Optically active point defects in crystals have gained widespread attention as photonic systems that can find use in quantum information technologies. However challenges remain in the placing of individual defects at desired locations, an essential element of device fabrication. Here we report the controlled generation of single nitrogen-vacancy (NV) centres in diamond using laser writing. The use of aberration correction in the writing optics allows precise positioning of vacancies within the diamond crystal, and subsequent annealing produces single NV centres with up to 45% success probability, within about 200 nm of the desired position. Selected NV centres fabricated by this method display stable, coherent optical transitions at cryogenic temperatures, a pre-requisite for the creation of distributed quantum networks of solid-state qubits. The results illustrate the potential of laser writing as a new tool for defect engineering in quantum technologies.Comment: 21 pages including Supplementary informatio

A nitrogen-vacancy (NV−) centre in a nanodiamond, levitated in high vacuum, has recently been proposed as a probe for demonstrating mesoscopic centre-of-mass superpositions and for testing quantum gravity. Here, we study the behaviour of optically levitated nanodiamonds containing NV− centres at sub-atmospheric pressures and show that while they burn in air, this can be prevented by replacing the air with nitrogen. However, in nitrogen the nanodiamonds graphitize below ≈10 mB. Exploiting the Brownian motion of a levitated nanodiamond, we extract its internal temperature (Ti) and find that it would be detrimental to the NV− centre’s spin coherence time. These values of Ti make it clear that the diamond is not melting, contradicting a recent suggestion. Additionally, using the measured damping rate of a levitated nanoparticle at a given pressure, we propose a new way of determining its size.

Optical trapping at high vacuum of a nanodiamond containing a nitrogen vacancy centre would provide a test bed for several new phenomena in fundamental physics. However, the nanodiamonds used so far have absorbed too much of the trapping light, heating them to destruction (above 800 K) except at pressures above ∼10 mbar where air molecules dissipate the excess heat. Here we show that milling diamond of 1000 times greater purity creates nanodiamonds that do not heat up even when the optical intensity is raised above 700 GW m −2 below 5 mbar of pressure.

The scheme recently proposed in [M. Scala et al., Phys Rev Lett 111, 180403 (2013)], where a gravity-dependent phase shift is induced on the spin of a nitrogen-vacancy (NV) center in a trapped nanodiamond by the interaction between its magnetic moment and the quantized motion of the particle, provides a way to detect spatial quantum superpositions by means of spin measurements only. Here, the effect of unwanted coupling with other motional degrees of freedom is considered and we show that it does not affect the validity of the scheme. Both this coupling and the additional error source due to misalignment between the quantization axis of the NV center spin and the trapping axis are shown not to change the qualitative behavior of the system, so that a proof-ofprinciple experiment can be neatly performed. Our analysis, which shows that the scheme retains the important features of not requiring ground state cooling and of being resistant to thermal fluctuations, can be useful for the several schemes which have been proposed recently for testing macroscopic superpositions in trapped microsystems.