We calculate the force of a near-resonant guided light field of an ultrathin optical fiber on a two-level atom. We show that, if the atomic dipole rotates in the meridional plane, the magnitude of the force of the guided light depends on the field propagation direction. The chirality of the force arises as a consequence of the directional dependencies of the Rabi frequency of the guided driving field and the spontaneous emission from the atom. This provides a unique method for controlling atomic motion in the vicinity of an ultrathin fiber.
We calculate analytically and numerically the axial orbital and spin torques of guided light on a two-level atom near an optical nanofiber. We show that the generation of these torques is governed by the angular momentum conservation law in the Minkowski formulation. The orbital torque on the atom near the fiber has a contribution from the average recoil of spontaneously emitted photons. Photon angular momentum and atomic spin angular momentum can be converted into atomic orbital angular momentum. The orbital and spin angular momenta of the guided field are not transferred separately to the orbital and spin angular momenta of the atom.
We study the force of light on a two-level atom near an ultrathin optical fiber using the mode function method and the Green tensor technique. We show that the total force consists of the driving-field force, the spontaneous-emission recoil force, and the fiber-induced van der Waals potential force. Due to the existence of a nonzero axial component of the field in a guided mode, the Rabi frequency and, hence, the magnitude of the force of the guided driving field may depend on the propagation direction. When the atomic dipole rotates in the meridional plane, the spontaneous-emission recoil force may arise as a result of the asymmetric spontaneous emission with respect to opposite propagation directions. The van der Waals potential for the atom in the ground state is off-resonant and opposite to the off-resonant part of the van der Waals potential for the atom in the excited state. Unlike the potential for the ground state, the potential for the excited state may oscillate depending on the distance from the atom to the fiber surface.
Between mirrors, the density of electromagnetic modes differs from the one in free space. This changes the radiation properties of an atom as well as the light forces acting on an atom. It has profound consequences in the strong-coupling regime of cavity quantum electrodynamics. For a single atom trapped inside the cavity, we investigate the atom-cavity system by scanning the frequency of a probe laser for various atom-cavity detunings. The avoided crossing between atom and cavity resonance is visible in the transmission of the cavity. It is also visible in the loss rate of the atom from the intracavity dipole trap. On the normal-mode resonances, the dominant contribution to the loss rate originates from dipole-force fluctuations which are dramatically enhanced in the cavity. This conclusion is supported by Monte-Carlo simulations.
In the work, the thermal and vacuum fluctuation is predicted capable of generating a Casimir thrust force on a rotating chiral particle, which will push or pull the particle along the rotation axis. The Casimir thrust force comes from two origins: i) the rotation-induced symmetry-breaking in the vacuum and thermal fluctuation and ii) the chiral cross-coupling between electric and magnetic fields and dipoles, which can convert the vacuum spin angular momentum (SAM) to the vacuum force. Using the fluctuation dissipation theorem (FDT), we derive the analytical expressions for the vacuum thrust force in dipolar approximation and the dependences of the force on rotation frequency, temperature and material optical properties are investigated. The work reveals a new mechanism to generate a vacuum force, which opens a new way to exploit zero-point energy of vacuum.
We study the spontaneous emission of an excited atom close to an optical nanofiber and the resulting scattering forces. For a suitably chosen orientation of the atomic dipole, the spontaneous emission pattern becomes asymmetric and a resonant Casimir--Polder force parallel to the fiber axis arises. For a simple model case, we show that the such a lateral force is due to the interaction of the circularly oscillating atomic dipole moment with its image inside the material. With the Casimir--Polder energy being constant in the lateral direction, the predicted lateral force does not derive from a potential in the usual way. Our results have implications for optical force measurements on a substrate as well as for laser cooling of atoms in nanophotonic traps.