Control of the NV-centers fluorescence lifetime in resonant diamond particles (Conference Presentation)
Dmitry A. Zuev, Anastasia Zalogina, Roman S. Savelev, Elena V. Ushakova, Georgiy Zograf, Комиссаренко Филипп Эдуардович, Valentin A. Milichko, Sergey Makarov, Yuri S. Kivshar, Ilya V. Shadrivov
The resonant high-index nanostructures open opportunities for control many optical effects via optically-induced electric and magnetic Mie resonances, mostly localized inside the structures. Especial interest such nanostructures represent for quantum emitters placed inside, that makes possible enhancement of quantum source emission through resonant coupling to localized modes. We have proposed the concept of active dielectric nanoantennas based on nanodiamonds with embedded NV-centers. The study of theoretically dependence of optical properties of this system on the spectral position of the resonant modes has demonstrated that that at some sizes of the diamond spherical particles and certain position of the dipole in the sphere the Purcell factor can achieve the value of 30. We have demonstrated experimentally that the photoluminescence properties of the NV-centers can be controlled via scattering resonances and observed a decrease of the NV-centers lifetime in the studied diamond particles, as compared to nonresonant nanodiamonds. These results are in a good agreement with our theoretical calculations for the average Purcell factor for multiple NV-centers within a nanoparticle. The simplicity of the proposed concept compared to existing photonic cavity systems and applicability for a wide range of color centers in diamond make active diamond nanoantenna an effective tool for creating controllable emitting elements in the visible range for future nanophotonic devices.
The resonant high-index nanostructures open opportunities for control many optical effects via optically-induced electric and magnetic Mie resonances, mostly localized inside the structures. Especial interest such nanostructures represent for quantum emitters placed inside, that makes possible enhancement of quantum source emission through resonant coupling to localized modes. We have proposed the concept of active dielectric nanoantennas based on nanodiamonds with embedded NV-centers. The study of theoretically dependence of optical properties of this system on the spectral position of the resonant modes has demonstrated that that at some sizes of the diamond spherical particles and certain position of the dipole in the sphere the Purcell factor can achieve the value of 30. We have demonstrated experimentally that the photoluminescence properties of the NV-centers can be controlled via scattering resonances and observed a decrease of the NV-centers lifetime in the studied diamond particles, as compared to nonresonant nanodiamonds. These results are in a good agreement with our theoretical calculations for the average Purcell factor for multiple NV-centers within a nanoparticle. The simplicity of the proposed concept compared to existing photonic cavity systems and applicability for a wide range of color centers in diamond make active diamond nanoantenna an effective tool for creating controllable emitting elements in the visible range for future nanophotonic devices.
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 properties of luminescent diamond particles of different sizes (up to ~1.5 μ m) containing multiple NV-centers. We theoretically predict that the average liftetime in such particles is decreased by several times as compared to optically small subwavelength nanodiamonds. In our experiments, samples were obtained by milling the plasma-enhanced chemical vapor deposited diamond film, and characterized by Raman spectroscopy and dark- field spectroscopy methods. Time-resolved luminescence measurements of the excited state of NV-centers showed that their average lifetime varies from 10 to 17 ns in different samples. By comparing this data to the values of the lifetime of the NV-centers in optically small nanodiamonds, known from literature, we confirm a severalfold decrease of the lifetime in resonant particles.
Diamond particles with color centers have found numerous applications in quantum optics, bioimaging and nanosensing. Here, we report on an experimental study of the optical Mie resonances of subwavelength diamond particles and their effect on the fluorescence of nitrogen-vacancy centers. We employ single-particle scattering spectroscopy to reveal the fundamental optical resonances of individual diamond particles and measure the fluorescence saturation curves using continuous-wave excitation to evidence the difference in the spontaneous emission rate of the color centers in different particles. A simple analytical model has been used to predict the dependence of the saturation intensity on the particle size for a free-standing spherical diamond. Experimentally, we have shown that the magnetic dipole and quadrupole modes are excited in the fluorescence spectral range for particles of approximately 250-350 nm in size and that the saturation intensity for such particles is by an order of magnitude higher than for a smaller one, which is in agreement with our calculations. The results demonstrate that the efficiency of diamond-based sensors and single-photon sources can be improved by simply choosing particles of a proper size.
With their ability to process and transfer quantum information, large-scale entanglement-based quantum networks could be at the heart of a new age of quantum information, enabling fundamentally new applications such as distributed quantum computation, quantum communication, and quantum enhanced sensing. Due to their long spin coherence, controllable local qubit registers and optically active spins, color centers in diamond are prime candidates for nodes of such a network, and have enabled some of the most advanced quantum network demonstrations to date. These demonstrations include the distribution of a 3-node GHZ state across a quantum network, entanglement swapping, entanglement distillation, and memory-enhanced quantum communication. To move beyond current proof-of-principle networks, a further increase of entanglement generation rates is crucial. This thesis presents theoretical and experimental work on enhancing the spin-photon interface of color centers in diamond to achieve this goal, making use of the Purcell effect. The discussed work follows two main directions: embedding of color centers in open, tuneable Fabry-Perot micro-cavities, and in all-diamond photonic crystal cavities. First, we describe theoretical and experimental progress towards cavity-enhanced quantum networks based on nitrogen-vacancy (NV) centers in diamond. Due to their first order sensitivity to electric fields, we choose to embed NV centers in microns-thin diamond membranes that can be integrated into open fiber-based micro-cavities. We develop analytical methods to optimize the design of such open cavity systems for maximum Purcell enhancement of embedded color centers. We demonstrate a method to fabricate optically coherent NV centers in microns-thin diamond membranes, and use such structures to demonstrate the resonant excitation and detection of coherent, Purcell enhanced NV emission. A theoretical model in excellent agreement with our results suggests our system can improve entanglement rates between distant NV centers by two orders of magnitude with near-term improvements to the setup. Second, we describe progress towards an efficient spin-photon interface of group-IV color centers in diamond by coupling them to photonic nanostructures, allowing for large-scale integration. Due to their first-order insensitivity to electric fields, group-IV color centers can be brought in close proximity to surfaces (~ 100 nm), allowing for sub-wavelength mode volumes and thus very high Purcell factors. We numerically optimize photonic crystal cavity designs to maximize the Purcell enhancement of embedded emitters, test the robustness of our designs to real-world fabrication imperfections, and devise a method to efficiently interface nanophotonic structures. We then proceed to fabricate all-diamond photonic crystal cavities, making use of a dry etching technique that is selective to different crystallographic directions, and characterize the resulting optical quality factors. Finally, we marry the developed fabrication methods to fabricate microns-sized diamond platelets that can be transferred from a holding frame in a controlled fashion. This capability could be crucial for the realization of hybrid photonic circuits that we expect to be at the heart of future large-scale quantum networks.
Nitrogen–vacancy (NV) centers in diamond are generally recognized as highly promising as indefinitely stable highly efficient single-photon sources. We report an experimental quantification of the brightness, radiative decay rate, nonradiative decay rate and quantum efficiency of single NV centers in diamond nanocrystals. Our experiments show that the commonly observed large spread in fluorescence decay rates of NV centers in nanodiamond is inconsistent with the common explanation of large nanophotonic mode-density variations in the ultra-small high-index crystals at near-unity quantum efficiency. We report that NV centers in 25 nm nanocrystals are essentially insensitive to local density of optical states (LDOS) variations that we induce at a dielectric interface by using liquids to vary the refractive index, and propose that quantum efficiencies in such nanocrystals are widely distributed between 0 and 20%. For single NV centers in larger 100 nm nanocrystals, we show that decay rate changes can be reversibly induced by nanomechanically approaching a mirror to change the LDOS. Using this scanning mirror method, for the first time we report calibrated quantum efficiencies of NV centers, and show that different but nominally identical nanocrystals have widely distributed quantum efficiencies between 10 and 90%. Our measurements imply that nanocrystals that are to be assembled into hybrid photonic structures for cavity QED should first be individually screened to assess fluorescence properties in detail.
The negatively-charged nitrogen vacancy (NV(-)) center in diamond is of great interest for quantum information processing and quantum key distribution applications due to its highly desirable long coherence times at room temperature. One of the challenges for their use in these applications involves the requirement to further optimize the lifetime and emission properties of the centers. Our results demonstrate the reduction of the lifetime of NV(-) centers, and hence an increase in the emission rate, achieved by modifying the refractive index of the environment surrounding the nanodiamond (ND). By coating the NDs in a polymer film, experimental results and numerical calculations show an average of 63% reduction in the lifetime and an average enhancement in the emission rate by a factor of 1.6. This strategy is also applicable for emitters other than diamond color centers where the particle refractive index is greater than the refractive index of the surrounding media.