The most promising candidate as an everyday alternative to lithium-ion batteries (LIBs) are sodium-ion batteries (NIBs). This is not only due to Na abundance, but also because the main principles and cell structure are very similar to LIBs. Due to these benefits, NIBs are expected to be used in applications related to large-scale energy storage systems and other applications not requiring top-performance in terms of volumetric capacity. One important issue that has hindered the large scale application of NIBs is the anode material. Graphite and silicon, which have been widely applied as anodes in NIBs, do not show great performance. Hard carbons look very promising in terms of their abundance and low cost, but they tend to suffer from instability, in particular over the long term. In this work we explore a carbon-coated TiO2 nanoparticle system that looks very promising in terms of stability, abundance, low-cost, and most importantly that safety of the cell, since it does not suffer from potential sodium plating during cycling. Maintaining a nano-size and consistent morphology of the active material is a crucial parameter for maintaining a well-functioning cell upon cycling. In this work we applied Anomalous Small Angle X-Ray Scattering (ASAXS) for the first time at the Ti K-edge of TiO2 anatase nanoparticles on different cycled composite electrodes in order to have a complete morphological overview of the modifications induced by sodiation and desodiation. This work also demonstrates for the first time that the nanosize of the TiO2 is maintained upon cycling, which is in agreement with the electrochemical stability.

Supercapacitors are nowadays considered to be one of the most important electrochemical storage devices. These devices display high power and extraordinary cycle life, and they are currently used in an increasing number of applications. However, in order to further increase the applications of supercapacitors, an increase in their energy capacity appears to be necessary. Moreover, the development of safe and environmentally friendly supercapacitors is also required. In this article, we illustrate the contributions ionic liquids (ILs) might play in the development of high energy and safe supercapacitors. First, the use of ILs as electrolytes in supercapacitors is considered, and the advantages as well as challenges related to the use of this kind of electrolyte are analyzed. Next, the interaction between ILs and electrode materials is taken into account, with particular attention paid to inactive components of supercapacitor electrodes. The introduction of natural cellulose as a binder is used as an example of the contribution ILs might provide to the development of environmentally friendly supercapacitors.

Ionic liquids (ILs) are a very interesting new class of fluid materials because of their unique characteristics, such as wide chemical, thermal, and electrochemical stability, high ion conduction, non-detectable vapor pressure, nonflammability, and good-to-excellent capability to dissolve inorganic, organic, and polymer compounds. ILs are proposed for a very wide variety of applications, including electrochemical devices. However, high purity ILs, particularly for high-energy electrochemical applications, are not widely available commercially. In addition, solvent restriction and environmental impact, as well as the possibility to fully recycle chemicals and reagents, represent the most stringent requirements for the future synthesis processes of ILs. This article reviews synthesis route improvements in terms of environment impact solvents, chemical recycling and cost, and process yield for obtaining high purity (below 50 ppm) ILs.

A progress report of the MASTER project is presented here. MASTER is a system of three heterodyne receivers based on SIS (superconductor–insulator–superconductor) tunnel junction mixers. In our instrument these mixers will allow direct down-conversion from 94, 225, and 345 to 1.5 GHz, the IF where the signal will be detected. This instrument, coupled to a 2–4 m telescope like the one proposed for the DOME C base in Antarctica and in conjunction with an Acusto Optical Spectrometer, can be used to detect emission lines associated with molecular clouds in the interstellar medium. The current status of a 94 GHz receiver, the prototype of MASTER, will be presented too. The study of the optical coupling between the receiver and MITO telescope in the Italian Alps will also be described.

Field and laboratory trials were undertaken to determine effects and efficacy of neem extracts on the Sahelian grasshopper, Kraussaria angulifera (Krauss). Formulations of aqueous extracts were sprayed in field experiments. Concentrations of 0.5% and 1% were effective in reducing grasshopper feeding. Neem kernel powder applied systematically, partially protected millet against K. angulifera. The residual activity of the botanical insecticide was at least seven days. Analysis of plant selection behaviour showed that neem is primarily an antifeedant rather than a repellent for this insect. On first to third instar nymphs, growth regulating activity, expressed as difficulty in moulting or an incompleteness of sclerotization, may occur.

An improved cathodic material has been obtained by doping vanadium oxide hydrogel with silver. Silver-doped vanadium pentoxides with a silver molar fraction ranging from 0.01 to 1 were synthesized. With the successful doping, the electronic conductivity of V2O5 was increased by 2 to 3 orders of magnitude. The electrochemical performance of the silver doped materials is very high, up to 4 moles of lithium per mole of silver-doped V2O5 were found to be reversibly intercalated. In addition, the lithium diffusion coefficient is found to be high in the silver-doped material and with a smaller dependence on the lithium intercalation level. These enhancements resulted in high rates of insertion and delivered capacities.

Nickel oxide sputtered electrodes can undergo a reversible lithium intercalationdeintercalation process which is accompanied by a net electrochromic effect. The characteristics of this type of electrode and the mechanism of the related electrochromic process are discussed on the basis of results obtained by cyclic voltammetry and optical transmittance. The results show that nickel oxide is electrochromically activated by insertion of lithium in the oxide structure. The lithium intercalation process may be promoted by cyclic voltammetry or, more extensively, by polarizing cathodically the nickel oxide electrode in a non-aqueous electrolyte containing a lithium salt. Activated nickel oxide electrodes are of considerable interest for the realization of new types of efficient solid state electrochromic windows..