We use a bulk acoustic wave resonator to demonstrate coherent control of the excited orbital states in a diamond nitrogen-vacancy ( N V ) center at cryogenic temperature. Coherent quantum control is an essential tool for understanding and mitigating decoherence. Moreover, characterizing and controlling orbital states is a central challenge for quantum networking, where optical coherence is tied to orbital coherence. We study resonant multiphonon orbital Rabi oscillations in both the frequency and time domain, extracting the strength of the orbital-phonon interactions and the coherence of the acoustically driven orbital states. We reach the strong-driving limit, where the physics is dominated by the coupling induced by the acoustic waves. We find agreement between our measurements, quantum master-equation simulations, and a Landau-Zener transition model in the strong-driving limit. Using perturbation theory, we derive an expression for the orbital Rabi frequency versus the acoustic drive strength that is nonperturbative in the drive strength and agrees well with our measurements for all acoustic powers. Motivated by continuous-wave spin-resonance-based decoherence protection schemes, we model the orbital decoherence and find good agreement between our model and our measured few-to-several-nanoseconds orbital decoherence times. We discuss the outlook for orbital decoherence protection. Published by the American Physical Society 2024
We use a bulk acoustic wave resonator to demonstrate coherent control of the excited orbital states in a diamond nitrogen-vacancy ( N V ) center at cryogenic temperature. Coherent quantum control is an essential tool for understanding and mitigating decoherence. Moreover, characterizing and controlling orbital states is a central challenge for quantum networking, where optical coherence is tied to orbital coherence. We study resonant multiphonon orbital Rabi oscillations in both the frequency and time domain, extracting the strength of the orbital-phonon interactions and the coherence of the acoustically driven orbital states. We reach the strong-driving limit, where the physics is dominated by the coupling induced by the acoustic waves. We find agreement between our measurements, quantum master-equation simulations, and a Landau-Zener transition model in the strong-driving limit. Using perturbation theory, we derive an expression for the orbital Rabi frequency versus the acoustic drive strength that is nonperturbative in the drive strength and agrees well with our measurements for all acoustic powers. Motivated by continuous-wave spin-resonance-based decoherence protection schemes, we model the orbital decoherence and find good agreement between our model and our measured few-to-several-nanoseconds orbital decoherence times. We discuss the outlook for orbital decoherence protection. Published by the American Physical Society 2024
We study the resonant optical transitions of a single nitrogen-vacancy (NV) center that is coherently dressed by a strong mechanical drive. Using a gigahertz-frequency diamond mechanical resonator that is strain coupled to a NV center's orbital states, we demonstrate coherent Raman sidebands out to the ninth order and orbital-phonon interactions that mix the two excited-state orbital branches. These interactions are spectroscopically revealed through a multiphonon Rabi splitting of the orbital branches which scales as a function of resonator driving amplitude and is successfully reproduced in a quantum model. Finally, we discuss the application of mechanical driving to engineering NV-center orbital states.
Optically addressable spin defects in solid-state materials have shown great potential for applications ranging from metrology to quantum information processing. Many of these experiments require a detailed understanding of the full Hamiltonian dynamics in order to develop precise quantum control. Here we use picosecond resonant optical pulses to investigate the coherent orbital and spin dynamics of the nitrogen-vacancy (NV) center in diamond, over timescales spanning six orders of magnitude. We implement an ultrafast optical pump-probe technique to study the NV center’s orbital-doublet, spin-triplet excited state at cryogenic temperatures (T < 20 K), where the excited state becomes stable and optically coherent with the ground state. This technique, coupled with optical polarization selection rules, allows us to probe the coherent orbital dynamics of the NV center’s excited state [1]. These experiments reveal dynamics on femtosecond to nanosecond timescales due to the interplay between the ground and excited state orbital levels. This all-optical technique also provides a method to dynamically control the spin state of the NV center by harnessing the excited state structure. Through studying the spin dynamics of the NV center with coherent pulses of light, we are able to rotate the spin state on sub-nanosecond timescales. Furthermore, by tuning the excited-state spin Hamiltonian with an external magnetic eld, we demonstrate arbitrary-axis spin rotations through controlled unitary evolution of the spin state. Extending this to the full excited-state manifold, we develop a time-domain quantum tomography technique to precisely map the NV center’s excited state Hamiltonian. These techniques generalize to other systems and can be a powerful tool in characterizing and controlling qubits in other optically addressable spin systems.
We investigate coherent quantum control of a nitrogen vacancy (NV) center in diamond with microwave fields generated from a nanoscale magnet that is proximal to the NV center. Our results show remarkable coherent control with high contrast Rabi oscillations using nearfield microwaves from shape anisotropic nanomagnets of lateral dimensions down to 200 nm x 180 nm, driven remotely by surface acoustic wave (SAW) excitation that is at least 400 times and potentially 4 orders of magnitude more energy efficient than generating microwaves with an antenna. Furthermore, we show that varying the acoustic power driving such nanomagnets can achieve control over Rabi frequency. We also report spin-lattice relaxation time T1 is 103 +/-0.5 micro-seconds, the spin-spin relaxation time T2 is 1.23+/-0.29 micro-seconds, and the Ramsey coherence time T2* is 218+/-27 nanoseconds measured using microwave pulses generated by such nanomagnets. The use of the nanoscale magnets to implement highly localized and energy efficient coherent quantum control can replace thermally noisy microwave circuits and demonstrate a path to scalable quantum computing and sensing with NV-defects in diamond and other spin qubits.
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.
Surface acoustic wave (SAW) phonon coupling with nitrogen-vacancy (NV) center spins in diamond offers a promising platform for on-chip quantum phononic manipulations. Although an ensemble of NV centers coupled to a common SAW phonon mode enables superradiance and collective quantum control, achieving a tunable superradiant phase transition remains challenging. Here, we show that optically driving NV centers level transitions enhances the effective spin-phonon coupling, triggering a SAW phonon superradiant phase transition in the weak-coupling regime. We also demonstrate that above a critical threshold, the driving light rapidly switches on the phonon superradiance--a dynamic effect that persists in finite-number NV ensembles. Our results provide a controllable route to coherent phonon-NV spin manipulation in solid state quantum devices.
The nitrogen-vacancy (NV) center in diamond has emerged as a versatile atom-like system, finding diverse applications at both ambient and cryogenic temperatures. At room temperature, the NV center's spin-triplet electronic ground state has a long coherence time and can be read out and initialized using nonresonant optical excitation, which has enabled a wide range of metrology and quantum information applications. At cryogenic temperatures, the NV center exhibits a variety of narrow, atom-like optical transitions, which has made the NV center a promising platform for quantum optics applications. We use coherent optical manipulation of the NV center at cryogenic temperatures to probe its internal dynamics and aspects of its interactions with its environment.\nFirst, we investigate the intersystem crossing (ISC) process, which is a spin-dependent nonradiative decay mechanism that enables the electronic spin state to be optically initialized and read out at room temperature. We measure the ISC rates from different excited states as well as the rate at which interactions with phonons redistribute population between these states. Based on these measurements, we develop a theoretical model that unifies the phonon-induced mixing and ISC mechanisms. We find that our model is in excellent agreement with experiment and that it can be used to predict unknown elements of the NV center's electronic structure.\nSecond, we investigate a novel method of using coherent optical manipulation of the NV center's electronic spin to control a nearby nuclear spin. Coherent interactions between the NV center and nearby nuclear spins have enabled the development of NV center-based, multi-qubit quantum registers, but these techniques have generally required the application of microwave or radio-frequency radiation. We demonstrate control of the nuclear spin using an all-optical Raman technique and theoretically evaluate the extent to which the intrinsic physics of the NV center limits the coherence of this Raman-based manipulation technique.