National Institute Of Materials Physics - Romania

This study investigates the effects of neutron irradiation on tungsten (W) and copper-chromium-zirconium (CuCrZr) joints under conditions mimicking the high neutron flux environment of a tokamak fusion reactor. Samples of W/CuCrZr joints were subjected to irradiation in the Belgian Reactor 2 (BR2) nuclear reactor at SCK CEN (Belgian Nuclear Research Centre) to simulate the intense neutron exposure characteristic for International Thermonuclear Experimental Reactor (ITER) and DEMOnstration power plant reactor (DEMO) operations. The primary objective was to evaluate changes in the mechanical properties and microstructure of these materials, which are critical for their potential use in plasma-facing components. It is revealed that a significant reduction in tensile elongation of the joint, indicating some degree of embrittlement, is observed after the irradiation. Importantly, this effect is independent of the irradiation temperature. Possible physical reasons for the observed phenomenon are discussed.

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.

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.

Expression of concern for 'Iron oxide magnetic nanoparticles with versatile surface functions based on dopamine anchors' by Mykola Mazur et al., Nanoscale, 2013, 5, 2692-2702, https://doi.org/10.1039/C3NR33506B.

This work investigates the influence of composition on the thermal properties of the high entropy alloy family Cu5Cr35Fe35V20-X-5 (at. %), where X = Ti, Ta, W or Mo in the framework of acting as a thermal barrier between the W-based plasma-facing elements and the CuCrZr or Cu-based heat sink components of the fusion reactor. The alloys were produced by arc melting and their microstructure and mechanical properties were previously characterized by XRD, SEM, and Vickers hardness measurements. Thermal properties have been measured on as-cast at thermally treated alloys using the laser flash method in the temperature range 25 degrees C to 600 degrees C to determine the thermal diffusivity, alpha, thermal conductivity, lambda, and specific heat, C-p. Dilatometry experiments were also carried out to obtain the linear thermal expansion coefficient, CTE, as a function of temperature. For all materials, the thermal conductivity increases with temperature from 15 W/mK at RT to 28 W/mK at 600 degrees C and does not significantly depend on the thermal treatment for the Mo-HEA and W-HEA, but increases after aging for the Ta-HEA and Ti-HEA. These values are lower than those of W (similar to 122 W/mK at 600 degrees C) and much lower than for CuCrZr-IG (similar to 354 W/mK at 400 degrees C). The thermal expansion coefficients of these HEAs, similar to 10 x 10(-6) degrees C-1 at RT and similar to 2 x 10(-6) degrees C-1 at 650 degrees C are between those of CuCrZr and the W for the entire operative temperature range. These results indicate that the Cu5Cr35Fe35V20-X-5 (X = Ti, Ta, W, Mo) HEAs have a promising combination of the thermophysical properties, lambda, C-p and CTE, to act as thermal barrier in plasma-facing components that require the union of W- and Cu-based materials.

The synthesis of polycrystalline TiFe2Sn samples by a route including arc melting and spark plasma sintering with Hf, Y, and In substitutions at the Ti and Sn sites is investigated. For a reduced amount of substitution, around 2 at%, the samples are single phase, while for increased amounts, secondary phases segregate. As is characteristic of these compounds, the Fe-Ti atomic disorder generates a weak ferromagnetic ordering, which is also influenced by the type of substitutional atoms and the secondary phases in the samples with a higher Hf content. The Seebeck coefficient values show an increase for Ti0.98Hf0.02Fe2Sn and for samples with an adjusted Sn content, resulting in slightly increased power factor values. These values reach a maximum for Ti0.98Hf0.02Fe2Sn at approximately 300 K and for TiFe2Sn1.05 at approximately 325 K, namely, 2.69 x 10(-)(4) Wm(-1)K(-2) and 2.52 x 10(-)(4) Wm(-1)K(-2), respectively. The thermal conductivity of all the samples with substitutions increases with respect to the pristine sample. The highest figure of merit value of 0.016 is also obtained for Ti0.98Hf0.02Fe2Sn at 325 K.

This study investigates polycrystalline samples of TiFe2-xRexSn (with x = {0, 0.02, 0.04, 0.06, 0.2}) synthesized using conventional arc-melting and spark plasma sintering. Structural and morphological analysis shows that low Re substitutions result in good phase purity with minor traces of secondary phases, while higher Re content leads to the segregation of additional phases. The magnetism and electrical resistivity of the samples are affected by inherent Fe-Ti atomic disorder, with the effects of secondary phases becoming more prominent in the samples with higher Re content. The Seebeck coefficient values increase only for TiFe1.98Re0.02Sn, while the power factor increases for x = {0, 0.02, 0.04}, reaching maximal values for x = 0.02 at similar to 300 K and x = 0.04 at similar to 325 K, i.e., (2.22 +/- 0.2) x 10(-4) Wm(-1) K-2. The thermal conductivity of the samples increases with x, resulting in modest values of the figure of merit, with the maximum achieved for x = 0.02 at 325 K, i.e., 0.015 +/- 0.002. (c) The Author(s) 2024

Iron oxide nanoparticles were synthesized using a vortex microfluidic system and subsequently functionalized with a primary shell of salicylic acid, recognized for its ability to increase the stability and biocompatibility of coated materials. In the second stage, the vortex platform was placed in a magnetic field to facilitate the growth and development of a porous silica shell. The selected drug for this study was micafungin, an antifungal agent well regarded for its effectiveness in combating fungal infections and identified as a priority compound by the World Health Organization (WHO). The resulting nanocomposite system was characterized using various techniques, including Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), transmission electron microscopy (TEM), dynamic light scattering (DLS), Brunauer-Emmett-Teller (BET) analysis, UV-Vis spectroscopy, and Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS). The synthesis method produced nanoparticles with dimensions of 5-7 nm, highlighting the advantages of the chosen approach. A desorption profile was established using a continuous-flow, UV-Vis analysis system, indicating that the bioactive compound was released slowly; after two hours, approximately 50% of the loaded micafungin was detected in the release medium. Furthermore, the results obtained from the FT-ICR MS analysis provided molecular-level confirmation, thereby supporting the release mechanism of micafungin from the nanosystem.

In the present work, we report the synthesis and investigations of La0.9K0.1MnO3 and La0.8K0.1Pb0.1MnO3 bulk samples which could be potential magnetocaloric materials for magnetic refrigeration close to room temperature. A flash combustion reaction and sintering at 1200 degrees C for 10 h are used to prepare the bulk materials. Both compounds crystallized into a rhombohedral structure with R3\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\overline{3 }$$\end{document}c space group confirmed by X-ray powder diffraction results. Scanning electron microscopy analysis, combined with XRD peak profiles is performed to estimate the particle/crystallite size of the samples. Moreover, the Curie temperature, TC, is found to be higher in lead-rich sample due to the enhancement of the grain size and the Mn3+-O-Mn4+ double exchange (DE) interaction. Therefore, the bulk sample La0.8K0.1Pb0.1MnO3 shows a room temperature phase transition of 289 K as well as a higher saturation magnetization. The La0.8K0.1Pb0.1MnO3 bulk compound exhibits a high and sharp peak in magnetic entropy change up to 5.5 Jkg-1 K-1 under 5 T at the magnetic transition temperature TC. To compare the magnetocaloric performances of the studied compounds, relative cooling power (RCP) was employed. The obtained experimental results revealed that the increase in particle size influences severely the magnetocaloric properties.