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Comprehensive Summary: Inorganic lead halide perovskite (LHP) nanostructures, represented by formula CsPbX3 (X = Cl, Br, I), have garnered considerable interest for their exceptional optical properties and diverse applications. Despite their potential, challenges such as environmental degradation persist. In‐situ synthesis within protective materials pores is a promising way to address this issue. However, confining perovskite nanostructures into porous matrices during the synthesis can limit their photoluminescence quantum yield (PL QY) and tunability of optical properties. Various post‐treatment approaches exist to improve the properties of LHP and achieve their desired functionalities, but these strategies have not been explored for LHP confined in mesoporous matrices. Here, we demonstrate the efficacy of in‐situ post‐synthetic treatments to improve the optical properties of CsPbBr3 nanocrystals grown in nanoporous silica microspheres. Surface passivation with Br– ion‐containing precursors boosts PL QY, while anion‐assisted cation doping with Mn2+ ions introduces a new PL band. The adjustment of precursor amount and doping duration enables precise control over the optical properties of LHP, while additional coating with a SiO2 shell enhances their stability in polar solvents, expanding the potential applications of these composites. [ABSTRACT FROM AUTHOR]

Polycaprolactone (PCL) is a highly regarded biodegradable and environmentally friendly material that is extensively researched and applied in the field of biomedicine due to its exceptional biodegradability, biocompatibility, and other advantageous properties. The monomer ε-Caprolactone (ε-CL) plays a critical role in the synthesis of PCL, making it a key focus of study. This paper describes the preparation of hydrotalcite HT-Zn and SBA-15 through simple synthetic methods, and the subsequent creation of a hydrotalcite/SBA-15 composite catalyst, named HT-Zn/SBA-15, through a post-generation approach combining hydrotalcite and SBA-15. Scanning electron microscopy (SEM), wide-angle X-ray diffraction (XRD), and infrared spectroscopy (FT-IR) were employed to analyze the structures of the synthesized materials. The catalytic effects in Baeyer–Villiger oxidation were then investigated to examine the impact of various catalysts, solvents, and reaction conditions. The results indicated that utilizing HT-Zn/SBA-15 as the catalyst, acetonitrile as the solvent, and H2O2 as the oxidant, led to a conversion rate of cyclohexanone exceeding 80% and a selectivity of ε-CL surpassing 90% under the ideal reaction conditions. Additionally, the catalyst demonstrated excellent reusability, being able to be reused up to six times. [ABSTRACT FROM AUTHOR]

[Display omitted] Atmospheric water harvesting through reticular materials is an innovation that has the potential to change the world. Here, this study offers a technique for creating a solar-powered hygroscopic polymer material for atmospheric water harvesting with the reticular materials. The results show that the porous hygroscopic polymer materials can achieve high performance with high vapor capture (up to ac. 28.8–49.7 mg/g at 28–38 %RH and 25 ℃), rapid photothermal conversion efficiency (up to 32.2 ℃ within 15 min under 1000 W/m−2 light at 25 ℃), a low desorption temperature (lower than 40 ℃), and an effective water release rate. Besides, the material also has excellent water-retention properties, which can effectively store desorbed liquid water in polymer networks for use by vegetation during water demand periods. The strategy opens new avenues for atmospheric water-harvesting materials, which will hopefully solve the global crisis of freshwater shortages. [ABSTRACT FROM AUTHOR]

A process of CO2 decomposition in dielectric barrier discharge reactor using mesoporous CeO2-NiO catalysts was studied. Mesoporous materials of MCM-41, SBA-15 and MCF types were used in this study to investigate the influence of the material structure on CO2 decomposition efficiency. The obtained catalysts were characterized by physico-chemical methods: low temperature N2 adsorption, X-Ray diffraction and X-Ray photoelectron spectroscopy. CO2 conversion, CO yield and CO selectivity as well as energy efficiency and specific energy input were calculated. The comparison of process efficiency was conducted with that in the absence of any catalyst (plasma-only reactor). It was shown that in the presence of Ce-based catalysts, the conversion of CO2 (from 11 to 19%) and CO yield rise significantly, while CeNi samples show minor performance in CO2 plasma-catalytic dissociation. Porous characteristics affected the performance of CO2 decomposition. Using wide-porous MCF-type material as a support, it was possible to achieve the highest conversion due to enhanced CO2 adsorption in pores and subsequent plasma-catalytic decomposition. The combination of mesoporous silica material as a support and a CeO2 as an active component is promising for the plasma-catalytic CO2 splitting. [ABSTRACT FROM AUTHOR]

Woody biomass is an abundant renewable resource. In this study, aerogels for versatile triboelectric devices are fabricated from poplar biomass via a dissolution‐and‐regeneration method with concentrated lithium bromide solution as the solvent. To improve the aerogels' structural homogeneity, two treatments—ball‐milling the raw poplar woody biomass before its dissolution, and, separately, ultrasonication following its dissolution—were applied. These treatments altered the porous structures and mechanical properties of the resulting aerogels, leading to a marked increase in their triboelectric performance. Removing the majority of the lignin from the aerogels was also explored, and resulted in triboelectric output ≈5 times greater than that of pristine woody biomass aerogel (i.e., without ball milling, ultrasonication, or lignin reduction). The underlying mechanisms of such increases were found to be both chemical and physical. Next, triboelectric devices were fabricated using the optimal (i.e., low‐lignin) aerogel for energy harvesting and biomechanical monitoring. These devices were able to: 1) respond sensitively to force, likely due to the aerogel's porous structures; 2) capture mechanical energy, charge capacitors, and power small portable electronics; and 3) monitor biomechanical movements including respiration, joint motions, and gait‐pattern changes. [ABSTRACT FROM AUTHOR]

Porous clay heterostructures are a hybrid precursor between the pillaring process and organoclays. In this study, the organoclay was substituted by an aluminium intercalated species clay or pillared alumina clays. A porous clay heterostructure was successfully achieved from an aluminium intercalated species clay, due to the easy exchange of the aluminium species by the cosurfactant and silica species. However, using alumina pillared clays, the porous clay heterostructures were not formed; the alumina species were strongly attached to clay sheets which made difficult their exchange with cosurfactant molecules. In this case, the silica species were polymerized and decorated the surface of the used materials as indicated by different characterization techniques. The specific surface area of the porous clay heterostructure material reached 880 m2/g, and total pore volume of 0.258 cc/g, while the decorated silica alumina pillared clays exhibited lower specific surface area values of 244–440 m2/g and total pore volume of 0.315 to 0.157 cc/g. The potential of the synthesized materials was evaluated as a basic blue-41 dye removal agent. Porous clay heterostructure material has a removal capacity of 279 mg/g; while the other materials exhibited lower removal capacities between 75 mg/g and 165 mg/g. The used regeneration method was related to the acidity of the studied materials. The acidity of the materials possessed an impact on the adopted regeneration procedure in this study, the removal efficiency was maintained at 80% of the original performance after three successive regeneration cycles for the porous clay heterostructure. The Langmuir isotherm characteristics were used to propose a single-stage batch design. Porous clay heterostructures with a higher removal capacity resulted in a decrease in the quantities needed to achieve the target removal percentage of the BB-41 dye from an aqueous solution. [ABSTRACT FROM AUTHOR]

This study employed lignin-sulfonated (LS) to develop biobased carbon materials (LS-Cs) through a sulfur-doping approach to enhance their physicochemical properties, adsorption capabilities, and energy storage potentials. Various characterization techniques, including BET surface area analysis, SEM imaging, XPS, Raman spectroscopy, and elemental composition (CHNS), were employed to assess the quality of the LS-Cs adsorbent and electrode samples. Response Surface Methodology (RSM) was utilized for optimizing the two main properties (specific surface area, ABET, and mesopore area, AMESO) by evaluating three independent factors (i.e., activation temperature, ZnCl2:LS ratio, and sulfur content). According to the statistical analysis, ABET and AMESO were affected by ZnCl2 and sulfur content, while the pyrolysis temperature did not affect the responses in the studied conditions. It was found that increasing the ZnCl2 and sulfur contents led to an increment of the ABET and AMESO values. The LS-C materials exhibited very high ABETvalues up to 1993 m2 g−1 and with predominantly mesoporous features. The S-doping resulted in LS-Cs with high sulfur contents in their microstructures up to 15% (wt%). The LS-C materials were tested as adsorbents for sodium diclofenac (DCF) adsorption and reactive orange 16 dye (RO-16) and as electrodes for supercapacitors. The LS-Cs exhibited excellent adsorption capacity values for both molecules (197–372 mg g−1) for DCF, and (223–466 mg g−1) for RO-16. When tested as electrodes for supercapacitors, notably, LS-C3, which is a doped sample with sulfur, exhibited the best electrochemical performance, e.g. high specific capacitance (156 F/g at 50 mV/s), and delivered an excellent capacitance after 1000 cycles (63 F/g at 1 A/g), which denotes the noteworthy capacitive behavior of the S-doped electrode. Thus, the present work suggests an eco-friendly resource for developing effective, productive carbon materials for adsorbent and electrodes for SC application. However, further studies on the complete application of these materials as adsorbents and electrodes are needed for a deeper understanding of their behavior in environmental and energy storage applications. [ABSTRACT FROM AUTHOR]

Immobilization of the reactive metal sites over high surface area porous nanomaterial is a very demanding route in designing novel nanocatalysts for the synthesis of valuable fine chemicals. Here we report an efficient, eco‐friendly and sustainable route for the synthesis of aminophenoxazinone derivatives via oxidative coupling of o‐aminophenols catalysed by a novel mesoporous highly ordered Ni(II)‐complex functionalized mesoporous heterogeneous organosilica catalyst. A novel structurally characterized Ni(II)‐complex derived from 2‐(I‐(2‐(piperizin‐1‐yl) ethylimino) methyl)‐5‐methylphenol ligand has been immobilised over a 2D‐hexagonally ordered functionalized mesoporous SBA‐15 synthesized via surface functionalization of SBA‐15 material with 3‐aminopropyltriethoxysilane (APTES) to obtain the Ni(II)‐nanocatalyst SANI. Its catalytic activity has been explored for three different substrates like o‐aminophenol (OAP), 3‐amino‐4‐hydroxybenzoic acid (CAP) and 2‐amino‐4‐methylphenol (MAP) that produces corresponding phenoxazinone derivatives having the yields of 92, 81 and 85 %, respectively. suggesting wide scope of this supported mesoporous nanocatalyst. [ABSTRACT FROM AUTHOR]

Silica mesoporous materials have been the subject of wide scientific interest with various applications. However, the environmental impacts associated with their preparation have scarcely been studied. In the present work, we applied the Life Cycle Assessment (LCA) methodology to the materials MCM-41, MCM-48, UVM-7, mesoporous Stober particles, SBA-15, SBA-16, HMS, KIT-5, KIT-6, MSU, FDU, nano-MCM-41 and nano-MCM-48 for small- (grams) and large-scale (several kilograms) production. Furthermore, various improvements are proposed, and the impact associated with each of them is quantified. The results show that the values of a single score, a normalized and weighed combination of the damage categories, and net greenhouse gas emissions (NGHGE) are highly dependent on the synthesis procedures. On a small scale, the main impact is due to the use of energy and solvents. By contrast on a large scale, the use of solvents, tetraethylorthosilicate and the structure directing agent are the main determinants. From the values obtained for the different materials and scenarios, we estimate that the preparation of this class of materials could have an NGHGE of 54 ± 30 and 31 ± 18 kg CO2 eq. per kg of mesoporous material for small- and large-scale production, respectively. The use of calcination versus extraction, the incorporation of renewable energy and distillation/rectification are initiatives that can contribute to a significant reduction of the environmental impact. [ABSTRACT FROM AUTHOR]

This study investigates the adsorption of pollutants with different chemical structures; organic Naphtol Green B (NGB) dye and copper on a nanocomposite material with a hexagonal structure of the SBA-15 type. This research is divided into two main parts: the first carries out the synthesis of SBA-15 (Santa Barbra Amourphous) and its derivatives phases functionalized by 3-aminopropyl-triethoxylane (APTES) and calcined at 823 K. The second part presents the influence of the adsorption conditions on the adsorption efficiency of NGB dye and copper. High-resolution X-ray diffractogram (XRD) showed three distinct peaks characteristic of highly ordered mesoporous material. Nitrogen adsorption–desorption isotherm of SBA-15 at 77 K° is type IV typical of mesoporous materials. In addition, Fourier transform infrared spectroscopy (FT-IR) was also used in the characterization before and after the adsorption of the selected pollutants. At optimal conditions of pH 5.2, initial concentration of 50 mg/L, adsorbent dosage of 20 mg, and at adsorption time of 90 min the maximum removal of pollutants reached 76% and the adsorption capacity was 227.25 mg/g for NGB dye and 221.006 mg/g for copper. Furthermore, the adsorption kinetics followed the pseudo-second-order model, indicating that chemisorption was the dominant mechanism and the Sips isotherm model best described the adsorption data. Our research demonstrates that the SBA-15 material after modification is an effective adsorbent for removing effluents regardless of their different chemical structure (organic and inorganic). [ABSTRACT FROM AUTHOR]

This document provides a summary of a collection of articles on porous nanomaterials. It discusses the importance and applications of these materials, such as catalysis, drug delivery, and energy storage. The document highlights recent advancements in the synthesis and characterization of porous nanomaterials, focusing on silica, carbon-based materials, metal-organic frameworks (MOFs), and zeolites. It also presents specific studies on the synthesis and application of these materials, as well as their potential in various industries. The summary acknowledges the contributions of the authors to the Special Issue and emphasizes the need for continued research in this field. [Extracted from the article]

Since early developments in the field of mesoporous materials, mesoporous silica has attracted large interest in drug delivery, as they display an ordered array of pores with diameters ranging from 2 to 50 nm, which can be loaded with drugs. Mesoporous silica dissolves at physiological pH, triggering the release of loaded drugs. Several studies have focused on determining the key factors that determine the biodistribution, biocompatibility, and toxicity both in vitro or in vivo. However, in vivo studies focused on the degradation of mesoporous silica materials are very scarce, despite its relevance for drug release. In this perspective, recent works addressing mesoporous materials degradation in the context of drug delivery are discussed, first from a physicochemical point of view, and secondly in in vivo settings, in animal models that are the closest conditions to the encountered when the mesoporous materials are administered to humans. Finally, further discussion about the future directions in the design of mesoporous nanomaterials for therapy and for the study of their biological fate are presented. [ABSTRACT FROM AUTHOR]

Background: Therapeutic approaches that combine conventional photodynamic therapy (PDT) with gas therapy (GT) to sensitize PDT are an attractive strategy, but the molecular structure design of the complex lacks effective guiding strategies. Results: Herein, we have developed a nanoplatforms Cy-NMNO@SiO2 based on mesoporous silica materials loaded NIR-activatable small-molecule fluorescent probe Cy-NMNO for the synergistic treatment of photodynamic therapy/gas therapy (PDT/GT) in antibacterial and skin cancer. The theoretical calculation results showed that the low dissociation of N-NO in Cy-NMNO enabled it to dissociate effectively under NIR light irradiation, which is conducive to produce Cy and NO. Cy showed better 1O2 generation performance than Cy-NMNO. The cytotoxicity of Cy-NMNO obtained via the synergistic effect of GT and PDT synergistically enhances the effect of photodynamic therapy, thus achieving more effective tumor treatment and sterilization than conventional PDT. Moreover, the nanoplatforms Cy-NMNO@SiO2 realized efficient drug loading and drug delivery. Conclusions: This work not only offers a promising approach for PDT-GT synergistic drug delivery system, but also provides a valuable reference for the design of its drug molecules. [ABSTRACT FROM AUTHOR]

The transesterification reaction between ethylene carbonate (EC) and methanol is a sustainable method to produce dimethyl carbonate (DMC). As typical solid bases, carbon nitride (CN) materials have demonstrated catalytic application in many base-catalyzing reactions. In this work, in order to increase the surface area and improve the base intensity of the CN material, microporous MCM-22 was utilized to load CN, and then treated by NaOH (a.q.), thus enabling CN/MCM-22 composites being transferred into mesoporous CN-SiAlO materials. The physicochemical properties of the synthesized materials were analyzed by XRD, N2 adsorption–desorption, FT-IR, XPS, SEM, TG, and CO2-TPD. As mesoporous base catalysts, the CN-SiAlO materials showed superior catalytic activity to the bare CN and CN/MCM-22 in the transesterification reaction of EC with methanol. Under reaction temperature of 130 °C and reaction time of 3 h, the yield of DMC was up to 83.3%. [ABSTRACT FROM AUTHOR]

Hierarchically porous monolithic silica shows promise as a carrier material for immobilized organocatalysts. Conventional analysis usually includes physisorption, infrared spectroscopy and elemental analysis, among others, to elucidate the pore space and degree of functionalization of the material. However, these methods do not yield information about the spatial distribution of the organic species inside the monolithic reactor. In this work, time‐of‐flight secondary ion mass spectrometry has been applied to characterize the surface of organically functionalized silica monoliths. Cross sections of a silica monolith functionalized with 4‐dimethylaminopyridine were analyzed and the results were compared with physisorption and elemental analysis experiments of the same material. This way, insight into the radial distribution of the catalyst could be achieved, which might assist in interpreting the performance of such reactors in heterogeneous flow catalysis. [ABSTRACT FROM AUTHOR]

A porous, crosslinked aromatic polyamide having COCl and COOH groups (referred to as PA herein) prepared had a mesoporous structure and comprised agglomerates of particles with average diameters of approximately 30 nm. The PA was found to swell with significant deformation in response to water vapor, but was almost unchanged after exposure to toluene vapor. The polymeric structure returned to its original porous morphology after removal of the solvents, demonstrating that the PA possessed affinity for specific solvents and shape memory. The chemical composition and porous structure of the PA were also not affected by heating to 330 °C. The COCl groups in the PA could be modified by reaction with 2,4,6‐triaminopyrimidine (TAP), resulting in a doubly crosslinked structure based on the reaction with the TAP as well as the existing amide moieties in the polymer. The degree of modification was highly dependent on the reaction solvent used. The porous structure of the PA was essentially unchanged after this modification. The TAP‐based crosslinks in the modified PA could be selectively cleaved along with vaporization of the TAP by heating at 330 °C, which no change to the porous structure. Thus, the PA showed excellent heat resistance and structural stability. [ABSTRACT FROM AUTHOR]

Highly active transition metal oxides mesoporous materials have tremendous potential applications in energy storage and catalysis due to their great physicochemical performance. However, the regulation of porous structures still faces many challenges, and the synthesis of mesoporous materials is usually costly and long-time consuming. Herein, using CoO as the example, a strategy based on KOH activation and substitution reaction has been proposed to prepare CoO nanoarrays mesoporous material and improve its electrochemical performance. The CoCO3Co(OH)2 nanoarrays on Ni foam are transformed into a Co(OH)2 nanoarrays with high crystallinity through the substitution reaction in KOH solution. Meanwhile, the activation effect of KOH provides abundant porous structures for etching the nanoarrays. During the annealing process, the high crystallinity of Co(OH)2 effectively alleviates pore collapse, thereby obtaining a CoO nanoarrays mesoporous material with excellent electrochemical performance (denoted as A-CoO@NF). As the positive electrode material for supercapacitors, A-CoO@NF shows a high specific capacity of 775.6 C g−1, far higher than that of CoO@NF (416.5 C g−1). The enhanced electrochemical performance is attributed to its unique mesoporous structures, which positively promote electrolyte permeation and ion diffusion, and the ultrafine nanocrystals and smaller lattice parameters provide numerous edge active sites and enhance the conductivity. The strategy proposed here is expected to become a template-free, low-cost, and efficient preparation route for synthesizing more types of highly active metal oxide mesoporous materials. [ABSTRACT FROM AUTHOR]

In this work, a porous Co 3 O 4 anode material with capsule–shaped morphology is prepared by a simple solvothermal method and subsequent heat treatment process in air. The as–synthesized CoCO 3 precursor and Co 3 O 4 sample are systematically studied and analyzed by a series of testing technologies, such as XRD, FTIR, FESEM, (HR)TEM, TGA, XPS and N 2 adsorption/desorption measurement. As negative materials in Li–ion batteries, the Co 3 O 4 active material exhibits high charge/discharge specific capacity, good rate performance and satisfactory cycle stability. The excellent electrochemical properties are inevitably related to the structural characteristics of the electrode material itself, including regular morphology, rich pore structure, large specific surface area, high crystallinity, nanoscale particle size, etc. [ABSTRACT FROM AUTHOR]

In response to the ever increasing need to develop more efficient and sustainable methods for removing heavy metal contaminants from aqueous systems, the following article reports on the design of highly mesoporous alginate‐derived materials (Starbon®) and their application to the adsorption of heavy metals. Using the Starbon® process to expand, dry and pyrolyse an inherently porous polysaccharide precursor, it was possible to produce mesoporous materials (BJH mesopore volumes 0.81–0.94 cm3 g−1) with large surface areas (157–297 m2 g−1) across a range of low pyrolysis temperatures (200–300 °C). The mechanisms of thermal decomposition were explored in terms of chemical and structural changes using N2‐sorption porosimetry, thermogravimetric analysis, titration, FT‐IR spectroscopy and 13C NMR spectroscopy. It was found that, as a result of intermolecular dehydration and crosslinking, sufficient chemical stability is obtained by the intermediate temperature of 250 °C, with limited improvement seen at higher temperatures. In addition, the materials retained large metal adsorption capacities (0.70–1.72 mmol g−1) as well as strong selectivity for Cu2+ ions (over Co2+ and Ni2+), as compared to commercial petrochemical‐derived cation exchange resin Amberlite™ Mac 3H. Thus, highlighting the potential of Starbon® materials as a sustainable answer to the widespread problem of heavy metal‐contaminated wastewaters. [ABSTRACT FROM AUTHOR]

The fast developing world is in search of measures to control the accumulation of unused by‐products and waste materials generated during the production of useful commodities. Accordingly, wastes from agro‐industrial sectors can form raw materials for the production of various resources that are extensively used in many areas such as gas sorption and energy production. In the present work, cashew nut shell liquid (CNSL), the vesicant liquid present in the outer shell of cashew seed, forms the source material for the synthesis of porous organic polymers for carbon dioxide capture. Herein, novel types of hypercrosslinked polymers (HCPs) are synthesized via a simple Friedel–Crafts reaction with CNSL as the starting material. Polymerization of natural CNSL with dimethoxymethane/bis‐(chloromethyl)‐biphenyl as external crosslinker provides products in quantitative yield. One of the synthesized HCP is tuned to attain the required high porosity by carbonization at elevated temperatures using an activator. Thus, activated carbon material prepared at 700°C is found to have a high surface area of 880 m2/g with a good carbon dioxide adsorption capacity of 14.72 wt%. These porous materials had moderate isosteric heat of adsorption (23–31 kJ/mol) with excellent recycling capability. [ABSTRACT FROM AUTHOR]

The development of high‐performance catalysts for formic acid (FA) dehydrogenation is of extreme significance to the successful production of hydrogen under ambient conditions. Despite some encouraging progress, their activity is still unsatisfied than needed. In this work, it is presented that Lewis acidic VOx sites engineered ultrafine PdAu nanoclusters (PdAu‐VOx) perform perfectly for hydrogen production from FA dehydrogenation. Strikingly, the best catalyst — PdAu‐VOx embed in amino‐functionalized hollow mesoporous support (PdAu‐VOx/NHMS) discloses an impressive initial turnover frequency of 14155 h−1 and a low activation energy of 31.2 kJ mol−1 without additives at room temperature, and maintains 100% selectivity and conversion in the tenth cycle reaction. Mechanistic investigations illustrate that VOx species can serve as the Lewis acid sites, which not only regulate the adsorption strength of reactant and intermediate on PdAu, but also reinforce the C─H bond activation within FA molecule, thereby promoting the reaction kinetics for efficient hydrogen production. This work thus provides a strategy for the development of new‐style heterogeneous catalysts with Lewis acid‐base sites applied to a variety of energy‐related catalytic reactions. [ABSTRACT FROM AUTHOR]

Mesoporous materials find widespread applications due to their high specific surface area, contributing to enhanced performance. Scanning electron microscopy (SEM) observation of mesoporous materials provides valuable insights into their mesostructures. However, direct observation of the outermost surfaces, which often dictate material properties, remains challenging, especially for highly insulating and fragile compounds. In this study, utilizing SEM observation with ultra‐low‐voltage acceleration directed by Gemini column is proposed to achieve direct surface imaging of mesoporous organic materials with highly insulating and fragile characteristics. By observing mesostructured polymers obtained through a soft‐templating method without washing, stuffed pores are identified allowing the differentiation of micelle templates and polymer walls. Moreover, leveraging SEM measurements, a polymerization mechanism is proposed for dopamine on the polymer micelles adhered to the graphene oxide nanosheets. These findings demonstrate the potential of SEM measurements with ultra‐low accelerating voltage in facilitating surface observations of polymer‐derived nanomaterials characterized by high insulating properties and a fragile framework. [ABSTRACT FROM AUTHOR]

Aluminosilicate (Al‐SiO2) thin films with vertically aligned mesochannels were successfully synthesized on Indium Tin Oxide (ITO) electrodes and employed for the immobilization of a cationic Ru(II) water oxidation catalyst without requiring linker groups. Optimal synthesis conditions yielded uniform mesoporous Al‐SiO2 films with tunable Al content, high surface area (568 m2/g), 3.94 nm pore size, and 155 nm thickness. Electrochemical studies confirmed the presence of the immobilized Ru complex undergoing diffusion‐controlled Ru(III/II) and Ru(IV/III) electron transfer. The Ru loading reached 4.71 nmol/cm2 at Si/Al=9.6, with higher Al content enhancing loading amounts via cation exchange. The Ru‐modified electrode exhibited high electrocatalytic water oxidation activity, achieving 75.3 % Faradaic efficiency and a turnover number of 298.6 for O2 evolution for 1 hour. This work provides a new approach to construct porous environments on an electrode surface to immobilize positively charged transition‐metal complexes as catalysts, offering potential applications in the development of electrocatalytic systems for energy conversion. [ABSTRACT FROM AUTHOR]

Developing efficient catalysts for visible light reactions is vital in the field of photocatalysis. This study focuses on the synthesis of novel ternary composites (α-DMACoPc/TiO2/MIL-101 (Fe)) by leveraging the excellent adsorption properties of MIL-101 (Fe), the photosensitizing capabilities of phthalocyanine, and the photocatalytic potential of TiO2. The nanocomposites' structural and optical attributes were thoroughly analyzed. X-ray powder diffraction (XRD) was utilized to showcase the crystalline nature of the composites. Furthermore, Fourier transform infrared (FT-IR) studies confirmed the formation of ternary nanocomposites. Optical absorption investigations demonstrated the tuning of the optical band gap from the UV to the visible range. The results indicated that nearly 94% of the organic material was decomposed after 150 min of exposure to simulated sunlight from a xenon lamp. This high efficiency can be attributed to the synergistic interaction among the composites, enhancing light absorption. The composite's robust stability was evidenced through cyclic tests. Valuable information was provided to advance the design and synthesis of photocatalysts consisting of metal–organic frameworks synergized with semiconductors. Exploring the possibility of mesoporous materials was based on MOFs for photodegradation of organic pollutants. The photocatalytic degradation of organic pollutants by MOFs mesoporous materials was also investigated. The potential of composite materials in the field of dye degradation of industrial waste is confirmed. The good recycling photocatalytic reusability indicates the promising application of this photocatalyst. [ABSTRACT FROM AUTHOR]

In this study, Cu2O nanoparticles were synthesized using the sol–gel technique and subsequently functionalized with extracts from plants of the Rauvolfioideae subfamily and citrus fruits. Comprehensive characterization techniques, including UV-Vis spectroscopy, FT-IR, XRD, BET, SEM, and TEM, were employed to evaluate the structural and surface properties of the synthesized nanoparticles. The results demonstrated that both functionalized Cu2O nanoparticles exhibit mesoporous structures, as confirmed by nitrogen adsorption–desorption isotherms and the pore size distribution analysis. The green extract functionalized nanoparticles displayed a more uniform pore size distribution compared to those functionalized with the orange extract. The study underscores the potential of these functionalized Cu2O nanoparticles for applications in drug delivery, catalysis, and adsorption processes, highlighting the influence of the functionalization method on their textural properties and performance in antibacterial efficacy. [ABSTRACT FROM AUTHOR]

Diffusional limitations associated with zeolite microporous systems can be overcome by developing hierarchical zeolites, i.e., materials with a micro- and mesoporous framework. In this work, Y and ZSM-5 zeolites were modified using a surfactant-mediated hydrothermal alkaline method, with NaOH and cetyltrimethylammonium bromide (CTAB). For Y zeolite, after a mild acidic pretreatment, the effect of the NaOH+CTAB treatment time was investigated. For ZSM-5 zeolite, different concentrations of the base and acid solutions were tested in the two-step pretreatment preceding the hydrothermal treatment. The properties of the materials were studied with different physical–chemical techniques. Hierarchical Y zeolites were characterized by 3.3–5 nm pores formed during the alkaline treatment through the structure reconstruction around the surfactant aggregates. The effectiveness of the NaOH+CTAB treatment was highly dependent on the duration. For intermediate treatment times (6–12 h), both smaller and larger mesopores were also obtained. Hierarchical ZSM-5 zeolites showed a disordered mesoporosity, mainly resulting from the pretreatment rather than from the subsequent hydrothermal treatment. High mesoporosity was obtained when the concentration of the pretreating base solution was sufficiently high and that of the acid one was not excessive. Hierarchical materials can be obtained for both zeolite structures, but the pretreatment and treatment conditions must be tailored to the starting zeolite and the desired type of mesoporosity. [ABSTRACT FROM AUTHOR]

Mesoporous carbon nitride (MCN-K) was prepared using mesoporous KIT-6 material as a template and ethylenediamine and carbon tetrachloride as N and C sources, respectively. The synthesized MCN-K was treated with sulfuric acid under different experimental conditions, thus obtaining sulfonated MCN-KS adsorbents. The effects of initial solution pH, initial dye concentration, adsorbent amount, and temperature on Rhodamine-B (Rh-B) dye removal were investigated. The XRD, FT-IR, and N2 adsorption–desorption analyses confirmed that the mesoporous carbon nitride structure was successfully synthesized. The high nitrogen content (C/N molar ratio: 4.0) of the MCN-K sample was confirmed by (carbon, hydrogen, nitrogen and sulfur) CHNS elemental analysis. The XPS analysis was used to characterize the chemical states of the C, N and S atoms in the MCN-K and MCN-KS sorbents. It was found that there was not much difference between the removal percentages (93.13–89.92%) obtained in the pH range (4–12) studied. This result was attributed to the zwitter-ion form of Rh-B. The exothermic nature of the adsorption process of Rh-B on the MCN-K sorbent was determined by adsorption experiments performed at different temperatures. Adsorption capacities obtained from the Langmuir model were 185.2–104.2 mg/g in the studied temperature range. The kinetic behavior of the adsorption process was explained by the pseudo-second-order kinetic model in terms of both correlation coefficients (R2 > 0.91) and qe (35.59–190.26 mg/g) values. When the percentages of dye removal of the un-sulfonated and sulfonated samples were compared, it was found that sulfonation increased the adsorption rate considerably but did not contribute positively to the dye removal percentage. [ABSTRACT FROM AUTHOR]

Poly-aluminium chloride (PAC) sludge is a waste product created during drinking water treatment, usually generated in large quantities and typically landfilled. More attention must be directed to environmental-friendly management and economically sustainable of Al-based sludge. In this work, a low-cost and environmental-friendly adsorbent prepared by sodium alginate coated PAC sludge (SPS) was investigated for fluoride removal. Basic preparing parameters including heating temperature (200–800°C), sodium alginate concentration (0.5–5 wt%), particle size (1–2 mm, 2–3 mm, 3–4 mm) and operating parameters including dosage (1–14 g/L), solution pH (4–11), temperature (10–35°C), co-existing anions (NO3−, Cl−, SO42-, PO43-) were examined to evaluate the optimum defluoridation capacity. The prepared SPS adsorbents reached a high removal efficiency of 95.6% with initial fluoride concentration of 10 mg/L, dose of 8 g/L, contact time of 24 h, pH value of 7 and temperature of 10°C. The kinetic study indicated that fluoride adsorption followed the pseudo-second-order kinetics well (R2 = 0.9942), and adsorption isotherms can be well described by Freundlich model (R2 = 0.9952). Thermodynamic studies showed the fluoride adsorption was spontaneous and exothermic. The elements and functional groups of SPS adsorbents were analysed by using EDS and FTIR, respectively. The adsorption mechanism involved physisorption, ligand-exchange and electrostatic attraction. According to N2 adsorption–desorption isotherm, the SPS was mesoporous material which facilitated the adsorption of fluoride ions. Also, aluminium presented in form of Al-OH in SPS adsorbents had significant contribution in fluoride adsorption. The concentration of the residual aluminium ions was 4.48 × 10−3 mg/L which is lower than the China Drinking Water Standard. The encouraging results of this preliminary study indicated that SPS is an environmental-friendly and cost-effective treatment option for groundwater with fluoride pollution. [ABSTRACT FROM AUTHOR]

Boron-doped ordered mesoporous carbons (B-OMCs) were synthesized by a onepot soft-templating strategy, where resorcinol and formaldehyde were used as carbon sources, boric acid was used as boron source, and Pluronic F127 was used as structure directing agent. The effect of temperature and the boric acid content on the physical and electrochemical properties of the resultant materials were investigated. Inductively coupled plasma atomic emission spectroscopy (ICP-OES) was used for elemental analysis of the samples. The synthesis temperature did not have an overall positive effect on the doping of boron with a fixed amount of boron source. However, there was a clear increase in the doped-boron content when both the temperature and the boric acid content were increased. Nitrogen adsorption analysis isotherms showed that the samples had similar ordered mesoporous structures with surface areas varying between 535 and 712 m²/g. The uniform morphology in transmission electron microscopy (TEM) also confirmed the ordered mesoporous structure. Employing cyclic voltammetry analysis, the highest oxygen reduction activity (-0.28 mA/cm²) was achieved with the highest boron-doping percentage (0.29%) for a synthesis temperature of 77°C and boric acid to carbon ratio of 2. These results show that the boron-doped ordered mesoporous carbon is a promising material as catalyst support for improving the oxygen reduction reaction activity. [ABSTRACT FROM AUTHOR]

Recent improvements in advanced technology for toxic chemical remediation have involved the application of titanium oxide nanoparticles as a photocatalyst. However, the large energy bandgap associated with titanium oxide nanoparticles (3.0–3.20 eV) is a limitation for their application as a photocatalyst within the solar spectrum. Various structural modification methods have led to significant reductions in the energy bandgap but not without their disadvantages, such as electron recombination. In the current investigation, biochar was made from the leaves of an invasive plant (Acacia saligna) and subsequently applied as a support in the synthesis of titanium oxide nanoparticles. The characterization of biochar-supported titanium oxide nanoparticles was performed using scanning electron microscopy, Fourier transformer infrared, X-ray diffraction, and Brunauer–Emmett–Teller analyses. The results showed that the titanium oxide was successfully immobilized on the biochar's external surface. The synthesized biochar-supported titanium oxide nanoparticles exhibited the phenomenon of small hysteresis, which represents the typical type IV isotherm attributed to mesoporous materials with low porosity. Meanwhile, X-ray diffraction analysis revealed the presence of a mixture of rutile and anatase crystalline phase titanium oxide. The synthesis of biochar-supported titanium oxide nanoparticles was highly efficient in the degradation of Orange II Sodium dye under solar irradiation. Moreover, 83.5% degradation was achieved when the biochar-supported titanium oxide nanoparticles were used as photocatalysts in comparison with the reference titanium oxide, which only achieved 20% degradation. [ABSTRACT FROM AUTHOR]

There has been a growing interest in ecofriendly enzymatic processes. However, enzyme solubility limits the application of many biocatalysts in continuous systems, requiring the development of cost‐effective strategies for enzyme immobilization. Based on this premise, this study investigated the application of lipase immobilized in starch–alginate beads for oil transesterification in a tubular reactor. An economical derivative was produced by immobilizing Eversa Transform 2.0 in 50:50 (w/w) starch–alginate beads using the jet‐cutting technique. The biocatalyst had a particle size of about 500 μm and activity of 138.67 ± 18.53 U g−1. X‐ray photoelectron spectroscopy showed nitrogen content ranging from 6.38% to 7.29%, with uniform distribution of lipase throughout the beads. Nitrogen isotherms were characteristic of mesoporous materials, with an average pore diameter of 48.09 Å and low surface area (0.69 m2 g−1). A face‐centered central composite design was used to study soybean oil transesterification. In the best four runs, the process achieved a mean triglyceride conversion of 45%. High ester productivity levels (2.05 × 10−2% ester g−1 biocatalyst min−1 or 1.5 × 10−4% ester U−1 min−1) were obtained. Biocatalyst reuse led to a twofold increase in ester concentration (14.57% vs 7.7%). These findings confirm the successful development of a low‐cost biocatalyst suitable for use in continuous reactions. [ABSTRACT FROM AUTHOR]

The field of oncology has transformed in recent years, with treatments shifting from traditional surgical resection and radiation therapy to more diverse and customized approaches, one of which is immunotherapy. ICD (immunogenic cell death) belongs to a class of regulatory cell death modalities that reactivate the immune response by facilitating the interaction between apoptotic cells and immune cells and releasing specific signaling molecules, and DAMPs (damageassociated molecular patterns). The inducers of ICD can elevate the expression of specific proteins to optimize the TME (tumor microenvironment). The use of nanotechnology has shown its unique potential. Nanomaterials, due to their tunability, targeting, and biocompatibility, have become powerful tools for drug delivery, immunomodulators, etc., and have shown significant efficacy in clinical trials. In particular, these nanomaterials can effectively activate the ICD, trigger a potent anti-tumor immune response, and maintain long-term tumor suppression. Different types of nanomaterials, such as biological cell membrane-modified nanoparticles, self-assembled nanostructures, metallic nanoparticles, mesoporous materials, and hydrogels, play their respective roles in ICD induction due to their unique structures and mechanisms of action. Therefore, this review will explore the latest advances in the application of these common nanomaterials in tumor ICD induction and discuss how they can provide new strategies and tools for cancer therapy. By gaining a deeper understanding of the mechanism of action of these nanomaterials, researchers can develop more precise and effective therapeutic approaches to improve the prognosis and quality of life of cancer patients. Moreover, these strategies hold the promise to overcome resistance to conventional therapies, minimize side effects, and lead to more personalized treatment regimens, ultimately benefiting cancer treatment. [ABSTRACT FROM AUTHOR]

Functionalized mesoporous materials have become a promising carrier for enzyme immobilization. In this study, Santa Barbara Amorphous 15 (SBA-15) was modified by N-aminoethyl-γ-aminopropyl trimethoxy (R). R-SBA-15 was employed to purify and immobilize recombinant β-glucosidase from Terrabacter ginsenosidimutans (BgpA) in one step for the first time. Optimum pH of the constructed R-SBA-15@BgpA were 7.0, and it has 20 ℃ higher optimal temperature than free enzyme. Relative activity of R-SBA-15@BgpA still retained > 70% at 42 ℃ after 8-h incubation. The investigation on organic reagent resistance revealed that the immobilized enzyme can maintain strong stability in 15% DMSO. In leaching test and evaluation of storage stability, only trace amount of protein was detected in buffer of the immobilized enzyme after storage at 4 ℃ for 33 days, and the immobilized BgpA still maintained > 50% relative activity. It also demonstrated good reusability, with 76.1% relative activity remaining after fourteen successive enzymatic hydrolyses of epimedin A to sagittatoside A. The newly proposed strategy is an effective approach for the purification and immobilization of BgpA concurrently. In addition, R-SBA-15@BgpA was demonstrated to have high efficiency and stability in this application, suggesting its great feasibility and potential to produce bioactive compounds such as secondary glycosides or aglycones from natural products. [ABSTRACT FROM AUTHOR]

Covalent immobilization of chiral dienes in mesoporous solids for asymmetric heterogeneous catalysis is highly attractive. In order to study confinement effects in bimolecular vs monomolecular reactions, a series of pseudo‐C2‐symmetrical tetrahydropentalenes was synthesized and immobilized via click reaction on different mesoporous solids (silica, carbon, covalent organic frameworks) and compared with homogeneous conditions. Two types of Rh‐catalyzed reactions were studied: (a) bimolecular nucleophilic 1,2‐additions of phenylboroxine to N‐tosylimine and (b) monomolecular isomerization of isoxazole to 2H‐azirne. Polar support materials performed better than non‐polar ones. Under confinement, bimolecular reactions showed decreased yields, whereas yields in monomolecular reactions were only little affected. Regarding enantioselectivity the opposite trend was observed, i. e. effective enantiocontrol for bimolecular reactions but only little control for monomolecular reactions was found. [ABSTRACT FROM AUTHOR]

Comprehensive Summary: We present a facile synthetic strategy to create mesoporous Cu2O nanocrystals with tunable pore structures and surface functional groups of amine derivatives for efficient and preferable electrochemical conversion of CO2 into ethylene. The structural characteristics of these Cu2O nanocrystals can be manipulated using a set of amine derivatives, such as pyridine, 4,4'‐bipyridine, and hexamethylenetetramine, during the oxidative etching process of Cu nanocrystals by bubbling gaseous oxygen in N,N‐dimethylformamide solution. These amine derivatives not only serve as surface functional groups but also significantly affect the resulting pore structures. The synergistic effect of pore structure confinement and surface amine functionalization leads to the superb Faradaic efficiency (FE) of 51.9% for C2H4, respectively, together with the C2H4 partial current density of –209.4 mA·cm−2 at –0.8 V vs. reversible hydrogen electrode (RHE). The relatively high selectivity towards C2H4 was investigated using DFT simulations, where 4,4'‐bipyridine functionalized Cu2O seemed to favor the C2H4 formation with the low free energy of the intermediates. This study provides a feasible strategy to manipulate the pore structure and surface functionalization of mesoporous Cu2O nanocrystals by regulating the oxidative etching process, which sheds light on the rational preparation of high‐performance CO2RR electrocatalysts. [ABSTRACT FROM AUTHOR]

[Display omitted] Metal-phenolic networks (MPNs) have emerged as a versatile and multifunctional platform applied in bioimaging, disease treatment, electrocatalysis, and water purification. The synthesis of MPNs with mesoporous frameworks and ultra-small diameters (<200 nm), crucial for post-modification, cargo loading, and mass transport, remains a formidable challenge. Inspired by mussel chemistry, mesoporous metal-phenolic nanospheres (MMPNs) are facilely prepared by direct deposition of the metal-polyphenol complex on the interface of oil nano-droplets composed of block copolymers/1,3,5-trimethylbenzene followed by a spontaneous template-removal process. Due to the penetrable and stable networks, the oil nano-droplets gradually leak from the networks driven by shear stress during the stirring process. As a result, MMPNs are obtained without additional template removal procedures such as solvent extraction or high-temperature calcination. The materials have a large pore size (∼12.1 nm), uniform spherical morphology with a small particle size (∼99 nm), and a large specific surface area (49.8 m2 g−1). Due to the abundant phenolic hydroxyl groups, the MMPNs show excellent antioxidative property. The MMPNs also have excellent photothermal property, whose photothermal conversion efficiency was 40.9 %. Moreover, the phenolic hydroxyl groups can reduce Ag+ in situ to prepare Ag nanoparticles loaded MMPNs composites, which have excellent inhibition performance of drug-resistant bacteria biofilm. [ABSTRACT FROM AUTHOR]

Enhancing the accessibility and utilization of active sites through mesopores in carbon anode materials is crucial for developing high‐power potassium‐ion hybrid supercapacitors (PIHCs). Here, a multiscale phase separation method combining block copolymer (BCP) microphase‐ and homopolymer (HP) macrophase‐separation is utilized to produce two model carbon materials with controlled mesopore orientation: open‐end (oe‐MCS) and closed‐end mesoporous carbon sphere (ce‐MCS). BCPs form identical cylindrical micelles, and HPs encapsulate these cylindrical micelles within spheres and control their orientations relative to the interface. This approach manipulates only the degree of mesopore openings in the MCS materials while maintaining all other factors at similar levels. Opening mesopores in carbon anode materials primarily enhances K+ adsorption capacity, reduces K+ diffusion length, and improves ion transport. Thus, oe‐MCS anode exhibits a higher specific capacity with a significant capacitive‐controlled contribution. The resulting PIHC device displays maximum energy and power densities of 103 Wh kg−1 and 12 300 W kg−1, respectively, along with capacity retention of 86.1% after 20 000 cycles at 2.0 A g−1. This study significantly advances the understanding of mesopore design to improve capacitive K+ storage in hard carbon materials, paving the way for the development of high‐power PIHCs. [ABSTRACT FROM AUTHOR]

The extensive use of sulfonamide antibiotics (SAs) proved to be harmful to humans and the environment; thus, the treatment of SAs in water is imminent. In this work, mesoporous SBA-15 silicon was modified using N-[3-(trimethoxysilyl)propyl]ethylenediamine (AAPTMS) through the formation of AAPTMS-SBA-15. The adsorption performance of AAPTMS-SBA-15 toward sulfamethizole (SIZ) was investigated in the absence and presence of various metal ions, and the results reveal that the introduction of Ni2+ substantially improved the adsorption capacity for SIZ. To maximize the adsorption performance toward SIZ, AAPTMS-SBA-15 was then combined with the heavy metal Ni2+ to prepare Ni-AAPTMS-SBA-15. Subsequently, the adsorption performance and behavior of Ni-AAPTMS-SBA-15 were studied in terms of pH, adsorbent dosage, kinetics, isothermal adsorption, and thermodynamics. SIZ exhibited spontaneous and exothermic adsorption on Ni-AAPTMS-SBA-15, which rapidly reached equilibrium within 2 min; the maximum adsorption capacity was 188.68 mg g−1 at pH = 5.0 and adsorbent dosage of 8 mg. The effective adsorption of SIZ was attributed to the combined mechanisms of electrostatic interaction, complexation and pore-filling. [ABSTRACT FROM AUTHOR]

Continuous manufacturing of platform chemicals from lignocellulose is highly desirable for a fossil fuel independent future. We demonstrate highly selective production of para-xylene (pX) from ethylene and 2,5-dimethylfuran (DMF) in a packed bed microreactor using phosphorous-decorated zeolite beta (P-BEA), with pX selectivity up to 97% at 80% DMF conversion. We map the effect of reactor temperature, space velocity, concentration, gas-to-liquid ratio, and process pressure. Time-on-stream (TOS) and in situ regeneration studies show minimal productivity degradation over ∼5 h TOS and full productivity restoration upon regeneration for multiple cycles. Most non-selective Brønsted acidity occurs at low TOS and is attributed to the remaining trace Al bridge site. External mass transfer limitations are implicated at low space velocities. We combine the TOS data with NMR, XRD, and Raman to develop structure–performance insights into the catalyst behavior. A comparison with mesoporous P-supported materials illustrates that P-BEA is an excellent catalyst for size selectivity and long-term stability. [ABSTRACT FROM AUTHOR]

The correlation of the particle size with the magnetic property and that of the photocatalytic property has always garnered strong interest. Magnetic nanoparticles (MNPs) of Mn-doped Fe3O4 dispersed in KIT-6 (mesoporous silica) were synthesized by a hydrothermal method, and a facile recipe for dispersion of these MNPs was developed. These materials were characterized with different techniques like small-angle X-ray scattering (SAXS), X-ray diffraction, X-ray photoelectron spectroscopy, high-resolution transmission electron microscopy, field emission scanning electron microscopy, etc. The SAXS study shows that KIT-6 possesses a three-dimensional cylindrical pore system, and these pores get filled without affecting the pore size or pore ordering as a function of dispersion of Mn-doped Fe3O4 present as clusters within the channel structures of the mesoporous material. The magnetic properties along with the photocatalytic property of these MNPs were understood as a function of the particle size. The photocatalytic studies for the degradation studies of para-chlorophenol (p-CP) showed these MNPs to be very good photocatalysts with substantial apparent quantum efficiencies and turnover frequencies. The mechanism for the degradation of the p-CP solution as a function of particle size is postulated under the light of variation of magneto-photocatalytic property for the present series of MNPs. [ABSTRACT FROM AUTHOR]

In recent years, algae have emerged as a promising feedstock for biofuel production, due to their eco-friendly, sustainable, and renewable nature. Various methods, including chemical, biochemical, and thermochemical processes, are used to convert algal biomass into biofuels. Pyrolysis, a widely recognized thermochemical technique, involves high temperature and pressure to generate biochar and bio-oil from diverse algal sources. Various pyrolytic processes transform algal biomass into biochar and bio-oil, including low pyrolysis, fast pyrolysis, catalytic pyrolysis, microwave-assisted pyrolysis, and hydropyrolysis. These methods are utilized to convert a range of microalgae and cyanobacteria into biochar and bio-oil. In this publication, we will discuss catalytic pyrolysis using mesoporous materials, such as SBA-15. Mesoporous catalysts have earned significant attention for catalytic reactions, due to their high surface area, facilitating the better distribution of impregnated metal. Pyrolysis conducted in the presence of a mesoporous catalyst is viewed more as efficient, compared to reactions occurring within the smaller microporous cavities of traditional zeolites. SBA-15 supports with incorporated Zr and/or Ce were synthesized using the direct hydrothermal synthesis method. The catalyst was characterized using structural and morphological technical analysis and utilized for the pyrolysis reaction of the algal biomass. [ABSTRACT FROM AUTHOR]

The oral pathway is the preferred drug administration route in pharmaceutical sciences, however, the most employed 'highly active' drug candidates suffer from poor water solubility. The aim of this study was to develop repaglinide (RL)-loaded chitosan-grafted mesoporous silica material (MSM) to enhance drug dissolution. Such enhanced dissolution was investigated in in vitro and in vivo conditions. Our results showed successful grafting of chitosan (CN) on the surface of the MSM and the loading of RL into the mesopores of the silica host. Furthermore, the obtained drug dissolution profiles were fitted to mathematical models to characterize and compare drug dissolution profiles. Cytotoxicity evaluation against the human colorectal adenocarcinoma (Caco-2) cell line showed concentration-dependent toxicity for the MSN-based particles. Various liver and kidney mitochondrial functional parameters including lipid peroxidation assay, complex II activity, mitochondrial glutathione (GSH) level assay, ferric reducing antioxidant power (FRAP) assay, protein carbonyl level, and reactive oxygen species (ROS) formation, were used to investigate the biosafety of the silica-based dissolution enhancer. A significant reduction in blood glucose was observed after oral administration of the biocomposites for 24 h. The histopathological studies of the kidney and liver indicated no MSM-related adverse effects. We believed that our achievements can help the use of the hybrid organic–inorganic MSMs in improving the bioavailability of PWSDs in the one hand and, on the other hand, open a novel avenue to develop biocompatible and nontoxic MSMs in oral bioavailability of PWSDs. [ABSTRACT FROM AUTHOR]

The whimsical Las Vegas/Monte Carlo cubic dice are generalized to construct the combinatorial problem of enumerating all n-dimensional hypercube dice and dice of other shapes that exhibit cubic, icosahedral, and higher symmetries. By utilizing powerful generating function techniques for various irreducible representations, we derive the combinatorial enumerations of all possible dice in n-dimensional space with hyperoctahedral symmetries. Likewise, a number of shapes that exhibit icosahedral symmetries such as a truncated dodecahedron and a truncated icosahedron are considered for the combinatorial problem of dice enumerations with the corresponding shapes. We consider several dice with cubic symmetries such as the truncated octahedron, dodecahedron, and Rubik's cube shapes. It is shown that all enumerated dice are chiral, and we provide the counts of chiral pairs of dice in the n-dimensional space. During the combinatorial enumeration, it was discovered that two different shapes of dice exist with the same chiral pair count culminating to the novel concept of isochiral polyhedra. The combinatorial problem of dice enumeration is generalized to multi-coloring partitions. Applications to chirality in n-dimension, molecular clusters, zeolites, mesoporous materials, cryptography, and biology are also pointed out. Applications to the nonlinear n-dimensional hypercube and other dicey encryptions are exemplified with romantic, clandestine messages: "I love U" and "V Elope at 2". [ABSTRACT FROM AUTHOR]

The ever-growing demand for hydrogen peroxide (H2O2) makes large-scale production via environmentally-friendly strategies necessary. The electrochemical oxygen reduction reaction stands out as an efficient and green approach for H2O2 production. Here, nitrogen-doped mesoporous carbon materials (NMCM) with a hollow semispherical morphology are synthesized for H2O2 generation, which exhibit remarkable electrocatalytic stability, selectivity (94.5%), and onset potential (~ 0.6 V) toward the H2O2 formation in neutral environment. The distinct H2O2 production performance of NMCM can be attributed to synergistic effect of two factors, that is, the pyrrolic N to optimize the work function and the hollow semispherical morphology to facilitate mass transfer and expose abundant electrocatalytic active sites. This work offers a facile way to prepare metal-free electrocatalysts for realizing high-performance H2O2 production in neutral solutions. Nitrogen-doped mesoporous carbon materials with a hollow semispherical morphology and high pyrrolic N contents are synthesized for efficient H2O2 production. [ABSTRACT FROM AUTHOR]

The hydrothermal/soft templating method is an effective way to synthesize ordered mesoporous carbon (OMC), yet the mechanism of this strategy is not well illustrated. Herein, a hydrothermal temperature‐controlled approach is developed to precisely synthesize OMCs with well‐defined morphologies from liquefied wood (LW). As the hydrothermal temperature increases from 130 to 210°C, the hydrophilicity of the hydrophilic blocks decreases accompanied by the increase of the relative volume of the hydrophobic block, resulting in the packing parameter p of micelles changing from p ≤ 1/3 to 1/3 < p < 1/2, which transforms the micelle's structure from spherical to cylindrical. Additionally, accelerated nucleation occurred with the increased hydrothermal temperature. When the rate of nucleation is matched to the self‐assembly of the composite micelles, the composite micelles grow into worm‐like morphology and an ordered p6m mesostructure. This hydrothermal temperature‐controlled strategy provides a straightforward and effective approach for synthesizing OMCs with various morphologies from LW, addressing the previously insufficiently elucidated micelle formation mechanism in the hydrothermal/soft templating method. [ABSTRACT FROM AUTHOR]

To meet the growing emission of water contaminants, the development of new materials that enhance the efficiency of the water treatment system is urgent. Ordered mesoporous materials provide opportunities in environmental processing applications due to their exceptionally high surface areas, large pore sizes, and enough pore volumes. These properties might enhance the performance of materials concerning adsorption/ catalysis capability, durability, and stability. In this review, we enumerate the ordered mesoporous materials as adsorbents/catalysts and their modifications in water pollution treatment from the past decade, including heavy metals (Hg2+, Pb2+, Cd2+, Cr6+, etc.), toxic anions (nitrate, phosphate, fluoride, etc.), and organic contaminants (organic dyes, antibiotics, etc.). These contributions demonstrate a deep understanding of the synergistic effect between the incorporated framework and homogeneous active centers. Besides, the challenges and perspectives of the future developments of ordered mesoporous materials in wastewater treatment are proposed. This work provides a theoretical basis and complete summary for the application of ordered mesoporous materials in the removal of contaminants from aqueous solutions. [ABSTRACT FROM AUTHOR]

Antioxidants are essential for reducing oxidative stress, protecting cells from damage, and supporting overall well-being. Functionalized mesoporous silica materials have garnered interest due to their flexible uses in diverse domains, such as drug delivery systems. This review aims to thoroughly examine and evaluate the progress made in utilizing functionalized mesoporous silica materials as a possible approach to enhancing antioxidant activity. The authors performed a thorough search of reliable databases, including Scopus, PubMed, Google Scholar, and Clarivate Web of Science, using precise keywords linked to functionalized mesoporous silica nanoparticles and antioxidants. The identified journals serve as the major framework for the main discussion in this study. Functionalized mesoporous silica nanoparticles have been reported to greatly enhance antioxidant activity by allowing for an increased loading capacity, controlled release behavior, the targeting of specific drugs, improved biocompatibility and safety, and enhanced penetration. The results emphasize the significant capacity of functionalized mesoporous silica (FSM) to bring about profound changes in a wide range of applications. FSM materials can be designed as versatile nanocarriers, integrating intrinsic antioxidant capabilities and augmenting the efficacy of current drugs, offering substantial progress in antioxidant therapies and drug delivery systems, as well as enhanced substance properties in the pharmaceutical field. Functionalized mesoporous silica materials are a highly effective method for enhancing antioxidant activity. They provide new opportunities for the advancement of cutting-edge treatments and materials in the field of antioxidant research. The significant potential of FSM materials to change drug delivery methods and improve substance properties highlights their crucial role in future breakthroughs in the pharmaceutical field and antioxidant applications. [ABSTRACT FROM AUTHOR]

Asymmetric electrosynthesis provides an efficient and controllable route for chiral synthesis. In comparison to traditional symmetric synthesis methods, asymmetric electrosynthesis typically operates under milder conditions, reducing waste generation and energy consumption. This aligns with the current trend in green chemistry, contributing to the development of environmentally friendly synthetic pathways. Apart from reactions initiated with chiral substrates, introducing appropriate chiral factors during the electrochemical process is crucial. In this context, chiral electrodes have garnered significant attention due to their advantages such as high catalytic activity, enantioselectivity, and reusability. This concept aims to introduce the preparation of three main types of chiral electrodes over the past decade, including chiral modified electrodes, chiral immobilized electrodes and chiral imprinted electrodes, and their applications in asymmetric electrosynthesis. The article provides insights into the current state of the field and outlines prospects for future research. [ABSTRACT FROM AUTHOR]