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D. B. Bucher

Publications and source records attributed to D. B. Bucher.

3 recordsLinked to original sources

Nanoscale Sensing of Solid-State Samples with High Frequency Resolution

To meet the growing demand for nanoscale surface analysis, nitrogen-vacancy (NV) centers offer a high-sensitivity alternative by leveraging their ability to operate in immediate proximity to the sample. In this work, we propose a quantum control protocol designed to overcome the inherent challenges of solid-state environments, specifically by mitigating anisotropy and strong dipole-dipole interactions to enable the detection of isotropic chemical shifts at the nanoscale. To achieve this, our scheme synchronizes a slowly rotating magnetic field with tailored RF decoupling and MW control of the NV sensors. We provide an analytical mapping that explicitly links the measured spectrum to the control sequence features and the underlying system parameters, enabling a straightforward characterization of the sample.

quant-ph

Imaging local diffusion in microstructures using NV-based pulsed field gradient NMR

Understanding diffusion in microstructures plays a crucial role in many scientific fields, including neuroscience, cancer or energy research. While magnetic resonance (MR) methods are the gold standard for diffusion measurements, spatial encoding in MR imaging has limitations. Here, we introduce nitrogen-vacancy (NV) center based nuclear magnetic resonance (NMR) spectroscopy as a powerful tool to probe diffusion with an optical readouts. We have developed an experimental scheme combining pulsed gradient spin echo (PGSE) with optically detected NV-NMR spectroscopy, which allows for the local quantification of molecular diffusion and flow within microscopic sample volumes. We demonstrate correlated optical imaging with spatially resolved PGSE NV-NMR experiments probing anisotropic water diffusion within a model microstructure. Our optically detected PGSE NV-NMR technique opens up prospects for extending the current capabilities of investigating diffusion processes with the future potential of probing single cells, tissue microstructures, or ion mobility in thin film materials for battery applications.

physics.app-ph

Polarization transfer from optically-pumped NV center ensembles to multinuclear spin baths

NV-diamonds have attracted keen interest for nanoscale sensing and spin manipulation. In particular, the non-equilibrium electron spin polarization after optical excitation of single NV centers has successfully been transferred to nuclear spin baths in the surrounding of the defects. However, these experiments need to be extended to NV-ensembles which have promising practical applications in the hyperpolarization of bulk sample volumes for NMR signal enhancement. Here, we use a dense, shallow ensemble of NV-centers to demonstrate polarization transfer to nuclear spins in a well-defined composite diamond sample system. This allows us to address three different types of nuclear spins in different positions with respect to the NV polarization source: from the close proximity of $^{13}$C inside the diamond lattice to the self-assembled molecular system consisting of $^{1}$H and $^{19}$F spins outside the diamond and over multiple interfaces. We show that ensemble NV experiments face problems different from single NV experiments. In particular, using spinlock pulses, the inhomogeneously broadened ESR line of the NV ensemble limits the minimal resonance linewidth with which the transfer protocol can occur. Furthermore, we compare the NV spin-polarization losses and polarization transfer rates to the different nuclear baths and discuss the role of spin-diffusion as detrimentally affecting the direct observation of nuclear polarization build-up within the detection volume of nanoscale NV-NMR experiments.

cond-mat.mes-hall