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Spontaneous emission of a sodium Rydberg atom close to an optical nanofibre

Erwan Stourm, Y Zhang, Maxence Lepers, R. Guérout, Jacques Robert, Síle Nic Chormaic, Klaus Mølmer, E. Brion

Published Jan 1, 2019• 11 citations
OpenAlex

Abstract

We report on numerical calculations of the spontaneous emission rate of a Rydberg-excited sodium atom in the vicinity of an optical nanofibre. In particular, we study how this rate varies with the distance of the atom to the fibre, the fibre's radius, the symmetry s or p of the Rydberg state as well as its principal quantum number. We find that a fraction of the spontaneously emitted light can be captured and guided along the fibre. This suggests that such a setup could be used for networking atomic ensembles, manipulated in a collective way due to the Rydberg blockade phenomenon.

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Spontaneous emission of a sodium Rydberg atom close to an optical nanofibre

Erwan Stourm, Y Zhang, Maxence Lepers +5 more

We report on numerical calculations of the spontaneous emission rate of a Rydberg-excited sodium atom in the vicinity of an optical nanofibre. In particular, we study how this rate varies with the distance of the atom to the fibre, the fibre's radius, the symmetry s or p of the Rydberg state as well as its principal quantum number. We find that a fraction of the spontaneously emitted light can be captured and guided along the fibre. This suggests that such a setup could be used for networking atomic ensembles, manipulated in a collective way due to the Rydberg blockade phenomenon.

arXiv:1810.06887•Journal of Physics B Atomic Molecular and Optical Physics•Jan 2, 2019•13 citations

Spontaneous emission and energy shifts of a Rydberg rubidium atom close to an optical nanofiber

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In this paper, we report on numerical calculations of the spontaneous emission rates and Lamb shifts of a $^{87}\mathrm{Rb}$ atom in a Rydberg-excited state $\left(n\ensuremath{\le}30\right)$ located close to a silica optical nanofiber. We investigate how these quantities depend on the fiber's radius, the distance of the atom to the fiber, the direction of the atomic angular momentum polarization, as well as the different atomic quantum numbers. We also study the contribution of quadrupolar transitions, which may be substantial for highly polarizable Rydberg states. Our calculations are performed in the macroscopic quantum electrodynamics formalism, based on the dyadic Green's function method. This allows us to take dispersive and absorptive characteristics of silica into account; this is of major importance since Rydberg atoms emit along many different transitions whose frequencies cover a wide range of the electromagnetic spectrum. Our work is an important initial step toward building a Rydberg atom-nanofiber interface for quantum optics and quantum information purposes.

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Abstract We consider two rubidium atoms, prepared in the same S or P Rydberg states, near an optical nanofibre, and we determine their van der Waals interaction potential as a function of their separation along the nanofibre axis, their distance to the nanofibre axis, and their relative azimuthal angle. We compare results obtained through direct diagonalisation of the Hamiltonian (including quadrupolar interaction terms) with second-order perturbation calculations, and we identify which couplings mainly contribute to the potential in the presence of the nanofibre and in free-space. We relate the appearance of new allowed couplings to the broken rotation symmetry around the interatomic axis due to the presence of the fibre. These couplings induce novel features and cause a reshaping of the interaction anisotropy and formation of an interaction potential well for P states near the nanofibre. Our work constitutes an important step in the assessment of Rydberg atom-nanofibre quantum interfaces and devices.

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We show that single atoms can be detected using a sub-wavelength-diameter silica-fibre, an optical nanofibre, and the fact that single photons spontaneously emitted from the atoms can be readily guided into a single-mode optical fibre. Moreover, we find that single atoms around the nanofibre reveal a very prominent spectral feature, that is, the excitation spectrum splits into two peaks with a very small separation, smaller than the natural linewidth.

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Interaction of two Rydberg atoms in the vicinity of an optical nanofibre

Erwan Stourm, Maxence Lepers, Jacques Robert +3 more

We consider two rubidium atoms, prepared in the same S or P Rydberg states, near an optical nanofibre, and we determine their van der Waals interaction potential as a function of their separation along the nanofibre axis, their distance to the nanofibre axis, and their relative azimuthal angle. We compare results obtained through direct diagonalisation of the Hamiltonian (including quadrupolar interaction terms) with second-order perturbation calculations, and we identify which couplings mainly contribute to the potential in the presence of the nanofibre and in free-space. We relate the appearance of new allowed couplings to the broken rotation symmetry around the interatomic axis due to the presence of the fibre. These couplings induce novel features and cause a reshaping of the interaction anisotropy and formation of an interaction potential well for P states near the nanofibre. Our work constitutes an important step in the assessment of Rydberg atom-nanofibre quantum interfaces and devices.

•Feb 16, 2023•0 citations
We report on numerical calculations of the spontaneous emission rate of a Rydberg-excited sodium atom in the vicinity of an optical nanofibre. In particular, we study how this rate varies with the distance of the atom to the fibre, the fibre's radius, the symmetry s or p of the Rydberg state as well as its principal quantum number. We find that a fraction of the spontaneously emitted light can be captured and guided along the fibre. This suggests that such a setup could be used for networking atomic ensembles, manipulated in a collective way due to the Rydberg blockade phenomenon.
We report on numerical calculations of the spontaneous emission rate of a Rydberg-excited sodium atom in the vicinity of an optical nanofibre. In particular, we study how this rate varies with the distance of the atom to the fibre, the fibre's radius, the symmetry s or p of the Rydberg state as well as its principal quantum number. We find that a fraction of the spontaneously emitted light can be captured and guided along the fibre. This suggests that such a setup could be used for networking atomic ensembles, manipulated in a collective way due to the Rydberg blockade phenomenon.
In this paper, we report on numerical calculations of the spontaneous emission rates and Lamb shifts of a 87Rb^{87}\mathrm{Rb}87Rb atom in a Rydberg-excited state $\left(n\ensuremath{\le}30\right)$ located close to a silica optical nanofiber. We investigate how these quantities depend on the fiber's radius, the distance of the atom to the fiber, the direction of the atomic angular momentum polarization, as well as the different atomic quantum numbers. We also study the contribution of quadrupolar transitions, which may be substantial for highly polarizable Rydberg states. Our calculations are performed in the macroscopic quantum electrodynamics formalism, based on the dyadic Green's function method. This allows us to take dispersive and absorptive characteristics of silica into account; this is of major importance since Rydberg atoms emit along many different transitions whose frequencies cover a wide range of the electromagnetic spectrum. Our work is an important initial step toward building a Rydberg atom-nanofiber interface for quantum optics and quantum information purposes.
Abstract We consider two rubidium atoms, prepared in the same S or P Rydberg states, near an optical nanofibre, and we determine their van der Waals interaction potential as a function of their separation along the nanofibre axis, their distance to the nanofibre axis, and their relative azimuthal angle. We compare results obtained through direct diagonalisation of the Hamiltonian (including quadrupolar interaction terms) with second-order perturbation calculations, and we identify which couplings mainly contribute to the potential in the presence of the nanofibre and in free-space. We relate the appearance of new allowed couplings to the broken rotation symmetry around the interatomic axis due to the presence of the fibre. These couplings induce novel features and cause a reshaping of the interaction anisotropy and formation of an interaction potential well for P states near the nanofibre. Our work constitutes an important step in the assessment of Rydberg atom-nanofibre quantum interfaces and devices.
We consider two rubidium atoms, prepared in the same S or P Rydberg states, near an optical nanofibre, and we determine their van der Waals interaction potential as a function of their separation along the nanofibre axis, their distance to the nanofibre axis, and their relative azimuthal angle. We compare results obtained through direct diagonalisation of the Hamiltonian (including quadrupolar interaction terms) with second-order perturbation calculations, and we identify which couplings mainly contribute to the potential in the presence of the nanofibre and in free-space. We relate the appearance of new allowed couplings to the broken rotation symmetry around the interatomic axis due to the presence of the fibre. These couplings induce novel features and cause a reshaping of the interaction anisotropy and formation of an interaction potential well for P states near the nanofibre. Our work constitutes an important step in the assessment of Rydberg atom-nanofibre quantum interfaces and devices.