A two-level atom cannot emit more than one photon at a time. As early as the 1980s, this quantum feature was identified as a gateway to "single-photon sources", where a regular excitation sequence would create a stream of light particles with photon number fluctuations below the shot noise [1]. Such an intensity squeezed beam of light would be desirable for a range of applications such as quantum imaging, sensing, enhanced precision measurements and information processing [2,3]. However, experimental realizations of these sources have been hindered by large losses caused by low photon collection efficiencies and photophysical shortcomings. By using a planar metallo-dielectric antenna applied to an organic molecule, we demonstrate the most regular stream of single photons reported to date. Measured intensity fluctuations reveal 2.2 dB squeezing limited by our detection efficiency, equivalent to 6.2 dB intensity squeezing right after the antenna.Single-photon sources (SPS) have attracted a great deal of attention in the past two decades. One of the common methods for generating single photons is based on parametric down conversion in nonlinear materials, whereby a pair of photons are produced and separated using spectral, spatial, or polarization filters. Advantages of this approach are its large wavelength tunability and the possibility to herald the detection of one photon by the other one of the pair. However, the emission statistics in this method remains Poissonian, and it cannot produce single photons on demand.To exclude the generation of two simultaneous photons, and more importantly, to achieve deterministic production of single photons at a given time, the antibunched radiation of an isolated quantum emitter offers the best choice [4][5][6]. However, so far random losses in the emission, collection, and detection processes have made it impossible to register one single photon at a particular time [7], so that the common terminologies of "single-photon" source or photon "gun" used in the literature greatly fall short of their expectations.Three sources of loss have to be controlled. First, photophysical losses caused by a non-unity quantum efficiency (e.g. for color centers [8]) or unforseeable transitions to dark states (e.g. in colloidal quantum dots [9]) spoil a deterministic emission. Second, it is a great challenge to collect all the photons, which are usually emitted in a nearly isotropic fashion. Third, the quantum efficiency of the detectors and losses in the optical path limit the final performance. Here, we present a substantial progress in remedying these issues by using single organic molecules with very high quantum efficiency as emitter, optimizing the excitation pulse scheme, careful choice of the optical elements, and employing a new design of metallo-dielectric antennas [10, 11].1 arXiv:1608.07980v1 [quant-ph]