Due to their attractive properties, such as high energy and power density, Lithium-ion batteries are currently the most suitable energy storage system for powering portable electronic equipment, electric vehicles, etc. However, they are still affected by safety and stability problems that need to be solved to allow a wider range of applications, especially for critical areas such as power networks and aeronautics. In this paper, the issue of overdischarge abuse has been addressed on Lithium-ion cells with different anode materials: a graphite-based anode and a Lithium Titanate Oxide (LTO)-based anode model. Tests were carried out at different depths of discharge (DOD%) in order to determine the effect of DOD% on cell performance and the critical conditions that often make the cell fail irreversibly. Tests on graphite anode cells have shown that at DOD% higher than 110% the cell is damaged irreversibly; while at DOD% lower than 110% electrolyte deposits form on the anodic surface and structural damage affects the cathode during cycling after the overdischarge. Furthermore, at any DOD%, copper deposits are found on the anode. In contrast with the graphite anode, it was always possible to recharge the LTO-based anode cells and restore their operation, though in the case of DOD% of 140% a drastic reduction in the recovered capacity was observed. In no case was there any venting of the cell, or any explosive event.

Activated hard carbons, obtained from the pyrolysis of various waste biomasses, were prepared and characterized for use as the active material for the fabrication of battery electrodes. The preparation consisted of a pyrolysis process, followed by an activation with KOH and a further high-temperature thermal process. TG and DTA were used to discriminate the steps of the activation process, while SEM, XRD, and Raman characterization were employed to evaluate the effects of activation. The activated carbons were tested as electrodes in lithium-sulfur and lithium-ion batteries. The carbonaceous materials coming from cherry stones and walnut shells have proved to be particularly suitable as electrode components. When used as anodes in lithium-ion batteries, both carbons exhibited a high first cycle discharge capacity, which was not restored during the next charge. After the first two cycles, in which there was a marked loss of capacity, both electrodes showed good reversibility. When used as cathodes in lithium-sulfur batteries, both carbons exhibited good catalytic activity against the redox reaction involving sulfur species with good cycle stability and satisfactory Coulombic efficiency.

Cycling high temperature CO₂ capture using CaO–based solid sorbents, known as the calcium looping (CaL) process, is gaining considerable scientific and industrial interest due to the high theoretical sorbent capacity (0.78 gCO₂/gCaO), the low specific cost, and the negligible environmental impact of the employed materials. In this work, we investigated the self–combustion synthesis of CaO–CaZrO₃ sorbents with different CaO contents (40, 60, and 80 wt%) for use in the CaL process. CaZrO₃ was used as a spacer to avoid CaO grains sintering at high temperature and to reduce the diffusional resistances of CO₂ migrating towards the inner grains of the synthetic sorbent. Samples were characterized by X–ray diffraction (XRD), Brunauer–Emmett–Teller (BET), and scanning electron microscopy (SEM) analyses. The reaction between CO₂ and CaO (i.e., carbonation) was carried out in 20 vol% CO₂ at 650 °C and calcination (i.e., decomposition of CaCO₃ to CaO and CO₂) at 900 °C in pure Ar or with 85 vol% CO₂ using a thermogravimetric analyzer (thermogravimetric/differential thermal analysis (TG–DTA)). The most stable sorbent was with 40 wt% of CaO showing a CO₂ uptake of up to 0.31 g CO₂/g_sorbent and 0.26 g CO₂/g_sorbent operating under mild and severe conditions, respectively. The experimental data corroborated the prediction of the shrinking core spherical model in the first phase of the carbonation. A maximum reaction rate of 0.12–0.13 min⁻¹ was evaluated in the first cycle under mild and severe conditions of regeneration.

A study was conducted to explore the effects of Sr doping on the electrical properties of perovskite LaFeO₃ thin-film protective conversion coatings grown onto a K41 ferritic stainless steel, a typical interconnect material for intermediate temperature solid oxide cell (SOC) applications. The Sr-doped coatings were prepared in La₂O₃- and SrO-containing molten carbonate baths with minor added amounts of nitrate salt for accelerated coating formation. For comparison purposes, undoped coatings were obtained using the same carbonate bath, with the only difference being that SrO was replaced by inert MgO. SEM/EDX and XRD analyses were used for coating characterization and confirmed the effective incorporation of Sr but not of Mg into the LaFeO₃ layer. Although both the Sr-doped and undoped coatings consisted of a LaFeO₃ layer grown above an inner Fe-Cr spinel, the coating thickness of the Sr-doped coating was distinctly higher, approximately 2 µm, which is twice that of the undoped coating. Electrical measurements in terms of Area-Specific Resistance (ASR) were conducted at 700 °C in air and showed that Sr-doping significantly improved the electrical conductivity of the coated K41 steel. Due to the Sr-doping, the ASR values of the coated steel dropped from 60 to 37 mΩ cm² after 300 h of exposure, in spite of the higher Sr-doped coating thickness. The study concludes that Sr-doped thin-film perovskite coatings appear to be a promising solution for improved SOCs steel interconnect stability at intermediate temperatures.