Layers of transparent and conductive Sn-doped zinc oxide (ZnO) have been prepared using chemical reactive liquid phase (spray) method on glass substrates. X-ray diffraction analysis shows that the obtained layers show preferential grains orientation along the direction (002). Microstructural analysis indicates that the thickness of the deposited films is independent of Sn content, i.e. 408 nm, and that the average grain size increases with increasing Sn content, ranging from 31 nm to 42 nm. The value of the optical gap obtained using UV-visible transmission spectroscopy method increases slightly from 3.1 eV to 3.3 eV. Moreover, transmission curves reveal that the prepared thin films are transparent in the visible domain
SnS films have been prepared by electrodeposition technique onto Cu and ITO substrates using acidic solutions containing tin chloride and sodium thiosulfate with sodium citrate as an additive. The effects of sodium citrate on the electrochemical behavior of electrolyte bath containing tin chloride and sodium thiosulfate were investigated by cyclic voltammetry and chronoamperometry techniques. Deposited films were characterized by XRD, FTIR, SEM, optical, photoelectrochemical, and electrical measurements. XRD data showed that deposited SnS with sodium citrate on both substrates were polycrystalline with orthorhombic structures and preferential orientations along (111) directions. However, SnS films with sodium citrate on Cu substrate exhibited a good crystalline structure if compared with that deposited on ITO substrates. FTIR results confirmed the presence of SnS films at peaks 1384 and 560 cm-1. SEM images revealed that SnS with sodium citrate on Cu substrate are well covered with a smooth and uniform surface morphology than deposited on ITO substrate. The direct band gap of the films is about 1.3 eV. p-type semiconductor conduction of SnS was confirmed by photoelectrochemical and Hall Effect measurements. Electrical properties of SnS films showed a low electrical resistivity of 30 Ω cm, carrier concentration of 2.6 × 10
The realization of an optical-fiber corrosion sensor (OFCS) has been achieved using two different methods. In the first method, a plastic clad silica (PCS) fiber whose uncladded part (2 cm in length) has been metallized through deposition using nickelphosphorus. In the second method, metallization used gold and nickel-phosphorus. The light power [PðÞ] at the exit end of the fiber is recorded as a function of the angle (, angle of incidence) made by the axis of the fiber and a beam from a laser diode at a 670 nm wavelength applied at the entrance of the fiber. It is observed that the corrosion of the coating material (nickel-phosphorus) modifies the PðÞ curves, be it by immersion in phosphoric acid solutions. The full width at halfmaximum of these curves increases with increasing corrosion pit density. Kinetic curves of corrosion have been obtained for different concentrations of phosphoric acid. This type of sensor is important because it can be inserted in metallic infrastructures to monitor the corrosion state of the structure in situ.
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