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Physical review. B, Condensed matter

Quantum optics of localized light in a photonic band gap

Sajeev John, Jian Wang

Published Jun 1, 1991• 395 citations
Publisher

Abstract

We describe the quantum electrodynamics of photons interacting with hydrogenic atoms and molecules in a class of strongly scattering dielectric materials. These dielectrics consist of an ordered or nearly ordered array of spherical scatterers with real positive refractive index and exhibit a complete photonic band gap or pseudogap for all directions of electromagnetic propagation. For hydrogenic atoms with a transition frequency in the forbidden optical gap, we demonstrate both the existence and stability of a photon-atom bound state. For a band gap to center frequency ratio \ensuremath{\Delta}\ensuremath{\omega}/${\mathrm{\ensuremath{\omega}}}_{0}$\ensuremath{\sim}5%, the photon localization length ${\ensuremath{\xi}}_{\mathrm{loc}}$\ensuremath{\ge}10L, where L is the lattice constant of dielectric array. This strong self-dressing of the atom by its own localized radiation field leads to anomalous Lamb shifts and a splitting of the excited atomic level into a doublet when the transition frequency lies near a photonic band edge. We estimate the magnitude of this splitting to be ${10}^{\mathrm{\ensuremath{-}}6}$ at the vacuum transition energies.The stability of this photon-bound state with respect to electromagnetic as well as vibrational decay mechanisms is examined. For an isolated molecule embedded in the solid fraction of the dielectric structure, the dominant mechanism for absorption and spontaneous emission is via optically driven electron-phonon interactions and the resulting phonon-absorption and -emission sidebands. Raman or Brillouin scattering of a localized photon into a propagating mode, or vice versa, directly by photon-phonon interaction is forbidden. For atoms not in contact with the solid fraction of the dielectric host, the electromagnetic two-photon spontaneous emission rate is on the scale of several days. For two identical atoms separated by a distance R within the photonic band gap, energy transfer from an excited atom to an unexcited atom occurs by a phase-shifted resonance dipole-dipole interaction which vanishes exponentially for R>${\ensuremath{\xi}}_{\mathrm{loc}}$. This leads to the formation of a narrow photonic impurity band within the gap when a finite density of atoms is present. This impurity band exhibits a different kind of nonlinear optical properties. When two neighboring atoms are both excited, single-photon spontaneous emission at \ensuremath{\sim}2\ensuremath{\Elzxh}${\mathrm{\ensuremath{\omega}}}_{0}$ occurs by a third-order electromagnetic process with rate \ensuremath{\Gamma}\ensuremath{\sim}${\mathrm{\ensuremath{\alpha}}}^{3}$${\mathrm{\ensuremath{\omega}}}_{0}$(${\mathit{a}}_{0}$/R${)}^{8}$, where ${\mathit{a}}_{0}$ is the atomic Bohr radius and \ensuremath{\alpha} is the fine-structure constant.

DOI
10.1103/physrevb.43.12772

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We describe the quantum electrodynamics of photons interacting with hydrogenic atoms and molecules in a class of strongly scattering dielectric materials. These dielectrics consist of an ordered or nearly ordered array of spherical scatterers with real positive refractive index and exhibit a complete photonic band gap or pseudogap for all directions of electromagnetic propagation. For hydrogenic atoms with a transition frequency in the forbidden optical gap, we demonstrate both the existence and stability of a photon-atom bound state. For a band gap to center frequency ratio \ensuremath{\Delta}\ensuremath{\omega}/\ensuremathω0{\mathrm{\ensuremath{\omega}}}_{0}\ensuremathω0​\ensuremath{\sim}5%, the photon localization length \ensuremathξloc{\ensuremath{\xi}}_{\mathrm{loc}}\ensuremathξloc​\ensuremath{\ge}10L, where L is the lattice constant of dielectric array. This strong self-dressing of the atom by its own localized radiation field leads to anomalous Lamb shifts and a splitting of the excited atomic level into a doublet when the transition frequency lies near a photonic band edge. We estimate the magnitude of this splitting to be 10\ensuremath−6{10}^{\mathrm{\ensuremath{-}}6}10\ensuremath−6 at the vacuum transition energies.The stability of this photon-bound state with respect to electromagnetic as well as vibrational decay mechanisms is examined. For an isolated molecule embedded in the solid fraction of the dielectric structure, the dominant mechanism for absorption and spontaneous emission is via optically driven electron-phonon interactions and the resulting phonon-absorption and -emission sidebands. Raman or Brillouin scattering of a localized photon into a propagating mode, or vice versa, directly by photon-phonon interaction is forbidden. For atoms not in contact with the solid fraction of the dielectric host, the electromagnetic two-photon spontaneous emission rate is on the scale of several days. For two identical atoms separated by a distance R within the photonic band gap, energy transfer from an excited atom to an unexcited atom occurs by a phase-shifted resonance dipole-dipole interaction which vanishes exponentially for R>\ensuremathξloc{\ensuremath{\xi}}_{\mathrm{loc}}\ensuremathξloc​. This leads to the formation of a narrow photonic impurity band within the gap when a finite density of atoms is present. This impurity band exhibits a different kind of nonlinear optical properties. When two neighboring atoms are both excited, single-photon spontaneous emission at \ensuremath{\sim}2\ensuremath{\Elzxh}\ensuremathω0{\mathrm{\ensuremath{\omega}}}_{0}\ensuremathω0​ occurs by a third-order electromagnetic process with rate \ensuremath{\Gamma}\ensuremath{\sim}{\mathrm{\ensuremath{\alpha}}}^{3}$${\mathrm{\ensuremath{\omega}}}_{0}(a0{\mathit{a}}_{0}a0​/R)8{)}^{8})8, where a0{\mathit{a}}_{0}a0​ is the atomic Bohr radius and \ensuremath{\alpha} is the fine-structure constant.
It is shown that in dielectrics exhibiting a complete photonic band gap, quantum electrodynamics predicts the occurrence of bound states of photons to hydrogenic atoms. When the atomic transition frequency lies near a photonic band edge, the excited atomic level experiences an anomalous Lamb shift and splits into a doublet. One member of this doublet exhibits resonance fluorescence whereas the other level is dressed by the emission and reabsorption of near-resonant photons whose amplitude decays exponentially from the vicinity of the atom.
Summary form only given. Unlike semiconductors which facilitate the coherent propagation of electrons, photonic band gap (PBG) materials execute their novel functions through the coherent localization of photons. When a PBG material is doped with impurity atoms which have an electronic transition that lies within the gap, spontaneous emission of light from the atom is inhibited. Inside the gap, the photon forms a bound state to the atom. Outside the gap, radiative dynamics in the colored vacuum is highly nonMarkovian. I discuss the influence of these memory effects on laser action. When spontaneous emission is absent, the next order radiative effect (resonance dipole-dipole interaction between atoms) must be incorporated, leading to anomalous nonlinear optical effects which occur at a much lower threshold than in ordinary vacuum. I describe the collective switching of two-level atoms near a photonic band edge, by external laser field, from a passive stare to one exhibiting population inversion. This effect is forbidden in ordinary vacuum. Finally, I discuss the prospects for a phase sensitive, single (3-level) atom quantum memory device, onto which information may be written by an external laser pulse. By scattering polarized photons (flying qubit) this system may execute certain quantum logic operations.
We study the resonance Raman scattering of light from a three-level atom embedded in a photonic band-gap material or in a frequency dispersive medium whose photon spectrum exhibits a gap due to photon coupling to medium excitations such as excitons and optical phonons. We demonstrate that the one-particle spectrum of the system consists of either a continuous part with energy lying outside the gap or a single discrete mode with energy lying inside the gap. The discrete mode, which occurs when both of the allowed atomic transitions of the $\ensuremath{\Lambda}$ configuration lie inside the gap, can be treated as a photon-atom bound state in which the radiation is localized in the vicinity of the atom. In the case of the continuous spectrum, the Rayleigh and Stokes lines are shifted as well as narrowed (or broadened) as the corresponding transition frequencies are shifted relative to the upper band edge, providing a distinctive experimental signature of atom-photon interactions near a photonic band edge.
Introduction The propagation of light in periodically ordered photonic crystals bears a strong analogy to the wave propagation of conduction electrons in atomic crystals. The development of Bloch modes and dispersion are determined by the interference of waves that are diffracted by lattice planes [19, 52]. The periodicity commensurate with the wavelength (a ≈ λ/2) gives rise to Bragg diffraction that is associated with frequency windows for which waves are forbidden to propagate in a particular direction. Such stop gaps have long been known to arise for electromagnetic waves, notably for X-rays in atomic crystals [214]. At optical frequencies, the stop gaps that occur in one-dimensional periodic structures, known as Bragg stacks, are widely used in optical laboratories as broadband highly reflecting dielectric mirrors [556]. The distinguishing feature of three-dimensional (3D) photonic crystals is that a common stop gap can be achieved for all directions and for all polarizations simultaneously: the widely pursued 3D photonic band gap . Historically a 3D band gap has never been considered for the propagation of X-rays in periodic media, since a gap requires a high refractive index contrast of order unity, whereas the refractive index varies by less then 10 −4 in the X-ray range. At frequencies inside the 3D photonic band gap, the density of optical states (DOS) completely vanishes. As the density of states can also be interpreted as the density of vacuum fluctuations [334], a 3D band gap thus serves as an effective shield to these fluctuations. The total absence of optical modes in a photonic band gap has implications beyond classical optics that break the analogy between the behavior of light in photonic crystals and the behavior of electrons in atomic crystals. 3D photonic band gap crystals play an important role in cavity quantum electrodynamics (cQED) [64, 549], where they offer at least five prospects for new physics. Firstly, probably the most eagerly pursued phenomenon is the complete inhibition of spontaneous emission: an excited quantum emitter – such as an atom, molecule, or quantum dot – embedded in a crystal with its transition frequency tuned to within the 3D band gap remains forever excited since it cannot decay to the ground state by emitting a photon.
We present a comprehensive quantum electrodynamical analysis of the interaction between a continuum with photonic band gaps (PBGs) or frequency cut-off and an excited two-level atom, which can be either ‘bare’ or ‘dressed’ by coupling to a near-resonant field mode. A diversity of novel features in the atom and field dynamics is shown to arise from the non-Markovian character of radiative decay into such a continuum of modes. Firstly the excited atom is shown to evolve, by spontaneous decay, into a superposition of non-decaying single-photon dressed states, each having an energy in a different PBG, and a decaying component. This superposition is determined by the atomic resonance shift, induced by the spontaneously emitted photon, into or out of a PBG. The main novel feature exhibited by the decaying excited-state component is the occurrence of beats between the shifted atomic resonance frequency and the PBG cut-off frequencies, corresponding to a non-Lorentzian emission spectrum. Secondly the induced decay of a resonantly driven atom into such a continuum exhibits a cascade of transitions down the ladder of dressed states, which are labelled by decreasing photon numbers of the driving mode. Remarkably, this cascade is terminated at the dressed-state doublet, from which all subsequent transitions to lower doublets are forbidden because they fall within the PBG. This doublet then becomes an attractor state for the populations of higher-lying doublets. As a result, the photon-number distribution of the driving mode becomes strongly sub-Poissonian.
Radiative coupling between identical atoms sharing an excitation is studied in media where dispersion creates photonic band gaps, i.e., forbidden bands of light propagation for all directions and polarizations. Photonic band gaps can exist in media whose dielectric index exhibits strong three-dimensionally periodic modulations (``photonic crystals'') or in bands of polaritonic media. It is shown that the resonant dipole-dipole interaction as well as cooperative fluorescence of two-atom systems can be strongly enhanced or suppressed, to the extent of being essentially eliminated, by one of the following mechanisms: (a) dependence on location of the atoms within a unit cell of a photonic crystal, i.e., sensitivity to the spatial variation of the field normal modes; (b) dependence on the density of normal modes in allowed bands and on the density of virtual (evanescent) modes in band gaps. The ability to suppress the dipole-dipole interactions at interatomic separations characterizing quasimolecules would have far-reaching implications on their dissociative or collisional dynamics, spectroscopy, and rates of energy transfer.