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Authentication of a product's originality by anticounterfeiting labels represents a crucial point toward protection against forgery. Fast and scalable fabrication methods of original labels with a high degree of protection are in high demand for the protection of valuable goods. Here, we propose a simple strategy for fabrication of hidden security tags with IR luminescent readout by the direct femtosecond laser patterning of silicon-erbium-silicon sandwiched thin films. The choice of laser processing parameters makes possible the creation of random or quasi-regular self-organized surface nanotextures. The controlled laser-driven oxidation accompanying this process provides simultaneous regulation of the film's optical properties and spontaneous emission yield of the embedded Er atoms. The regimes are detected when optically similar patterned areas demonstrate different Er emission intensities, allowing us to create hidden security tags with facile readout at the C-band telecommunication wavelengths. The obtained results take another step toward the application of IR-luminescent erbium-based anticounterfeiting labels for covert and/or forensic security levels.

It has been experimentally shown for the first time that metallic copper in glasses can play the role of a reducing agent for other metallic ions, in particular, resulting in the formation of metal nanoparticles. Silver ions have been introduced into an alkali silicate glass containing copper nanoparticles by ion exchange. This has resulted in the formation of silver nanoparticles accompanied by the disappearance of copper nanoparticles initially contained in the glass. Such a process has never been observed and described anywhere. The process has been explained by the redox reaction Cu 0 + Ag + → Cu + + Ag 0 taking place in silver ion exchange. It has been shown that this reaction can go only in one direction (from left to right) as a result of the relative positions of copper and silver in the activity series.

For the first time, we demonstrated that additional poling at room temperature (cold repoling) of a soda-lime glass thermally poled in open anode configuration causes an increase of the optical second harmonic signal by more than an order of magnitude. Performed experiments allow relating this increase in the optical nonlinearity of the glass to the orientation of hydrogenated dipoles in the vicinity of the glass surface. This indicates that both frozen electric field and dipole orientation are responsible for the nonlinearity of thermally poled alkali-containing glasses. Observed dipole orientation in glasses is of interest for molecular physics and electrodynamic studies.

Dissociation of a ligand isoniazid from a protein catalase was investigated using all-atom molecular dynamics (MD) simulations. Random acceleration MD (τ-RAMD) was used, in which a random artificial force applied to the ligand facilitates its dissociation. We have suggested a novel approach to extrapolate such obtained dissociation times to the zero-force limit assuming never before attempted universal exponential dependence of the bond strength on the applied force, allowing direct comparison with experimentally measured values. We have found that our calculated dissociation time was equal to 36.1 s with statistically significant values distributed in the interval of 0.2-72.0 s, which quantitatively matches the experimental value of 50 ± 8 s despite the extrapolation over 9 orders of magnitude in time.