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Environment spectroscopy with an NV center in diamond

Santiago Hernández-Gómez, Francesco Poggiali, Nicole Fabbri, Paola Cappellaro

Published Jan 1, 2020• 0 citations
Publisher

Abstract

Nitrogen-vacancy (NV) centers in diamond have emerged in the last decade as a prominent platform for quantum technologies. As for any qubit system, a good understanding of their local environment is crucial to build quantum devices protected from detrimental noise. Here, we describe in detail a method to spectroscopically characterize the spin bath around an NV center, even when the NV coherence time is short, and identify the coherent coupling with the nearest nuclear spins. In the regime of weak qubit-bath coupling, the acquired knowledge of the bath reliably predicts the qubit dynamics under different controls.

DOI
10.3254/enfi200027

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•Jun 6, 2014•1 citation
Nitrogen-vacancy (NV) centers in diamond have emerged in the last decade as a prominent platform for quantum technologies. As for any qubit system, a good understanding of their local environment is crucial to build quantum devices protected from detrimental noise. Here, we describe in detail a method to spectroscopically characterize the spin bath around an NV center, even when the NV coherence time is short, and identify the coherent coupling with the nearest nuclear spins. In the regime of weak qubit-bath coupling, the acquired knowledge of the bath reliably predicts the qubit dynamics under different controls.
The nitrogen-vacancy (NV) center in diamond is a promising candidate for development of quantum communication and simulation devices which are based on the control of coupled quantum systems. It offers an optical readout of its spin state, exhibits long coherence times and allows to coherently control nearby nuclear spins, e.g. from 13C nuclei, even at room-temperature. For successful demonstration of such systems however, controlling the nuclear spin environment, and thus tuning the coupling strengths is crucial to allow the fabrication of a scalable platforms. The combination of Chemical Vapor Deposition (CVD) of diamond as a method with isotopic control on the diamond composition and ion implantation as a tool to reliably create NV centers is a perfect toolkit to study the realization such quantum systems.
We theoretically investigate spin decoherence of a single nitrogen-vacancy (NV) center in diamond. Using the spin coherent-state PPP-representation method, we simulate coherence evolution of the NV center coupled to surrounding nitrogen electron (N) spins. In the system, the strength of N-N coupling is the same order as that of NV-N coupling (the strong intrabath coupling regime). We find that spin decoherence time as well as free-induction decay of the NV center depend on the spatial configuration of N spins. Both the spin decoherence rate (1/T21/{T}_{2}1/T2​) and dephasing rate (1/T2∗)1/{T}_{2}^{*})1/T2∗​) of the NV center increase linearly with the concentration of the N spins. Using the PPP-representation method, we also demonstrate extracting the noise spectrum of the N spin bath. The capability to calculate the noise spectrum will provide promising pathways to suppress decoherence of spin systems in the strong intrabath coupling regime.
Knowing a quantum system's environment is critical for its practical use as a quantum device. Qubit sensors can reconstruct the noise spectral density of a classical bath, provided long enough coherence time. Here, we present a protocol that can unravel the characteristics of a more complex environment, comprising both unknown coherently coupled quantum systems, and a larger quantum bath that can be modeled as a classical stochastic field. We exploit the rich environment of a nitrogen-vacancy center in diamond, tuning the environment behavior with a bias magnetic field, to experimentally demonstrate our method. We show how to reconstruct the noise spectral density even when limited by relatively short coherence times, and identify the local spin environment. Importantly, we demonstrate that the reconstructed model can have predictive power, describing the spin qubit dynamics under control sequences not used for noise spectroscopy, a feature critical for building robust quantum devices. At lower bias fields, where the effects of the quantum nature of the bath are more pronounced, we find that more than a single classical noise model are needed to properly describe the spin coherence under different controls, due to the back action of the qubit onto the bath.
The nitrogen vacancy (NV) center in diamond, a well-studied, optically active spin defect, is the prototypical system in many state of the art quantum sensing and communication applications. In addition to the enticing properties intrinsic to the NV center, its diamond host's nuclear and electronic spin baths can be leveraged as resources for quantum information, rather than considered solely as sources of decoherence. However, current synthesis approaches result in stochastic defect spin positions, reducing the technology's potential for deterministic control and yield of NV-spin bath systems, as well as scalability and integration with other technologies. Here, we demonstrate the use of theoretical calculations of electronic central spin decoherence as an integral part of an NV-spin bath synthesis workflow, providing a path forward for the quantitative design of NV center-based quantum sensing systems. We use computationally generated coherence data to characterize the properties of single NV center qubits across relevant growth parameters to find general trends in coherence time distributions dependent on spin bath dimensionality and density. We then build a maximum likelihood estimator with our theoretical model, enabling the characterization of a test sample through NV T2* measurements. Finally, we explore the impact of dimensionality on the yield of strongly coupled electron spin systems. The methods presented herein are general and applicable to other qubit platforms that can be appropriately simulated.
Abstract Nitrogen-vacancy (NV) centers in diamond have been developed into essential hardware units for a wide range of solid-state-based quantum technology applications. While such applications require the long spin coherence times of the NV centers, they are often limited due to decoherence. In this study, we theoretically investigate the decoherence of NV-spin ensembles induced by nitrogen impurities (P1 centers), which are one of the most dominant and inevitable magnetic field noise sources in diamond. We combined cluster correlation expansion and density functional theory to compute the Hahn-echo spin-coherence time of the NV centers for a broad range of P1 concentrations. Results indicate a clear linear dependence of T2 on P1 concentrations on a log scale with a slope of −1.06, which is in excellent agreement with previous experimental results. The interplay between the Jahn–Teller effect and the hyperfine interaction in the P1 center plays a critical role in determining the bath dynamics and the resulting NV decoherence. Our results provide a theoretical upper bound for the NV-spin T2 over a wide range of P1 densities, serving as a key reference for materials optimization and spin bath characterization to develop highly coherent NV-based devices for quantum information technology.
The nitrogen vacancy (NV) center in diamond is a unique quantum system that combines solid state spin qubits with coherent optical transitions. The spin states of the NV center can be initialized, read out, and controlled with RF fields at room temperature. It can be coupled to other spin systems in the environment while at the same time maintaining an extraordinary degree of quantum coherence. Experiments utilizing the NV center's spin states have led to a wide range of demonstrations from quantum error correction to high-sensitivity magnetometry. This thesis, however, focuses on creating an interface between NV centers and light in the visible domain by making use of its optical transitions. Such an interface connects the quantum system consisting of NV centers and nuclear spins to photons, which can then be used to both manipulate the spin qubits themselves or transport quantum information over large distances.