Search Results (1,209)

An inorganic–organic hybrid nano-adsorbent was prepared by chemical immobilisation of an organic Schiff base Cu (II) ion receptor, DHB ((E)-N-(1-(2-hydroxy-6-methyl-4-oxo-4H-pyran-3-yl) ethylidene) benzohydrazide), a selective dehydroacetic acid-based chemosensor, onto a mesoporous silica support. In order to prepare the sorbent, the silylating agent was anchored onto the silica. During this procedure, 3-Chloropropyl trimethoxy silane (CPTS) was attached to the surface, increasing hydrophobicity. By immobilising DHB onto the CPTS platform, the silica surface was activated, and as a result the coordination chemistry of the Schiff base generated a hybrid adsorbent with the capability to rapidly sequestrate Cu (II) ions from wastewater, as an answer to combat growing Waste Electrical and Electronic Equipment (WEEE) contamination in water supplies, in the wake of a prolonged consumerism mentality and boom in cryptocurrency mining. The produced hybrid materials were characterised by FTIR, proximate and ultimate analysis, nitrogen physisorption, PXRD, SEM, and TEM. The parameters influencing the removal efficiency of the sorbent, including pH, initial metal ion concentration, contact time, and adsorbent dosage, were optimised to achieve enhanced removal efficiency. Under optimal conditions (pH 7.0, adsorbent dosage 3 mg, contact time of 70 min, and 25 °C), Cu (II) ions were quantitatively sequestered from the sample solution; 93.1% of Cu (II) was removed under these conditions. The adsorption was found to follow pseudo-second-order kinetics, and Langmuir model fitting affirmed the monolayer adsorption. Full article

Organic optoelectronic devices receive appreciable attention due to their low cost, ecology, mechanical flexibility, band-gap engineering, brightness, and solution process ability over a broad area. In this study, we designed and studied organic light-emitting diodes (OLEDs) consisting of an assembly of natural dyes, extracted from noble fir leaves (evergreen) and blue hydrangea flowers mixed with poly-methyl methacrylate (PMMA) as light emitters. We experimentally demonstrate the effective conversion of blue light emitted by an inorganic laser/photodiode into longer-wavelength red and green tunable photoluminescence due to the excitation of natural dye–PMMA nanostructures. UV-visible absorption and photoluminescence spectroscopy, ellipsometry, and Fourier transform infrared methods, together with optical microscopy, were performed for confirming and characterizing the properties of light-emitting diodes based on natural dyes. We highlighted the optical and physical properties of two different natural dyes and demonstrated how such characteristics can be exploited to make efficient LED devices. A strong pure red emission with a narrow full-width at half maximum (FWHM) of 23 nm in the noble fir dye–PMMA layer and a green emission with a FWHM of 45 nm in blue hydrangea dye–PMMA layer were observed. It was revealed that adding monolayer MoS₂ to the nanostructures can significantly enhance the photoluminescence of the natural dye due to a strong correlation between the emission bands of the inorganic–organic emitters and back mirror reflection of the excitation blue light from the monolayer. Based on the investigation of two natural dyes, we demonstrated viable pathways for scalable manufacturing of efficient hybrid OLEDs consisting of assembly of natural-dye polymers through low-cost, purely ecological, and convenient processes. Full article

This work explores a novel and efficient synthetic approach to a new class of boron cluster derivatives via the nucleophilic addition of stabilized phosphorus ylides, Ph₃P=CHR² (R² = COOEt, CN), to a series of nitrilium salts of the closo-decaborate anion, [2-B₁₀H₉NCR¹]⁻ (R¹ = Me, Et, ⁿPr, ⁱPr, Ph). The reaction proceeds regio- and stereospecifically, affording a diverse range of iminoacyl phosphorane derivatives, [2-B₁₀H₉NH=C(R¹)C(PPh₃)R²]⁻, in high isolated yields (up to 95%). The obtained compounds (10 examples) were isolated as tetrabutylammonium or tetraphenylphosphonium salts and thoroughly characterized by multinuclear NMR (¹¹B, ¹H, ¹³C, ³¹P), high-resolution mass spectrometry, and single-crystal X-ray diffraction. The reaction feasibility was found to be strongly influenced by the steric hindrance of the R¹ group. Furthermore, the practical utility of these novel hybrids was demonstrated by employing the [2-B₁₀H₉NH=C(CH₃)C(COOC₂H₅)=PPh₃]⁻ anion as a highly effective membrane-active component in ion-selective electrodes. The developed tetraphenylphosphonium (TPP⁺) sensor exhibited a near-Nernstian response, a low detection limit of 3 × 10⁻⁸ M, and excellent selectivity over a range of common inorganic and organic cations, showcasing the potential of closo-borate-based ionophores in analytical chemistry. Full article

The industrial application of free sucrose phosphorylase (SPase) is significantly limited due to cost, stability issues, and poor reusability. In this study, we employed organic–inorganic hybrid nanoflowers to achieve cell immobilization by co-assembling metal ions with cells. The surface of cells was coated with nanoflowers via chitosan-regulated biomimetic mineralization, thereby enhancing the activity of immobilized cells while providing a protective structure to improve stability. The relative activity of the immobilized cells was 30% higher than that of the free cells. After placing at 4 °C in 15 days, the relative activity of immobilized cells (80%) was substantially higher than that of free cells (40%). Moreover, the immobilized cells retained approximately 85% of their relative activity after 10 cycles. In summary, the novel biocatalysts developed in this study combine high catalytic performance with excellent reusability, demonstrating significant advantages in E. coli cell immobilization and providing a solid foundation for their application in industrial biocatalysis and related fields. Full article

Constructed wetlands (CWs), which combine biological and physicochemical processes and adhere to circular economy principles, are increasingly recognized as nature-based wastewater treatment solutions. With an emphasis on resource valorization and pollutant removal efficiency, this review assessed the use of organic residues as substrates in CWs. In total, 44 peer-reviewed open-access case studies in English were obtained from 325 documents that were retrieved from Scopus using PRISMA-based eligibility criteria. Information about the wastewater source, substrate, CW type, and results was extracted. The results indicated that biochar (66.7%) predominated because of its high adsorption capacity and microbial support, while shell or forest residues and agricultural residues (20.5%) helped remove micropollutants and phosphorus. CWs with vertical subsurface flow were most prevalent (54%). According to studies, the removal efficiencies of biochar and agricultural or shell residues were 10–15% higher than those of inorganic substrates for phosphorus, TSS (total suspended solids), NH₄⁺ (ammonium), and BOD (biochemical oxygen demand) in wastewater. Through innovative designs and the application of circular economy strategies, including revalorize, reuse, reutilize, reintegrate, rethink and reconnect, organic substrates enhance pollutant removal and improve the overall sustainability of CWs. Overall, CWs with organic residues provide cost-effective and environmentally sustainable wastewater treatment; further research on local resources, hybrid systems, and supportive policies is recommended to promote broader implementation. Full article

In recent years, hybrid polymer/POSS (Polyhedral Oligomeric Silsesquioxane) systems have attracted particular attention, combining the advantages of organic and inorganic components. This paper reports on the thermal and thermo-oxidative degradation and weathering processes of these materials, as well as their impact on mechanical, chemical, and morphological properties. The paper discusses the physical and chemical changes occurring during degradation, the mechanisms of autoxidation, and the influence of environmental factors such as UV radiation, temperature, and humidity. Particular attention is paid to the role of POSS nanoparticles in polymer stabilization—their barrier function, free radical scavenging, and oxygen diffusion limitation. Methods for analyzing ageing processes are presented, including thermogravimetry coupled with infra-red spectroscopy (TG-FTIR), mechanical property testing, and yellowness index assessment. Material durability prediction models and their importance in designing composite lifespans in the context of the circular economy are also discussed. It is demonstrated that the appropriate type and concentration of POSS (typically 2–6 wt.%) can significantly improve polymer composites’ resistance to heat, radiation, and oxidizing agents, extending their service life and enabling more sustainable lifecycle management of products. Full article

The increasing impact of global warming is predominantly driven by the extensive use of fossil fuels, which release significant amounts of greenhouse gases into the atmosphere. This has led to a critical need for alternative, sustainable energy sources that can mitigate environmental impacts. Photovoltaic technology has emerged as a promising solution by harnessing renewable energy from the sun, providing a clean and inexhaustible power source. Perovskite solar cells (PSCs) are a class of hybrid organic–inorganic solar cells that have recently attracted significant scientific attention due to their low cost, relatively high efficiency, low–temperature processing routes, and longer carrier lifetimes. These characteristics make them a viable alternative to traditional fossil fuels, reducing the carbon footprint and contributing to the fight against global warming. In this study, the SCAPS–1D numerical simulator was used in the computational analysis of a PSC device with the configuration FTO/ETL/BaZr(S_0.6Se_0.4)₃/HTL/Ir. Different hole transport layer (HTL) and electron transport layer (ETL) material were proposed and tested. The HTL materials included copper (I) oxide (Cu₂O), 2,2′,7,7′–Tetrakis(N,N–di–p–methoxyphenylamine)9,9′–spirobifluorene (spiro–OMETAD), and poly(3–hexylthiophene) (P₃HT), while the ETLs included cadmium suphide (CdS), zinc oxide (ZnO), and [6,6]–phenyl–C₆₁–butyric acid methyl ester (PCBM). Finally, BaZr(S_0.6Se_0.4)₃ was proposed as an absorber, and a fluorine–doped tin oxide glass substrate (FTO) was proposed as an anode. The metal back contact used was iridium. Photovoltaic parameters such as short circuit density (I_sc), open circuit voltage (V_oc), fill factor (FF), and power conversion efficiency (PCE) were used to evaluate the performance of the device. The initial simulated primary device with the configuration FTO/CdS/BaZr(S_0.6Se_0.4)₃/spiro–OMETAD/Ir gave a PCE of 5.75%. Upon testing different HTL materials, the best HTL was found to be Cu₂O, and the PCE improved to 9.91%. Thereafter, different ETLs were also inserted and tested, and the best ETL was established to be ZnO, with a PCE of 10.10%. Ultimately an optimized device with a configuration of FTO/ZnO/BaZr(S_0.6Se_0.4)₃/Cu₂O/Ir was achieved. The other photovoltaic parameters for the optimized device were as follows: FF = 31.93%, J_sc = 14.51 mA cm⁻², and V_oc = 2.18 V. The results of this study will promote the use of environmentally benign BaZr(S_0.6Se_0.4)₃–based absorber materials in PSCs for improved performance and commercialization. Full article

The development of emerging high-tech technologies comes with a growing demand for composite materials with outstanding mechanical properties and wear resistance. Herein, we fabricated organic-inorganic self-stratifying gradient coatings based on silicon density by chemically bonding octa- and mono-amino polyhedral oligomeric silsesquioxane (POSS) onto the polyimide (PI) resin. The microstructure and chemical characteristics of POSS-PI-based composite coatings were investigated. The enhancements to the mechanical properties and wear resistance of the PI-based composites due to the gradient structure were also investigated. As expected, the addition of POSS significantly increased the composites’ thermal stability and mechanical properties. In particular, the tensile strength and nano-indentation hardness of the 4 wt.% POSS-PI composites were enhanced by 28.6% and 68.4%, respectively. Furthermore, compared with that of pure PI, the wear rate of the POSS-PI self-stratifying coatings decreased by 78.9%, which was due to the enhanced cross-linking density and gradient structure that resulted from the self-stratifying of POSS. Full article

Tandem white organic light-emitting diodes (OLEDs), formed by stacking red, green, and blue organic electroluminescent units, offer a promising route toward high-resolution microdisplays. However, their performance is constrained by the intrinsically short lifetime of blue OLED sub-units. Replacing the unstable blue OLED with a long-lived GaN-based LED could address this limitation, but practical hybridization remains difficult because of incompatible fabrication routes and significant current imbalance between the inorganic and organic units. Here, we demonstrate the first hybrid GaN–OLED tandem white LEDs enabled by an interface-engineered charge-generation unit (CGU). By introducing an ITO/HAT-CN/LiNH₂-doped Bphen CGU, we simultaneously enhance the work function, strengthen the built-in electric field, and smooth the interfacial morphology. These synergistic effects promote efficient charge generation, yielding near-ideal voltage summation and well-balanced electron–hole injection. As a result, the hybrid tandem device shows a nearly twofold increase in current efficiency (from 28.1 to 58.6 cd A^–1) and significantly reduced spectral shift under varying current densities. We further demonstrate the generality of this approach by integrating the GaN emission with yellow OLEDs to produce stable blue–yellow hybrid white emission. This work establishes an applicable strategy for integrating GaN-LEDs and OLEDs, opening a pathway toward efficient, stable, and compact white light engines for next-generation microdisplay technologies. Full article

Phenolic aerogel holds great promise for applications in thermal protection against ablation, and constructing inorganic–organic hybrid networks is an effective strategy to enhance its oxidation and ablation resistance. This study introduces a stepwise hybridization strategy for the preparation of SiO₂–ZrO₂–phenolic resin aerogels (SZPA). First, nano-silica sol and nanometer-scale zirconia were physically blended to form a uniformly dispersed mixture. Subsequently, the modified silica was incorporated into a phenolic resin solution to construct a three-dimensional hybrid silica–phenolic network framework. Nano-sized zirconia was then uniformly dispersed within the matrix as a physical reinforcing phase through high-shear dispersion. Finally, the SZPA with a hierarchical nanoporous structure was obtained via ambient-pressure drying. Owing to its unique hybrid network structure, the aerogel exhibits markedly improved properties: the thermal conductivity is as low as 0.0419–0.0431 W/(m·K) (a reduction of approximately 24%), and the specific surface area is as high as 190–232 m²/g (an increase of approximately 83%). Meanwhile, the inorganic network considerably enhances the residual mass at elevated temperatures, as well as the oxidation resistance and thermal stability of the matrix. Among the tested materials, the SZPA-4 exhibited outstanding thermal insulation capability at high temperatures; its back surface temperature reached only 74.4 °C after 600 s of exposure to a 1200 °C butane flame. This study provides a feasible route for the preparation of high-performance phenolic-based composite aerogels for aerospace thermal protection systems, thereby expanding their potential applications in extreme thermal environments. Full article

Supercapacitors are widely studied for their high energy density, low cost, and exceptional cycling durability. However, the decisive factor in determining the performance of supercapacitors is the electrode material. Among emerging materials, metal glycerates stand out as tunable organic-inorganic hybrids with well-controlled structures. Yet, progress in tailoring metal glycerates for supercapacitors has not been organized or consolidated into a coherent framework. Herein, we systematically summarize recent advances in the synthesis, structural evolution, and electrochemical applications of metal glycerates and their derivatives (including hydroxides, oxides, sulfides, phosphides, selenides, and composites) as electrodes for supercapacitors, emphasizing the intrinsic structure-performance correlations. Finally, the key challenges and future prospects, covering controlled synthesis, interfacial stability, mechanistic insight, and device-level integration, are discussed to guide the rational design of next-generation MG-based materials for high-performance, sustainable supercapacitor technologies. Full article

To increase the use of the near-infrared (NIR) light from In₂O₃, a nanocomposite of In₂O₃/reduced graphene oxide was synthesised. To improve adhesion to the substrates, a small amount of PVA (polyvinyl alcohol) was added to the nanocomposite. Results showed that adding an appropriate amount of PVA to the nanocomposite remarkably enhanced the ability to extract photogenerated carriers due to interface optimisation based on the grain boundary filling with PVA and charge tunnelling effects. The nanocomposites exhibited photoconductive switching responses from the visible light region to the near-infrared range. Meanwhile, the organic/inorganic hybrid coating on silk fibres exhibited mutual conversion of positive and negative photoconductivity, as well as electrical switching responses to applied strain. Furthermore, it was found that a photoelectric signal could still be determined with zero bias after the In₂O₃/reduced graphene oxide nanocomposite had been stored for over four years. This reflects that the nanocomposites have an internal electric field that promotes the transfer of photogenerated carriers and prevents the recombination of photogenerated electrons and holes. Similar results were also obtained by adding an appropriate amount of other non-conjugated polymers, such as dendrimers. Physical mechanisms are discussed. This study provides reference values for the development of multifunctional organic/inorganic hybrids integrating non-conjugated polymer components to enhance specific properties. Full article

Hydrogen sulfide (H₂S) is a gasotransmitter that plays a crucial role in regulating pathological processes following injury to the central and peripheral nervous systems. This review systematizes current data on various classes of H₂S donors and inhibitors of its biosynthesis in neurotrauma and related experimental models. Inorganic donors (e.g., NaHS, Na₂S, and STS) rapidly suppress oxidative stress and inflammation, supporting the recovery of synaptic plasticity and cognitive function. Organic donors (e.g., GYY4137, ACS67, ACS84, SPRC, ADT-OH and its derivatives, S-memantine, and MTC) provide sustained H₂S release, stabilize the blood–brain barrier, and exhibit antiapoptotic activity. Natural donors (e.g., DADS, DATS, and SAMe) demonstrate high biocompatibility, inhibit pyroptosis, and enhance antioxidant defense mechanisms. Hybrid systems—including nanoparticles and hydrogels—enable targeted delivery and prolonged action, thereby stimulating regeneration and angiogenesis. Thiol-activated donors (e.g., COS/H₂S and AlaCOS) allow controlled H₂S release, offering broad opportunities for precise modulation of its concentration within target tissues. Inhibitors (e.g., AOAA, PAG, oxamic hydrazide 1, L-aspartic acid, benserazide, and NSC4056) of H₂S biosynthesis underscore the physiological importance of this gasotransmitter, as their administration enhances neuroinflammation and diminishes neuroprotection. The analysis reveals a general pattern: all classes of H₂S donors effectively modulate key pathological mechanisms, differing in their rate, duration, and specificity of action. These findings highlight the therapeutic promise of H₂S-based pharmacological agents in clinical neurotraumatology, while emphasizing the need for further research to optimize delivery systems, enhance efficacy, and minimize adverse effects. Full article

Rapid progress on the fabrication of lead halide perovskite has led to the development of high performance optoelectronic devices, particularly in the field of solar cell technologies. This initial success has subsequently inspired investigations into layered 2D-halide perovskite structures, motivated in part by their good environmental stability, but more significantly by their intriguing fundamental photo-physics. They have recently been used to improve the photoresponsivity of monolayer transition metal dichalcogenides in hybrid heterostructures. In this paper, we report on the synthesis of the (PEA)₂(MA)_n−1Pb_nI_3n+1 series (with n = 1, 2, 3) of 2D-halide perovskites, in order to develop a platform that provides ultra-thin layers for the fabrication of hybrid heterostructures. The crystal synthesis method and its basic structural and optical characterization are shown, highlighting the differences in the crystal synthesis processes. Furthermore, we explore the preparation of 2D halide perovskite ultra-thin flakes using the mechanical exfoliation method, and few-layer-areas of n = 1 member of the series are identified using atomic force microscopy. Finally, we study the deposition of thin and ultra-thin films using the spin coating technique to provide an alternative process to the exfoliation. Full article

In the continuous demand for high-performance lithium-ion batteries (LIBs), thermal management control is, these days, crucial with respect to safety, performance, and longevity. As a promising passive solution, Phase Change Materials (PCMs) have been implemented to overcome the conventional battery thermal management (BTM) approaches, including air cooling, liquid cooling, or refrigerant-based systems. Their ability to transfer the heat during phase change processes makes them ideal candidates for further thermal buffers, thus allowing compact and energy-efficient temperature control without extra power consumption. This work encompasses the recent progress in PCM-based battery thermal management systems, with a particular focus on material selection, structural design, and experimental validation. Current advances in composite PCMs, including the use of high-conductivity additives, porous supports, and encapsulation methods, are here appraised in terms of their thermal conductivity, cycling stability, leakage prevention, and overall safety. Comparisons between organic, inorganic, and hybrid PCM types demonstrate the benefits and drawbacks of each class. Ongoing discussion is also directed towards challenges that include low thermal conductivity, limited heat storage capacity, scalability, cost, and flammability. Future development opportunities are also identified in the areas of multifunctional PCMs, hybrid passive–active cooling approaches, scalable processing, and life-cycle considerations. Full article