Abstract. In this study, lead iodide (PbI 2 ) thin films were deposited on glass substrates by spin coating a solution of 0.2 M PbI 2 dissolved in dimethylformamide, varying the deposition time and the spin speed. The thickness of the thin films decreased with increase in spin speed and deposition time, as examined by profilometry measurements. The structure, morphology, optical and electrical properties of the thin films were analysed using various techniques. X-ray diffraction patterns revealed that the thin films possessed hexagonal structures. The thin films were grown highly oriented to [001] direction of the hexagonal lattice. Raman peaks detected at 96 and 136 cm −1 were corresponding to the characteristic vibration modes of PbI 2 . The X-ray photoelectron spectroscopy detected the presence of Pb and I with core level binding energies corresponding to that in PbI 2 . Atomic force microcopy showed smooth and compact morphology of the thin films. From UV-Vis transmittance and reflectance spectral analysis, the bandgap of the thin films ∼2.3 eV was evaluated. The dark conductivity of the thin films was computed and the value decreased as the deposition time and spin speed increased.
Size-selected TiN nanoclusters in the range of 4 to 20 nm have been produced by an ionized cluster beam, which combines a glow-discharge sputtering with an inert gas condensation technique. With this method, by controlling the experimental conditions, it was possible to produce nanoparticles with a high control in size. The size distribution of TiN nanoparticles was determined before deposition by mass spectroscopy and confirmed by atomic force microscopy. The size distribution was also analyzed using a high-resolution transmission electron micrograph. The photoluminescence [PL] spectra of TiN nanoparticles at different sizes were also experimentally investigated. We reported, for the first time, the strong visible luminescence of TiN nanoparticles on Si (111) wafer due to the reduced size. We also discussed the PL intensity as a function of the nanoparticle size distribution.
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