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arXiv:cond-mat/0401332 · Physical Review B

Spontaneous-decay dynamics in atomically doped carbon nanotubes

Igor V. Bondarev, Ph. Lambin

Published Jul 15, 2004• 45 citations

Abstract

We report a strictly nonexponential spontaneous decay dynamics of an excited two-level atom placed inside or at different distances outside a carbon nanotube (CN). This is the result of strong non-Markovian memory effects arising from the rapid variation of the photonic density of states with frequency near the CN. The system exhibits vacuum-field Rabi oscillations, a principal signature of strong atom-vacuum-field coupling, when the atom is close enough to the nanotube surface and the atomic transition frequency is in the vicinity of the resonance of the photonic density of states. Caused by decreasing the atom-field coupling strength, the nonexponential decay dynamics gives place to the exponential one if the atom moves away from the CN surface. Thus, atom-field coupling and the character of the spontaneous decay dynamics, respectively, may be controlled by changing the distance between the atom and CN surface by means of a proper preparation of atomically doped CNs. This opens routes for new challenging nanophotonics applications of atomically doped CN systems as various sources of coherent light emitted by dopant atoms.

DOI: 10.1103/physrevb.70.035407

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We report a strictly nonexponential spontaneous decay dynamics of an excited two-level atom placed inside or at different distances outside a carbon nanotube (CN). This is the result of strong non-Markovian memory effects arising from the rapid variation of the photonic density of states with frequency near the CN. The system exhibits vacuum-field Rabi oscillations, a principal signature of strong atom-vacuum-field coupling, when the atom is close enough to the nanotube surface and the atomic transition frequency is in the vicinity of the resonance of the photonic density of states. Caused by decreasing the atom-field coupling strength, the nonexponential decay dynamics gives place to the exponential one if the atom moves away from the CN surface. Thus, atom-field coupling and the character of the spontaneous decay dynamics, respectively, may be controlled by changing the distance between the atom and CN surface by means of a proper preparation of atomically doped CNs. This opens routes for new challenging nanophotonics applications of atomically doped CN systems as various sources of coherent light emitted by dopant atoms.

Spontaneous decay process of an excited two-level atom placed inside or outside a single-wall carbon nanotube is analyzed for both weak and strong atom-radiation-field coupling regime. In the weak coupling regime, the effect of the nanotube surface has been demonstrated to dramatically increase the spontaneous decay rate -- by 4 to 5 orders of magnitude compared with that of the same atom in vacuum. Such an increase is associated with the nonradiative decay via surface quasiparticle excitations in the nanotube. In the strong coupling regime, the decay of the upper atomic state proceeds via damped Rabi oscillations with the frequency assigned by the density of final photonic states of the system. Possible applications of the effect predicted are discussed.

A theory of the spontaneous decay process of an excited atom placed inside or outside (near the surface) of a carbon nanotube has been developed. Numerical calculations of the atomic spontaneous decay enhancement factor have been performed for various achiral nanotubes. The effect of the nanotube surface has been demonstrated to dramatically increase the spontaneous decay rate—by 6–7 orders of magnitude—compared with that of the same atom in a vacuum. Such an increase is associated with nonradiative decay via surface excitations in the nanotube. Possible applications of the predicted effect are discussed.

Quantum optics phenomena, including light absorbtion and atomic states entanglement, are discussed for carbon nanotubes doped with atoms (ions). It has been shown that, similar to semiconductor microcavities and photonic band-gap materials, carbon nanotubes may qualitatively change the character of the atom-electromagnetic-field interactions, yielding strong atom-field coupling regime with the formation of quasi-one-dimensional atomic polaritons. These may be observed experimentally via the effect of the absorption line splitting (Rabi splitting) in the frequency range close to the atomic transition frequency. A scheme for entangling atomic polaritons is investigated using the photon Green function formalism for quantizing electromagnetic fields in the presence of quasi-one-dimensional absorbing and dispersing media. Small-diameter metallic nanotubes are shown to result in sizable amounts of the two-qubit atomic entanglement with no damping for sufficiently long times, thus challenging novel applications of atomically doped carbon nanotubes in quantum information science.

In this work we study the spontaneous emission of a two-level atom placed inside a hollow cylindrical waveguide of infinite length and with perfectly electric conducting walls. The atom, whose electric dipole moment is assumed to be oriented along the symmetry axis of the waveguide, couples to a photonic band structure with a non-linear dispersion relation. We address two different regimes of coupling between the atom and the photonic band structure. In particular, we refer to the regime where the internal frequency of the a.tom is close to a band edge as the strong coupling regime and to the regime where the internal frequency is far from a band edge as the weak coupling regime. In the weak coupling regime, we find that the a.tom decays exponentially with a modified decayed rate due to the presence of the waveguide, and that the line-shape of the emitted photons within every band takes the form of a Lorentzian. In the strong coupling regime, we find a non-exponential decay of the atom, which is due to non-Markovian dynamics of the system. Moreover, the population of the atom presents oscillations in time and it converges to a non-zero positive value, indicating that the a.tom never fully decays. In this regime the spectrum of the emitted photons becomes more involved.