The aim of this work was to investigate how chemical functionalization affects the electronic properties of multi-walled carbon nanotubes, altering the electrophoretic deposition process: a method of choice for the fabrication of high quality, all-carbon nanotube (CNT) layers. Wet chemistry methods were applied to modify the surfaces of CNTs by insertion of various oxygen- and nitrogen-containing groups. Transmission electron microscopy revealed no significant changes in the material morphology, while X-ray photoelectron spectroscopy and Raman spectroscopy showed that changes in the chemical composition did not translate to the changes in the structure. Molecularly modelled optimized surface functional group geometries and electron density distributions allowed the calculation of the dipole moments (–COOH = 0.77; –OH = 1.65; –CON(CH₃CH₂)₂ = 3.33; –CONH₂ = 2.00; –NH₂ = 0.78). Due to their polarity, the introduction of surface functional groups resulted in significant modifications of the electronic properties of CNTs, as elucidated by work function measurements via the Kelvin method and ultraviolet photoelectron spectroscopy. The work function changed from 4.6 eV (raw CNTs) to 4.94 eV for the –OH functionalized CNTs and 4.3 eV for the CNTs functionalized with –CON(CH₃CH₂), and was inversely proportional to the dipole moment values. Finally, using CNT dispersions, electrophoretic deposition was conducted, allowing the correlation of the work function of CNTs and the measured electrophoretic current with the impact on the deposits' qualities. Thus, a rational background for the development of carbon-based biomaterials was provided.

Synthesis of spinel zinc ferrite ultrafine needle-like particles that exhibit exceptional stability in aqueous dispersion (without any surfactants) and superparamagnetic response is reported. Comprehensive structural and magnetic characterization of the particles is performed using X-ray and electron diffraction, small angle X-ray scattering, transmission electron microscopy, dynamic light scattering, vibrating sample magnetometry, Mössbauer spectroscopy and high-resolution X-ray spectroscopy. It reveals nearly stoichiometric ZnFe₂O₄ nanorods with mixed spinel structure and unimodal size distribution of mean length of 20 nm and diameter of 5 nm. Measurements performed in aqueous and dried form shows that particles’ properties are significantly changed as a result of drying.

In this manuscript, we describe the results of our recent studies on carbon aerogels derived from natural starches. A facile method for the fabrication of carbon aerogels is presented. Moreover, the complete analysis of the carbonization process of different starch aerogels (potato, maize, and rice) was performed using thermogravimetric studies combined with a detailed analysis of evolved decomposition products. The prepared carbon aerogels were studied in terms of their morphology and electrical properties to relate the origin of starch precursor with final properties of carbon materials. The obtained results confirmed the differences in carbon aerogels’ morphology, especially in materials’ specific surface areas, depending on the botanical origin of precursors. The electrical conductivity measurements suggest that carbon aerogels with the best electrical properties can be obtained from potato starch.

In this study, we perform quantitative characterization of precipitates and oxide inclusions in Inconel 625 additively manufactured by the laser powder-bed fusion (L-PBF) process. The application of different microscopy techniques allowed us to characterize the microstructure at micro- and nano-scale in the as-built and stress-relieved condition and correlate the features of grains and cellular substructure with parameters of particles along the planes parallel and perpendicular to the build direction. The optimized imaging conditions and image analysis procedure allowed easily distinguishing precipitates and oxide inclusions and performing their quantitative analysis. The results showed that intercellular areas are the preferential sites of precipitation of the Laves phase and NbC carbides with diameters in the range of 10 to 440 nm. Moreover, aluminum oxide inclusions with diameters in the range of 30 to 300 nm are randomly distributed. Regardless of the processing conditions of the examined samples, the influence of the stress-relief annealing on the secondary phases was not observed. In both the as-built and stress-relieved samples, the size of precipitates is in submicrometer scale. The analysis provided detailed information about the parameters of particles depending on the orientation versus the build direction. It was demonstrated that despite the tendency for columnar grain morphology and the anisotropy of the cellular substructure, the particle distribution is almost uniform throughout the volume of the additively manufactured L-PBF Inconel 625.Graphical Abstract