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Register a new userQuantum control of nuclear spin qubits in a rapidly rotating diamond
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Nuclear spins in certain solids couple weakly to their environment, making them attractive candidates for quantum information processing and inertial sensing. When coupled to the spin of an optically-active electron, nuclear spins can be rapidly polarized, controlled and read via lasers and radiofrequency fields. Possessing coherence times of several milliseconds at room temperature, nuclear spins hosted by a nitrogen-vacancy center in diamond are thus intriguing systems to observe how classical physical rotation at quantum timescales affects a quantum system. Unlocking this potential is hampered by precise and inflexible constraints on magnetic field strength and alignment in order to optically induce nuclear polarization, which restricts the scope for further study and applications. In this work, we demonstrate optical nuclear spin polarization and rapid quantum control of nuclear spins in a diamond physically rotating at $1,$kHz, faster than the nuclear spin coherence time. Free from the need to maintain strict field alignment, we are able to measure and control nuclear spins in hitherto inaccessible regimes, such as in the presence of a large, time-varying magnetic field that makes an angle of more than $100^circ$ to the nitrogen-lattice vacancy axis. The field induces spin mixing between the electron and nuclear states of the qubits, decoupling them from oscillating rf fields. We are able to demonstrate that coherent spin state control is possible at any point of the rotation, and even for up to six rotation periods. We combine continuous dynamical decoupling with quantum feedforward control to eliminate decoherence induced by imperfect mechanical rotation. Our work liberates a previously inaccessible degree of freedom of the NV nuclear spin, unlocking new approaches to quantum control and rotation sensing.
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A controlled qubit in a rotating frame opens new opportunities to probe fundamental quantum physics, such as geometric phases in physically rotating frames, and can potentially enhance detection of magnetic fields. Realising a single qubit that can be measured and controlled during physical rotation is experimentally challenging. In this work, we demonstrate quantum control of a single nitrogen-vacancy (NV) centre within a diamond rotated at 200,000rpm, a rotational period comparable to the NV spin coherence time $T_2$. We stroboscopically image individual NV centres that execute rapid circular motion in addition to rotation, and demonstrate preparation, control and readout of the qubit quantum state with lasers and microwaves. Using spin-echo interferometry of the rotating qubit, we are able to detect modulation of the NV Zeeman shift arising from the rotating NV axis and an external DC magnetic field. Our work establishes single NV qubits in diamond as quantum sensors in the physically rotating frame, and paves the way for the realisation of single-qubit diamond-based rotation sensors.
Hybrid quantum registers, such as electron-nuclear spin systems, have emerged as promising hardware for implementing quantum information and computing protocols in scalable systems. Nevertheless, the coherent control of such systems still faces challenges. Particularly, the lower gyromagnetic ratios of the nuclear spins cause them to respond slowly to control fields, resulting in gate times that are generally longer than the coherence time of the electron spin. Here, we demonstrate a scheme for circumventing this problem by indirect control: We apply a small number of short pulses only to the electron spin and let the full system undergo free evolution under the hyperfine coupling between the pulses. Using this scheme, we realize robust quantum gates in an electron-nuclear spin system, including a Hadamard gate on the nuclear spin and a controlled-NOT gate with the nuclear spin as the target qubit. The durations of these gates are shorter than the electron spin coherence time, and thus additional operations to extend the system coherence time are not needed. Our demonstration serves as a proof of concept for achieving efficient coherent control of electron-nuclear spin systems, such as NV centers in diamond. Our scheme is still applicable when the nuclear spins are only weakly coupled to the electron spin.
We introduce an optical tweezer platform for assembling and individually manipulating a two-dimensional register of nuclear spin qubits. Each nuclear spin qubit is encoded in the ground $^{1}S_{0}$ manifold of $^{87}$Sr and is individually manipulated by site-selective addressing beams. We observe that spin relaxation is negligible after 5 seconds, indicating that $T_1gg5$ s. Furthermore, utilizing simultaneous manipulation of subsets of qubits, we demonstrate significant phase coherence over the entire register, estimating $T_2^star = left(21pm7right)$ s and measuring $T_2^text{echo}=left(42pm6right)$ s.
We use the electronic spin of a single Nitrogen-Vacancy (NV) defect in diamond to observe the real-time evolution of neighboring single nuclear spins under ambient conditions. Using a diamond sample with a natural abundance of $^{13}$C isotopes, we first demonstrate high fidelity initialization and single-shot readout of an individual $^{13}$C nuclear spin. By including the intrinsic $^{14}$N nuclear spin of the NV defect in the quantum register, we then report the simultaneous observation of quantum jumps linked to both nuclear spin species, providing an efficient initialization of the two qubits. These results open up new avenues for diamond-based quantum information processing including active feedback in quantum error correction protocols and tests of quantum correlations with solid-state single spins at room temperature.
The interaction between a central qubit spin and a surrounding bath of spins is critical to spin-based solid state quantum sensing and quantum information processing. Spin-bath interactions are typically strongly anisotropic, and rapid physical rotation has long been used in solid-state nuclear magnetic resonance to simulate motional averaging of anisotropic interactions, such as dipolar coupling between nuclear spins. Here, we show that the interaction between electron spins of nitrogen-vacancy centers and a bath of $^{13}$C nuclear spins in a diamond rotated at up to 300,000rpm introduces decoherence into the system via frequency-modulation of the nuclear spin Larmor precession. The presence of an off-axis magnetic field necessary for averaging of the dipolar coupling leads to a rotational dependence of the electron-nuclear hyperfine interaction, which cannot be averaged out with experimentally achievable rotation speeds. Our findings offer new insights into the use of physical rotation for quantum control with implications for quantum systems having motional and rotational degrees of freedom that are not fixed.
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