Ashok Ajoy

Stable three-axis nuclear-spin gyroscope in diamond

We propose a sensitive and stable three-axis gyroscope in diamond. We achieve high sensitivity by exploiting the long coherence time of the N14 nuclear spin associated with the Nitrogen-Vacancy center in diamond, and the efficient polarization and measurement of its electronic spin. While the gyroscope is based on a simple Ramsey interferometry scheme, we use coherent control of the quantum sensor to improve its coherence time as well as its robustness against long-time drifts, thus achieving a very robust device with a resolution of 0.5mdeg/s/(Hz mm^3)^(1/2). In addition, we exploit the four axes of delocalization of the Nitrogen-Vacancy center to measure not only the rate of rotation, but also its direction, thus obtaining a compact three-axis gyroscope.

Quantum simulation via filtered Hamiltonian engineering: application to perfect quantum transport in spin networks.

We propose a method for Hamiltonian engineering that requires no local control but only relies on collective qubit rotations and field gradients. The technique achieves a spatial modulation of the coupling strengths via a dynamical construction of a weighting function combined with a Bragg grating. As an example, we demonstrate how to generate the ideal Hamiltonian for perfect quantum information transport between two separated nodes of a large spin network. We engineer a spin chain with optimal couplings starting from a large spin network, such as one naturally occurring in crystals, while decoupling all unwanted interactions. For realistic experimental parameters, our method can be used to drive almost perfect quantum information transport at room temperature. The Hamiltonian engineering method can be made more robust under decoherence and coupling disorder by a novel apodization scheme. Thus, the method is quite general and can be used to engineer the Hamiltonian of many complex spin lattices with different topologies and interactions.

Svetlichny's inequality and genuine tripartite nonlocality in three-qubit pure states

The violation of the Svetlichnys inequality (SI) [Phys. Rev. D 35, 3066 (1987)] is sufficient but not necessary for genuine tripartite nonlocal correlations. Here we quantify the relationship between tripartite entanglement and the maximum expectation value of the Svetlichny operator (which is bounded from above by the inequality) for the two inequivalent subclasses of pure three-qubit states: the Greenberger-Horne-Zeilinger (GHZ) class and the W class. We show that the maximum for the GHZ-class states reduces to Mermins inequality [Phys. Rev. Lett. 65, 1838 (1990)] modulo a constant factor, and although it is a function of the three tangle and the residual concurrence, large numbers of states do not violate the inequality. We further show that by design SI is more suitable as a measure of genuine tripartite nonlocality between the three qubits in the W-class states,and the maximum is a certain function of the bipartite entanglement (the concurrence) of the three reduced states, and only when their sum attains a certain threshold value do they violate the inequality.

Decay of spin coherences in one-dimensional spin systems

Strategies to protect multi-qubit states against decoherence are difficult to formulate because of their complex many-body dynamics. A better knowledge of the decay dynamics would help in the construction of dynamical decoupling control schemes. Here we use solid-state nuclear magnetic resonance techniques to experimentally investigate decay of coherent multi-spin states in linear spin chains. Leveraging on the quasi-one-dimension geometry of fluorapatite crystal spin systems, we can gain a deeper insight on the multi- spin states created by the coherent evolution, and their subsequent decay, than it is possible in three-dimensional (3D) systems. We are then able to formulate an analytical model that captures the key features of the decay. We can thus compare the decoherence behavior for different initial states of the spin chain and link their decay rate to the state characteristics, in particular their coherence and long-range correlation among spins. Our experimental and theoretical study shows that the spin chains undergo a rich dynamics, with a slower decay rate than for the 3D case, and thus might be more amenable to decoupling techniques.

Quantum interpolation for high-resolution sensing

Significance Nanoscale magnetic resonance imaging enabled by quantum sensors is a promising path toward the outstanding goal of determining the structure of single biomolecules at room temperature. We develop a technique, which we name “quantum interpolation,” to improve the frequency resolution of these quantum sensors far beyond limitations set by the experimental controlling apparatus. The method relies on quantum interference to achieve high-fidelity interpolation of the quantum dynamics between hardware-allowed time samplings, thus allowing high-resolution sensing. We demonstrate over two orders of magnitude resolution gains, and discuss applications of our work to high-resolution nanoscale magnetic resonance imaging. Recent advances in engineering and control of nanoscale quantum sensors have opened new paradigms in precision metrology. Unfortunately, hardware restrictions often limit the sensor performance. In nanoscale magnetic resonance probes, for instance, finite sampling times greatly limit the achievable sensitivity and spectral resolution. Here we introduce a technique for coherent quantum interpolation that can overcome these problems. Using a quantum sensor associated with the nitrogen vacancy center in diamond, we experimentally demonstrate that quantum interpolation can achieve spectroscopy of classical magnetic fields and individual quantum spins with orders of magnitude finer frequency resolution than conventionally possible. Not only is quantum interpolation an enabling technique to extract structural and chemical information from single biomolecules, but it can be directly applied to other quantum systems for superresolution quantum spectroscopy.

Perfect quantum transport in arbitrary spin networks

Spin chains have been proposed as wires to transport information between distributed registers in a quantum information processor. Unfortunately, the challenges in manufacturing linear chains with engineered couplings has hindered experimental implementations. Here we present strategies to achieve perfect quantum information transport in arbitrary spin networks. Our proposal is based on the weak coupling limit for pure state transport, where information is transferred between two end spins that are only weakly coupled to the rest of the network. This regime allows ignoring the complex, internal dynamics of the bulk network and relying on virtual transitions or on the coupling to a single bulk eigenmode. We further introduce control methods capable of tuning the transport process and achieve perfect fidelity with limited resources, involving only manipulation of the end qubits. These strategies could be thus applied not only to engineered systems with relaxed fabrication precision, but also to naturally occurring networks; specifically, we discuss the practical implementation of quantum state transfer between two separated nitrogen vacancy (NV) centers through a network of nitrogen substitutional impurities.

Mixed-state quantum transport in correlated spin networks

Quantum spin networks can be used to transport information between separated registers in a quantum information processor. To find a practical implementation, the strict requirements of ideal models for perfect state transfer need to be relaxed, allowing for complex coupling topologies and general initial states. Here we analyze transport in complex quantum spin networks in the maximally mixed state and derive explicit conditions that should be satisfied by propagators for perfect state transport. Using a description of the transport process as a quantum walk over the network, we show that it is necessary to phase correlate the transport processes occurring along all the possible paths in the network. We provide a Hamiltonian that achieves this correlation, and use it in a constructive method to derive engineered couplings for perfect transport in complicated network topologies.

Bright nanowire single photon source based on SiV centers in diamond

The practical implementation of many quantum technologies relies on the development of robust and bright single photon sources that operate at room temperature. The negatively charged silicon-vacancy (SiV-) color center in diamond is a possible candidate for such a single photon source. However, due to the high refraction index mismatch to air, color centers in diamond typically exhibit low photon out-coupling. An additional shortcoming is due to the random localization of native defects in the diamond sample. Here we demonstrate deterministic implantation of Si ions with high conversion efficiency to single SiV- centers, targeted to fabricated nanowires. The co-localization of single SiV- centers with the nanostructures yields a ten times higher light coupling efficiency than for single SiV- centers in bulk diamond. This enhanced photon out-coupling, together with the intrinsic scalability of the SiV- creation method, enables a new class of devices for integrated photonics and quantum science.

Algorithmic approach to simulate Hamiltonian dynamics and an NMR simulation of quantum state transfer

We propose an iterative algorithm to simulate the dynamics generated by any n-qubit Hamiltonian. The simulation entails decomposing the unitary time evolution operator U (unitary) into a product of different time-step unitaries. The algorithm product-decomposes U in a chosen operator basis by identifying a certain symmetry of U that is intimately related to the number of gates in the decomposition. We illustrate the algorithm by first obtaining a polynomial decomposition in the Pauli basis of the n-qubit quantum state transfer unitary by Di Franco et al. [Phys. Rev. Lett. 101, 230502 (2008)] that transports quantum information from one end of a spin chain to the other, and then implement it in nuclear magnetic resonance to demonstrate that the decomposition is experimentally viable. We further experimentally test the resilience of the state transfer to static errors in the coupling parameters of the simulated Hamiltonian. This is done by decomposing and simulating the corresponding imperfect unitaries.

Atomic-Scale Nuclear Spin Imaging Using Quantum-Assisted Sensors in Diamond

Nuclear spin imaging at the atomic level is essential for the understanding of fundamental biological phenomena and for applications such as drug discovery. The advent of novel nano-scale sensors has given hope of achieving the long-standing goal of single-protein, high spatial-resolution structure determination in their natural environment and ambient conditions. In particular, quantum sensors based on the spin-dependent photoluminescence of Nitrogen Vacancy (NV) centers in diamond have recently been used to detect nanoscale ensembles of external nuclear spins. While NV sensitivity is approaching single-spin levels, extracting relevant information from a very complex structure is a further challenge, since it requires not only the ability to sense the magnetic field of an isolated nuclear spin, but also to achieve atomic-scale spatial resolution. Here we propose a method that, by exploiting the coupling of the NV center to an intrinsic quantum memory associated with the Nitrogen nuclear spin, can reach a tenfold improvement in spatial resolution, down to atomic scales. The spatial resolution enhancement is achieved through coherent control of the sensor spin, which creates a dynamic frequency filter selecting only a few nuclear spins at a time. We propose and analyze a protocol that would allow not only sensing individual spins in a complex biomolecule, but also unraveling couplings among them, thus elucidating local characteristics of the molecule structure.