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Yttrium-doped ZnO thin films were deposited on silica glass substrates by the sol–gel method. The structural, electrical and optical properties of yttrium-doped ZnO thin films were investigated systematically and in detail. All the thin films have a preferred (0 0 2) orientation. When compared with the electrical resistivity values of films without annealing treatment, the values of films annealed in the reducing atmosphere were decreased by about three orders of magnitude. The lowest electrical resistivity value was 6.75 × 10−3 Ω cm, which was obtained in the 0.5 at% yttrium-doped ZnO thin film annealed in nitrogen with 5% hydrogen at 500 °C. In room-temperature photoluminescence (PL) spectra, two PL emission peaks are found in the pure ZnO thin film; one is the near-band-edge (NBE) emission at 3.22 eV and the other is a green emission at about 2.38 eV. Nevertheless, the green emission is not found in the PL of the yttrium-doped ZnO thin films. The low-temperature PL spectrum of the undoped ZnO thin film at 83 K is split into well-resolved free and bound excition emission peaks in the ultraviolet region, but the NBE emission of the 5 at% yttrium-doped ZnO thin film at 83 K has only one broad emission peak.

A novel ZnO nanorod array (NR)/CuAlO2 nanofiber (NF) heterojunction nanostructure was grown on a substrate of Ni plates using sol–gel synthesis for the NFs and hydrothermal reaction for the NRs. Compared with a traditional ZnO/CuAlO2 laminar film nanostructure, the photocurrent of this fibrous network heterojunction is significantly increased. A significant blue-shift of the absorption edge and a favorable forward current to reverse current ratio at applied voltages of − 2t o+2 V were observed in this heterojunction with the increase of Zn 2+ ion concentration in the hydrothermal reaction. Furthermore, the photoelectrochemical properties were investigated and the highest photocurrent of 3.1 mA cm −2 was obtained under AM 1.5 illumination with 100 mW cm −2 light intensity at 0.71 V (versus Ag/AgCl). This novel 3D fibrous network nanostructure plays an important role in the optoelectronic field and can be extended to other binary or ternary oxide compositions for various applications. (Some figures in this article are in colour only in the electronic version)

One dimensional (1D), self-organized TiO2 nanotube arrays are known to have excellent charge transport properties and a NiO/TiO2 junction is efficient in separating electron–hole pairs. This paper describes the synthesis of a NiO/TiO2 junction electrode constructed using self-organized TiO2 nanotube arrays combining the above two properties. The self-organized TiO2 nanotube arrays used in this study were prepared by anodizing titanium films, which resulted in closely packed n-type TiO2 tubes with an inner pore diameter of 60–90 nm, a wall thickness of approximately 15 nm and a length of 600 nm. The NiO/TiO2 junction was synthesized by electroless plating and annealing which resulted in TiO2 nanotube arrays coated with a layer (about 200 nm in thickness) of NiO particles (20–40 nm). The resulting NiO/TiO2 junction electrode enabled us to obtain an enhanced photocurrent (3.05 mA cm−2) as compared with a TiO2 electrode based on TiO2 nanotube arrays (0.92 mA cm−2) under AM 1.5 G (100 mw cm−2) at a bias of 0.65 V.

Large-scale aggregative flowerlike ZnO nanostructures, consisting of many bunches of nanorods at different orientations with a diameter of about 60 nm and a length of 1 µm, have been synthesized through a simple hydrothermal process at a lower temperature. The x-ray power diffraction pattern indicates that the novel flowerlike ZnO nanostructures are hexagonal, and the selected area electron diffraction reveals that the ZnO nanorods are single crystal in nature and preferentially grow along [0 0 1]. Raman spectrum, room-temperature photoluminescence and UV–vis absorption spectra are also discussed. Furthermore, the influence of the reaction time on the morphology of the ZnO nanostructures is investigated, and a possible growth model is proposed. Finally, the gas sensor based on the ZnO nanostructures exhibits high sensitivity for ethanol as well as quick response and recovery time due to the high surface-to-volume ratio.