Publications

Lithium-ion batteries (LIBs) are fundamental to modern technology, powering everything from portable electronics to electric vehicles and large-scale energy storage systems. As their use expands across various industries, ensuring the reliability and safety of these batteries becomes paramount. This review explores the multifaceted aspects of LIB reliability, highlighting recent advancements and ongoing challenges. The importance of safety has been underscored by numerous incidents, such as the well-known smartphone battery explosions and more than 10,000 fires a year at facilities throughout Australia, both linked to LIB failures. These events emphasize the need for robust reliability and safety measures to ensure consistent performance and longevity. Factors like battery chemistry, design, manufacturing, and operating conditions can all influence the reliability of LIBs. Despite their widespread use, the mechanisms of failure, failure rates, and consequences of LIB failures are still not well understood, raising significant safety concerns. Current reliability assessment techniques include experimental methods, computational models, and data-driven approaches. Emerging trends, such as advanced characterization techniques and standardized testing protocols, advocate for improved practices to enhance the reliability and safety of LIBs across all applications.

Hydroxyapatite (HAp), resembling human bone tissue, is a promising biomaterial for dental and hip prosthetics. Incorporating fluorine ions enhances HAp properties, particularly in dental restoration. This new study examines the physicochemical and biological properties of fluorine substituted hydroxyapatite (FHAp) coatings. Structural and morphological properties of the coatings were investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM) and atomic force microscopy (AFM). The elemental composition of the FHAp coatings was studied using energy-dispersive X-ray spectroscopy (EDS) and X-ray photoelectron spectroscopy. Fourier Transform Infrared spectroscopy (FTIR) investigations were also conducted. The typical peaks identified in XRD patterns of the FHAp were associated with pure hydroxyapatite with hexagonal structure. The general XPS spectrum of FHAp coatings shows peaks corresponding to the constituent elements of stoichiometric HAp as well as the presence of F that was used as a substituent. Consequently, the FTIR studies results underlined the presence of hydroxyapatite in the FHAp coatings. The SEM images reveal the presence of a uniform and continuous layer of particle conglomerates evenly distributed across the FHAp surface. Valuable information about the FHAp coating's wettability, adhesion and coating thickness were also obtained. Also, the AFM images suggest the absence of the significant irregularities from the surface of the FHAp coatings. Investigations of FHAp coatings reveal promising outcomes for cell viability and proliferation. Detailed analysis of FHAp's 3D surface characteristics and roughness, following ISO 25178-2:2012 standards, highlights their favorable biocompatibility, supporting MG63 cell proliferation. The surface roughness parameters of FHAp coatings were found to vary, with Sa values spanning from 0.029 +/- 0.004 mu m to 0.778 +/- 0.007 mu m, while Sq ranged from 0.035 +/- 0.005 mu m to 0.907 +/- 0.011 mu m. Furthermore, FHAp exhibits skewness (Ssk) from -0.048 +/- 0.006 to 0.195 +/- 0.009, kurtosis (Sku) from -0.600 +/- 0.011 to -1.050 +/- 0.021, and fractal dimension from 2.14 +/- 0.01 to 2.19 +/- 0.01, indicating consistent surface complexity and favorable properties. The Minkowski Functionals mirror the morphological observations from AFM images, emphasizing their dynamic influence on the samples' surfaces.

Ruthenium-based catalysts were prepared through a deposition-precipitation approach, taking beta zeolites with Si/Al ratios of 12.5, 18.5, and 150, respectively, as supports, and 1-3 wt% loadings of metal. Their activation was performed in the presence of either H2 or NaBH4. The dispersion of the Ru species and the acid-base properties were influenced by both the preparation method and the activation protocol. The catalysts reduced under H2 flow presented well-dispersed Ru(0) and RuOx nanoparticles, while the reduction with NaBH4 led to larger RuOx crystallites and highly dispersed Ru(0). These characteristics exerted an important role in the hydrogenation of levulinic acid (LA) to gamma-valerolactone (GVL). The H2 dissociation occurred via a heterolytic mechanism involving Lewis acid-base pairs associated with RuOx and the framework oxygen (Si-O-Al) located near the zeolite pore edge. The Ru(0) nanoparticles activated the -C=O bond of the LA substrate, while the presence of the carrier zeolite Br & oslash;nsted acid sites promoted the ring-closure esterification of the 4-hydroxyvaleric acid (4-HVA) intermediate to GVL. An optimal combination of these features was achieved for the catalyst with 3 wt% Ru and a Si/Al ratio of 150, which selectively converted LA (XLA = 96.5%) to GVL (SGVL = 97.8%) at 130 degrees C and 10 bars of H2.

In this work, three methods for the synthesis of composites based on poly(ortho-toluidine) (POT) and WS2 are reported: (a) the solid-state interaction (SSI) of POT with WS2 nanoparticles (NPs); (b) the in situ chemical polymerization (ICP) of ortho-toluidine (OT); and (c) the electrochemical polymerization (ECP) of OT. The preparation of WS2 sheets was performed by the ball milling of the WS2 NPs followed by ultrasonication in the solvent N,N'-dimethyl formamide. During the synthesis of the POT/WS2 composites by SSI and ICP, an additional exfoliation of the WS2 NPs was reported. In this work, we demonstrated the following: (a) the ICP method leads to POT/WS2 composites, which contain repeating units of POT in the leucoemeraldine salt (LS) state, while (b) the ECP method leads to POT/WS2 composites, which contain repeating units of POT in the emeraldine salt (ES) state. Capacitances equal to 123.5, 465.76, and 751.6 mF cm-2 in the cases of POT-ES/WS2 composites, synthesized by SSI, ICP, and ECP, respectively, were reported.

This study examined the gradual replacement of Ca2+ with a small amount of Mg2+ ions (0-1 wt%) in selected calcium phosphates commonly used in regenerative medicine: hydroxyapatite Ca10(PO4)6(OH)2, brushite CaHPO4 center dot 2H2O, and (3-tricalcium phosphate ((3TCP) Ca3(PO4)2. These compounds were obtained using precipitation reactions from aqueous solutions, followed by appropriate thermal treatment (drying or furnace heating). The microstructure and physicochemical properties of the materials were thoroughly analysed using powder X-ray diffraction (PXRD), scanning and transmission electron microscopy (SEM and TEM), and mid-infrared spectroscopy (FT-IR). Additionally, the release of Mg2+ ions from the selected materials was investigated, and a preliminary in vitro toxicity assessment was performed. The results showed that the introduction of magnesium ions up to 1 wt% was achieved with relatively high efficiency (63-82 % for brushite, 77-97 % for hydroxyapatite, and 88-100 % for (3-tricalcium phosphate). The entire series of hydroxyapatites was phase-homogeneous, but monetite was observed as an additional phase in the case of brushite samples. In contrast, several (3TCP samples were contaminated with a small amount of calcium oxide and hydroxide. The incorporation of Mg2+ ions significantly impacted the unit cell parameters of each type of calcium phosphate and the ultrastructure of the obtained powders. With an increase in the amount of introduced magnesium, the resulting crystals became smaller and showed a greater tendency to form aggregates. The obtained results indicate that it is possible to obtain calcium phosphate materials containing Mg2+ ions with a gradual release of ions. The fastest ions release occurred from the brushite sample, while the slowest was from the apatitic powder, which is in great accordance with the solubility of the materials. All samples, except for Mg0.5-Bru, were non-cytotoxic.

The purpose of this work is to obtain different kinds of advanced nanostructures with four materials of interest: carbon, titanium, aluminum and silicon, deposited by Thermionic Vacuum Arc (TVA) technology on the Si substrate, in two cases: C/Ti/C/Al/C/Si multilayer film and C+Ti/C+Al/C+Si composite film with inclusion of nitrogen. Also, for each type of samples some parameters varied: substrates temperature (Room Temperature, 200 degrees C, 300 degrees C, 400 degrees C) and the bias voltage applied on the substrates, i.e. - 400 V. Thermal Desorption Spectroscopy (TDS) analyses revealed the presence of nitrogen in all cases. The Raman spectra reveal that the film nitrogen treatments leads to the formation of nitrides for each compound. The infrared absorption spectra are dominated by the formation of C-N bonds, which are the same as in the Raman spectra. EDX and Elemental composition show the values of atomic percentage depending on the substrate deposition temperature. TEM and XPS depth profiles are studied. Based on nanoindentation studies, the Young modulus and hardness are measured. The tribology measurements are also performed.

The present study aims to develop and investigate the biological response of a bone substitute based on electrospun polyvinylidene fluoride (PVDF) fibres, which are either embedded or coated with a silicate bioglass belonging to SiO2-P2O5-CaO-Na2O oxide system. This bioglass is substituted with antibacterial agents, silver (Ag) and cerium (Ce), while deposition methods utilized include pulsed laser deposition (PLD) and matrixassisted pulsed laser evaporation (MAPLE). The results showed the inhomogeneous distribution of the glassy particulate phase in the polymer fibres when using electrospinning as single processing technique. In contrast, the materials achieved by combining the electrospinning with laser ablation displayed a continuous coating of glass at the polymer fibres surface. The thickness and roughness of this layer can be easily tuned as a function of deposition conditions, as it was demonstrated when changing the dispersion medium or working pressure. Good results were obtained for all coated PVDF fibres, but especially in the case of PLD processing with a thicker layer of silicate glass, the imaging evaluation suggested a superior beneficial impact on cellular metabolism. Such scaffolds, with controlled porosity, engineered surface and potential piezoelectric properties represent important candidates for the field of personalized bone substitutes.

This work investigates the gelation behavior and phase stability of E7 liquid crystals using a series of mesogenic benzoylthiourea (BTU) gelators with different alkyl chain lengths (6, 10, 12) at concentrations as low as 2.5 wt.%. Polarized optical microscopy (POM) and differential scanning calorimetry (DSC) confirm that the BTU gelators effectively stabilize the E7/gel composites through hydrogen bonding and pi-pi interactions. DSC studies reveal a concentration-dependent shift in transition temperatures, with evidence of distinct LC-isotropic and isotropic-gel transitions. Rheological and dielectric studies further demonstrate a reversible gel-sol transition and enhanced dipolar relaxation times (37.7 ns), indicating strong interactions between E7 and the BTU network.

In this contribution, we review the recent results from the INDRA and FAZIA Collaborations. It will cover the results from INDRA-VAMOS experiments at GANIL, the first two INDRA-FAZIA campaigns at GANIL and FAZIA experiments at LNS Catania. Recent detector upgrades and developpements will also be discussed. Those results are better explained and more detailed in the following report presentations of this issue and just a brief overview will be mentionned here, with mostly the main conclusions addressed.

The present study is focused on describing the influence of the sintering method (fast field-assisted Spark Plasma Sintering vs. conventional sintering) on the functional properties of BaTi0.90Hf0.10O3 ceramics with polymorph superposition around room temperature. Dense ceramics, derived from nanopowders synthesized via Pechini method, with grain size downscaled from 3.7 to 0.07 mu m were prepared using different sintering strategies. XRD data at room temperature revealed the presence of mixtures of dissimilar structural modifications either for the starting nanopowder, as well as for the related ceramics. The Landau-based calculations indicated that different amounts of polymorphs are stable in these ceramics, by considering the grain size reduction and the strain-stress fields produced by the fast sintering method, thus confirming the experimental results of the structural and Raman analyses. By decreasing the average grain size from micro-to nanoscale, a slight decrease of the Curie temperature, accompanied by the increase of the diffuseness of the ferroelectric-to-paraelectric phase transition and the decrease of both the permittivity maxima and the dielectric losses was detected. Both the dielectric response and the ferroelectric P(E) loops indicated a ferroelectric-relaxor crossover as the grain size decreased in the nanometre range. The beneficial effect of the nanostructuring on the energy storage efficiency was also revealed.