Vladimira Petrakova, Andrew J. Taylor, Irena Kratochvilova, Frantisek Fendrych, Jiri Vacik, Jan Kucka, Jan Stursa, Petr Cigler, Miroslav Ledvina, Anna Fiserova, Peter Kneppo, Milos Nesladek
High biocompatibility, variable size ranging from ~ 5 nm, stable luminescence from its color centers and simple carbon chemistry for biomolecule grafting make nanodiamond (ND) particles an attractive alternative to molecular dyes for drug-delivery. Here we present a novel method for remote monitoring of chemical processes in biological environment based on color changes from photo-luminescent NV centers in ND. We propose to drive the NV luminescence chemically, by alternating the surface electric field developed by interacting atoms and molecules with the diamond surface. Due to the small ND size, the developed electric field penetrates into the bulk of the nanoparticle and intermingles with the electronic NV states. This allows construction of optical chemo-biosensors operating in cells, visible in classical confocal microscopes. We demonstrate this phenomenon on oxidized and hydrogenated ND as well as single crystal diamond containing engineered NV centers. Hydrogenation of NDs leads to quenching of luminescence related to negatively charged (NV-) centers and by this way produces color shifts from NV- (636 nm) to neutral NV0 (575nm) luminescence. We model how the reduction of diamond size increases the magnitude of NV color shift phenomena.
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http://arxiv.org/abs/1103.1397
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