the DDI.

DOI
10.48550/arxiv.1806.06546

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The effect of the dipole polarization on the quantum dipole dipole interaction near an Ag nanosphere (ANS) is investigated. A theoretical formalism in terms of classical Green function is developed for the transfer rate and the potential energy of the dipole dipole interaction (DDI) between two polarized dipoles. It is found that a linear transition dipole can couple to a left circularly polarized transition dipole much stronger than to a right circularly polarized transition dipole. This polarization selectivity exists over a wide frequency range and is robust against the variation of the dipoles' position or the radius of the ANS. In contrast, a right circularly polarized transition dipole, can change sharply from coupling strongly to another right circularly polarized dipole to coupling strongly to a left circularly polarized dipole with varying frequency. However, if the two dipoles are placed in the same radial direction of the sphere, the right circularly polarized transition dipole can only couple to the dipole with the same polarization while not to the left circularly polarized transition dipole. These findings may be used in solid-state quantum-information processing based on the DDI.
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Abstract We investigate the enhanced electric dipole–dipole interaction of surface plasmon polaritons (SPPs) supported by a planar metal film waveguide. By taking two nitrogen-vacancy (NV) center electric dipoles in diamond as an example, both the coupling strength and collective relaxation of two dipoles are studied with the numerical Green Function method. Compared to two-dipole coupling on a planar surface, metal film provides stronger and tunable coupling coefficients. Enhancement of the interaction between coupled NV center dipoles could have applications in both quantum information and energy transfer investigation. Our investigation provides systematic results for experimental applications based on a dipole–dipole interaction mediated with SPPs on a planar metal film.
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We present a theoretical study for the Kerr nonlinearity of a four-level double-V-type quantum system near a two-dimensional array of metal-coated dielectric nanospheres. In the quantum system under study one V-type transition is influenced by the interaction with surface plasmons while the other V-type transition interacts with free-space vacuum. The quantum system interacts with a linearly polarized weak laser field that couples the lowest state with the upper states in the free-space transitions. We show that the Kerr nonlinearity is strongly influenced by the presence of the plasmonic nanostructure and is particularly sensitive to the distance between the quantum system and the plasmonic nanostructure.
We show that the quantum interference between two spontaneous emission channels can be greatly enhanced when a three-level V-type atom is placed near plasmonic nanostructures such as metallic slabs, nanospheres, or periodic arrays of metal-coated spheres. The spontaneous emission rate is calculated by a rigorous first-principles electromagnetic Green's tensor technique. The enhancement of quantum interference is attributed to the strong dependence of the spontaneous emission rate on the orientation of an atomic dipole relative to the surface of the nanostructure at the excitation frequencies of surface plasmons.