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Spin-based quantum information processing makes extensive use of spin-state manipulation. This ranges from dynamical decoupling of nuclear spins in quantum sensing experiments to applying logical gates on qubits in a quantum processor. Fast manipulation of spin states is highly desirable for accelerating experiments, enhancing sensitivity, and applying elaborate pulse sequences. Strong driving using intense radio-frequency (RF) fields can, therefore, facilitate fast manipulation and enable broadband excitation of spin species. In this work, we present an antenna for strong driving in quantum sensing experiments and theoretically address challenges of the strong driving regime. First, we designed and implemented a micron-scale planar spiral RF antenna capable of delivering intense fields to a sample. The planar antenna is tailored for quantum sensing experiments using the diamond’s nitrogen-vacancy (NV) center and should be applicable to other solid-state defects. The antenna has a broad bandwidth of 22 MHz, is compatible with scanning probes, and is suitable for cryogenic and ultrahigh vacuum conditions. We measure the magnetic field induced by the antenna and estimate a field-to-current ratio of $113 \pm 16$ G/A, representing a six-fold increase in efficiency compared to the state-of-the-art, crucial for cryogenic experiments. We demonstrate the antenna by driving Rabi oscillations in ^1 H spins of an organic sample on the diamond surface and measure ^1 H Rabi frequencies of over 500 kHz, i.e. $\mathrm{\pi}$ -pulses shorter than 1 $\mu\mathrm{s}$ —an order of magnitude faster than previously reported in NV-based nuclear magnetic resonance (NMR). Finally, we discuss the implications of driving spins with a field tilted from the transverse plane in a regime where the driving amplitude is comparable to the spin-state splitting, such that the rotating wave approximation does not describe the dynamics well. We present a simple recipe to optimize pulse fidelity in this regime based on a phase and offset-shifted sine drive, which may be optimized in situ without numerical optimization procedures or precise modeling of the experiment. We consider this approach in a range of driving amplitudes and show that it is particularly efficient in the case of a tilted driving field. The results presented here constitute a foundation for implementing fast nuclear spin control in various systems.

We present a novel method for engineering an optical clock transition that is robust against external field fluctuations and is able to overcome limits resulting from field inhomogeneities. The technique is based on the application of continuous driving fields to form a pair of dressed states essentially free of all relevant shifts. Specifically, the clock transition is robust to magnetic field shifts, quadrupole and other tensor shifts, and amplitude fluctuations of the driving fields. The scheme is applicable to either a single ion or an ensemble of ions, and is relevant for several types of ions, such as ${}^{40}{\mathrm{Ca}}^{+}$ , ${}^{88}{\mathrm{Sr}}^{+}$ , ${}^{138}{\mathrm{Ba}}^{+}$ and ${}^{176}{\mathrm{Lu}}^{+}$ . Taking a spherically symmetric Coulomb crystal formed by 400 ${}^{40}{\mathrm{Ca}}^{+}$ ions as an example, we show through numerical simulations that the inhomogeneous linewidth of tens of Hertz in such a crystal together with linear Zeeman shifts of order 10 MHz are reduced to form a linewidth of around 1 Hz. We estimate a two-order-of-magnitude reduction in averaging time compared to state-of-the art single ion frequency references, assuming a probe laser fractional instability of ${10}^{-15}$ . Furthermore, a statistical uncertainty reaching 2.9 × 10 ^−16 in 1 s is estimated for a cascaded clock scheme in which the dynamically decoupled Coulomb crystal clock stabilizes the interrogation laser for an ${}^{27}{\mathrm{Al}}^{+}$ clock.

The sensitivity of magnetic resonance imaging (MRI) depends strongly on nuclear spin polarisation and, motivated by this observation, dynamical nuclear spin polarisation has recently been applied to enhance MRI protocols (Kurhanewicz et al 2011 Neoplasia http://dx.doi.org/10.1593/neo.101102 13 http://dx.doi.org/10.1593/neo.101102 ). Nuclear spins associated with the ^13 C carbon isotope (nuclear spin I = 1/2) in diamond possess uniquely long spin lattice relaxation times (Reynhardt and High 2011 Prog. Nucl. Magn. Reson. Spectrosc. http://dx.doi.org/10.1016/s0079-6565(00)00025-x 38 http://dx.doi.org/10.1016/s0079-6565(00)00025-x ). If they are present in diamond nanocrystals, especially when strongly polarised, they form a promising contrast agent for MRI. Current schemes for achieving nuclear polarisation, however, require cryogenic temperatures. Here we demonstrate an efficient scheme that realises optically induced ^13 C nuclear spin hyperpolarisation in diamond at room temperature and low ambient magnetic field. Optical pumping of a nitrogen-vacancy centre creates a continuously renewable electron spin polarisation which can be transferred to surrounding ^13 C nuclear spins. Importantly for future applications we also realise polarisation protocols that are robust against an unknown misalignment between magnetic field and crystal axis.

We present a new method of constructing a fully robust qubit in a three-level system. By the application of continuous driving fields, robustness to both external and controller noise is achieved. Specifically, magnetic noise and power fluctuations do not operate within the robust qubit subspace. Whereas all the continuous driving based constructions of such a fully robust qubit considered so far have required at least four levels, we show that in fact only three levels are necessary. This paves the way for simple constructions of a fully robust qubit in many atomic and solid state systems that are controlled by either microwave or optical fields. We focus on the NV-center in diamond and analyze the implementation of the scheme, by utilizing the electronic spin sub-levels of its ground state. In current state-of-the-art experimental setups the scheme leads to improvement of more than two orders of magnitude in coherence time, pushing it towards the lifetime limit. We show how the fully robust qubit can be used to implement quantum sensing, and in particular, the sensing of high frequency signals.

We construct Lindbladians associated with controlled stochastic Hamiltonians in the weak coupling regime. This construction allows us to determine the power spectrum of the noise from measurements of dephasing rates. Moreover, by studying the derived equation it is possible to optimize the control as well as to test numerical algorithms that solve controlled stochastic Schrödinger equations. A few examples are worked out in detail.

A proposal for a phase gate and a Mølmer–Sørensen gate in the dressed state basis is presented. In order to perform the multi-qubit interaction, a strong magnetic field gradient is required to couple the phonon-bus to the qubit states. The gate is performed using resonant microwave driving fields together with either a radio-frequency (RF) driving field, or additional detuned microwave driving fields. The gate is robust to ambient magnetic field fluctuations due to an applied resonant microwave driving field. Furthermore, the gate is robust to fluctuations in the microwave Rabi frequency and is decoupled from phonon dephasing due to a resonant RF or a detuned microwave driving field. This makes this new gate an attractive candidate for the implementation of high-fidelity microwave based multi-qubit gates. The proposal can also be realized in laser-based set-ups.

We propose a set of techniques that enable universal quantum computing to be carried out using dressed states. This applies in particular to the effort of realizing quantum computation in trapped ions using long-wavelength radiation, where coupling enhancement is achieved by means of static magnetic-field gradient. We show how the presence of dressing fields enables the construction of robust single and multi-qubit gates despite the unavoidable presence of magnetic noise, an approach that can be generalized to provide shielding in any analogous quantum system that relies on the coupling of electronic degrees of freedom via bosonic modes.

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.

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.

Realizing controlled quantum dynamics via the magnetic interactions between colour centres in diamond remains a challenge despite recent demonstrations for nanometre separated pairs. Here we propose to use the intrinsic acoustical phonons in diamond as a data bus for accomplishing this task. We show that for nanodiamonds the electron–phonon coupling can take significant values that together with mode frequencies in the THz range can serve as a resource for conditional gate operations. Based on these results, we analyse how to use this phonon-induced interaction for constructing quantum gates among the electron-spin triplet ground states, introducing the phonon dependence via Raman transitions. Combined with decoupling pulses this offers the possibility for creating entangled states within nanodiamonds on the scale of several tens of nanometres, a promising prerequisite for quantum sensing applications.

The detection of a nuclear spin in an individual molecule represents a key challenge in physics and biology whose solution has been pursued for many years. The small magnetic moment of a single nucleus and the unavoidable environmental noise present the key obstacles for its realization. In this paper, we demonstrate theoretically that a single nitrogen-vacancy center in diamond can be used to construct a nano-scale single-molecule spectrometer that is capable of detecting the position and spin state of a single nucleus and can determine the distance and alignment of a nuclear or electron spin pair. The proposed device would find applications in single-molecule spectroscopy in chemistry and biology, for example in determining the protein structure or in monitoring macromolecular motions, and can thus provide a tool to help unravel the microscopic mechanisms underlying bio-molecular function.

We study experimentally and theoretically the properties of structural defects (kink solitons) in two-dimensional ion Coulomb crystals. We show how different types of kink solitons with different physical properties can be realized, and transformed from one type into another by varying the aspect ratio of the trap confinement. Further, we discuss how impurities in ion Coulomb crystals, such as mass defects, can modify the dynamics of kink creation and their stability. For both pure and impure crystals, the experimentally observed kink dynamics are analysed in detail and explained theoretically by numerical simulations and calculations of the Peierls–Nabarro potential. Finally, we demonstrate that static electric fields provide a handle to vary the influence of mass defects on kinks in a controlled way and allow for deterministic manipulation and creation of kinks.

The loss of coherence is one of the main obstacles for the implementation of quantum information processing. The efficiency of dynamical decoupling schemes, which have been introduced to address this problem, is limited itself by the fluctuations in the driving fields which will themselves introduce noise. We address this challenge by introducing the concept of concatenated continuous dynamical decoupling, which can overcome not only external magnetic noise but also noise due to fluctuations in driving fields. We show theoretically that this approach can achieve relaxation limited coherence times, and demonstrate experimentally that already the most basic implementation of this concept yields an order of magnitude improvement to the decoherence time for the electron spin of nitrogen vacancy centers in diamond. The proposed scheme can be applied to a wide variety of other physical systems, including trapped atoms and ions and quantum dots, and may be combined with other quantum technologies challenges such as quantum sensing and quantum information processing.

We investigate the performance of inhomogeneously broadened spin ensembles as quantum memories under continuous dynamical decoupling. The role of the continuous driving field is twofold: firstly, it decouples individual spins from magnetic noise; secondly, and more importantly, it suppresses and reshapes the spectral inhomogeneity of spin ensembles. We show that a continuous driving field, which itself may also be inhomogeneous over the ensemble, can considerably enhance the decay of the tails of the inhomogeneous broadening distribution. This fact enables a spin-ensemble-based quantum memory to exploit the effect of cavity protection and achieve a much longer storage time. In particular, for a spin ensemble with a Lorentzian spectral distribution, our calculations demonstrate that continuous dynamical decoupling has the potential to improve its storage time by orders of magnitude for the state-of-the-art experimental parameters.

Setting off from the classic input–output formalism, we develop a theoretical framework to characterize the Gaussian quantum channels relating the initial correlations of an open bosonic system to those of properly identified output modes. We then proceed to apply our formalism to the case of quantum harmonic oscillators, such as the motional degrees of freedom of trapped ions or nanomechanical oscillators, interacting with travelling electromagnetic modes through cavity fields and subject to external white noise. We thus determine the degree of squeezing that can be transferred from an intra-cavity oscillator to light and show that the intra-cavity squeezing can be transformed into distributed optical entanglement if one can access both output fields of a two-sided cavity.

We examine the time-dependent dynamics of ion crystals in radiofrequency traps. The problem of stable trapping of general three-dimensional crystals is considered and the validity of the pseudopotential approximation is discussed. We analytically derive the micromotion amplitude of the ions, rigorously proving well-known experimental observations. We use a recently proposed method to find the modes that diagonalize the linearized time-dependent dynamical problem. This allows one to obtain explicitly the (‘Floquet–Lyapunov’) transformation to coordinates of decoupled linear oscillators. We demonstrate the utility of the method by analyzing the modes of a small ‘peculiar’ crystal in a linear Paul trap. The calculations can be readily generalized to multispecies ion crystals in general multipole traps, and time-dependent quantum wavefunctions of ion oscillations in such traps can be obtained.

The quest for experimental platforms that allow for the exploration, and even control, of the interplay of low dimensionality and frustration is a fundamental challenge in several fields of quantum many-body physics, such as quantum magnetism. Here, we propose the use of cold crystals of trapped ions to study a variety of frustrated quantum spin ladders. By optimizing the trap geometry, we show how to tailor the low dimensionality of the models by changing the number of legs of the ladders. Combined with a method for selectively hiding ions provided by laser addressing, it becomes possible to synthesize stripes of both triangular and Kagome lattices. Besides, the degree of frustration of the phonon-mediated spin interactions can be controlled by shaping the trap frequencies. We support our theoretical considerations by initial experiments with planar ion crystals, where a high and tunable anisotropy of the radial trap frequencies is demonstrated. We take into account an extensive list of possible error sources under typical experimental conditions, and describe explicit regimes that guarantee the validity of our scheme.