A better control over processes responsible for the photocurrent generation in semiconductors and nanocomposites is essential in the fabrication of photovoltaic devices, efficient photocatalysts and optoelectronic elements. Therefore, new approaches towards photochemical properties tuning are intensively searched for. Among numerous parameters, the photocurrent polarity is of great importance to the overall performance of a device. Usually, the polarity is controlled through an alignment of electronic states/bands, tailoring of applied potential or suitable selection of incident light wavelengths. In most scenarios though, the influence of light intensity is somehow neglected and either some arbitrarily chosen, natural conditions are mimicked or this parameter is varied only in a narrow range. Here we present a ternary nanocomposite in which the persistent photocurrent polarity switching is achieved through changes in the light intensity. We also present arguments suggesting this behaviour is of a general character and should be considered also in other photochemical systems.

This review focuses on the synthesis, properties and selected applications of heavy pnictogen chalcohalides, i.e. compounds of the MQX stoichiometry, where M = As, Sb, and Bi; Q = O, S, Se, and Te; and X = F, Cl, Br and I. The first section focuses on their synthesis and crystal structures, and the second section discusses the electronic structure on the basis of quantum chemical modelling and selected experimental data. Finally, the third section discusses their electrical, photoelectrochemical and photocatalytic properties and applications. In contrast to perovskites, chalcopyrites and kesterites, chalcohalides have attracted relatively less attention, but their structure and properties are well suited for numerous applications.

In vitro cytotoxicity assessment is indispensable in developing new biodegradable implant materials. Zn, which demonstrates an ideal corrosion rate between Mg‐ and Fe‐based alloys, has been reported to have excellent in vivo biocompatibility. Therefore, modifications aimed at improving Zn's mechanical properties should not degrade its biological response. As sufficient strength, ductility and corrosion behavior required of load‐bearing implants has been obtained in plastically deformed Zn‐3Ag‐0.5Mg, the effect of simultaneous Ag and Mg additions on in vitro cytocompatibility and antibacterial properties was studied, in relation to Zn and Zn‐3Ag. Direct cell culture on samples and indirect extract‐based tests showed almost no significant differences between the tested Zn‐based materials. The diluted extracts of Zn, Zn‐3Ag, and Zn‐3Ag‐0.5Mg showed no cytotoxicity toward MG‐63 cells at a concentration of ≤12.5%. The cytotoxic effect was observed only at high Zn²⁺ ion concentrations and when in direct contact with metallic samples. The highest LD₅₀ (lethal dose killing 50% of cells) of 13.4 mg/L of Zn²⁺ ions were determined for the Zn‐3Ag‐0.5Mg. Similar antibacterial activity against Escherichia coli and Staphylococcus aureus was observed for Zn and Zn alloys, so the effect is attributed mainly to the released Zn²⁺ ions exhibiting bactericidal properties. Most importantly, our experiments indicated the limitations of water‐soluble tetrazolium salt‐based cytotoxicity assays for direct tests on Zn‐based materials. The discrepancies between the WST‐8 assay and SEM observations are attributed to the interference of Zn²⁺ ions with tetrazolium salt, therefore favoring its transformation into formazan, giving false cell viability quantitative results.

Co-Mo and Co-Mo-C Alloys Deposited in a Magnetic Field of High Intensity and their Electrocatalytic Properties: The article presents results of tests on electrodeposition in a magnetic field of Co-Mo and Co-Mo-C alloys characterised by low overvoltage of hydrogen evolution. Addition of molybdenum and carbon was to lower the values of overvoltage of hydrogen evolution on cobalt. The influence of a magnetic field of high intensity (1 - 12 T) on the deposits composition, structure and morphology was determined. The deposition was conducted in a magnetic field of parallel orientation of the magnetic field forces lines in relation to the working electrode. Electrocatalytic properties of the obtained alloy coatings within the range of hydrogen evolution were tested in a concentrated solution of NaOH. The obtained alloys were analysed with the XRD method, their composition was tested with the WDXRF technique and they underwent observation applying scanning electron microscopy (SEM). The comparison of electrocatalytic properties of Co-Mo alloys with properties of Co-Mo-C ones enabled determining the influence of carbon presence in cathodic deposits on the overvoltage value of hydrogen evolution on them.