S. Murugesan

Functionalized Silicate Sol−Gel-Supported TiO2−Au Core−Shell Nanomaterials and Their Photoelectrocatalytic Activity

The N-[3-(trimethoxysilyl)propyl]ethylenediamine (EDAS) derived silicate matrix supported core-shell TiO(2)-Au nanoparticles (EDAS/(TiO(2)-Au)(nps)) were prepared by NaBH(4) reduction of HAuCl(4) precursor on preformed TiO(2) nanoparticles in the presence of EDAS monomer. The core-shell (TiO(2)-Au)(nps) nanoparticles were stabilized by the amine functional group of the EDAS silicate sol-gel network. The potential application of this EDAS/(TiO(2)-Au)(nps) modified electrode toward the photoelectrochemical oxidation of methanol was explored. The EDAS/(TiO(2)-Au)(nps) modified electrode showed a 12-fold enhancement in the catalytic activity toward photoelectrooxidation of methanol when compared to TiO(2) dispersed in EDAS silicate sol-gel matrix. This improved photoelectrochemical performance is explained on the basis of beneficial promotion of interfacial charge transfer processes of the EDAS/(TiO(2)-Au)(nps) nanocomposite. A methanol oxidation peak current density of 12.3 mA cm(-2) was achieved at an optimum loading of Au(nps) on TiO(2) particles. This novel amine functionalized EDAS silicate sol-gel stabilized core-shell (TiO(2)-Au)(nps) nanomaterial could be an excellent candidate for the photocatalytic and photoelectrochemical applications.

Nanostructured CuO Thin Films Prepared through Sputtering for Solar Selective Absorbers

Nanostructured cupric oxide (CuO) thin films have been deposited on copper (Cu) substrates at different substrate temperatures and oxygen to argon gas ratios through direct current (DC) reactive magnetron sputtering. The deposited CuO thin films are characterized by using X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), profilometry, and spectrophotometry techniques. The crystalline phases, morphology, optical properties, and photothermal conversion efficiency of the CuO thin films are found to be significantly influenced by the change in substrate temperature and oxygen to argon gas ratio. The variations in the substrate temperature and oxygen to argon gas ratio have induced changes in Cu