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Register a new userCoupling of Nitrogen-Vacancy Centers to Photonic Crystal Cavities in Monocrystalline Diamond
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The zero-phonon transition rate of a nitrogen-vacancy center is enhanced by a factor of ~70 by coupling to a photonic crystal resonator fabricated in monocrystalline diamond using standard semiconductor fabrication techniques. Photon correlation measurements on the spectrally filtered zero-phonon line show antibunching, a signature that the collected photoluminescence is emitted primarily by a single nitrogen-vacancy center. The linewidth of the coupled nitrogen-vacancy center and the spectral diffusion are characterized using high-resolution photoluminescence and photoluminescence excitation spectroscopy.
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The photoluminescence of nitrogen-vacancy (NV) centers in diamond nanoparticles exhibits specific properties as compared to NV centers in bulk diamond. For instance large fluctuations of lifetime and brightness from particle to particle have been reported. It has also been observed that for nanocrystals much smaller than the mean luminescence wavelength, the particle size sets a lower threshold for resolution in Stimulated Emission Depletion (STED) microscopy. We show that all these features can be quantitatively understood by realizing that the absorption-emission of light by the NV center is mediated by the diamond nanoparticle which behaves as a dielectric nanoantenna.
We study the phenomenon of controllable localization-delocalization transition in a quantum many-body system composed of nitrogen-vacancy centers coupled to photonic crystal cavities, through tuning the different detunings and the relative amplitudes of two optical fields that drive two nondegenerate transitions of the $Lambda $-type configuration. We not only characterize how dissipation affects the phase boundary using the mean-field quantum master equation, but also provide the possibility of observing this photonic quantum phase transition (QPT) by employing several experimentally observable quantities, such as mean intracavity photon number, density correlation function and emitted spectrum, exhibiting distinct optical signatures in different quantum phases. Such a spin-cavity system opens new perspectives in quantum simulation of condensed-matter and many-body physics in a well-controllable way.
We demonstrate optical coupling between a single tin-vacancy (SnV) center in diamond and a free-standing photonic crystal nanobeam cavity. The cavities are fabricated using quasi-isotropic etching and feature experimentally measured quality factors as high as ~11,000. We investigate the dependence of a single SnV centers emission by controlling the cavity wavelength using a laser-induced gas desorption technique. Under resonance conditions, we observe an intensity enhancement of the SnV emission by a factor of 12 and a 16-fold reduction of the SnV lifetime. Based on the large enhancement of the SnV emission rate inside the cavity, we estimate the Purcell factor for the SnV zero-phonon line to be 37 and the coupling efficiency of the SnV center to the cavity, the beta factor, to be 95%. Our work paves the way for the realization of quantum photonic devices and systems based on efficient photonic interfaces using the SnV color center in diamond.
The optical coupling of guided modes in a GaP waveguide to nitrogen-vacancy (NV) centers in diamond is demonstrated. The electric field penetration into diamond and the loss of the guided mode are measured. The results indicate that the GaP-diamond system could be useful for realizing coupled microcavity-NV devices for quantum information processing in diamond.
We propose an experiment to generate deterministic entanglement between separate nitrogen vacancy (NV) centers mediated by the mode of a photonic crystal cavity. Using numerical simulations the applicability and robustness of the entanglement operation to parameter regimes achievable with present technology is investigated. We find that even with moderate cavity Q-factors of $10^{4}$ a concurrence of $c>0.6$ can be achieved within a time of $t_{max}approx150$~ns, while Q-factors of $10^{5}$ promise $c>0.8$. Most importantly, the investigated scheme is relative insensitive to spectral diffusion and differences between the optical transitions frequencies of the used NV centers.
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