arXiv subjects

Fedor Jelezko

Publications and source records attributed to Fedor Jelezko.

At least 91 records · Page 5Linked to original sources

arXiv2019

Experimental measurement of the quantum geometric tensor using coupled qubits in diamond

Geometry and topology are fundamental concepts, which underlie a wide range of fascinating physical phenomena such as topological states of matter and topological defects. In quantum mechanics, the geometry of quantum states is fully captured by the quantum geometric tensor. Using a qubit formed by an NV center in diamond, we perform the first experimental measurement of the complete quantum geometric tensor. Our approach builds on a strong connection between coherent Rabi oscillations upon parametric modulations and the quantum geometry of the underlying states. We then apply our method to a system of two interacting qubits, by exploiting the coupling between the NV center spin and a neighboring $^{13}$C nuclear spin. Our results establish coherent dynamical responses as a versatile probe for quantum geometry, and they pave the way for the detection of novel topological phenomena in solid state.

quant-ph↗

arXiv2019

Preparing single SiV$^{-}$ center in nanodiamonds for external, optical coupling with access to all degrees of freedom

Optical coupling enables intermediate- and long-range interactions between distant quantum emitters. Such interaction may be the basic element in bottom-up approaches of coupled spin systems or for integrated quantum photonics and quantum plasmonics. Here, we prepare nanodiamonds carrying single, negatively-charged silicon-vacancy centers for evanescent optical coupling with access to all degrees of freedom by means of atomic force nanomanipulation. The color centers feature excellent optical properties, comparable to silicon-vacancy centers in bulk diamond, resulting in a resolvable fine structure splitting, a linewidth close to the Fourier-Transform limit under resonant excitation and a good polarization contrast. We determine the orbital relaxation time $T_{1}$ of the orbitally split ground states and show that all optical properties are conserved during translational nanomanipulation. Furthermore, we demonstrate the rotation of the nanodiamonds. In contrast to the translational operation, the rotation leads to a change in polarization contrast. We utilize the change in polarization contrast before and after nanomanipulation to determine the rotation angle. Finally, we evaluate the likelihood for indistinguishable, single photon emission of silicon-vacancy centers located in different nanodiamonds. Our work enables ideal evanescent, optical coupling of distant nanodiamonds containing silicon-vacancy centers with applications in the realization of quantum networks, quantum repeaters or complex quantum systems.

cond-mat.mtrl-sci↗

arXiv2019

Revealing the emergence of classicality in nitrogen-vacancy centers

The origin of classical reality in our quantum world is a long-standing mystery. Here, we examine a nitrogen vacancy center evolving naturally in the presence of its environment to study quantum Darwinism - the proliferation of information about preferred quantum states throughout the world via the environment. This redundantly imprinted information accounts for the perception of objective reality, as it is independently accessible by many without perturbing the system of interest. To observe the emergence of redundant information, we implement a novel dynamical decoupling scheme that enables the measurement/control of several nuclear spins (the environment E) interacting with a nitrogen vacancy (the system S). In addition to showing how to create entangled SE states relevant to quantum metrology, we demonstrate that under the decoherence of S, redundant information is imprinted onto E, giving rise to classical objectivity - a consensus of the nuclear spins about the state of S. This provides the first laboratory verification of the objective classical world emerging from the underlying quantum substrate.

quant-ph↗

arXiv2019

Discovery of ST1 centers in natural diamond

The ST1 center is a point defect in diamond with bright fluorescence and a mechanism for optical spin initialization and readout. The center has impressive potential for applications in diamond quantum computing as a quantum bus to a register of nuclear spins. This is because it has an exceptionally high readout contrast and, unlike the well-known nitrogen-vacancy center, it does not have a ground state electronic spin that decoheres the nuclear spins. However, its chemical structure is unknown and there are large gaps in our understanding of its properties. We present the discovery of ST1 centers in natural diamond. Our experiments identify interesting power dependence of the center's optical dynamics and reveal new electronic structure. We also present a theory of its electron-phonon interactions, which we combine with previous experiments, to shortlist likely candidates for its chemical structure.

quant-ph↗

arXiv2019

Nano-NMR based flow meter

Microfludic channels are now a well established platform for many purposes, including bio-medical research and Lab on a Chip applications. However, the nature of flow within these channels is still unclear. There is evidence that the mean drift velocity in these channels deviates from the regular Navier-Stokes solution with `no slip' boundary conditions. Understanding these effects, is not only of value for fundamental fluid mechanics interest, but it also has practical importance for the future development of microfluidic and nanofludic infrastructures. We propose a nano-NMR based setup for measuring the drift velocity near the surface of a microfludic channel in a non-intrusive fashion. We discuss different possible protocols, and provide a detailed analysis of the measurement's sensitivity in each case. We show that the nano-NMR scheme outperforms current fluorescence based techniques.

quant-ph↗

arXiv2019

Unidirectional single-photon emission from germanium-vacancy zero-phonon lines: Deterministic emitter-waveguide interfacing at plasmonic hot spots

Striving for nanometer-sized solid-state single-photon sources, we investigate atom-like quantum emitters based on single germanium vacancy (GeV) centers isolated in crystalline nanodiamonds (NDs). Cryogenic characterization indicated symmetry-protected and bright (> 10^6 counts/s with off-resonance excitation) zero-phonon optical transitions with up to 6-fold enhancement in energy splitting of their ground states as compared to that found for GeV centers in bulk diamonds (i.e., up to 870 GHz in highly strained NDs vs 150 GHz in bulk). Utilizing lithographic alignment techniques, we demonstrate an integrated nanophotonic platform for deterministic interfacing plasmonic waveguides with isolated GeV centers in NDs that enables 10-fold enhancement of single-photon decay rates along with the emission direction control by judiciously designing and positioning a Bragg reflector. This approach allows one to realize the unidirectional emission from single-photon dipolar sources introducing a novel method that is alternative to the propagation-direction-dependent techniques based on chiral interactions or topological protection. The developed plasmon-based nanophotonic platform opens thereby new perspectives for quantum nanophotonics in general and for realizing entanglement between single photons and spin qubits, in particular.

physics.app-ph↗

arXiv2019

Randomisation of Pulse Phases for Unambiguous and Robust Quantum Sensing

We develop theoretically and demonstrate experimentally a universal dynamical decoupling method for robust quantum sensing with unambiguous signal identification. Our method uses randomisation of control pulses to suppress simultaneously two types of errors in the measured spectra that would otherwise lead to false signal identification. These are spurious responses due to finite-width $π$ pulses, as well as signal distortion caused by $π$ pulse imperfections. For the cases of nanoscale nuclear spin sensing and AC magnetometry, we benchmark the performance of the protocol with a single nitrogen vacancy centre in diamond against widely used non-randomised pulse sequences. Our method is general and can be combined with existing multipulse quantum sensing sequences to enhance their performance.

quant-ph↗

arXiv2019

Mixed Dynamical Decoupling

We propose a scheme for mixed dynamical decoupling (MDD), where we combine continuous dynamical decoupling with robust sequences of phased pulses. Specifically, we use two fields for decoupling, where the first continuous driving field creates dressed states that are robust to environmental noise. Then, a second field implements a robust sequence of phased pulses to perform inversions of the dressed qubits, thus achieving robustness to amplitude fluctuations of both fields. We show that MDD outperforms standard concatenated continuous dynamical decoupling in realistic numerical simulations for dynamical decoupling in NV centers in diamond. Finally, we also demonstrate how our technique can be utilized for improved sensing.

quant-ph↗

arXiv2019

Initialization and Readout of Nuclear Spins via negatively charged Silicon-Vacancy Center in Diamond

In this work, we demonstrate initialization and readout of nuclear spins via a negatively charged silicon-vacancy (SiV) electron spin qubit. Under Hartmann-Hahn conditions the electron spin polarization is coherently transferred to the nuclear spin. The readout of the nuclear polarization is observed via the fluorescence of the SiV. We also show that the coherence time of the nuclear spin (6 ms) is limited by the electron spin-lattice relaxation due to the hyperfine coupling to the electron spin. This work paves the way towards realization of building blocks of quantum hardware with an efficient spin-photon interface based on the SiV color center coupled to a long lasting nuclear memory.

quant-ph↗

arXiv2019

Limits on Spectral Resolution Measurements by Quantum Probes

The limits of frequency resolution in nano-NMR experiments have been discussed extensively in recent years. It is believed that there is a crucial difference between the ability to resolve a few frequencies and the precision of estimating a single one. Whereas the efficiency of single frequency estimation gradually increases with the square root of the number of measurements, the ability to resolve two frequencies is limited by the specific timescale of the signal and cannot be compensated for by extra measurements. Here we show theoretically and demonstrate experimentally that the relationship between these quantities is more subtle and both are only limited by the Cramér-Rao bound of a single frequency estimation.

quant-ph↗

arXiv2018

Single SiV$^-$ centers in low-strain nanodiamonds with bulk-like spectral properties and nano-manipulation capabilities

We report on the isolation of single SiV$^-$ centers in nanodiamonds. We observe the fine-structure of single SiV$^-$ center with improved inhomogeneous ensemble linewidth below the excited state splitting, stable optical transitions, good polarization contrast and excellent spectral stability under resonant excitation. Based on our experimental results we elaborate an analytical strain model where we extract the ratio between strain coefficients of excited and ground states as well the intrinsic zero-strain spin-orbit splittings. The observed strain values are as low as best values in low-strain bulk diamond. We achieve our results by means of H-plasma treatment of the diamond surface and in combination with resonant and off-resonant excitation. Our work paves the way for indistinguishable, single photon emission. Furthermore, we demonstrate controlled nano-manipulation via atomic force microscope cantilever of 1D- and 2D-alignments with a so-far unreached accuracy of about 10nm, as well as new tools including dipole rotation and cluster decomposition. Combined, our results show the potential to utilize SiV$^-$ centers in nanodiamonds for the controlled interfacing via optical coupling of individually well-isolated atoms for bottom-up assemblies of complex quantum systems.

cond-mat.mes-hall↗

arXiv2018

Controllable Non-Markovianity for a Spin Qubit in Diamond

We present a flexible scheme to realize non-artificial non-Markovian dynamics of an electronic spin qubit, using a nitrogen-vacancy center in diamond where the inherent nitrogen spin serves as a regulator of the dynamics. By changing the population of the nitrogen spin, we show that we can smoothly tune the non-Markovianity of the electron spin's dynamic. Furthermore, we examine the decoherence dynamics induced by the spin bath to exclude other sources of non-Markovianity. The amount of collected measurement data is kept at a minimum by employing Bayesian data analysis. This allows for a precise quantification of the parameters involved in the description of the dynamics and a prediction of so far unobserved data points.

quant-ph↗

arXiv2018

Observation of Floquet Raman transition in a driven solid-state spin system

We experimentally observe Floquet Raman transitions in the weakly driven solid state spin system of nitrogen-vacancy center in diamond. The periodically driven spin system simulates a two-band Wannier-Stark ladder model, and allows us to observe coherent spin state transfer arising from Raman transition mediated by Floquet synthetic levels. It also leads to the prediction of analog photon-assisted Floquet Raman transition and dynamical localisation in a driven two-level quantum system. The demonstrated rich Floquet dynamics offers new capabilities to achieve effective Floquet coherent control of a quantum system with potential applications in various types of quantum technologies based on driven quantum dynamics. In particular, the Floquet-Raman system may be used as a quantum simulator for the physics of periodically driven systems.

quant-ph↗

arXiv2018

Quantum spectroscopy of single spins assisted by a classical clock

Quantum spectroscopy with single two level systems has considerably improved our ability to detect weak signals. Recently it was realized that for classical signals, precision and resolution of quantum spectroscopy is limited mainly by coherence of the signal and stability of the clock used to measure time. The coherence time of the quantum probe, which can be significantly shorter, is not a major limiting factor in resolution measurements. Here, we address a similar question for spectroscopy of quantum signals, for example a quantum sensor is used to detect a single nuclear spin. We present and analyze a novel correlation spectroscopy technique with performance that is limited by the coherence time of the target spins and the stability of the clock.

quant-ph↗

arXiv2018

Magnetic-field-learning using a single electronic spin in diamond with one-photon-readout at room temperature

Nitrogen-vacancy (NV) centres in diamond are appealing nano-scale quantum sensors for temperature, strain, electric fields and, most notably, for magnetic fields. However, the cryogenic temperatures required for low-noise single-shot readout that have enabled the most sensitive NV-magnetometry reported to date, are impractical for key applications, e.g. biological sensing. Overcoming the noisy readout at room-temperature has until now demanded repeated collection of fluorescent photons, which increases the time-cost of the procedure thus reducing its sensitivity. Here we show how machine learning can process the noisy readout of a single NV centre at room-temperature, requiring on average only one photon per algorithm step, to sense magnetic field strength with a precision comparable to those reported for cryogenic experiments. Analysing large data sets from NV centres in bulk diamond, we report absolute sensitivities of $60$ nT s$^{1/2}$ including initialisation, readout, and computational overheads. We show that dephasing times can be simultaneously estimated, and that time-dependent fields can be dynamically tracked at room temperature. Our results dramatically increase the practicality of early-term single spin sensors.

quant-ph↗

arXiv2018

Probing quantum thermalization of a disordered dipolar spin ensemble with discrete time-crystalline order

We investigate thermalization dynamics of a driven dipolar many-body quantum system through the stability of discrete time crystalline order. Using periodic driving of electronic spin impurities in diamond, we realize different types of interactions between spins and demonstrate experimentally that the interplay of disorder, driving and interactions leads to several qualitatively distinct regimes of thermalization. For short driving periods, the observed dynamics are well described by an effective Hamiltonian which sensitively depends on interaction details. For long driving periods, the system becomes susceptible to energy exchange with the driving field and eventually enters a universal thermalizing regime, where the dynamics can be described by interaction-induced dephasing of individual spins. Our analysis reveals important differences between thermalization of long-range Ising and other dipolar spin models.

quant-ph↗

arXiv2018

Clock transition by continuous dynamical decoupling of a three-level system

We present a novel continuous dynamical decoupling scheme for the construction of a robust qubit in a three-level system. By means of a clock transition adjustment, we first show how robustness to environmental noise is achieved, while eliminating drive-noise, to first-order. We demonstrate this scheme with the spin sub-levels of the NV-centre's electronic ground state. By applying drive fields with moderate Rabi frequencies, the drive noise is eliminated and an improvement of 2 orders of magnitude in the coherence time is obtained compared to the pure dephasing time. We then show how the clock transition adjustment can be tuned to eliminate also the second-order effect of the environmental noise with moderate drive fields. A further improvement of more than 1 order of magnitude in the coherence time is expected and confirmed by simulations. Hence, our scheme prolongs the coherence time towards the lifetime-limit using a relatively simple experimental setup.

quant-ph↗

arXiv2018

Pulsed polarisation for robust DNP

Dynamical nuclear polarisation (DNP) is an important technique that uses polarisation transfer from electron to nuclear spins to achieve nuclear hyperpolarisation. As the electron spin of the nitrogen vacancy (NV) centres in diamond can be optically initialised nearly perfectly even at room temperature and ambient conditions, new opportunities become possible by the combination of efficient DNP with optically polarised NV centres. Among such applications are nanoscale nuclear magnetic resonance spectroscopy of liquids, hyperpolarised nanodiamonds as MRI contrast agents as well as the initialisation of nuclear spin based diamond quantum simulators. Current realisations of DNP perform the polarisation transfer by achieving energetic resonance between electrons and nuclei via carefully tuned microwave fields or by using quasi-adiabatic sweep-based schemes across resonance points. The former limits robustness against control errors while the latter limits polarisation rates, making the realisation of the applications extremely challenging. Here we introduce the concept of Hamiltonian engineering by pulse sequences and use it for the systematic design of polarisation sequences that are simultaneously robust and fast. We derive sequences theoretically and demonstrate experimentally that they are capable of efficient polarisation transfer from an optically polarised nitrogen-vacancy centre in diamond to the surrounding $^{13}$C nuclear spin bath even in the presence of control errors, making it an ideal tool for the realisation of the above NV centre based applications.

quant-ph↗