Zn₃V₂O₈ and Mg₃V₂O₈ pseudo binary nanomaterials were obtained at 250°C by the hydrothermal method. A morphological and an optical characterization of the obtained nanomaterials were proceeded through different techniques as: X-ray diffraction, SEM, AFM and UV-VIS measurements. The optical band gap values for both nanomaterials were determined. For Zn₃V₂O₈ was obtained a value equal to 3.50 eV for the band gap and for the Mg₃V₂O₈ nanomaterial was obtained a value equal with 3.60 eV for the band gap.

The optimization of the photoactive electrode based on TiO₂ with a complex architecture for UV dyes along with water-based electrolyte has successfully allowed us (i) to obtain a photovoltaic efficiency of the dye-sensitized solar cell with 1.45 times higher than the best efficiency reported for synthetic dye and 3 times for curcumin dye so far; (ii) transparency on the entire Photosynthetic Active Radiation domain; (iii) preserving high efficiency for lighting 1 sun (summer) and shading, especially for 60 mW/cm², which represents the maximum illumination in the rest of the seasons. Our water-based dye-sensitized solar cells loaded with synthetic and natural UV dyes have revealed that the implementation of a dye-sensitized solar cell in autonomous greenhouses is a viable and inexpensive concept.

Six new bio-inspired flavylium salts were synthesized and investigated by a combined computational and experimental study for dye-sensitized solar cell applications. The compounds were characterized by FT–IR, UV–Vis, NMR spectroscopy, and LC–MS spectrometry techniques. The pH-dependent photochromic properties of the flavylium dyes were investigated through a UV–Vis spectroscopy study and revealed that they follow the same network of chemical reactions as anthocyanins upon pH changes. The structural and electronic properties of the dyes were investigated using density functional theory (DFT) and time-dependent density functional theory (TD–DFT). Geometry optimization calculation revealed that all dyes, regardless of the specie, flavylium cations or quinoidal bases, present a planar geometry. The photovoltaic performances of the dyes, in both flavylium and quinoidal base forms, were evaluated by the HOMO and LUMO energies and by calculating the light-harvesting efficiencies, the free energy change of electron injection, and the free energy change regeneration. The MO analysis showed that all dyes can inject electrons into the conduction band of the TiO₂ upon excitation and that the redox couple can regenerate the oxidized dyes. The results obtained for the free energy change of electron injection suggest that the quinoidal bases should inject electrons into the semiconductor more efficiently than the flavylium cations. The values for the free energy change regeneration showed that the redox electrolyte can easily regenerate all dyes. Dipole moment analysis was also performed. DSSCs based on the dyes, in both flavylium and quinoidal base forms, were assembled, and their photovoltaic performances were evaluated by measuring the open-circuit voltage, the short circuit current density, the fill factor, and the energy conversion efficiency. Results obtained by both experimental and computational studies showed that the overall performances of the DSSCs with the quinoidal forms were better than those obtained with the flavylium cations dyes.

The rapid spread of the Internet of Things (IoT) along with the development of innovative low-power electronic devices has also driven the development of indoor photovoltaics. In this paper, we propose a simple and economically feasible solution that can improve the efficiency of dye-sensitized solar cells (DSSCs) under indoor light conditions by ~112%, without requiring a complex TiO₂ photoanode architecture or the design of new dyes. The ball milling process of the TiO₂ paste was optimized for indoor light conditions for the first time, both in terms of efficiency and production costs, by developing a rapid preparation method that can be used industrially for the application of DSSCs. A simple use of 12 mm diameter balls caused beneficial structural modifications, decreasing the size of the crystallites, and leading to a high OH generation on the TiO₂ surface responsible for the improvement of energy conversion efficiency.