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Due to its physical and chemical properties, the n-type tungsten oxide (WO3) semiconductor is a suitable photoanode for water decomposition reaction. The responses of the photoelectrochemical PEC water-splitting properties as an effect of structural and optical changes of WO3 thin films, as well as the nature of electrolyte solutions, were studied in this work. The WO3 thins films have been obtained by pulsed laser deposition (PLD) on silicon (Si(001)) covered with platinum substrates using three different laser wavelengths. As the XRD (X-ray diffraction) and XTEM (cross-section transmission electron microscopy) analysis shows, the formation of highly crystalline monocline WO3 phase is formed for the film deposited at 1064 nm wavelength and poor crystalline phases with a large ordering anisotropy, characteristic of 2D structures for the films deposited at 355 nm and 193 nm wavelengths, respectively. The photogenerated current densities Jph depend on the laser wavelength, in both alkaline and acidic electrolyte. The maximum values of the photocurrent density have been obtained for the sample prepared with laser emitting at 355 nm. This behavior can be correlated with the coherent crystallized atomic ordering that appear for long distances (10&ndash, 15 nm) in the (001) plane of the monoclinic WO3 phase structure films obtained at 355 nm laser wavelength. All the samples show poor current density in dark conditions and they are very stable in both acidic and alkaline solutions. The highest photocurrent density value is obtained in acidic solution for the WO3 thin film prepared by 355 nm laser (29 mA/cm2 at 1.6 V vs. RHE (1.35 V vs. Ag/AgCl)).

The active layer of the bulk heterojunction organic photovoltaic cells is typically based on a polymeric blend containing a donor polymer and a fullerene-based polymer electron acceptor. However, in the last decade non-fullerene polymer-based solar cells have seen a rapid progress, due to their extraordinary chemical, thermal and photo stability, and because of their ability to decrease the voltage loss. The conventional Organic Photovoltaic Cells (OPVs), structures based on either P3HT:PCBM bulk heterojunction (BHJ) polymeric blend or P3HT/PCBM bilayer heterojunction, have limited efficiency and stability, in principal due to the fullerene derivatives used as acceptor component. PCBM for example, as many other fullerene derivatives, exhibits some deficiencies, such as: limited chemical and energetic tunability, small range of absorption spectra, morphological instability and relatively high production costs. That is why in the last years, novel non-fullerene materials started to be used in order to overcome the above limits associated with the fullerene acceptors. In this paper two different non-fullerene acceptor materials have been tested as potential candidates for the efficient OPVs based on P3HT donor polymer as main absorber: a new conjugated polymer containing chelating ligands like 1,10-Phenanthroline (Phen), and a small-molecule acceptor like 5,10,15,20-Tetra(4-pyridyl)-21H,23H-porphine (TPyP). For both cell configurations a decrease of the voltage loss was obtained, and it was also observed that the thickness of the P3HT donor layer has an important contribution to the output power ( P max ) and fill factor ( FF ) of the OPV structures ( FF and P max increased almost two times by decreasing the thickness of the P3HT donor layer).