Surface-enhanced Raman spectroscopy (SERS) of living cells has rapidly become a powerful trend in biomedical diagnostics. It is a common belief that highly ordered, artificially engineered substrates are the best future decision in this field. This paper, however, describes an alternative successful solution, a new effortless chemical approach to the design of nanostructured silver and heterometallic continuous coatings with a stochastic “coffee ring” morphology. The coatings are formed from an ultrasonic mist of aqueous diamminesilver hydroxide, free of reducing agents and nonvolatile pollutants, under mild conditions, at about 200–270 °C in air. They consist of 30–100 micrometer wide and 100–400 nm high silver rings composed, in turn, of a porous silver matrix with 10–50 nm silver grains decorating the sponge. This hierarchic structure originates from ultrasonic droplet evaporation, contact-line motion, silver(I) oxide decomposition and evolution of a growing ensemble of silver rings. The fabricated substrates are a remarkable example of a new scalable and low cost material suitable for SERS analyses of living cells. They evoke no hemolysis and reduce erythrocyte lateral mobility due to suitable “coffee ring” sizes and a tight contact with the silver nanostructure. A high SERS enhancement, characteristic of pure silver rings, made it possible to record Raman scattering spectra from submembrane hemoglobin in its natural cellular environment inside single living erythrocytes, thus making the substrates promising for various biosensor chips.

Natural polyelectrolytes, humic substances, are suggested to control in situ growth of feroxyhyte nanoparticles of a highly reduced mean size and with enhanced colloidal stability in salt solutions. The feroxyhyte is formed as 2–5 nm thick and 20 × 20 nm wide nanoflakes due to the blocking of developing facets of feroxyhyte and constraints caused by diffusion limitations of ionic constituents across partially charged branches of humic substances.

A novel, facile, and versatile microwave-assisted method of high-yield synthesis of layered rare earth hydroxo compounds (LRHs) is proposed. Layered yttrium hydroxonitrates synthesized by the microwave-assisted technique crystallize in the form of thin hexagonal plates aggregated into spheroidal particles. Depending on the conditions of microwave-assisted hydrothermal synthesis, the formation of several phases differing in interplanar spacing along the [00l] direction is possible. The materials obtained are shown to possess good anion-exchange properties. This work provides a route to large-scale synthesis of LRH-based advanced materials.

A boost in the development of flexible and wearable electronics facilitates the design of new materials to be applied as transparent conducting films (TCFs). Although single-walled carbon nanotube (SWCNT) films are the most promising candidates for flexible TCFs, they still do not meet optoelectronic requirements demanded for their successful industrial integration. In this study, we proposed and thoroughly investigated a new approach that comprises simultaneous bilateral (outer and inner surface) SWCNT doping after their opening by thermal treatment at 400 °C under an ambient air atmosphere. Doping by a chloroauric acid (HAuCl₄) ethanol solution allowed us to achieve the record value of equivalent sheet resistance of 31 ± 4 Ω sq⁻¹ at a transmittance of 90% in the middle of the visible spectrum (550 nm). The strong p-doping was examined by open-circuit potential (OCP) measurements and confirmed by ab initio calculations demonstrating a downshift of the Fermi level of around 1 eV for the case of bilateral doping.