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Reversible solid oxide cell (RSOC) technology allows use of a single device to efficiently derive chemicals from power (power-to-fuel) and power from chemicals (fuel-to-power). Fuel flexibility is a key aspect, as developing SOCs able to operate on fuels other than hydrogen can ease their integration into existing infrastructure. In addition, H2O and/or CO2 reduction is favorable in SOECs as polarization losses are reduced at high temperature. Here, a composite fuel electrode, 60 wt.% La0.6Sr0.4Fe0.8Mn0.2O3-δ (LSFMn) and 40 wt.% (5 wt.% Ni)-containing Ce0.85Sm0.15O2-δ (Ni-SDC) was investigated in H2-fueled, CO-fueled SOFCs and for CO2 reduction in SOEC mode. In reducing conditions, Fe exsolved from the LSFMn perovskite formed a Ni-Fe alloy with Ni present on SDC. The composite fuel electrode showed remarkable activity for CO2 reduction with a current density output of 1.40 A cm-2 (1.5 V) at 850 °C. SOFC/SOEC cell reversibility was obtained in different CO2:CO mixtures. Electrochemical impedance spectroscopy analysis was used to better understand cell mechanisms in SOFC and SOEC mode.

The production of electric energy from solar radiation is nowadays one of the most investigated and developed “carbon free” technology. A throughout investigation of the ceramics most commonly used as heat transfer fluids and/or heat storage materials for concentrating solar power systems (i.e. alkaline and heart alkaline nitrate/nitrite mixtures) is here reported. The study stems by the need to base materials selection on an accurate and critical knowledge of all their characteristics, including their thermophysical, environmental compatibility, and economic features. At this purpose, a rating criterion have been established, to readily show the advantages and disadvantages of each material, and to highlight which characteristics of the examined materials need to be further investigated and improved. Nitrate/nitrite mixtures have also been compared with other ceramics used for thermal storage, such as solid fillers, liquid metals, other salt mixtures, or phase change materials.

Nanostructured scheelite (CaWO4) was synthesized directly from enriched wolframite (Fe1-xMnxWO4) ore (55.18 % WO3) and lime (CaO) by energetic planetary milling, with no need of high-temperature calcination. After 48 h milling, wolframite was fully converted into nanostructured CaWO4. The mechanochemically derived products, when refluxed overnight in boiling Na2CO3 0.7 M at atmospheric pressure, showed practically complete (> 95 %) dissolution of the calcium tungstate, leaving CaCO3 in the solid residue. In contrast, the very same leaching treatment, when applied to either bare enriched wolframite or pure micro-crystalline CaWO4, did cause a scarse or little solubilization of tungsten. These results confirm the much higher reactivity of nanostructured scheelite in leaching treatments. The observed mechanochemical synthetic route may lead to less energy-intensive and lower environmental impact of tungsten-bearing minerals processing.

Chemical storage systems are a promising innovative route to overcome the issue of the solar irradiation storage, resulting as cost effective and with high energy density. A main problem with these kinds of materials is to design a synthesis method for preparing stable reactive structures, presenting at the same time a high volumetric charging/discharging enthalpy. At this purpose, a size controlled spinel was produced, characterized and investigated regarding its thermophysical and kinetics properties. The obtained powder presents an average diameter between 100 and 200 µm and an energy density of 133 J/g and an experimental test was carried out to verify the spinel morphology stability under thermal cycles. The specific heat is similar to other structured chemical storage system and makes the spinel feasible to be used also as sensible accumulation medium. Despite the relatively high particles size, and the expected small exposed reactive area, the charging, and especially discharging reaction rates resulted particularly favourable and comparable with the reported behaviour of micrometric powders. The particularly simple preparation method plus the cost effectiveness of the precursors leads to a quite convenient expected cost for the storage material, absolutely similar to commercially available accumulation systems.

Ta2O5 nanopowders to be used as sensing electrodes in high temperature electrochemical gas sensors for hydrocarbons detection were synthesized using a sol-gel method and their structural and microstructural properties were investigated. The as-synthesized powders were heated at different temperatures in the range 250-1000 degrees C and characterized by TG-DTA, XRD, SEM, TEM and FT-IR. This investigation allowed to identify the correct thermal treatments to achieve the microstructural, textural and functional stability of materials working at high temperature, preserving their nano-metric grain size. Planar sensors fabricated by using Ta2O5 powders treated at 750 degrees C showed promising results for the selective detection of propylene at high temperature (700 degrees C). The good stability of the sensing response after gas exposure at high temperature was correlated to the stable microstructure the electrodes. Thus, Ta2O5 powders seems good candidate as sensing electrode for sensors for automotive exhausts monitoring.

Sulfonated poly ether ether ketone (SPEEK) with a high degree of sulfonation (DS = 0.9) was mixed with a modified silane bearing a sulfonic acid function (sulfonated diphenylsilanediole, SDPDO).Homogeneous composite membranes with several SPEEK:SDPDO ratios, were obtained. The addition of the ormosil significantly improved the water uptake and solubility properties of pure SPEEK.The structural and electrochemical characteristics of the composite membranes were investigated by means of thermogravimetric analysis (TG), field emission scanning electron microscopy (FE-SEM), and electrochemical impedance spectroscopy (EIS). The conductivity values of the composites SPEEK/SDPDO demonstrated that they possess good proton transport characteristics, thus being suitable for application in Polymer Electrolyte Fuel Cells operating at intermediate temperature.

Diphenylsilanediol (DPDO) reacts with triethoxysilane (TREOS) in anhydrous conditions and in the presence of pyridine, to form complex mixtures of linear and cyclic condensation products which were identified by 29Si NMR and ATR/FTIR spectroscopies. The distribution of products can be varied by modifying the reaction conditions. Spectroscopic analysis allowed to identify the optimal reagents ratio and concentration for the production of hetero-condensation products minimizing the number of residual –OH groups whose presence would affect the performance of optical waveguides based on the synthesised nano building blocks.