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Register a new userSuper-extended nanofiber-guided field for coherent interaction with hot atoms
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We fabricate an extremely thin optical fiber that supports a super-extended mode with a diameter as large as 13 times the optical wavelength, residing almost entirely outside the fiber and guided over thousands of wavelengths (5 mm), in order to couple guided light to warm atomic vapor. This unique configuration balances between strong confinement, as evident by saturation powers as low as tens of nW, and long interaction times with the thermal atoms, thereby enabling fast and coherent interactions. We demonstrate narrow coherent resonances (tens of MHz) of electromagnetically induced transparency for signals at the single-photon level and long relaxation times (10 ns) of atoms excited by the guided mode. The dimensions of the guided modes evanescent field are compatible with the Rydberg blockade mechanism, making this platform particularly suitable for observing quantum non-linear optics phenomena.
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We investigate the electric quadrupole interaction of an alkali-metal atom with guided light in the fundamental and higher-order modes of a vacuum-clad ultrathin optical fiber. We calculate the quadrupole Rabi frequency, the quadrupole oscillator strength, and their enhancement factors. In the example of a rubidium-87 atom, we study the dependencies of the quadrupole Rabi frequency on the quantum numbers of the transition, the mode type, the phase circulation direction, the propagation direction, the orientation of the quantization axis, the position of the atom, and the fiber radius. We find that the root-mean-square (rms) quadrupole Rabi frequency reduces quickly but the quadrupole oscillator strength varies slowly with increasing radial distance. We show that the enhancement factors of the rms Rabi frequency and the oscillator strength do not depend on any characteristics of the internal atomic states except for the atomic transition frequency. The enhancement factor of the oscillator strength can be significant even when the atom is far away from the fiber. We show that, in the case where the atom is positioned on the fiber surface, the oscillator strength for the quasicircularly polarized fundamental mode HE$_{11}$ has a local minimum at the fiber radius $asimeq 107$ nm, and is larger than that for quasicircularly polarized higher-order hybrid modes, TE modes, and TM modes in the region $a<498.2$ nm.
We experimentally study the ground state coherence properties of cesium atoms in a nanofiber-based two-color dipole trap, localized 200 nm away from the fiber surface. Using microwave radiation to coherently drive the clock transition, we record Ramsey fringes as well as spin echo signals and infer a reversible dephasing time $T_2^ast=0.6$ ms and an irreversible dephasing time $T_2^prime=3.7$ ms. By theoretically modelling the signals, we find that, for our experimental parameters, $T_2^ast$ and $T_2^prime$ are limited by the finite initial temperature of the atomic ensemble and the heating rate, respectively. Our results represent a fundamental step towards establishing nanofiber-based traps for cold atoms as a building block in an optical fiber quantum network.
We dispersively interface an ensemble of one thousand atoms trapped in the evanescent field surrounding a tapered optical nanofiber. This method relies on the azimuthally-asymmetric coupling of the ensemble with the evanescent field of an off-resonant probe beam, transmitted through the nanofiber. The resulting birefringence and dispersion are significant; we observe a phase shift per atom of $sim$,1,mrad at a detuning of six times the natural linewidth, corresponding to an effective resonant optical density per atom of 0.027. Moreover, we utilize this strong dispersion to non-destructively determine the number of atoms.
Photons are nonchiral particles: their handedness can be both left and right. However, when light is transversely confined, it can locally exhibit a transverse spin whose orientation is fixed by the propagation direction of the photons. Confined photons thus have chiral character. Here, we employ this to demonstrate nonreciprocal transmission of light at the single-photon level through a silica nanofibre in two experimental schemes. We either use an ensemble of spin-polarised atoms that is weakly coupled to the nanofibre-guided mode or a single spin-polarised atom strongly coupled to the nanofibre via a whispering-gallery-mode resonator. We simultaneously achieve high optical isolation and high forward transmission. Both are controlled by the internal atomic state. The resulting optical diode is the first example of a new class of nonreciprocal nanophotonic devices which exploit the chirality of confined photons and which are, in principle, suitable for quantum information processing and future quantum optical networks.
Optical nanofibers confine light to subwavelength scales, and are of interest for the design, integration, and interconnection of nanophotonic devices. Here we demonstrate high transmission (> 97%) of the first family of excited modes through a 350 nm radius fiber, by appropriate choice of the fiber and precise control of the taper geometry. We can design the nanofibers so that these modes propagate with most of their energy outside the waist region. We also present an optical setup for selectively launching these modes with less than 1% fundamental mode contamination. Our experimental results are in good agreement with simulations of the propagation. Multimode optical nanofibers expand the photonic toolbox, and may aid in the realization of a fully integrated nanoscale device for communication science, laser science or other sensing applications.
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