No Arabic abstract
Ordered ensembles of atoms, such as atomic arrays, exhibit distinctive features from their disordered counterpart. In particular, while collective modes in disordered ensembles show a linear optical response, collective subradiant excitations of subwavelength arrays are endowed with an intrinsic non-linearity. Such non-linearity has both a coherent and a dissipative component: two excitations propagating in the array scatter off each other leading to formation of correlations and to emission into free space modes. We show how to take advantage of such non-linearity to coherently prepare a single excitation in a subradiant (dark) collective state of a one dimensional array as well as to perform an entangling operation on dark states of parallel arrays. We discuss the main source of errors represented by disorder introduced by atomic center-of-mass fluctuations, and we propose a practical way to mitigate its effects.
We determine the transmission of light through a planar atomic array beyond the limit of low light intensity that displays optical bistability in the mean-field regime. We develop a theory describing the intrinsic optical bistability, which is supported purely by resonant dipole-dipole interactions in free space, showing how bistable light amplitudes exhibit both strong cooperative and weak single-atom responses and how they depend on the underlying low light intensity collective excitation eigenmodes. Similarities of the theory with optical bistability in cavities are highlighted, while recurrent light scattering between atoms takes on the role of cavity mirrors. Our numerics and analytic estimates show a sharp variation in the extinction, reflectivity, and group delays of the array, with the incident light completely extinguished up to a critical intensity well beyond the low light intensity limit. Our analysis paves a way for collective nonlinear optics with cooperatively responding dense atomic ensembles.
We report on a simple method to prepare optical pulses with exponentially rising envelope on the time scale of a few ns. The scheme is based on the exponential transfer function of a fast transistor, which generates an exponentially rising envelope that is transferred first on a radio frequency carrier, and then on a coherent cw laser beam with an electro-optical phase modulator (EOM). The temporally shaped sideband is then extracted with an optical resonator and can be used to efficiently excite a single Rb-87 atom.
Improving the precision of measurements is a significant scientific challenge. The challenge is twofold: first, overcoming noise that limits the precision given a fixed amount of a resource, N, and second, improving the scaling of precision over the standard quantum limit (SQL), 1/sqrt{N}, and ultimately reaching a Heisenberg scaling (HS), 1/N. Here we present and experimentally implement a new scheme for precision measurements. Our scheme is based on a probe in a mixed state with a large uncertainty, combined with a post-selection of an additional pure system, such that the precision of the estimated coupling strength between the probe and the system is enhanced. We performed a measurement of a single photons Kerr non-linearity with an HS, where an ultra-small Kerr phase of around 6 *10^{-8} rad was observed with an unprecedented precision of around 3.6* 10^{-10} rad. Moreover, our scheme utilizes an imaginary weak-value, the Kerr non-linearity results in a shift of the mean photon number of the probe, and hence, the scheme is robust to noise originating from the self-phase modulation.
A setup to frequency-convert an arbitrary image encoded in the spatial profile of a probe field onto a signal field using four-wave mixing in a thermal atom vapor is proposed. The atomic motion is exploited to cancel diffraction of both signal and probe fields simultaneously. We show that an incoherent probe field can be used to enhance the transverse momentum bandwidth which can be propagated without diffraction, such that smaller structures with higher spatial resolution can be transmitted. It furthermore compensate linear absorption with non-linear gain, to improve the four-wave mixing performance since the propagation dynamics of the various field intensities is favorably modified.
We propose an efficient free-space scheme to create single photons in a well-defined spatiotemporal mode. To that end, we first prepare a single source atom in an excited Rydberg state. The source atom interacts with a large ensemble of ground-state atoms via a laser-mediated dipole-dipole exchange interaction. Using an adiabatic passage with a chirped laser pulse, we produce a spatially extended spin wave of a single Rydberg excitation in the ensemble, accompanied by the transition of the source atom to another Rydberg state. The collective atomic excitation can then be converted to a propagating optical photon via a coherent coupling field. In contrast to previous approaches, our single-photon source does not rely on the strong coupling of a single emitter to a resonant cavity, nor does it require the heralding of collective excitation or complete Rydberg blockade of multiple excitations in the atomic ensemble.