Composite coatings containing reduced graphene oxide (rGO) and 3-(aminopropyl)triethoxysilane functionalised rGO (APTES-rGO) were prepared by sol-gel technology and deposited on Al 2024 T-3. Covalent functionalisation of GO by APTES occurred by formation of amide bonds, accompanied by GO reduction. The thin sheets were retained. The hydrophilicity of the coating increased when APTES-rGO was added. The opposite was observed when GO was added. A key finding is that the rGO flakes agglomerate and lie in a random orientation in the coating, whereas the APTES-rGO flakes are more evenly distributed in the matrix and appear to lie along the plane of the substrate.
Ta3N5 nanotubes (NTs) were obtained from nitridation of Ta2O5 NTs, which were grown directly on Ta foil through a 2-step anodization procedure. With Co(OH)x decoration, a photocurrent density as high as 2.3 mA cm-2 (1.23 V vs. NHE) was reached under AM1.5G simulated solar light; however, the electrode suffered from photocorrosion. More stable photoelectrochemical (PEC) performance was achieved by first loading Co(OH)x, followed by loading cobalt phosphate (Co-Pi) as double co-catalysts. The Co(OH)x/Co-Pi double co-catalysts may act as a hole storage layer that slows down the photocorrosion caused by the accumulated holes on the surface of the electrode. A "waggling" appearance close to the "mouth" of Ta2O5 NTs was observed, and may indicate structural instability of the "mouth" region, which breaks into segments after nitridation and forms a top layer of broken Ta3N5 NTs. A unique mesoporous structure of the walls of the Ta3N5 NTs, which is reported here the first time, is also a result of the nitridation process. We believe that the mesoporous structure makes it difficult for the nanotubes to be fully covered by the co-catalyst layer, hence rationalizing the remaining degradation by photocorrosion.
Herein, we demonstrate the shape- and size-selective growth of ZnO nanostructures on indium tin oxide-coated glass substrates by using a microwave-assisted chemical bath deposition method. By systematically controlling the deposition parameters, it is possible to produce shape- and size-selective nanostructures with high alignment and uniformity. Specifically, the pH of the bath can be used to control the shape of rods from bundled structures to tapered and flat tips. Furthermore, the deposition temperature can be used to control the size of the ZnO array from 770 to 125â nm. The prepared rods were active catalysts in the degradation of methylene blue under UV radiation, and exhibited size-dependent activity.
TiO2 nanoparticles modified with nitrogen and sulfur were prepared from titania nanotubes by a facile wet chemistry method. The samples synthesized with different thiourea/TiO2 ratios showed a uniform nanoparticle size distribution centred at approximately 10 nm with a developed specific surface area of 246 m2 g-1. These modified nanosized photocatalysts exhibited higher photocatalytic activity for the degradation of gaseous isopropanol than unmodified titania nanotubes under visible illumination. This could be attributed to the synergistic effects of a large specific surface area, strong absorption in the visible region, a redshift in the adsorption edge, and surface adsorption modification induced by nitrogen and sulfur compounds.
