Mirosław Jakub Kruszewski

This study compares five Si–Me infiltration coatings, Si:Mo (1:4), Si:Ti (1:1), Si:Zr (1:5), Si:Ta (1:1), and Si:W (1:5), deposited on C/C sonotrodes for ultrasonic atomization of CuSn8. The coatings were evaluated in terms of phase constitution, microstructure, wettability, nanoindentation response, and powder-production performance. XRD showed that the coatings formed distinct multiphase reaction layers, with Si:Ta (1:1) being the most silicide-dominated system, while the other coatings contained carbide or silicide–carbide phases. Metallization strongly improved the surface wettability of C/C, especially for Si:Zr (1:5) and Si:W (1:5). Nanoindentation indicated the most favorable H/E* and H³/E*² descriptors for Si:W (1:5) and Si:Mo (1:4). All coatings enabled high powder yields in single-run atomization tests, while apparent differences in particle-size distribution were observed among the coating conditions. Overall, the results show that coating selection for ultrasonic atomization should combine phase constitution, surface-state descriptors, near-surface mechanical response, layer retention, and process performance. Within the investigated conditions and the limitation of single-run atomization experiments, Si:W (1:5) emerged as the most promising and best-balanced coating candidate, while Si:Ta (1:1) and Si:Mo (1:4) remained relevant alternatives.

The development of thermoelectric modules based on skutterudite materials requires stable, low-resistance interfaces between segments operating at different temperature ranges. This study investigates the microstructure, thermoelectric performance, and thermal stability of the following two joints: In_0.4Co₄Sb₁₂/Co₄Sb_10.8Te_0.6Se_0.6 (n-type) and CeFe₃Co_0.5Ni_0.5Sb₁₂/In_0.25Co₃FeSb₁₂ (p-type), fabricated by pulse plasma sintering (PPS). Scanning electron microscopy (SEM) and energy-dispersive spectroscopy (EDS) analyses confirmed the formation of well-bonded interfaces without pores or cracks. Aging at 773 K for 168 h did not result in morphological or chemical degradation, and phase composition remained unchanged according to X-ray diffraction (XRD). Surface Seebeck coefficient mapping and contact resistance measurements showed negligible changes after annealing, confirming electrical stability. To provide context for potential applications, theoretical energy conversion efficiencies were estimated based on measured thermoelectric properties, yielding 13.2% and 10.1% for the n- and p-type segmented legs, respectively. Additionally, measured coefficients of thermal expansion (CTE) indicated low mismatch between jointed materials, supporting good mechanical compatibility. The results demonstrate that the selected material combinations are thermally, chemically, and electrically stable and can be effectively used in segmented thermoelectric legs for intermediate-temperature applications.

The aim of this work was to investigate the possibility of doping copper sulfide Cu₂S with selected fifth-group elements, potentially having a positive effect on the thermoelectric properties of the resulting materials. For the selected model structures, theoretical calculations and an analysis of the electronic structure and changes in the enthalpy of formation due to doping were performed using the WIEN2k package employing the Full-Potential Linearized Augmented Plane Wave (FP-LAPW) method within density functional theory (DFT) formalism. Polycrystalline materials with the nominal composition of Cu₃₂S₁₅X₁ (X = P, As, Sb, Bi) were synthesized in quartz ampoules, then sintered using the spark plasma sintering (SPS) technique and “SPS melting” method. The chemical and phase compositions of the obtained sinters were studied by X-Ray diffraction (XRD) and scanning electron microscopy (SEM). Additionally, investigations of thermoelectric properties, i.e., electrical conductivity, Seebeck coefficient and thermal conductivity in the temperature range 300–920 K, were performed. The results of this study indicate that only phosphorus is successfully incorporated into the Cu₂S structure.

Magnesium (Mg) and its alloys offer promise for aerospace, railway, and 3D technology applications, yet their inherent limitations, including inadequate strength, pose challenges. Magnesium matrix composites, particularly with metallic reinforcements like titanium (Ti) and its alloys, present a viable solution. Therefore, this study investigates the impact of Ti6Al4V reinforcement on AZ31 magnesium alloy composites produced using pulse plasma sintering (PPS). Results show enhanced microhardness of the materials due to improved densification and microstructural refinement. However, Ti6Al4V addition decreased corrosion resistance, leading to strong microgalvanic corrosion and substrate dissolution. Understanding these effects is crucial for designing Mg-based materials for industries like petrochemicals, where degradation-resistant materials are vital for high-pressure environments. This research provides valuable insights into developing Mg-Ti6Al4V composites with tailored properties for diverse industrial applications, highlighting the importance of considering corrosion behavior in material design. Further investigation is warranted to establish predictive correlations between Ti6Al4V content and corrosion rate for optimizing composite performance.