Search Results (1,235)

Tuning structural heterogeneity in metallic glasses is key to improving their mechanical performance. Here we examine how carbon micro-alloying modulates the relaxation dynamics and creep of Fe-based amorphous ribbons. Increasing carbon content lowers the crystallization temperature, amplifies β-relaxation, and reduces hardness, consistent with enhanced atomic mobility. Nanoindentation creep, fitted with a stretched-exponential model, shows a decreasing exponent with carbon addition, indicating broader relaxation–time distributions and stronger dynamic heterogeneity. Nanoscale force-mapping further reveals a larger fraction of liquid-like regions and pronounced viscoelastic heterogeneity in carbon-rich samples. These changes facilitate the activation of shear-transformation zones and promote room-temperature creep flow. Together, the results establish a direct link between structural heterogeneity, relaxation processes, and mechanical response, providing guidance for the design of ductile metallic glasses. Full article

Background: Clonazepam is a benzodiazepine drug indicated in all clinical forms of epileptic seizures, various forms of myoclonic seizures, myoclonus and other abnormal movements. At present, it is classified as a hazardous drug requiring special precautions for personnel at reproductive risk, according to a technical document produced by the Spanish National Institute for Safety and Health at Work (INSST), in collaboration with the Spanish Society of Hospital Pharmacy (SEFH). The commercial solutions of clonazepam, for oral and parenteral administration, are supplied by laboratories in glass containers. Repacking in pre-filled polypropylene (PP) syringes, made in the pharmacy service, and in aseptic conditions, may facilitate its administration and reduce the risks to the health or safety of nursing personnel. Nevertheless, there is a lack of stability studies of clonazepam in pre-filled PP syringes. Objectives: To evaluate the physicochemical stability of commercial clonazepam 2.5 mg/mL oral solution and 1 mg/mL parenteral solution repackaged in pre-filled PP syringes under various storage conditions. Methods: A rapid, linear, precise and sensitive high-performance liquid chromatography (HPLC) method for chemical stability studies of Clonazepam 1 mg/mL (parenteral use) and 2.5 mg/mL (oral use) in solution was implemented after repackaging in pre-filled PP syringes. The studies were conducted by measuring concentrations of oral and parenteral clonazepam in pre-filled syringes, at various time points, over 30 days in several different storage conditions: oral clonazepam protected from light in refrigerator and at controlled room temperature exposed to ambient light; parenteral clonazepam protected from light in a refrigerator and at controlled room temperature protected or unprotected from light. Visual aspects and pH change as well as crystal formation were checked to determine physical stability. Results: The degradation of the active ingredient in all groups was less than 10% after 30 days. No evidence of crystal formation, pH and visual aspect changes were observed. Conclusions: Clonazepam 1 mg/mL parenteral solution and 2.5 mg/mL oral solution in pre-filled PP syringes are stable for up to 30 days in the tested conditions. The centralized repackaging of clonazepam in pre-filled PP syringes, connected to a closed safety system, in the pharmacy service, reduces drug manipulation by nursing staff decreasing the risk of occupational exposure. Full article

NASICON-type Li_1+XFe_XTi_2-X(PO₄)₃ (x = 0.1, 0.3, 0.4) solid electrolytes for all-solid-state Li-ion batteries were synthesized using a sol–gel method. This study investigated the impact of substituting Fe³⁺ (0.645 Å), a trivalent cation, for Ti⁴⁺ (0.605 Å) on ionic conductivity. Li_1+XFe_XTi_2-X(PO₄)₃ samples, subjected to various sintering temperatures, were characterized using TG-DTA, XRD with Rietveld refinement, XPS, FE-SEM, and AC impedance to evaluate composition, crystal structure, fracture-surface morphology, densification, and ionic conductivity. XRD analysis confirmed the formation of single-crystalline NASICON-type Li_1+XFe_XTi_2-X(PO₄)₃ at all sintering temperatures. However, impurities in the secondary phase emerged owing to the high sintering temperature above 1000 °C and increased Fe content. Sintered density increased with the densification of Li_1+XFe_XTi_2-X(PO₄)₃, as evidenced by FE-SEM observations of sharper edges of larger quasi-cubic grains at elevated sintering temperatures. At 1000 °C, with Fe content exceeding 0.4, grain coarsening resulted in additional grain boundaries and internal cracks, thereby reducing the sintered density. Li_1.3Fe_0.3Ti_1.7(PO₄)₃ sintered at 900 °C exhibited the highest density among the other conditions and achieved the maximum total ionic conductivity of 1.51 × 10⁻⁴ S/cm at room temperature, with the lowest activation energy for Li-ion transport at 0.37 eV. In contrast, Li_1.4Fe_0.4Ti_1.6(PO₄)₃ sintered at 1000 °C demonstrated reduced ionic conductivity owing to increased complex impedance associated with secondary phases and grain crack formation. Full article

The synthesis of two series of poly(lactic acid) (PLA)-based polymer nanocomposites (PNCs) filled with small amounts (0.5 and 1%) of Ag and Cu nanoparticles (NPs) was performed. Moreover, two methods for the PNC synthesis were performed, namely, ‘conventional mixing techniques’ and ‘in situ ring opening polymerization (ROP)’. The latter method was employed for the first time; moreover, it was found to be more effective in achieving very good NP dispersion in the polymer matrix as well as the formation of interfacial polymer–NP interactions. The in situ ROP for PLA/Cu was not productive due to the oxidation of Cu NPs being faster than the initiation of ROP. The presence of NPs resulted in suppression of the glass transition temperature, T_g (23–60 °C), with the effects being by far stronger in the case of ROP-based PNCs, e.g., exhibiting T_g decrease by tens of K. Due to that surprising result, the ROP-based PLA/Ag PNCs exhibited elevated ionic conductivity phenomena (at room temperature). This can be exploited in specific applications, e.g., mimicking the facilitated small molecules permeation. The effects of NPs on crystallinity (2–39%) were found opposite between the two series. Crystallinity was facilitated/suppressed in the mixing/ROP -based PNCs, respectively. The local and segmental molecular mobility map was constructed for these systems for the first time. Combining the overall data, a concluding scenario was employed, that involved the densification of the polymer close to the NPs’ surface and the free volume increase away from them. Finally, an exceptional effect was observed in PLA + 0.5% Ag (ROP). The crystallization involvement resulted in a severe suppression of T_g (−25 °C). Full article

Metallic glass alloys exhibit excellent properties, yet suffer from poor room-temperature plasticity, a limitation that restricts their engineering applications. Bulk metallic glass matrix composites (BMGMCs) have proven effective in enhancing the plasticity of metallic glasses, and the addition of alloying elements serves as a key strategy to regulate their microstructure and optimize the properties of these composites. This study aims to investigate the effects of a vanadium (V) addition on the mechanical properties and microstructure of Ti-based BMGMCs, while exploring the underlying mechanism of V’s influence. Using (Ti₅₁Zr₂₅Cu₆Be₁₈)_100−xV_x (x = 0, 4, 8, 12, 16, 20) BMGMCs as test specimens, microstructural characterization was performed via X-ray diffraction (XRD) and scanning electron microscopy (SEM), and compressive mechanical properties were tested. The results indicate that a V addition refines dendrites without altering the phase composition, which remains composed of β-Ti crystals and an amorphous matrix. With the increase in V content, the compressive plastic strain shows a trend of first increasing and then decreasing; when x = 12, the specimen exhibits the maximum compressive plastic strain, reaching 7.9%. Additionally, the volume fraction of the crystalline phase gradually increases with increasing V content. This study clarifies the mechanism by which V regulates the microstructure and properties of Ti-based BMGMCs, thereby providing theoretical and experimental insights for optimizing alloy compositions to enhance the mechanical performance. Full article

The citrate–nitrate method was employed to synthesize the magnesium chromite (MgCr₂O₄) spinel, followed by calcination at 700 °C for 3 h. The synthesized compound was analyzed using techniques including powder XRD, SEM-EDAX, FTIR, UV-DRS, and LCR Meter. The structural analysis was conducted using an X-ray diffractometer, which revealed the formation of the cubic crystal symmetry of the sample with the corresponding Fd-3 m space group. The average crystallite size of the sample was calculated around 15.38 nm. Using tetrahedral and octahedral positions, the lattice vibrations of the associated chemical bonds were identified using Fourier transform infrared (FTIR) spectroscopy. SEM (scanning electron microscopy) micrographs showed that the spherical nature of the particles and the constituent particles were between 10 and 40 nm in size. The optical bandgap value was evaluated using Tauc’s plot. Pellets of the powdered sample were prepared for determining the dielectric aspects, such as the dielectric constant (ε′) and tangent loss (tanδ), in the frequency range of 10 Hz–8 MHz at room temperature. The charge transport mechanism was explored from the complex impedance spectroscopy study. The obtained results indicate that magnesium chromite may be a potential candidate in the fabrication of sensors, micro-electronic devices, etc. Full article

The present study concentrates on the role and underlying mechanisms of in situ crystallization (employed for nanocrystal formation) in influencing the solidification microstructure and properties of aluminum alloys. By systematically analyzing the effects on α-Al refinement, silicon phase modification, and secondary phase control, as well as exploring the impact on room-temperature mechanical properties, high-temperature deformation behavior, and fatigue performance, this work reveals the potential physical mechanisms of improving mechanical properties by providing nucleation sites and inhibiting grain growth, such as fine-grain strengthening and dispersion strengthening. Moreover, stabilization of the second phase optimizes high-temperature deformation behavior, and a reduction in stress concentration improves fatigue performance. Compared with traditional microstructure control methods, in situ crystallization can achieve deeper grain refinement from micron to nanometer scale, ensuring high uniformity of grain distribution and showing good compatibility with existing processes. By defining the regulation of in situ crystallization on the microstructure and properties of aluminum alloy, the existing research provides a feasible material solution for high stress, high temperature, and high reliability. Its core significance lies in breaking through the performance bottlenecks of traditional modification technology, such as unstable refining effect, element segregation, and so on. The co-promotion of “strength–plasticity–stability” of aluminum alloys and the consideration of process compatibility and cost controllability lay a theoretical and technical foundation for the industrialization of high-performance aluminum alloys. Full article

All-solid-state lithium batteries (ASSLBs) employing Li-rich layered oxide (LLO) cathodes are regarded as promising next-generation energy storage systems owing to their outstanding energy density and intrinsic safety. Polymer-in-salt solid electrolytes (PISSEs) offer advantages such as high room-temperature ionic conductivity, enhanced Li anode interfacial compatibility, and low processing costs; however, their practical deployment is hindered by poor oxidative stability especially under high-voltage conditions. In this study, we report the rational design of a bilayer electrolyte architecture featuring an in situ solidified LiClO₄-doped succinonitrile (LiClO₄–SN) plastic–crystal interlayer between a Li_1.2Mn_0.6Ni_0.2O₂ (LMNO) cathode and a poly (vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP)-based PISSE. This PISSE/SN–LiClO₄ configuration exhibits a wide electrochemical stability window up to 4.7 V vs. Li⁺/Li and delivers a high ionic conductivity of 5.68 × 10⁻⁴ S cm⁻¹ at 25 °C. The solidified LiClO₄-SN layer serves as an effective physical barrier, shielding the PVDF-HFP matrix from direct interfacial contact with LMNO and thereby suppressing its oxidative decomposition at elevated potentials. As a result, the bilayer polymer-based cells with the LMNO cathode demonstrate an initial discharge capacity of ∼206 mAh g⁻¹ at 0.05 C and exhibit good cycling stability with 85.7% capacity retention after 100 cycles at 0.5 C under a high cut-off voltage of 4.6 V. This work not only provides a promising strategy to enhance the compatibility of PVDF-HFP-based electrolytes with high-voltage cathodes through the facile in situ solidification of plastic interlayers but also promotes the application of LMNO cathode material in high-energy ASSLBs. Full article

Metal hydrides are an attractive way to store hydrogen in a compact and safe manner under low pressure. However, one of the hurdles to the widespread use of this method is the difficulty of the first hydrogenation, which increases the material cost. In this paper, we report the effect of substituting Zr with Ti in Zr_1−xTi_xCr₂ alloys (x = 0, 0.25, 0.5, 0.75, and 1) on the first hydrogenation. All the substituted alloys had similar microstructures and crystallized in the metastable C14 Laves phase. For x = 0, the first hydrogenation was possible at room temperature under 2 MPa of hydrogen pressure. As x increased, the hydrogen capacity decreased. For x = 0.75 and 1, first hydrogenation was practically impossible. Full article

This study investigates the influence of RE elements on the room- and high-temperature properties of magnesium alloys. The effects of RE type, addition level, and multi-element alloying strategies were systematically analyzed to clarify the underlying strengthening mechanisms and processing pathways for optimizing Mg–RE alloys. RE elements enhance the mechanical and thermal properties of Mg alloys through crystal structure modification, formation of thermally stable dispersed phases, precipitation strengthening, and solid-solution strengthening. Compared with conventional alloying elements, RE additions offer distinct advantages in strengthening efficiency and overall performance. To fully exploit these benefits, new research paradigms that integrate machine learning and other advanced techniques are required, enabling the intelligent design of multicomponent alloy systems tailored to specific application requirements. Full article

Organic phase change materials (OPCMs) offer high energy density for thermal storage but suffer from crystallization kinetics dependent on ambient temperature, leading to uncontrolled heat release and limited storage lifetime. Although doping OPCMs with azobenzene (Azo) derivatives enables optically controlled energy storage and release, existing systems require UV irradiation for E-to-Z isomerization. This UV dependency seriously hinders their development in practical solar applications. Herein, we develop a visible-light-responsive Azo@OPCM composite by doping tetra-ortho-fluorinated azobenzene into eicosane. Systematic characterization of composites with different dopant ratios via UV–visible spectroscopy and differential scanning calorimetry reveals that green-light irradiation drives E-to-Z isomerization, achieving 97–99% Z-isomer conversion. This photoisomerization could introduce supercooling through photo-responsive energy barriers generated by Z-isomer, allowing thermal energy storage at lower temperatures. Subsequent blue-light irradiation triggers Z-to-E reversion to eliminate supercooling and enable optically controlled heat release. Additionally, by regulating the molar ratios of dopant, the optimized composites achieved 280.76 J/g energy density at 20% molar doping ratio, which surpassed that of pure eicosane and the reported Azo-based photothermal energy storage system. This work establishes a complete visible-light-controlled energy harvesting–storage–release cycle with significant potential for near-room-temperature solar thermal storage applications. Full article

It was demonstrated that various defects can be induced in halide crystals by irradiation with swift heavy ions. Here, we irradiated barium fluoride (BaF₂) single crystals with 220 MeV xenon ions at room temperature and performed stepwise thermal annealing up to the temperature of 825 K to study the kinetics of ion-induced defects at different temperatures. Optical spectroscopy was utilized for the measurement of the wide range of absorption spectra from NIR to VUV. A sharp decrease in the F₂ absorption peak was observed for the samples annealed in the temperature range of 400–450 K. This result can be explained by their recombination with anion interstitials during thermal decay of the complex hole centers. The mobile interstitials, those did not recombine with the F₂ centers, increase the absorption peaks in the 9–10 eV region, which can be associated with interstitial aggregates. Full article

In the light of increasing research into amorphous composites and their applications, as-cast specimens of multicomponent Ti₄₈Zr₁₈V₁₂Cu₅Be₁₇ amorphous composites were prepared via water-cooled copper mold suction casting. Subsequently, the as-cast specimens were subjected to semi-solid isothermal treatment to obtain semi-solid specimens. Taking the semi-solid specimens as the research object, room temperature compressive deformation behavior was investigated by analyzing the shear band characteristics on the side surfaces of the compressed specimens. The evolution of shear bands at various stages of plastic deformation was investigated via scanning electron microscopy (SEM). Additionally, significant work hardening was observed after yielding. Surface deformation morphologies indicate that the work-hardening behavior is associated with plastic deformation, interactions between shear bands, and interactions between shear bands and β-Ti crystals. Experiments have demonstrated that at a specific deformation extent, shear bands preferentially initiate at the crystal–amorphous matrix interface. In the final stage of plastic deformation, shear bands propagate through work-hardened β-Ti crystals into the amorphous matrix, with their propagation retarded by the β-Ti crystals. When shear bands in the amorphous matrix are obstructed by β-Ti crystals and can no longer propagate, some evolve into cracks. These cracks then propagate exponentially, leading to eventual fracturing of the specimens and termination of plastic deformation. The research findings provide a theoretical basis for analyzing the deformation capacities of various amorphous composites. Full article

Amorphous indium gallium zinc oxide (a-IGZO) is widely used as an oxide semiconductor in the electronics industry due to its low leakage current and high field-effect mobility. However, a-IGZO suffers from notable limitations, including crystallization at temperatures above 600 °C and the high cost of indium. To address these issues, nitrogen-doped zinc oxynitride (ZnON), which can be processed at room temperature, has been proposed. Nitrogen in ZnON effectively reduces oxygen vacancies (V_O), resulting in enhanced field-effect mobility and improved stability under positive bias stress (PBS) compared to IGZO. In this study, selective deep ultraviolet femtosecond (DUV fs) laser annealing was applied to the channel region of ZnON thin-film transistors (TFTs), enabling rapid threshold voltage (Vth) modulation within microseconds, without the need for vacuum processing. Based on the electrical characteristics of both Vth-modulated and pristine ZnON TFTs, an NMOS inverter was fabricated, demonstrating reliable performance. These results suggest that laser annealing is a promising technique, applicable to various logic circuits and electronic devices. Full article

A single-crystal magnesium oxide (MgO) dual-Fabry–Perot (FP)-cavity sensor based on MEMS technology and laser micromachining is proposed for simultaneous measurement of temperature and pressure. The pressure sensitive cavity is processed by wet chemical etching and direct bonding, which can improve machining efficiency, ensure the quality of the reflection surface and achieve thermal stress matching. Femtosecond laser and micromachining technologies are used to fabricate a rough surface and a through hole to reduce the reflect surface and fix the optical fiber. The bottom surface of the pressure cavity and the upper surface of the MgO wafer form a temperature cavity. A cross-correlation signal demodulation algorithm combined with a temperature decoupling method is proposed to achieve dual-cavity demodulation and eliminate the cross-sensitivity between temperature and pressure, improving the accuracy of pressure measurement. Experimental results show that the proposed sensor can stably operate at an ambient environment of 22–800 °C and 0–0.5 MPa with a pressure sensitivity of approximately 0.20 µm/MPa (room temperature), a repeatability error of 2.06% and a hysteresis error of 1.90%. After temperature compensation, thermal crosstalk is effectively eliminated and the pressure measurement accuracy is 2.01%F.S. Full article