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This work aims to contribute to the industrial development of safer and advanced leathers using nanomaterials (NMs) that are based in titanium oxide doped with silver (Ag-TiO2NMs). These NMs present an ecological alternative to volatile organic biocides and organic solvents, frequently used nowadays. Safe application of these NMs brings added value to footwear and leather products and reduces the bulk chemical wide pollution. These newly developed materials are expected to be useful for footwear manufacturing (for common or professional use) with advanced protection against bacteria and fungus, which are the most common cause of feet infections, for either common or professional use. Hence, the main aim of this work is the improvement of leather footwear in order to overcome the feet infections and ensure minimum risk of human skin penetration. In order to accomplish the main aim, the cytotoxicity, antimicrobial and self-cleaning properties of leather surface, treated with Ag-TiO2NMs by sputtering deposition were assessed. The Ag-TiO2 coatings were deposited onto leather substrates by DC-pulsed reactive magnetron sputtering using two targets, Ti and Ag, in an Ar + O2 atmosphere. Compositional analysis was achieved by X-ray energy dispersive spectrometry (EDX). Contact angle of the coatings was measured and the results show that with the introduction of silver in TiO2 microstructure promotea an increase in hydrophobicity. The antibacterial activity of the samples was assessed by agar diffusion method and the results point out to a silver antibacterial activity.

Electroactive polymers are the most interesting class of polymers used as smart materials in various applications, such as the development of sensors and actuators for biomedical applications in areas as smart prosthesis, implantable biosensors and biomechanical signal monitoring, among others. For acquiring or applying the electrical signal from/to the piezoelectric material, suitable electrodes can be produced from Ti based coatings with tailored multifunctional properties, as conductivity and antibacterial characteristics, obtained by the inclusion of Ag. This work reports on Ti1-xAgx electrodes and Ag-TiNy electrodes deposited by d. c. and pulsed magnetron sputtering at room temperature on poly(vinylidene fluoride)(PVDF). In the first system (Ti1-xAgx electrodes), silver content was varied from 0-100 at. %. For the second system (Ag-TiNy electrodes), the nitrogen content changed between 0 to 40.3 at. % by increasing the nitrogen gas flow between 0 sccm and 15 sccm and the ratio Ti/Ag changed from 13.4 to 2.2 being clearly the visible decrease on the Ti content in the reactive mode. The X-Ray Diffraction (XRD) results revealed that the deposition conditions preserve the polymer structure and suggested the presence of crystalline Ti phase in pure titanium coating and fcc-Ag phase in pure silver coating for the Ti1-xAgx system. For the Ag-TiNy system it is possible to detect a fcc TiN structure and a fcc Ag phase. Sheet resistivity values show a typical behavior of a binary alloy system, varying between 0.12 and 28.5 /sq for the Ti1-xAgx electrodes. For the second system the sheet resistivity decrease with the nitrogen content from 12.0 /sq with 0 at. % to 2.8 /sq for 40.3 at. % of N. The piezoelectricity of the different samples show similar values, showing values from 19.6 to 27.6 pCN-1 for the Tix-1Agx system and 13.6 pCN-1 as minimum for the Ag- TiNy system, achieved for the highest N content. In order to assess the mechanical behavior of the as-sputtered films, the film/substrate system was loaded unidirectionally using a tensile machine. The stress-strain curves were analyzed and correlated with the structural data. Moreover, the antibacterial activity of the samples was assessed and it was verified that samples from the second series (Ag-TiNy) present antibacterial activity, in contrast of the first series (Ti1-xAgx).

Development of new self-lubricant coating systems with control of the lubricous species diffusion have enormous potential to be used in the protection of surfaces in components for machining. In the last years, vanadium rich coatings have been introduced as possible candidates for self-lubrication due to their optimum tribological properties. This work is devoted on the study of V additions on the morphology, structure and on the tribological properties of TiSiN films deposited by HiPIMS in Deep Oscillation Magnetron Sputtering (DOMS) mode. Two different peak powers were used on the deposition of coatings in order to produce films with different morphology. The tribological properties of coatings were evaluated at room temperature against Al2O3 balls on a pin-on-disc apparatus. Increasing of peak power showed to change the cross section morphology of films from columnar type to compact structure. V additions improved the tribological properties of TiSiN coatings. This research is sponsored by FEDER funds through the program COMPETE – Programa Operacional Factores de Competitividade – and by national funds through FCT – Fundação para a Ciência e a Tecnologia, under the projects: PTDC/EMETME/ 122116/2010 and PTDC/EMS-TEC/1805/2012. The authors acknowledge the Master student Melkamu A. Mekicha (co-author of this paper) from the International Joint European Master in Tribology of Surfaces and Interfaces (TRIBOS) program, doing his thesis in the mechanical engineering department of the University of Coimbra, for his special dedication on the development of this research.

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Mo–Se–C films were deposited by sputtering from a carbon target with pellets of MoSe2. In addition to the standard evaluation of their chemical composition, structure, morphology, hardness and cohesion/adhesion, the core objective of this paper was to analyze the tribological behavior of these films, particularly in the high-load regime. The carbon content varied from 29 to 68 at.% which led to a progressive increase of the Se/Mo ratio and the hardness. The friction coefficient of Mo–Se–C coatings clearly decreased with load from 0.15 to 0.05. The excellent friction properties were attributed to the formation of a thin molybdenum diselenide film on the top of the wear track of the coating and on the counterpart surface, while the role of the carbon in the sliding process is only secondary by increasing the coating hardness and thus its wear resistance.

The stability of nanostructured metal alloys is currently being extensively investigated, and several mathematical models have been developed to describe the thermodynamics of these systems. However, model capability in terms of thermal stability predictions strongly relies on grain boundary-related parameters that are difficult to measure or estimate accurately. To overcome this limitation, a novel theoretical approach is proposed and adopted in this work to identify W-based nanocrystalline alloys which are potentially able to show thermodynamic stability. A comparison between model outcomes and experimental findings is reported for two selected alloys, namely W-Ag and W-Al. Experimental results clearly highlight that W-Ag mixtures retain a segregated structure on relatively coarse length scales even after prolonged mechanical treatments. Moreover, annealing at moderate temperatures readily induces demixing of the constituent elements. In contrast, homogeneous nanostructured W-Al solid solutions are obtained by ball milling of elemental powders. These alloys show enhanced thermal stability with respect to pure W even at high homologous temperatures. Experimental evidences agree with model predictions for both the investigated systems.

Among the members of the transition metal dichalcogenides (TMD) family, molybdenum disulfide has the most consolidated application outcomes in tribological fields. However, despite the growing usage as nanostructured solid lubricant due to its lamellar structure, little is known about the atomistic interactions taking place at the interface between two MoS2 sliding layers, especially at high loads. By means of ab initio modeling of the static potential energy surface and charge distribution analysis, we demonstrate how electrostatic interactions, negligible in comparison with van der Waals and Pauli contributions at zero load, progressively affect the sliding motion at increasing loads. As such, they discriminate the relative stability and the frictional behavior of bilayers where the two monolayers defining the interface have a different relative orientation. In particular, for antiparallel sliding layers we observed a load-induced increase of both the depth of the minima and the height of the energy barriers compared to parallel ones, which may have important consequences for the fabrication of more efficient ultralow friction devices at the nanoscale.

Nanostructured materials are essential building blocks for the fabrication of new devices for energy harvesting/storage, sensing, catalysis, magnetic, and optoelectronic applications. However, because of the increase of technological needs, it is essential to identify new functional materials and improve the properties of existing ones. The objective of this Viewpoint is to examine the state of the art of atomic-scale simulative and experimental protocols aimed to the design of novel functional nanostructured materials, and to present new perspectives in the relative fields. This is the result of the debates of Symposium I "Atomic-scale design protocols towards energy, electronic, catalysis, and sensing applications", which took place within the 2018 European Materials Research Society fall meeting.