The novel effect of self-excitation of an atomic beam propagating above a metal surface is predicted and a theory is developed. Its underlying mechanism is positive feedback provided by the reflective surface for the atomic polarization. Under certain conditions the atomic beam flying in the near field of the metal surface acts as an active device that supports sustained atomic dipole oscillations, which generate, in their turn, an electromagnetic field. This phenomenon does not exploit stimulated emission and therefore does not require population inversion in atoms. An experiment with Rydberg atoms in which this effect should be most pronounced is proposed and the necessary estimates are given.
The novel effect of self-excitation of an atomic beam propagating above a metal surface is predicted and a theory is developed. Its underlying mechanism is positive feedback provided by the reflective surface for the atomic polarization. Under certain conditions the atomic beam flying in the near field of the metal surface acts as an active device that supports sustained atomic dipole oscillations, which generate, in their turn, an electromagnetic field. This phenomenon does not exploit stimulated emission and therefore does not require population inversion in atoms. An experiment with Rydberg atoms in which this effect should be most pronounced is proposed and the necessary estimates are given.
We study the optomechanical coupling of a oscillating effective mirror with a Rydberg atomic gas, mediated by the dynamical atom-mirror Casimir-Polder force. This coupling may produce a near-field resonant atomic excitation whose probability scales as ∝(d(2)an(4)t)(2)/z(0)(8), where z(0) is the average atom-surface distance, d the atomic dipole moment, a the mirror's effective oscillation amplitude, n the initial principal quantum number, and t the time. We propose an experimental configuration to realize this system with a cold atom gas trapped at a distance ∼2×10 μm from a semiconductor substrate whose dielectric constant is periodically driven by an external laser pulse, hence realizing an effective mechanical mirror motion due to the periodic change of the substrate from transparent to reflecting. For a parabolic gas shape, this effect is predicted to excite about ∼10(2) atoms of a dilute gas of 10(3) trapped Rydberg atoms with n=75 after about 0.5 μs, which is high enough to be detected in typical Rydberg gas experimental conditions.
A theory of evanescent mode atomic mirrors utilising a metallic sheet on a dielectric substrate is described. The emphasis here is on the role of the metallic sheet and on the evaluation of atomic trajectories using the field- dipole orientation picture. At low intensity, the atomic reflection process is controlled by two separate mechanisms both of which are modified by the presence of the metallic sheet and influenced by the use of the field-dipole orientation picture. The first mechanism involves the spontaneous force which accelerates the atom parallel to the sheet plane. The second mechanism involves the combined dipole plus van der Waals force which acts to repel the atom from the surface, decelerating its motion until it attains an instantaneous halt before changing direction away from the surface at an appr opriate turning point in the trajectory. Various quantitative features arising from varying the controllable parameters of the system, including screening effects as well as desirable enhancement effects, are pointed out and discussed.
This thesis reports the first controlled study of the interactions of Rydberg atoms with a metal surface. In these experiments, a collimated beam of potassium Rydberg atoms is directed at a plane surface at near grazing incidence. Positive ions formed by surface ionization are attracted to the surface by their image charge, which is counterbalanced by an external electric field applied perpendicular to the surface. The ions are detected by a position-sensitive detector (PSD). At some critical value of the external field, the ion trajectories just miss the surface, suggesting that analysis of the dependence of the ion signals on external electric field can be used to determine the distance from the surface at which ionization occurs. This distance, and thus the corresponding critical electric field, is expected to be n-dependent. Experimentally, however, it was observed that the ion signal had a sudden n-independent onset when only a small positive perpendicular electric field was applied at the surface. This observation requires, surprisingly, that the ions produced by surface ionization can readily escape from the surface. The data do, however, show that Rydberg atoms are efficiently ionized in collisions with the surface. This process may provide a useful new detection technique for Rydberg atoms.
Highly excited (Rydberg) atoms have exaggerated properties making them extremely sensitive to external electromagnetic fields and interacting strongly with their environment. Atomic vapor cells represent an attractive platform for studying Rydberg atoms and fabricating quantum devices. For example, Rydberg atoms in vapor cells have been used as sensitive detectors of electric fields of frequencies ranging from DC up to the THz range but also as single photon sources for quantum technology applications exploiting collective phenomena due to the Rydberg blockade effect [1]. Rydberg atoms also find applications in fundamental physics, in particular for the measurement of dispersive interactions of the Casimir-Polder type (atom-surface interactions) [2]. One major advantage of Rydberg atoms is that they expose limitations in the traditional perturbative approach of Casimir-Polder (CP) theory [3, 4]. Indeed, in the extreme near-field, the dipole approximation breaks down and higher-order terms need to be considered. We report on extensive experimental measurements of the Rydberg-surface interaction using spectroscopy in cesium vapor nanocells of a thickness ranging roughly from 200-700nm, as well as selective reflection spectroscopy on a macroscopic cesium all-sapphire cell. Atoms are first excited to the Cs(6P) level with a 894nm pump laser and subsequently a green laser ≈ 510nm probes Rydberg nD or nS states, where the principal quantum number n ranges between 15-17. Our experiments evidence the dipole-dipole term of the Casimir-Polder interaction providing a measurement of the C3 coefficient for cesium Rydberg states. Furthermore, our experiment clearly evidences an additional interaction that induces shifts and broadens the linewidth of the probed transitions in the vicinity of the dielectric windows of our cells. We believe that this interaction is due to electric fields that are either generated by patch charges (trapped on the surface or induced by the excitation lasers), or by cesium adsorbants. We show that the different polarizability (of opposing sign) between S and D Rydberg states can be exploited to extract quantitative measurements of the strength and distance scaling (z-dependence) of such parasitic electrostatic interactions.Our experiments suggest that the sensitivity of Rydberg atoms to external electric fields could provide a unique tool for probing electrostatic interactions in the vicinity of surfaces. This could allow systematic error corrections in Casimir-Polder experiments with excited or even ground state atoms that aim at putting bounds on the existence of non-Newtonian gravity [5]. We are currently exploring the possibility of coating the internal window interfaces with conducting 2D material such as graphene to reduce the influence of parasitic charges. This could allow us to probe atoms closer to the surface, where quadrupole interactions could be experimentally attainable for the first time [4].References[1] H. Kubler, J. P. Shaffer, T. Baluktsian, R. Loew, T. Pfau, Nat. Photon., 4, 112–116 (2013).[2] V. Sandoghdar et al., Phys. Rev. Lett 68, 3432–3435 (1993).[3] J. A. Crosse et al., Phys. Rev. A 82, 3010901 (2010).[4] B. Dutta et al., Phys. Rev. Res. 6, L022035 (2024).[5] A. Laliotis, B-S. Lu, M. Ducloy, D. Wilkowski, AVS Quantum Sci. 3, 043501 (2021).
It is shown that spontaneous emission of an excited atom is suppressed, and electromagnetic instability of the ground state is possible, if an atom is located in the vicinity of an active medium which amplifies the propagating radiation. The effect is due to a modified and phase-shifted near field of an oscillating atomic dipole, which prevails over the usual radiation reaction field related to the wave zone. The necessary conditions for the reversal of the total electromagnetic back reaction are found, and possible experimental realizations are discussed.
A theory of lasing in an optically thin layer of active centers disposed at a metal surface is developed from first principles. The approach is based on a rigorous account of the local field in the close vicinity of a reflective surface, which provides feedback for dipole oscillations in active centers. It is demonstrated that the gain medium thickness plays a crucial role in the lasing condition and controls switching from conventional lasing to lasing without inversion. The numerical calculations are carried out for erbium doped glass bordering a gold surface where radiation at telecom wavelength (1532 nm) can be generated.