Search Results (19)

Bismuth ferrite (BiFeO₃, BFO) is one of the few single-phase crystalline compounds exhibiting strong multiferroic properties at room temperature, which makes it promising for use in various fields of science and technology. The remarkable characteristics of BFO at the nanoscale position it as a compelling candidate for enhancing the functionalities of polymeric nanocomposite materials. In this study, we explore the fabrication of polyvinylidene fluoride (PVDF) nanocomposites with a variable content of BFO nanopowders (0, 5, 10, 15, 20, and 25 wt%) by solution casting in the form of thin films with the thickness of ~60 µm. Our findings reveal that the presence of BFO nanoparticles slightly facilitates the formation of β- and γ-phases of PVDF, known for their enhanced piezoelectric properties, thereby potentially expanding the utility of PVDF-based materials in sensors, actuators, and energy harvesting devices. On the other hand, the increase in filler concentration leads to enlarged spherulite diameter and porosity of PVDF, as well as an increase in filler content above 20 wt% resulting in a decrease in the degree of crystallinity. The structural changes in the surface were found to increase the hydrophobicity of the nanocomposite surface. Magnetometry indicates that the magnetic properties of nanocomposite are influenced by the BFO nanoparticle content with the saturation magnetization at ~295 K ranging from ~0.08 emu/g to ~0.8 emu/g for samples with the lowest and higher BFO content, respectively. Full article

Bismuth ferrite, BiFeO₃, a multiferroic perovskite oxide, has gained significant attention in the field of materials science due to its unique combination of ferroelectric and antiferromagnetic properties. This inherent dual nature makes it essential for various cutting-edge technologies, including non-volatile memories, spintronics, and energy-harvesting devices. However, realizing its full potential requires the precise synthesis of high-purity bismuth ferrite nanoparticles. In this scholarly endeavor, we present a comprehensive exploration of the meticulous fabrication of bismuth ferrite nanoparticles using a microwave-assisted combustion method conducted in the solid-state regime. We utilized bismuth nitrate and iron nitrate as precursor materials, combined with an organic fuel amalgam consisting of ammonium nitrate and glycine. Achieving complete combustion through microwave irradiation required a detailed optimization process for the oxidant-to-fuel ratio and absolute quantities. Our research systematically investigated various fuel-to-oxidant ratios, including 1:1, 3:6, 6:3, and 12:12, all conducted under rigorously controlled microwave irradiation conditions. Subsequent characterization through infrared spectroscopy (IR), X-Ray Diffraction (XRD), and scanning electron microscopy (SEM) confirmed the successful synthesis of high-purity bismuth ferrite nanoparticles. Furthermore, optimizing the synthesis conditions resulted in nanoparticles with superior purity and structural integrity. In conclusion, we meticulously evaluated the photocatalytic properties of the synthesized bismuth ferrite nanoparticles, with a specific focus on their effectiveness in degrading malachite green. Our findings highlight the significant impact of carefully tailored combustion parameters on the photocatalytic performance of bismuth ferrite nanoparticles, positioning them as promising candidates for various environmental remediation and catalytic applications. This study advances our understanding of the custom synthesis of advanced photocatalytic materials, potentially fostering sustainable technological advancements. Full article

The creation of multi-stimuli-sensitive composite polymer–inorganic materials is a practical scientific task. The combination of photoactive magneto-piezoelectric nanomaterials and ferroelectric polymers offers new properties that can help solve environmental and energy problems. Using the doctor blade casting method with the thermally induced phase separation (TIPS) technique, we synthesized a hybrid polymer–inorganic nanocomposite porous membrane based on polyvinylidene fluoride (PVDF) and bismuth ferrite (BiFeO₃/BFO). We studied the samples using transmission and scanning electron microscopy (TEM/SEM), infrared Fourier spectroscopy (FTIR), total transmission and diffuse reflection, fluorescence microscopy, photoluminescence (PL), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), vibrating-sample magnetometer (VSM), and piezopotential measurements. Our results demonstrate that the addition of BFO increases the proportion of the polar phase from 76.2% to 93.8% due to surface ion–dipole interaction. We also found that the sample exhibits laser-induced fluorescence, with maxima at 475 and 665 nm depending on the presence of nanoparticles in the polymer matrix. Furthermore, our piezo-photocatalytic experiments showed that under the combined actions of ultrasonic treatment and UV–visible light irradiation, the reaction rate increased by factors of 68, 13, 4.2, and 1.6 compared to sonolysis, photolysis, piezocatalysis, and photocatalysis, respectively. This behavior is explained by the piezoelectric potential and the narrowing of the band gap of the composite due to the mechanical stress caused by ultrasound. Full article

In this study, multifunctional lithium-doped bismuth ferrite [BiFe_1−xLi_xO₃]-graphene nanocomposites (x = 0.00, 0.02, 0.04, 0.06) were synthesized by a sol-gel and ultrasonication assisted chemical reduction method. X-ray diffraction and FESEM electron microscopy techniques disclosed the nanocomposite phase and nanocrystalline nature of [BiFe_1−xLi_xO₃]-graphene nanocomposites. The FESEM images and the EDX elemental mapping revealed the characteristic integration of BiFe_1−xLi_xO₃ nanoparticles (with an average size of 95 nm) onto the 2D graphene layers. The Raman spectra of the [BiFe_1−xLi_xO₃]-graphene nanocomposites evidenced the BiFe_1−xLi_xO₃ and graphene nanostructures in the synthesized nanocomposites. The photocatalytic performances of the synthesized nanocomposites were assessed for ciprofloxacin (CIP) photooxidation under UV-visible light illumination. The photocatalytic efficiencies of [BiFe_1−xLi_xO₃]-graphene nanocomposites were measured to be 42%, 47%, 43%, and 10%, for x = 0.00, 0.02, 0.04, 0.06, respectively, within 120 min illumination, whereas the pure BiFeO₃ nanoparticles were 21.0%. BiFe_1−xLi_xO₃ nanoparticles blended with graphene were explored as cathode material and tested in a microbial fuel cell (MFC). The linear sweep voltammetry (LSV) analysis showed that the high surface area of BiFeO₃ was attributed to efficient oxygen reduction reaction (ORR) activity. The increasing loading rates of (0.5–2.5 mg/cm²) [BiFe_1−xLi_xO₃]-graphene composite on the cathode surface showed increasing power output, with 2.5 and 2 mg/cm² achieving the maximum volumetric power density of 8.2 W/m³ and 8.1 W/m³, respectively. The electrochemical impedance spectroscopy (EIS) analysis showed that among the different loading rates used in this study, BiFeO₃, with a loading rate of 2.5 mg/cm², showed the lowest charge transfer resistance (R_ct). The study results showed the potential of [BiFe_1−xLi_xO₃]-graphene composite as a cost-effective alternative for field-scale MFC applications. Full article

Developing a simple and efficient method for removing organic micropollutants from aqueous systems is crucial. The present study describes the preparation and application, for the first time, of novel MXene-decorated bismuth ferrite nanocomposites (BiFeO₃/MXene) for the removal of six sulfonamides including sulfadiazine (SDZ), sulfathiazole (STZ), sulfamerazine (SMZ), sulfamethazine (SMTZ), sulfamethoxazole (SMXZ) and sulfisoxazole (SXZ). The properties of BiFeO₃/MXene are enhanced by the presence of BiFeO₃ nanoparticles, which provide a large surface area to facilitate the removal of sulfonamides. More importantly, BiFeO₃/MXene composites demonstrated remarkable sulfonamide adsorption capabilities compared to pristine MXene, which is due to the synergistic effect between BiFeO₃ and MXene. The kinetics and isotherm models of sulfonamide adsorption on BiFeO₃/MXene are consistent with a pseudo-second-order kinetics and Langmuir model. BiFeO₃/MXene had appreciable reusability after five adsorption–desorption cycles. Furthermore, BiFeO₃/MXene is stable and retains its original properties upon desorption. The present work provides an effective method for eliminating sulfonamides from water by exploiting the excellent texture properties of BiFeO₃/MXene. Full article

The acetone-sensing performance of BiFeO₃ is related to structural phase transformation, morphology and band gap energy which can be modulated by rare-earth ions doping. In this work, Bi_1−xEr_xFeO₃ nanoparticles with different amounts of Er doping were synthesized via the sol-gel method. The mechanism of Er doping on acetone-sensing performance of Bi_1−xEr_xFeO₃ (x = 0, 0.05, 0.1 and 0.2) sensors was the focus of the research. The optimal working temperature of Bi_0.9Er_0.1FeO₃ (300 °C) was decreased by 60 °C compared to BiFeO₃ (360 °C). The Bi_0.9Er_0.1FeO₃ sample demonstrated the optimal response to 100 ppm acetone (43.2), which was 4.8 times that of pure BFO at 300 °C. The primary reason, which enhances the acetone-sensing performance, could be the phase transformation induced by Er doping. The lattice distortions induced by phase transformation are favorable to increasing the carrier concentration and mobility, which will bring more changes to the hole-accumulation layer. Thus, the acetone-sensing performance of Bi_0.9Er_0.1FeO₃ was improved. Full article

This paper presents the results of the synthesis of samarium-doped bismuth ferrite (BFO) nanoparticles by the solution combustion method. The dependence of BFO properties on the amount of the samarium (Sm) in the composition was studied. The synthesized nanocomposites were characterized by scanning electron microscopy SEM), X-ray diffractometry (XRD), Raman, Electron Diffuse Reflectance Spectroscopy (EDRS) and Electron Magnetic Resonance (EMR). The photocatalytic (PC) measurements showed the absence of a strict correlation between the PC activity and the crystallite size and band gap. An increase in the PC activity of BFO samples with 10 and 15% doping was observed and it was concluded that in controlling the PC properties in doped BFO, the processes of interfacial polarization at the boundaries of the morphotropic phase transition are of decisive importance. It was supposed that the internal electric field formed at these boundaries contributes to the efficient separation of photogenerated charge carriers. Full article

Photocatalytic biomass valorization has proven to be a valuable approach for sustainably constructing value—added products from waste materials. The present study aimed to know about Bismuth ferrite (BiFeO₃) nanoparticles combined into carboxymethyl cellulose (CMC) obtained from oil palm empty fruit bunch waste (OCMC) and used as a catalyst composite for the degradation of anionic dyes, specifically on methyl orange (MO) and congo red (CR). The parameter that affects the formation of OCMC, such as the degree of substitution (DS), depends upon the alkalization reaction time and NaOH concentrations. The highest DS was obtained at 1.562 and found at 60% NaOH with 9 h of alkalization, very close to that of the commercial CMC (CCMC) DS value. X-ray diffraction (XRD) analysis revealed that OCMC as a semi-crystalline phase and the tensile strength of OCMC film increased significantly from 0.11 MPa to 3.54 MPa as compared to CCMC. The comparative study on photocatalytic degradation of MO and CR using OCMC and CCMC reinforced with 0.8% BiFeO₃ showed a minor difference in removal percentage. The efficiency removal for CCMC/BFO towards CR and MO was enhanced to 95.49% and 92.93% after a 3-h treatment, and a similar result was obtained in the case of OCMC/BiFeO₃ at 92.50% for CR and 89.56% for MO, respectively. Nevertheless, it is interesting that OCMC film exhibits remarkable stability with an improvement in terms of tensile strength and stays more intact than that of CCMC. Full article

Currently, organic dyes and other environmental contaminants are focal areas of research, with considerable interest in the production of stable, high-efficiency, and eco-friendly photocatalysts to eliminate these contaminants. In the present work, bismuth-doped zinc ferrite (Bi-ZnFe₂O₄) nanoparticles (NPs) and bismuth-doped zinc ferrites supported on sulfur-doped graphitic carbon nitride (Bi-ZnFe₂O₄/S-g-C₃N₄) (BZFG) photocatalysts were synthesized via a hydrothermal process. SEM, XRD, and FTIR techniques were used to examine the morphological, structural, and bonding characteristics of the synthesized photocatalysts. The photocatalytic competence of the functional BZFG nanocomposites (NCs) was studied against MB under sunlight. The influence of Bi (0.5, 1, 3, 5, 7, 9, and 11 wt.%) doping on the photocatalytic performance of ZnFe₂O₄ was verified, and the 9%Bi-ZnFe₂O₄ nanoparticles exhibited the maximum MB degradation. Then, 9%Bi-ZnFe₂O₄ NPs were homogenized with varying amounts of S-g-C₃N₄ (10, 30, 50, 60, and 70 wt.%) to further enhance the photocatalytic performance of BZFG NCs. The fabricated Bi-ZnFe₂O₄/30%S-g-C₃N₄ (BZFG-30) composite outperformed ZnFe₂O₄, S-g-C₃N₄ and other BZFG NCs in terms of photocatalytic performance. The enriched photocatalytic performance of the BZFG NCs might be ascribed to a more efficient transfer and separation of photo-induced charges due to synergic effects at the Bi-ZnFe₂O₄/S-g-C₃N₄ interconnection. The proposed modification of ZnFe₂O₄ using Bi and S-g-C₃N₄ is effective, inexpensive, and environmentally safe. Full article

Visible light-driven photocatalyst BiFeO₃ (BFO) nanoparticles were synthesised by the auto-combustion method. The honey was used to fuel the auto combustion method to synthesise the BFO nanoparticles. The structural, optical and morphological activities of the bismuth loaded BFO nanoparticles were characterised by X-ray diffraction (XRD), FTIR, UV, photoluminescence (PL) and SEM analysis, respectively. The bismuth content modifies the lattice parameters of XRD and reduces the bandgap energy. The observed crystallite size varies from 19 to 27 nm and the bandgap region is 2.07 to 2.21 eV. The photo-charge carriers increased upon the BFO nanoparticles and their emission at 587 nm in the visible region of the PL spectrum. The 2% bismuth loaded BFO nanoparticles showed better morphology than 0% and 5% bismuth loaded BFO nanoparticles. The oxidation state of BFO nanoparticles and their binding energies were characterised by X-ray Photoelectron Spectroscopy (XPS) analysis. The methylene blue dye (MB) degradation against 2% BFO nanoparticles showed enhanced catalytic activity (81%) than the remaining samples of BFO nanoparticles. The bacterial activity of BFO nanoparticles was assessed against Gram-positive and Gram-negative bacteria, including S. aureus and E. coli. 2% Excess bismuth BFO nanoparticles exhibit better antibacterial activity. Comparatively, 2% Excess bismuth BFO nanoparticles derived an outstanding crystallinity, charge separation, and reduced bandgap activities. Based on these findings, BFO nanoparticles may be applicable in drug delivery and water remediation applications. Full article

The present work was carried out to synthesize bismuth ferrite (BFO) nanoparticles by combustion synthesis, and to evaluate the photocatalytic activity of synthesized bismuth ferrite nanoparticles against cefixime trihydrate. BFO nanoparticles were successfully synthesized using bismuth (III) nitrate and iron (III) nitrate by a combustion synthesis method employing different types of fuels such as maltose, succinic acid, cinnamic acid, and lactose. The effects of the different types of fuels on the morphology and size of the bismuth ferrite nanoparticles were investigated. Characterization of the as-obtained bismuth ferrite nanoparticles was carried out by different techniques such as X-ray diffraction (XRD), scanning electron microscopy (SEM), Energy-Dispersive Spectroscopy (EDS), N₂-sorption analysis, Fourier-transform infrared spectroscopy (FT-IR), and ultraviolet-visible (UV–vis) spectroscopy. Photoluminescence studies were also carried out for the various bismuth ferrite nanoparticles obtained. Degradation of cefixime trihydrate was investigated under sunlight to evaluate the photocatalytic properties of the bismuth ferrite nanoparticles, and it was found that the bismuth ferrite nanoparticles followed first-order degradation kinetics in solar irradiation in the degradation of antibiotic, cefixime trihydrate. Full article

Semiconductor-based photocatalysis is a probable approach to overcoming many pollution problems and eradicating toxic organic materials from wastewater. This research endeavor aimed to explore the synergistic potential of different semiconductor nanocomposites for photocatalytic degradation of organic pollutants in contaminated water. A facile hydrothermal approach was employed to synthesize bismuth oxide and cobalt ferrite nanoparticles from their precursors—bismuth nitrate pentahydrate, ferric chloride hexahydrate and cobalt chloride hexahydrate—with various concentrations and conditions to optimize the product. Subsequently, nanocomposites of bismuth oxide and cobalt ferrite were prepared by solid-state mixing in varying concentrations followed by calcination. UV/visible diffuse reflectance spectroscopy, X-ray diffraction, scanning electron microscopy and elemental dispersive X-ray spectroscopic techniques have corroborated the successful synthesis of nanocomposites. The energy gaps of bismuth oxide and cobalt ferrite nanocomposites were computed in the range of 1.58–1.62 eV by Tauc plots. These nanocomposite materials were ascertained for photocatalytic potential to degrade methyl orange organic dye in water. A nanocomposite with equiquantic proportions has shown the best photocatalytic degradation activity, which may be attributed to the type-II band configuration and a synergistic effect, because Bi₂O₃ acts as an electron sink. This synergism has reduced the cogent band gap, hindered electron hole recombination and increased electron hole availabilities for photodegradation reactions, thus ensuing an efficient photodegradation co-work of Bi₂O₃/CoFe₂O₄ nanocomposites. Full article

In the direct current electric field, the surface of epoxy resin (EP) insulating material is prone to charge accumulation, which leads to electric field distortion and damages the overall insulation of the equipment. Nano-doping is an effective method to improve the surface insulation strength and DC flashover voltage of epoxy resin composites. In this study, pure bismuth ferrite nanoparticles (BFO), as well as BFO nanofillers, which were doped by La element, Cr element as well as co-doped by La + Cr element, were prepared by the sol-gel method. Epoxy composites with various filler concentrations were prepared by blending nano-fillers with epoxy resin. The morphology and crystal structure of the filler were characterized by scanning electron microscopy (SEM) and X-ray diffraction (XRD) tests. The effects of different filler types and filler mass fraction on the surface flashover voltage, charge dissipation rate, and trap characteristics of epoxy resin composites were studied. The results showed that element doping with bismuth ferrite nanofillers could further increase the flash voltage of the composites. The flashover voltage of La + Cr elements co-doped composites with the filler mass fraction of 4 wt% was 45.2% higher than that of pure epoxy resin. Through data comparison, it is found that the surface charge dissipation rate is not the only determinant of the flashover voltage. Appropriately reducing the surface charge dissipation rate of epoxy resin composites can increase the flashover voltage. Finally, combining with the distribution characteristics of the traps on the surface of the materials to explain the mechanism, it is found that the doping of La element and Cr element can increase the energy level depth and density of the deep traps of the composite materials, which can effectively improve the flashover voltage along the surface of the epoxy resin. Full article

Bismuth ferrite nanoparticles with an average particle diameter of 45 nm and spatial symmetry R3c were obtained by combustion of organic nitrate precursors. BiFeO₃-silicone nanocomposites with various concentrations of nanoparticles were obtained by mixing with a solution of M10 silicone. Models of piezoelectric generators were made by applying nanocomposites on a glass substrate and using aluminum foil as contacts. The thickness of the layers was about 230 μm. There was a proportional relationship between the different concentrations of nanoparticles and the detected potential. The output voltages were 0.028, 0.055, and 0.17 V with mass loads of 10, 30, and 50 mass%, respectively. Full article

Herein we report on novel multiferroic core–shell nanostructures of cobalt ferrite (CoFe₂O₄)–bismuth, sodium titanate doped with barium titanate (BNT–BT_0.08), prepared by a two–step wet chemical procedure, using the sol–gel technique. The fraction of CoFe₂O₄ was varied from 1:0.5 to 1:1.5 = BNT–BT_0.08/CoFe₂O₄ (molar ratio). X–ray diffraction confirmed the presence of both the spinel CoFe₂O₄ and the perovskite Bi_0.5Na_0.5TiO₃ phases. Scanning electron microscopy analysis indicated that the diameter of the core–shell nanoparticles was between 15 and 40 nm. Transmission electron microscopy data showed two–phase composite nanostructures consisting of a BNT–BT_0.08 core surrounded by a CoFe₂O₄ shell with an average thickness of 4–7 nm. Cole-Cole plots reveal the presence of grains and grain boundary effects in the BNT–BT_0.08/CoFe₂O₄ composite. Moreover, the values of the dc conductivity were found to increase with the amount of CoFe₂O₄ semiconductive phase. Both X-ray photoelectron spectroscopy (XPS) and Mössbauer measurements have shown no change in the valence of the Fe³⁺, Co²⁺, Bi³⁺ and Ti⁴⁺ cations. This study provides a detailed insight into the magnetoelectric coupling of the multiferroic BNT–BT_0.08/CoFe₂O₄ core–shell composite potentially suitable for magnetoelectric applications. Full article