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Emission dipole imaging in diamond single emitters

Stefania Castelletto, Ahanorovich, I., Brant C. Gibson, Brett C. Johnson, Steven Prawer

Published Jan 1, 2010• 0 citations
OpenAlex

Abstract

We present direct imaging of the emission pattern of Cr-based individual single photon emitters in monolithic diamond and a measurement of their quantum efficiency. By imaging the excited state transition dipole intensity distribution of single Cr centres in bulk diamond and nano diamonds, we reconstructed their 3D orientation.

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We present direct imaging of the emission pattern of individual chromium-based single photon emitters in diamond and measure their quantum efficiency. By imaging the excited state transition dipole intensity distribution in the back focal plane of high numerical aperture objective, we determined its 3D orientation. Employing ion implantation techniques, the emitters were placed at various distances from the diamond-air interface. By comparing the decay rates from the single chromium emitters at different depths in the diamond crystal, we measured an average quantum efficiency of 28%.
We present direct imaging of the emission pattern of individual chromium-based single photon emitters in diamond and measure their quantum efficiency. By imaging the excited state transition dipole intensity distribution in the back focal plane of high numerical aperture objective, we determined that the emission dipole is oriented nearly orthogonal to the diamond-air interface. Employing ion implantation techniques, the emitters were engineered with various proximities from the diamond-air interface. By comparing the decay rates from the single chromium emitters at different depths in the diamond crystal, an average quantum efficiency of 28% was measured.
Controlled fabrication and identification of bright single-photon emitters is at the heart of quantum optics. Here we demonstrate controlled engineering of a chromium bright single-photon source in bulk diamond by ion implantation. The Cr center has fully polarized emission with a zero-phonon line centered at 749 nm, full width at half maximum of 4 nm, an extremely short lifetime of $\ensuremath{\sim}1\text{ }\text{ns}$, and a count rate of $0.5\ifmmode\times\else\texttimes\fi{}{10}^{6}\text{ }\text{counts}/\text{s}$. By combining the polarization measurements and the vibronic spectra, a model of the center has been proposed consisting of one interstitial chromium atom with a transition dipole along one of the ⟨100⟩⟨100⟩⟨100⟩ directions.
Diamond is emerging as an optical supermaterial, due to its wide transparency bandwidth, excellent thermooptic properties and most notably its stable, large dipole moment, room temperature, single photon emitting colour centres. In this paper we present recent progress in the characterization of non radiative and radiative decay in single impurities and the fabrication of hybrid diamond-tellurite optical structures.. First, we present direct imaging of the emission pattern of individual ion implanted chromium-based single photon emitters in diamond and measure their quantum efficiency. By comparing the decay rates from the single chromium emitters at different depths in the diamond crystal, we measured an average quantum efficiency of 28%. Second, a hybrid approach involving a soft glass tellurite host material has been introduced, allowing nitrogen-vacancy (NV-) diamond emitters to be built into an optical fibre. The potential of integrating Cr-related centres in hybrid optical structures is also discussed.
On-demand, high repetition rate sources of indistinguishable, polarized single photons are the key component for future photonic quantum technologies (O'Brien et al 2009 Nat. Photonics 3 687–95). Colour centres in diamond offer a promising solution, and the narrow linewidth of the recently identified nickel-based NE8 centre makes it particularly appealing for realizing the transform-limited sources necessary for quantum interference. Here, we report the characterization of dipole orientation and coherence properties of a single NE8 colour centre in a diamond nanocrystal at room temperature. We observe a single-photon coherence time of 0.21 ps and an emission lifetime of 1.5 ns. Combined with an emission wavelength that is ideally suited for applications in existing quantum optical systems, these results show that NE8 is a far more promising source than the more commonly studied nitrogen-vacancy centre and point the way to the realization of a practical diamond colour centre-based single-photon source.