Search Results (930)

Driven by the growing demand for functional textiles featuring excellent waterproofness, moisture permeability and mechanical robustness in outdoor sportswear, medical protection and technical apparel, traditional pongee—despite its desirable softness, high wrinkle resistance and good stability as an ideal substrate fabric—is severely restricted in further application by its intrinsically poor hydrostatic pressure resistance in extremely wet environments. Accordingly, we developed a modified waterborne polyurethane (WPU) coating for pongee substrates to fabricate functional textiles that maintain high hydrostatic pressure resistance while possessing good mechanical properties and increased UV absorption. In this study, by using the sol–gel method, an amorphous silicon dioxide (SiO₂) coating layer was constructed on the surface of titanium dioxide (TiO₂) particles, forming silica-modified titania particles (SiO₂/TiO₂). These SiO₂-modified particles were subsequently physically blended with an anionic waterborne polyurethane system that had been previously modified with a polyester-type modifier A to enhance its hydrostatic pressure resistance. The resulting composite coating was designed to combine the high hydrostatic pressure resistance inherited from the modified WPU matrix, the mechanical reinforcement and increased UV absorption contributed by SiO₂/TiO₂, and satisfactory water repellency on fabric substrates. The results indicate that the incorporation of an appropriate amount of modifier A into the prepolymer system significantly enhances hydrostatic pressure resistance while maintaining high elongation at break. At a SiO₂/TiO₂ loading of 0.2 wt%, the composite film exhibits optimal comprehensive performance, characterized by superior mechanical properties, low water absorption, and static water contact angles exceeding 100° for coated fabrics. SiO₂/TiO₂ composite WPU coatings substantially improve hydrostatic pressure resistance across various fabrics, with 380T polyester taffeta demonstrating the best performance. This resistance remains remarkably stable after standard washing, indicating excellent wash fastness and practical applicability. Full article

Laser-induced damage of sol–gel SiO₂ antireflection coatings remains a key reliability issue in high-power laser systems because porous networks, residual hydroxyl groups, and defect-related absorption centers can trigger localized heating and stress concentration under nanosecond irradiation. In this work, continuous-wave CO₂ laser conditioning was used as a localized post-treatment method to regulate the microstructure of sol–gel SiO₂ coatings on fused silica substrates. The revised manuscript clarifies the processing window, scanning parameters, laser damage testing protocol, and the sample-specific nature of the reported LIDT values. Laser conditioning induces partial densification of the porous coating, dehydration of Si-OH groups, relaxation of the Si-O-Si network, and enhancement of mechanical properties. Under the optimized conditioning condition, the surface roughness decreases from 14.08 nm to 9.76 nm, and the LIDT at 1064 nm increases from 4.8 J/cm² to 7.0 J/cm². The LIDT values are discussed as a relative microstructure–property comparison for the present coating system rather than as the upper technological limit of sol–gel silica coatings. Combined FTIR analysis, thermal simulation, morphology observation, and damage probability analysis indicate that the improvement originates from the combined effects of reduced defect absorption, moderated porosity, improved heat dissipation, and enhanced resistance to thermally induced cracking. The results provide a mechanism-guided strategy for using CO₂ laser conditioning to tune sol–gel silica coatings while also identifying the need for further validation on higher-LIDT coatings and at application-relevant wavelengths. Full article

SiO_x anodes are highly promising for next-generation lithium-ion batteries due to their superior theoretical capacity. However, issues such as drastic volume expansion and low initial Coulombic efficiency (ICE) impede their practical use. While macroporous architectures can mitigate these challenges, traditional fabrication often depends on tedious hard templating methods and significant organic solvent consumption. In this work, we report a sustainable, emulsion-self-templated and organic solvent-free strategy to synthesize a carbon-coated 3D macroporous SiO_x/C composite (3DM-SiO_x/C@C). Our approach uniquely integrates radical polymerization with a water-in-oil emulsion and sol–gel process, followed by chemical vapor deposition (CVD). The 3D macroporous framework is generated via in-situ emulsion droplets acting as self-templates, effectively eliminating the need for external sacrificial templates and toxic etchants. Notably, this organic solvent-free process achieves an exceptional precursor to (precursor + organic solvent) mass ratio of 1.0, contrasting sharply with conventional methods (0.0044–0.17). The resulting hierarchical structure, characterized by interconnected macropores and a uniform carbon coating, significantly enhances structural integrity and electronic conductivity. Electrochemical evaluations reveal that 3DM-SiO_x/C@C exhibits an improved ICE of 74.32% and long-term cycling stability even at a high current density of 1.0 A g⁻¹ compared to non-porous and uncoated counterparts. This integrated synthesis offers a green and scalable pathway for developing high-performance silicon-based anodes for large-scale energy storage. Full article

Lithium-ion batteries require cathode materials with high capacity and cycling stability. Li₃V₂(PO₄)₃ (LVP) offers a theoretical capacity of 197 mAh/g but suffers from poor electronic conductivity. In this study, a Li₃V₂(PO₄)₃/carbon (LVP/C) composite was synthesized via a citric acid-assisted sol–gel method. The effects of pyrolysis temperature (700–1000 °C) and citric acid-to-salt ratio (1:1, 0.5:1, 0.25:1) were systematically investigated. The optimal composite was obtained at 900 °C with a 1:1 ratio. This material exhibited a well-crystallized monoclinic structure (space group P2₁/c) with unit cell volume of 890.61 ų. The amorphous carbon coating provided a specific surface area of 33.03 m²/g. Electrochemically, the optimal LVP/C_1:1 composite delivered an initial specific capacity of 114 mAh/g at C/10 rate—twice that of samples with lower carbon content. It also demonstrated 100% capacity retention after 25 cycles with favorable coulombic efficiency (67%) and reduced charge-transfer resistance. These results show that pyrolysis at 900 °C with a 1:1 citric acid-to-salt ratio provides an optimal balance between crystallinity, carbon coating uniformity, and electrochemical performance for high-performance LVP/C composite cathodes. Full article

Cobalt-free Li-rich Mn-based layered oxides are promising cathode materials for next-generation lithium-ion batteries because of their high capacity and reduced reliance on cobalt resources. However, their practical application is still limited by low initial Coulombic efficiency, sluggish reaction kinetics, severe voltage decay, and progressive structural degradation during cycling. In this work, a Na-assisted sol–gel strategy was developed to construct a cobalt-free Li-rich Mn-based cathode with multiple twin boundaries, and the optimized sample with the composition of Li_1.13Na_0.06Mn_0.594Ni_0.219O₂ was denoted as SG-TB. Unlike conventional surface coating or elemental doping, this strategy focuses on regulating the bulk crystal framework through crystallographic defect engineering. Structural characterizations indicate that SG-TB contains repeatedly distributed twin-boundary-related interfaces, supporting the presence of multiple twin boundaries within the layered cathode. Benefiting from this structural feature, SG-TB delivers an initial Coulombic efficiency of 96%, an initial discharge capacity of 256 mAh/g, a discharge capacity of 167 mAh/g at 5 C, and a capacity retention of 77% after 200 cycles at 1 C. Further analyses suggest that the multiple twin boundaries help reduce electrochemical polarization, enhance Li⁺ diffusion kinetics, and improve structural retention during cycling. This work demonstrates that Na-assisted multiple twin-boundary engineering is an effective strategy for improving the reaction reversibility and structural stability of cobalt-free Li-rich Mn-based cathodes. Full article

As anodized aluminum components are increasingly deployed in high-power optical and precision industrial systems operating in non-vacuum environments, their outgassing behavior has emerged as a critical material reliability concern. In contamination-sensitive optical assemblies, released volatiles can accumulate on nearby surfaces, leading to haze formation, scattering, and progressive optical degradation. The porous anodic oxide layer retains water, hydrogen, dyes, and processing residues that are released under thermal, photonic, and environmental stresses typical of industrial operation. While most qualification data remain vacuum-centric, equivalent evaluation frameworks for ambient environments are limited. This review analyzes surface-driven desorption mechanisms relevant to non-vacuum systems and provides practical guidance for material and process engineers by evaluating mitigation strategies across the anodizing process chain, including fine-grain substrate selection, controlled anodizing with nickel acetate sealing, post-bake stabilization, and alternative dense coatings such as electroless nickel, sol–gel films, and Acktar. The analysis underscores the need for non-vacuum-specific qualification standards to support reliable material selection and long-term system performance. Full article

Hafnia (hafnium oxide) nanostructures, both unmodified and silica-modified with minor and major silica content, were synthesized using an adapted sol–gel method with D-L tartaric acid as an internal template. After thermal treatment, structural non-stoichiometry and light absorptive properties were identified in the resulting hafnium-based nanostructures, indicating their potential for various applications, including photocatalysis. The ability of these materials to photogenerate reactive oxygen species (ROS), namely superoxide anion radicals (•O₂₋) under simulated solar light (AM 1.5) and singlet oxygen (¹O₂) under visible light (λ > 390 nm), was evaluated and monitored by UV–Vis and photoluminescence spectroscopy. Functionalization of hafnium-based oxides with protoporphyrin IX was employed to enhance singlet oxygen photogeneration. The reactivity of the generated (¹O₂) was assessed by quenching of DL α-tocopherol photoluminescence under visible light irradiation. Photocatalytic experiments conducted under anaerobic conditions demonstrated the ability of the hafnia-based nanostructures to reduce 1,4-benzoquinone (BQ) to 1,4-hydroquinone (H₂Q). Furthermore, embedding the hafnia-based powders into polyvinyl alcohol hydrogels enabled the obtainment of photoactive coatings on glass substrates, for which their mechanical properties were evaluated using force–distance spectroscopy measurements. Morphological and structural characterization of the materials was performed using scanning electron microscopy (SEM), scanning transmission electron microscopy (STEM), atomic force microscopy (AFM), X-ray diffraction and fluorescence (XRD, XRF), X-ray photoelectron spectroscopy (XPS), N₂ adsorption–desorption measurements, UV–Vis spectroscopy, photoluminescence (PL) spectroscopy, and zeta potential measurements. These investigations revealed that adding silica induces significant modifications in the morphology, texture, and structure of the hafnia, thereby enhancing the functional properties of the resulting materials. Full article

CuO thin layers were synthesized using the sol–gel method and deposited onto glass substrates through the dip-coating technique. The impact of annealing temperatures on the structural, optical, and electrical characteristics of the developed CuO thin layers was comprehensively assessed through X-ray diffraction, UV–visible spectrophotometry, and four-point techniques, respectively. X-ray diffraction analysis revealed the formation of CuO thin layers with a distinctive monoclinic tenorite phase structure. The UV–visible spectrophotometer results demonstrated a decrease in transmittance from approximately 30% to about 7% as the annealing temperature increased from 200 °C to 400 °C. The semiconducting properties exhibited temperature-dependent variations, with the band gap narrowing from 1.70 to 1.48 eV as the temperature increased from 200 to 400 °C. Additionally, the electrical conductivity of the CuO layers exhibited a significant increase from 48 to 61 S.m⁻¹ over the same temperature range. Collectively, the findings suggest that an annealing temperature of 400 °C is optimal for achieving well-crystallized CuO layers with desirable characteristics, including high absorbance, low transmittance, a reduced energy band gap, and enhanced electrical conductivity. These results underscore our ability to manipulate CuO properties, offering insights for tailoring them to meet specific requirements, particularly in the context of gas sensor applications. Full article

Self-powered photodetectors have attracted widespread attention in Internet of Things applications due to their low power consumption and high sensitivity. In this study, plasmonic self-powered poly(3-hexylthiophene)/zinc oxide (P3HT/ZnO) heterojunction photodetectors incorporating silver triangular nanoplates (AgTNPs) were fabricated using sol–gel and spin-coating techniques. The experimental results demonstrate that the incorporation of AgTNP nanostructures significantly enhances the photoelectric conversion efficiency of the plasmonic P3HT/AgTNPs/ZnO photodetectors across both the ultraviolet and visible spectral regions. The responsivity enhancement ratio of the plasmonic devices reached its maximum under illumination at a wavelength of 525 nm. Compared with the reference P3HT/ZnO device, the responsivity values of the P3HT/AgTNPs-1/ZnO and P3HT/AgTNPs-2/ZnO devices increased by factors of 3.24 and 4.21, respectively. The optimal P3HT/AgTNPs-2/ZnO device exhibited responsivity values of 9.49, 10.80, and 10.47 mA/W under irradiation at wavelengths of 440 nm, 460 nm, and 525 nm, respectively. The mechanism of performance enhancement induced by the plasmonic AgTNPs is also discussed. This work demonstrates that embedding triangular plasmonic metal nanoplates within semiconductor heterojunctions constitutes an effective strategy for performance enhancement, providing new insights for the rational design of high-performance optoelectronic devices. Full article

Mg-doped ZnO (Zn_1−xMg_xO, x = 0.00–0.05) thin films were successfully grown on glass substrates with a c-axis orientation at 600 °C using the sol–gel dip-coating technique. The structural features, defect-related photoluminescence, and optical constants of the films were systematically investigated as a function of Mg concentration. X-ray diffraction (XRD) patterns confirmed a single-phase hexagonal wurtzite structure with a preferential (₀₀₂) orientation for all compositions, indicating the successful substitution of Mg²⁺ ions into the ZnO lattice. The crystallite size (D₀₀₂) was found to vary between 28.49 and 41.18 nm, while microstrain and stress exhibited non-monotonic behavior depending on Mg content. This behavior reveals a transition from compressive to tensile stress due to lattice distortion and defect formation. Photoluminescence (PL) spectra showed a dominant near-band-edge (NBE) ultraviolet emission, along with broad visible emissions extending from violet to red. Optical constants were accurately extracted using a double-facet-coated substrate (DFCS) model, combined with nonlinear curve fitting using the Nelder–Mead optimization algorithm. The films showed a strong absorption edge at about 370 nm and exceptional optical transparency (≈60–80%) in the visible spectrum. The systematic blue shift in the extinction coefficient with increasing Mg content confirms bandgap engineering in Zn_1−xMg_xO thin films. The refractive index dispersion was successfully modeled using the Cauchy relation, demonstrating composition-dependent tunable optical properties. Depending on the Mg content, the optical bandgap values ranged from approximately 3.265 to 3.315 eV. The band-edge states and optical constants are strongly affected by the combined effects of defect development, Mg-induced lattice distortion, and changes in optical dispersion. These results indicate that sol–gel-derived Mg-doped ZnO thin films with composition-dependent stress states, defect states, and tunable optical properties are promising candidates for UV photodetectors, optical coatings, and transparent optoelectronic devices. Full article

Stone heritage deteriorates through physical, chemical, and biological processes driven by water, climate, and microbial colonization. Multifunctional polymeric coatings combining hydrophobic and antimicrobial moieties have emerged as a promising conservation strategy, yet a substantial gap remains between laboratory innovation and real-world performance. This review critically examines advances from 2021 to 2026, covering wetting theory, antimicrobial mechanisms, and material architectures, including molecularly integrated systems, Sol–Gel hybrids, nanocomposites, and layered systems. Long-term studies on the Aurelian Walls in Rome and stone in Reims show that biocidal efficacy typically declines within one to two years despite the chemical persistence of the coatings. In parallel, hydrophobic performance often deteriorates over time due to UV exposure, particulate deposition, and surface chemical changes, leading to increased wettability and reduced protective efficiency. Substrate porosity governs durability and visual compatibility (ΔE* < 5 threshold), while treatments can reshape microbial communities, favoring stress-tolerant meristematic fungi. Regulatory pressure on fluorinated compounds drives the development of more sustainable alternatives. Emerging directions include stimuli-responsive systems, self-healing materials, slippery interfaces, and precision polymer architectures. However, future progress will depend on tailoring formulations to major lithotypes, improving compatibility with porous substrates, and validating performance through standardized accelerated aging and multi-year field trials. Bridging laboratory design with environmental exposure data and conservation practice will be essential for achieving durable and culturally acceptable protection strategies. Full article

Thin-film cobalt oxides have attracted increasing attention due to their visible-light activity and potential environmental applications. In this work, Co₃O₄ coatings were prepared on glass substrates through a sol–gel dip-coating process followed by thermal treatment at 450, 500, and 550 °C. Structural characterization was carried out using X-ray diffraction (XRD) and Raman spectroscopy. Diffraction patterns, together with the Raman spectra, indicate the formation of the cubic spinel phase of Co₃O₄, while sharper diffraction peaks appeared at higher annealing temperatures, indicating improved crystallinity of the films. Surface morphology was analyzed by scanning electron microscopy (SEM) and atomic force microscopy (AFM). SEM observations revealed continuous polycrystalline coatings, whereas AFM measurements showed clear variations in surface topography and roughness produced by thermal treatment. Wettability measurements obtained from contact angle (CA) analysis indicate modifications in the surface properties of the films as the annealing temperature changes. Optical characterization performed by ultraviolet–visible spectroscopy (UV–Vis) showed strong absorption in the visible region with an indirect band gap close to 1.58 eV. Photocatalytic activity was evaluated through the degradation of methylene blue under visible-light irradiation. Degradation efficiencies of approximately 93.9%, 97.4% and 98.7% were obtained after 5 h for films annealed at 450, 500, and 550 °C, respectively. Full article

Since their discovery in 2009, perovskite solar cells (PSCs) have demonstrated rapid progress. Ambient-processed, carbon-based PSCs utilizing a pre-heating step offer a cost-effective fabrication route. Nevertheless, the role of the compact titanium dioxide (TiO₂-c) layer in ambient conditions has remained under-explored and inconsistently reported in the literature. This study then investigated the impact of TiO₂-c layer thickness, ranging from 70 nm to 155 nm, on the performance of PSCs fabricated entirely in ambient air with high relative humidity (RH > 70%). The layers were deposited via the sol-gel spin-coating method. Experimental results then revealed that the thinnest layer (70 nm) yielded the lowest average power conversion efficiency (PCE) of 2.05% due to diminished J_sc and V_oc values. The optimized TiO₂-c thickness was also identified at 95 nm, achieving an average PCE of 2.95% and a peak efficiency of 4.5%. Structural analysis via XRD confirmed the presence of both anatase and brookite phases. Notably, increasing the thickness from 70 nm to 155 nm resulted in a slight reduction in the anatase peak and a corresponding increase in the brookite peak. The superior performance at 95 nm could be attributed to a balanced crystal intensity between these two phases. Furthermore, TiO₂-c thickness was found to correlate with larger aggregate formation, better uniform shape grains, and reduced surface roughness, significantly influencing the morphology of the subsequent mesoporous TiO₂-m layer. These findings then provided critical insights into how thickness variation in the TiO₂-c layer could influence the performance of ambient-processed carbon-based PSCs. Full article

Selenium nanoparticles (SeNPs) represent promising bioactive agents due to their reduced toxicity and multifunctional biological properties. In this study, SeNPs were synthesized via an eco-friendly phytosynthesis approach using Curcuma longa extract, yielding curcumin-functionalized selenium nanoparticles (cur–SeNPs). The composites (cur–SeNPs), either in native extract form or isolated, were incorporated into siloxane hybrid matrices prepared by the sol–gel method from tetraethyl orthosilicate: dimethyldimethoxysilane precursors, with polyvinylpyrrolidone (PVP) as a structural modifier. The host matrices were differentiated by the ratios between the precursors of the siloxane network, 3:1 for CS0–CS4, respectively, 1:1 for CS5, modified with PVP in the case of CS2 and CS3. These were loaded with cur–SeNPs–T in the cases of CS1, CS2, CS5 or with cur–SeNPs for CS3 and CS4. FTIR, XRD, SEM, and EDX analyses confirmed the formation of amorphous siloxane networks with well-dispersed SeNPs (up to ~12 wt%). PVP incorporation generated ordered mesoporous structures, increasing total pore volume sixfold and enlarging the average pore diameter to 9.26 nm. Studies about selenium ion release demonstrate that mesoporosity significantly enhances diffusion-controlled release. Antimicrobial assays against Staphylococcus aureus, Escherichia coli, and Candida albicans reveal a synergistic effect between curcuminoids and SeNPs, particularly in matrices with higher nanoparticle loading. The sol–gel technique for obtaining hybrid materials is very versatile regarding the supports on which the resulting materials or the compounds hosted in these host networks can be deposited. The dynamics of the development of hybrid materials is also reflected in the multitude of applications in various fields such as bio-medical, electronics, agriculture or food. Results obtained in this work highlight the potential of the developed systems for antimicrobial coatings on glass substrates and targeted delivery applications. Full article

The practical application of inorganic ferroelectric fillers in flexible piezoelectric composites is critically constrained by low polarization efficiency and severe interfacial incompatibility with polymer matrices. Herein, we report a multi-level in situ surface modification strategy that simultaneously addresses both limitations. High-purity one-dimensional tetragonal barium titanate nanofibers (BTO NFs) are first synthesized via sol–gel electrospinning combined with a two-step gradient annealing process, which precisely controls phase evolution and preserves structural continuity. To overcome the detrimental acid-induced degradation of BTO NFs during functionalization, a polydopamine (PDA) buffer layer is first conformally coated, followed by the liquid-phase deposition of a conductive polypyrrole (PPy) shell, forming a robust core–shell PPy@PBT NFs architecture. Incorporating only 4 wt% of these multifunctional fillers into a poly(vinylidene fluoride) (PVDF) matrix yields a dramatic enhancement in electromechanical performance. The resulting flexible piezoelectric energy harvesters achieve a piezoelectric coefficient (d₃₃) of 28.7 pC/N, an output voltage of 13 V, and an output current of 0.7 μA, representing substantial improvements over unmodified filler systems. This synergistic enhancement originates from the PDA-mediated interfacial stress transfer and the PPy-induced Maxwell–Wagner polarization intensification, establishing a robust and generalizable paradigm for high-performance flexible piezoelectric composites in self-powered wearable electronics. Full article