2014

We propose an all-optical scheme to prolong the quantum coherence of a negatively charged nitrogen-vacancy (NV) center in diamond at cryogenic temperatures. Optical control of the NV spin suppresses energy fluctuations of the $^{3}{{{\rm A}}_{2}}$ ground states and forms an energy gap protected subspace. By optical control, the spectral linewidth of magnetic resonance is much narrower and the measurement of the frequencies of magnetic field sources has higher resolution. The optical control also improves the sensitivity of the magnetic field detection and can provide measurement of the directions of signal sources.
H Landa, Retzker, A, Schaetz, T, and Reznik, B. 7/30/2014. Entanglement Generation Using Discrete Solitons In Coulomb Crystals. Physical Review Letters, 113, 5. https://doi.org/10.1103/PhysRevLett.113.053001. Publisher's Version
Laser-cooled and trapped ions can crystallize and feature discrete solitons that are nonlinear, topologically protected configurations of the Coulomb crystal. Such solitons, as their continuum counterparts, can move within the crystal, while their discreteness leads to the existence of a gap-separated, spatially localized motional mode of oscillation above the spectrum. Suggesting that these unique properties of discrete solitons can be used for generating entanglement between different sites of the crystal, we study a detailed proposal in the context of state-of-the-art experimental techniques. We analyze the interaction of periodically driven planar ion crystals with optical forces, revealing the effects of micromotion in radio-frequency traps inherent to such structures, as opposed to linear ion chains. The proposed method requires Doppler cooling of the crystal and sideband cooling of the soliton’s localized modes alone. Since the gap separation of the latter is nearly independent of the crystal size, this approach could be particularly useful for producing entanglement and studying system-environment interactions in large, two- and possibly three-dimensional systems.
A proposal to use trapped ions to implement spin-one XXZ antiferromagnetic chains as an experimental tool to explore the Haldane phase is presented. We explain how to reach the Haldane phase adiabatically, demonstrate the robustness of the ground states to noise in the magnetic field and Rabi frequencies, and propose a way to detect them using their characteristics: an excitation gap and exponentially decaying correlations, a nonvanishing nonlocal string order, and a double degenerate entanglement spectrum. Scaling up to higher dimensions and more frustrated lattices, we obtain richer phase diagrams, and we can reach spin liquid phase, which can be detected by its entanglement entropy which obeys the boundary law.
G Arrad, Vinkler, Y, Aharonov, D, and Retzker, A. 4/16/2014. Increasing Sensing Resolution With Error Correction. Physical Review Letters, 112, 15. https://doi.org/10.1103/PhysRevLett.112.150801. Publisher's Version
The signal to noise ratio of quantum sensing protocols scales with the square root of the coherence time. Thus, increasing this time is a key goal in the field. By utilizing quantum error correction, we present a novel way of prolonging such coherence times beyond the fundamental limits of current techniques. We develop an implementable sensing protocol that incorporates error correction, and discuss the characteristics of these protocols in different noise and measurement scenarios. We examine the use of entangled versue untangled states, and error correction’s reach of the Heisenberg limit. The effects of error correction on coherence times are calculated and we show that measurement precision can be enhanced for both one-directional and general noise.
Interferometry with massive particles may have the potential to explore the limitations of standard quantum mechanics, in particular where it concerns its boundary with general relativity and the yet to be developed theory of quantum gravity. This development is hindered considerably by the lack of experimental evidence and testable predictions. Analyzing effects that appear to be common to many of such theories, such as a modification of the energy dispersion and of the canonical commutation relation within the standard framework of quantum mechanics, has been proposed as a possible way forward. Here we analyze in some detail the impact of a modified energy-momentum dispersion in a Ramsey-Bordé setup and provide achievable bounds of these correcting terms when operating such an interferometer with nanodiamonds. Thus, taking thermal and gravitational disturbances into account will show that without specific prerequisites, quantum gravity modifications may in general be suppressed requiring a revision of previously estimated bounds. As a possible solution we propose a stable setup which is rather insensitive to these effects. Finally, we address the problems of decoherence and pulse errors in such setups and discuss the scalings and advantages with increasing particle mass.
A Albrecht, Koplovitz, G, Retzker, A, Jelezko, F, Yochelis, S, Porath, D, Nevo, Y, Shoseyov, O, Paltiel, Y, and Plenio, MB . 9/4/2014. Self-Assembling Hybrid Diamond-Biological Quantum Devices. New Journal Of Physics, 16. https://iopscience.iop.org/article/10.1088/1367-2630/16/9/093002. Publisher's Version
The realization of scalable arrangements of nitrogen vacancy (NV) centers in diamond remains a key challenge on the way towards efficient quantum information processing, quantum simulation and quantum sensing applications. Although technologies based on implanting NV-centers in bulk diamond crystals or hybrid device approaches have been developed, they are limited by the achievable spatial resolution and by the intricate technological complexities involved in achieving scalability. We propose and demonstrate a novel approach for creating an arrangement of NV-centers, based on the self-assembling capabilities of biological systems and their beneficial nanometer spatial resolution. Here, a self-assembled protein structure serves as a structural scaffold for surface functionalized nanodiamonds, in this way allowing for the controlled creation of NV-structures on the nanoscale and providing a new avenue towards bridging the bio–nano interface. One-, two- as well as three-dimensional structures are within the scope of biological structural assembling techniques. We realized experimentally the formation of regular structures by interconnecting nanodiamonds using biological protein scaffolds. Based on the achievable NV-center distances of 11 nm, we evaluate the expected dipolar coupling interaction with neighboring NV-centers as well as the expected decoherence time. Moreover, by exploiting these couplings, we provide a detailed theoretical analysis on the viability of multiqubit quantum operations, suggest the possibility of individual addressing based on the random distribution of the NV intrinsic symmetry axes and address the challenges posed by decoherence and imperfect couplings. We then demonstrate in the last part that our scheme allows for the high-fidelity creation of entanglement, cluster states and quantum simulation applications.