Abstract The Nitrogen-Vacancy (NV) defect in diamond is a unique quantum system that offers precision sensing of nanoscale physical quantities at room temperature beyond the current state-of-the-art. The benchmark parameters for nanoscale magnetometry applications are sensitivity, spectral resolution, and dynamic range. Under realistic conditions the NV sensors controlled by conventional sensing schemes suffer from limitations of these parameters. Here we experimentally show a new method called dynamical sensitivity control (DYSCO) that boost the benchmark parameters and thus extends the practical applicability of the NV spin for nanoscale sensing. In contrast to conventional dynamical decoupling schemes, where π pulse trains toggle the spin precession abruptly, the DYSCO method allows for a smooth, analog modulation of the quantum probe’s sensitivity. Our method decouples frequency selectivity and spectral resolution unconstrained over the bandwidth (1.85 MHz–392 Hz in our experiments). Using DYSCO we demonstrate high-accuracy NV magnetometry without |2π| ambiguities, an enhancement of the dynamic range by a factor of 4 · 103, and interrogation times exceeding 2 ms in off-the-shelf diamond. In a broader perspective the DYSCO method provides a handle on the inherent dynamics of quantum systems offering decisive advantages for NV centre based applications notably in quantum information and single molecule NMR/MRI.
Abstract The Nitrogen-Vacancy (NV) defect in diamond is a unique quantum system that offers precision sensing of nanoscale physical quantities at room temperature beyond the current state-of-the-art. The benchmark parameters for nanoscale magnetometry applications are sensitivity, spectral resolution, and dynamic range. Under realistic conditions the NV sensors controlled by conventional sensing schemes suffer from limitations of these parameters. Here we experimentally show a new method called dynamical sensitivity control (DYSCO) that boost the benchmark parameters and thus extends the practical applicability of the NV spin for nanoscale sensing. In contrast to conventional dynamical decoupling schemes, where π pulse trains toggle the spin precession abruptly, the DYSCO method allows for a smooth, analog modulation of the quantum probe’s sensitivity. Our method decouples frequency selectivity and spectral resolution unconstrained over the bandwidth (1.85 MHz–392 Hz in our experiments). Using DYSCO we demonstrate high-accuracy NV magnetometry without |2π| ambiguities, an enhancement of the dynamic range by a factor of 4 · 103, and interrogation times exceeding 2 ms in off-the-shelf diamond. In a broader perspective the DYSCO method provides a handle on the inherent dynamics of quantum systems offering decisive advantages for NV centre based applications notably in quantum information and single molecule NMR/MRI.
The Nitrogen-Vacancy (NV) defect in diamond is a unique quantum system that offers precision sensing of nanoscale physical quantities beyond the current state-of-the-art. Here we present a method to controllably encode the interactions in the population of the spin states, thereby introducing a way to control the sensitivity of a single spin as a continuum in contrast to free-evolution based methods. By adopting this feature we demonstrate high-accuracy NV magnetometry without 2pi ambiguities, enhance the dynamic range by a factor of 4*10^3 achieve interaction times exceeding 2 ms in off-the-shelf diamond. We perform nuclear spin-noise spectroscopy in the frequency domain by dynamically controlling the NV spin's sensitivity piecewise and in a smooth manner thereby precluding harmonic artefacts and undesired interactions. On a broader perspective dynamical sensitivity control provides an elegant handle on the inherent dynamics of quantum systems, while offering decisive advantages for NV centre applications notably in quantum controls and single molecule NMR/MRI.
As a demand from developing nanotechnology and quantum information technology based on mesoscopic material, quantum sensors with better spatial resolution and sensitivity are required. \n \nHowever, few material meets the requirements of nanoscale sensors including stability and small size. Single spin of Nitrogen-Vacancy(NV) centers in diamond crystal is one kind of the ideal quantum sensors for magnetometry that has been investigated in recent years. It provides a potential way to study the dynamics in a mesoscopic system with high sensitivity at room temperature. This thesis proposes a theoretical method to realize spin interaction detection based on NV centers on an atomic force-microscopy(AFM) tip. To realize this method, a robust control on NV centers and target electron spins at zero magnetic field is necessary. A pulse control technique for NV centers is proposed to realize transitions between two degenerate states at zero magnetic field, which is an important part of the sensing method. The key to realizing this transition is a circularly polarized microwave pulse generated by two parallel wires. Combined with optimal control techniques, this pulse can achieve a gate fidelity over 99.95% theoretically.
Nuclear magnetic resonance (NMR) schemes can be applied to micron-, and nanometer-sized samples by the aid of quantum sensors such as nitrogen vacancy (NV) color centers in diamond. These minute devices allow for magnetometry of nuclear spin ensembles with high spatial and frequency resolution at ambient conditions, thus having a clear impact in different areas such as chemistry, biology, medicine, and material sciences. In practice, NV quantum sensors are driven by microwave (MW) control fields with a twofold objective: On the one hand, MW fields bridge the energy gap between NV and nearby nuclei which enables a coherent and selective coupling among them while, on the other hand, MW fields remove environmental noise on the NV leading to enhanced interrogation time. In this work we review distinct MW radiation patterns, or dynamical decoupling techniques, for nanoscale NMR applications.
Quantum technologies are expected to significantly change our world in the next decades and the possible applications are diverse – ranging from quantum computation and encryption to metrology with unprecedented sensitivity. This thesis focuses on quantum sensing and imaging based on single nitrogen-vacancy (NV) centres in diamond to measure magnetic fields. Its electronic spin qualifies this point defect as a highly sensitive quantum sensor and its atomic size offers nanoscale spatial resolution. The simple optical initialisation and readout, together with the relatively long coherence time at ambient conditions, make NV centres promising candidates for biological applications and in particular for nuclear magnetic resonance (NMR) on the nanoscale. Recording the spectral information on the nanoscale allows to determine the structure of single or just a few molecules. However, the current main problems and challenges include insufficient spectral resolution, artificial signals and overall poor performance. In this thesis new spectroscopic techniques which tackle these issues are presented. First, it is shown that by randomisation of control pulse phases spurious harmonic signals can be suppressed, which otherwise complicate spectrum interpretation and can lead to false signal identification. At the same time the effects of pulse imperfections are mitigated. Furthermore, a protocol allowing to measure with a coherence independent spectral resolution is presented. It is demonstrated that linewidths below 1mHz are possible, which is an improvement of more than seven orders of magnitude compared to traditional methods. Due to its simple implementation, the protocol is relevant for many applications. Initially developed to measure signals oscillating up to several megahertz, it is further shown that modifications allow to extend the frequency range into the gigahertz domain. Finally, quantum frequency discrimination with the task to differentiate between two frequency distributions using a quantum sensor is analysed. An optimised protocol is introduced and the influences of different readout strategies are discussed with respect to the probability to make an incorrect decision. These findings are useful for diagnostic tests in NMR.
The nitrogen-vacancy (NV) center in diamond is a quantum defect in diamond with unique properties for use in high-sensitive, high-resolution quantum sensors of magnetic fields. One of the most interesting and challenging application of NV quantum sensors is nanoscale magnetic resonance imaging (nano-MRI), which would enable to address single biomolecules. To this goal, improving the sensitivity of the NV sensor is a crucial task. Here, we present a quantum optimal control method that optimizes the sensitivity of NV sensor to specific weak magnetic signals with biologically-relevant, complex spectrum. The method, based on the mapping of the sensing problem on a problem of energy optimization of an Ising chain, allows us to improve sensitivity by three orders of magnitude compared to standard control sequences.
In nanoscale metrology, dissipation of the sensor limits its performance. Strong dissipation has a negative impact on sensitivity, and sensor-target interaction even causes relaxation or dephasing of the latter. The weak dissipation of nitrogen-vacancy (NV) sensors in room temperature diamond enables detection of individual target nuclear spins, yet limits the spectral resolution of nuclear magnetic resonance (NMR) spectroscopy to several hundred Hertz, which typically prevents molecular recognition. Here, we use the NV intrinsic nuclear spin as a nonvolatile classical memory to store NMR information, while suppressing sensor back-action on the target using controlled decoupling of sensor, memory, and target. We demonstrate memory lifetimes up to 4 min and apply measurement and decoupling protocols, which exploit such memories efficiently. Our universal NV-based sensor device records single-spin NMR spectra with 13 Hz resolution at room temperature.Dissipation of the sensor is a limiting factor in metrology. Here, Pfender et al. suppress this effect employing the nuclear spin of an NV centre for robust intermediate storage of classical NMR information, allowing then to record single-spin NMR spectra with 13 Hz resolution at room temperature.