Fe_1-xCo_x nanowires are obtained by electrochemical deposition into the pores of track-etched membranes. The characteristics of the growth process that allow controlling the length and aspect ratio of the nanowires are established. The elemental composition and magnetic properties of the nanowires depend on the diameter of the track-etched pores, which varies from 30 to 200 nm, and the electrochemical potential U (650–850 mV), which determines the nanowire growth rate. According to the results of elemental analysis and the Mössbauer spectroscopy data, the Co content in Fe_1-xCo_x lies in the range of x=0.20−0.25. It is found that the orientation of the magnetic moment of Fe–Co nanoparticles in the wires depends both on the track pore size d and on the nanowire growth rate. Thus, the magnetic moments in nanowires grown in 50-nm-diameter pores are oriented within 0°–40° with respect to the nanowire axis. The magnetic properties of the nanowires are explained in the framework of a theoretical model describing the magnetic dynamics of nanocomposites, which was extended to include the relaxation of the magnetization vector and to take into account interaction between the particles. The key physical parameters important for the technological applications of the nanowires are determined, their dependence on the nanowire growth conditions is traced, and the possibility of controlling them is established.

Background: The alignment of liquid crystals by surfaces is crucial for applications. It determines the director configuration in the bulk, its stability against defects and electro-optical switching scenarios. The conventional planar alignment of rubbed polymer layers can be locally flipped to vertical by irradiation with a focused ion beam on a scale of tens of nanometers.Results: We propose a digital method to precisely steer the liquid crystal director tilt at polymer surfaces by combining micrometer-size areas treated with focused ion beam and pristine areas. The liquid crystal tends to average the competing vertical and planar alignment actions and is stabilized with an intermediate pretilt angle determined by the local pattern duty factor. In particular, we create micrometer-sized periodic stripe patterns with this factor gradually varying from 0 to 1. Our optical studies confirm a predictable alignment of a nematic liquid crystal with the pretilt angle continuously changing from 0° to 90°. A one-constant model neglecting the difference between the elastic moduli reproduces the results quantitatively correctly.Conclusion: The possibility of nanofabrication of polymer substrates supporting an arbitrary (from planar to vertical) spatially inhomogeneous liquid crystal alignment opens up prospects of “imprinting” electrically tunable versatile metasurfaces constituting lenses, prisms and q-plates.

The development of advanced methods for the synthesis of nano- and microparticles in the field of biomedicine is of high interest due to a range of reasons. The current synthesis methods may have limitations in terms of efficiency, scalability, and uniformity of the particles. Here, we investigate the synthesis of submicron calcium carbonate using a microfluidic chip with a T-shaped oil supply for droplet-based synthesis to facilitate control over the formation of submicron calcium carbonate particles. The design of the chip allowed for the precise manipulation of reaction parameters, resulting in improved porosity while maintaining an efficient synthesis rate. The pore size distribution within calcium carbonate particles was estimated via small-angle X-ray scattering. This study showed that the high porosity and reduced size of the particles facilitated the higher loading of a model peptide: 16 vs. 9 mass.% for the particles synthesized in a microfluidic device and in bulk, correspondingly. The biosafety of the developed particles in the concentration range of 0.08–0.8 mg per plate was established by the results of the cytotoxicity study using mouse fibroblasts. This innovative approach of microfluidically assisted synthesis provides a promising avenue for future research in the field of particle synthesis and drug delivery systems.