Organometal halide perovskite solar cells have demonstrated high conversion efficiency but poor long-term stability against ultraviolet irradiation and water. We show that rapid light-induced free-radical polymerization at ambient temperature produces multifunctional fluorinated photopolymer coatings that confer luminescent and easy-cleaning features on the front side of the devices, while concurrently forming a strongly hydrophobic barrier toward environmental moisture on the back contact side. The luminescent photopolymers re-emit ultraviolet light in the visible range, boosting perovskite solar cells efficiency to nearly 19% under standard illumination. Coated devices reproducibly retain their full functional performance during prolonged operation, even after a series of severe aging tests carried out for more than 6 months.

Nowadays, dye-sensitized solar cells (DSSCs) are the most extensively investigated systems for the conversion of solar energy into electricity, particularly for implementation in devices where low cost and good performance are required. Nevertheless, a key aspect is still to be addressed, being considered strongly harmful for a long time, which is the presence of water in the cell, either in the electrolyte or at the electrode/electrolyte interface. Here comes the present review, in the course of which we try our best to address the highly topical role of water in DSSCs, trying to figure out if it is a poisoner or the keyword to success, by means of a thoroughly detailed analysis of all the established phenomena in an aqueous environment. Actually, in the last few years the scientific community has suddenly turned its efforts in the direction of using water as a solvent, as demonstrated by the amount of research articles being published in the literature. Indeed, by means of DSSCs fabricated with water-based electrolytes, reduced costs, non-flammability, reduced volatility and improved environmental compatibility could be easily achieved. As a result, an increasing number of novel electrodes, dyes and electrolyte components are continuously proposed, being highly challenging from the materials science viewpoint and with the golden thread of producing truly water-based DSSCs. If the initial purpose of DSSCs was the construction of an artificial photosynthetic system able to convert solar light into electricity, the use of water as the key component may represent a great step forward towards their widespread diffusion in the market.

Here we demonstrate that by regulating the mobility of classic −EO− based backbones, an innovative polymer electrolyte system can be architectured. This polymer electrolyte allows the construction of all solid lithium-based polymer cells having outstanding cycling behaviour in terms of rate capability and stability over a wide range of operating temperatures. Polymer electrolytes are obtained by UV-induced (co)polymerization, which promotes an effective interlinking between the polyethylene oxide (PEO) chains plasticized by tetraglyme at various lithium salt concentrations. The polymer networks exhibit sterling mechanical robustness, high flexibility, homogeneous and highly amorphous characteristics. Ambient temperature ionic conductivity values exceeding 0.1 mS cm−1 are obtained, along with a wide electrochemical stability window (>5 V vs. Li/Li+), excellent lithium ion transference number (>0.6) as well as interfacial stability. Moreover, the efficacious resistance to lithium dendrite nucleation and growth postulates the implementation of these polymer electrolytes in next generation of all-solid Li-metal batteries working at ambient conditions.

Main DSSC components, along with their most critical materials and related issues are reviewed and feasible alternatives are envisaged.

Safety issues rising from the use of conventional liquid electrolytes in lithium-based batteries are currently limiting their application to electric vehicles and large-scale energy storage from renewable sources. Polymeric electrolytes represent a solution to this problem due to their intrinsic safety. Ideally, polymer electrolytes should display both high lithium transference number (t Li + ) and ionic conductivity. Practically, strategies for increasing t Li + often result in low ionic conductivity and vice versa. Herein, networked polymer electrolytes simultaneously displaying t Li + approaching unity and high ionic conductivity (σ ≈ 10 −4 S cm −1 at 25 °C) are presented. Lithium cells operating at room temperature demonstrate the promising prospect of these materials.