Fedor Jelezko

In this work, we experimentally demonstrate a novel and simple approach that uses off-the-shelf optical elements to enhance the collection efficiency from a single emitter. The key component is a solid immersion lens made of diamond, the host material for single color centers. We improve the excitation and detection of single emitters by one order of magnitude, as predicted by theory.

Optical detection of single defect centers in the solid state is a key element of novel quantum technologies. This includes the generation of single photons and quantum information processing. Unfortunately the brightness of such atomic emitters is limited. Therefore we experimentally demonstrate a novel and simple approach that uses off-the-shelf optical elements. The key component is a solid immersion lens made of diamond, the host material for single color centers. We improve the excitation and detection of single emitters by one order of magnitude, as predicted by theory.

Probed But Not Perturbed: The processing and manipulation of quantum information holds great promise in terms of outperforming classical computers and secure communication. However, quantum information is delicate, and even reading the information is a destructive and probabilistic process requiring a number of measurements to home in on the information stored as a quantum state. For the nitrogen vacancy in diamond, Neumann et al. (p. 542 , published online 1 July) show that these limitations can be eliminated. A measurement protocol was designed and implemented where the spin state of the nuclear spin of the vacancy could be mapped onto and read out from the surrounding electronic spins in a single-shot measurement nondestructively.

A new fabrication method to produce homogeneously fluorescent nanodiamonds with high yields is described. The powder obtained by high energy ball milling of fluorescent high pressure, high temperature diamond microcrystals was converted in a pure concentrated aqueous colloidal dispersion of highly crystalline ultrasmall nanoparticles with a mean size less than or equal to 10 nm. The whole fabrication yield of colloidal quasi-spherical nanodiamonds was several orders of magnitude higher than those previously reported starting from microdiamonds. The results open up avenues for the industrial cost-effective production of fluorescent nanodiamonds with well-controlled properties.

Photon interference among distant quantum emitters is a promising method to generate large scale quantum networks. Interference is best achieved when photons show long coherence times. For the nitrogen-vacancy defect center in diamond we measure the coherence times of photons via optically induced Rabi oscillations. Experiments reveal a close to Fourier-transform (i.e., lifetime) limited width of photons emitted even when averaged over minutes. The projected contrast of two-photon interference (0.8) is high enough to envisage applications in quantum information processing. We report 12 and 7.8 ns excited state lifetimes depending on the spin state of the defect.

Coherent coupling between single quantum objects is at the heart of modern quantum physics. When coupling is strong enough to prevail over decoherence, it can be used for the engineering of correlated quantum states. Especially for solid-state systems, control of quantum correlations has attracted widespread attention because of applications in quantum computing. Such coherent coupling has been demonstrated in a variety of systems at low temperature1, 2. Of all quantum systems, spins are potentially the most important, because they offer very long phase memories, sometimes even at room temperature. Although precise control of spins is well established in conventional magnetic resonance3, 4, existing techniques usually do not allow the readout of single spins because of limited sensitivity. In this paper, we explore dipolar magnetic coupling between two single defects in diamond (nitrogen-vacancy and nitrogen) using optical readout of the single nitrogen-vacancy spin states. Long phase memory combined with a defect separation of a few lattice spacings allow us to explore the strong magnetic coupling regime. As the two-defect system was well-isolated from other defects, the long phase memory times of the single spins was not diminished, despite the fact that dipolar interactions are usually seen as undesirable sources of decoherence. A coherent superposition of spin pair quantum states was achieved. The dipolar coupling was used to transfer spin polarisation from a nitrogen-vacancy centre spin to a nitrogen spin, with optical pumping of a nitrogen-vacancy centre leading to efficient initialisation. At the level anticrossing efficient nuclear spin polarisation was achieved. Our results demonstrate an important step towards controlled spin coupling and multi-particle entanglement in the solid state.

Summary form only given. Fluorescence excitation method of single molecule spectroscopy has been applied recently to study individual nitrogen-vacancy (N-V) defect centers in diamond. These objects are of great interest owing to the proposal to build quantum computer at /sup 13/C nuclear spins neighboring the N-V center. Based on new spectroscopic information we have developed simple models of the N-V center and used them to describe a wide range of experiments dealing both with single centers and with their ensembles. The first model emphasizes possible tunneling of N atom into vacancy and describes that in terms of double well potentials. The second model takes into account the spin-triplet character of the ground electronic state of the center and allows to describe a variety of fluorescence detected magnetic resonance phenomena.

Detection and manipulation of single electron spin states in solids has recently been given much attention for applications to quantum computing. In this architecture, the inter-atomic spacing of spins in a solid is an important parameter. One way to control the inter-atomic spacing is to implant spin impurities in pairs via ion implantation. Here, we discuss a proof-of-principle demonstration in synthetic diamond, wherein N₂ was implanted to create pairs of nitrogen-vacancy (NV) color centers.