Unraveling Charge State of Supported Au Single-Atoms during CO Oxidation.

Thermally stable Au single-atoms supported by monolayered CuO grown at Cu(110) have been successfully prepared. The charge transfer from the CuO support to single Au atoms is confirmed to play a key role in tuning the activity for CO oxidation. Initially, the negatively charged Au single-atom is active for CO oxidation with its adjacent lattice O atom depleted to generate an O vacancy in the CuO monolayer.

Effect of the Hydrogen Bond in Photoinduced Water Dissociation: A Double-Edged Sword.

Photoinduced water dissociation on rutile-TiO2 was investigated using various methods. Experimental results reveal that the water dissociation occurs via transferring an H atom to a bridge bonded oxygen site and ejecting an OH radical to the gas phase during irradiation. The reaction is strongly suppressed as the water coverage increases.

Microstructure and cytotoxicity evaluation of duplex-treated silver-containing antibacterial TiO₂ coatings.

Implant-related infection is one of the most common and serious complications associated with biomedical implantation. To prevent bacterial adhesion, a series of porous TiO2 coatings with different concentrations of silver (designated as M0, M1, M2 and M3) were prepared on pure titanium substrates by a duplex-treatment technique combining magnetron sputtering with micro-arc oxidation. All coatings are porous with pore size less than 5 μm and the concentrations of silver in the M0, M1, M2 and M3 are 0, 0.