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Register a new userFast Phase-manipulation of the Single Nuclear Spin in Solids by Rotating Fields
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We propose fast phase-gates of single nuclear spins interacting with single electron spins. The gate operation utilizes geometric phase shifts of the electron spin induced by fast/slow rotating fields; the path difference depending on nuclear spin states enables nuclear phase shifts. The gate time is inversely proportional to the frequency of the slow rotating field. As an example, we use nitrogen-vacancy centers in diamond, and show the phase-gate time orders of magnitude shorter than previously reported. We also show the robustness of the gate against decoherence and systematic errors.
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A precessing spin observed in a rotating frame of reference appears frequency-shifted, an effect analogous to the precession of a Foucault pendulum observed on the rotating Earth. This frequency shift can be understood as arising from a magnetic pseudo-field in the rotating frame that nevertheless has physically significant consequences, such as the Barnett effect. Detecting these pseudo-fields is experimentally challenging, as a rotating-frame sensor is required. Previous work has realised classical rotating-frame detectors. Here we use quantum sensors, nitrogen-vacancy (NV) centres, in a rapidly rotating diamond to detect pseudo-fields in the rotating frame. While conventional magnetic fields induce precession at a rate proportional to the gyromagnetic ratio, rotation shifts the precession of all spins equally, and thus primarily affect nearby $^{13}$C nuclear spins. We are thus able to explore these effects via quantum sensing in a rapidly rotating frame, and define a new approach to quantum control using rotationally-induced nuclear spin-selective magnetic fields. This work provides an integral step towards realising precision rotation sensing and quantum spin gyroscopes.
Precise characterization of a hyperfine interaction is a prerequisite for high fidelity manipulations of electron and nuclear spins belonging to a hybrid qubit register in diamond. Here, we demonstrate a novel scheme for determining a hyperfine interaction, using single-quantum and zero-quantum Ramsey fringes, by applying it to the system of a Nitrogen Vacancy (NV) center and a $^{13}$C nuclear spin in the 1$^{mathrm{st}}$ shell. The zero-quantum Ramsey fringe, analogous to the quantum beat in a $Lambda$-type level structure, particularly enhances the measurement precision for non-secular hyperfine terms. Precisions less than 0.5 MHz in the estimation of all the components in the hyperfine tensor were achieved. Furthermore, for the first time we experimentally determined the principal axes of the hyperfine interaction in the system. Beyond the 1$^{mathrm{st}}$ shell, this method can be universally applied to other $^{13}$C nuclear spins interacting with the NV center.
We use single-spin resonant spectroscopy to study the spin structure in the orbital excited-state of a diamond nitrogen-vacancy center at room temperature. We find that the excited state spin levels have a zero-field splitting that is approximately half of the value of the ground state levels, a g-factor similar to the ground state value, and a hyperfine splitting ~20x larger than in the ground state. In addition, the width of the resonances reflects the electronic lifetime in the excited state. We also show that the spin-splitting can significantly differ between NV centers, likely due to the effects of local strain, which provides a pathway to control over the spin Hamiltonian and may be useful for quantum information processing.
Magnetic solitons can constitute a means for manipulating qubits from a distance. This would overcome the necessity of directly applying selective magnetic fields, which is unfeasible in the case of a matrix of qubits embedded in a solid-state quantum device. If the latter contained one-dimensional Heisenberg spin chains coupled to each qubit, one can originate a soliton in a selected chain by applying a time-dependent field at one end of it, far from the qubits. The generation of realistic solitons has been simulated. When a suitable soliton passes by, the coupled qubit undergoes nontrivial operations, even in the presence of moderate thermal noise.
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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