Search Results (13)

The influence of Zn²⁺, Ca²⁺ and Co²⁺ doping on the thermal, structural, morphological, and magnetic characteristics of CdBi_0.1Fe_1.9O₄ nanoparticles synthetized via the sol–gel technique and calcined at 300, 600, 900 and 1200 °C was investigated. Thermal analysis revealed the initial formation of metallic glyoxylates up to 300 °C, followed by their decomposition into metal oxides and subsequent ferrite formation. X-ray diffraction revealed that the ferrites were poorly crystallized at lower temperatures, whereas at higher calcination temperatures all nanocomposites exhibited well-crystalized ferrites coexisting with the SiO₂ matrix, except for the Co_0.1Cd_0.9Bi_0.1Fe_1.9O₄@SiO₂ nanocomposite, which formed a single, well-defined crystalline phase. Atomic force microscopy images revealed spherical ferrite particles encapsulated within an amorphous layer, with particle size, surface area, and coating thickness influenced by both the type of dopant ion and the calcination temperature. The structural parameters estimated by X-ray diffraction, as well as the magnetic characteristics, were strongly influenced by the dopant type and thermal treatment. These results demonstrate that the structural and magnetic characteristics of CdBi₀.₁Fe₁.₉O₄ ferrites can be effectively tuned through controlled doping and calcination, providing insights for the design of tailored functional applications. Full article

High-performance dielectric materials that can be processed at ultra-low temperatures are essential for next-generation LTCC technologies and compact RF–microwave components. In this work, a multicomponent Bi–Fe–Nb oxide system was synthesized using a modified citrate sol–gel method and thermally treated at only 400 °C to investigate its structural evolution and dielectric behavior. XRD and Raman analysis revealed the coexistence of a well-crystallized BiOCl phase embedded within a partially amorphous Bi–Fe–Nb–O matrix. SEM and EDS mapping confirmed the presence of two distinct microstructural regions, reflecting differences in local composition and crystallization kinetics. Microwave measurements at 2.7 and 5.0 GHz showed low dielectric losses and a stable dielectric response. Impedance spectroscopy in the RF range revealed strong Maxwell–Wagner polarization at low frequencies and thermally activated relaxation evidenced by the temperature shift in the modulus and impedance peaks. Arrhenius analysis of the relaxation frequencies yielded similar activation energies from both modulus and impedance formalisms, indicating a single underlying relaxation mechanism. Equivalent-circuit fitting confirmed non-Debye behavior, with nearly temperature-independent capacitance and decreasing resistance consistent with thermally activated conduction. These results demonstrate that the Bi–Fe–Nb system exhibits promising dielectric stability and functional behavior even when processed at exceptionally low temperatures. Full article

This review analyzes TiO₂-based coatings formed by the plasma electrolytic oxidation (PEO) process of titanium for the photocatalytic degradation of methyl orange (MO) under simulated solar irradiation conditions. PEO is recognized as a useful technique for creating oxide coatings on various metals, particularly titanium, to assist in the degradation of organic pollutants. TiO₂-based photocatalysts in the form of coatings are more practical than TiO₂-based photocatalysts in the form of powder because the photocatalyst does not need to be recycled and reused after wastewater degradation treatment, which is an expensive and time-consuming process. In addition, the main advantage of PEO in the synthesis of TiO₂-based photocatalysts is its short processing time (a few minutes), as it excludes the annealing step needed to convert the amorphous TiO₂ into a crystalline phase, a prerequisite for a possible photocatalytic application. Pure TiO₂ coatings formed by PEO have a low photocatalytic efficiency in the degradation of MO, which is due to the rapid recombination of the photo-generated electron/hole pairs. In this review, recent advances in the sensitization of TiO₂ with narrow band gap semiconductors (WO₃, SnO₂, CdS, Sb₂O₃, Bi₂O₃, and Al₂TiO₅), doping with rare earth ions (example Eu³⁺) and transition metals (Mn, Ni, Co, Fe) are summarized as an effective strategy to reduce the recombination of photo-generated electron/hole pairs and to improve the photocatalytic efficiency of TiO₂ coatings. Full article

The potential of aerogels as catalysts for the synthesis of a relevant class of bis-heterocyclic compounds such as bis(indolyl)methanes was investigated. In particular, the studied catalyst was a nanocomposite aerogel based on nanocrystalline nickel ferrite (NiFe₂O₄) dispersed on amorphous porous silica aerogel obtained by two-step sol–gel synthesis followed by gel drying under supercritical conditions and calcination treatments. It was found that the NiFe₂O₄/SiO₂ aerogel is an active catalyst for the selected reaction, enabling high conversions at room temperature, and it proved to be active for three repeated runs. The catalytic activity can be ascribed to both the textural and acidic features of the silica matrix and of the nanocrystalline ferrite. In addition, ferrite nanocrystals provide functionality for magnetic recovery of the catalyst from the crude mixture, enabling time-effective separation from the reaction environment. Evidence of the retention of species involved in the reaction into the catalyst is also pointed out, likely due to the porosity of the aerogel together with the affinity of some species towards the silica matrix. Our work contributes to the study of aerogels as catalysts for organic reactions by demonstrating their potential as well as limitations for the room-temperature synthesis of bis(indolyl)methanes. Full article

In this work, to promote the separation of photogenerated carriers, prevent the catalyst from photo-corrosion, and improve the photo-Fenton synergistic degradation of organic pollutants, the coating structure of FeOOH/BiO_2−x rich in oxygen vacancies was successfully synthesized by a facile and environmentally friendly two-step process of hydrothermal and chemical deposition. Through a series of degradation activity tests of synthesized materials under different conditions, it was found that FeOOH/BiO_2−x demonstrated outstanding organic pollutant degradation activity under visible and near-infrared light when hydrogen peroxide was added. After 90 min of reaction under photo-Fenton conditions, the degradation rate of Methylene Blue by FeOOH/BiO_2−x was 87.4%, significantly higher than the degradation efficiency under photocatalysis (60.3%) and Fenton (49.0%) conditions. The apparent rate constants of FeOOH/BiO_2−x under photo-Fenton conditions were 2.33 times and 3.32 times higher than photocatalysis and Fenton catalysis, respectively. The amorphous FeOOH was tightly coated on the layered BiO_2−x, which significantly increased the specific surface area and the number of active sites of the composites, and facilitated the improvement of the separation efficiency of the photogenerated carriers and the prevention of photo-corrosion of BiO_2−x. The analysis of the mechanism of photo-Fenton synergistic degradation clarified that ·OH, h⁺, and ·O₂⁻ are the main active substances involved in the degradation of pollutants. The optimal degradation conditions were the addition of the FeOOH/BiO_2−x composite catalyst loaded with 20% Fe at a concentration of 0.5 g/L, the addition of hydrogen peroxide at a concentration of 8 mM, and an initial pH of 4. This outstanding catalytic system offers a fresh approach to the creation and processing of iron-based photo-Fenton catalysts by quickly and efficiently degrading various organic contaminants. Full article

The oxygen evolution reaction (OER) is a key half-reaction in electrocatalytic water splitting. Large-scale water electrolysis is hampered by commercial noble-metal-based OER electrocatalysts owing to their high cost. To address these issues, we present a facile, one-pot, room-temperature co-precipitation approach to quickly synthesize carbon-nanotube-interconnected amorphous NiFe-layered double hydroxides (NiFe-LDH@CNT) as cost-effective, efficient, and stable OER electrocatalysts. The hybrid catalyst NiFe-LDH@CNT delivered outstanding OER activity with a low onset overpotential of 255 mV and a small Tafel slope of 51.36 mV dec⁻¹, as well as outstanding long-term stability. The high catalytic capability of NiFe-LDH@CNT is associated with the synergistic effects of its room-temperature synthesized amorphous structure, bi-metallic modulation, and conductive CNT skeleton. The room-temperature synthesis can not only offer economic feasibility, but can also allow amorphous NiFe-LDH to be obtained without crystalline boundaries, facilitating long-term stability during the OER process. The bi-metallic nature of NiFe-LDH guarantees a modified electronic structure, providing additional catalytic sites. Simultaneously, the highly conductive CNT network fosters a nanoporous structure, facilitating electron transfer and O₂ release and enriching catalytic sites. This study introduces an innovative approach to purposefully design nanoarchitecture and easily synthesize amorphous transition-metal-based OER catalysts, ensuring their cost effectiveness, production efficiency, and long-term stability. Full article

The potential of glass ceramics as applicable materials in various fields including fillers for dental restorations is our guide to present a new procedure for improvements of the mechanical properties of dental composites. This work aims to use Zn₂SiO₄ and SiO₂–ZnO nano-materials as fillers to improve the mechanical properties of Bis-GMA/TEGDMA mixed dental resins. Zn₂SiO₄ and SiO₂–ZnO samples were prepared and characterized by using XRD, FE-SEM, EDX, and FT-IR techniques. The XRD pattern of the SiO₂–ZnO sample shows that ZnO crystallized in a hexagonal phase, while the SiO₂ phase was amorphous. Similarly, the Zn₂SiO₄ sample crystallized in a rhombohedral crystal system. The prepared samples were used as fillers for the improvement of the mechanical properties of Bis-GMA/TEGDMA mixed dental resins. Five samples of dental composites composed of Bis-GMA/TEGDMA mixed resins were filled with 2, 5, 8, 10, and 15 wt% of SiO₂–ZnO, and similarly, five samples were filled with Zn₂SiO₄ samples (2, 5, 8, 10, and 15 wt%). All of the 10 samples (A₁–A₁₀) were characterized by using different techniques including FT-IR, FE-SEM, EDX, and TGA analyses. According to the TGA analysis, all samples were thermally stable up to 200 °C, and the thermal stability increased with the filler percent. Next, the mechanical properties of the samples including the flexural strength (FS), flexural modulus (FM), diameter tensile strength (DTS), and compressive strength (CS) were investigated. The obtained results revealed that the samples filled with 8 wt% of SiO₂–ZnO and 10 wt% of Zn₂SiO₄ had higher FS values of 123.4 and 136.6 MPa, respectively. Moreover, 8 wt% of both fillers displayed higher values of the FM, DTS, and CS parameters. These values were 8.6 GPa, 34.2 MPa, and 183.8 MPa for SiO₂–ZnO and 11.3 GPa, 41.2 MPa, and 190.5 MPa for the Zn₂SiO₄ filler. Inexpensive silica-based materials enhance polymeric mechanics. Silica–metal oxide nanocomposites improve dental composite properties effectively. Full article

Al₂O₃ coatings are the most promising candidate material for mitigating (lead-bismuth eutectic) LBE corrosion at elevated temperatures, but preventing inward diffusion of Pb, Bi, and O for the ceramic coating remains a critical challenge. Here, we have fabricated an amorphous Al₂O₃ coating with an ultra-dense structure by continuous high-power magnetron sputtering (C-HPMS). After LBE corrosion at 550 °C for 2000 h, nanocavities induced by the phase transformation from amorphous to γ-Al₂O₃ provide the diffusion path for Fe, O, Pb, and Bi in which the corrosion products, such as Fe₃O₄, PbO₂, or their mixed oxides, form. Furthermore, the diffusion of Pb to the substrate and Cr segregation at the interface between the coating and substrate are observed for the sample exposed to LBE at 550 °C for 4000 h. Additionally, the hardness and interface bonding strength are enhanced after LBE corrosion. Moreover, pit corrosion was found to be the main failure mode of coating, and pits that merged with each other induced large area failure at a temperature of 650 °C. The corrosion mechanism of Al₂O₃ includes element diffusion, phase transformation, and chemical reaction. This work not only provides a deep understanding of the corrosion mechanism of amorphous Al₂O₃ coatings, but also shows the optimization method on the corrosion resistance of Al₂O₃ coating. Full article

Industrial wastewater contains diverse toxic dyes and drugs, which pollute the environment and poison creatures. Utilizing photocatalysts has been accepted to be an effective method to degrade water pollutions using solar light. Crystalline bismuth ferrite (Bi₂Fe₄O₉) with a band gap of 1.9–2.0 eV is expected to be one of the most promising candidates for photocatalysts in the visible light region. Amorphous graphene is also a promising candidate as a photocatalyst owing to its excellent electronic and optical properties. Herein, a composite of Bi₂Fe₄O₉/graphene aerogels (GAs) was prepared with a two-step hydrothermal method. The prepared Bi₂Fe₄O₉ powders were confirmed to be successfully doped into GAs and evenly dispersed between graphene sheets. The Bi₂Fe₄O₉/GA composite was utilized to perform photodegradation for organic dyes and antibiotic drugs under visible light irradiation, yielding efficiencies of 90.22%, 92.3%, 71.8% and 78.58% within 330 min for methyl orange, methylene blue, Rhodamine B and tetracycline hydrochloride, respectively. Such distinct photocatalytic activities overwhelmed the pure Bi₂Fe₄O₉ powders of 14.10%, 22.19%, 13.98% and 48.08%, respectively. Additionally, the composite produced a degradation rate constant of 0.00623 min⁻¹ for methylene blue, which is significantly faster than that of 0.00073 min⁻¹ obtained by the pure powder. These results provide an innovative strategy for designing 3D visible-light-responsive photocatalysts combined with graphene aerogel for water purification. Full article

In this work, different electrodes were employed for the determination of Cr(VI) by the cathodic square-wave voltammetry (SWV) technique and the square-wave adsorptive stripping voltammetry (SWAdSV) technique in combination with diethylenetriaminepentaacetic acid. Using SWV, a comparison of the analytical performance of the bare glassy carbon electrode (GCE), ex situ electrodes (antimony-film—SbFE, copper-film—CuFE, and bismuth-film—BiFE), and the GCE modified with a new magnetic nanocomposite (MNC) material was performed. First, the MNC material was synthesized, i.e., MNPs@SiO₂@Lys, where MNPs stands for magnetic maghemite nanoparticles, coated with a thin amorphous silica (SiO₂) layer, which was additionally functionalized with derived lysine (Lys). The crystal structure of the prepared MNCs was confirmed by X-ray powder diffraction (XRD), while the morphology and nano-size of the MNCs were investigated by field emission scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM), where TEM was additionally used to observe the MNP core and silica layer thickness. The presence of functional groups of the MNCs was investigated by attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR) and surface analysis was performed by X-ray photoelectron spectroscopy (XPS). The hydrophilicity of the modified electrodes was also tested by static contact angle measurements. Then, MNPs@SiO₂@Lys was applied onto the electrodes and used with the SWV and SWAdSV techniques. All electrodes tested with the SWV technique were effective for Cr(VI) trace determination. On the other hand, the SWAdSV technique was required for ultra-trace determination of Cr(VI). Using the SWAdSV technique, it was shown that a combination of ex situ BiFE with the deposited MNPs@SiO₂@Lys resulted in excellent analytical performance (LOQ = 0.1 µg/L, a linear concentration range of 0.2–2.0 µg/L, significantly higher sensitivity compared to the SWV technique, an RSD representing reproducibility of 9.0%, and an average recovery of 98.5%). The applicability of the latter system was also demonstrated for the analysis of a real sample. Full article

Tetragonal CuBi₂O₄/amorphous BiFeO₃ (T-CBO/A-BFO) composites are prepared via a one-step solvothermal method at mild conditions. The T-CBO/A-BFO composites show expanded visible light absorption, suppressed charge recombination, and consequently improved photocatalytic activity than T-CBO or A-BFO alone. The T-CBO/A-BFO with an optimal T-CBO to A-BFO ratio of 1:1 demonstrates the lowest photoluminescence signal and highest photocatalytic activity. It shows a removal rate of 78.3% for the photodegradation of methylene orange under visible light irradiation for 1 h. XPS test after the cycle test revealed the reduction of Bi³⁺ during the photocatalytic reaction. Moreover, the as prepared T-CBO/A-BFO show fundamentally higher photocatalytic activity than their calcinated counterparts. The one-step synthesis is completed within 30 min and does not require post annealing process, which may be easily applied for the fast and cost-effective preparation of photoactive metal oxide heterojunctions. Full article

A mononuclear iron(II) complex bearing the linear pentadentate N₅ Schiff-base ligand containing two 1,2,3-triazole moieties and the MeCN monodentate ligand, [Fe^IIMeCN(L_3-Me-3^Ph)](BPh₄)₂·MeCN·H₂O (1), have been prepared (L_3-Me-3^Ph = bis(N,N′-1-Phenyl-1H-1,2,3-triazol-4-yl-methylideneaminopropyl)methylamine). Variable-temperature magnetic susceptibility measurements revealed an incomplete one-step spin crossover (SCO) from the room-temperature low-spin (LS, S = 0) state to a mixture of the LS and high-spin (HS, S = 2) species at the higher temperature of around 400 K upon first heating, which is irreversible on the consecutive cooling mode. The magnetic modulation at around 400 K was induced by the crystal-to-amorphous transformation accompanied by the loss of lattice MeCN solvent, which was evident from powder X-ray diffraction (PXRD) studies and themogravimetry. The single-crystal X-ray diffraction studies showed that the complex is in the LS state (S = 0) between 296 and 387 K. In the crystal lattice, the complex-cations and B(1)Ph₄⁻ ions are alternately connected by intermolecular CH···π interactions between the methyl group of the MeCN ligand and phenyl groups of B(1)Ph₄⁻ ions, forming a 1D chain structure. The 1D chains are further connected by P4AE (parallel fourfold aryl embrace) interactions between two neighboring complex-cations, constructing a 2D extended structure. B(2)Ph₄⁻ ions and MeCN lattice solvents exist in the spaces of the 2D layer. DFT calculations verified that the 1,2,3-triazole-containing ligand L_3-Me-3^Ph gives a stronger ligand field around the octahedral coordination environment of the iron(II) ion than the analogous imidazole-containing ligand H₂L^2Me (= bis(N,N′-2-methylimidazol-4-yl-methylideneaminopropyl)methylamine) of the known compound [Fe^IIMeCN(H₂L^2Me)](BPh₄)_1.5·Cl_0.5·0.5MeCN (2) reported by Matsumoto et al. (Nishi, K.; Fujinami, T.; Kitabayashi, A.; Matsumoto, N. Tetrameric spin crossover iron(II) complex constructed by imidazole⋯chloride hydrogen bonds. Inorg. Chem. Commun. 2011, 14, 1073–1076), resulting in the much higher spin transition temperature of 1 than that of 2. Full article

In this study, carbonized kelp biochar (AKB) modified by KOH impregnation and photocatalytic Bi₂MoO₆/AKB composite (BKBC) nanomaterials were the first time successfully synthesized for efficient removal of dyes in aqueous solution. BET, XRD, FT-IR, and SEM were employed to characterize as-prepared samples. UV-vis and other test results indicated that the removal efficiency of methylene blue (MB) was 61.39% and 94.12% for BKBC and AKB, respectively, which was up to 13 times and 20 times higher in comparison with pure Bi₂MoO₆ (PBM). In addition, the equilibrium adsorption capacity of MB could reach up to 324.1 mg/g for AKB. This high dyes adsorption performance could be likely attributed to its high specific surface area (507.177 m²/g) and its abundant presence of various functional groups such as –OH and =C–H on AKB. Particularly, the existing of amorphous carbon and transition metal oxides, such as Fe₂O₃ and Mn₅O₈, could be beneficial for the photodegradation of MB for AKB. Meanwhile, experimental data indicated that adsorption kinetics complied with the pseudo-second order model well, and all of the tests had satisfactory results in terms of the highly efficient adsorption and photodegradation activity of AKB nanomaterials, which suggested its great potential in wastewater treatment. Full article