Each natural mode of the electromagnetic field within a parabolic mirror exhibits spatial localization and polarization properties that can be exploited for the quantum control of its interaction with atomic systems. The region of localization is not restricted to the focus of the mirror leading to a selective response of atomic systems trapped on its vicinity. We report calculations of the spontaneous emission rates for an atom trapped inside the mirror accounting for all atomic polarizations and diverse trapping regions. It is shown that electric dipole transitions can be enhanced near the focus of a deep parabolic mirror with a clear identification of the few vectorial modes involved. Out of the focus the enhancement vanishes gradually, but the number of relevant modes remains small. Ultimately this represents a quantum electrodynamic system where internal and external degrees of freedom cooperate to maximize a selective exchange and detection of single excitations.
Focusing with a 4$pi$ parabolic mirror allows for concentrating light from nearly the complete solid angle, whereas focusing with a single microscope objective limits the angle cone used for focusing to half solid angle at maximum. Increasing the solid angle by using deep parabolic mirrors comes at the cost of adding more complexity to the mirrors fabrication process and might introduce errors that reduce the focusing quality. To determine these errors, we experimentally examine the focusing properties of a 4$pi$ parabolic mirror that was produced by single-point diamond turning. The properties are characterized with a single $^{174}$Yb$^{+}$ ion as a mobile point scatterer. The ion is trapped in a vacuum environment with a movable high optical access Paul trap. We demonstrate an effective focal spot size of 209 nm in lateral and 551 nm in axial direction. Such tight focusing allows us to build an efficient light-matter interface. Our findings agree with numerical simulations incorporating a finite ion temperature and interferometrically measured wavefront aberrations induced by the parabolic mirror. We point at further technological improvements and discuss the general scope of applications of a 4$pi$ parabolic mirror.
We investigate the emission of single photons from CdSe/CdS dot-in-rods which are optically trapped in the focus of a deep parabolic mirror. Thanks to this mirror, we are able to image almost the full 4$pi$ emission pattern of nanometer-sized elementary dipoles and verify the alignment of the rods within the optical trap. From the motional dynamics of the emitters in the trap we infer that the single-photon emission occurs from clusters comprising several emitters. We demonstrate the optical trapping of rod-shaped quantum emitters in a configuration suitable for efficiently coupling an ensemble of linear dipoles with the electromagnetic field in free space.
We study spontaneous emission from a rubidium atom into the fundamental and higher-order modes of a vacuum-clad ultrathin optical fiber. We show that the spontaneous emission rate depends on the magnetic sublevel, the type of modes, the orientation of the quantization axis, and the fiber radius. We find that the rate of spontaneous emission into the TE modes is always symmetric with respect to the propagation directions. Directional asymmetry of spontaneous emission into other modes may appear when the quantization axis does not lie in the meridional plane containing the position of the atom. When the fiber radius is in the range from 330 nm to 450 nm, the spontaneous emission into the HE$_{21}$ modes is stronger than into the HE$_{11}$, TE$_{01}$, and TM$_{01}$ modes. At the cutoff for higher-order modes, the rates of spontaneous emission into guided and radiation modes undergo steep variations, which are caused by the changes in the mode structure. We show that the spontaneous emission from the upper level of the cyclic transition into the TM modes is unidirectional when the quantization axis lies at an appropriate azimuthal angle in the fiber transverse plane.
We provide an estimate on the absolute values of the emission rate of photon pairs produced by spontaneous parametric down conversion in a bulk crystal when all interacting fields are in single transverse Gaussian modes. Both collinear and non-collinear configurations are covered, and we arrive at a fully analytical expression for the collinear case. Our results agree reasonably well with values found in typical experiments, which allows this model to be used for understanding the dependency on the relevant experimental parameters.
The polarizations of optical fields, besides field intensities, provide more degrees of freedom to manipulate coherent light-matter interactions. Here we propose how to achieve a coherent switch of optomechanical entanglement in a polarized-light-driven cavity system. We show that by tuning the polarizations of the driving field, the effective optomechanical coupling can be well controlled and, as a result, quantum entanglement between the mechanical oscillator and the optical transverse electric (TE) mode can be coherently and reversibly switched to that between the same phonon mode and the optical transverse magnetic (TM) mode. This ability of switching optomechanical entanglement with such a vectorial device can be important for building a quantum network being capable of efficient quantum information interchanges between processing nodes and flying photons.
R. Gutierrez-Jauregui
,R. Jauregui
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(2020)
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"Spontaneous transition rates near the focus of a parabolic mirror with identification of the vectorial modes involved"
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Ricardo Gutierrez-Jauregui
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