Pure and Cu-doped NiO films were synthesized via a soft chemical process. They were deposited on glass substrates heated to 400 °C. Different atomic percentage ratios (2, 4, 6, 8, and 10%) of Cu-doping were used. The prepared samples were characterized by several techniques such as X-ray diffraction for crystallographic study, SEM and AFM for microstructural and morphological properties, and UV-Visible spectroscopy for optical and photocatalytical analysis. XRD results of pure and Cu-doped NiO films indicated the formation of NiO polycrystalline phases under a cubic structure with a favored orientation along the (200) plane noticed in all sprayed films. SEM images revealed the formation of NiO nanoparticles of spherical forms whose sizes increase and agglomerate with increasing Cu-doping. At 10% Cu-doping, NiO agglomeration was extended to the whole surface. AFM images showed a textured and rough surface composed of NiO nanoparticles of average size varying from 16 to 10 nm depending on Cu-doping concentration. UV-visible spectroscopy confirmed the transparency of NiO films and their semiconducting character with a band gap ranging from 3.4450 eV to 2.8648 eV. The photocatalytical properties of pure and Cu-NiO films were enhanced by Cu-doping particles as revealed by the degradation of methylene blue (MB) solution subjected to irradiation.

Pure and Mg-doped manganese oxide thin films were synthesized on heated glass substrates using the spray pyrolysis technique. The surface chemical composition was investigated by the use of X-ray photoelectron spectroscopy (XPS). Structural and morphological properties were studied by using X-ray diffraction (XRD), scanning electron microscope (SEM) and atomic force microscopy (AFM). Optical properties were characterized by UV-visible spectroscopy. XPS spectra showed typical Mn (2p3/2), (2p1/2) and O (1s) peaks of Mn₃O₄ with a slight shift attributed to the formation of different chemical states of manganese. XRD analysis revealed the tetragonal phase of Mn₃O₄ with a preferred (211) growth orientation that improved with Mg-doping; likewise, grain size is observed to increase with the Mg doping. SEM images of Mn₃O₄ films showed rough surfaces composed of uniformly distributed nanograins whose size decreases with the Mg-doping. The manganese oxide films surface observed in AFM show a textured, rough and porous surface. The combination of transmittance and absorption data in the UV-visible range allowed determining the energy values of the Eg band gap (1.5–2.5 eV). The decrease of the band gap with the Mg-doping increase is attributed to the influence of the greater size of the Mg²⁺ ion in the manganese oxide lattice.

ZnO thin films were synthesized on silicon and glass substrates using the plasma-enhanced chemical vapor deposition (PECVD) technique. Three samples were prepared at substrates temperatures of 200, 300, and 400 °C. The surface chemical composition was analyzed by the use of X-Ray Photoelectron spectroscopy (XPS). Structural and morphological properties were studied by using X-ray diffraction (XRD) and scanning electron microscopy (SEM). Optical properties were carried out by UV-visible spectroscopy. XPS spectra showed typical peaks of Zn(2p3/2), Zn(2p1/2), and O(1s) of ZnO with a slight shift attributed to the substrate temperature. XRD analysis revealed hexagonal wurtzite phases with a preferred (002) growth orientation that improved with temperature. Calculation of grain size and dislocation density revealed the crystallization improvement of ZnO when the substrate temperature varied from 200 to 400 °C. SEM images of ZnO films showed textured surfaces composed of grains of spherical shape uniformly distributed. The transmittance yields are reaching 80%, and the values of the band-gap energy indicate that the ZnO films prepared by PECVD present transparent and semiconducting properties.

We report on the photocatalytical properties of pure and barium-doped nickel oxide nanofilms synthesised on glass substrates using a simple spray pyrolysis method. The nanofilms were prepared from different solution concentrations obtained from pure nickel chloride hexahydrate (NiCl₂:6H₂O) powder in distilled water. Doping has been obtained at various concentrations of barium (0–5%) by simultaneously dissolving (BaCl₂:2H₂O) in the distilled water. The structure and the morphology of the NiO and Ba-NiO nanofilms were investigated by means of X-ray diffraction and atomic force microscopy. The observed principal (111), (200) and (220) XRD patterns peaks correspond to cubic NiO adopting the NaCl-type structure. AFM observations revealed a textured and rough surface. Optical reflectance and transmittance measurements showed an optical band gap corresponding to that of NiO, only slightly affected by the barium doping. The photocatalytic properties of the films were enhanced by barium doping as revealed by the degradation of methylene blue (MB) aqueous solution under ultraviolet irradiation. Between 70–80% of MB was consumed after 300 min ultraviolet irradiation with the addition NiO with Ba concentrations in the range 0–3%.

Pure and Li-doped CuO nanofilms were synthesized on heated glass substrates using the spray-pyrolysis technique. The deposited pure CuO nanofilms were achieved at a precursor molarity of 0.2 M using a solution prepared from copper nitrate trihydrate (Cu(NO₃)₂·3H₂O). Doped Li–CuO nanofilms were obtained using several doping concentrations (3, 6, 9, 12 and 15%) by adding a solution prepared from lithium nitrate (LiNO₃). The pure and Li–CuO samples were investigated by different techniques. XRD revealed three dominant peaks (-111), (111) and (211), which are the properties of monoclinic CuO. The increase in Li-doping concentration showed the appearance of other peaks of low intensities detected at 2θ ranging from 49 to 68°. AFM images showed a textured and inhomogeneous surface composed of spherical grains whose size decreased with increasing Li doping. UV–visible spectroscopy showed that the CuO samples were of low transparency; the transmittance was less than 50%. The band-gap energy determined from Tauc’s equation plot increased from 2.157 to 3.728 eV with the increase in Li doping. These values correspond well to the band gap of semiconducting CuO. The photocatalytic properties were accelerated by Li doping, as revealed by the discoloration of aqueous methylene-blue (MB) solution under ultraviolet irradiation.

In this paper, we try to study the effect of two different ionic and nonionic amines dodecylamine (DDA) and hexadecyldimethylamine (DMHA) considered as weak bases and surfactant on the growth of ZnO nanorods using hydrothermal synthesis technique. The self-assembly of oriented attachment (OA) of ZnO nano- and microrods has been successfully obtained by this technique at temperatures greater than 150 °C. The ZnO nano/microrods were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), Raman scattering spectroscopy, Fourier transform infrared (FTIR) and photoluminescence. The XRD measurements show that ZnO prepared by DDA amine presents small grain size in comparison to ZnO obtained from DMHA amine. From SEM characterization, we show that DDA amine has a great effect on the OA of several homogenous ZnO microrods building blocks. The growth process is explained by the formation of ZnO OA in microstructures scale which is depending on ionic character of amines. Optic measurements (Raman, FTIR and photoluminescence) are presented and commented.