Ingmar Jakobi

High-precision nanoscale temperature sensing using single defects in diamond.

Measuring local temperature with a spatial resolution on the order of a few nanometers has a wide range of applications in the semiconductor industry and in material and life sciences. For example, probing temperature on the nanoscale with high precision can potentially be used to detect small, local temperature changes like those caused by chemical reactions or biochemical processes. However, precise nanoscale temperature measurements have not been realized so far owing to the lack of adequate probes. Here we experimentally demonstrate a novel nanoscale temperature sensing technique based on optically detected electron spin resonance in single atomic defects in diamonds. These diamond sensor sizes range from a micrometer down to a few tens of nanometers. We achieve a temperature noise floor of 5 mK/Hz(1/2) for single defects in bulk sensors. Using doped nanodiamonds as sensors the temperature noise floor is 130 mK/Hz(1/2) and accuracies down to 1 mK for nanocrystal sizes and therefore length scales of a few tens of nanometers. This combination of precision and position resolution, combined with the outstanding sensor photostability, should allow the measurement of the heat produced by chemical interactions involving a few or single molecules even in heterogeneous environments like cells.

Room-temperature entanglement between single defect spins in diamond

Entanglement is the central yet fleeting phenomenon of quantum physics. Once being considered a peculiar counter-intuitive property of quantum theory1, it has developed into the most central element of quantum technology. Consequently, there have been a number of experimental demonstrations of entanglement between photons2, atoms3, ions4 and solid-state systems such as spins or quantum dots5, 6, 7, superconducting circuits8, 9 and macroscopic diamond10. Here we experimentally demonstrate entanglement between two engineered single solid-state spin quantum bits (qubits) at ambient conditions. Photon emission of defect pairs reveals ground-state spin correlation. Entanglement (fidelity = 0.67±0.04) is proved by quantum state tomography. Moreover, the lifetime of electron spin entanglement is extended to milliseconds by entanglement swapping to nuclear spins. The experiments mark an important step towards a scalable room-temperature quantum device being of potential use in quantum information processing as well as metrology.

High-fidelity spin entanglement using optimal control

Precise control of quantum systems is of fundamental importance in quantum information processing, quantum metrology and high-resolution spectroscopy. When scaling up quantum registers, several challenges arise: individual addressing of qubits while suppressing cross-talk, entangling distant nodes and decoupling unwanted interactions. Here we experimentally demonstrate optimal control of a prototype spin qubit system consisting of two proximal nitrogen-vacancy centres in diamond. Using engineered microwave pulses, we demonstrate single electron spin operations with a fidelity F≈0.99. With additional dynamical decoupling techniques, we further realize high-quality, on-demand entangled states between two electron spins with F>0.82, mostly limited by the coherence time and imperfect initialization. Crosstalk in a crowded spectrum and unwanted dipolar couplings are simultaneously eliminated to a high extent. Finally, by high-fidelity entanglement swapping to nuclear spin quantum memory, we demonstrate nuclear spin entanglement over a length scale of 25 nm. This experiment underlines the importance of optimal control for scalable room temperature spin-based quantum information devices.

Perfect alignment and preferential orientation of nitrogen-vacancy centers during chemical vapor deposition diamond growth on (111) surfaces

Synthetic diamond production is a key to the development of quantum metrology and quantum information applications of diamond. The major quantum sensor and qubit candidate in diamond is the nitrogen-vacancy (NV) color center. This lattice defect comes in four different crystallographic orientations leading to an intrinsic inhomogeneity among NV centers, which is undesirable in some applications. Here, we report a microwave plasma-assisted chemical vapor deposition diamond growth technique on (111)-oriented substrates, which yields perfect alignment (94% ± 2%) of as-grown NV centers along a single crystallographic direction. In addition, clear evidence is found that the majority (74% ± 4%) of the aligned NV centers were formed by the nitrogen being first included in the (111) growth surface and then followed by the formation of a neighboring vacancy on top. The achieved homogeneity of the grown NV centers will tremendously benefit quantum information and metrology applications.

Nanoscale detection of a single fundamental charge in ambient conditions using the NV - Center in diamond

conditions using the NV− center in diamond Florian Dolde, ∗ Marcus W. Doherty, Julia Michl, Ingmar Jakobi, Boris Naydenov, Sebastien Pezzagna, Jan Meijer, Philipp Neumann, Fedor Jelezko, Neil B. Manson, and Jörg Wrachtrup 3. Physikalisches Institut, Research Center SCoPE and IQST, Universität Stuttgart, Pfaffenwaldring 57. D-70550 Stuttgart, Germany Laser Physics Centre, Research School of Physics and Engineering, Australian National University, Australian Capital Territory 0200, Australia Institut für Quantenoptik and IQST, Universität Ulm, Ulm D-89073, Germany Physikalisches Institut, Universität Leipzig, 04103 Leipzig, Germany

Enhancing quantum sensing sensitivity by a quantum memory

In quantum sensing, precision is typically limited by the maximum time interval over which phase can be accumulated. Memories have been used to enhance this time interval beyond the coherence lifetime and thus gain precision. Here, we demonstrate that by using a quantum memory an increased sensitivity can also be achieved. To this end, we use entanglement in a hybrid spin system comprising a sensing and a memory qubit associated with a single nitrogen-vacancy centre in diamond. With the memory we retain the full quantum state even after coherence decay of the sensor, which enables coherent interaction with distinct weakly coupled nuclear spin qubits. We benchmark the performance of our hybrid quantum system against use of the sensing qubit alone by gradually increasing the entanglement of sensor and memory. We further apply this quantum sensor-memory pair for high-resolution NMR spectroscopy of single 13C nuclear spins.

Quantum Simulation of Helium Hydride Cation in a Solid-State Spin Register

Ab initio computation of molecular properties is one of the most promising applications of quantum computing. While this problem is widely believed to be intractable for classical computers, efficient quantum algorithms exist which have the potential to vastly accelerate research throughput in fields ranging from material science to drug discovery. Using a solid-state quantum register realized in a nitrogen-vacancy (NV) defect in diamond, we compute the bond dissociation curve of the minimal basis helium hydride cation, HeH(+). Moreover, we report an energy uncertainty (given our model basis) of the order of 10(-14) hartree, which is 10 orders of magnitude below the desired chemical precision. As NV centers in diamond provide a robust and straightforward platform for quantum information processing, our work provides an important step toward a fully scalable solid-state implementation of a quantum chemistry simulator.

Measuring the defect structure orientation of a single NV− centre in diamond

The negatively charged nitrogen-vacancy (NV−) centre in diamond has many exciting applications in quantum nano-metrology, including magnetometry, electrometry, thermometry and piezometry. Indeed, it is possible for a single NV− centre to measure the complete three-dimensional vector of the local electric field or the position of a single fundamental charge in ambient conditions. However, in order to achieve such vector measurements, near complete knowledge of the orientation of the centreʼs defect structure is required. Here, we demonstrate an optically detected magnetic resonance (ODMR) technique employing rotations of static electric and magnetic fields that precisely determines the orientation of the centreʼs major and minor trigonal symmetry axes. Thus, our technique is an enabler of the centreʼs existing vector sensing applications and also motivates new applications in multi-axis rotation sensing, NV growth characterization and diamond crystallography.

Measuring broadband magnetic fields on the nanoscale using a hybrid quantum register

The generation and control of fast switchable magnetic fields with large gradients on the nanoscale is of fundamental interest in material science and for a wide range of applications. However, it has not yet been possible to characterize those fields at high bandwidth with arbitrary orientations. Here, we measure the magnetic field generated by a hard-disk-drive write head with high spatial resolution and large bandwidth by coherent control of single electron and nuclear spins. We are able to derive field profiles from coherent spin Rabi oscillations close to the gigahertz range, measure magnetic field gradients on the order of 1 mT nm-1 and quantify axial and radial components of a static and dynamic magnetic field independent of its orientation. Our method paves the way for precision measurement of the magnetic fields of nanoscale write heads, which is important for future miniaturization of these devices.The generation and control of nanoscale magnetic fields are of fundamental interest in material science and a wide range of applications. Nanoscale magnetic resonance imaging quantum spintronics for example require single spin control with high precision and nanoscale spatial resolution using fast switchable magnetic fields with large gradients. Yet, characterizing those fields on nanometer length scales at high band width with arbitrary orientation has not been possible so far. Here we demonstrate single electron and nuclear spin coherent control using the magnetic field of a hard disc drive write head. We use single electron spins for measuring fields with high spatial resolution and single nuclear spins for large band width measurements. We are able to derive field profiles from coherent spin Rabi oscillations close to GHz in fields with gradients of up to 10 mT/nm and measure all components of a static and dynamic magnetic field independent of its orientation. Our method paves the way for precision measurement of the magnetic fields of nanoscale write heads important for future miniaturization of the devices.

Efficient creation of dipolar coupled nitrogen-vacancy spin qubits in diamond

Coherently coupled pairs or multimers of nitrogen-vacancy defect electron spins in diamond have many promising applications especially in quantum information processing (QIP) but also in nanoscale sensing applications. Scalable registers of spin qubits are essential to the progress of QIP. Ion implantation is the only known technique able to produce defect pairs close enough to allow spin coupling via dipolar interaction. Although several competing methods have been proposed to increase the resulting resolution of ion implantation, the reliable creation of working registers is still to be demonstrated. The current limitation are residual radiation-induced defects, resulting in degraded qubit performance as trade-off for positioning accuracy. Here we present an optimized estimation of nanomask implantation parameters that are most likely to produce interacting qubits under standard conditions. We apply our findings to a well-established technique, namely masks written in electron-beam lithography, to create coupled defect pairs with a reasonable probability. Furthermore, we investigate the scaling behavior and necessary improvements to efficiently engineer interacting spin architectures.