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Physical Review Letters

Switching Control of Spontaneous Emission by Polarized Atoms in Two-Dimensional Photonic Crystals

Yun-Song Zhou, Xuehua Wang, Ben–Yuan Gu, Fu-He Wang

Published Mar 17, 2006• 29 citations
Publisher

Abstract

We calculate the lifetime distribution function of an assembly of polarized atoms in two-dimensional (2D) photonic crystals (PCs) at different polarization orientations of atomic dipole moments. We reveal a switching effect of atomic spontaneous emission (SE) and find a significant change of atomic lifetime, up to a factor of 33, by tuning the polarized orientation of the atoms. These observations suggest that the tuning of the polarized orientation of atoms provides a new way for the effective control of atomic SE processes in 2D PCs.

DOI
10.1103/physrevlett.96.103601

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We calculate the lifetime distribution function of an assembly of polarized atoms in two-dimensional (2D) photonic crystals (PCs) at different polarization orientations of atomic dipole moments. We reveal a switching effect of atomic spontaneous emission (SE) and find a significant change of atomic lifetime, up to a factor of 33, by tuning the polarized orientation of the atoms. These observations suggest that the tuning of the polarized orientation of atoms provides a new way for the effective control of atomic SE processes in 2D PCs.
The lifetime distribution functions of the spontaneous emission (SE) of the excited atoms embedded in two-dimensional (2D) photonic crystals (PCs) with square lattice, consisting of square air rods in dielectric medium with different filling factors, are calculated by using the plane wave expansion method. The numerical results show that the SE in the 2D PCs cannot be prohibited completely but it can be inhibited intensively by the pseudo-PBG of the PCs. In the pseudoband edges, the SE is accelerated obviously. The reduced average lifetime of the excited atoms and the extension of the reduced lifetime distribution in the 2D PCs both are the same as those in the 3D PCs in the order of magnitude. Our results provide an available way to control the behavior of the SE by changing the structures of the 2D PCs.
Spontaneous decay behaviors from an assembly of atoms (or molecules) in 3D photonic crystals (PC's) with pseudogaps are investigated. Theoretically, a lifetime distribution function for these atoms or molecules is defined to reveal decay kinetics. Our calculations show that quite wide or narrow lifetime distributions can occur for different spread configurations of the atoms (or molecules). The pure PC effect may lead to coexistence of both accelerated and inhibited decay processes. These results provide theoretical clarification for substantial discrepancies in the recent reported experiments.
Being motivated by the controversial results based on two dispersion models and Weisskopf–Wigner approximation (WWA), we introduce, for the first time to our knowledge, the position-dependent photon-atom interaction into the Green function method of the evolution operator and develop a universal theoretical approach to study spontaneous emission of atoms in photonic crystals (PCs). A position-sensitive generalized Lorentzian formalism (non-Lorentzian shape) for the decay of an excited atom in PCs is derived, and an exact numerical method for calculating the local coupling strength, proportional to the photonic local density of state (LDOS), is presented. For weak interaction PCs with pseudo gaps, the generalized Lorentzian formalism may be reduced to the famous Lorentzian spectrum. In this case, we introduce a lifetime distribution function for an assembly of atoms and find that it depends strongly on the atomic configuration in space, which clarifies successfully the tremendous discrepancy between different experiments. For the PCs with large full gaps, we find that the atomic position can fundamentally change the decay behavior of an excited atom: in strong interaction positions, the atomic decay is non-classical or exhibits an envelope-damped Rabi oscillation, while in weak interaction positions the WWA is valid. Recently, we also predicted giant Lamb shifts for hydrogen atoms in PCs, and revealed that in inhomogeneous electromagnetic environment, the dominant contribution to the Lamb shift comes from real photon emission, while the contribution from emission and reabsorption of virtual photon is negligible, in vast contrast with the case of free space where the virtual photon processes play a key role.
We theoretically investigate the spontaneous emission light of an excited three-level atom embedded in an anisotropic photonic crystal with two asymmetric bands. The property of spontaneous emission relating to the atomic position in a unit cell of the crystal is described with a position-dependent phase difference. The atomic transition in free space can be manipulated by the other associated transition coupling to photonic crystal. The result shows that the spontaneous emission spectra are effectively shifted and tuned by the atomic position-dependent phase, which results in the asymmetric distribution of the photonic density of states between two bands, and the increasing band can push the emitted light towards the other band. The physical process can be further illuminated through analyzing the emitted field in photonic crystal. The result perhaps offers an interesting route towards tunable photonic devices.