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Conference on Lasers and Electro-Optics Europe & European Quantum Electronics Conference (CLEO/Europe-EQEC)

Nanostructured Control of Interactions of Quantum Emitters Beyond Electric Dipole Approximation

Miriam Kosik, O. Burlayenko, Karolina Słowik

Published Jun 1, 2019• 0 citations
Publisher

Abstract

Summary form only given. In the pioneering work of Purcell, the possibility to control spontaneous emission lifetimes of quantum emitters by tailoring their electromagnetic surroundings was widely investigated and verified in various types of cavities or band-gap environments. This includes semiconductor microstructures, photonic crystals, and plasmonic nanoparticles. Due to the extraordinary ability of plasmonic nanostructures to confine light into subwavelength spatial domains, steps beyond the paradigmatic electric dipole approximation in the theoretical description of this process may be necessary. In this contribution, we focus on the case of multiple in general nonidentical two-level emitters, sharing the same electromagnetic surroundings, whose local density of states could be tailored by a neighbouring nanostructure. In this case, the surroundings may serve as a long-distance emitter-emitter interaction carrier, or it may trigger collective emission processes, in analogy to Dicke superradiance. We describe these phenomena taking into account the electric dipole, magnetic dipole and electric quadrupole components of light-matter interaction Hamiltonian.

DOI
10.1109/cleoe-eqec.2019.8871846

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Summary form only given. In the pioneering work of Purcell, the possibility to control spontaneous emission lifetimes of quantum emitters by tailoring their electromagnetic surroundings was widely investigated and verified in various types of cavities or band-gap environments. This includes semiconductor microstructures, photonic crystals, and plasmonic nanoparticles. Due to the extraordinary ability of plasmonic nanostructures to confine light into subwavelength spatial domains, steps beyond the paradigmatic electric dipole approximation in the theoretical description of this process may be necessary. In this contribution, we focus on the case of multiple in general nonidentical two-level emitters, sharing the same electromagnetic surroundings, whose local density of states could be tailored by a neighbouring nanostructure. In this case, the surroundings may serve as a long-distance emitter-emitter interaction carrier, or it may trigger collective emission processes, in analogy to Dicke superradiance. We describe these phenomena taking into account the electric dipole, magnetic dipole and electric quadrupole components of light-matter interaction Hamiltonian.
The photonic environment can significantly influence emission properties and interactions among atomic systems. In such scenarios, frequently the electric dipole approximation is assumed that is justified as long as the spatial extent of the atomic system is negligible compared to the spatial variations of the field. While this holds true for many canonical systems, it ceases to be applicable for more contemporary nanophotonic structures. To go beyond the electric dipole approximation, we propose and develop in this article an analytical framework to describe the impact of the photonic environment on emission and interaction properties of atomic systems beyond the electric dipole approximation. Particularly, we retain explicitly magnetic dipolar and electric quadrupolar contributions to the light-matter interactions. We exploit a field quantization scheme based on electromagnetic Green’s tensors, suited for dispersive materials. We obtain expressions for spontaneous emission rate, Lamb shift, multipole-multipole shift and superradiance rate, all being modified with dispersive environment. The considered influence could be substantial for suitably tailored nanostructured photonic environments, as demonstrated exemplarily.
The photonic environment can significantly influence emission properties and interactions among atomic systems. In such scenarios, frequently the electric dipole approximation is assumed that is justified as long as the spatial extent of the atomic system is negligible compared to the spatial variations of the field. While this holds true for many canonical systems, it ceases to be applicable for more contemporary nanophotonic structures. To go beyond the electric dipole approximation, we propose and develop in this article an analytical framework to describe the impact of the photonic environment on emission and interaction properties of atomic systems beyond the electric dipole approximation. Particularly, we retain explicitly magnetic dipolar and electric quadrupolar contributions to the light-matter interactions. We exploit a field quantization scheme based on electromagnetic Green's tensors, suited for dispersive materials. We obtain expressions for spontaneous emission rate, Lamb shift, multipole-multipole shift and superradiance rate, all being modified with dispersive environment. The considered influence could be substantial for suitably tailored nanostructured photonic environments, as demonstrated exemplarily.
In this paper, we study the collective effects which appear as a pair of quantum emitters is positioned in close vicinity to a plasmonic nanoparticle. These effects include multipole-multipole interaction and collective decay, the strengths and rates of which are modified by the presence of the nanoparticle. As a result, entanglement is generated between the quantum emitters, which survives in the stationary state. To evaluate these effects, we exploit the Green's tensor-based quantization scheme in the Markovian limit, taking into account the corrections from light-matter coupling channels higher than the electric dipole. We find these higher-order channels to significantly influence the collective rates and degree of entanglement, and in particular, to qualitatively influence their spatial profiles. Our findings indicate that, apart from quantitatively modifying the results, the higher-order interaction channels may introduce asymmetry into the spatial distribution of the collective response.
The rate of spontaneous emission is known to depend on the environment of a emitter, and the enhancement of one-photon emission in a resonant cavity is known as the Purcell effect. Here we develop a theory of spontaneous two-photon emission for a general electromagnetic environment including inhomogeneous dispersive and absorptive media. This theory is used to evaluate the two-photon Purcell enhancement in the vicinity of metallic nanoparticles and demonstrates that the surface-plasmon resonances supported by these particles can increase the emission rate by more than two orders of magnitude. The control over two-photon Purcell enhancement given by tailored nanostructured environments could provide an emitter with any desired spectral response and may serve as an ultimate route for designing light sources with novel properties.
Frontier quantum engineering tasks require reliable control over light-matter interaction dynamics, which could be obtained by introducing electromagnetic structuring. Initiated by the Purcell's discovery of spontaneous emission acceleration in a cavity, the concept of electromagnetic modes' design have gained a considerable amount of attention due to development of photonic crystals, micro-resonators, plasmonic nanostructures and metamaterials. Those approaches, however, offer qualitatively different strategies for tailoring light-matter interactions and are based on either high quality factor modes shaping, near field control, or both. Remarkably, rigorous quantum mechanical description might address those processes in a different fashion. While traditional cavity quantum electrodynamics tools are commonly based on mode decomposition approach, few challenges rise once dispersive and lossy nanostructures, such as noble metals (plasmonic) antennas or metamaterials, are involved. The primary objective of this review is to introduce key methods and techniques while aiming to obtain comprehensive quantum mechanical description of spontaneous, stimulated and higher order emission and interaction processes, tailored by nanostructured material environment. The main challenge and the complexity here are set by the level of rigorousity, up to which materials should be treated. While relatively big nanostructured features (10 nm and larger) could be addressed by applying fluctuation–dissipation theorem and corresponding Green functions' analysis, smaller objects will require individual approach. Effects of material granularity, spatial dispersion, tunneling over small gaps, material memory and others will be reviewed. Quantum phenomena, inspired and tailored by nanostructured environment, plays a key role in development of quantum information devices and related technologies. Rigorous analysis is required for both examination of experimental observations and prediction of new effects.
We present a novel photonic model that enables an efficient computation of the two-photon Purcell effect of a quantum emitter in the vicinity of an arbitrary photonic structure. Our framework is relevant for the plasmonic nanocavities used to enhance higher-order light-matter interactions, as it goes beyond the dipolar approximation. The computation of Purcell factors through classical electromagnetic simulations determines the influence of the environment without tedious analytic calculations. We demonstrate that placing a hydrogen-like emitter close to a silver nanodisk enhances the transition rate by 5 and 11 orders of magnitude via electric dipole and quadrupole two-photon transitions, respectively. This process has exciting implications for future research, including the potential for efficient entangled two-photon sources.