Shallow, negatively
charged nitrogen-vacancy centers (NV
–
) in diamond
have been proposed for high-sensitivity magnetometry
and spin-polarization transfer applications. However, surface effects
tend to favor and stabilize the less useful neutral form, the NV
0
centers. Here, we report the effects of green laser irradiation
on ensembles of nanometer-shallow NV centers in flat and nanostructured
diamond surfaces as a function of laser power in a range not previously
explored (up to 150 mW/μm
2
). Fluorescence spectroscopy,
optically detected magnetic resonance (ODMR), and charge-photoconversion
detection are applied to characterize the properties and dynamics
of NV
–
and NV
0
centers. We demonstrate
that high laser power strongly promotes photoconversion of NV
0
to NV
–
centers. Surprisingly, the excess
NV
–
population is stable over a timescale of 100
ms after switching off the laser, resulting in long-lived enrichment
of shallow NV
–
. The beneficial effect of photoconversion
is less marked in nanostructured samples. Our results are important
to inform the design of samples and experimental procedures for applications
relying on ensembles of shallow NV
–
centers in diamond.