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Register a new userQuantum coherence between two atoms beyond Q=10^15
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We place two atoms in quantum superposition states and observe coherent phase evolution for 3.4x10^15 cycles. Correlation signals from the two atoms yield information about their relative phase even after the probe radiation has decohered. This technique was applied to a frequency comparison of two Al+ ions, where a fractional uncertainty of 3.7+1.0-0.8x10^-16/sqrt{tau/s} was observed. Two measures of the Q-factor are reported: The Q-factor derived from quantum coherence is 3.4+2.4-1.1x10^16, and the spectroscopic Q-factor for a Ramsey time of 3 s is 6.7x10^15. As part of this experiment, we demonstrate a method to detect the individual quantum states of two Al+ ions in a Mg+-Al+-Al+ linear ion chain without spatially resolving the ions.
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We demonstrate experimentally that a single Rb atom excited to the $79d_{5/2}$ level blocks the subsequent excitation of a second atom located more than $10 murm m$ away. The observed probability of double excitation of $sim 30%$ is consistent with a theoretical model based on calculations of the long range dipole-dipole interaction between atoms.
We study the photonic interactions between two distant atoms which are coupled by an optical element (a lens or an optical fiber) focussing part of their emitted radiation onto each other. Two regimes are distinguished depending on the ratio between the radiative lifetime of the atomic excited state and the propagation time of a photon between the two atoms. In the two regimes, well below saturation the dynamics exhibit either typical features of a bad resonator, where the atoms act as the mirrors, or typical characteristics of dipole-dipole interaction. We study the coherence properties of the emitted light and show that it carries signatures of the multiple scattering processes between the atoms. The model predictions are compared with the experimental results in J. Eschner {it et al.}, Nature {bf 413}, 495 (2001).
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.
As a physically motivated and computationally simple model for cold atomic and molecular collisions, the multichannel quantum defect theory (MQDT) with frame transformation (FT) formalism provides an analytical treatment of scattering resonances in an arbitrary partial wave between alkali-metal atoms, leading to the experimental observation of $p-$ and $d-$wave resonances. However, the inconsistency of quantum defects for describing scattering resonances shows up when compared with experiments. Here, with two heteronuclear atoms in the ground state of an optical tweezer, the energy dependence of quantum defects is obviously revealed by comparing the measured s-wave scattering length with the prediction of MQDT-FT. By dividing the quantum defects into energy sensitive and insensitive categories, the inconsistency is ultimately removed while retaining the analytic structure of MQDT-FT. This study represents a significant improvement in the analytical MQDT-FT and demonstrates that a clean two-particle system is valuable to the test of collisional physics.
Over the past few years we have built an apparatus to demonstrate the entanglement of neutral Rb atoms at optically resolvable distances using the strong interactions between Rydberg atoms. Here we review the basic physics involved in this process: loading of single atoms into individual traps, state initialization, state readout, single atom rotations, blockade-mediated manipulation of Rydberg atoms, and demonstration of entanglement.
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