Publications

In this study, we developed a ternary nanocomposite using graphene oxide (GO), multiwalled carbon nanotubes (MWCNTs), and tungsten trioxide (WO3), nanostructures, synthesized via a straightforward chemical process with ultrasound assistance. The initial composition was GO/MWCNT, later combined with WO3 to form the GO/ MWCNT: WO3 (25/25:50) structure. Characterization was performed using X-ray diffraction, which revealed the multiphase nature of the WO3 nanostructures. Scanning Electron Microscopy showed the one-dimensional CNTs interwoven with graphene oxide sheets decorated with densely populated WO3 nanopetals. Fourier transform infrared and Raman spectroscopy confirmed the chemical composition of the system. The photocatalytic degradation of Rhodamine-B in water under visible light irradiation was significantly enhanced using the GO/

Ag8SnS6 (ATS) nanoparticles, with a band gap of 1.35 eV, which is located exactly at the Schockley-Queisser optimal value for a single-junction solar cell, were utilized as a photoabsorber component in solid state photovoltaic devices. The as-made particles were capped with long aliphatic chains of oleic acid and oleylamine. After surface functionalization of the shorter and extremely basic formamidinium cations, an increase of the absorption coefficient throughout the visible spectrum range was observed. The ligand exchange led also to a slight increase of the band gap, by a value of 0.05 eV. XRD, XPS, UPS, diffuse reflectance, TEM and EDX characterization studies revealed the structure of the nanoparticles and finally proof-of-concept thin film solar cells were fabricated. A maximum photoconversion efficiency of 0.22% was achieved for the as-made particles.

The present paper evidences the beneficial effect that the combination of Pt with WO3 and silicotungstic acid (STA) brings to the methanol oxidation electroactivity. To avoid substrate interferences boron doped diamond (BDD) was used as the electrocatalysts support. SEM measurements have shown that the use of a STA/WO3/BDD substrate allows the electrodeposition of smaller Pt clusters, exhibiting better dispersion, higher homogeneity in terms of size and enhanced electrochemically active surface area. Cyclic voltammetry, polarization and EIS experiments demonstrated than STA addition on the WO3/BDD support induces to the deposited Pt higher activity and improved resistance to fouling during methanol anodic oxidation. Based on the XPS results such behavior was tentatively ascribed to the higher surface concentration of Pt(OH)2 species and adsorbed water that STA presence enables, which may assist in the oxidative desorption of reaction intermediates.

We investigate the second-order Floquet topological (SOFT) phase transitions, from the perspective of spatial symmetries. In this respect, we consider a generic honeycomb lattice Floquet topological insulator (FTI), realized by circularly polarized light irradiation, in the presence of spin-orbit coupling (Kane-Mele model). We find that our studied FTI presents chiral symmetry on a preferential direction in Fourier space, the same property that protects the topological phases in the Su-Schrieffer-Heeger (SSH) model. Thus we were allowed to characterize the SOFT phases in terms of mirror-graded winding numbers (Zak phase). Moreover, our model exhibits C2 and C3 symmetry in Fourier space, a property which lead us to investigate two finite structures having the aforementioned symmetries, namely, rhombic and triangular shapes. Indeed, we find that both of them undergo SOFT phase transitions, characterized by the appearance of 0D corner states symmetrically localized over the whole sheet. Finally, we investigate the C2 and C3 symmetry breaking. Interestingly, we reveal that the corner states are not destroyed, but localize at preferential corners instead, giving rise to a corner polarization.

Developing new glass electrolytes with the necessary room-temperature ionic conductivity (similar to 10(-3) Scm(-1)) for solid-state batteries, especially sodium-ion (Na+) batteries, has been impeded by the lack of a clear relationship between composition, structure, and conductivity in glass materials. This study highlights the impact of the mixed glass formers on the structure, Na+-ion dynamics, and glass conductivity. To this end, we substituted SiO2 for P2O5 in sodium alumino-phosphate glass while maintaining a constant molar concentration of Al2O3 and Na2O. A detailed analysis combining molecular simulations and experiments revealed that the glass containing 15 mol% SiO2 exhibited the highest DC ionic conductivity of similar to 9 x 10(-6) Scm(-1) at 473 K, followed by a decrease for 20 mol% SiO2. To understand this behavior, microscopic characteristic length such as critical hopping distance and Na+ diffusion coefficients were correlated with structural changes using AC conductivity analysis. Altogether, we elucidate the composition-dependent Na+ ion dynamics in the alumino-phosphate glass system, with factors like mobile charge carrier concentration, ion mobility, and coulombic forces influenced by the structure of different glass compositions.

Chalcogenide glasses (ChGs) are a class of amorphous materials presenting remarkable mechanical, optical, and electrical properties, making them promising candidates for advanced photonic and optoelectronic applications. With the increasing integration of artificial intelligence in modern materials design, we are able to systematically select, prepare, and optimize appropriate compositions for desired applications in a manner that was unachievable before. This study employs various machine learning models to reliably predict the refractive index at 20 degrees C using a small dataset of 541 samples extracted from the SciGlass database. The input for the algorithms consists of a selected set of physico-chemical features computed for the chemical composition of each entry. Additionally, these algorithms served as inner models for an ensemble logistic regression estimator that achieved a superior R2 value of 0.8985. SHAP feature analysis of the second-best model, CatBoostRegressor (R2 = 0.8920), revealed the importance of elemental density, atomic weight, ground state atomic gap, and fraction of p valence electrons in tuning the value of the refractive index of a chalcogenide compound.

The catalytic hydrodeoxygenation (HDO) of lignocellulose-derived pyrolysis oil is a critical process for producing high-quality biofuels. This study investigates the effect of the Mg/Al molar ratio on the catalytic performance of CuMg(Al)O mixed oxide catalysts in the HDO reaction of benzyl alcohol as a model oxygenated compound. They were synthesized by coprecipitation with a fixed Cu content of 15 at. %, with respect to cations, and different Mg/Al molar ratios (0/1, 1/1, 3/1, 5/1, and 1/0). The catalysts were characterized using X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDX), X-ray photoelectron spectroscopy (XPS), diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS), UV-vis spectroscopy, nitrogen adsorption-desorption isotherms, temperature-programmed reduction with hydrogen (H2-TPR), and temperature-programmed desorption (TPD) of CO2 and NH3. It has been shown that the Mg/Al molar ratio strongly influences the physicochemical characteristics of the CuMg(Al)O mixed oxides and, hence, their catalytic performance. Catalytic tests were conducted in a stainless-steel autoclave reactor and the obtained results indicated that the systems with Mg/Al molar ratios of 3/1 and 5/1, issued from layered double hydroxide precursors, exhibited the highest activity, with yields to toluene higher than 85%. This superior performance is attributed to the well-dispersed copper species on the catalyst surface combined with appropriate acid-base properties. As the CuMg(Al)O system with Mg/Al molar ratio of 5/1 was the best in terms of benzyl alcohol conversion, i.e., ca. 98% at 230 degrees C, under 5 atm of H2, for 3 h of reaction time, with high selectivity to toluene of ca. 87%, the influence of the reaction time, temperature and reusability over multiple reaction cycles on its performance were investigated.

The search for advanced materials has been growing, and high entropy alloys (HEAs) are emerging as promising candidates for application in the fusion domain. This work investigates the effect of Cr on the FeTaTiW medium entropy alloy to form (CrFeTaTi)70W30 high entropy alloy, comparing the experimental production and characterization with the simulation (molecular dynamics and hybrid molecular dynamics-Monte Carlo) of the phases formed. The alloys were produced by mechanical alloying and sintered by spark plasma sintering. Both simulations have shown that a body-centered cubic structure is formed for both compositions. Monte Carlo simulation provides a more precise prediction of microstructural formation and element segregation. Microstructural examination of the consolidated material revealed the presence of a W-rich phase and a Ti-rich phase, consistent with the phase separation observed in the MC simulations. Moreover, X-ray diffraction analysis of the milled powder for FeTaTiW and (CrFeTaTi)70W30 confirmed the formation of a bcc (body-centered cubic)-type structure with a low fraction of intermetallic phases. Mechanical testing showed ductile behavior at 1000 degrees C where (CrFeTaTi)70W30 showed a stress magnitude almost double that of FeTaTiW. Additionally, the thermal diffusivity between 20 and 1000 degrees C of both alloys increases as the temperature rises. (CrFeTaTi)70W30 exhibits an increase from 3 to 5 mm2/s, while FeTaTiW increases from 4 to 9 mm2/s. Still, both system's thermal diffusivity values are lower than those of CuCrZr and pure tungsten. Despite this, the study underscores the promising attributes of HEAs and highlights areas for further optimization to enhance its suitability for extreme conditions.

The gas sensitivity of field-effect structures with 2D-MoS2 channels selectively grown between Mo electrodes using the Mo-CVD method was investigated by measuring the effect of molecular adsorption from air on the device source-drain current (Isd). The channels were composed of interconnected atomically thin MoS2 grains, with their density and average thickness varied by choosing two different distances (15 and 20 mu m) between the Mo contacts. A high response to the tested stimuli, including molecule adsorption, illumination and gate voltage changes, was observed. A significant, persistent photoconduction was induced by positive charge accumulation on traps, most likely at grain boundaries and associated defects. Isd increased under high vacuum, both in the dark and under illumination. The relative dark current response to the transition from air to high vacuum reached up to 1000% at the turn-on voltage. When monitored during the gradual change in air pressure, Isd exhibited a non-monotonic function, sharply peaking at about 10-2 mbar, suggesting molecular adsorption on different defect sites and orientations of adsorbed H2O molecules, which were capable of inducing electron accumulation or depletion. Despite the screening of disorder by extra electrons, the #20 mu m sample remained more sensitive to air molecules on its surface. The high vacuum state was also investigated by annealing devices at temperatures up to 340 K in high vacuum, followed by measurements down to 100 K. This revealed thermally stimulated currents and activation energies of trapping electronic states assigned to sulfur vacancies (230 meV) and other shallow levels (85-120 meV), possibly due to natural impurities, grain boundaries or disorder defects. The results demonstrate the high sensitivity of these devices to molecular adsorption, making the technology promising for the easy fabrication of chemical sensors.

The transition from planar to three-dimensional (3D) magnetic nanostructures represents a significant advancement in both fundamental research and practical applications, offering vast potential for next-generation technologies like ultrahigh-density storage, memory, logic, and neuromorphic computing. Despite being a relatively new field, the emergence of 3D nanomagnetism presents numerous opportunities for innovation, prompting the creation of a comprehensive roadmap by leading international researchers. This roadmap aims to facilitate collaboration and interdisciplinary dialogue to address challenges in materials science, physics, engineering, and computing. The roadmap comprises eighteen sections, roughly divided into three blocks. The first block explores the fundamentals of 3D nanomagnetism, focusing on recent trends in fabrication techniques and imaging methods crucial for understanding complex spin textures, curved surfaces, and small-scale interactions. Techniques such as two-photon lithography and focused electron beam-induced deposition enable the creation of intricate 3D architectures, while advanced imaging methods like electron holography and synchrotron x-ray tomography provide nanoscale spatial resolution for studying magnetization dynamics in three dimensions. Various 3D magnetic systems, including coupled multilayer systems, artificial spin-ice, magneto-plasmonic systems, topological spin textures, and molecular magnets are discussed. The second block introduces analytical and numerical methods for investigating 3D nanomagnetic structures and curvilinear systems, highlighting geometrically curved architectures, interconnected nanowire systems, and other complex geometries. Finite element methods are emphasized for capturing complex geometries, along with direct frequency domain solutions for addressing magnonic problems. The final block focuses on 3D magnonic crystals and networks, exploring their fundamental properties and potential applications in magnonic circuits, memory, and spintronics. Computational approaches using 3D nanomagnetic systems and complex topological textures in 3D spintronics are highlighted for their potential to enable faster and more energy-efficient computing.