Search Results (254)

MXenes, a family of two-dimensional transition metal carbides and nitrides, exhibit exceptional electrical conductivity, tunable surface chemistry, and strong broadband light absorption. However, their practical implementation is often limited by structural instability, such as restacking and surface oxidation. In this study, we propose a strategy for the design of hybrid nanocomposites based on exfoliated Ti₃C₂T_x MXene embedded within a porous silica (SiO₂) matrix and further functionalized with cerium dioxide (CeO₂) nanoparticles. The SiO₂ matrix, synthesized via a sol–gel approach, ensures homogeneous dispersion, increased porosity, and thermal stability, effectively reducing MXene restacking. Simultaneously, CeO₂ nanoparticles create surface oxygen vacancies and enhance interfacial reactivity. Comprehensive structural, morphological, surface, and optical characterizations confirm the formation of stable, light-responsive nanoarchitectures with tailored textural properties. Furthermore, the obtained material exhibit promising photothermal-catalytic properties. This work offers a materials-oriented approach for engineering multifunctional MXene-based architectures with enhanced photothermal performance, exemplified by their potential application in the photothermo-catalytic CO₂ conversion into solar fuels, showcasing the broader possibilities enabled by these materials. Full article

Metallogels constitute a rapidly expanding class of hybrid soft materials in which metal ions, metal complexes, or metal-containing nanoparticles play a decisive structural and functional role within a three-dimensional gel network. Their unique combination of supramolecular assembly, metal-ligand coordination, and dynamic network behaviour provides tunable mechanical, optical, electrical, redox, and catalytic properties that are not accessible in conventional hydrogels or organogels. This review systematically summarises current knowledge on metallogels, beginning with a classification based on matrix type, dominant metal interaction and functional output, spanning metallohydrogels, metal-organic gels, metal-phenolic gels, nanoparticle-based gels, polymer-based metallogels and low-molecular-weight metallogels. Key synthesis pathways are discussed, including coordination-chemistry-driven formation, metal-ligand self-assembly, in situ reduction, diffusion-mediated strategies, sol-gel-like polymerisation, enzyme-assisted routes, and bio-derived fabrication. Particular emphasis is placed on structure-function relationships that enable the development of catalytic, conductive, luminescent, antimicrobial, and biomedical metallogels. The examples compiled here highlight the versatility and transformative potential of metallogels in next-generation soft technologies, including sensing, energy conversion, wound healing, drug delivery, and emerging applications such as soft electronics and on-skin catalytic or bioactive patches. By mapping current progress and emerging design principles, this review aims to support the rational engineering of metallogels for advanced technological and biomedical applications Full article

Gel-based routes, particularly sol–gel processes, offer a versatile pathway to generate uniform inorganic networks and gel-derived functional ceramics with controlled composition and interfacial coverage. In this study, we employ a citrate-assisted sol–gel coating strategy to form a precursor gel containing Li, La, Zr, and Ge species on lithium-rich manganese-based layered oxide (LMLO) cathode particles, followed by drying/thermal conversion to obtain a Ge-substituted garnet-type Li₇La₃Zr₂O₁₂ (Ge-LLZO) ceramic coating. Structural and surface analyses (FE-SEM/EDS, XPS, and FE-TEM) confirm the presence of surface-deposited coating-related species and coating-induced changes in surface chemistry, while bulk XRD is primarily used to verify that the layered LMLO host structure is preserved after the gel-to-ceramic treatment. Electrochemical testing indicates that the gel-derived Ge-LLZO coating can influence interfacial kinetics and resistance evolution, as reflected by differential capacity behavior, impedance responses, and rate capability trends, alongside microstructural observations suggesting reduced damage compared with bare LMLO after cycling. Overall, this work demonstrates that gelation-assisted deposition and gel-to-ceramic conversion enable Ge-LLZO surface coatings on LMLO cathodes that modulate interfacial kinetics and resistance evolution. Under the harsh 4.8–2.0 V/1C condition, the bare LMLO shows an abrupt capacity drop after ~60 cycles, while the coated LMLO exhibits a more gradual decay up to 100 cycles; further optimization is required for robust long-term stability. Full article

The synthesis of Mn-TiO₂/TiO₂, together with its application as a photoanode for solar flow batteries (SFBs), is reported herein. Both the pure TiO₂ electrode and the Mn-TiO₂/TiO₂ based composite electrode were prepared using the sol–gel spin-coating technique. The incorporation of a Mn-TiO₂ layer led to the enhancement of the built-in electric field within the composite photoanode. This enhancement not only improved the light-harvesting capability of the photoanode but also suppressed the recombination of charge carriers, consequently enhancing the photocatalytic efficiency. Furthermore, the optimal annealing temperature and the optimum TiO₂ loading were systematically controlled and optimized to maximize the photoelectric conversion efficiency of the composite photoanode. Ultimately, the optimized Mn-TiO₂ composite photoanode was integrated into a monolithic solar flow battery. The results demonstrate that the battery’s photocharging current density reaches 300 μA·cm⁻². The photocharging current density was relatively increased by 150%. Full article

The catalytic removal of toluene, a representative aromatic volatile organic compound (VOC), requires efficient and stable catalysts. This study systematically investigated the effect of B-site doping with transition metals (Fe, Cu, and Ni) on the catalytic performance of LaMnO₃ perovskite for toluene oxidation. The LaMn_0.5X_0.5O₃ catalysts were synthesized via a sol–gel method and evaluated. The LaMn_0.5Ni_0.5O₃ catalysts exhibited the optimal catalytic performance, achieving toluene conversion temperatures of 243 °C at 50% conversion (T₅₀) and 296 °C at 90% conversion (T₉₀). Comprehensive characterization revealed that Ni doping effectively refined the catalyst’s microstructure (grain size decreased to 19.21 nm), increased the concentration of surface-active oxygen species (142.7%), elevated the Mn⁴⁺/Mn³⁺ ratio to 0.65, and enhanced lattice oxygen mobility. These modifications collectively contributed to its outstanding catalytic activity. The findings demonstrate that targeted B-site doping, particularly with Ni, is a promising strategy for engineering efficient perovskite catalysts for VOC abatement. Full article

Up-conversion nanoparticles (UCNPs) are materials that convert near-infrared (NIR) photons into ultraviolet (UV) or visible emissions. To enhance their optical properties, UCNPs are often synthesized with oxide (Y₂O₃) or fluoride (NaYF₄) support matrices, useful for energy storage applications. In this study, NaYF₄-UCNPs were synthesized via coprecipitation and heat-treated at 400 °C. Then, a tetraethyl orthosilicate (TEOS) film was synthesized by the sol–gel technique at varying pH and temperatures from 25 °C to 80 °C. Characterization using scanning electron microscopy (SEM), X-ray diffraction (XRD), and confocal microscopy (CM) confirmed the up-conversion properties. These materials show promise for enhancing solar radiation density in polymer degradation. Full article

Membrane electrolytes play a critical role in energy conversion devices. The development of stable, efficient membrane electrolytes is urgent and demands paramount attention for the successful commercialization of fuel cells. Chitosan, a naturally occurring material, and silica particles were used as precursors for organic–inorganic membrane polymers. The silica nanoparticles were prepared by the sol–gel and Stober methods and characterized using various techniques, including XRD, FTIR, etc. The silica-incorporated membranes show improved properties, with the sulfur-functionalized membranes having optimal proton conductivity, ion-exchange capacity, and tensile strength of 0.0238 S/cm, 2.86 meq/g, and 7.3 MPa, respectively. It also showed the lowest methanol permeability. This was clear proof that membrane functionalization has a positive impact on tuning the properties of electrolyte membranes and should be further explored in membrane development. Full article

Lithium–sulfur (Li-S) batteries are renowned for their high theoretical energy density and low cost, yet their practical implementation is hampered by the polysulfide shuttle effect and sluggish redox kinetics. Herein, a sol–gel strategy is proposed to engineer a multifunctional MXene/Fe₃O₄ composite as an efficient mediator for the cathode interlayer. The synthesized composite features Fe₃O₄ nanospheres uniformly anchored on the highly conductive Ti₃C₂T_x MXene lamellae, forming a unique 0D/2D conductive network. This structure not only provides abundant polar sites for strong chemical adsorption of polysulfides but also significantly enhances charge transfer, thereby accelerating the conversion kinetics. As a result, the Li-S battery based on the MXene/Fe₃O₄ interlayer delivers a high initial discharge capacity of 1367.1 mAh g⁻¹ at 0.2 C and maintains a stable capacity of 1103.4 mAh g⁻¹ after 100 cycles, demonstrating an exceptionally low capacity decay rate of only 0.19% per cycle. Even at a high rate of 1 C, a remarkable capacity of 1066.1 mAh g⁻¹ is retained. Electrochemical analyses confirm the dual role of the composite in effectively suppressing the shuttle effect and catalyzing the polysulfide conversion. This sol–gel engineering approach offers valuable insight into the design of high-performance mediators for advanced Li-S batteries. Full article

Corrosion induced by defective oxide scales severely compromises the durability of concrete structures. This study develops a dual-mechanism sol-gel protection strategy based on La³⁺/Ni²⁺/2-Methylimidazole (2-MI). First, 2-Methylimidazole-catalyzed epoxy ring-opening constructs defect-minimized Si–O–Si/C–O–C networks through 60 °C low-temperature curing, reducing microcrack formation and curing energy consumption compared to conventional 130 °C processing. Second, utilizing 400 °C waste heat from hot-rolled steel triggers pH-modulated La₂O₃/NiO co-deposition within oxide scale defects, enhancing corrosion resistance. After a 40-day immersion in SCP + 0.1 M NaCl, the coated reinforcement exhibits a low-frequency impedance modulus of 25.6 kΩ·cm², achieving a 10.4-fold increase over untreated steel. Specimens embedded in 3.5 wt% NaCl mortar demonstrate a 120-day impedance modulus of 74.63 kΩ·cm², exceeding the control by 8.03-fold. This strategy integrates efficient industrial waste heat utilization with energy-saving low-temperature curing, providing long-term corrosion protection for marine concrete structures. Full article

Multinary metal oxides are widely applied in energy storage and conversion, heterogeneous catalysis and environmental technologies, but their wide band gaps, low intrinsic electronic conductivity and limited density of active sites severely restrict their practical efficiency. This review examines non-metallic doping via the substitutional, interstitial or mixed incorporation of light elements such as B, C, N, F, P and S as a versatile strategy to overcome these fundamental limitations. We begin by outlining the primary synthesis methodologies for doped oxides, such as sol–gel, chemical vapor deposition, and hydrothermal routes, followed by a critical discussion of the multi-technique characterization framework required to verify successful dopant incorporation and elucidate its structural and electronic consequences. We focus on the fundamental principles of how doping parameters—such as mode, element type, and concentration—can be tuned to regulate material properties. The key mechanisms for performance enhancement, including synergistic lattice reconstruction, defect engineering, and electronic structure modulation, are emphasized. Significant advancements are highlighted in applications like energy storage, fuel cells, water splitting, and CO₂ reduction. Finally, we assess current challenges, such as the precise control of doping sites and long-term stability, and offer perspectives on the rational design of next-generation oxide materials. Full article

Recently, the state of the art of aerogels (AGs) has been reviewed, reporting first on their classification, based on the chemical origin of their precursors and the different methods existing to prepare them. Additionally, AGs of inorganic origin (IAGs) were contemplated, deeply discussing the properties, specific synthesis, and possible uses of silica and metal oxide-based AGs, since they are the most experimented and patented AGs already commercialized in several sectors. In this second part review, IAGs are examined again, but chalcogenide and metals AGs (CAGs and MAGs) are debated, since they are still too little studied, patented, and marketed, despite their nonpareil properties and vast range of possible applications. First, to give readers unaware of the previous work on AGs, a background about IAGs, all their main subclasses have been reported and their synthesis, including sol–gel, epoxide addition (EA), and dispersed inorganic (DIS) methods, as well as procedures involving the use of pre-synthesized nanoparticles as building blocks, have been discussed. Morphology and microstructure images of materials prepared by such synthetic method have been supplied. Conversely, the methods needed to prepare CAGs and MAGs, topics of this study, have been debated separately in the related sections, with illustrative SEM images. Their possible uses, properties, and some comparisons of their performance with that of other AGs and not AG materials traditionally tested for the same scopes, have also been disserted, reporting several case studies in reader-friendly tables. Full article

A novel metal oxide catalyst, PdO_x/CuO-ST, was prepared by calcining a Pd-embedded CuBTC precursor and compared with a PdO_x/CuO-SG catalyst synthesized via a sol–gel method. Characterization results indicated that in both catalysts, Pd species were incorporated into the CuO lattice, forming synergistic interactions that lowered the reduction temperature of CuO. The PdO_x/CuO-ST catalyst exhibited superior catalytic activity in the oxidative carbonylation of phenol to diphenyl carbonate when calcined at low temperature, which was attributed to well-dispersed Cu atoms and enhanced Pd–Cu integration. However, high-temperature calcination led to catalyst sintering and the formation of surface-adsorbed oxygen species, which reacted with PdO on CuO to generate inactive Pd_xCu_yO phases, thereby reducing the active Pd²⁺ content and degrading catalytic performance. Under optimized reaction conditions (100 °C, 7 h, Pd/phenol molar ratio = 1/425, and 6.6 MPa), the PdO_x/CuO-ST catalyst achieved a maximum phenol conversion of 79.5% and a diphenyl carbonate selectivity of 84.5%. Stability tests revealed that although the catalyst structure remained intact, deactivation occurred due to Pd leaching and the reduction in active PdO to metallic Pd⁰. Full article

In recent years CO₂ reforming of methane has attracted great interest as it produces high CO/H₂ ratio syngas suitable for the synthesis of higher hydrocarbons and oxygenated derivatives since it is a way for disposing and recycling two greenhouse gases with high environmental impact, CH₄ and CO₂, and because it is regarded as a potential route to store and transmit energy due to its strong endothermic effect. Along with noble metals, all the group VIII metals except for osmium have been studied for catalytic CO₂ reforming of methane. It was found that the catalytic activity of Ni, though lower than those of Ru and Rh, was higher than the catalytic activities of Pt and Pd. Although noble metals have been proven to be insensitive to coke, the high cost and restricted availability limit their use in this process. It is therefore valuable to develop stable Ni-based catalysts. In this contribution, we show how their activity and coking resistivity are greatly related to the size and dispersion of Ni particles. Well-dispersed Ni nanoparticles were achieved by multistep impregnation on a mesoporous silica support, namely SBA-15, obtained through a sol-gel method, using acetate as a nickel precursor and keeping the Ni loading between 5% and 11%. Significant catalytic activity was obtained at temperatures as low as 450 °C, a temperature well below their deactivation temperature, i.e., 700 °C. For the pre-reduced samples, a CO₂ conversion higher than 99% was obtained at approximately 680 °C. As such, their deactivation by sintering and coke formation was prevented. To the best of our knowledge, no Ni-based catalysts with complete CO₂ conversion at temperatures lower than 800 °C have been reported so far. Full article

In this work, we present the first report on the synthesis via the sol–gel method of a high-entropy (Fe_0.2Co_0.2Cu_0.2Ni_0.2Mn_0.2)Nb₂O₆ with columbite–orthorhombic structure. Polyvinylpyrrolidone (PVP), ammonium niobium oxalate, and equimolar amounts of Fe, Co, Cu, Ni, and Mn ions were used. The refinement of the XRD pattern showed the presence of niobate crystallites with an average size of 48.4 nm and a fraction of 7.6 wt% of a spinel-like phase. At temperatures below 5 K, the DC and AC magnetometry results revealed the presence of a ferromagnetic-like phase due to the niobate phase. The Mössbauer spectrum at 300 K showed a paramagnetic and two magnetically ordered components corresponding to the niobate and the spinel-like phases, respectively. The spectral components were typical of Fe³⁺, indicating the presence of cation vacancies. The elemental mapping obtained from EDS measurements showed compositional homogeneity. The XRF measurements confirmed a composition consistent with nominal values. These results confirm the feasibility of synthesizing entropy-stabilized columbite oxides via the sol–gel route, opening new opportunities for the design of multifunctional ceramics with tunable structural and magnetic properties for high-performance thermal barrier coatings and energy conversion applications. Full article

The chemical looping steam reforming of methane (CLSR) employing Fe-containing oxygen carriers can produce syngas and hydrogen simultaneously. However, Fe-based oxygen carriers exhibit low CH₄ activation ability and cyclic stability. In this work, oxygen carriers with fixed Fe content and different Fe/Ni ratios were synthesized by the sol–gel method to investigate the effects of Ni-Fe-Al interactions on CLSR performance. Ni-Fe-Al interactions promote the growth of the spinel structure and regulate both the catalytic sites and the available lattice oxygen, resulting in the CH₄ conversion and CO selectivity being maintained at 96–98% and above 98% for the most promising oxygen carrier, with an Fe₂O₃ content of 20 wt% and Fe/Ni molar ratio of 10. The surface, phase, and particle size were kept the same over 90 cycles, leading to high stability. During the CLSR cycles, conversion from Fe³⁺ to Fe²⁺/Fe⁰ occurs, along with transformation between Ni²⁺ in NiAl₂O₄ and Ni⁰. Overall, the results demonstrate the feasibility of using spinel containing earth-abundant elements in CLSR and the importance of cooperation between oxygen release and CH₄ activation. Full article