CuO nanocrystals were prepared by thermal decomposition of Cu-oxalate at 400 °C; then CuO/TiO2 core/shell nanocrystals were formed via the hydrolysis of titanium isopropoxide (TIP) on the surface of CuO nanocrystals. The characteristics of the synthesized nanocrystals were systematically studied using appropriate techniques, namely the morphology by using scanning electron microscopy (SEM), and the crystalline structure by x-ray powder diffraction (XRD) and Raman spectroscopy. The structure, shape and size of the CuO and CuO/TiO2 nanocrystals could be tuned by changing various technological parameters: (i) the reaction/growth time (from several minutes to several hours), (ii) reaction temperature (from room temperature to 90 °C) and (iii) the molar ratios of the precursors. The results showed that the reaction temperature and the molar ratio of the precursors play important roles in controlling the morphology and size of both CuO and CuO/TiO2 nanocrystals. With increasing reaction temperature, nano-CuO evolved from spherical shaped nanoparticles to microspheres. By shelling the large-bandgap TiO2 layers on CuO nanocrystals, the core/shell structure is formed and the narrow-bandgap nano-CuO core is expected to be resistant to photocorrosion.
This paper reports on the fabrication of non-chapped, vertically well aligned titanium dioxide nanotubes (TONTs) by using electrochemical etching method and further heat treatment. Very highly ordered metallic titanium nanotubes (TNTs) were formed by directly anodizing titanium foil at room temperature in an electrolyte composed of ammonium fluoride (NH 4 F), ethylene glycol (EG), and water. The morphology of as-formed TNTs is greatly dependent on the applied voltage, NH 4 F content and etching time. Particularly, we have found two interesting points related to the formation of TNTs: (i) the smooth surface without chaps of the largely etched area was dependent on the crystalline orientation of the titanium foil; and (ii) by increasing the anodizing potential from 15 V to 20 V, the internal diameter of TNT was increased from about 50 nm to 60 nm and the tube density decreased from 403 tubes μm −2 down to 339 tubes μm −2 , respectively. For the anodizing duration from 1 h to 5 h, the internal diameter of each TNT was increased from ∼30 nm to 60 nm and the tube density decreased from 496 tubes μm −2 down to 403 tubes μm −2 . After annealing at 400 °C in open air for 1 h, the TNTs were transformed into TONTs in anatase structure; further annealing at 600 °C showed the structural transformation from anatase to rutile as determined by Raman scattering spectroscopy.
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