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Bulletin of the American Physical Society

Control of multiple excited Rydberg states around segmented carbon nanotubes

Peter Schmelcher, H. R. Sadeghpour, Johannes Knörzer, Christian Fey

Published May 26, 2016• 0 citations
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Igor V. Bondarev, Gregory Ya. Slepyan, С. А. Максименко

The spontaneous decay process of an excited atom placed inside or outside a carbon nanotube is analyzed. Calculations have been performed for various achiral nanotubes. The effect of the nanotube surface is shown to increase the atomic spontaneous decay rate by up to 6 orders of magnitude compared with that of the same atom in vacuum. This increase is associated with nonradiative decay via surface excitations in the nanotube.

arXiv:cond-mat/0204433•Physical Review Letters•Aug 23, 2002•53 citations
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.