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arXiv:0812.4505 · Optics Express

Coherent interference effects in a nano-assembled diamond NV center cavity-QED system

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

Published Apr 29, 2009• 162 citations
arXivHTMLPDF

Abstract

Diamond nanocrystals containing NV color centers are positioned with 100-nanometer-scale accuracy in the near-field of a high-Q SiO(2) microdisk cavity using a fiber taper. The cavity modified nanocrystal photoluminescence is studied, with Fano-like quantum interference features observed in the far-field emission spectrum. A quantum optical model of the system is proposed and fit to the measured spectra, from which the NV(-) zero phonon line coherent coupling rate to the microdisk is estimated to be 28 MHz for a nearly optimally placed nanocrystal.

DOI
10.1364/oe.17.008081

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Diamond nanocrystals containing NV color centers are positioned with 100-nanometer-scale accuracy in the near-field of a high-Q SiO(2) microdisk cavity using a fiber taper. The cavity modified nanocrystal photoluminescence is studied, with Fano-like quantum interference features observed in the far-field emission spectrum. A quantum optical model of the system is proposed and fit to the measured spectra, from which the NV(-) zero phonon line coherent coupling rate to the microdisk is estimated to be 28 MHz for a nearly optimally placed nanocrystal.
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We theoretically investigate a cavity quantum electrodynamics system in which a high-QQQ whispering-gallery-mode (WGM) microresonator interacts with multiple diamond nanocrystals each containing a single nitrogen-vacancy (NV) center. With a tapered fiber waveguide coupling the WGMs, the transmission spectrum of the system exhibits a twofold-splitting phenomenon, where the first fold of splitting originates from the nanocrystals' Rayleigh scattering and the second fold stems from the NV center dipole coupling with the WGMs. The interacting system can serve as a platform to generate quantum entanglement between two NV centers embedded in distant diamond nanocrystals. Our further study reveals that the Rayleigh scattering of the nanocrystals plays a positive role in generating entanglement in some cases. The analytical results show that the relatively strong scattering leads to a larger concurrence for the fixed dipole-cavity detunings. This investigation may hold potential for solid-state quantum information processing applications.
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.
Nitrogen–vacancy (NV) centers in diamond are generally recognized as highly promising as indefinitely stable highly efficient single-photon sources. We report an experimental quantification of the brightness, radiative decay rate, nonradiative decay rate and quantum efficiency of single NV centers in diamond nanocrystals. Our experiments show that the commonly observed large spread in fluorescence decay rates of NV centers in nanodiamond is inconsistent with the common explanation of large nanophotonic mode-density variations in the ultra-small high-index crystals at near-unity quantum efficiency. We report that NV centers in 25 nm nanocrystals are essentially insensitive to local density of optical states (LDOS) variations that we induce at a dielectric interface by using liquids to vary the refractive index, and propose that quantum efficiencies in such nanocrystals are widely distributed between 0 and 20%. For single NV centers in larger 100 nm nanocrystals, we show that decay rate changes can be reversibly induced by nanomechanically approaching a mirror to change the LDOS. Using this scanning mirror method, for the first time we report calibrated quantum efficiencies of NV centers, and show that different but nominally identical nanocrystals have widely distributed quantum efficiencies between 10 and 90%. Our measurements imply that nanocrystals that are to be assembled into hybrid photonic structures for cavity QED should first be individually screened to assess fluorescence properties in detail.