Surface Tamm States of 2–5 nm Nanodiamond via Raman Spectroscopy

We observed resonance effects in the Raman scattering of nanodiamonds with an average size of 2–5 nm excited at a wavelength of 1064 nm (1.16 eV). The resonant Raman spectrum of the 2–5 nm nanodiamonds consists of bands at wavelengths of 1325 and 1600 cm(−1), a band at 1100–1250 cm(−1), and a plateau in the range from 1420 to 1630 cm(−1). When excited away from the resonance (at a wavelength of 405 nm, 3.1 eV), the Raman spectrum consists of only three bands at 1325, 1500, and 1600 cm(−1). It is important to note that the additional lines (1500 and 1600 cm(−1)) belong to the sp(3)-hybridized carbon bonds. The phonon density of states for the nanodiamonds (~1 nm) was calculated using moment tensor potentials (MTP), a class of machine-learning interatomic potentials. The presence of these modes in agreement with the lattice dynamics indicates the existence of bonds with force constants higher than in single-crystal diamonds. The observed resonant phenomena of the Raman scattering and the increase in the bulk modulus are explained by the presence of Tamm states with an energy of electronic transitions of approximately 1 eV, previously observed on the surface of single-crystal diamonds.