Sol-gel Procedure Research Articles

Zn2Mo3O8/ZnMo8O10/Mo8O23 nanocomposites; structural properties, synthesis and its emerging application in electrochemical hydrogen storage

Electrode materials based on zinc molybdenum oxides were designed by the saccharide-assisted sol-gel procedure for electrochemical hydrogen storage (EHS). By using different characterization methods to observe the formation of nanostructures, it was possible to determine that carbon texture was present on the nanostructured surfaces of zinc molybdenum oxides. The effects of employing various saccharides (mono, di, and poly saccharides) as carbon sources and fuel on the microstructure, electrochemical behaviors, and purity of synthesized samples were compared. The growth of nanocomposites including Zn2Mo3O8, ZnMo8O10, and Mo8O23 phases was facilitated by the saccharide. A charge-discharge method was used to build three-electrode cells and expose them to galvanostatic cycling. To ascertain the stability of electrode architectures, cycling performance at various rates was carried out. The samples' hydrogen storage capabilities were examined, and the sample generated with glucose showed an optimum capacity about 1017 mAhg−1 after 15th cycle.

Superior performance of asymmetric supercapacitor based on Cu doped bismuth ferrite electrode

Electrochemical energy storage devices, like supercapacitors and batteries, are needed to meet the constantly increasing demands of portable energy devices. Many types of supercapacitor electrodes were synthesized and reported which include carbon-based materials, polymers, oxides and perovskites. In this work, we report on the fabrication of Cu doped bismuth ferrite (Cu-BiFeO3, Cu-BFO) nanoparticles via sol-gel procedure. In most of the doping cases the costly rare earth elements like La, Nd, Sm, Ce and Yb are used to replace Bi. Electrodes of Bi1-xCuxFeO3 where x have the values 0.0, 0.025, 0.05, 0.075, 0.1 and 0.15 were deposited on graphitic sheets. Optimum Cu doping value was found to be at x = 0.05. Cu2+ ions doping in place of Bi3+ ions will reveal the roles of oxygen vacancies, as determined from XPS. The estimated values of specific capacitance was found to be 732 F/g at 0.5 A/g for the electrode at x = 0.05 in three electrode system. 5%Cu-BFO//Carbon black asymmetric supercapacitor (ASC) device can be charged and discharged reversibly at cell voltage of 0.0 up to 1.5 V when using a 0.5 M Na2SO4 aqueous electrolyte. This configuration allows the ASC device to deliver a great energy density of 37.25 Wh/kg at a power density of 752 W/kg. The ASC device demonstrates excellent cycling stability, retaining 88.64 % of its initial specific capacitance after 5000 cycles. Increasing the Cu content up to 15 % causes instability in the crystal structure of BFO resulting on phase segregation into Bi2Fe4O9 along with BFO and deterioration in the electrode overall performance. XPS showed that replacement of Cu2+ in place of Bi3+ disturbs the neutrality and the chemical environment of the compound. Hence to achieve neutrality and ionic balance, oxygen vacancies increase and the Fe2+/Fe3+ ratio increases as well. Both oxygen vacancies and the change in the Fe ions ratio reduce electrochemical impedance and give rise to charge density. The homogenous distribution of the pores at x = 0.05 contributed greatly to its fast electrolyte ion diffusion that improved the observed capacitive properties. One has to mention here, that despite doping that contains ions with different ionic size and/or different oxidation state is unfavorable, to some extent, due to the changes they produce in the electronic structure and the chemical environment, nevertheless it is sometimes beneficial in creating new parameters in the structure that promote specific application like in the case of the current work, oxygen vacancies, increase in surface area and the mixed state valency.

Research on preparation of micron-scale orthogonally aligned HMS patterns based on soft lithography

The soft lithography enables the fabrication of microfluidic honeycombs, which are micron-scale, orthogonally aligned hexagonal mesoporous silica (HMS) patterns with channels embedded within them, on silicon substrates. The process entails meticulous cleaning, precise master mold design (including features for channel alignment) using electron-beam lithography, generation of polydimethylsiloxane (PDMS) mold creation, ink formulation, and pattern transfer. Subsequent steps include the sol-gel transition, hardening, alignment verification, characterization, and optional functionalization. It is of the utmost importance to optimize these steps and the master design in order to achieve success. Therefore, the paper examines the creation of micron-scale HMS patterns with orthogonal alignment through the innovative application of soft lithography. The technique encompasses the strategic design of hexagonal motifs, precision master mold crafting, the PDMS stamps, and a meticulous sol-gel procedure, resulting in HMS structures that exhibit remarkable precision and adaptability. This paper underscores the transformative potential of soft lithography in the realm of advanced materials, which offers a controlled and uniform approach to size and uniformity. The refined soft lithography process not only achieves the precise orthogonal alignment of HMS patterns but also highlights its adaptability and economic viability in nanotechnology ventures.

Enhancing solar cell productivity with MgAl2O4–ZnAl2O4 blended anti-reflection coatings

The enhancement of productivity in solar cells primarily relies on the application of anti-reflection coatings. The current research employs coating materials such as MgAl2O4, ZnAl2O4 and blended MgAl2O4–ZnAl2O4 as an anti-reflective layer on the monocrystalline Si solar cells by employing RF sputter coating method. Magnesium nitrate hexahydrate and aluminium nitrate nonahydrate were utilized for the synthesis of MgAl2O4 by the sol-gel technique. ZnAl2O4 was synthesized using zinc nitrate hexahydrate and aluminum nitrate nonahydrate by sol–gel procedure. The performance of coated photovoltaic cells was evaluated through different characterization techniques. From the optical study, the blended MgAl2O4-ZnAl2O4 coating shows the maximum absorbance of around 93 % and lowest reflectance of 9 %. The MgAl2O4–ZnAl2O4 blend achieves a maximum power conversion efficiency (PCE) of 22.12 % in a controlled light source and 19.21 % in direct sunlight. Compared to other solar cells, blended MgAl2O4–ZnAl2O4 demonstrates low resistivity (4.23 × 10−3 Ω-cm), high carrier concentration (35.81 × 1020 cm−3) and maximum hall mobility (12.96 cm2/Vs). From the surface temperature measurement, it is evident that the MgAl2O4–ZnAl2O4 blend coated solar cell exhibits lowest temperature of 38.2 °C under simulated light. The experimental results indicate that the blended MgAl2O4–ZnAl2O4 coated photovoltaic cells exhibits superior productivity than the various coated and uncoated solar cells. Therefore, it can be stated that MgAl2O4–ZnAl2O4 blends are the excellent antireflective materials for achieving desired PCE in solar photovoltaic cells.

Oxygen-deficient annealing boosts performance of CoNiFe oxide electrocatalyst in oxygen evolution reaction

Mixed oxides of transition metals have emerged as promising catalysts for the oxygen evolution (OER) reaction in alkaline water electrolysis. Since OER is significantly slower than hydrogen evolution, developing stable and easily accessible materials that effectively promote OER is one of the keys to improving overall efficiency. In this context, we present a promising method for preparing Co-Ni-Fe oxides which is based on a straightforward sol–gel procedure. Key to success is a thermal treatment under oxygen-deficient atmosphere, which renders superior electrocatalytic properties compared to a treatment under reductive and aerobic conditions, respectively. Attractive performance characteristics are thereby obtained, e.g., a η10 value of 291 mV and a Tafel slope of 32 mV dec−1. The impact of the annealing conditions on the material properties has been elaborated using cyclic voltammetry, impedance spectroscopy, and structural analyses. Stability and strong performance under practical conditions were confirmed in long-term studies using an AEM electrolyzer.

Exploring the structural, magnetic and shielding performance of Mn doped Yb2O3 and Eu2O3 nanostructures

Re2-xMnxO3 (ReYb or Eu, x = 0.0, 0.05, 0.1, 0.15) nanostructures were produced utilizing the sol-gel procedure. The crystal structure and microstructure of all samples were analyzed based on XRD measurements using the Rietveld profile approach. The lattice parameter, cation distribution of different cations between different crystallographic sites, bond lengths of different polyhedrons, crystallite size, micro-strain and distortion index of the different polyhedrons of the formed sample were determined. Mn cations were found to prefer the 8b sites of the cubic bixbyite structure. The average crystallite size decreased following doping, while the microstrain experienced a significant increase. The low temperature dependent magnetizations for Yb1.85Mn0.15O3 and Eu1.85M0.15O3 nanostructures under a magnetic field of 200 Oe were investigated. Curie–Weiss law was employed to determine the magnetic configuration of the samples. The values of the effective magnetic moments μeff are 4.89 μB and 3.77 μB for Yb1.85Mn0.15O3 and Eu1.85M0.15O3, whereas the calculated values are 4.531 μB and 3.535 μB, respectively. The shielding properties of Re2-xMnxO3 (ReYb or Eu) nanostructures were studied using the Phy-X/PSD simulation program. The linear attenuation coefficients (LAC) and mass attenuation coefficients (MAC) values of the Yb2-xMnxO3 samples are greater than those of the Eu2-xMnxO3 samples. The half value length (HVL) and tenth value length (TVL) values increased as Mn was added to Re1.85Mn0.15O3 nanostructures. Yb1.85Mn0.05O3 and Eu1.85Mn0.05O3 nanostructures have the highest mean free path (MFP) values of 3 cm and 4 cm, respectively, at an energy of 5 MeV. The exposure build-up factor (EBF), and energy absorption build-up factor (EABF) values affected by the host rare earth oxide and the amount of Mn doping. The Re1.85Mn0.15O3 nanostructures exhibit a greater capacity to absorb photons with lower energy rather than higher energy. Yb1.85Mn0.15O3 nanostructure demonstrates exceptional neutron shielding capacities.

Exploring the Structural, Optical and Photoluminescence Performances of CuCo2O4 and ZnMn2O4 Alloying

The performance of the structural, linear/ nonlinear optical and photoluminescent properties of CuCo2O4 and ZnMn2O4 alloying was investigated. (1−x)CuCo2O4/(x)ZnMn2O4 (x = 0, 0.10, 0.15, 0.2) samples were prepared by the sol-gel and hydrothermal procedures. Synchrotron X-ray diffraction measurements were employed to investigate the structural and microstructural properties applying the Rietveld refinement method. Fourier transform infraed and Raman techniques were applied to explore the structures’ variation and chemical bonding of the obtained phases. Ultraviolet–visible diffuse reflectance spectroscopy measurements were collected to explore the optical properties. The optical band gap values were determined using the Kubelka-Munk method. All samples exhibited two band gaps in the visible-NIR regions. Upon composing with ZnMn2O4, the band gaps of CuCo2O4 declined for x = 0.1 and 0.15, followed by an increase at x = 0.2. The possible electronic band structure of the samples and the photoluminescent performance of the prepared samples was investigated. The observed PL patterns manifest wide and asymmetrical emissions. The CIE chromaticity diagram for all samples was plotted. The obtained findings of (1−x)CuCo2O4/(x)ZnMn2O4 nominate their efficient role in optical device fabrication and photocatalyst applications.

Facile Fabrication of Hydrophobic and Elastic Silica Aerogels with Enhanced Anti/De-Icing Performance

The anti/de-icing methods are mainly divided into two types: active method and passive method. The passive method generally adopts three ideas: reducing water contact, inhibiting water icing and reducing ice adhesion. Silica aerogels, which have adjustable surface wettability, thermal conductivity and porosity, would be designed to satisfy the requirement for passive anti/de-icing methods. In this work, the organic–inorganic hybrid aerogels based on organosilicon were facilely prepared in a sol–gel procedure, which showed hydrophobic and elastic properties. It could be seen that the thermal insulation effect originating from aerogel-like porous network endowed the efficient anti-icing property. Moreover, the lowest ice adhesion strengths of the above silica aerogels and the related oil-based lubricant-filled aerogels were 7.1[Formula: see text]kPa and 5[Formula: see text]kPa, respectively, which belonged to the icephobic surface. Besides, the ice adhesion strength only increased to 15.6[Formula: see text]kPa after 30 icing–deicing cycles, showing that hydrophobic and elastic silica aerogels had efficient deicing durability.

Novel binary regulated silicon-carbon materials as high-performance anodes for lithium-ion batteries

The massive volume dilation, unsteady solid electrolyte interphase, and weak conductivity about Si have failed to bring it to practical applications, although its potential capacity is up to 4200 mAh g−1. For solving these problems, novel binary regulated silicon–carbon materials (Si/BPC) were done by a sol–gel procedure combined with single carbonization. Analytical techniques were systematically utilized to examine the effects of element doping at several gradients on morphology, structure and electrochemical properties of composites, thus the optimal content was identified. Si/BPC preserves a discharge specific capacity of 1021.6 mAh g−1 with a coulomb efficiency of 99.27% after 180 cycles at 1000 mA g−1, within the upgrade than single-doped and undoped. In rate test, it has a specific capacity of 1003.2 mAh g−1 at a high current density of 5000 mA g−1, quickly back towards 2838.6 mAh g−1 at 200 mA g−1. The inclusion of B and P elements is linked to the electrochemical characteristics. In the co-doped carbon layers, the synergistic impact of doping B and P accelerates the diffusion kinetics of lithium ions, boosts diffusion rate of Li+, offers low electrochemical impedance (45.75 Ω). This brings more defects to provide transport carriers and induces a substantial amount of electrochemically active sites, which fosters the storage of Li+, thus making silicon material electrochemically more active and potential.

Construction of n-n heterojunction copper manganese spinel/mesoporous WO3 photocatalyst for efficient H2 evolution rate from aqueous glycerol

Mesoporous metal oxides can expedite charge separation and mobility and give enormous active sites for H2 production. Herein, n-n heterojunction CuMn2O4/WO3 nanocomposites were constructed by a sol-gel procedure employing F-127 surfactant. The synthesized CuMn2O4/WO3 photocatalysts have been evaluated for H2 evolution from aqueous glycerol as an electron donor under visible illumination. XRD patterns of the synthesized CuMn2O4/WO3 nanocomposite manifested the formation of the monoclinic structure of WO3 and crystalline cubic CuMn2O4 spinel. The TEM image of WO3 NPs showed quasi-spherical ∼10–20 nm and CuMn2O4 NPs ∼10 nm were regularly dispersed on the surface of WO3. The optimum 12%CuMn2O4/WO3 nanocomposite exhibited a significant enhancement photocatalytic ability with the maximal H2 evolution rate (2856.6 μmol h−1g−1), which is about of 14.4 -fold higher than WO3 NPs. The optimal photocatalyst dosage is 2.4 g/L with a large evolution rate of 3427.2 μmol h−1g−1. The close interfacial connection existing between CuMn2O4 and WO3 with S-scheme mechanism and active charge separation generated the high H2 yield. The H2 evolution experiments for 45 h using CuMn2O4/WO3 nanocomposite are stable with high efficiency after five cyclings. This superb H2 evolution rate was utilized from the design of proper bandgap energy; the fostered light harvest, and the enhancement of separation efficiency photocarriers. The resultant CuMn2O4/WO3 nanocomposites exhibit a favorable photocatalyst for sustainability where it is effectively utilized in glycerol by-product through the renewable solar illumination to produce H2 and cleanly water concomitantly.

Comparing magnetic characteristics of CoSe3xFe2–4xO4 (x ≤ 0.10) spinel ferrite nanoparticles synthesized via Sol-Gel and hydrothermal approaches

In this study, Se substituted Co spinel ferrite nanoparticles (CoSe3xFe2–4xO4 (x ≤ 0.10), CoSe SFNPs) have been synthesized via sol-gel (SG) and hydrothermal (HT) routes and their structural, magnetic and morphological features have been compared. The effect of both the Se substitution and the method of synthesis on the structural, morphological and magnetic features of the host CoFe2O4 have been investigated. The structure and morphology of the SFNPs were examined using XRD, EDX, SEM, TEM and HR-TEM methods. XRD analysis confirmed the single-phase formation of CoSe SFNPs for both HT and SG routes. A TEM study for the HT process demonstrated the development of spherical nanoparticles with uniform size, whereas the SG procedure produced NPs with an indeterminate shape. By examining the hysteresis loops at 300 and 20 K and analysing the temperature-dependent changes in magnetization (M), the magnetic characteristics of CoSe (x ≤ 0.10) SFNPs prepared by the SG and HT methods were investigated. CoSe SFNPs possess magnetically soft and hard natures at 300 and 20 K, respectively. Under each synthesis condition, at 20 K, the SQR values are above 0.5, which signifies well-ordered magnetic domains at this temperature. Across all the materials, as the temperature decreases, zero field cooling (ZFC) branches exhibit a non-linear decline in magnetization which becomes nearly stable in the field cooling (FC) branches. The deviation of the ZFC curve with respect to FC one is more pronounced in the case of SFNPs prepared by the HT process. Our findings demonstrate that by employing the desired synthesis method, Se dopants can be applied to achieve particular magnetic characteristics of CoFe2O4 NPs.

Enhancing the Electrical, Dielectric, and Structural Properties of CeO2-ZrO2 Nanocomposites

For enhancing the breakdown strength and increase the capacity of high voltage power supply with high oxidation stability and good electric properties, Ceramic nanomaterials like zirconia (ZrO2) and Ceria (CeO2) preferred due to their strong insulating property and high relative permittivity. In this article, we have reported the synthesis of CeO2/ZrO2 nanocomposite by chemical method. The use of surfactants during synthesis have an adverse effect on the catalytic activity of CeO2 with different morphologies like nanorods, nanocubes, and nano-octahedra. In addition, zirconia can be synthesized via a variety of techniques, including sol-gel, hydrothermal, and precipitation procedures, and combined with other metal oxide nanoparticles. The synthesized nanocomposites were analyzed by X-ray diffraction (XRD), scanning electron microscope (SEM). The crystalline nature and mixed phase of CeO2/ZrO2 nanoparticles have been confirmed by the findings of XRD and SEM analysis. At various frequencies and temperatures, the dielectric constant and dielectric loss of the synthesized nanoparticles were determined. The conductivity and dielectric characteristics of the synthesized samples exhibited temperature and frequency dependency, indicating that the dopant concentration had a significant impact. As frequency increased, the nanoparticles' tangent loss and dielectric constant dropped sharply. These nano-composites can be used as a metal oxide semiconductor for memory devices as well as fuel cells.

Effect of preparation conditions of nanocrystalline Pd/MgO catalysts on their performance in selective hydrogenation of acetylene

In the present work, an alkoxide sol-gel method was applied to prepare Pd/MgO catalysts. The sol-gel procedure was followed by supercritical drying (aerogels) or conventional drying (xerogels) in a furnace. These materials were compared with the impregnated samples. The Pd loading was 1 wt% in all the cases. The as-prepared catalysts were characterized by a set of physicochemical methods. Both the type of the Pd precursor and the preparation route were found to affect the porous structure of the materials as well as the dispersion of the palladium particles and their localization over the MgO support. Both the xerogel and incipient wetness impregnation methods lead to a narrower pore size distribution in comparison to the aerogel technique. The most dispersed particles with an average size of ∼ 2.0–2.2 nm were observed for the samples prepared by xerogel and impregnation methods. In the case of aerogel-prepared samples, metallic palladium particles possess bimodal distribution with average diameters of 4.3 and 8.4 nm. The best catalytic performance in acetylene hydrogenation to ethylene (50 % acetylene conversion at 37 °C with selectivity ∼60 %) was observed for the Pd/MgO catalyst prepared via the aerogel route using [Pd(NH3)4](NO3)2. Compared to other samples, this material is characterized by relatively weak metal-support interactions and the availability of active sites for reactants, which ensures the kinetic mode of the hydrogenation reaction (Ea = 74.9 kJ/mol).

Assessment and Optimization of the Insecticidal Properties of γ-Al2O3 Nanoparticles Derived from Mentha pulegium By-Products to Xylosandrus crassiusculus (Carob Beetle).

This study concentrates on assessing the insecticidal attributes of the γ-Al2O3 nanoparticles derived from the remnants of Mentha pulegium, which include essential oil, ethanolic extract, and plant waste. The synthesis of the γ-Al2O3 nanoparticles was executed using a direct sol-gel procedure, affirming the crystal structure according to extensive physicochemical analyses such as UV-Vis, XRD, FTIR, and SEM. Evaluation of the insecticidal activity in vitro was conducted against Xylosandrus crassiusculus, a pest that infests carob wood, utilizing strains from diverse forests in the Khenifra region, situated in the Moroccan Middle Atlas. The lethal doses 50 ranged from 40 mg/g to 68 mg/g, indicating moderate effectiveness compared to the commercial insecticide Permethrin. Optimization of the conditions for the efficiency of the γ-Al2O3 nanoparticles was determined using experimental plans, revealing that time, humidity, and temperature were influential factors in the lethal dose 50 of these nanomaterials. Moreover, this study encompasses the establishment of correlations using Principal Component Analysis (PCA) and Ascending Hierarchical Classification (AHC) among various geographic, biological, and physical data, amalgamating geographic altitude and γ-Al2O3 nanoparticle insecticide parameters, as well as the attributes of the mechanical tests conducted on the carob wood affected by insects. The correlations highlight the close connections between the effectiveness of the insecticide, mountain altitude, and the mechanical parameters that were examined. Ultimately, these nanoparticles demonstrate promising potential as alternative insecticides, thus opening up encouraging prospects for safeguarding against carob wood pests.

Preparation and Thermoluminescence Properties of Polycrystalline Na2SO4/SiO2 composite

A sodium sulphate/silica (Na2SO4/SiO2) composite was prepared by a sol-gel procedure using a geode as the silica source. The prepared sample was characterized by XRD, XRF and IR techniques. The Na2SO4/SiO2 has an orthorhombic phase, and an average crystalline size is about 51 nm. Thermoluminescence characteristics of Na2SO4/SiO2 were studied at different parameters. The glow curve resulting from Na2SO4/SiO2 showed one clear peak between 150 oC to 200 oC, depending on the energy. The general peak structure of the TL glow curve remains unchanged as a result of repeated cycles of irradiation at various X–ray energies, and exhibits good linearity over the used exposure. There were no significant changes in the TL reading after ten times of reuse, and the fading was observed at 56% after 15 days of irradiation and after one month about 82.3% of the TL signal was lost, and the value of Zeff of Na2SO4/SiO2 was found to be 13.56.

A novel potassium‐containing layered oxide for the cathode of sodium‐ion batteries

AbstractLayered oxides are successful cathode materials for sodium‐ion batteries. Many of these oxides show interesting kinetic behavior but have poor structural stability. To overcome this limitation, an alternative material containing potassium in the interlayer space in trigonal prismatic coordination is studied here. The transition‐metal layers are formed by sustainable transition elements such as iron and manganese. The solid was prepared using a sol–gel procedure that led to a product with relatively high purity, with a Pʹ3‐type structure indexable in the C2/m space group of the monoclinic system. Its electrochemical behavior was studied in sodium metal half‐cells. When the cell is charged up to 4.3 V, it is observed that the potassium extraction is not complete. The subsequent discharge of the cell is associated with the intercalation of sodium from the electrolyte. Thus, it is possible to incorporate a greater number of alkaline ions than those extracted in the previous charge. The residual potassium in the structure was found to be favorable to maintaining the structural integrity of the compound upon cycling. This can be explained by the beneficial effect of potassium, which would act as a structural “pillar” in the interlayer, which would reduce structural degradation during cycling.

A review of pore-forming agents on the structures, porosities, and mechanical properties of porous ceramics

<p>This review article provided a thorough examination of porous ceramic materials, concentrating on production, characteristics, and the involvement of pore-forming agents. The primary objective of this research was to evaluate the effects of various ceramic materials and pore-forming agents on the structure, porosity, and mechanical characteristics of porous ceramics. The study's scope included a thorough investigation of key sources of literature, such as academic publications, review articles, and industry reports, to provide a comprehensive understanding of porous ceramic technology. According to the literature review, the selection of ceramic material and pore-forming agents has a significant influence on the pore size distribution, porosity, and mechanical strength of porous ceramics. Various manufacturing methods, including foaming, sintering, and sol-gel procedures, were explored in terms of their influence on porous ceramic microstructure and characteristics. Furthermore, the study emphasized the need to optimize processing settings and select pore-forming agents to obtain the necessary qualities in porous ceramic materials. Overall, this review is useful for researchers, engineers, and practitioners who desire to learn more about porous ceramic manufacturing, characteristics, and applications.</p>

Exploring the Properties and Applications of Nanomaterials in Environmental Technology: A review

Because of their unique properties and potential uses in a wide range of industries, nanomaterials have attracted a lot of attention. The many characteristics of nanomaterials and their uses in environmental technology are examined in this article. Different kinds of nanomaterials, such as nanoparticles, nanowires, and nanosheets, as well as their fabrication techniques—such as chemical vapour deposition, sol-gel procedures, and green synthesis—are methodically examined in this review. The use of nanomaterials in water purification, pollution control, and environmental remediation are some of the key applications that are covered. The review focusses on the developments in nanomaterial technology as well as how they can revolutionise the way environmental issues are resolved. This analysis offers insights into the efficient application of nanomaterials for sustainable environmental solutions by examining recent research and advancements.

Hybrid calcium magnesium ferrite: A multifaceted nanomaterial for energy, sensing, and environmental applications

The current work employs the urea aided conventional sol–gel procedure to synthesize hybrid calcium magnesium ferrite (CMF – CaO/MgFe2O4) nanomaterial. To verify the existence of synthesized nanomaterials, X-ray diffraction analysis (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), and UV diffuse reflectance spectroscopy (UV-DRS) are employed. The observed crystalline size of the nanomaterials is 44.14 nm. The estimated band gap is 2.36 eV, which is validated using UV-DRS equipment. The investigation's findings are supported by actual applications in electrochemical studies and photocatalytic degradation of synthesized hybrid CMF. It was also investigated how to modify the working electrode's surface to detect heavy metals, drugs, and biomolecules like uric acid, paracetamol, creatinine, cadmium and mercury. Electrochemical research was done to determine the ideal properties of CMF as an electrode material for use in batteries, supercapacitors, and sensors applications. Furthermore, synthesized hybrid CMF exhibits excellent photocatalytic activity, employed as a catalyst to decolorize acid red 88(AR-88) dyes at room temperature under visible light illumination, with a 120-minute photocatalytic activity with the degradation efficiencyof 60.40 %.

Investigation of catalytic activation of peroxydisulfate on cu-doped mesoporous silica-based particles (Cu-BMS) for efficient degradation of methylene blue

The Cu-doped mesoporous silica-based particles (Cu-BMS) were prepared using an evaporation-induced self-assembly sol-gel procedure as a heterogeneous catalyst for the activation of peroxydisulfate (PDS). The formation of well-organized mesoporous structures with amorphous nature and high surface area of 286 m2/g was demonstrated. The catalytic activity of Cu-BMS in the degradation of Methylene Blue (MB) and the effects of operating parameters, including Cu-BMS dosage, initial PDS amount, initial MB concentration, temperature and initial pH, were investigated in details. The Cu-BMS demonstrated a remarkable catalytic activity (93.5% degradation efficiency within 60 min) and good stability.