Using a nanomanipulation technique a nanodiamond with a single nitrogen vacancy center is placed directly on the surface of a gallium phosphide photonic crystal cavity.A Purcell-enhancement of the fluorescence emission at the zero phonon line (ZPL) by a factor of 12.1 is observed. The ZPL coupling is a first crucial step towards future diamond-based integrated quantum optical devices.

An alignment free, micrometer-scale single photon source consisting of a single quantum emitter on an optical fiber operating at room temperature is demonstrated. It easily integrates into fiber optic networks for quantum cryptography or quantum metrology applications.(1) Near-field coupling of a single nitrogen-vacancy center is achieved in a bottom-up approach by placing a preselected nanodiamond directly on the fiber facet. Its high photon collection efficiency is equivalent to a far-field collection via an objective with a numerical aperture of 0.82. Furthermore, simultaneous excitation and re-collection through the fiber is possible by introducing a fiber-connected single emitter sensor.

Integrated quantum optical hybrid devices consist of fundamental constituents such as single emitters and tailored photonic nanostructures. A reliable fabrication method requires the controlled deposition of active nanoparticles on arbitrary nanostructures with highest precision. Here, we describe an easily adaptable technique that employs picking and placing of nanoparticles with an atomic force microscope combined with a confocal setup. In this way, both the topography and the optical response can be monitored simultaneously before and after the assembly. The technique can be applied to arbitrary particles. Here, we focus on nanodiamonds containing single nitrogen vacancy centers, which are particularly interesting for quantum optical experiments on the single photon and single emitter level.

We introduce a theory to analyze the behavior of light emitters in nanostructured environments rigorously. Based on spectral theory, the approach opens the possibility to quantify precisely how an emitter decays to resonant states of the structure and how it couples to a background, also in the presence of general dispersive media. Quantification on this level is essential for designing and analyzing topical nanophotonic setups, e.g., in quantum technology applications. We use a numerical implementation of the theory for computing modal and background decay rates of a single-photon emitter in a diamond nanoresonator.

Single photon emi ers in two-dimensional materials are promising candidates for future generation of quantum photonic technologies. In this work, we experimentally determine the quantum e ciency (QE) of single photon emi ers (SPE) in few-layer hexagonal boron nitride (hBN). We employ a metal hemisphere that is attached to the tip of an atomic force microscope to directly measure the lifetime variation of the SPEs as the tip approaches the hBN. is technique enables non-destructive, yet direct and absolute measurement of the QE of SPEs. We nd that the emi ers exhibit very high QEs approaching (87 ± 7) % at wavelengths of ≈ 580 nm, which is amongst the highest QEs recorded for a solid state single photon emi er.