Search Results (225)

Memristors with resistive switching capabilities are vital for information storage and brain-inspired computing, making them a key focus in current research. This study demonstrates non-volatile analog resistive switching behavior in Al/TiO_x/TiN/Si(n⁺⁺)/Al memristive devices. Analog resistive switching offers gradual, controllable conductance changes, which are essential for mimicking brain-like synaptic behavior, unlike digital/abrupt switching. The amorphous titanium oxide (TiO_x) active layer was deposited using the pulsed-DC reactive magnetron sputtering technique. The impact of increasing the oxide thickness on the electrical performance of the memristors was investigated. Electrical characterizations revealed stable, forming-free analog resistive switching, achieving endurance beyond 300 DC cycles. The charge conduction mechanisms underlying the current–voltage (I–V) characteristics are analyzed in detail, revealing the presence of ohmic behavior, Schottky emission, and space-charge-limited conduction (SCLC). Experimental results indicate that increasing the TiO_x film thickness from 31 to 44 nm leads to a notable change in the current conduction mechanism. The results confirm that the memristors have good stability (>1500 s) and are capable of exhibiting excellent long-term potentiation (LTP) and long-term depression (LTD) properties. The analog switching driven by oxygen vacancy-induced barrier modulation in the TiO_x/TiN interface is explained in detail, supported by a proposed model. The remarkable switching characteristics exhibited by the TiO_x-based memristive devices make them highly suitable for artificial synapse applications in neuromorphic computing systems. Full article

The development of multifunctional conductive hydrogels with rapid self-healing capabilities and powerful sensing functions is crucial for advancing wearable electronics. This study designed and prepared a polyvinyl alcohol (PVA)–borax hydrogel incorporating carbon nanotubes (CNTs) and biomass carbon nanospheres (CNPs) as dual-carbon fillers. This hydrogel exhibits excellent conductivity, mechanical flexibility, and self-recovery properties. Serving as a highly sensitive piezoresistive sensor, it efficiently converts mechanical stimuli into reliable electrical signals. Sensing tests demonstrate that the CNT/CNP/PVA–borax hydrogel sensor possesses an extremely fast response time (88 ms) and rapid recovery time (88 ms), enabling the detection of subtle and rapid human motions. Furthermore, the hydrogel sensor also exhibits outstanding cyclic stability, maintaining stable signal output throughout continuous loading–unloading cycles exceeding 3200 repetitions. The hydrogel sensor’s characteristics, including rapid self-healing, fast-sensing response/recovery, and high fatigue resistance, make the CNT/CNP/PVA–borax conductive hydrogel an ideal choice for multifunctional wearable sensors. It successfully monitored various human motions. This study provides a promising strategy for high-performance self-healing sensing devices, suitable for next-generation wearable health monitoring and human–machine interaction systems. Full article

Plasma-derived fibrin hydrogels are widely used in tissue engineering because of their excellent biological properties. Specifically, human plasma-derived fibrin hydrogels serve as 3D matrices for autologous skin graft production, skeletal muscle repair, and bone regeneration. Nevertheless, for advanced applications such as in vitro skin equivalents and engineered grafts, the intrinsic limitations of native fibrin hydrogels in terms of long-term mechanical stability and resistance to degradation need to be addressed to enhance the usefulness and application of these hydrogels in tissue engineering. In this study, we chemically modified plasma-derived fibrin by incorporating succinimidyl alginate (SA), a version of alginate chemically modified to introduce reactive succinimidyl groups. These NHS ester groups (N-hydroxysuccinimide esters), attached to the alginate backbone, are highly reactive toward the primary amine groups present in plasma proteins such as fibrinogen. When mixed with plasma, the NHS groups covalently bond to the amine groups in fibrin, forming stable amide linkages that reinforce the fibrin network during hydrogel formation. This chemical modification improved mechanical properties, reduces contraction, and enhanced the stability of the resulting hydrogels. Hydrogels were prepared with a final fibrinogen concentration of 1.2 mg/mL and SA concentrations of 0.5, 1, 2, and 3 mg/mL. The objective was to evaluate whether this modification could create a more stable matrix suitable for supporting skin tissue development. The mechanical and microstructure properties of these new hydrogels were evaluated, as were their biocompatibility and potential to create 3D skin models in vitro. Dermo-epidermal skin cultures with primary human fibroblast and keratinocyte cells on these matrices showed improved dermal stability and better tissue structure, particularly SA concentrations of 0.5 and 1 mg/mL, as confirmed by H&E (Hematoxylin and Eosin) staining and immunostaining assays. Overall, these results suggest that SA-functionalized fibrin hydrogels are promising candidates for creating more stable in vitro skin models and engineered skin grafts, as well as for other types of engineered tissues, potentially. Full article

Prussian blue and its analogs (PBAs), considered potential cathode materials for sodium-ion batteries (SIBs), still confront multiple challenges. For example, many defect vacancies and high crystal water content are generated during the fast crystallization of PBAs, impairing the rate performance. The stress accumulation during Na⁺ insertion/extraction destabilizes the lattice framework and then damages the electrochemical performance. Herein, iron-based Prussian blue with an open-pore skeleton structure (PB-3) is prepared using a facile template method which employs PVP and sodium citrate to control the crystallization rate and adjust the particle morphology. The prepared materials exhibit excellent kinetic properties and are conducive to mitigate the volume changes during ion insertion/extraction processes. PB-3 electrode not only exhibits a superior rate performance (92 mAh g⁻¹ reversible capacity at 2000 mA g⁻¹), but also presents superior cycling performance (capacity retention remained at 90.2% after 600 cycles at a current density of 500 mA g⁻¹). The highly reversible sodium ion insertion/extraction mechanism of PB-3 is investigated by ex situ XRD tests, which proves that the stabilized lattice structure can enhance the long cycling performance. In addition, the considerable capacitance contributes to the rate performance. This study provides valuable insights for the subsequent development of high-performance and stable cathodes for SIBs. Full article

This study focused on the preparation of poly(ε-caprolactone)/carbon nanotubes (PCL/CNTs) composite membranes via electrospinning technology and investigated their performance in oil–water separation. The effects of varying CNTs contents and spinning parameters on the structure and properties of the membrane materials were systematically studied. A highly uniform diameter distribution of the PCL fiber was achieved by using the dichloromethane/dimethylformamide (DCM/DMF) composite solvent with volume ratio of 7:3, as well as a PCL concentration of ca. 17 wt.%. The optimal electrospinning parameters were identified as an applied voltage of 18 kV and a syringe pump flow rate of 1 mL·h⁻¹, which collectively ensured uniform fiber morphology under the specified processing conditions. The critical threshold concentration of CNTs in the composite system was determined to be 1 wt.%, above which the composite fibers exhibit a significant increase in diameter heterogeneity. Both pristine PCL fibrous membranes and PCL/CNTs composite membranes demonstrated excellent and stable oil–water separation performance, with separation efficiencies consistently around 90%. Notably, no significant attenuation in separation efficiency was observed after ten consecutive separation cycles. Furthermore, when incorporating 0.5 wt.% CNTs, the PCL/CNT composite membranes exhibited a 20% increase in separation flux for heavy oils compared to pristine PCL membranes. Additionally, CNTs, as a prototypical class of nanofillers for polymer matrix reinforcement, can potentially enhance the mechanical properties of composite films, thus effectively prolonging their service life. Full article

Carbon nanotubes (CNTs) functionalized with metal oxides exhibit synergistic properties that enhance their performance across various applications, particularly in electrochemistry. Recent advancements have highlighted the potential of CNT–metal oxide heterostructures, with a specific focus on their electrochemical properties, which are pivotal for applications in sensors, supercapacitors, batteries, and catalytic systems. Among these, nickel oxide (NiO)-modified CNTs have garnered significant attention due to their cost-effectiveness, facile synthesis, and promising gas-sensing capabilities. This study employs quantum-chemical calculations within the framework of density functional theory (DFT) to elucidate the interaction mechanisms between CNTs and NiO. The results demonstrate that the adsorption process leads to the formation of stable CNT-NiO complexes, with detailed analysis of adsorption energies, equilibrium distances, and electronic structure modifications. The single-electron spectra and density of states (DOS) of the optimized complexes reveal significant alterations in the electronic properties, particularly the modulation of the energy gap induced by surface and edge functionalization. Furthermore, the interaction of CNT-NiO composites with acetone (C₃H₆O) and carbon dioxide (CO₂) is modeled, revealing a physisorption-dominated mechanism. The adsorption of these gases induces notable changes in the electronic properties and charge distribution within the system, underscoring the potential of CNT-NiO composites for gas-sensing applications. This investigation provides a foundational understanding of the role of metal oxide modifications in tailoring the sensory activity of CNTs toward trace amounts of diverse substances, including metal atoms, inorganic molecules, and organic compounds. The findings suggest that CNT-NiO systems can serve as highly sensitive and selective sensing elements, with potential applications in medical diagnostics and environmental monitoring, thereby advancing the development of next-generation sensor technologies. Full article

Recently, research has increasingly focused on the introduction of non-precious metals and developing highly stable carriers to enhance catalyst performance. In this study, we successfully synthesized copper (Cu)-modified biochar catalysts utilizing a sequential approach involving enzymatic treatment, liquid impregnation, and activation processes, which effectively enhanced the dispersion and introduction efficiency of Cu onto the biochar, thereby reducing the requisite Cu loading while maintaining high catalytic activity. The experimental results showed that the toluene degradation of 10%Cu@BCL was three times higher than that of unmodified activated carbon (AC) at 290 °C. A more uniform distribution of Cu was obtained by the enzymatic and activation treatments, optimizing the catalyst’s structural properties and reducing the amount of Cu on the biochar. Moreover, the transformation between various oxidation states of Cu (from Cu⁰/Cu(I) to Cu(II)) facilitated the electron transfer during the degradation of toluene. To further understand the catalytic mechanisms, density functional theory (DFT) calculations were employed to elucidate the interactions between toluene molecules and the Cu-modified biochar surface. These findings reveal that the strategic modification of biochar as a carrier not only enhances the dispersion and stability of active metal species but contributes to improved catalytic performance, thereby enhancing its degradation efficiency for VOCs in high-temperature conditions. Full article

To mitigate the serious environmental impact caused by the persistent accumulation of plastics, replacing conventional plastics with paper-based alternatives has emerged as a promising trend. In response to the environmental and health concerns associated with petrochemical-based plastic meal boxes and fluorinated water- and oil-repellent agents, this study proposes a sustainable, fluorine-free coating technology based on chitosan to enhance the water and oil resistance of molded-paper pulp meal boxes. By adjusting the degree of deacetylation and the solution concentration of chitosan, coated meal boxes were fabricated via a spraying method. The results demonstrate that coatings prepared with highly deacetylated (>95%) and concentrated (4% w/v) chitosan significantly improve barrier properties, achieving a water contact angle of 114.9° ± 3°, the highest oil-resistance rating (12/12) according to TAPPI standards, and stable resistance to 95 °C hot oil for up to 30 min without leakage. In addition, the coated samples exhibit enhanced mechanical strength (21.26 MPa) and excellent biodegradability. This work provides a cost-efficient and eco-friendly disposable food packaging solution, facilitating the sustainable substitution of petrochemical-based plastics. Full article

Alkali-activated materials, as a low-carbon cementitious material, are widely known for their excellent durability and mechanical properties. In recent years, the modification of alkali-activated materials using biochar has gradually attracted attention. Fibrous biochar has a highly porous structure and large specific surface area, which can effectively adsorb alkaline ions in alkali-activated materials, thereby improving their pore structure and density. Additionally, the surface of the biochar contains abundant functional groups and chemically reactive sites. These can interact with the active components in alkali-activated materials, forming stable composite phases. This interaction further enhances the material’s mechanical strength and durability. Moreover, the incorporation of biochar endows alkali-activated materials with special adsorption capabilities and environmental remediation functions. For instance, they can adsorb heavy metal ions and organic pollutants from water, offering significant environmental benefits. However, research on biochar-modified alkali-activated materials is still in the exploratory phase. There are several challenges, such as the unclear mechanisms of how biochar preparation conditions and performance parameters affect the modification outcomes, and the need for further investigation into the compatibility and long-term stability of biochar with alkali-activated materials. Future research should focus on these issues to promote the widespread application of biochar-modified alkali-activated materials. Full article

Polyaryletherketone (PAEK) materials, including polyetheretherketone (PEEK) and polyetherketoneketone (PEKK), possess excellent mechanical properties and biocompatibility; however, their inherently low surface energy limits effective bonding with resin cements. This study investigated the effects of hydrofluoric acid (HF) etching and handheld nonthermal plasma (HNP) treatment on enhancing the adhesive performance of PAEK surfaces. Disk-shaped PEEK (BP) and PEKK (PK) specimens were divided into four groups: APA (airborne-particle abrasion), PLA (nonthermal plasma treatment), LHF (5.0% HF), and HHF (9.5% HF). Surface characterization was performed using a thermal field emission scanning electron microscope (FE-SEM). Surface wettability was evaluated using contact angle goniometry. Cytotoxicity was evaluated using HGF-1 cells exposed to conditioned media and analyzed via PrestoBlue assays. Shear bond strength (SBS) was measured after three aging conditions—NT (no aging), TC (thermocycling), and HA (highly accelerated aging)—using a light-curing resin cement. Failure modes were categorized, and statistical analysis was performed using one-way and two-way ANOVA with Tukey’s HSD test (α = 0.05). Different surface treatments did not affect surface characterization. PLA treatment significantly improved surface wettability, resulting in the lowest contact angles among all groups, followed by HF etching (HHF > LHF), while APA showed the poorest hydrophilicity. Across all treatments, PK exhibited better wettability than BP. Cytotoxicity results confirmed that all surface treatments were nontoxic to HGF-1 cells, indicating favorable biocompatibility. SBS testing demonstrated that PLA-treated specimens achieved the highest and most stable bond strength across all aging conditions. Although HF-treated groups exhibited lower bond strength overall, BP samples treated with HF showed relatively less reduction following aging. Failure mode analysis revealed a shift from mixture and cohesive failures in the NT aging condition to predominantly adhesive failures after TC and HA aging conditions. Notably, the PLA-treated groups retained mixture failure patterns even after aging, suggesting improved interfacial durability. Among the tested methods, PLA treatment was the most effective strategy, enhancing surface wettability, bond strength, and aging resistance without compromising biocompatibility. In summary, the PLA demonstrated the greatest clinical potential for improving the adhesive performance of PAEK when used with light-curing resin cements. Full article

Despite substantial research on how environmental factors affect fungal diversity, the mechanisms shaping regional-scale diversity patterns remain poorly understood. This study employed ITS high-throughput sequencing to evaluate soil fungal diversity, community composition, and co-occurrence networks across alpine meadows, desert steppes, and alpine shrublands in the southwestern Tibetan Plateau. We found significantly higher fungal α-diversity in alpine meadows and desert steppes than in alpine shrublands. Random forest and CAP analyses identified the mean annual temperature (MAT) and normalized difference vegetation index (NDVI) as major ecological drivers. Mantel tests revealed that soil physicochemical properties explained more variation than climate, indicating an indirect climatic influence via soil characteristics. Distance–decay relationships suggested that environmental heterogeneity and species interactions drive community isolation. Structural equation modeling confirmed that the MAT and NDVI regulate soil pH and carbon/nitrogen availability, thereby influencing fungal richness. The highly modular fungal co-occurrence network depended on key nodes for connectivity. Vegetation coverage correlated positively with network structure, while soil pH strongly affected network stability. Spatial heterogeneity constrained stability and diversity through resource distribution and niche segregation, whereas stable networks concentrated resources among dominant species. These findings enhance our understanding of fungal assemblage processes at a regional scale, providing a scientific basis for the management of soil fungal resources in plateau ecosystems. Full article

With the increasing demand for thermal management in electronic devices, highly efficient and controllable phase change materials have attracted significant attention. The compound 2-amino-2-methyl-1,3-propanediol (AMPD), as a solid–solid phase change material, exhibits remarkable supercooling behavior and a high latent heat storage (ΔH_endo = 247.9 J/g). However, its phase transition kinetics and mechanically triggered properties have not been systematically investigated. In this study, the phase transition behavior of AMPD under different cooling rates and thermal cycling conditions was systematically analyzed using differential scanning calorimetry (DSC). Furthermore, the mechanical triggering characteristic of AMPD under a supercooled state was also studied. The results demonstrated that AMPD can maintain a supercooled state for an extended period, and the exothermic enthalpy change (ΔH_exo) increased by 17.8% (from 154.1 to 181.6 J/g) during thermal cycling. Additionally, mechanical triggering could induce rapid heat release from AMPD, enabling the on-demand regulation of heat utilization. This study revealed that AMPD enables stable supercooling and controllable heat release via thermal or mechanical triggers, offering a novel strategy for tunable solid–solid phase change materials. Full article

Recycling carbon-fiber-reinforced plastics (CFRPs) is crucial for sustainable material utilization, particularly in aerospace applications, where large quantities of prepreg waste are generated. This study investigated the mechanical properties of highly oriented recycled CFRP (rCFRP) molded using vacuum-assisted resin transfer molding (VaRTM), wet-layup, and traditional RTM methods. Recycled carbon fibers (rCFs) obtained via solvolysis and pyrolysis were processed into nonwoven preforms to ensure fiber alignment through carding. The influence of molding methods, fiber recycling techniques, and fiber orientation on mechanical performance was examined through tensile tests, fiber volume fraction (Vf) analysis, and scanning electron microscopy observations. The results indicated that the solvolysis-recycled rCF exhibited superior interfacial adhesion with the resin, leading to a higher tensile strength and stiffness, particularly in the RTM process, where a high Vf was achieved. Wet-layup molding effectively reduced the void content owing to autoclave curing, maintaining stable properties even with pyrolyzed rCF. VaRTM, while enabling vacuum-assisted resin infusion, exhibited a higher void content, limiting improvements in mechanical performance. This study highlights that tailoring the molding method according to the desired performance, such as increasing stiffness potential by enhancing Vf in RTM or improving tensile strength by improving fiber–matrix adhesion in wet-layup molding, is critical for optimizing rCFRP properties, providing important insights into sustainable CFRP recycling and high-performance material design. Full article

High-entropy alloys (HEAs) represent a paradigm-shifting material system offering vast compositional space for tailoring mechanical properties. The yield strength and hardness are critical performance metrics, yet their interrelationships in diverse HEAs remain incompletely understood, partly due to data limitations. This work employs an integrated machine learning framework to investigate the compressive yield strength (σ_y) and hardness (HV) correlation across a dataset of cast HEAs. Random forest models are successfully developed for phase structure classification (accuracy = 92%), hardness prediction (test R² = 0.90), and yield strength prediction (test R² = 0.91), enabling data imputation to expand the analysis dataset. Correlation analysis on the expanded dataset reveals a general positive trend between σ_y and HV (overall Pearson r = 0.75) but highlights a strong dependence on the predicted phase structure. The single-phase BCC alloys exhibit the strongest linear correlation between σ_y and HV (r = 0.88), whereas the single-phase FCC alloys show a weaker linear dependence (r = 0.59), and multiphase alloy systems display varied behavior. The specific ranges of compositional parameters (highly negative mixing enthalpy ΔH, low atomic size difference δ, high mixing entropy ΔS, and intermediate-to-high valence electron concentration VEC) are associated with a stronger σ_y-HV correlation, potentially linked to the formation of stable solid solutions. Furthermore, artificial neural network modeling confirms the varying complexity of the σ_y-HV relationship across different phases, outperforming simple models for some multiphase systems. This work provides robust predictive models for HEA properties and advances the fundamental understanding of the composition- and phase-dependent coupling between yield strength and hardness, aiding rational HEA design. Full article

Sandy red clay, abundant in clay minerals, exhibits a marked sensitivity to variations in water content. Several of its properties are highly prone to deterioration due to wet–dry cycling, potentially leading to slope instability. To investigate the multi-scale deterioration patterns and the underlying chain mechanism of sandy red clay subjected to wet–dry cycles, this study conducted systematic tests on remolded sandy red clay specimens through 0 to 5 wet–dry cycles, with the number of cycles (N) as the variable. The study’s results indicated the following, under wet–dry cycling: (1) Regarding the expansion and shrinking properties, the absolute expansion rate (δ_a) progressively increased, whereas the absolute shrinkage rate (η_a) gradually decreased. Concurrently, the relative expansion rate (δ_r) and relative shrinkage rate (η_r) gradually declined. (2) At the microscale, wet–dry cycles induced significant changes in the microstructure, characterized by increased particle rounding, disrupted stacked aggregates, altered inter-particle contacts, enlarged and interconnected pores, increased number of pores, and a reduction in clay mineral content. (3) At the mesoscale, cracks initiated and propagated. The evolution of cracks undergoes stages of initiation stage, propagation stage, and stable stage, and with the crack rate increasing to 2.0% after five cycles. (4) At the macroscale, the shear strength exhibited a continuous decline. After five cycles, cohesion decreased by as much as 49.6%, whereas the internal friction angle only decreased by 4.3%. This indicates that the loss of cohesion was the primary factor contributing to the strength deterioration. (5) A 19.4% decrease in the slope factor of safety (F_v) occurred after five cycles. This reduction was primarily attributed to the decrease in material cohesion and the upward shift in the potential sliding surface. Under the influence of wet–dry cycles, slope failures typically transitioned from overall or deep sliding to localized or shallow sliding. Full article