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Frontiers in Optics

Engineering Nitrogen-Vacancy Centers Near The Surface Of Diamond For Coupling To Optical Microcavities

Kai‐Mei C. Fu, Charles Santori, Paul E. Barclay, Raymond G. Beausoleil

Published Jan 1, 2010• 0 citations
Publisher

Abstract

The optical properties of nitrogen-vacancy centers created nanometers from the surface of diamond are investigated. Deterministic control of the charge state is demonstrated and recent progress toward coupling single centers to cavities is presented.
DOI
10.1364/fio.2010.ftut1

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The nitrogen-vacancy (NV) center is a point defect in diamond and has been championed as a promising solid-state "artificial atom." NV center properties such as its bright luminescence, room-temperature optical readout of spin states, and long spin decoherence lifetime make it an excellent system for applications in quantum information processing, high sensitivity magnetometry, and biotagging. In all applications, near-surface NVs are desirable. However, it has been found that the favorable properties of the NV center are significantly diminished as the NV center nears the surface. \nThis dissertation presents efforts in understanding the effect of the surface on the luminescence of NV centers less than a wavelength of light from the surface. We use plasma assisted etching to, independently, change the surface termination and bring the NV closer to the surface. We find that treating the surface with CF4 plasma results in a deposited polymerous fluorocarbon which helps stabilize nearby NVs. We propose using a downstream etcher to bring NVs closer to the surface, while minimizing damage and maintaining NV luminescence. Finally, we enhance emission of these near-surface NVs by coupling them into a hybrid diamond plasmonic cavity. The fabricated devices result in a measured Q of 170, higher than other previously fabricated diamond plasmonic devices.
The combination of the long electron state spin coherence time and the optical coupling of the ground electronic states to an excited state manifold makes the nitrogen-vacancy (NV) center in diamond an attractive candidate for quantum information processing. To date the best spin and optical properties have been found in centers deep within the diamond crystal. For useful devices it will be necessary to engineer NVs with similar properties close to the diamond surface. We report on properties including charge state control and preferential orientation for near surface NVs formed either in CVD growth or through implantation and annealing.
Scalable quantum information processing using nitrogen-vacancy (NV) centers in diamond will be difficult without the ability to couple the centers to optical microcavities and waveguides. Here we present our preliminary result of coupling a single NV center in a nanoparticle to a silica microdisk at cryogenic temperatures. The cavity-coupled NV photoluminescence is coupled out of the cavity through a tapered fiber. Although the current system is limited by the spectral properties of the NV center and the Q of the cavity, efficient particle-cavity and cavity-waveguide coupling should lead to the realization of a "one-dimensional atom" as needed for CQED, enable single-shot electron-spin readout, and increase the probability of success in entanglement schemes based on single-photon detection.
Scalable realizations of quantum network technologies utilizing the nitrogen vacancy center in diamond require creation of optically coherent NV centers in close proximity to a surface for coupling to optical structures. We create single NV centers by 15^{15}15N ion implantation and high-temperature vacuum annealing. Origin of the NV centers is established by optically detected magnetic resonance spectroscopy for nitrogen isotope identification. Near lifetime-limited optical linewidths (<<< 60 MHz) are observed for the majority of the normal-implant (7∘^\circ∘, ≈\approx≈ 100 nm deep) 15^{15}15NV centers. Long-term stability of the NV−^-− charge state and emission frequency is demonstrated. The effect of NV-surface interaction is investigated by varying the implantation angle for a fixed ion-energy, and thus lattice damage profile. In contrast to the normal implant condition, NVs from an oblique-implant (85∘^\circ∘, ≈\approx≈ 20 nm deep) exhibit substantially reduced optical coherence. Our results imply that the surface is a larger source of perturbation than implantation damage for shallow implanted NVs. This work supports the viability of ion implantation for formation of optically stable NV centers. However, careful surface preparation will be necessary for scalable defect engineering.