arXiv subjects

Benedikt Tratzmiller

Publications and source records attributed to Benedikt Tratzmiller.

7 recordsLinked to original sources

arXiv2023

Towards a unified picture of polarization transfer -- pulsed DNP and chemically equivalent PHIP

Nuclear spin hyperpolarization techniques, such as dynamic nuclear polarization (DNP) and parahydrogen-induced polarization (PHIP), have revolutionized nuclear magnetic resonance and magnetic resonance imaging. In these methods, a readily available source of high spin order, either electron spins in DNP or singlet states in hydrogen for PHIP, is brought into close proximity with nuclear spin targets, enabling efficient transfer of spin order under external quantum control. Despite vast disparities in energy scales and interaction mechanisms between electron spins in DNP and nuclear singlet states in PHIP, a pseudo-spin formalism allows us to establish an intriguing equivalence. As a result, the important low-field polarization transfer regime of PHIP can be mapped onto an analogous system equivalent to pulsed-DNP. This establishes a correspondence between key polarization transfer sequences in PHIP and DNP, facilitating the transfer of sequence development concepts. This promises fresh insights and significant cross-pollination between DNP and PHIP polarization sequence developers.

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arXiv2021

Parallel selective nuclear spin addressing for fast high-fidelity quantum gates

Due to their long coherence times, nuclear spins have gained considerable attention as physical qubits. Two-qubit gates between nuclear spins of distinct resonance frequencies can be mediated by electron spins, usually employing a sequence of electron-nuclear gates. Here we present a different approach inspired by, but not limited to, NV centers in diamond and discuss possible applications. To this end we generalize external electron spin control sequences for nuclear spin initialization and hyperpolarization to achieve the simultaneous control of distinct nuclear spins via an electron spin. This approach results in efficient entangling gates that, compared to standard techniques, reduce the gate time by more than 50% when the gate time is limited by off-resonant coupling to other spins, and by up to 22% when the gate time is limited by small electron-nuclear coupling.

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arXiv2020

Limited-control metrology approaching the Heisenberg limit without entanglement preparation

Current metrological bounds typically assume full control over all particles that are involved in the protocol. Relaxing this assumption we study metrological performance when only limited control is available. As an example, we measure a static magnetic field when a fully controlled quantum sensor is supplemented by particles over which only global control is possible. We show that even for a noisy quantum sensor, a protocol that maps the magnetic field to a precession frequency can achieve transient super-Heisenberg scaling in measurement time and Heisenberg scaling in the particle number. This leads to an estimation uncertainty that approaches that achievable under full control to within a factor independent of the particle number for a given total time. Applications to hybrid sensing devices and the crucial role of the quantum character of the sensor are discussed.

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arXiv2020

On the robustness of the NV-NMR spectrometer setup to magnetic field inhomogeneities

The NV-NMR spectrometer is a promising candidate for detection of NMR signals at the nano scale. Field inhomogeneities, however, are a major source of noise that limits spectral resolution in state of the art NV - NMR experiments and constitutes a major bottleneck in the development of nano scale NMR. Here we propose, a route in which this limitation could be circumvented in NV-NMR spectrometer experiments, by utilising the nanometric scale and the quantumness of the detector.

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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.

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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.

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arXiv2017

Blueprint for nanoscale NMR

Nitrogen vacancy (NV) centers in diamond have been used as ultrasensitive magnetometers to perform nuclear magnetic resonance (NMR) spectroscopy of statistically polarized samples at 1 - 100 nm length scales. However, the spectral linewidth is typically limited to the kHz level, both by the NV sensor coherence time and by rapid molecular diffusion of the nuclei through the detection volume which in turn is critical for achieving long nuclear coherence times. Here we provide a blueprint for a set-up that combines a sensitivity sufficient for detecting NMR signals from nano- to micron-scale samples with a spectral resolution that is limited only by the nuclear spin coherence, i.e. comparable to conventional NMR. Our protocol detects the nuclear polarization induced along the direction of an external magnetic field with near surface NV centers using lock-in detection techniques to enable phase coherent signal averaging. Using NV centers in a dual role of NMR detector and optical hyperpolarization source to increase signal to noise, and in combination with Bayesian interference models for signal processing, nano/microscale NMR spectroscopy can be performed on sub-millimolar sample concentrations, several orders of magnitude better than the current state of the art.

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