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The generation and manipulation of entanglement between isolated particles has precipitated rapid progress in quantum information processing. Entanglement is also known to play an essential role in the optical properties of atomic ensembles, but fundamental effects in the controlled emission and absorption from small, well-defined numbers of entangled emitters in free space have remained unobserved. Here we present the control of the spontaneous emission rate of a single photon from a pair of distant, entangled atoms into a free-space optical mode. Changing the length of the optical path connecting the atoms modulates the emission rate with a visibility $V = 0.27 pm 0.03$ determined by the degree of entanglement shared between the atoms, corresponding directly to the concurrence $mathcal{C_{rho}}= 0.31 pm 0.10$ of the prepared state. This scheme, together with population measurements, provides a fully optical determination of the amount of entanglement. Furthermore, large sensitivity of the interference phase evolution points to applications of the presented scheme in high-precision gradient sensing.
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
We present a novel approach to engineer the photon correlations emerging from the interference between an input field and the field scattered by a single atom in free space. Nominally, the inefficient atom-light coupling causes the quantum correlatio
Photon interference among distant quantum emitters is a promising method to generate large scale quantum networks. Interference is best achieved when photons show long coherence times. For the nitrogen-vacancy defect center in diamond we measure the
We investigate the emission of single photons from CdSe/CdS dot-in-rods which are optically trapped in the focus of a deep parabolic mirror. Thanks to this mirror, we are able to image almost the full 4$pi$ emission pattern of nanometer-sized element
A diamond nano-crystal hosting a single nitrogen vacancy (NV) center is optically selected with a confocal scanning microscope and positioned deterministically onto the subwavelength-diameter waist of a tapered optical fiber (TOF) with the help of an