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Composite membranes made-up of sulphonated polyetheretherketone (SPEEK, DS = 0.5) and of a sulphonated and silylated hybrid organic–inorganic derivative of polyphenylsulphone (SiSPPSU, DS = 2) were prepared and characterised. The water and methanol uptake, as well as thermal properties, of blend membranes containing 5 and 10 wt.-% SiSPPSU were evaluated. The electrochemical performance of the membranes was evaluated by electrochemical impedance spectroscopy (EIS) and tested in a direct methanol fuel cell (DMFC) station. The presence of SiSPPSU modified the properties of SPEEK, allowing to increase its performance in terms of proton conductivity, thermal and hydrolytic stability. These blends appeared to be suitable electrolytes for DMFC applications.

Hybrid membranes based on highly sulfonated poly(ether ether ketone) (SPEEK, DS = 0.9) where titania network was dispersed by in situ sol–gel reactions were prepared and characterized. The syntheses were carried out using either a basic catalyst (pyridine) or a chelating agent (2,4-pentandione) to control the features of the inorganic network in the polymeric matrix. Membranes were characterized by thermogravimetric analysis (TG), field emission scanning electron microscopy (FE-SEM), and electrochemical impedance spectroscopy (EIS). The formation of the inorganic component did not introduce any porosity in the final material and both syntheses led to membranes with enhanced thermal stability, reduced water uptake and good proton conductivity ( σ = 5.8 × 10 −2 S cm −1 ) up to 120 °C, thus making the samples suitable for application as polymeric electrolytes at intermediate temperature.

Bilayer electrolytes made of barium cerate covered with a thin film of barium zirconate deposited by pulsed laser deposition show promise for improving chemical stability without greatly affecting electrochemical performance in fuel cell operation.

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The ALTEA project studies the problems related to possible functional damage to the Central Nervous System (CNS) due to particle radiation in space environment. The project is a large international and multi-disciplinary collaboration. The ALTEA instrumentation is an helmet-shaped multi-sensor device that will measure concurrently the dynamics of the functional status of the visual system and the passage of each particle through the brain within a pre-determined energy window. ALTEA is scheduled to fly in the International Space Station in February 2003. One part of the multi-sensor device, one of the advanced silicon telescopes, will be launched in the ISS in early 2002 and serve as test for the final device and as discriminating dosimeter for the particle fluences within the ISS.

Highly performing perovskite-based anodes for methane mixtures-fueled solid oxide fuel cells (SOFC) are proposed. Catalytic activities of La0.6Sr0.4Fe1-xPdxO3-δ (LSFPd) with x = 0.05, 0.1 toward dry reforming of methane (DMR) and partial oxidation of methane (POM) reactions are investigated. The addition of (30wt%) Ce0.85Gd0.15O2-δ (GDC) and of (30wt%) Ni(5wt%)-GDC to the perovskite compounds was evaluated to enhance both electrocatalytic and electrochemical properties. Electrolyte-supported cells based on La0.8Sr0.2Ga0.8Mg0.2O3-δ (LSGM) pellets and LSFPd perovskite oxides at both electrodes are fabricated and tested using CH4, CH4/Ar and CH4/CO2 mixtures in the 750–850°C temperature range. Fuel cell tests using anodic mixtures such as LSFPd/GDC and LSFPd/Ni-GDC are also performed. A discussion based on the comparison between catalytic and electrochemical results and on the possible reforming and/or oxidation reactions taking place at the anode is detailed.

The development of low-melting mixtures is crucial for the diffusion of sustainable and green alternative energy sources, namely, CSP. Ternary mixtures containing sodium, potassium, and calcium are extremely promising as thermal fluids due to their good thermophysical properties, low toxicity and cost. Most literature studies on ternary mQ4ixtures refer to a particular commercial composition and there are few data regarding ternary phase diagrams. Thus, for improving the current understanding on this topic, further theoretical and experimental investigation on ternary mixtures is of utmost interest. An experimental campaign was conducted to study the binary subsystems of the ternary mixtures and develop a regular solution model for simulating the ternary phase diagram. To validate the model, several data were determined using an innovative experimental rheometric method. The results showed that a ternary contribution in the regular solution model is necessary and an empirical expression for this ternary parameter was proposed and validated.

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.

The study and development of multi-component alkaline nitrates systems is of utmost interest to investigate low melting and low cost HTFs and HSMs, to be used in CSP plants. At this aim, several binary and ternary mixtures have been proposed as feasible and promising materials in the scientific literature. In order to evaluate the most feasible HTF and HSM, the simulation campaign proposed in this work was focused on economical and readily available compounds, ruling out rare and costly species. A semi-predictive model, based on the regular solution theory, was employed to draw the ternary phase diagrams of LiNO3/NaNO3/Ca(NO3)2 and LiNO3/KNO3/Ca(NO3)2, from which it was possible to select the lower melting zones and the compositions. The binary sub-systems were the starting point for the employed approach. The results showed a good agreement with literature experimental data, and new low melting compositions were simulated and experimentally validated. It is noteworthy that it was possible to identify in great detail the zones of the two ternaries presenting the lowest freezing points and this can allow the design of interesting and cost-effective low melting mixtures.

Enzymatic hydrolysis of poly(1,4-butylene 2,5-thiophenedicarboxylate) (PBTF) and poly(1,4-butylene 2,5-furandicarboxylate) (PBF) by Humicola insolens (HiC) and Thermobifida cellulosilytica (Cut) cutinases is investigated. For the first time, the different depolymerization mechanisms of PBTF (endo-wise scission) and PBF (exo-wise cleavage) has been unveiled and correlated to the chemical structure of the two polyesters. Keywords: Poly(1,4-butylene 2,5-thiophenedicarboxylate) (PBTF), Poly(1,4-butylene 2,5-furandicarboxylate) (PBF), Enzymatic hydrolysis, Endo/exo chain scission, Cutinases, Polyesters degradation

Dense micrometric La0.8Sr0.2Ga0.8Mg0.2O3-δ (LSGM) films were deposited by spin-coating on porous LSGM scaffolds characterized by homogeneous pore structure. Porous anodes were infiltrated with aqueous nickel and nickel/copper nitrate solutions, dried and fired at 700 °C. Homogeneous metal coating with proper interconnection was observed by SEM, chemical stability confirmed by XRD, and electrical characterization of anodic substrates was performed. Catalytic activity of different anodes was evaluated ex-situ in a quartz micro-reactor fed with CH4:CO2 mixture at range 650 and 700 °C. To investigate the redox properties of the metallic phases, the anodic substrates were subjected to redox ageing cycles and characterized by H2-TPR.

Perovskite solar cells employing CH3NH3PbI3-xClx active layers show power conversion efficiency (PCE) as high as 20% in single cells and 13% in large area modules. However, their operational stability has often been limited due to degradation of the CH3NH3PbI3-xClx active layer. Here, we report a perovskite solar module (PSM, best and av. PCE 10.5 and 8.1%), employing solution-grown TiO2 nanorods (NRs) as the electron transport layer, which showed an increase in performance (∼5%) even after shelf-life investigation for 2500 h. A crucial issue on the module fabrication was the patterning of the TiO2 NRs, which was solved by interfacial engineering during the growth process and using an optimized laser pulse for patterning. A shelf-life comparison with PSMs built on TiO2 nanoparticles (NPs, best and av. PCE 7.9 and 5.5%) of similar thickness and on a compact TiO2 layer (CL, best and av. PCE 5.8 and 4.9%) shows, in contrast to that observed for NR PSMs, that PCE in NPs and CL PSMs dropped by ∼50 and ∼90%, respectively. This is due to the fact that the CH3NH3PbI3-xClx active layer shows superior phase stability when incorporated in devices with TiO2 NR scaffolds. (Figure Presented).