No Arabic abstract
We formulate a theory of slow polaritons in atomic gases and apply it to the slowing down, storing, and redirecting of laser pulses in an EIT medium. The normal modes of the coupled matter and radiation are determined through a full diagonalization of the dissipationless Hamiltonian. Away from the EIT resonance where the polaritons acquire an excited-state contribution, lifetimes are introduced as a secondary step. With detuning included various four-wave mixing possibilities are analyzed. We investigate specifically the possibility of reverting a stopped polariton by reversing the control beam.
Coherent diffusion pertains to the motion of atomic dipoles experiencing frequent collisions in vapor while maintaining their coherence. Recent theoretical and experimental studies on the effect of coherent diffusion on key Raman processes, namely Raman spectroscopy, slow polariton propagation, and stored light, are reviewed in this Colloquium.
We describe a new type of spatially periodic structure (lattice models): a polaritonic crystal (PolC) formed by a two-dimensional lattice of trapped two-level atoms interacting with quantised electromagnetic field in a cavity (or in a one-dimensional array of tunnelling-coupled microcavities), which allows polaritons to be fully localised. Using a one-dimensional polaritonic crystal as an example, we analyse conditions for quantum degeneracy of a low-branch polariton gas and those for quantum optical information recording and storage.
We study systems of fully polarized ultracold atomic gases obeying Fermi statistics. The atomic transition interacts dispersively with a mode of a standing-wave cavity, which is coherently pumped by a laser. In this setup, the intensity of the intracavity field is determined by the refractive index of the atomic medium, and thus by the atomic density distribution. Vice versa, the density distribution of the atom is determined by the cavity field potential, whose depth is proportional to the intracavity field amplitude. In this work we show that this nonlinearity leads to an instability in the intracavity intensity that differs substantially from dispersive optical bistability, as this effect is already present in the regime, where the atomic dipole is proportional to the cavity field. Such instability is driven by the matter waves fluctuations and exhibits a peculiar dependence on the fluctuations in the atomic density distribution.
We investigate the sympathetic relaxation of a free-standing, vibrating carbon nano-tube that is mounted on an atom chip and is immersed in a cloud of ultra-cold atoms. Gas atoms colliding with the nano-tube excite phonons via a Casimir-Polder potential. We use Fermis Golden Rule to estimate the relaxation rates for relevant experimental parameters and develop a fully dynamic theory of relaxation for the multi-mode phononic field embedded in a thermal atomic reservoir. Based on currently available experimental data, we identify the relaxation rates as a function of atom density and temperature that are required for sympathetic ground state cooling of carbon nano-tubes.
Light-induced states are commonly observed in the photoionization spectra of laser-dressed atoms. The properties of autoionizing polaritons, entangled states of light and Auger resonances, however, are largely unexplored. We employ attosecond transient-absorption spectroscopy to study the evolution of autoionizing states in argon, dressed by a tunable femtosecond laser pulse. The avoided crossings between the $3s^{-1}4p$ and several light-induced states indicates the formation of polariton multiplets. We measure a controllable stabilization of the polaritons against ionization, in excellent agreement with emph{ab initio} theory. Using an extension of the Jaynes-Cummings model to autoionizing states, we show that this stabilization is due to the destructive interference between the Auger decay and the radiative ionization of the polaritonic components. These results give new insights into the optical control of electronic structure in the continuum, and unlock the door to applications of autoionizing polaritons in poly-electronic systems.