Search Results (324)

The formation of carbon nanostructures and silicon carbide (SiC) using a single-source precursor offers a simplified route for material synthesis; however, the factors governing the transition between CNT-like structure formation and SiC growth remain unclear. In this study, the growth behavior of carbon-related structures using vinylsilane was systematically investigated by hot-wall chemical vapor deposition (CVD) on various substrates, including Fe bulk substrates and Fe thin films on SiO₂/Si. CNT-like structures were preferentially formed on Fe bulk substrates, whereas Fe thin-film substrates exhibited CNT-like growth at the initial stage followed by increased Si–C-related phase formation with increasing growth temperature and growth time. In contrast, on Fe thin films with limited catalyst amounts, CNT-like growth occurred initially, followed by increased Si–C-related phase formation with increasing growth temperature and growth time. These observations are consistent with a growth transition associated with the balance between Si uptake into the metal and surface SiC formation processes. By controlling catalyst amount, growth temperature, and growth time, the relative formation of CNT-like structures, SiC-rich coatings, and intermediate morphologies could be tuned within a single process. Furthermore, a SiC/CNT-like composite structure was directly formed on a conductive Fe substrate in a one-step CVD process. Electrochemical measurements showed an enhanced current response compared with a bare Fe substrate, indicating preliminary electrochemical activity and suggesting potential applicability as a high-surface-area electrode platform. Full article

Background: Late-onset preeclampsia (LO-PE) is the most prevalent clinical phenotype of preeclampsia and, although traditionally considered less strongly associated with placental dysfunction than early-onset disease, increasing evidence supports the presence of relevant placental alterations. The extracellular matrix (ECM) is a key regulator of villous architecture, tissue mechanics, trophoblast behavior, vascular remodeling, and angiogenesis. This study aimed to characterize ECM remodeling in placentas from women with LO-PE. Patients and Methods: A prospective observational study was conducted in 111 pregnant women, including 68 with LO-PE and 43 healthy controls. Placental samples were collected immediately after delivery. Gene expression of elastogenesis-related markers, cross-linking enzymes, fibrillar collagens, matrix-remodeling regulators, and endothelial–matrix signaling molecules was assessed by RT-qPCR. Protein expression was evaluated by immunohistochemistry. Differences between groups were analyzed using non-parametric tests with Benjamini–Hochberg correction, and correlations among ECM markers were explored using Spearman analysis. Results: LO-PE placentas showed significantly increased expression of tropoelastin (TE), fibulin-4 (FBLN-4), fibulin-5 (FBLN-5), fibrillin-1 (FBN-1), lysyl oxidase (LOX), lysyl oxidase-like 1 (LOXL-1), collagen type I (COL-I), collagen type III (COL-III), and matrix metalloproteinase-2 (MMP-2) at both gene and protein levels. Conversely, gene and protein expression of tissue inhibitor of metalloproteinase-2 (TIMP-2) and epidermal growth factor-like domain 7 (EGFL7) showed a marked decrease in the placentas of pregnant women with LO-PE. These findings indicate enhanced elastogenesis, increased matrix cross-linking, greater fibrillar collagen deposition, and an imbalance in matrix turnover. Correlation analysis further suggested that, although the FBLN-4/FBLN-5 axis remained preserved, LO-PE placentas displayed partial disruption of the broader ECM transcriptional network. Conclusions: LO-PE placentas exhibit a coordinated but dysregulated ECM remodeling phenotype involving elastic, collagenous, proteolytic, and endothelial–matrix regulatory pathways. These alterations support ECM remodeling as a relevant biological feature of LO-PE placental pathophysiology. Full article

Maintaining a conductive network is essential for achieving high energy density and long-term reliability in lithium-ion batteries. However, its stability is often compromised by structural non-uniformity, and under high-voltage operation, by the oxidative degradation of carbon-based conductive additives. To address these issues, we propose a composite cathode design that combines multi-component electrophoretic deposition (EPD) with a chemically stable Ti₄O₇ conductive oxide. The EPD conditions were systematically investigated, and an applied voltage of 100 V was identified as the standard voltage for controlling electrode loading while avoiding cracking and delamination under severe deposition conditions. The electrochemical performance of the EPD-derived electrodes depended strongly on the Ti₄O₇ content in the initial EPD suspension. Ti-0 and Ti-1, prepared from suspensions containing 0 and 1 wt% Ti₄O₇, respectively, maintained stable capacity delivery over a wide loading range, with areal capacities in good agreement with the theoretical values. In contrast, Ti-5, prepared from a suspension containing 5 wt% Ti₄O₇, exhibited significant capacity degradation and failed under high-loading conditions. High-voltage cycling over 50 cycles and impedance analysis further showed that Ti-1 exhibited better cycling behavior than Ti-0, with less pronounced resistance growth, whereas Ti-5 displayed poor cycling performance. These results suggest that multi-component EPD with an appropriate amount of Ti₄O₇ can provide a balanced hybrid conductive network for improving the relative high-voltage cycling behavior of cathodes within the tested condition. Full article

Regenerated cellulose is a promising tribopositive material for sustainable triboelectric nanogenerators (TENGs), although its electrical output remains sensitive to surface and interfacial properties. In this study, regenerated cellulose was modified using atomic layer deposition (ALD) of Al₂O₃, TiO₂, and ZnO to investigate how nanoscale oxide coatings influence triboelectric performance against a tribonegative PTFE counter layer. Two deposition regimes were examined: 7 ALD cycles, representing the early stage of ALD growth, and 200 cycles, representing a more developed coating regime. Triboelectric measurements, dielectric spectroscopy, structural characterization and contact angle analysis, were used to evaluate how ALD modification influences the electrical response of regenerated cellulose. All ALD-modified samples exhibited increased surface charge density and power output compared to unmodified cellulose, while also showing improved retention of triboelectric performance at elevated relative humidity. The 7-cycle samples consistently outperformed the corresponding 200-cycle coatings under low-humidity conditions, whereas the 200-cycle ZnO sample exhibited the highest humidity stability. No direct correlation between wettability and triboelectric output was observed. The results suggest that relatively small interfacial modifications introduced by ALD are sufficient to influence both the triboelectric response and humidity-dependent charge dissipation behavior of regenerated cellulose. Full article

Mg-based thin films are promising candidates for hydrogen-responsive optical devices. However, their performance is strongly influenced by microstructural evolution during deposition. In this work, Mg thin films were deposited onto glass substrates placed on different substrate-holder materials (Si and 304 stainless steel) to investigate the influence of substrate-holder configuration on microstructure formation. Fluorocarbon (FC)/Pd/Mg multilayer films were subsequently fabricated to evaluate hydrogenation and dehydrogenation behaviors. The results show that the substrate-holder material significantly affects film morphology and hydrogenation performance. Mg films prepared using the Si holder exhibit relatively uniform hexagonal-like surface morphologies, whereas those prepared using the stainless-steel holder show a transition from granular to hexagonal-like morphologies with increasing sputtering power. Hydrogenation measurements reveal that FC/Pd/Mg films prepared using the stainless-steel holder exhibit superior performance, including a reflectance modulation of approximately 70%, a transmittance modulation exceeding 40%, and a hydrogenation time of about 30 s. In contrast, films prepared using the Si holder show reduced optical modulation and slower hydrogenation kinetics. The observed differences in hydrogenation behavior are closely correlated with variations in film microstructure induced by different substrate-holder configurations. The results suggest that substrate-holder-dependent growth conditions may influence defect formation and hydrogen diffusion pathways in Mg-based thin films. This study highlights the importance of substrate-holder configuration as a processing parameter affecting microstructure evolution and hydrogen-responsive performance in FC/Pd/Mg multilayer films. Full article

This work reports the combination of pentagonal grain morphology, high phase purity, and non-monotonic thermal conductivity behavior over a wide temperature range (25–1200 °C). The SrZrO₃ coatings with different processing parameters are deposited using atmospheric plasma spraying (APS). Unlike conventional atmospheric plasma-sprayed oxide coatings, distinct pentagonal-shaped grains with multi-directional orientation suggest a unique solidification pathway and anisotropic growth mechanism. The pentagonal morphology may come from the impingement of five radially columnar grain sectors during rapid solidification of a highly undercooled melt splat, constrained by local thermal gradients. This atypical morphology, not commonly reported for SrZrO₃ coatings, is further supported by electron backscatter diffraction (EBSD) results, which confirm a remarkably high phase fraction (~94.5%) of SrZrO₃ despite rapid quenching inherent to APS processing. The combination of high phase purity and unusual grain geometry represents a significant advancement in tailoring the microstructures of environmental barrier materials. Moreover, the non-linear thermal conductivity response with temperature shows a pronounced decrease up to ~800 °C (0.737 W·m⁻¹·K⁻¹) stabilization between 800 and 900 °C, and a subsequent increase at higher temperatures. This behavior indicates a complex interplay between phonon scattering, defect structures, and possible radiative heat transfer contributions at elevated temperatures. Full article

Nickel ferrite (NiFe₂O₄) is one of the most studied inverse-spinel ferrites because it combines moderate saturation magnetization, comparatively high electrical resistivity, chemical stability, and broad synthesis flexibility. Yet the literature shows that the measured structure and magnetism of NiFe₂O₄ are not intrinsic constants; they evolve strongly with dimensionality, size, thickness, strain state, cation distribution, surface spin disorder, and synthesis pathway. This review develops a unified theoretical and literature-based interpretation of how dimensionality reshapes the structural and magnetic behavior of NiFe₂O₄ across bulk ceramics, nanoparticles, one-dimensional nanostructures, polycrystalline thin films, and ultrathin epitaxial films. The review is anchored in the two uploaded nickel ferrite attachments and expanded using internet-sourced journal literature on spinel inversion, surface effects, mechanochemical synthesis, sputtered and pulsed laser deposited thin films, and epitaxial ultrathin-film anomalies. The central novelty of this article is the formulation of a dimensionality-dependent framework in which the observed magnetic response is governed by a competition among three coupled factors: (i) the cation-distribution function, which controls the A–B superexchange balance and therefore the net ferrimagnetic moment; (ii) the microstructural coherence function, which measures how crystallinity, strain, defects, and anti-phase boundaries preserve or degrade exchange continuity; and (iii) the surface/interface spin-order parameter, which quantifies the loss or reconfiguration of magnetic order at free surfaces and buried interfaces. Within this framework, bulk NiFe₂O₄ behaves as a near-equilibrium inverse spinel with relatively stable magnetization, whereas nanoscale NiFe₂O₄ experiences strong spin canting and finite-size suppression due to the growing fraction of disordered surface spins. Thin films introduce a distinct regime in which strain, texture, anti-phase boundaries, substrate mismatch, and growth kinetics determine both anisotropy and magnetization. In ultrathin epitaxial films, off-equilibrium cation redistribution and interface-controlled electronic reconstruction may even generate magnetization values far above bulk expectations. The review also compares major synthesis routes—solid-state reaction, sol–gel, co-precipitation, hydrothermal growth, reactive milling, combustion, pulsed laser deposition, and radio-frequency sputtering—and explains why each route biases the final dimensionality-dependent properties differently. A set of word-style equations is provided to formalize spinel inversion, finite-size suppression, anisotropy scaling, coercivity trends, and superparamagnetic crossover. Beyond summarizing the field, the review proposes a regime map linking dimensionality to characteristic structural defects and magnetic signatures, and it identifies unresolved questions concerning the true origin of enhanced magnetization in ultrathin NiFe₂O₄, the interplay between anti-phase boundaries and strain, and the distinction between intrinsic inversion changes and extrinsic substrate artifacts. The resulting article offers a submission-ready, originality-focused review that positions dimensionality as the master variable governing structure–magnetism correlations in nickel ferrite. Full article

Fluorocarbon (FC)/Pd/Mg multilayer thin films have attracted considerable attention as hydrogen-responsive optical materials. However, their performance is strongly limited by interfacial instability and structural degradation during deposition and hydrogen cycling. In this study, Pt/FC/Pd/Mg multilayer thin films were obtained during focused ion beam (FIB) sample preparation, and transmission electron microscopy (TEM) was employed to investigate the FC layer–mediated interfacial effects. The results reveal that Pt deposition on FC leads to the formation of a confined nanocrystalline interfacial region accompanied by a reduced apparent FC thickness and the development of a Pt–FC intermixing zone. This behavior indicates that the FC layer functions as a “soft landing” medium, dissipating kinetic energy and modifying nucleation and growth behavior. Motivated by this finding, the mechanical properties of FC films and their influence on hydrogen-cycling performance in FC/Pd/Mg/FC structures are further examined. The hardness of FC layers can be tuned from 3.03 MPa to 42.8 MPa by adjusting sputtering parameters. Hydrogen-cycling experiments reveal a strong and non-monotonic dependence on FC mechanical properties. When the FC buffer layer is relatively hard, the initial hydrogenation kinetics are improved; however, prolonged cycling leads to poor adhesion and interfacial degradation. In contrast, when the FC buffer layer is soft, hydrogenation kinetics degrade rapidly during cycling, while long-term interfacial adhesion and structural integrity are significantly improved. These results demonstrate a dual and competing role of FC layers in governing hydrogen transport and mechanical stability, highlighting a critical trade-off for the design of durable hydrogen-responsive multilayer thin films. Full article

Zinc oxide (ZnO) nanoparticles have attracted increasing attention in wood science due to their multifunctional properties, including antimicrobial activity, UV absorption, and photocatalytic behavior. Water-based deposition protocols offer clear advantages yet typically struggle with nanoparticle aggregation and limited adhesion to lignocellulosic substrates. This work introduces a rapid and scalable waterborne protocol combining catalyst-free aqueous seeding with microwave-assisted (MWA) growth under mild conditions. Pinus pinaster veneer samples were treated via dip-coating and spraying, with single and double seeding cycles, followed by MWA growth. Protocol efficiency was assessed through ZnO retention, SEM, and EDS analysis, while the impact of the substrate was assessed via mechanical testing, ATR-FTIR spectroscopy, and colorimetry. Dip-coating achieves significantly higher precursor uptake than spraying, while repeated seeding cycles further increase ZnO loading. Results suggest that incorporation may proceed through zinc–carboxylate bonds within the wood matrix, followed by localized ZnO nanostructures development. The effective integration did not weaken the mechanical properties, while color changes were significant for dip-coated samples and noticeable for sprayed ones. Overall, this methodology provides a fast, water-based, and minimally invasive route for ZnO incorporation into wood and a scalable pathway with retained mechanical and chemical properties and limited visual impact. Full article

To address the uneven deposition of zirconium conversion coatings on multiphase 55AlZnMg under short pretreatment cycles, this study investigated the time-dependent formation behavior of ZrCC in a selected H₂ZrF₆ bath. By precisely controlling the immersion time (20–90 s) and utilizing SEM-EDS and AFM characterization techniques, this study systematically revealed the growth kinetics and film-forming mechanisms of ZrCC on complex alloy surfaces. The results indicate that the Zn-rich phase on the surface of the 55AlZnMg coating, due to its relatively positive potential, preferentially induces the deposition of the film-forming material. Subsequently, dealloying occurs in the Al-rich phase and the Mg/Zn enriched regions, forming Zn-enriched regions that promote the continuous deposition of the film-forming material, ultimately achieving complete surface coverage; the film morphology evolves from an initial needle-like structure to a network structure, eventually forming a nanosheet structure. The film-forming process of ZrCC on the 55AlZnMg substrate surface is primarily driven by selective growth, with electrochemical properties of the alloy phases, significantly enhancing adhesion between the aluminum-zinc-magnesium coating and the overcoat and providing practical guidance for improving surface uniformity and interfacial adhesion of Al-Zn-Mg-coated steel. Full article

The interfacial behavior of hybrid nanoparticles on biological substrates governs their functional performance. Here, we investigate how surface properties and colloidal stability dictate the pH-dependent adhesion of oxybenzone-loaded palygorskite nanohybrids to hair—a model biological interface. A series of hybrids with 5–50% oxybenzone loadings were prepared via melt impregnation. XRD and FTIR analyses confirm hydrogen bonding between oxybenzone and palygorskite, forming stable organic–inorganic hybrids. The colloidal stability of these nanohybrids varies non-monotonically with oxybenzone loading, governed by surface hydrophilicity and zeta potential, exhibiting a network-like behavior upon pH change. Optimal stability is achieved at an intermediate loading with a favorable balance of surface properties. While pristine hybrids show no affinity for hair, surface modification with cationic polyquaternium-7 (PQ-7) or non-ionic polyvinylpyrrolidone (PVP) enables effective deposition through distinct pH-dependent mechanisms: PQ-7 operates optimally at pH 10 via electrostatic attraction, whereas PVP performs best at pH 4 through hydrogen bonding, forming a protective coating layer on the hair surface. Deposition fails for PVP-modified hybrids at 50% loading due to excessive surface hydrophobicity. The deposited hybrids provide exceptional UV protection, significantly mitigating cuticle damage, suppressing photo-yellowing, and minimizing protein oxidation. Among the hybrids, hybrid-35 exhibited the best colloidal stability, whereas PQ-7-modified hybrid-50 gave the highest UV protection (color difference ΔE reduced from 10.51 to 1.60). The adhesion rates of the two best-performing hybrids were 2.70% and 2.85%, respectively. Beyond hair protection, we evaluate the environmental interface of these materials. While free oxybenzone is highly toxic to Chlorella vulgaris, hybridization drastically reduces its ecotoxicity. Remarkably, palygorskite and the hybrids promote algal growth, likely by acting as nutrient adsorbents and attachment sites. This work provides fundamental insights into particle–biointerface interactions and offers a strategy for designing functional hybrid materials with tailored surface properties for bio-related applications. Full article

Developing zinc oxide-based nano-bactericides as alternatives to conventional chemical bactericides for controlling rice bacterial diseases has become a major research focus. In this study, ZnO nanoparticles were initially surface-modified and subsequently covalently conjugated with chitooligosaccharide (COS) via imine bonds to get a pH-responsive zinc oxide–chitooligosaccharide (ZnO–COS) delivery system. A series of physicochemical characterizations, including FTIR, UV-vis, XRD, and TGA, confirmed the successful synthesis of ZnO–COS NPs. Building on this foundation, the pH-responsive release behavior, foliar deposition performance, antibacterial activity, and biosafety of the nanoparticles were systematically investigated. The prepared ZnO–COS NPs exhibited pronounced acid-triggered Zn²⁺ release, together with enhanced wettability, spreadability, and retention on rice leaf surfaces, owing to COS incorporation. In both in vitro and in vivo assays against Xanthomonas oryzae pv. oryzae (Xoo), ZnO–COS NPs demonstrated effective antibacterial activity associated with bacterial cell damage and the activation of antioxidant defense responses in plants. Consequently, ZnO–COS NPs achieved a preventive efficacy of 56.0% against rice bacterial blight, surpassing those of ZnO (33.3%) and COS (14.3%). Furthermore, safety assessment confirmed the good biocompatibility of ZnO–COS NPs towards rice seed germination and seedling growth. In summary, the synthesised ZnO–COS NPs integrated pH-responsive release, improved foliar deposition, and enhanced antioxidant capacity of rice, offering a promising strategy for mitigating bacterial diseases in rice. Full article

Diabetic foot ulceration is a severe and common chronic complication of diabetes, accompanied by excessive reactive oxygen species (ROS) accumulation, persistent bacterial infection, prolonged inflammation, and insufficient angiogenesis. Traditional single-function wound dressings fail to simultaneously resolve these pathological barriers, leading to unsatisfactory healing outcomes. In this study, we developed a multifunctional composite hydrogel (E/MGel) by introducing mussel adhesive protein (MAP) into methacrylated hyaluronic acid (mHA) to construct an antibacterial and antioxidant delivery system, which was further loaded with epidermal growth factor (EGF) to promote angiogenesis. The as-prepared E/MGel exhibited a uniform porous structure, favorable rheology, high swelling ratio, and sustained protein release behavior. In vitro results demonstrated that E/MGel exerted potent antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA) and Escherichia coli (E.coli), high ROS scavenging efficiency, good cytocompatibility, and remarkable pro-angiogenic effect on endothelial cells. In a mouse model of diabetic MRSA-infected full-thickness skin defect, E/MGel significantly accelerated wound closure, reduced bacterial burden, downregulated pro-inflammatory cytokines, promoted collagen deposition, and enhanced neovascularization. Meanwhile, no obvious systemic toxicity was observed. Taken together, this multifunctional hydrogel integrates antibacterial, antioxidant, and pro-angiogenic capacities to break the pathological vicious cycle of diabetic wounds, providing a promising and safe strategy for the clinical treatment of diabetic infected wounds. Full article

Polymer-engineered MXene composites have emerged as a versatile materials platform for electrochemical energy storage, offering a means to address key limitations associated with ion transport, structural instability, and interfacial reactivity. This review provides a unified perspective on how polymer integration modifies the structure–transport–stability relationships of MXene-based systems across Na-ion batteries, aqueous Zn-ion batteries, and supercapacitors. In Na-ion systems, polymer-mediated interlayer engineering and porosity control improve ion accessibility and mitigate diffusion limitations arising from the large ionic radius of Na⁺. In aqueous Zn-ion systems, polymer electrolytes and interfacial layers regulate Zn²⁺ solvation and deposition behavior, suppressing dendritic growth and parasitic reactions. In supercapacitors, polymer–MXene hybrids establish coupled ionic–electronic transport pathways and mechanically compliant architectures, enabling stable electrochemical performance under high-rate and deformable conditions. Particular emphasis is placed on the underlying mechanisms responsible for suppressing oxidation, preserving structural integrity, and extending cycle life, including interfacial passivation, desolvation regulation, and structural confinement. These coupled effects govern long-term electrochemical stability across different energy storage systems. Finally, recent advances in operando characterization, data-driven materials design, and scalable processing are discussed in the context of future development. By linking material design strategies to fundamental mechanisms, this review outlines a coherent framework for the rational development of polymer–MXene composites toward practical energy storage applications. Full article

In this study, cathodic arc deposition was employed to synthesize CrAlN/TiSiN nanostructured multilayer coatings on silicon wafer substrates. The effects of the multilayer architecture on the microstructure and corrosion resistance of the coatings were systematically investigated. The structural characteristics and performance of the deposited films were analyzed using scanning electron microscopy (SEM), energy-dispersive spectroscopy (EDS), X-ray diffraction (XRD), and electrochemical polarization measurements. The experimental results demonstrate that various CrAlN/TiSiN multilayer configurations were successfully deposited, forming dense multilayer coatings with a thickness of approximately 1–2 μm and a dominant FCC β₁-NaCl crystalline structure. The presence of nanostructured multilayer interfaces effectively inhibited columnar grain growth and contributed to microstructural refinement. XRD analysis revealed competitive growth between the (111) and (200) crystallographic orientations, indicating that the crystallization behavior is influenced by the interplay between surface energy minimization and strain energy accumulation. Contact angle measurements showed that all the coatings exhibited water contact angles exceeding 90°, indicating hydrophobic characteristics and potential anti-fouling capacity. In particular, the CrAlN outer layer structure presented lower surface free energy, which further enhances the coating system’s anti-fouling capacity. Electrochemical polarization results indicate that the corrosion current density of all the coatings remained in the order of 10⁻⁷ A/cm², demonstrating excellent chemical stability. Overall, the CrAlN/TiSiN nanostructured multilayer coatings exhibit pronounced interface strengthening and densification growth mechanisms, which effectively enhance the chemical stability of silicon-based material surfaces. These results could provide valuable insights for the structural design and optimization of high-performance protective coatings. Full article