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The ferroelectric switching behaviour and piezoelectric response of poly(vinylidene fluoride) (PVDF) prepared by drawing at stretching ratios from 1 to 5 and temperatures from 80 to 140 • C has been studied. Stretching ratio and temperature deeply influence the α (non-ferroelectric) to β (ferroelectric) phase transformation. The variations in the phase content are accompanied by changes in the degree of crystallinity and the microstructure, all of them influencing the macroscopic piezoelectric and ferroelectric response of the material. This work shows how the piezo-and ferroelectric behaviour of PVDF depends on the aforementioned parameters and, in particular, on the crystalline β-phase content. Coercive electric field, remnant polarization and saturation polarization increase with increasing ferroelectric β-phase content in the sample. In a similar way, samples with higher β-phase content show higher d 33 piezoelectric coefficients.

Polymer‐based magnetoelectric (ME) materials are an interesting, challenging and innovative research field, that will bridge the gap between fundamental research and applications in the near future. Here, the current state of the art on the different materials, the used configurations for the development of sensors and actuators, as well as the main values of the ME coupling obtained for the different polymer‐based systems are summarized. Further, some of the specific applications that are being developed for those polymer‐based ME materials are addressed as well as the main advantages and remaining challenges in this research field.

Magnetic nanoparticles (NPs) are emerging as an important class of biomedical functional nanomaterials in areas such as hyperthermia, drug release, tissue engineering, theranostic, and lab-on-a-chip, due to their exclusive chemical and physical properties. Although some works can be found reviewing the main application of magnetic NPs in the area of biomedical engineering, recent and intense progress on magnetic nanoparticle research, from synthesis to surface functionalization strategies, demands for a work that includes, summarizes, and debates current directions and ongoing advancements in this research field. Thus, the present work addresses the structure, synthesis, properties, and the incorporation of magnetic NPs in nanocomposites, highlighting the most relevant effects of the synthesis on the magnetic and structural properties of the magnetic NPs and how these effects limit their utilization in the biomedical area. Furthermore, this review next focuses on the application of magnetic NPs on the biomedical field. Finally, a discussion of the main challenges and an outlook of the future developments in the use of magnetic NPs for advanced biomedical applications are critically provided.

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Poly(vinylidene fluoride), PVDF, based nanocomposites with different clays structures have been processed by solvent casting and melt crystallisation. Depending on the melting temperature of the polymer, the nanocomposite recrystalises in the electroactive γ or non electroactive α-phase of the polymer. This fact is related to the thermal behaviour of the clay.For montmorillonite clay, the full crystallisation of the electroactive γ-phase occurs for clay contents lower than 0.5 wt%, allowing the nanocomposites to maintain the mechanical properties of the polymer matrix. The electroactivity of the material has been proven by measuring the piezoelectric d 33 response of the material. The obtained value of d 33 is -7 pC/N, lower than in β-PVDF obtained by mechanical stretching, but still among the largest coefficients obtained for polymers. Further, the optical transmittance in the visible range is strongly enhanced with respect to the transmittance of the pure polymer. Finally, it is demonstrated that the nucleation of the γ-phase can be also obtained in other clays, such as in kaolinite and laponite.

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The effect of filler size and content in the thermal, mechanical and electrical response of poly(vinylidene fluoride) (PVDF)/ BaTiO 3 nanocomposites has been investigated. Dielectric constant increases significantly with increasing filler content and decreasing filler size. Space charge effects at the interface between BaTiO 3 and PVDF strongly influence the dielectric response. The electroactive -phase of PVDF is nucleated by the presence of the ceramic filler, the effect being strongly dependent on filler size and independent on filler content. This filler/matrix interaction is also responsible for the variations observed in the activation energy of the thermal degradation of the polymer. Smaller particles lead to larger relative contact areas and are responsible for the main variations observed in the thermal, mechanical and electrical properties of the composites.