a b s t r a c tCommercial titania photocatalysts were modified with 2 wt% of silver by photodeposition. The properties of the samples were characterized by DRS, XPS, XRD, FE-SEM and STEM. The modified samples exhibited activity under visible light and enhanced activity under UV irradiation for 2-propanol and acetic acid oxidation, respectively. The time-resolved microwave conductivity (TRMC) analysis indicated that enhanced activity (2.5-8-fold enhancement depending on titania) under UV irradiation was caused by an electron storage in metallic nanoparticles (NPs), and therefore decreasing the recombination between charge carriers. The action spectrum (AS) analysis proved that localized surface plasmon resonance (LSPR) of silver NPs induced the photocatalytic activity under visible light irradiation. The increase of antimicrobial properties under visible light irradiation indicated that not only intrinsic properties of silver in the dark, but also plasmonic properties of Ag@TiO 2 were responsible for overall bacteria killing. The evolution of carbon dioxide under both irradiation ranges indicated mineralization of bacteria cells, and therefore possible application of silver-modified titania for decomposition of chemical and biological pollutants.

In going from oxo-via nitrido-to carbometalates the oxidation states of transition-metal elements participating in the formation of respective ternary and higher compounds are significantly lowered.[1] Based on these observations, we started to investigate the effect of elemental carbon as additive to selected nitridometalate systems. By using excess nitrogen during the high-temperature reactions (so-called oxidizing conditions) nitridometalate cyanamides are preferably formed (e.g. [6]

Commercial titania photocatalysts were modified with silver and gold by photodeposition, and characterized by diffuse reflectance spectroscopy (DRS), X-ray powder diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and scanning transmission electron microscopy (STEM). It was found that silver co-existed in zero valent (core) and oxidized (shell) forms, whereas gold was mainly zero valent. The obtained noble metal-modified samples were examined with regard to antibacterial (Escherichia coli (E. coli)) and antifungal (Aspergillus niger (A. niger), Aspergillus melleus (A. melleus), Penicillium chrysogenum (P. chrysogenum), Candida albicans (C. albicans)) activity under visible-light irradiation and in the dark using disk diffusion, suspension, colony growth (“poisoned food”) and sporulation methods. It was found that silver-modified titania, besides remarkably high antibacterial activity (inhibition of bacterial proliferation), could also decompose bacterial cells under visible-light irradiation, possibly due to an enhanced generation of reactive oxygen species and the intrinsic properties of silver. Gold-modified samples were almost inactive against bacteria in the dark, whereas significant bactericidal effect under visible-light irradiation suggested that the mechanism of bacteria inactivation was initiated by plasmonic excitation of titania by localized surface plasmon resonance of gold. The antifungal activity tests showed efficient suppression of mycelium growth by bare titania, and suppression of mycotoxin generation and sporulation by gold-modified titania. Although, the growth of fungi was hardly inhibited through disc diffusion (inhibition zones around discs), it indicates that gold does not penetrate into the media, and thus, a good stability of plasmonic photocatalysts has been confirmed. In summary, it was found that silver-modified titania showed superior antibacterial activity, whereas gold-modified samples were very active against fungi, suggesting that bimetallic photocatalysts containing both gold and silver should exhibit excellent antimicrobial properties.

Überraschende Eigenschaften hält der trigonal‐planare Komplex [Co(CN)3]6− bereit (siehe Strukturbild; Co rot, C grau, N grün, Erdalkalimetall‐Gegenionen gelb). Bindungslängen und Ladungen der CN‐Liganden variieren, und das Co‐Zentrum verfügt über eine geschlossenschalige (d10‐)Konfiguration.