Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userAnisotropic electron-nuclear interactions in a rotating quantum spin bath
368
0
0.0
(
0
)
Ask ChatGPT about the research
No Arabic abstract
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.
rate research
Read More
A major problem facing the realisation of scalable solid-state quantum computing is that of overcoming decoherence - the process whereby phase information encoded in a qubit is lost as the qubit interacts with its environment. Due to the vast number of environmental degrees of freedom, it is challenging to accurately calculate decoherence times $T_2$, especially when the qubit and environment are highly correlated. Hybrid or mixed electron-nuclear spin qubits, such as donors in silicon, possess optimal working points (OWPs) which are sweet-spots for reduced decoherence in magnetic fields. Analysis of sharp variations of $T_2$ near OWPs was previously based on insensitivity to classical noise, even though hybrid qubits are situated in highly correlated quantum environments, such as the nuclear spin bath of $^{29}$Si impurities. This presented limited understanding of the decoherence mechanism and gave unreliable predictions for $T_2$. I present quantum many-body calculations of the qubit-bath dynamics, which (i) yield $T_2$ for hybrid qubits in excellent agreement with experiments in multiple regimes, (ii) elucidate the many-body nature of the nuclear spin bath and (iii) expose significant differences between quantum-bath and classical-field decoherence. To achieve these, the cluster correlation expansion was adapted to include electron-nuclear state mixing. In addition, an analysis supported by experiment was carried out to characterise the nuclear spin bath for a bismuth donor as the hybrid qubit, a simple analytical formula for $T_2$ was derived with predictions in agreement with experiment, and the established method of dynamical decoupling was combined with operating near OWPs in order to maximise $T_2$. Finally, the decoherence of a $^{29}$Si spin in proximity to the hybrid qubit was studied, in order to establish the feasibility for its use as a quantum register.
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.
We apply the time-convolutionless (TCL) projection operator technique to the model of a central spin which is coupled to a spin bath via nonuniform Heisenberg interaction. The second-order results of the TCL method for the coherences and populations of the central spin are determined analytically and compared with numerical simulations of the full von Neumann equation of the total system. The TCL approach is found to yield an excellent approximation in the strong field regime for the description of both the short-time dynamics and the long time behavior.
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.
In this paper, we study the electron spin decoherence of single defects in silicon carbide (SiC) nuclear spin bath. We find that, although the natural abundance of $^{29}rm{Si}$ ($p_{rm{Si}}=4.7%$) is about 4 times larger than that of $^{13}{rm C}$ ($p_{rm{C}}=1.1%$), the electron spin coherence time of defect centers in SiC nuclear spin bath in strong magnetic field ($B>300~rm{Gauss}$) is longer than that of nitrogen-vacancy (NV) centers in $^{13}{rm C}$ nuclear spin bath in diamond. The reason for this counter-intuitive result is the suppression of heteronuclear-spin flip-flop process in finite magnetic field. Our results show that electron spin of defect centers in SiC are excellent candidates for solid state spin qubit in quantum information processing.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
