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nitrogen-Vacancy (nV) centers in diamonds have been shown in recent years to be excellent magnetometers on the nanoscale. one of the recent applications of the quantum sensor is retrieving the nuclear Magnetic Resonance (nMR) spectrum of a minute sample, whose net polarization is well below the Signal-to-noise Ratio (SnR) of classic devices. the information in the magnetic noise of diffusing particles has also been shown in decoherence spectroscopy approaches to provide a method for measuring different physical parameters. Similar noise is induced on the NV center by a flowing liquid. However, when the noise created by diffusion effects is more dominant than the noise of the drift, it is unclear whether the velocity can be efficiently estimated. Here we propose a non-intrusive setup for measuring the drift velocity near the surface of a flow channel based on magnetic field quantum sensing using NV centers. We provide a detailed analysis of the sensitivity for different measurement protocols, and we show that our nanoscale velocimetry scheme outperforms current fluorescence based approaches even when diffusion noise is dominant. Our scheme can be applied for the investigation of microfluidic channels, where the drift velocity is usually low and the flow properties are currently unclear. A better understanding of these properties is essential for the future development of microfluidic and nanofluidic infrastructures.

Nano nuclear magnetic resonance (nano‐NMR) spectroscopy with nitrogen‐vacancy (NV) centers holds the potential to provide high‐resolution spectra of minute samples. This is likely to have important implications for chemistry, medicine, and pharmaceutical engineering. One of the main hurdles facing the technology is that diffusion of unpolarized liquid samples broadens the spectral lines thus limiting resolution. Experiments in the field are therefore impeded by the efforts involved in achieving high polarization of the sample which is a challenging endeavor. Here, a scenario where the liquid is confined to a small volume is examined. It is shown that the confinement “counteracts” the effect of diffusion, thus overcoming a major obstacle to the resolving abilities of the NV‐NMR spectrometer.

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