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Physical Review B

Quantitative modeling of fluorescent emission in photonic crystals

Johannes Gutmann, Hans P. Zappe, Jan Christoph Goldschmidt

Published Nov 13, 2013• 22 citations
Publisher

Abstract

Photonic crystals affect the photon emission of embedded emitters due to an altered local density of photon states (LDOS). We review the calculation of the LDOS from eigenmodes in photonic crystals and propose a rate equation model for fluorescent emitters to determine the changes in emission induced by the LDOS. We show how to calculate the modifications of three experimentally accessible characteristics: emission spectrum (spectral redistribution), emitter quantum yield, and fluorescence lifetime. As an example, we present numerical results for the emission of the dye Rhodamine B inside an opal photonic crystal. For such photonic crystals with small permittivity contrast, the LDOS is only weakly modified, resulting in rather small changes. We point out that in experiments, however, usually only part of the emitted light is detected, which can have a very different spectral distribution (e.g., due to a photonic band gap in the direction of detection). We demonstrate the calculation of this detected spectrum for a typical measurement setup. With this reasoning, we explain the previously not fully understood experimental observation that strong spectral modifications occurred, while at the same time only small changes in lifetime were found. With our approach, the mentioned effects can be quantitatively calculated for fluorescent emitters in any photonic crystal.

DOI
10.1103/physrevb.88.205118

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Photonic crystals affect the photon emission of embedded emitters due to an altered local density of photon states (LDOS). We review the calculation of the LDOS from eigenmodes in photonic crystals and propose a rate equation model for fluorescent emitters to determine the changes in emission induced by the LDOS. We show how to calculate the modifications of three experimentally accessible characteristics: emission spectrum (spectral redistribution), emitter quantum yield, and fluorescence lifetime. As an example, we present numerical results for the emission of the dye Rhodamine B inside an opal photonic crystal. For such photonic crystals with small permittivity contrast, the LDOS is only weakly modified, resulting in rather small changes. We point out that in experiments, however, usually only part of the emitted light is detected, which can have a very different spectral distribution (e.g., due to a photonic band gap in the direction of detection). We demonstrate the calculation of this detected spectrum for a typical measurement setup. With this reasoning, we explain the previously not fully understood experimental observation that strong spectral modifications occurred, while at the same time only small changes in lifetime were found. With our approach, the mentioned effects can be quantitatively calculated for fluorescent emitters in any photonic crystal.
A photonic crystal, defined as a periodic dielectric structure, can influence the radiation rate of an embedded dipolar emitter. A theory of this effect is developed and the efficiency of a dipolar photonic source is calculated for a realistic three-dimensional crystal. Taking as a starting point the photonic band structure and its associated eigenfields, it is shown that the emission rate is strongly correlated with the density of modes, but also that the density of modes alone cannot explain all features found in the emission spectrum. For an infinite crystal, the computation of the field propagator confirms that the emission rate falls to zero in the frequency range defined by the photonic band gap. The emitter lifetime changes with the dipole location and orientation, leading to a radiation rate enhancement or inhibition according to the direction of the emission. These results may open routes to photonic sources with very high quantum efficiency.
We have measured spectrally resolved fluorescence lifetimes of dye incorporated in high-quality photonic crystals, made of colloidal spheres. The emission spectrum shows a pronounced Bragg notch. In contrast, the fluorescence lifetime does not depend on the interaction between light and the photonic crystal. The results are explained with a simple model of an atom in a cavity. The effects of homogeneous and inhomogeneous broadening of the emission spectrum of dye inside photonic crystals are discussed.
In certain three-dimensional crystals, a frequency range exist for all polarizations for which light is not allowed to propagate in any direction, called the 3D photonic band gap: a frequency range where the density of vacuum fluctuations vanishes in an ideal infinitely large and perfect system. The complete absence of vacuum fluctuations can be interpreted as zero density of states and vice versa. It is well known that the characteristics of spontaneous emission of light depend strongly on the environment of the light source. According to quantum electrodynamics, the emission rate of a two-level quantum emitter as described by Fermi’s “golden rule”, is factorized into one part describing the emitter’s properties and a second part describing the effect of the environment on the light field via the local density of optical state (LDOS). The radiative decay rate of the emitters is proportional to the LDOS. The absence of vacuum fluctuations or the zero LDOS leads to complete inhibition of the spontaneous emission. While many great advances towards a band gap have been made, no complete inhibition has ever been observed to date. In this thesis, for the first time, we have studied the spontaneous emission of PbS quantum dots inside real 3D photonic band gap crystal as a function of frequency throughout the band gap. In our experiments we have observed an inhibited emission of 18x in the band gap. The time-resolved decay curves show evidence for intriguing finite-size effects whereby vacuum fluctuations tunnel into the band gap. Unfortunately, most theories assume crystals of infinite extent, where the inhibition in the band gap is also infinite, as vacuum fluctuations don’t exist inside the crystal. Here we propose an original model to calculate the LDOS in the band gap of a finite photonic crystal based on tunneling of the vacuum fluctuations into the crystal. We validate our model for the one-dimensional situation with a direct comparison to the analytic calculations which exist for one-dimensional photonic crystals. For three dimensional crystals, the theory shows an excellent match to the experiment.
Quantum electrodynamics of atom spontaneous emission from a three-dimensional photonic crystal is studied in a full vectorial framework. The electromagnetic fields are quantized via solving the eigenproblem of photonic crystals with use of a plane-wave expansion method. It is found that the photon density of states and local density of states (LDOS) with a full band gap vary slowly near the edge of band gap, in significant contrast to the singular character predicted by the previous isotropic model. Therefore, the spontaneous emission can be solved by conventional Weisskopf-Wigner approximate theory, which yields a pure exponentially decaying behavior with a rate proportional to the LDOS.
We present the first experiments that demonstrate strong angle-independent modification of spontaneous emission spectra from laser dyes in photonic crystals, made of inverse opals in titania. We show that both the fluorescence quantum efficiency and weak disorder play a key role in interpreting the experimental data. We compare the angle-independent emission spectra of dye in photonic crystals with spectra from such crystals with much smaller lattice spacings, for which emission is in the long wavelength limit. The ratio of emission power spectra shows inhibition of emission up to a factor ∼ 5 over a large bandwidth of 13% of the first order Bragg resonance frequency. The inhibition shifts to increasing wavelength with the lattice parameter, confirming the photonic nature of the phenomenon. The center frequency and bandwidth of the inhibition agree with the calculated total density of states, but the measured inhibition of the vacuum fluctuations is much larger. This result is confirmed by experiments using different dyes. We likely probe the strongly modulated local photonic density of states, due to the spatially nonuniform distribution of dye molecules over the unit cell.