ABSTRACT
The location of the Pd atoms in Pd2Au36(SC2H4Ph)24, is studied both experimentally and theoretically. X-ray photoelectron spectroscopy (XPS) indicates oxidized Pd atoms. Palladium K-edge extended X-ray absorption fine-structure (EXAFS) data clearly show Pd-S bonds, which is supported by far infrared spectroscopy and by comparing theoretical EXAFS spectra in R space and circular dichroism spectra of the staple, surface and core doped structures with experimental spectra.
ABSTRACT
Photocatalytic activity of Ag/TiO(2) composites obtained by photoreduction treatment (PRT) was investigated. The composite materials, containing various ratio of silver nanoparticles (0.6-3.7 wt %) were obtained by depositing silver on the Evonic-Degussa P25 titania surface. Selected samples whose color varied between light rose and purple brown were examined by SEM, TEM, XPS, DRS, and BET techniques. Flat band potential was determined using Roy method. TEM analysis showed spherically shaped silver nanoparticles of the diameter 4-12 nm. The XPS measurements revealed that silver particles were obtained mainly in metallic form. DRS spectra and photovoltage measurements showed that silver nanoparticles modified the P25 spectral properties but they changed neither the band gap nor the location of flat band potential. The photocatalytic activity of Ag/P25 composite was compared to the photocatalytic activity of pure P25 in the photooxidation reaction of an important potable water contaminant humic acid (HA) and two model compounds, oxalic acid (OxA) and formic acid (FA). The photodecomposition reaction was investigated in a batch reactor containing aqueous suspension of a photocatalyst illuminated by either UV or artificial sunlight (halogen lamp). The tests proved that a small amount of silver nanoparticles deposited on the titania surface triggers the increase in photocatalytic activity; this increase depends, however, on the decomposed substance.
