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New Journal of Physics

Creation and nature of optical centres in diamond for single-photon emission—overview and critical remarks

Sébastien Pezzagna, Detlef Rogalla, Dominik Wildanger, Jan Meijer, Alexander M. Zaitsev

Published Mar 29, 2011• 249 citations
Publisher

Abstract

A huge variety of optical colour centres can be found in diamond, emitting in its whole wide transparency range. Although several of these centres have been demonstrated as single-photon emitters, none of them meets all of the requirements of an ideal single-photon source. In this view, we discuss the properties of prominent optical centres, such as the nitrogen vacancy, the silicon vacancy or the so-called NE8 centre, as well as recently found centres ascribed to defects containing Ni, Si, Cr and Xe. Besides suitable intrinsic properties, it is necessary for practical applications that optical centres can be created artificially on demand. Of all known methods, only ion implantation allows for the most controlled creation of such defect centres. In this paper, we discuss how nanoscalability, that is, the nanometre placement and the deterministic creation of optical centres, can, could or cannot be achieved by the available ion implantation techniques. A fine analysis of individual optical centres is now possible, thanks to the recently developed subdiffraction optical microscopy methods.

DOI
10.1088/1367-2630/13/3/035024

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A huge variety of optical colour centres can be found in diamond, emitting in its whole wide transparency range. Although several of these centres have been demonstrated as single-photon emitters, none of them meets all of the requirements of an ideal single-photon source. In this view, we discuss the properties of prominent optical centres, such as the nitrogen vacancy, the silicon vacancy or the so-called NE8 centre, as well as recently found centres ascribed to defects containing Ni, Si, Cr and Xe. Besides suitable intrinsic properties, it is necessary for practical applications that optical centres can be created artificially on demand. Of all known methods, only ion implantation allows for the most controlled creation of such defect centres. In this paper, we discuss how nanoscalability, that is, the nanometre placement and the deterministic creation of optical centres, can, could or cannot be achieved by the available ion implantation techniques. A fine analysis of individual optical centres is now possible, thanks to the recently developed subdiffraction optical microscopy methods.
Abstract We present a high throughput and systematic method for the screening of colour centres in diamond with the aim of searching for and reproducibly creating new optical centres down to the single defect level, potentially of interest for a wide range of diamond-based quantum applications. The screening method presented here should, moreover, help to identify some already indexed defects among hundreds in diamond (Zaitsev 2001 Optical Properties of Diamond (Berlin: Springer)) but also some promising defects of a still unknown nature, such as the recently discovered ST1 centre (Lee et al 2013 Nat. Nanotechnol . 8 487; John et al 2017 New J. Phys . 19 053008). We use ion implantation in a systematic manner to implant several chemical elements. Ion implantation has the advantage of addressing single atoms inside the bulk with defined depth and high lateral resolution, but the disadvantage of producing intrinsic defects. The implanted samples are annealed in vacuum at different temperatures (between 600 °C and 1600 °C with 200 °C steps) and fully characterised at each step in order to follow the evolution of the defects: formation, dissociation, diffusion, re-formation and charge state, at the ensemble level and, if possible, at the single centre level. We review the unavoidable ion implantation defects (such as the GR1 and 3H centres), discuss ion channeling and thermal annealing and estimate the diffusion of the vacancies, nitrogen and hydrogen. We use different characterisation methods best suited for our study (from widefield fluorescence down to sub-diffraction optical imaging of single centres) and discuss reproducibility issues due to diamond and defect inhomogeneities. Nitrogen is also implanted for reference, taking advantage of the considerable knowledge on NV centres as a versatile sensor in order to retrieve or deduce the conditions and local environment in which the different implanted chemical elements are embedded. We show here the preliminary promising results of a long-term study and focus on the elements O, Mg, Ca, F and P from which fluorescent centres were found.
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.
Single-photon sources are a fundamental element for developing quantum technologies, and sources based on colour centres in diamonds are among the most promising candidates. The well-known nitrogen vacancy centres are characterized by several limitations, and thus few other defects have recently been considered. In the present work, we characterize, in detail, native efficient single colour centres emitting in the near infra-red ( λ = 740–780 nm) in both standard IIa single-crystal and electronic-grade polycrystalline commercial chemical vapour deposited (CVD) diamond samples. In the former case, a high-temperature ( T > 1000 °C) annealing process in vacuum is necessary to induce the formation/activation of luminescent centres with good emission properties, while in the latter case the annealing process has marginally beneficial effects on the number and performance of native centres in commercially available samples. Although displaying significant variability in several photo-physical properties (emission wavelength, emission rate instabilities, saturation behaviours), these centres generally display appealing photophysical properties for applications as single photon sources: short lifetimes (0.7–3 ns), high emission rates (∼50–500 × 10 3 photons s −1 ) and strongly (>95%) polarized light. The native centres are tentatively attributed to impurities incorporated in the diamond crystal during the CVD growth of high-quality type-IIa samples, and offer promising perspectives in diamond-based photonics.
Ni-related optical centres in diamond are promising as alternatives to the nitrogen vacancy (NV) centre for quantum applications and biomarking. In order to achieve the reliability and reproducibility required, a method for producing the Ni-related centres in a controllable manner needs to be established. In this study, we have attempted this control by implanting high purity CVD diamond samples with Ni and N followed by thermal annealing. Samples implanted with Ni show a new Ni-related PL peak centered at 711 nm and a well known doublet at 883/885 nm along with weak NV luminescence. The optical properties of the two Ni-related defects are investigated. In particular, an excited state lifetime of the 883/885 nm peak is measured to be 11.6 ns.
Silicon-vacancy (SiV) centers in diamond are gaining an increased interest for application, such as in quantum technologies and sensing. Due to the strong luminescence concentrated in its sharp zero-phonon line at room temperature, SiV centers are being investigated as single-photon sources for quantum communication, and also as temperature probes for sensing. Here, we discussed strategies for the fabrication of SiV centers in diamond based on Si-ion implantation followed by thermal activation. SiV color centers in high-quality single crystals have the best optical properties, but polycrystalline micro and nanostructures are interesting for applications in nano-optics. Moreover, we discuss the photoluminescence properties of SiV centers in phosphorous-doped diamond, which are relevant for the creation of electroluminescent devices, and nanophotonics strategies to improve the emission characteristics of the SiV centers. Finally, the optical properties of such centers at room and high temperatures show the robustness of the center and give perspectives for temperature-sensing applications.