Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userPolarizing the electronic and nuclear spin of the NV-center in diamond in arbitrary magnetic fields: analysis of the optical pumping process
347
0
0.0
(
0
)
Ask ChatGPT about the research
No Arabic abstract
Initializing a set of qubits to a given quantum state is a basic prerequisite for the physical implementation of quantum-information protocols. Here, we discuss the polarization of the electronic and nuclear spin in a single nitrogen vacancy center in diamond. Our initialization scheme uses a sequence of laser, microwave and radio-frequency pulses, and we optimize the pumping parameters of the laser pulse. A rate equation model is formulated that explains the effect of the laser pulse on the spin system. We have experimentally determined the population of the relevant spin states as a function of the duration of the laser pulse by measuring Rabi oscillations and Ramsey-type free-induction decays. The experimental data have been analyzed to determine the pumping rates of the rate equation model.
rate research
Read More
We propose a protocol that achieves arbitrary N-qubit interactions between nuclear spins and that can measure directly nuclear many-body correlators by appropriately making the nuclear spins interact with a nitrogen vacancy (NV) center electron spin. The method takes advantage of recently introduced dynamical decoupling techniques and demonstrates that action on the electron spin is sufficient to fully exploit nuclear spins as robust quantum registers. Our protocol is general, being applicable to other nuclear spin based platforms with electronic spin defects acting as mediators as the case of silicon carbide.
A rotation sensor is one of the key elements of inertial navigation systems and compliments most cellphone sensor sets used for various applications. Currently, inexpensive and efficient solutions are mechanoelectronic devices, which nevertheless lack long-term stability. Realization of rotation sensors based on spins of fundamental particles may become a drift-free alternative to such devices. Here, we carry out a proof-of-concept experiment, demonstrating rotation measurements on a rotating setup utilizing nuclear spins of an ensemble of NV centers as a sensing element with no stationary reference. The measurement is verified by a commercially available MEMS gyroscope.
We experimentally investigate the protection of electron spin coherence of nitrogen vacancy (NV) center in diamond by dynamical nuclear polarization. The electron spin decoherence of an NV center is caused by the magnetic ield fluctuation of the $^{13}$C nuclear spin bath, which contributes large thermal fluctuation to the center electron spin when it is in equilibrium state at room temperature. To address this issue, we continuously transfer the angular momentum from electron spin to nuclear spins, and pump the nuclear spin bath to a polarized state under Hartman-Hahn condition. The bath polarization effect is verified by the observation of prolongation of the electron spin coherence time ($T_2^*$). Optimal conditions for the dynamical nuclear polarization (DNP) process, including the pumping pulse duration and depolarization effect of laser pulses, are studied. Our experimental results provide strong support for quantum information processing and quantum simulation using polarized nuclear spin bath in solid state systems.
The negatively-charged nitrogen-vacancy (NV) center in diamond is at the frontier of quantum nano-metrology and bio-sensing. Recent attention has focused on the application of high-sensitivity thermometry using the spin resonances of NV centers in nano-diamond to sub-cellular biological and biomedical research. Here, we report a comprehensive investigation of the thermal properties of the centers spin resonances and demonstrate an alternate all-optical NV thermometry technique that exploits the temperature dependence of the centers optical Debye-Waller factor.
We introduce an alternate route to dynamically polarize the nuclear spin host of nitrogen-vacancy (NV) centers in diamond. Our approach articulates optical, microwave and radio-frequency pulses to recursively transfer spin polarization from the NV electronic spin. Using two complementary variants of the same underlying principle, we demonstrate nitrogen nuclear spin initialization approaching 80% at room temperature both in ensemble and single NV centers. Unlike existing schemes, our approach does not rely on level anti-crossings and is thus applicable at arbitrary magnetic fields. This versatility should prove useful in applications ranging from nanoscale metrology to sensitivity-enhanced NMR.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
