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Bulletin of the American Physical Society

Double quantum coherence control in NV- centers in Diamond at small fields

Osama Moussa, Ian Hincks, David G. Cory

Published Jun 7, 2013• 0 citations
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Nanoscale quantum probes such as the nitrogen-vacancy (NV) center in diamonds have demonstrated remarkable sensing capabilities over the past decade as control over fabrication and manipulation of these systems has evolved. The biocompatibility and rich surface chemistry of diamonds has added to the utility of these probes but, as the size of these nanoscale systems is reduced, the surface chemistry of diamond begins to impact the quantum properties of the NV center. In this work, we systematically study the effect of the diamond surface chemistry on the quantum coherence of the NV center in nanodiamonds (NDs) 50 nm in size. Our results show that a borane-reduced diamond surface can on average double the spin relaxation time of individual NV centers in nanodiamonds when compared to thermally oxidized surfaces. Using a combination of infrared and X-ray absorption spectroscopy techniques, we correlate the changes in quantum relaxation rates with the conversion of sp 2 carbon to C–O and C–H bonds on the diamond surface. These findings implicate double-bonded carbon species as a dominant source of spin noise for near surface NV centers. The link between the surface chemistry and quantum coherence indicates that through tailored engineering of the surface, the quantum properties and magnetic sensitivity of these nanoscale systems may approach that observed in bulk diamond.
High-fidelity quantum operation of qubits plays an important role in magnetometry based on nitrogen-vacancy (NV) centers in diamonds. However, the nontrivial spin-spin coupling of the NV center decreases signal contrast and sensitivity. Here, we overcome this limitation by exploiting the amplitude modulation of microwaves, which allows us to perfectly detect magnetic signals at low fields. Compared with the traditional double-quantum sensing protocol, the full contrast of the detection signal was recovered, and the sensitivity was enhanced three times in the experiment. Our method is applicable to a wide range of sensing tasks, such as temperature, strain, and electric field.
Abstract Nitrogen-vacancy (NV) centers in diamond have become an important tool for quantum technologies. All of these applications rely on long coherence times of electron and nuclear spins associated with these centers. Here, we study the energy level anti-crossings of an NV center in diamond coupled to a first-shell 13C nuclear spin in a small static magnetic field. These level anti-crossings (LACs) occur for specific orientations of the static magnetic field due to the strong non-secular components of the Hamiltonian. At these orientations we observe decoherence-free subspaces, where the electron spin coherence times ( T 2 * ) are 5–7 times longer than those at other orientations. Another interesting property at these LACs is that individual transition amplitudes are dominated by a single component of the magnetic dipole moment. Accordingly, this can be used for vector detection of microwave magnetic fields with a single NV center. This is particularly important to precisely control the center using numerical optimal control techniques.