Search Results (162)

The development of sustainable and functional nanocomposites has attracted considerable attention in recent years due to their broad spectrum of potential applications, including wood preservation. Also, a global goal is to reuse the large volumes of waste for environmental issues. In this context, the aim of the study was to obtain soda lignin particles, to graft ZnO nanoparticles onto their surface and to apply these hybrids, embedded into a biodegradable polymer matrix, as protection/preservation coating for oak wood. The organic–inorganic hybrids were characterized in terms of compositional, structural, thermal, and morphological properties that confirm the efficacy of soda lignin extraction and ZnO grafting by physical adsorption onto the decorating support and by weak interactions and coordination bonding between the components. The developed solution based on poly(3-hydroxybutyrate-co-3-hydroxyvalerate) and lignin-ZnO was applied to oak wood specimens by brushing, and the improvement in hydrophobicity (evaluated by water absorption that decreased by 48.8% more than wood, humidity tests where the treated sample had a humidity of 4.734% in comparison with 34.911% for control, and contact angle of 97.8° vs. 80.5° for untreated wood) and UV and fungal attack protection, while maintaining the color and aspect of specimens, was sustained. L.ZnO are well dispersed into the polymer matrix, ensuring a smooth and less porous wood surface. According to the results, the obtained wood coating using both a biodegradable polymeric matrix and a waste-based preservative can be applied for protection against weathering degradation factors, with limited water uptake and swelling of the wood, UV shielding, reduced wood discoloration and photo-degradation, effective protection against fungi, and esthetic quality. Full article

Hydrogels are three-dimensional network structures composed of hydrophilic polymers that can swell in water and are very similar to soft tissues such as connective tissue or the extracellular matrix. DNA hydrogels are particularly notable for biomedical applications due to their high biocompatibility, physiological stability, molecular recognition, biodegradability, easy functionalization, and low immunogenicity. Based on these advantages, stimuli-responsive DNA hydrogels that have the property of reversibly changing their structure in response to various microenvironments or molecules are attracting attention as smart nanomaterials that can be applied to biosensing and material transfer, such as in the case of cells and drugs. As DNA nanotechnology advances, DNA can be hybridized with a variety of nanomaterials, from inorganic nanomaterials such as gold nanoparticles (AuNPs) and quantum dots (QDs) to synthetic polymers such as polyacrylamide (PAAm) and poly(N-isopropylacrylamide) (pNIPAM). These hybrid structures exhibit various optical and chemical properties. This review discusses recent advances and remaining challenges in biomedical applications of stimuli-responsive smart DNA hydrogel-based systems. It also highlights various types of hybridized DNA hydrogel, explores various response mechanism strategies of stimuli-responsive DNA hydrogel, and provides insights and prospects for biomedical applications such as biosensing and drug delivery. Full article

Anti-washout admixtures (AWAs) are a unique component of underwater non-dispersive concrete (UNDC), which gives the concrete the ability to remain undispersed in water. On some special occasions, freshly mixed underwater non-dispersive concrete is exposed to the erosion of moving water, and conventional acrylamide-based AWAs are only suitable for static water or the water flow rate is small. In this study, the inorganic component nanosilica (NS) is modified, treated, and copolymerized with the organic components acrylamide (AM) and acrylic acid (AA) to form an inorganic–organic hybrid polymer with a hyperbranched structure, which changes the linear structure of the original polyacrylamide molecule, and we optimize the synthesis process. The polymers are characterized at the microscopic level and their compatibility with polycarboxylic acid water-reducing agents (SP) is investigated. In addition, the polymers are compared and evaluated with commonly used PAM in terms of their working performance. The experimental results indicated that under specific process conditions, polymers endow cement mortar with good resistance to water erosion. At the same time, the polymers’ three-dimensional network structure is prominent, with good compatibility with SP and better anti-dispersity. The microstructure of the cement paste with added polymers is dense and flat, but its flowability and setting time are slightly worse. This study provides a new development direction for the development of AWAs under a dynamic water environment, which has specific engineering significance. Full article

The detection of hydrogen gas is crucial for both industrial fields, as a green energy carrier, and biomedical applications, where it is a biomarker for diagnosis. TiO₂ nanomaterials are stable and sensitive to hydrogen gas, but their gas response can be negatively affected by external factors such as humidity. Therefore, a strategy is required to mitigate these influences. The utilization of organic–inorganic hybrid gas sensors, specifically metal oxide gas sensors coated with ultra-thin copolymer films, is a relatively novel approach in this field. In this study, we examined the performance and long-term stability of novel TiO₂-based sensors that were coated with poly(trivinyltrimethylcyclotrisiloxane-co-tetrafluoroethylene) (P(V3D3-co-TFE)) co-polymers. The P(V3D3-co-TFE)/TiO₂ hybrid sensors exhibit high reliability even for more than 427 days. They exhibit excellent hydrogen selectivity, particularly in environments with high humidity. An optimum operating temperature of 300 °C to 350 °C was determined. The highest recorded response to H₂ was approximately 153% during the initial set of measurements at a relative humidity of 10%. The developed organic–inorganic hybrid structures open wide opportunities for gas sensor tuning and customization, paving the way for innovative applications in industry and biomedical fields, such as exhaled breath analysis, etc. Full article

Hybrid polymers combine the benefits of inorganic and organic material properties, offering superior thermal, mechanical, and chemical stability, making them ideal for optical applications. This study focuses on the fabrication and characterization of antireflective (AR) structures within hybrid polymers using reactive ion etching (RIE). The etching process produces nanopillars with controlled heights, achieving excellent AR performance across a broad spectral range from 450 nm to 2 µm. Optical characterization, including angle-resolved transmission and reflection measurements, shows that the structured samples maintain high transmission efficiency and reduced reflectance at varying incidence angles. Thermal stability tests reveal that the AR structures preserve their optical properties after exposure to temperatures up to 250 °C. Higher temperatures cause significant material yellowing, which is attributed to changes in the bulk material rather than damage to the structured surface. Hydrophobicity measurements show significant water repellency in structured samples, with contact angles more than twice those of unstructured layers. These findings highlight the potential of hybrid polymers with moth-eye-inspired nanostructures for high-performance, durable optical components in demanding environments. Full article

The efficient separation and removal of carbon dioxide (${CO}_2$) from its mixtures is an important technological challenge to limit effects resulting from the increase of the carbon dioxide concentration in the atmosphere. Membrane technology is an environmentally friendly approach, highly scalable and less energy-consuming than conventional methods such as adsorption, absorption and cryogenic separation. Hybrid membrane materials incorporating inorganic filler nanostructures in polymer matrices having polyethylene glycol (PEG) as a plasticized additive are promising membrane materials given the presence of ${CO}_2$-philic polar functional groups of PEGs and the structural refinements on the blend matrix consequent to the filler distribution. In this review, literature information on hybrid polymer/PEG membranes are critically reviewed to discuss how filler dispersion in the blend matrix gives rise to enhanced ${CO}_2$ separation performances with respect to those obtained with traditional mixed matrix membranes where filler nanostructures are dispersed in the neat polymer. The discussion will be focused on the correlation between the ${CO}_2$ transport properties, membrane structural properties and defect resulting from the polymer-filler incompatibility. It is shown that hybrid polymer/PEG membranes with dispersed filler nanostructures simultaneously offer improved ${CO}_2$ separation performances and enhanced mechanical properties compared with nanocomposite ones where filler particles are dispersed in the neat polymer matrix. PEG addition enhances the filler-matrix compatibility, delays filler aggregation and limits the formation of filler-matrix interface defects. Full article

A sol-gel approach was used to prepare a thin hydrogel membrane based on an organic-inorganic polymer matrix embedded with pre-synthesized gold nanoparticles (AuNPs). The organic polymers utilized were poly(vinyl alcohol) (PVA) and poly(ethylene oxide) 400 (PEO) while tetraethoxysilane (TEOS) served as a precursor for the inorganic silica polymer. AuNPs were synthesized using D-glucose as a reducing agent and starch as a capping agent. A mixture of PVA, PEO, pre-hydrolyzed TEOS, and AuNP dispersions was cast and dried at 50 °C to obtain the hybrid hydrogel membrane. The structure, morphology, and optical properties of the nanocomposite membrane were analyzed using TEM, SEM, XRD, and UV-Vis spectroscopy. The newly designed hybrid hydrogel membrane was utilized as an efficient sorbent for the simultaneous speciation analysis of valence species of chromium and manganese in water samples via solid-phase extraction. This study revealed that Cr(III) and Mn(II) could be simultaneously adsorbed onto the PVA/PEO/SiO₂/AuNP membrane at pH 9 while Cr(VI) and Mn(VII) remained in solution due to their inability to bind under these conditions. Under optimized parameters, detection limits and relative standard deviations were determined for chromium and manganese species. The developed analytical method was successfully applied for the simultaneous speciation analysis of chromium and manganese in drinking water and wastewater samples. Full article

Anion-conducting organic–inorganic polymers (OIPs), constructed using metal–organic framework (MOF)-like structures with non-toxic, non-rare catalytic metals (Fe³⁺, Zr⁴⁺), have been developed. The incorporation of MOF-like structures imparts porosity to the polymers, classifying them as porous organic polymers (POPs). The combination between catalytic activity, ion conduction, and porosity allows the material to act as one-component catalytic electrodes. A high catalytic activity is expected since the entire surface area contributes to electrocatalysis, rather than being restricted to triple-phase boundaries. The synthesis involved anchoring a synthon onto a commercial polymer, assembling organo-metallic moieties, and functionalizing with quaternary ammonium (QA) groups. Two hybrid materials, Zr-POP-QA and Fe-POP-QA, were thoroughly characterized by NMR, FTIR, XPS, BET surface area (≈200 m²/g), and TGA. The resulting electrodes demonstrated a high electrochemically active surface area and a high efficiency for the oxygen reduction reaction (ORR), a critical process for energy storage and conversion technologies. The performance was characterized by a 4-electron reduction pathway, a high onset potential (≈0.9 V vs. RHE), and a low Tafel slope (≈0.06 V). We attribute this efficiency to the high active surface area, which results from the simultaneous presence of catalytic transition metal ions (Zr or Fe) and ion conducting groups. Full article

Solid electrolytes, including polymer electrolytes, are a promising option for improving the performance of environmentally friendly batteries such as rechargeable lithium-ion batteries or fuel cells. Hydrogen–oxygen fuel cells producing only water under power generation are attracting widespread attention, and they need proton conductors as electrolytes. Fluoropolymer electrolytes such as Nafion^® have been utilized for hydrogen–oxygen fuel cells below 100 °C; however, they are not applicable over the working temperature. Therefore, other types of polymer electrolytes are demanded for hydrogen–oxygen fuel cells. Polyoxometalate (POM) inorganic clusters are known as proton conductors and are utilized to prepare POM–polymer composites for solid electrolyte application. In such POM–polymer composites, distinct compositions and structures are significant for improving the performance of proton conductivity. Recently, POM–polymer composites with distinct compositions and structures have been synthesized to obtain high proton conductivity. The key factor is to use single-crystalline compounds. Here, several examples are overviewed by classifying them into three categories: (i) single-crystalline POM–polymer composites, (ii) organically modified POM (org-POM) polymers, and (iii) POM hybrid polymers using polymerizable cations. The application of proton-conductive solid electrolytes is focused on. Full article

This review provides an overview of the synthesis, characterization and application of coordination polymers based on N,O-donor Schiff base ligands. The coordination polymers (CPs) represent a novel class of inorganic–organic hybrid materials with tunable compositions and fascinating structures. They are composed of metal ions and organic ligands. Therefore, the nature of the metal ion and type of organic ligand is the most significant factor in constructing targeted coordination polymers with the desired properties. Due to the versatile coordination modes, N,O-donor Schiff base ligands are also used to construct various CPs. Full article

Organic materials have emerged as promising candidates for cathode materials in lithium-ion batteries and supercapacitors, offering unique properties and advantages over traditional inorganic counterparts. This review investigates the use of organic compounds as cathode materials in energy storage devices, focusing on their application in lithium-ion batteries and supercapacitors. The review covers various types of organic materials, organosulfur compounds, organic free radical compounds, organic carbonyl compounds, conducting polymers, and imine compounds. The advantages, challenges, and ongoing developments in this area are examined and the potential of organic cathode materials to achieve higher energy density, improved cycling stability, and environmental sustainability is highlighted. The comprehensive analysis of organic cathode materials provides insights into their electrochemical performance, electrode reaction mechanisms, and design strategies such as molecular structure modification, hybridization with inorganic components, porous architectures, conductive additives, electrolyte optimization, binder selection, and electrode architecture to improve their efficiency and performance. In addition, future research in the field of organic cathode materials should focus on addressing current limitations such as low energy density, cycling stability, poor discharge capability, potential safety concerns and improving their performance. To do this, it will be necessary to improve structural stability, conductivity, cycle life, and capacity fading, explore new redox-active organic compounds, and pave the way for the next generation of high-performance energy storage devices. For organic cathode materials to be commercially viable, it is also essential to develop scalable and economical manufacturing processes. Full article

This review examines the recent advancements and unique properties of polymer–inorganic hybrid materials formed through coordination bonding (Class II hybrids), which enable enhanced functionality and stability across various applications. Here, we categorize these materials based on properties gained through complexation, focusing on electrical conductivity, thermal stability, photophysical characteristics, catalytic activity, and nanoscale self-assembly. Two major synthetic approaches to making these hybrids include homogeneous and heterogeneous methods, each with distinct tradeoffs: Homogeneous synthesis is straightforward but requires favorable mixing between inorganic and polymer species, which are predominantly water-soluble complexes. In contrast, heterogeneous methods are post-processing techniques that provide high area selectivity for inorganic precursors, allowing precise integration within polymer matrices. Finally, we highlight the role of hybrid linkers, namely metallosupramolecular polymers, in creating structural diversity. These can be organized into three main groups: metal–organic frameworks (MOFs), coordination polymers (CPs), and supramolecular coordination complexes (SCCs). Each of these groups introduces unique structural and functional properties that expand the potential applications of hybrid materials. Full article

Objective: It is hypothesized that the way nano- and micro-hybrid polymer-based composites are structured and cured impacts the way they respond to aging. Material and methods: A polymer–ceramic interpenetrating network composite (Vita Enamic/VE), an industrially polymerized (Brillinat CriosST/BC), and an in situ light-cured composite with discrete inorganic fillers (Admira Fusion5/AF5) were selected. Specimens (308) were either cut from CAD/CAM blocks (VE/BC) or condensed and cured in white polyoxymethylene molds (AF5) and subjected to four different aging conditions (n = 22): (a) 24 h storage in distilled water at 37 °C; (b) 24 h storage in distilled water at 37 °C followed by thermal cycling for 10,000 cycles 5/55 °C (TC); (c) TC followed by storage in a 75% ethanol–water solution; and (d) TC followed by a 3-week demineralization/remineralization cycling. CAD/CAM samples were also measured dry before the aging process. Three-point bending test, quantitative and qualitative fractography, instrumented indentation test (IIT), SEM, and reliability analyses were used. Uni- and multifactorial ANOVA, Tukey’s post hoc test, and Weibull analysis were performed for statistical analysis. Results: A significant (p < 0.001) and very strong effect of the parameter material was observed (η_P² > 0.9). VE exhibited two to three times higher elastic moduli and hardness parameters compared to BC and AF5, which were comparable. Strength was highest in BC but was accompanied by high beam deformation. The effect of aging was comparatively smaller and was more evident in the IIT parameters than in the flexural strength or modulus. Reliability was high (m > 15) in VE and BC, regardless of aging protocol, while it was significantly reduced in AF5 following aging protocols b-d. Conclusions: TC was the method of artificial aging with a significant impact on the measured parameters, while demineralization/remineralization cycling had little or no impact. Clinical relevance: The degradation of composites occurred irrespective of the structuring and curing method and manifested in a low deterioration in the measured properties. Full article

This paper reviews the recent development of organic–inorganic hybrid dielectric materials for application as gate dielectrics in thin-film transistors (TFTs). These hybrid materials consist of the blending of high-k inorganic dielectrics with polymers, and their resulting properties depend on the amount and type of interactions between the organic and inorganic phases. The resulting amorphous networks, characterized by crosslinked organic and inorganic phases, can be tailored for specific applications, including gate dielectrics in TFTs. As dielectric materials, they offer a synergistic combination of high dielectric constants, low leakage currents, and mechanical flexibility, crucial for next-generation flexible electronics. Furthermore, organic–inorganic hybrid materials are easily processed in solution, allowing for low-temperature deposition compatible with flexible substrates. Various configurations of these hybrid gate dielectrics, such as bilayer structures and polymer nanocomposites, are discussed, with an emphasis on their potential to enhance device performance. Despite the significant advancements, challenges remain in optimizing the performance and stability of these hybrid materials. This review summarizes recent progress and highlights the advantages and emerging applications of low-temperature, solution-processed hybrid dielectrics, with a focus on their integration into flexible, stretchable, and wearable electronic devices. Full article

Metal–organic frameworks (MOFs) are hybrid inorganic–organic 3D coordination polymers with metal sites and organic linkers, which are a “hot” topic in the research of sorption, separations, catalysis, sensing, and environmental remediation. In this study, we explore the molecular mechanism and kinetics of interaction of the new copper porphyrin aluminum metal–organic framework (actAl-MOF-TCPPCu) compound 4 with a vapor of the volatile organic sulfur compound (VOSC) diethyl sulfide (DES). First, compound 4 was synthesized by post-synthetic modification (PSM) of Al-MOF-TCPPH₂ compound 2 by inserting Cu²⁺ ions into the porphyrin ring and characterized by complementary qualitative and quantitative chemical, structural, and spectroscopic analysis. Second, the interaction of compound 4 with DES vapor was analyzed dynamically by the novel method of in situ time-dependent attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy at controlled humidity levels. The sorbent–adsorbate interactions, as analyzed by the shifts in IR peaks, indicate that the bonding includes the hydroxy O-H, carboxylate COO⁻, and phenyl groups. The kinetics of sorption obeys the Langmuir pseudo-first-order rate law. The pre-adsorption of water vapor by compound 4 at the controlled relative humidity under static (equilibrium) conditions yields the binary stoichiometric adsorption complex (Al-MOF-TCPPCu)_1.0(H₂O)_8.0. The pre-adsorption of water vapor makes the subsequent sorption of DES slower, while the kinetics obey the same rate law. Then, static pre-adsorption of water vapor was followed by static sorption of DES vapor, and the ternary adsorption complex (Al-MOF-TCPPCu)_1.0(H₂O)_8.0(DES)₃.₈ was obtained. Despite the pre-adsorption of significant amounts of water, the binary complex adsorbs a large amount of DES: ca. 36.6 wt. % (per compound 4). Finally, the ternary complex is facilely regenerated by gentle heating under vacuum. Compound 4 and related MOFs are promising for adsorptive removal of vapor of DES and related VOSCs from dry and humid air. Full article