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arXiv:1110.3329 · Physical Review Letters

Two-Photon Quantum Interference from Separate Nitrogen Vacancy Centers in Diamond

Hannes Bernien, Lilian Childress, Lucio Robledo, Matthew Markham, Daniel J. Twitchen, Ronald Hanson

Published Jan 26, 2012• 277 citations
arXivHTMLPDF

Abstract

We report on the observation of quantum interference of the emission from two separate nitrogen vacancy (NV) centers in diamond. Taking advantage of optically induced spin polarization in combination with polarization filtering, we isolate a single transition within the zero-phonon line of the nonresonantly excited NV centers. The time-resolved two-photon interference contrast of this filtered emission reaches 66%. Furthermore, we observe quantum interference from dissimilar NV centers tuned into resonance through the dc Stark effect. These results pave the way towards measurement-based entanglement between remote NV centers and the realization of quantum networks with solid-state spins.

DOI
10.1103/physrevlett.108.043604

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We report on the observation of quantum interference of the emission from two separate nitrogen vacancy (NV) centers in diamond. Taking advantage of optically induced spin polarization in combination with polarization filtering, we isolate a single transition within the zero-phonon line of the nonresonantly excited NV centers. The time-resolved two-photon interference contrast of this filtered emission reaches 66%. Furthermore, we observe quantum interference from dissimilar NV centers tuned into resonance through the dc Stark effect. These results pave the way towards measurement-based entanglement between remote NV centers and the realization of quantum networks with solid-state spins.
We demonstrate quantum interference between indistinguishable photons emitted by two nitrogen-vacancy centers in distinct diamond samples separated by two meters. Macroscopic solid immersion lenses are used to enhance photon collection efficiency. Quantum interference is verified by measuring a value of the second-order cross-correlation function g((2))(0)=0.35±0.04<0.5. In addition, optical transition frequencies of two separated nitrogen-vacancy centers are tuned into resonance with each other by applying external electric fields. An extension of the present approach to generate entanglement of remote solid-state qubits is discussed.
As a kind of hybrid spin system, nitrogen-vacancy (NV) centers in diamond have shown great advantages in implementing quantum registers for quantum information processing (QIP). When scaling up quantum registers to quantum networks for long-distance quantum communication and distributed quantum computation, determining how to entangle two registers in distant nodes is a basic challenge in the absence of direct interactions. In this paper, we present a scheme for entangling two distant NV centers based on the special optical absorption and emission of NV centers. In this demonstration, we transfer the entanglement information of a pair of photons to nuclear spins in NV centers and create remote NV–NV entanglement mediated by entangled photons. We then explain how to extract the entangled information from NV centers to prepare on-demand entangled photons for optical quantum information processing. The strategy of entanglement transfer between spins and photons demonstrated herein may pave the way for an NV-center-based quantum network.
Individual nitrogen vacancy (NV) centers in diamond have recently emerged as a leading candidate for a building block for quantum information processing systems. Individual NV centers have many properties that are desirable for qubits. For example their spin states can be manipulated, initialized and measured even at room temperature. In order to build a quantum information processing system that consists of more than a single NV center, these individual NV centers have to be connected via quantum channels that distribute entanglement and allow quantum state transfer between NV centers. This thesis explores how the optical properties of the NV center can be used and manipulated to form these quantum channels. Likewise we show how the same properties can be used to better control the nuclear spin environment surrounding the NV center. We first introduce, review and experimentally study the relevant optical properties of the NV center. These quantum optical techniques are then used to experimentally demonstrate spin-photon entanglement between the electronic spin of an individual NV center and a single photon. We next demonstrate quantum interference of two photons produced by NV centers in distinct diamond samples separated by two meters. These two demonstrations pave the way for entanglement generation, leading to quantum channels, between remote NV centers. Finally we demonstrate optical cooling, real-time measurement and conditional preparation of the nuclear spin environment around an NV center using all-optical manipulation of its electronic spin. This technique can lead to better control of individual NV centers and thus more robust quantum information processing systems.
The nitrogen-vacancy (NV) center in diamond has garnered great interest over the past decade as its electronic spin shows promise as a quantum bit (qubit) and nanoscale sensor. Consisting of a substitutional nitrogen adjacent to a vacant site within the carbon lattice of diamond, this defect exhibits millisecond-long spin coherence times extending beyond room temperature, spin-dependent optical addressability, coupling to intrinsic and nearby nuclear spins, and it can be controlled and manipulated through electrical, magnetic, and optical means. In particular, at cryogenic temperatures (T < 25 K), the NV center's excited state becomes sharp and optically resolvable, providing a solid-state quantum optical testbed. In this thesis, I describe several experiments that explore this quantum optical interface to facilitate the development of a photonic network of single spins linked and controlled by light. We begin by exploring how electric fields tune the orbital levels within the NV center through the DC Stark effect, finding a surprising photo-induced field that aids in the ability to tune multiple NV centers' optical transitions to degeneracy. We then develop techniques to fully control the spin state of the NV center by coupling through a lambda system, an energy configuration consisting of two lower levels coupled to one of higher energy. When a lambda system is optically driven, the spin becomes trapped in a dark state, or the eigenstate of the system that is not coupled to the light fields through destructive interference, forming the basis for the various types of control demonstrated. We demonstrate arbitrary-basis initialization and readout of the spin state through coherent population trapping, as well as the ability to rotate about any arbitrary basis through stimulated Raman transitions. Combining these techniques, we measure the NV center's spin coherence through a completely optical measurement. We then extend these lambda system techniques to adiabatically move the dark state in trajectories around the Bloch sphere. Such trajectories accumulate a quantum mechanical phase that depends only on the geometry of the path enclosed, not on the energetics or time of the interaction. We characterize the interaction, measure this phase, known as Berry phase, and explore the limits of its control and resilience to noise. Finally, we demonstrate another all-optical control technique that uses strong ultrafast pulses of light to transfer the spin between the ground and excited states, deriving spin manipulation from the excited state dynamics. This technique also provides time-resolved spectroscopy of the excited state and its various decay and decoherence mechanisms. These experiments advance the progress toward the development of photonic networks coupling and controlling defects through light-matter interactions.
For quantum information applications, nitrogen-vacancy (NV) centers in diamond combine many of the advantages of atomic systems (optical access, millisecond spin-coherence times) with the engineering flexibility of solid-state devices. Recent demonstrations of coherent coupling between photons and individual NV-center spins [1,2] provide a route to integrating NV-center qubits within photonic networks and for on-demand generation of entangled single-spin/single-photon pairs. Such applications require the ability to tune the NV-center zero-phonon optical transitions, to compensate for natural sample inhomogeneities which perturb the electronic orbital states. Here we demonstrate the ability to electrically control the orbitals of individual NV centers by applying voltages to micron-scale surface gates [3]. Surprisingly, the local electric field experienced by an NV center is significantly enhanced by a photoinduced space charge resulting from photoionization of deep donor impurities within the diamond, even in high-purity single-crystal material (< 5 ppb nitrogen content). Since the photoinduced electric fields are reproducible as a function of gate voltage and are predominantly directed perpendicular to the diamond surface, we can harness them to obtain three-dimensional control of the local electric field vector with surface gates alone. To demonstrate this technique, we tune the excited-state orbital doublet of a strained NV center to degeneracy, as required for some spin-photon entanglement protocols [2], and then adjust the optical transition frequency, showing that we can tune multiple NV centers to have the same degenerate transition energy. This method should enable the coherent coupling of multiple NV center spins to indistinguishable photons within a scalable photonic network.