Plasmon-assisted photocurrent generation from silver nanoparticle monolayers combined with porphyrins via their different chain-length alkylcarboxylates.

Three-typed porphyrin derivatives with a different chain-length alkylcarboxylic acid as their peripheral anchor group have been prepared. Anodic photocurrents were observed in a simple system where the porphyrin derivatives were directly anchored on an indium tin oxide (ITO) electrode. Cathodic photocurrents and their plasmon-assisted enhancement appeared from an Ag nanoparticle (Ag NP) composite monolayer combined with the porphyrin derivatives on the ITO electrode.

Direct transformation into silver nanoparticles via thermal decomposition of oxalate-bridging silver oleylamine complexes.

Silver(I) oxalate, Ag2(C2O4), reacts with two equivalents of oleylamine (Ag:oleylamine = 1:1 mole/mole) to form an oxalate-bridged silver-oleylamine complex, [(oleylamine)Ag(micro-C2O4)Ag(oleylamine)]. The precursor complex is thermally decomposed at approximately 150 degrees C with CO2 evolution to produce Ag nanoparticles with approximately 11 nm dimension. The Ag nanoparticles contain approximately 12 wt% of oleylamines as the surface stabilizer.