The formation of a lyotropic liquid crystal phase at the level of MXene-based aqueous dispersions due to the self-assembling capacity of these two-dimensional (2D) materials has been previously successfully reported. However, the influence of electrical external factors has been less studied in spite of the fact that understanding the electrical behaviour of 2D-based liquid crystal compounds is vital for fostering the development of new innovative applications. Consequently, within this paper, we report an in-depth evaluation of the dielectric properties of liquid crystalline phases in Ti₃C₂ MXene aqueous dispersions. The dependence on the low voltage of planar ε ⊥ ′ to homeotropic ε ∥ ′ orientational transition is emphasized and discussed, while the influence of the electric field frequency at the level of dielectric anisotropy is assessed in respect to various concentrations of MXene flakes within the same 2D-based compounds. Nonetheless, dielectric spectroscopy highlights the biphasic nature (containing both nematic and isotropic phases) of the studied aqueous Ti₃C₂ MXene inks visible up to 20% MXene. Above this concentration, the existence of a pure nematic phase in the dispersion of highMXene concentration (>20 wt%) was detected based on the evaluation of dielectric permittivity against various voltage values.

Flame-resistant polymer composites were prepared based on polyvinyl alcohol (PVA) as a polymer matrix and a polyphosphonate as flame retardant. Oxalic acid was used as crosslinking agent. LiClO₄, BaTiO₃, and graphene oxide were also incorporated into PVA matrix to increase the ionic conductivity. The obtained film composites were investigated by infrared spectroscopy, scanning electron microscopy, thermogravimetric analysis, differential scanning calorimetry and microscale combustion tests. Incorporating fire retardant (PFRV), BaTiO₃, and graphene oxide (GO) into a material results in increased resistance to fire when compared to the control sample. A thermogravimetric analysis revealed that, as a general trend, the presence of PFRV and BaTiO₃ nanoparticles enhances the residue quantity at a temperature of 700 °C from 7.9 wt% to 23.6 wt%. Their dielectric properties were evaluated with Broad Band Dielectric Spectroscopy. The electrical conductivity of the samples was determined and discussed in relation to the LiClO₄ content. The electrical properties, including permittivity and conductivity, are being enhanced by the use of LiClO₄. Additionally, a relaxation peak has been observed in the dielectric losses at frequencies exceeding 103 Hz. The electrical properties, including permittivity and conductivity, are being enhanced by the use of LiClO₄. Additionally, a relaxation peak has been observed in the dielectric losses at frequencies exceeding 103 Hz. Out of the various composites tested, the composite containing 35 wt% of LiClO₄ exhibits the highest alternating current (AC) conductivity, with a measured value of 2.46 × 10⁻³ S/m. Taking into consideration all the aspects discussed, these improved composites are intended for utilization in the manufacturing of Li-Ion batteries.

Controlling, orientating, and assembling 2D materials is critical for their successful exploitation as active elements in various applications, particularly for sensors. Despite the increased interest in exploiting the properties of MXenes, to date, the direct dielectrophoretic assembly of this category of materials has not been reported. Thus, this work presents an experimental study on dielectrophoretic assembly of pristine MXene flakes at the level of screen-printed interdigitated microelectrodes. The development of MXene uniaxial ‘bridges’ across electrode micro-gaps can be controlled by convenient dielectrophoretic parameters such as voltage and frequency, which are thoroughly discussed. Moreover, appropriate frequencies for avoiding parasitic electrokinetic phenomena (AC electro-osmosis, electrothermal effect) that hamper the application of dielectrophoresis were identified. Finally, the proposed methodology for assembling MXene flakes demonstrates its feasibility of being used for development of chemiresistors as of satisfactory response of pristine MXene ‘bridges’ to ethanol atmosphere.

PbTi_1−xFe_xO_3−δ (x = 0, 0.3, 0.5, and 0.7) ceramics were prepared using the classical solid-state reaction method. The investigated system presented properties that were derived from composition, microstructure, and oxygen deficiency. The phase investigations indicated that all of the samples were well crystallized, and the formation of a cubic structure with small traces of impurities was promoted, in addition to a tetragonal structure, as Fe³⁺ concentration increased. The scanning electron microscopy (SEM) images for PbTi_1−xFe_xO_3−δ ceramics revealed microstructures that were inhomogeneous with an intergranular porosity. The dielectric permittivity increased systematically with Fe³⁺ concentration, increasing up to x = 0.7. A complex impedance analysis revealed the presence of multiple semicircles in the spectra, demonstrating a local electrical inhomogeneity due the different microstructures and amounts of oxygen vacancies distributed within the sample. The increase of the substitution with Fe³⁺ ions onto Ti⁴⁺ sites led to the improvement of the magnetic properties due to the gradual increase in the interactions between Fe³⁺ ions, which were mediated by the presence of oxygen vacancies. The PbTi_1−xFe_xO_3−δ became a multifunctional system with reasonable dielectric, piezoelectric, and magnetic characteristics, making it suitable for application in magnetoelectric devices.