The Journal of Physical Chemistry C · 2014 · 35 citations · 37 references
Natural SciencesChemistryMaterials ScienceMaterials ChemistryNanomaterialsSpectroscopyCarbon NanomaterialsMolecular SpectroscopyNanomaterial CharacterizationSurface SpectroscopyBond LengthsCarbon Fraction DeterminationCarbon-13 Nuclear Magnetic ResonanceCross-polarizationHeat Treatment EffectsNanodiamondsX-ray Absorption Near Edge StructureX-ray Absorption Spectroscopy
The ability of solid-state 13 C NMR to detect and quantify small amounts of sp 2 -hybridized carbon on the surface of ∼5 nm diameter nanodiamond particles is demonstrated. The C═C carbon fraction is only 1.1 ± 0.4% in pristine purified detonation nanodiamond, while a full single-layer graphitic or “bucky diamond” shell would contain ca. 25% of all C in a 5 nm diameter particle. Instead of large aromatic patches repeatedly proposed in the recent literature, sp 3 -hybridized CH and COH carbons cover most of the nanodiamond particle surface, accounting for ∼5% each. C═O and COO groups also seen in X-ray absorption near-edge structure spectroscopy (XANES) but not detected in previous NMR studies make up ca. 1.5% of all C. They are removed by heat treatment at 800 °C, which increases the aromatic fraction. 13 C{ 1 H} NMR demonstrates that the various sp 2 -hybridized carbons are mostly not protonated, but cross-polarization shows that they are separated from 1 H by only a few bond lengths, which proves that they are near the protonated surface. Together, the observed C–H, C–OH, C═O, and C═C groups account for 12–14% of all C, which matches the surface fraction expected for bulk-terminated 5 nm diameter diamond particles.
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