High-Resolution NMR Spectroscopy at Large Fields with Nitrogen Vacancy Centers
arXiv:2205.04150 · doi:10.1103/PhysRevLett.130.133603
Abstract
Ensembles of nitrogen-vacancy (NV) centers are used as sensors to detect NMR signals from micron-sized samples at room temperature. In this scenario, the regime of large magnetic fields is especially interesting as it leads to a large nuclear thermal polarisation -- thus, to a strong sensor response even in low concentration samples -- while chemical shifts and J-couplings become more accessible. Nevertheless, this regime remains largely unexplored owing to the difficulties to couple NV-based sensors with high-frequency nuclear signals. In this work, we circumvent this problem with a method that maps the relevant energy shifts in the amplitude of an induced nuclear spin signal that is subsequently transferred to the sensor. This stage is interspersed with free-precession periods of the sample nuclear spins where the sensor does not participate. Thus, our method leads to high spectral resolutions ultimately limited by the coherence of the nuclear spin signal.
6 pages, 3 figures
References in corpus (5)
- Sub-millihertz magnetic spectroscopy with a nanoscale quantum sensor
- Quantum sensing with arbitrary frequency resolution
- Imaging mesoscopic nuclear spin noise with a diamond magnetometer
- Dynamical decoupling methods in nanoscale NMR
- Detection of Molecular Transitions with Nitrogen-Vacancy Centers and Electron-Spin Labels
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- Robust microwave cavity control for NV ensemble manipulation
- Pulse sequence design for high field NMR with NV centers in dipolarly coupled samples
- Enhanced microscale NMR spectroscopy of low-gyromagnetic ratio nuclei via hydrogen transfer
- Quantum Memory Enhanced Multipoint Correlation Spectroscopy for Statistically Polarized NMR
- Enhanced sensitivity in microscale high-field NMR via nuclear-spin locking with NV centers
- Microscale Sensing with Strongly Interacting NV Ensembles at High Fields