In this study, titania nanoparticles were obtained using the microwave-assisted technique. Moreover, different surfactants (PEG (M_n = 400), Pluronic P123 and Triton X−100) were used during the synthesis in order to determine their impact on the crystallinity and morphology of the final products. Subsequently, techniques such as XRD, SEM and TEM (performed in high contrast and high-resolution mode), diffuse reflectance spectroscopy (DRS), low temperature N₂ sorption (BET model), FTIR and TGA were carried out. Based on the crystallinity analysis of the obtained materials, it was established that the addition of surfactants results in greater (PEG and Triton X−100) or smaller (Pluronic P123) average crystallite size. The main purpose of this study was to use the synthesized nanomaterials in the photodegradation process (in the UV light range) of the model organic pollutants – phenol (20 mg/L) and etodolac (15 mg/L). Furthermore, it was also pointed out that the dye-sensitized solar cells can be a second application for the synthesized titania nanomaterials. The photo-oxidation and photovoltaic tests have shown that the titanium dioxide obtained using the surfactant-assisted microwave method is characterized not only by better photodegradation efficiency of phenol and etodolac, but also by higher photocurrent density compared to the reference titania samples—the pristine TiO₂ and commercial P25.

(2005). SYNTHESIS OF SUBSTITUTED 1,3,4-THIADIAZOLES USING LAWESSON'S REAGENT. Organic Preparations and Procedures International: Vol. 37, No. 3, pp. 213-222.

The charge recombination and exciton dissociation are generally recognized as the basic electronic processes limiting the efficiency of photovoltaic devices. In this work, we propose a detailed mechanism of photocurrent generation in dye-sensitized solar cells (DSSCs) examined by magnetic field effect (MFE) technique. Here we demonstrate that the magnitude of the MFE on photocurrent in DSSCs can be controlled by the radius and spin coherence time of electron-hole (e-h) pairs which are experimentally modified by the photoanode morphology (TiO₂ nanoparticles or nanotubes) and the electronic orbital structure of various dye molecules (ruthenium N719, dinuclear ruthenium B1 and fully organic squaraine SQ2 dyes). The observed MFE is attributed to magnetic-field-induced spin-mixing of (e-h) pairs according to the Δg mechanism.