No Arabic abstract
The nitrogen-vacancy (NV) center in diamond has been established as a prime building block for quantum networks. However, scaling beyond a few network nodes is currently limited by low spin-photon entanglement rates, resulting from the NV centers low probability of coherent photon emission and collection. Integration into a cavity can boost both values via the Purcell effect, but poor optical coherence of near-surface NV centers has so far prevented their resonant optical control, as would be required for entanglement generation. Here, we overcome this challenge, and demonstrate resonant addressing of individual, fiber-cavity-coupled NV centers, and collection of their Purcell-enhanced coherent photon emission. Utilizing off-resonant and resonant addressing protocols, we extract Purcell factors of up to 4, consistent with a detailed theoretical model. This model predicts that the probability of coherent photon detection per optical excitation can be increased to 10% for realistic parameters - an improvement over state-of-the art solid immersion lens collection systems by two orders of magnitude. The resonant operation of an improved optical interface for single coherent quantum emitters in a closed-cycle cryogenic system at T $sim$ 4 K is an important result towards extensive quantum networks with long coherence.
Optical microcavities are a powerful tool to enhance spontaneous emission of individual quantum emitters. However, the broad emission spectra encountered in the solid state at room temperature limit the influence of a cavity, and call for ultra-small mode volume. We demonstrate Purcell-enhanced single photon emission from nitrogen-vacancy (NV) centers in nanodiamonds coupled to a tunable fiber-based microcavity with a mode volume down to $1.0,lambda^{3}$. We record cavity-enhanced fluorescence images and study several single emitters with one cavity. The Purcell effect is evidenced by enhanced fluorescence collection, as well as tunable fluorescence lifetime modification, and we infer an effective Purcell factor of up to 2.0. With numerical simulations, we furthermore show that a novel regime for light confinement can be achieved, where a Fabry-Perot mode is combined with additional mode confinement by the nanocrystal itself. In this regime, effective Purcell factors of up to 11 for NV centers and 63 for silicon vacancy centers are feasible, holding promise for bright single photon sources and efficient spin readout under ambient conditions.
We employ a fiber-based optical microcavity with high finesse to study the enhancement of phonon sideband fluorescence of nitrogen-vacancy centers in nanodiamonds. Harnessing the full tunability and open access of the resonator, we explicitly demonstrate the scaling laws of the Purcell enhancement by varying both the mode volume and the quality factor over a large range. While changes in the emission lifetime remain small in the regime of a broadband emitter, we observe an increase of the emission spectral density by up to a factor of 300. This gives a direct measure of the Purcell factor that could be achieved with this resonator and an emitter whose linewidth is narrower than the cavity linewidth. Our results show a method for the realization of wavelength-tunable narrow-band single-photon sources and demonstrate a system that has the potential to reach the strong-coupling regime.
We experimentally demonstrate high degree of polarization of 13C nuclear spins weakly interacting with nitrogen-vacancy (NV) centers in diamond. We combine coherent microwave excitation pulses with optical illumination to provide controlled relaxation and achieve a polarity-tunable, fast nuclear polarization of degree higher than 85% at room temperature for remote 13C nuclear spins exhibiting hyperfine interaction strength with NV centers of the order of 600 kHz. We show with the aid of numerical simulation that the anisotropic hyperfine tensor components naturally provide a route to control spin mixing parameter so that highly efficient nuclear polarization is enabled through careful tuning of nuclear quantization axis by external magnetic field. We further discuss spin dynamics and wide applicability of this method to various target 13C nuclear spins around the NV center electron spin. The proposed control method demonstrates an efficient and versatile route to realize, for example, high-fidelity spin register initialization and quantum metrology using nuclear spin resources in solids.
We propose a hybrid quantum architecture for engineering a photonicMott insulator-superfluid phase transition in a two-dimensional (2D) square lattice of a superconducting transmission line resonator (TLR) coupled to a single nitrogen-vacancy (NV) center encircled by a persistent current qubit. The localization-delocalization transition results from the interplay between the on-site repulsion and the nonlocal tunneling. The phase boundary in the case of photon hopping with real-valued and complex-valued amplitudes can be obtained using the mean-field approach. Also, the quantum jump technique is employed to describe the phase diagram when the dissipative effects are considered. The unique feature of our architecture is the good tunability of effective on-site repulsion and photon-hopping rate, and the local statistical property of TLRs which can be analyzed readily using presentmicrowave techniques. Our work opens new perspectives in quantum simulation of condensed-matter and many-body physics using a hybrid spin circuit-QED system. The experimental challenges are realizable using currently available technologies.
Frequency-stabilized mid-infrared lasers are valuable tools for precision molecular spectroscopy. However, their implementation remains limited by complicated stabilization schemes. Here we achieve optical self-locking of a quantum cascade laser to the resonant leak-out field of a highly mode-matched two-mirror cavity. The result is a simple approach to achieving ultra-pure frequencies from high-powered mid-infrared lasers. For short time scales (<0.1 ms), we report a linewidth reduction factor of $3times10^{-6}$ to a linewidth of 12 Hz. Furthermore, we demonstrate two-photon cavity-enhanced absorption spectroscopy of an N$_{2}$O overtone transition near a wavelength of 4.53 $mu$m.