This news release is available in German.
But how are the electronic properties of nanodiamonds deposited on a solid-state substrate different from those displayed by nanodiamonds in aqueous solutions?
Dr. Tristan Petit working in the HZB team headed by Prof. Emad F. Aziz has now investigated this with the help of absorption and emission spectroscopy at BESSY II. Their results, just published in Nanoscale, demonstrate that nanodiamonds display valence holes in aqueous solutions, which are not observed when characterized as a thin film.
"The interaction between the nanodiamonds and the neighbouring molecules and ions is especially strong in water", say Petit. The adsorption of active pharmaceutical ingredients on nanodiamonds can be influenced, for example, by adding salts or changing the pH value. Petit and his colleagues have now discovered that the electronic signature of surface states of nanodiamonds in aqueous dispersions are considerably different from those of nanodiamonds on a solid-state substrate.
With the help of micro-jet technology developed by Emad Aziz at HZB, they examined liquid samples in vacuum using X-ray spectroscopy and developed a detailed picture of the filled and unfilled electron states in valence and conduction bands. Their results show that holes, i.e. missing electrons in the valence band, formed on the surfaces of the nanodiamonds in the aqueous dispersion. "This suggests that electrons at the surface of nanodiamonds are donated to the surrounding water molecules", Petit suggests. The physicists suspect they might also influence the nanoparticles' chemical, optical, and catalytic properties through changes to their electronic structure. They would like to determine in future studies whether the catalytic effect of nanodiamonds in aqueous environment can be increased in order to split water molecules into oxygen and hydrogen using light.
Reference: Valence holes observed in nanodiamonds dispersed in water, Tristan Petit, Mika Pflüger, Daniel Tolksdorf, Jie Xiao and Emad Flear Aziz, Nanoscale, 2015, DOI: 10.1039/C4NR06639A