RESUMEN
Resonance fluorescence as the emission of a resonantly-excited two-level quantum system promises indistinguishable single photons and coherent high-fidelity quantum-state manipulation of the matter qubit, which underpin many quantum information processing protocols. Real applications of the protocols demand high degrees of scalability and stability of the experimental platform, and thus favor quantum systems integrated on one chip. However, the on-chip solution confronts several formidable challenges compromising the scalability prospect, such as the randomness, spectral wandering and scattering background of the integrated quantum systems near heterogeneous and nanofabricated material interfaces. Here we report an organic-inorganic hybrid integrated quantum photonic platform that circuits background-free resonance fluorescence of single molecules with an ultrastable lifetime-limited transition. Our platform allows a collective alignment of the dipole orientations of many isolated molecules with the photonic waveguide. We demonstrate on-chip generation, beam splitting and routing of resonance-fluorescence single photons with a signal-to-background ratio over 3000 in the waveguide at the weak excitation limit. Crucially, we show the photonic-circuited single molecules possess a lifetime-limited-linewidth transition and exhibit inhomogeneous spectral broadenings of only about 5% over hours' measurements. These findings and the versatility of our platform pave the way for scalable quantum photonic networks.
RESUMEN
Single nanoscopic emitters embedded in the crystalline matrix have become a valuable resource for emerging nanophotonics and quantum technologies. The generally anisotropic nature of the matrix strongly affects the emission properties of the quantum emitters, in particular, when the matrix is assembled in nanophotonic structures. We report on rigorous analysis and engineering of spontaneous emission from single emitters coupled to nanoantenna and planar anisotropic antenna structures. By developing a convenient theoretical method with efficient numerical implementation, we show that accurate modeling of the anisotropy is essential in predicting the emission pattern for many important systems, such as single molecules in the solid-state matrix, isolated defects in 2D materials and so on. In particular, we illustrate the amplified effects of material anisotropy and geometrical anisotropy for emitters coupled to planar antenna and nanoantenna structures. We show that with an appropriate design of the anisotropy, a strong enhancement of the emission rate and a nearly collimated beam from single emitters can be simultaneously achieved.
