Improving the stability of perovskite solar cells: Inorganic-organic perovskite solar cells have poor long-term stability because ultraviolet light and humidity degrade these materials. Bella et al. show that coating the cells with a water-proof fluorinated polymer that contains pigments to absorb ultraviolet light and re-emit it in the visible range can boost cell efficiency and limit photodegradation. The performance and stability of inorganic-organic perovskite solar cells are also limited by the size of the cations required for forming a correct lattice. Saliba et al. show that the rubidium cation, which is too small to form a perovskite by itself, can form a lattice with cesium and organic cations. Solar cells based on these materials have efficiencies exceeding 20% for over 500 hours if given environmental protection by a polymer coating. Science , this issue pp. 203 and 206
Dye-sensitized solar cells (DSSCs), as emerging photovoltaic technology, have been thoroughly and extensively investigated in the last three decades. Since their first appearance in 1991, DSSCs have gained increasing attention and have been classified as feasible alternatives to conventional photovoltaic devices due to their numerous advantages, such as cheap and simple preparation methods, the possibility of being integrated in buildings and astonishing performances under indoor and diffuse illumination conditions. Photoconversion efficiencies of up to 14% and 8% have been obtained for lab-scale devices and modules, respectively. Albeit the efforts made, these values seem arduous to be outdone, at least under simulated solar radiation. Nevertheless, recent lab-scale systems have demonstrated photoconversion efficiencies of up to 33% under indoor illumination (i.e. 1000 lux) leading to an actual Renaissance (or Revival) of these devices. It is worth mentioning that scientists in this field are developing innovative materials aiming at long-term and efficient devices, being the concept of sustainability often set apart. However, in light of effective commercialization of this technology, stability, efficiency and sustainability should be considered as the essential keywords. Nowadays, DSSCs are finding a “new way back” towards sustainability and rather a huge number of reports have focused on the preparation of green and cost-effective materials to replace the standard ones. In this scenario, the present review aims to give an overview of the most adopted strategies to enhance the sustainability of materials in classical DSSC components (e.g. sensitizer, redox couple, electrolyte and counter-electrode), including smart synthesis and deposition procedures, which currently represent utmost important topics in the scientific community.
This review highlights the efforts towards the realization of an artificial photosynthetic system able to convert sunlight into electricity by using a unique solvent, water, the solvent of life.
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.