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.

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Bromobenzenethiol passivated gold nanoparticles were mixed with a poly(phenylene ethynylene) bearing thioester flexible sequences in order to obtain a fluorescent composite for optical biosensors. The particles and the composite were characterized by 1H, 13C NMR, UV-Vis and fluorescence spectroscopy, TEM and STEM. The particles are homogeneously dispersed in the polymer matrix as observed by electron microscopy. The NMR spectra suggest that the gold particles and the poly(phenylene ethynylene) are probably interacting through the sulfur atoms of the –C(O)S- and –CH2-S-CH2- moieties of the flexible sequences of the polymer as well as through  interactions between the aromatic ring of 4-bromobenzenthiol and the conjugated backbone of pPET3OC12-sqS. The quantum yield of the composite both in solution and in solid state films is slightly lower than that of pPET3OC12-sqS because of the quenching effect of gold. Nonetheless, a change of the fluorescence intensity of the composite films can be detected as a consequence of the contact with microorganisms. Preliminary microbiological assays indicate an antimicrobial effect of the composite film with the E. coli bacteria.