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arXiv:1401.6193 · Physical Review B

Reversible dynamics of single quantum emitters near metal-dielectric interfaces

Alejandro González-Tudela, Paloma A. Huidobro, Luis Martín-Moreno, C. Tejedor, Francisco José García-Vidal

Published Jan 9, 2014• 78 citations
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Abstract

Here we present a systematic study of the dynamics of a single quantum emitter near a flat metal-dielectric interface. We identify the key elements that determine the onset of reversibility in these systems by using a formalism suited for absorbing media and through an exact integration of the dynamics. Moreover, when the quantum emitter separation from the surface is small, we are able to describe the dynamics within a pseudomode description that yields analytical understanding and allows more powerful calculations.

DOI
10.1103/physrevb.89.041402

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Here we present a systematic study of the dynamics of a single quantum emitter near a flat metal-dielectric interface. We identify the key elements that determine the onset of reversibility in these systems by using a formalism suited for absorbing media and through an exact integration of the dynamics. Moreover, when the quantum emitter separation from the surface is small, we are able to describe the dynamics within a pseudomode description that yields analytical understanding and allows more powerful calculations.
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The presence of a metal nanoparticle (MNP) near a quantum dipole emitter, when a localized surface plasmon mode is excited via the resonant coupling with an excited quantum dipole, dramatically changes the relaxation dynamics: an exponential decay changes to step-like behavior. The main physical consequence of this relaxation process is that the emission, being largely determined by the MNP, comes out with a substantial delay. A large number of system parameters in our analytical description opens new possibilities for controlling quantum emitter dynamics.
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Here we present the theoretical foundation of the strong coupling phenomenon between quantum emitters and propagating surface plasmons observed in two-dimensional metal surfaces. For that purpose, we develop a quantum framework that accounts for the coherent coupling between emitters and surface plasmons and incorporates the presence of dissipation and dephasing. Our formalism is able to reveal the key physical mechanisms that explain the reported phenomenology and also determine the physical parameters that optimize the strong coupling. A discussion regarding the classical or quantum nature of this phenomenon is also presented.
Surface plasmon polaritons are charge density waves of electrons in a metal, which are coupled to an electromagnetic field at a metal-dielectric interface. The electro- magnetic field associated with surface plasmons is confined, resulting in increased field intensities near the interface. Optical emitters placed near a metal film interact strongly with the surface plasmon modes present, not only modifying the radiation rates, but also the radiation profile. These emitters may be used to store and process information, and understanding their behaviour in the presence of a lossy metal film is important in determining the advantages and limitations of using surface plasmons. In this thesis, we wish to understand how we can optically control atoms by exploring two physical phenomena: first, the influence of surface plasmons on collective effects in an ensemble of emitters. Secondly, the single photon excitation of an emitter near a metal film. In the first case, we analyze the collective radiative behaviour of multiple classical emitters near a metal film that radiatively couple to the far-field through surface plasmon modes. We demonstrate that the contributions of dipolar image charges within the metal film significantly affect the cooperative emission of nearby sources, generating sub- and super-radiant emission that can be controlled with a suitably detuned external driving field. In the second case, we determine the excitation probability of an atom near a metal film by a single photon pulse that is time reversed. Using a quantum electro- dynamic description of absorbing dielectrics, we show that non-radiative decay will limit the excitation probability to about half of the maximum that could be achieved in the absence of losses.