Search

Fluorination of diamonds modulates their optical and electromagnetic properties and creates surfaces with increased hydrophobicity. In addition, fluorination of diamonds and nanodiamonds has been recently shown to stabilize fluorescent nitrogen-vacancy centers, which can serve as extremely sensitive single atomic defects in a vast range of sensing applications from quantum physics to high-resolution biological imaging. Traditionally, fluorination of carbon nanomaterials has been achieved using harsh and complex experimental conditions, creating hydrophobic interfaces with difficult dispersibility in aqueous environments. Here, a mild benchtop approach to nanodiamond fluorination is described using selective Ag+-catalyzed radical substitution of surface carboxyls for fluorine. In contrast to other approaches, this high-yielding procedure does not etch diamond carbons and produces a highly hydrophilic interface with mixed C−F and C−OH termination. This dual functionalization of nanodiamonds suppresses detrimental hydrophobic interactions that would lead to colloidal destabilization of nanodiamonds. It is also demonstrated that even a relatively low surface density of fluorine contributes to stabilization of negatively charged nitrogen-vacancy centers and boosts their fluorescence. The simultaneous control of the surface hydrophilicity and the fluorescence of nitrogen-vacancy centers is an important issue enabling direct application of fluorescent nanodiamonds as nanosensors for quantum optical and magnetometry measurements operated in biological environment. [ABSTRACT FROM AUTHOR]