The present work reports the application of RF-magnetron sputtering technique to realize CsPbBr ${}_3$ 70 nm thick films on glass substrate by means of a one-step procedure. The obtained films show highly uniform surface morphology and homogeneous thickness as evidenced by AFM and SEM investigations. XRD measurements demonstrate the presence of two phases: a dominant orthorhombic CsPbBr ${}_3$ and a subordinate CsPb ${}_2$ Br ${}_5$ . Finally, XPS data reveals surface bromine depletion respect to the stoichiometrical CsPbBr ${}_3$ composition, nevertheless photoluminescence spectroscopy results confirm the formation of a highly luminescent film. These preliminary results demonstrate that our approach could be of great relevance for easy fabrication of large area perovskite thin films. Future developments, based on this approach, may include the realization of multijunction solar cells and multicolor light emitting devices.

When low temperature nitriding of austenitic stainless steels is carried out, it is very important to remove the surface passive layer for obtaining homogeneous incorporation of nitrogen. In the glow-discharge nitriding technique this surface activation is performed by cathodic sputtering pre-treatment, which can heat also the samples up to nitriding temperature. This preliminary study investigates the possibility of producing modified surface layers on austenitic stainless steels by performing low pressure glow-discharge treatments with nitrogen, similar to cathodic sputtering, so that surface activation, heating and nitrogen incorporation can occur in a single step having a short duration (up to about 10 min). Depending on treatment parameters, it is possible to produce different types of modified surface layers. One type, similar to that obtained with low temperature nitriding, consists mainly of S phase and it shows improved surface hardness and corrosion resistance in 5% NaCl solution in comparison with the untreated steel. Another type has large amounts of chromium nitride precipitates, which cause a marked hardness increase but a poor corrosion resistance. These surface treatments influence also water wetting properties, so that the apparent contact angle values become >90°, indicating a hydrophobic behavior.

Chromium deposits rank among the most widespread metal coatings for functional and decorative purposes. However, electrodeposition from Cr(VI) aqueous solution, which is the industrial process currently used to achieve thin chromium deposits, presents several environmental issues, urging the development of alternative solutions. In this study, which aims to compare the functional and aesthetical properties of decorative coatings, 800 nm thick chromium layers were deposited directly onto copper substrates by means of magnetron sputtering (MS) and direct current electrodeposition (ED). The obtained coatings were characterized regarding their thickness, morphology, color index, chemical composition, and corrosion resistance viewpoints. With respect to the electroplated samples, which constitute the benchmark, the magnetron sputtered ones appeared to be darker but showed a pleasing reflective appearance and superior thickness homogeneity, as well as the absence of voids and macrocracks, as evidenced by scanning electron microscopy (SEM) investigation. Regarding the anticorrosion performances of the chromium layers, electrochemical and standard salt spray test (NSS test) were carried out at room temperature in 3.5% NaCl solution, and evidenced similar, if not better, results for the magnetron sputtered coatings. On the whole, the data displayed here demonstrates the suitability of magnetron sputtering technology for use as an industrially feasible finishing technology for both aesthetic and mild-condition anticorrosion purposes.

Low-temperature nitriding of austenitic stainless steels produces modified surface layers, consisting mainly of the S phase, which improve surface hardness and corrosion resistance. Because of the localized plastic deformations, owing to modified layer formation, and ion bombardment occurring during the process itself, this treatment produces also modifications of surface morphology and roughness, which can affect wettability and corrosion behavior. In this study the effects of plasma nitriding, performed using different treatment conditions, on the surface morphology and roughness, and thus on wettability and corrosion resistance, of AISI 202 specimens with different initial finishings (2D and polished finishing) were investigated. Different probe liquids, having both high (bi-distilled water and solution of 3.5% NaCl) and low (ethanol and rapeseed oil) surface tension, were employed for assessing the wetting behavior with the sessile drop method. The contact angle values for water increased markedly when nitriding was performed on polished samples, while this increase was smaller for 2D samples, and on selected specimens a hydrophobic behavior was observed. Very low contact angle values were registered using low surface tension liquids, suggesting an oleophilic behavior. Corrosion resistance in a 5% NaCl solution was assessed, and it depended on the characteristics of the nitrided specimens.

Low-temperature nitriding allows to improve surface hardening of austenitic stainless steels, maintaining or even increasing their corrosion resistance. The treatment conditions to be used in order to avoid the precipitation of large amounts of nitrides are strictly related to alloy composition. When nickel is substituted by manganese as an austenite forming element, the production of nitride-free modified surface layers becomes a challenge, since manganese is a nitride forming element while nickel is not. In this study, the effects of nitriding conditions on the characteristics of the modified surface layers obtained on an austenitic stainless steel having a high manganese content and a negligible nickel one, a so-called nickel-free austenitic stainless steel, were investigated. Microstructure, phase composition, surface microhardness, and corrosion behavior in 5% NaCl were evaluated. The obtained results suggest that the precipitation of a large volume fraction of nitrides can be avoided using treatment temperatures lower than those usually employed for nickel-containing austenitic stainless steels. Nitriding at 360 and 380 °C for duration up to 5 h allows to produce modified surface layers, consisting mainly of the so-called expanded austenite or γ_N, which increase surface hardness in comparison with the untreated steel. Using selected conditions, corrosion resistance can also be significantly improved.

Due to global environmental concerns related to climate change, the need to improve the service life of structures and infrastructures is imminently urgent. Structural elements typically suffer service life reductions, leading to poor environmental sustainability and high maintenance costs. Graphene oxide nanosheets (GONSs) effectively dispersed in a cement matrix can promote hydration, refine the microstructure and improve interfacial bonding, leading to enhanced building materials’ performance, including mechanical strength and transport properties. Cement-based nanocomposites engineered with GONSs were obtained using two commercial nanofillers, a GO water suspension and a free-flowing GO nanopowder, characterized by fully comparable morphology, size and aspect ratio and different oxidation degrees (i.e., oxygen-to-carbon molar ratio), 0.55 and 0.45, respectively. The dosage of the 2D-nanofiller ranged between 0.01% and 0.2% by weight of cement. The electrical and thermal properties were assessed through electrochemical impedance spectroscopy (EIS) and a heat flow meter, respectively. The results were discussed and linked to micrometric porosity investigated by micro-computed tomography (μ-CT) and transport properties as determined by initial surface absorption test (ISAT), boil-water saturation method (BWS) and chloride ion penetration test. Extra-low dosage mortars, especially those loaded with a lower oxidation degree (i.e., 0.45GO), showed decreased permeability and improved barrier to chloride ion transport combined with enhanced thermal and electrical conductivity with respect to that of the control samples.