No Arabic abstract
We report on pulsed-laser induced generation of nitrogen-vacancy (NV) centers in diamond facilitated by a solid-immersion lens (SIL). The SIL enables laser writing at energies as low as 5.8 nJ per pulse and allows vacancies to be formed close to a diamond surface without inducing surface graphitization. We operate in the previously unexplored regime where lattice vacancies are created following tunneling breakdown rather than multiphoton ionization. We present three samples in which NV-center arrays were laser-written at distances between ~1 $mu$m and 40 $mu$m from a diamond surface, all presenting narrow distributions of optical linewidths with means between 62.1 MHz and 74.5 MHz. The linewidths include the effect of long-term spectral diffusion induced by a 532 nm repump laser for charge-state stabilization, thereby emphasizing the particularly low charge-noise environment of the created color centers. Such high-quality NV centers are excellent candidates for practical applications employing two-photon quantum interference with separate NV centers. Finally, we propose a model for disentangling power broadening from inhomogeneous broadening in the NV center optical linewidth.
Diamonds nitrogen vacancy (NV) center is an optically active defect with long spin coherence times, showing great potential for both efficient nanoscale magnetometry and quantum information processing schemes. Recently, both the formation of buried 3D optical waveguides and high quality single NVs in diamond were demonstrated using the versatile femtosecond laser-writing technique. However, until now, combining these technologies has been an outstanding challenge. In this work, we fabricate laser written photonic waveguides in quantum grade diamond which are aligned to within micron resolution to single laser-written NVs, enabling an integrated platform providing deterministically positioned waveguide-coupled NVs. This fabrication technology opens the way towards on-chip optical routing of single photons between NVs and optically integrated spin-based sensing.
Solid-state quantum emitters have emerged as robust single-photon sources and addressable spins: key components in rapidly developing quantum technologies for broadband magnetometry, biological sensing, and quantum information science. Performance in these applications, be it magnetometer sensitivity or quantum key generation rate, is limited by the number of photons detected. However, efficient collection of a quantum emitters photoluminescence (PL) is challenging as its atomic scale necessitates diffraction-limited imaging with nanometer-precision alignment, oftentimes at cryogenic temperatures. In this letter, we image an individual quantum emitter, an isolated nitrogen-vacancy (NV) center in diamond, using a dielectric metalens composed of subwavelength pillars etched into the diamonds surface. The metalens eliminates the need for an objective by operating as a high-transmission-efficiency immersion lens with a numerical aperture (NA) greater than 1.0. This design provides a scalable approach for fiber coupling solid-state quantum emitters that will enable the development of deployable quantum devices.
A study of the photophysical properties of nitrogen-vacancy (NV) color centers in diamond nanocrystals of size of 50~nm or below is carried out by means of second-order time-intensity photon correlation and cross-correlation measurements as a function of the excitation power for both pure charge states, neutral and negatively charged, as well as for the photochromic state, where the center switches between both states at any power. A dedicated three-level model implying a shelving level is developed to extract the relevant photophysical parameters coupling all three levels. Our analysis confirms the very existence of the shelving level for the neutral NV center. It is found that it plays a negligible role on the photophysics of this center, whereas it is responsible for an increasing photon bunching behavior of the negative NV center with increasing power. From the photophysical parameters, we infer a quantum efficiency for both centers, showing that it remains close to unity for the neutral center over the entire power range, whereas it drops with increasing power from near unity to approximately 0.5 for the negative center. The photophysics of the photochromic center reveals a rich phenomenology that is to a large extent dominated by that of the negative state, in agreement with the excess charge release of the negative center being much slower than the photon emission process.
Important discoveries have frequently been made through the studies of matter under high pressure. The conditions of the pressure environment are important for the interpretation of the experimental results. Due to various restrictions inside the pressure cell, detailed information relevant to the pressure environment, such as the pressure distribution, can be hard to obtain experimentally. Here we present the study of pressure distributions inside the pressure medium under different experimental conditions with NV centers in diamond particles as the sensor. These studies not only show a good spatial resolution, wide temperature and pressure working ranges, compatibility of the existing pressure cell design with the new method, but also demonstrate the usefulness to measure with these sensors as the pressure distribution is sensitive to various factors. The method and the results will benefit many disciplines such as material research and phase transitions in fluid dynamics.
We designed a nanoscale light extractor (NLE) for efficient outcoupling and beaming of broadband light emitted by shallow, negatively charged nitrogen-vacancy (NV) centers in bulk diamond. The NLE consists of a patterned silicon layer on diamond and requires no etching of the diamond surface. Our design process is based on adjoint optimization using broadband time-domain simulations and yields structures that are inherently robust to positioning and fabrication errors. Our NLE functions like a transmission antenna for the NV center, enhancing the optical power extracted from an NV center positioned 10 nm below the diamond surface by a factor of more than 35, and beaming the light into a +/-30{deg} cone in the far field. This approach to light extraction can be readily adapted to other solid-state color centers.