Ensembles of negatively charged nitrogen vacancy centers (NV-) in diamond have been proposed for sensing of magnetic fields and paramagnetic agents, and as a source of spin-order for the hyperpolarization of nuclei in magnetic resonance applications. To this end, strongly fluorescent nanodiamonds represent promising materials, with large surface areas and dense ensembles of NV-. However, surface effects tend to favor the less useful neutral form, the NV0 centers. Here, we study the fluorescence properties and optically detected magnetic resonance (ODMR) of NV- centers as a function of laser power in strongly fluorescent bulk diamond and in nanodiamonds obtained by nanomilling the native material. In bulk diamond, we find that increasing laser power increases ODMR contrast, consistent with a power-dependent increase in spin-polarization. Surprisingly, in nanodiamonds we observe a non-monotonic behavior, with a decrease in ODMR contrast at higher laser power that can be ascribed to more efficient NV-→NV0 photoconversion in nanodiamonds compared to bulk diamond, resulting in depletion of the NV- pool. We also studied this phenomenon in cell cultures following internalization of NDs in macrophages. Our findings show that surface effects in nanodiamonds substantially affect the NV properties and provide indications for the adjustment of experimental parameters.
Optically detected nuclear quadrupolar interaction ofN14in nitrogen-vacancy centers in diamond
