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Physical Review Letters

Decay Distribution of Spontaneous Emission from an Assembly of Atoms in Photonic Crystals with Pseudogaps

Xuehua Wang, Rongzhou Wang, Ben–Yuan Gu, Guo-Zhen Yang

Published Feb 13, 2002• 94 citations
Publisher

Abstract

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.

DOI
10.1103/physrevlett.88.093902

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Physical Review E•Oct 5, 2004•15 citations
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.
Photonic crystals (PCs) with relatively low dielectric contrast (i.e., with pseudogaps) have significant influence on the fluorescence decay of internal emitters. Fluorescence decays of ensembles of dye molecules measured at different positions in the PCs exhibit a nonexponential behavior, which is best fitted by a continuous distribution of decay rates. The most frequent decay rates of these distributions are smaller and their widths are narrower in a PC with a pseudogap acting in the emission range of the emitters than in a PC having the pseudogap out of this range. These experimental results have been well accounted for by calculations of the local density of states and rate constant for spontaneous emission.
Spontaneous decay behavior from an assembly of atoms (or molecules) in a dielectric slab sandwiched by two dielectric semi-infinite spaces with arbitrary refractive indices is investigated. We introduce a lifetime distribution function to describe decay kinetics. The zero-point fluctuations of the electromagnetic field are calculated as a function of the position of atom in the slab. They display a symmetric profile with respect to the central plane of the slab in symmetric structure sample and the contributions of the guided modes and the radiation modes components both exhibit cosinelike variation with a base but with a phase difference of \ensuremath{\pi}. With the increase of the thickness of the slab, the oscillations become dense. In contrast, for the asymmetric structure case, the related curves are asymmetric with respect to the middle plane of slab and exhibit considerably distorted cosinelike oscillations. The dependence of the spontaneous emission rate of atoms on the thickness of the slab and the refractive indices of substrate also is surveyed. Our calculations show that quite wide or narrow lifetime distribution can occur for different thicknesses of the slab. The coexistence of both accelerated and inhibited decay processes appears. The calculated results are in good agreement with experimental results.
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.
Motivated by the significant controversy between the two dispersion models and Weisskopf-Wigner approximation (WWA), for the first time to our knowledge, we introduce the position-dependent photon-atom interaction into the Green function method of the evolution operator and develop a universal theoretical treatment on spontaneous emission of atoms in photonic crystals (PCs). A position-sensitive generalized Lorentzian formulism (non-Lorentzian shape) for the decay of an excited atom in PCs is derived, 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 formulism may be reduced to the famous Lorentzian spectrum. In this case, we introduced a lifetime distribution function for an assembly of atoms and found that the lifetime distribution strongly depend on the spread configuration of these atoms in space, which clarifies successfully the tremendous discrepancy between different experiments. For the PCs with large full gaps, we found 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.