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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. [ABSTRACT FROM AUTHOR]

This work reports an approach of highly active sonophotocatalysts through the combined Zn-doping and heterojunction of CoFe2O4/α-Fe2O3 heterostructures. The novelty lies in the combined Zn-doping and α-Fe2O3 coupling strategy to tune the electronic structure and enhance charge separation of spinel-based magnetic nanocatalyst. A sol–gel auto-combustion method was used to synthesize Zn0.3Co0.7Fe2O4 nanoparticles with ~12% α-Fe2O3 content. The Zn-doping increased the magnetization saturation from ~65 to 86 emu/g and narrowed the optical bandgap from ~1.48 to 1.62 eV compared to undoped CoFe2O4, indicating a modified electronic structure. Under sonophotocatalysis, near complete methylene blue decomposition was achieved in 45 min for both catalysts, with a 30% synergistic effect observed. The Zn-doping also activated the semiconductor photocatalysis mechanism. The combined Zn-doping and heterojunction approach enables highly active sonophotocatalysts to effectively degrade dye pollutants and mitigate water pollution. [ABSTRACT FROM AUTHOR]

Ti3C2Tx MXene is one of the most comprehensively studied 2D materials in terms of its adsorptive, transport, and catalytic properties, cytotoxic performance, etc. Still, conventional MXene synthesis approaches provide low single-flake MXene yield and frequently uncontrollable properties, demanding further post-processing. The MXene family also lacks magnetism, which is helpful for producing effective nanoadsorbents as their magnetic decantation is the cheapest and most convenient way to remove the spent adsorbent from water. Composite materials consisting of magnetic nanoparticles grown on top of MXene flakes are commonly used to provide magnetic properties to the resulting nanocomposite. In this paper, we study the possibility to delaminate multilayer Ti3C2Tx MXene sheets directly by growing iron oxide magnetic nanoparticles inside their interlayer spacing. We find out that, with a mass fraction of particles comparable or exceeding that of MXenes, their growth is accompanied by an effective enhancement of single-layer MXene yield and suitable magnetic properties of the resulting composite. The developed approach can be further used for simplifying synthesis protocols to obtain magnetic MXene-based nanoadsorbents with tunable properties. [ABSTRACT FROM AUTHOR]

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. [ABSTRACT FROM AUTHOR]

New composite materials consisting of polymer matrix with PZT and NdFeB microparticles were prepared and investigated in the work. It was found that magnetic properties such as saturation magnetization, coercivity, permeability, depend on mass concentration of the ferromagnetic particles in the samples. Also it was found that all samples had electrical polarization in DC external electric field. The electric properties such as coercivity, remanent polarization, the maximum polarization value, had changes in the external constant magnetic field 1.1 kOe. These changes depended on both concentrations of ferromagnetic and ferroelectric particles. This type of magnetoelectric transformation allows us to classify new materials as multiferroic materials. These new composite materials can easily be prepared of any shape, the final materials are flexible and resistant to external chemical influences. The area of application of new multiferroic materials varies from sensors to autonomous energy sources.

Polymer-based multiferroics, combining magnetic and piezoelectric properties, are studied experimentally—from synthesis to multi-parameter characterization—in view of their prospects for fabricating biocompatible scaffolds. The main advantage of these systems is facile generation of mechanical deformations and electric signals in response to external magnetic fields. Herein, we address the composites based on PVDF-TrFE polymer matrices filled with a combination of piezoelectric (BaTiO3, BTO) and/or ferrimagnetic (Zn0.25Co0.75Fe2O4, ZCFO) particles. It is shown that the presence of BTO micron-size particles favors stripe-type structuring of the ZCFO filler and enhances the magnetoelectric response of the sample up to 18.6 mV/(cm∙Oe). Besides that, the admixing of BTO particles is crucial because the mechanical properties of the composite filled with only ZCFO is much less efficient in transforming magnetic excitations into the mechanical and electric responses. Attention is focused on the local surfacial mechanical properties since those, to a great extent, determine the fate of stem cells cultivated on these surfaces. The nano-indentation tests are accomplished with the aid of scanning probe microscopy technique. With their proven suitable mechanical properties, a high level of magnetoelectric conversion and also biocompatibility, the composites of the considered type are enticing as the materials for multiferroic-based polymer scaffolds. [ABSTRACT FROM AUTHOR]

Featured Application: Metallic nanoparticles with a high value of magnetization have potential interest for application in biomedicine, catalysis, composite permanent magnets, and other fields. Cobalt ferrite nanoparticles of different stoichiometries synthesized by a sol–gel autocombustion method were used as a starting material to obtain high-moment Fe50Co50 and Fe66Co34 metal nanoparticles by topochemical hydrogen reduction. Structural and magnetic investigations confirmed the formation of FeCo nanoparticles with crystallite sizes of about 30 nm and magnetization at 0.5 T of ~265 Am2/kg (0 K), which was larger than the expected bulk value, likely because of the incorporation in the body-centered cubic (bcc) FeCo structure of the residual C atoms present on the surface of the oxide particles. Temperature-dependent magnetization measurements in the H2 atmosphere were also performed to investigate in detail the reduction mechanism and the effect of an external magnetic field on the process efficiency. [ABSTRACT FROM AUTHOR]

Bi-magnetic core/shell nanoparticles were synthesized by a two-step high-temperature decomposition method of metal acetylacetonate salts. Transmission electron microscopy confirmed the formation of an ultrathin shell (~0.6 nm) of NiO and NiFe2O4 around the magnetically hard 8 nm CoFe2O4 core nanoparticle. Magnetization measurements showed an increase in the coercivity of the single-phase CoFe2O4 seed nanoparticles from ~1.2 T to ~1.5 T and to ~2.0 T for CoFe2O4/NiFe2O4 and CoFe2O4/NiO, respectively. The NiFe2O4 shell also increases the magnetic volume of particles and the dipolar interparticle interactions. In contrast, the NiO shell prevents such interactions and keeps the magnetic volume almost unchanged. [ABSTRACT FROM AUTHOR]