Serena Gagliardi

Hard carbons (HCs) are promising sodium-ion battery anodes but suffer capacity loss at high rates due to tortuous Na⁺ pathways. Here, a zeolite-templated carbon (ZTC) was introduced as a conductive, mesoporous additive (10 wt%) to a hazelnut-derived hard carbon (HEZ) to improve Na⁺ transport and rate performance. Structural and porosity analyses show complementary architectures: a microporous HEZ and a highly ordered ZTC with interconnected mesopores. Electrodes containing ZTC exhibit increased apparent ionic diffusion coefficients (from ~3.5 · 10⁻¹⁰ to ~16 · 10⁻¹⁰ cm²·s⁻¹ Cathodic) and enhanced rate capability. Galvanostatic intermittent titration technique (GITT) analysis indicates accelerated Na⁺ transport in the low-voltage plateau region, and galvanostatic cycling demonstrates a sustained plateau capacity of ~100 mAh·g⁻¹ for the ZTC-containing electrode after 50 cycles at 50 mA·g⁻¹ (vs. ~30 mAh·g⁻¹ for pristine HC). Although the ZTC increases the electrode surface area and lowers initial Coulombic efficiency, the addition markedly improves high-rate storage and capacity retention. These results demonstrate that a minor fraction of templated mesoporous carbon can effectively alleviate kinetic limitations in bio-derived HC anodes for sodium-ion batteries.

A comprehensive methodology is proposed for the quantitative analysis of microporosity in HC for SIBs anodes. SAXS coupled with the Ruland–Smarsly approach enables the detection of closed pores and accurate estimation of surface area and pore‐size distribution beyond BET limitations. Two representative materials, a petroleum‐based and a biowaste‐derived HC, were compared to correlate nanostructural features with electrochemical behavior. Complementary XRD, Raman spectroscopy, and SEM support the SAXS interpretation by revealing differences in crystallinity and morphology. The results show that sustainable biowaste‐derived carbons achieve performance comparable to commercial ones. This SAXS‐based framework provides a reproducible route to probe nanoscale disorder in carbon anodes and guides the rational design of efficient and low‐impact materials for next‐generation SIBs.

The vibrational properties of the chiral sulfoxide methyl-p-tolyl-sulfoxide (Metoso) were investigated by infrared and Raman spectroscopy in the solid, liquid and aqueous solution phases, for both the enantiopure compounds and their racemic mixture. Experimental data were complemented by DFT calculations on the isolated enantiomer and on the two RR and RS dimeric conformers to support spectral interpretation and mode assignment. The IR and Raman spectra of the crystalline enantiomer and racemic mixture are similar, indicating comparable molecular organization and intermolecular interactions in the solid state. Upon melting, band broadening and frequency shifts are observed, consistent with molecular disorder and the breaking of weak intramolecular interactions, accompanied by changes in the S-O, S-CH₃ and C-H stretching frequencies. In aqueous solution, further broadening and opposite shifts in these bands reflect the formation of Metoso-H₂O complexes through hydrogen bonds. Theoretical spectra reproduce the observed trends and confirm that either solvent or phase transitions control the balance between intra- and intermolecular interactions thus influencing the vibrational degrees of freedom of the model chiral sulfoxide.

The vibrational properties of the chiral sulfoxide methyl-p-tolyl-sulfoxide (Metoso) were investigated by infrared and Raman spectroscopy in the solid, liquid and aqueous solution phases, for both the enantiopure compounds and their racemic mixture. Experimental data were complemented by DFT calculations on the isolated enantiomer and on the two RR and RS dimeric conformers to support spectral interpretation and mode assignment. The IR and Raman spectra of the crystalline enantiomer and racemic mixture are similar, indicating comparable molecular organization and intermolecular interactions in the solid state. Upon melting, band broadening and frequency shifts are observed, consistent with molecular disorder and the breaking of weak intramolecular interactions, accompanied by changes in the S–O and S–CH₃ and C-H stretching frequencies. In aqueous solution, further broadening and opposite shifts of these bands reflect the formation of Metoso–H₂O complexes through hydrogen bonds. Theoretical spectra reproduce the observed trends and confirm that either solvent or phase transitions control the balance between intra- and intermolecular interactions thus influencing the vibrational degrees of freedom of the model chiral sulfoxide.

The coffee cherry processing produces various waste products, such as coffee husks, which are a valuable source of pectin and phenolic acids that can be used as high-value biomolecules in human and animal food, cosmetics, and pharmaceutical production chains. This study aims to optimize the eco-friendly extraction of polysaccharides, as pectin, and phenolic compounds from coffee peel using response surface methodology (RSM). This model was used to evaluate the extraction variables (temperature, time, pH, ionic strength, ultrasonic frequency, particle size, and solid/liquid ratio in water) to identify the critical factors. All responses were fitted to the RSM model, which revealed high estimation capabilities. Ionic strength and temperature were found to be critical process variables for pectin extraction, while the main factors responsible for phenolic extraction were ultrasonic frequency, pH, and solid/liquid ratio. Therefore, the operating conditions to optimize the extraction of both pectin and phenolic compounds were 80 °C, ultrasonic frequency 60 kHz, solid/liquid ratio 1:20, using pH 2 or 12 in the case of pectin or polyphenols, respectively. Direct Analysis in Real Time Mass Spectrometry (DART-MS) and Fourier-Transform Infrared Spectroscopy–Attenuated Total Reflectance (FTIR-ATR) analyses were performed to evaluate the chemical profile of the extracts and pectin. The recycling of coffee husk waste into bioproducts in view of the circular economy contributes to minimizing the impact on the environment and to generating additional income for coffee growers.

Femtosecond coherent Raman techniques have significant diagnostic value for the sensitive and non-intrusive measurement of temperature, pressure, and composition of gas mixtures. Due to the low density of samples, however, such measurements make use of high-energy amplified laser sources, with unwieldy and costly experimental setups. In this paper, we demonstrate an experimental setup equipped with a low-energy and low-average-power femtosecond oscillator allowing measurement of the pure-rotational spectrum of nitrogen down to atmospheric pressure using impulsive stimulated Raman scattering. Using a simplified model to analyze the experimental data we were able to derive the gas temperature with reasonable accuracy.

Nanostructured titania is one of the most commonly encountered constituents of nanotechnology devices for use in energy-related applications, due to its intrinsic functional properties as a semiconductor and to other favorable characteristics such as ease of production, low toxicity and chemical stability, among others. Notwithstanding this diffusion, the quest for improved understanding of the physical and chemical mechanisms governing the material properties and thus its performance in devices is still active, as testified by the large number of dedicated papers that continue to be published. In this framework, we consider and analyze here the effects of the material morphology and structure in determining the energy transport phenomena as cross-cutting properties in some of the most important nanophase titania applications in the energy field, namely photovoltaic conversion, hydrogen generation by photoelectrochemical water splitting and thermal management by nanofluids. For these applications, charge transport, light transport (or propagation) and thermal transport are limiting factors for the attainable performances, whose dependence on the material structural properties is reviewed here on its own. This work aims to fill the gap existing among the many studies dealing with the separate applications in the hope of stimulating novel cross-fertilization approaches in this research field.

Impulsive stimulated Raman scattering (ISRS) is a nonlinear pump–probe spectroscopy technique particularly suitable to study vibrational intermolecular and intramolecular modes in complex systems. For the latter, recent studies of ISRS microscopy with low-energy laser sources have attracted attention for investigation of photosensitive or biological samples. Following this stream of interest, in this paper, we report an investigation on the relationship between femtosecond ISRS data and pump–probe Z-scan measurements, showing that the latter technique is capable of capturing the Kerr nonlinearities induced by the molecular vibrational modes. To this aim, firstly, spectrally filtered and Raman-induced Kerr ISRS signals were simultaneously acquired to determine the sample nonlinear response and to establish the reference data for the Z-scan analysis. Then, by adopting a suitable experimental arrangement to avoid thermo-optical effects, we were able to unambiguously observe the Raman-induced effects in Z-scan measurements, thus obtaining a consistent picture between ISRS and Z-scan for the first time, to the best of our knowledge. Practical applications of the proposed method include calibrated measurements of the contribution of the internal (Raman) and external molecular modes to the nonlinear refractive index.

The need for compatible materials for the preservation of cultural heritage has resulted in the revival of lime-based mortar technology and other applications. This work investigates the cohesion and integrity of lime mortars added with fresh mucilage extracted from five plants and evaluates their bioreceptivity for long-term durability. Specimens of lime mortars added with 2.5% of fresh mucilage extracted from Aloe vera, Cylindropuntia californica, Opuntia engelmannii, Opuntia ficus-indica and Salvia hispanica mucilages were analyzed for color change (colorimetry), cohesion (ultrasound measurements), integrity (X-rays) and bioreceptivity (microbiological tests).The internal structure of the specimens added with Cacti mucilages shows better compactness, and no color change was noticed in the bio-mortars also after aging. The bioreceptivity response of mortars inoculated with bacteria, fungi and a photosynthetic biofilm was quite different. Specimens added with Aloe and Cylindropuntia mucilages showed a higher extent of bioreceptivity than the control; the specimens of bio-mortars added with Opuntia engelmannii, Opuntia ficus-indica and Salvia hispanica mucilages did not appear, up to threemonths after the contamination, any microbial growth. These results indicate that the addition of mucilage improves the mortar qualities, but the choice of the plant mucilage must be carefully evaluated since it can be responsible for changes in the bioreceptivity of the mortar.

Addiction of ceramic nanoparticles to acrylic polymers provides a simple and effective means to produce paints with important properties, such as mechanical resistance and tailored wettability, even though for optimal performances, an engineered nanoparticle distribution would be desirable. In this paper we report on the realization and on the morphological and functional characterization of nanocomposites where the nanophase is distributed on the surface of acrylic polymer films, in order to enhance the expression of surface-related properties. To this aim, commercial titanium oxide and silicon oxide nanopowders were dispersed in water and the suspensions were air-sprayed on polymeric films prepared by paint brushing, thus producing a nanostructured ceramic surface coating. Control of the pH of suspensions and acrylic acid functionalization of the surface of titania were used together with high power ultrasonic treatments in order to control dimension of the aggregates in the sprayed suspensions. Optical microscopy, mechanical profilometry, and atomic force microscopy were used to characterize the nanocomposite surface morphology and correlate it to the coating functional properties, evaluated through mechanical abrasion tests and contact angle measurements; also, colorimetry on coated stones was performed in order to test the impact of the coatings on the aesthetical appearance and their photostability under UV irradiation. Results show that the nanostructured ceramic layer slightly improves the resistance of coatings to mechanical abrasion in case of polymer films prepared from latexes. The nanocomposite surface layer does not affect the wettability of the polymer, which remained slightly hydrophilic; this behavior is likely due to inadequate distribution of the nanophase. On the other hand UV-induced superhydrophilicity was observed when the concentration of surface titania nanoparticles is about 0.6 mg/cm². Colorimetric analysis on historical and Carrara marbles before and after coating evidenced the good transparency of the nanocomposites. Accelerated aging tests permitted to demonstrate that, on the historical marbles, the presence of the nanoparticles has a protective action against UV-induced damage of the underlying polymer film, preventing photodegradation.