Abdallah F. Zedan

Ultrasmall Gold Nanoparticles Anchored to Graphene and Enhanced Photothermal Effects by Laser Irradiation of Gold Nanostructures in Graphene Oxide Solutions

In this work we demonstrate the coupling of the photothermal effects of gold nanostructures of controlled size and shape with graphene oxide nanosheets dispersed in water. The enhanced photothermal effects can be tuned by controlling the shape and size of the gold nanostructures, which result in a remarkable increase in the heating efficiency of the laser-induced size reduction of gold nanostructures. The Raman spectra of the Au-graphene nanosheets provide direct evidence for the presence of more structural defects in the graphene lattice induced by laser irradiation of graphene oxide nanosheets in the presence of Au nanostructures. The large surface areas of the laser-reduced graphene oxide nanosheets with multiple defect sites and vacancies provide efficient nucleation sites for the ultrasmall gold nanoparticles with diameters of 2-4 nm to be anchored to the graphene surface. This defect filling mechanism decreases the mobility of the ultrasmall gold nanoparticles and, thus, stabilizes the particles against the Ostwald ripening process, which leads to a broad size distribution of the laser-size-reduced gold nanoparticles. The Au nanostructures/graphene oxide solutions and the ultrasmall gold-graphene nanocomposites are proposed as promising materials for photothermal therapy and for the efficient conversion of solar energy into usable heat for a variety of thermal, thermochemical, and thermomechanical applications.

Silver Nanoparticles-Decorated Titanium Oxynitride Nanotube Arrays for Enhanced Solar Fuel Generation

We demonstrate, for the first time, the synthesis of highly ordered titanium oxynitride nanotube arrays sensitized with Ag nanoparticles (Ag/TiON) as an attractive class of materials for visible-light-driven water splitting. The nanostructure topology of TiO2, TiON and Ag/TiON was investigated using FESEM and TEM. The X-ray photoelectron spectroscopy (XPS) and the energy dispersive X-ray spectroscopy (EDS) analyses confirm the formation of the oxynitride structure. Upon their use to split water photoelectrochemically under AM 1.5 G illumination (100 mW/cm2, 0.1 M KOH), the titanium oxynitride nanotube array films showed significant increase in the photocurrent (6 mA/cm2) compared to the TiO2 nanotubes counterpart (0.15 mA/cm2). Moreover, decorating the TiON nanotubes with Ag nanoparticles (13 ± 2 nm in size) resulted in exceptionally high photocurrent reaching 14 mA/cm2 at 1.0 VSCE. This enhancement in the photocurrent is related to the synergistic effects of Ag decoration, nitrogen doping, and the unique structural properties of the fabricated nanotube arrays.

Tailoring the reducibility and catalytic activity of CuO nanoparticles for low temperature CO oxidation

Copper oxide (CuO) nanoparticles have received considerable interest as active and inexpensive catalysts for various gas–solid reactions. The CuO reducibility and surface reactivity are of crucial importance for the high catalytic activity. Herein, we demonstrate that the reducibility and stability of CuO nanoparticles can be controlled and tailored for the high catalytic activity of CO oxidation. The synthesized CuO nanoparticles possessed enhanced reducibility in CO atmosphere at lower reduction temperature of 126 °C compared to 284 °C for that of reference CuO particles. Moreover, the CuO catalysts with tailored reducibility demonstrated a reaction rate of 35 μmol s−1 g−1 and an apparent activation energy of 75 kJ mol−1. Furthermore, the tailored catalysts exhibited excellent long-term stability for CO oxidation for up to 48 h on stream. These readily-reducible CuO nanoparticles could serve as efficient, inexpensive and durable catalysts for CO oxidation at low temperatures.