01980nas a2200193 4500008004100000245011000041210006900151260001500220520137500235100001801610700001601628700001401644700001501658700001301673700002501686700002001711700001801731856003701749 2019 eng d00aFloquet engineering of optical lattices with spatial features and periodicity below the diffraction limit0 aFloquet engineering of optical lattices with spatial features an c06/18/20193 a
Floquet engineering or coherent time periodic driving of quantum systems has been successfully used to synthesize Hamiltonians with novel properties. In ultracold atomic systems, this has led to experimental realizations of artificial gauge fields, topological band structures, and observation of dynamical localization, to name just a few. Here we present a Floquet-based framework to stroboscopically engineer Hamiltonians with spatial features and periodicity below the diffraction limit of light used to create them by time-averaging over various configurations of a 1D optical Kronig-Penney (KP) lattice. The KP potential is a lattice of narrow subwavelength barriers spaced by half the optical wavelength (λ/2) and arises from the non-linear optical response of the atomic dark state. Stroboscopic control over the strength and position of this lattice requires time-dependent adiabatic manipulation of the dark state spin composition. We investigate adiabaticity requirements and shape our time-dependent light fields to respect the requirements. We apply this framework to show that a λ/4-spaced lattice can be synthesized using realistic experimental parameters as an example, discuss mechanisms that limit lifetimes in these lattices, explore candidate systems and their limitations, and treat adiabatic loading into the ground band of these lattices.
1 aSubhankar, S.1 aBienias, P.1 aTitum, P.1 aTsui, T-C.1 aWang, Y.1 aGorshkov, Alexey, V.1 aRolston, S., L.1 aPorto, J., V. uhttps://arxiv.org/abs/1906.0764601379nas a2200217 4500008004100000245005600041210005400097520077800151100001600929700001800945700001300963700001400976700002200990700001501012700002001027700001401047700002001061700001801081700002501099856003701124 2018 eng d00aCoherent optical nano-tweezers for ultra-cold atoms0 aCoherent optical nanotweezers for ultracold atoms3 aThere has been a recent surge of interest and progress in creating subwavelength free-space optical potentials for ultra-cold atoms. A key open question is whether geometric potentials, which are repulsive and ubiquitous in the creation of subwavelength free-space potentials, forbid the creation of narrow traps with long lifetimes. Here, we show that it is possible to create such traps. We propose two schemes for realizing subwavelength traps and demonstrate their superiority over existing proposals. We analyze the lifetime of atoms in such traps and show that long-lived bound states are possible. This work opens a new frontier for the subwavelength control and manipulation of ultracold matter, with applications in quantum chemistry and quantum simulation.
1 aBienias, P.1 aSubhankar, S.1 aWang, Y.1 aTsui, T-C1 aJendrzejewski, F.1 aTiecke, T.1 aJuzeliūnas, G.1 aJiang, L.1 aRolston, S., L.1 aPorto, J., V.1 aGorshkov, Alexey, V. uhttps://arxiv.org/abs/1808.0248701556nas a2200217 4500008004100000245006300041210006300104260001500167300001100182490000800193520094300201100002401144700001601168700001801184700001901202700001801221700002501239700002001264700001801284856003601302 2016 eng d00aAnomalous broadening in driven dissipative Rydberg systems0 aAnomalous broadening in driven dissipative Rydberg systems c2016/03/16 a1130010 v1163 aWe observe interaction-induced broadening of the two-photon 5s-18s transition in 87Rb atoms trapped in a 3D optical lattice. The measured linewidth increases by nearly two orders of magnitude with increasing atomic density and excitation strength, with corresponding suppression of resonant scattering and enhancement of off-resonant scattering. We attribute the increased linewidth to resonant dipole-dipole interactions of 18s atoms with spontaneously created populations of nearby np states. Over a range of initial atomic densities and excitation strengths, the transition width is described by a single function of the steady-state density of Rydberg atoms, and the observed resonant excitation rate corresponds to that of a two-level system with the measured, rather than natural, linewidth. The broadening mechanism observed here is likely to have negative implications for many proposals with coherently interacting Rydberg atoms.1 aGoldschmidt, E., A.1 aBoulier, T.1 aBrown, R., C.1 aKoller, S., B.1 aYoung, J., T.1 aGorshkov, Alexey, V.1 aRolston, S., L.1 aPorto, J., V. uhttp://arxiv.org/abs/1510.08710