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The low-cost material extrusion (MEX) additive manufacturing technology can offer an economical alternative to manufacture metal parts with complex geometry over traditional manufacturing or the more expensive powder bed fusion (PBF) techniques. In this work, a feedstock made of 316L stainless steel powder (65 % by volume) and a single component binder (LDPE) system was developed. The use of a single binder rather than two or more components, commonly used in metal MEX, introduces a novel and more sustainable solution in terms of costs and less use of chemicals. The rheology and processability of the feedstocks were studied, and samples were 3D printed. Debinding and sintering under a hydrogen atmosphere at 1380 °C were performed, and the resulting metallic parts have been characterized by a mechanical and microstructural point of view. The results show a sintered steel having 93 % of the theoretical density and an austenitic phase confirming that the post-processing under reductive atmosphere protected the samples from oxidation and other contamination. The sintered 3D parts show a grain size of ∼ 45 μm, a yield point of 250 MPa, a tensile strength of 520 MPa, and a Vickers microhardness of 285 HV typical of annealed steel.

Nitrogen can be electrochemically reduced to produce ammonia, which supplies an energy-saving and environmental-benign route at room temperature, but high-efficiency catalysts are sought to reduce the reaction barrier. Here, iron-doped α-MoO3 nanosheets are thus designed and proposed as potential catalysts for fixing N2 to NH3. The α-MoO3 band structure is intentionally modulated by the iron doping, which narrows the band gap of α-MoO3 and turns the semiconductor into a metal-like catalyst. Oxygen vacancies, generated by substituting Mo6+ for Fe3+ anions, are beneficial for nitrogen adsorption at the active sites. In 0.1 M Na2SO4, the Fe-doped MoO3 catalyst reached a high faradaic efficiency of 13.3% and an excellent NH3 yield rate of 28.52 μg h-1 mgcat-1 at -0.7 V versus reversible hydrogen electrode, superior to most of the other metal-based catalysts. Theoretical calculations confirmed that the N2 reduction reaction at the Fe-MoO3 surface followed the distal reaction path.

This work focuses on the replacement of mineral oils with bio-based waste cooking oils in rubber compounding. Two different waste cooking oils from potatoes and chicken frying process were analyzed by means of chemical and rheological tests to evaluate the chemical composition, the oxidative stability and the viscosity. Waste oils have been introduced in elastomeric compounds as substitute for typical processing aids (i.e. lubricants). Cure kinetics of rubber compounds was studied by rheological characterization. Mechanical properties of vulcanized samples were determined by means of tensile tests, hardness tests and dynamic mechanical analysis. The waste oils showed a rheological behavior very similar to the mineral oils conventionally employed in rubber manufacturing leading to almost the same processability of the resulting compound. The waste oils did not significantly affect the vulcanization kinetics of the rubber compound, as expected for conventional lubricants. Waste cooking oils and mineral oil show analogous influence on mechanical properties of cured compounds. At increasing oil content, the elongation at break and the tensile strength increased whereas the values of Elastic Modulus at 100% strain, the Storage Modulus and Shore A Hardness decreased with respect to the oil-free sample. These results are very promising, confirming the possibility to replace the mineral oils, in a good practice of circular economy.

Highly performing perovskite-based anodes for methane mixtures-fueled solid oxide fuel cells (SOFC) are proposed. Catalytic activities of La0.6Sr0.4Fe1-xPdxO3-δ (LSFPd) with x = 0.05, 0.1 toward dry reforming of methane (DMR) and partial oxidation of methane (POM) reactions are investigated. The addition of (30wt%) Ce0.85Gd0.15O2-δ (GDC) and of (30wt%) Ni(5wt%)-GDC to the perovskite compounds was evaluated to enhance both electrocatalytic and electrochemical properties. Electrolyte-supported cells based on La0.8Sr0.2Ga0.8Mg0.2O3-δ (LSGM) pellets and LSFPd perovskite oxides at both electrodes are fabricated and tested using CH4, CH4/Ar and CH4/CO2 mixtures in the 750–850°C temperature range. Fuel cell tests using anodic mixtures such as LSFPd/GDC and LSFPd/Ni-GDC are also performed. A discussion based on the comparison between catalytic and electrochemical results and on the possible reforming and/or oxidation reactions taking place at the anode is detailed.

Immiscible blends of ethylene‐propylene‐diene‐monomer (EPDM) and polyoxymethylene (POM), when EPDM is the major phase were compatibilized on the addition of an ionomer, poly(ethylene‐co‐methacrylic acid). The inclusion of the ionomer reduced the interfacial tension between the two phases, such that the diameter of the POM domains were significantly reduced to between 0.5 and 2 μm, typical of that required to toughen ductile polymers. The mechanical properties of the resultant compatibilized blends were significantly enhanced with increases in Young's modulus (↑54%), tensile strength (σ, ↑139%), elongation at break (e, ↑97%), and tensile toughness (↑500%) with increasing ionomer content, relative to EPDM rubber alone. The ShoreA hardness of the compatibilized blend was 70.1 compared with 56.8 for the immiscible binary blend and, 50.2 for neat EPDM rubber.

The impact of graphite nanoplatelets (GNPs) on the physical and mechanical properties of cementitious nanocomposites was investigated. A market-available premixed mortar was modified with 0.01% by weight of cement of commercial GNPs characterized by two distinctively different aspect ratios. The rheological behavior of the GNP-modified fresh admixtures was thoroughly evaluated. Hardened cementitious nanocomposites were investigated in terms of density, microstructure (Scanning Electron Microscopy, SEM and micro–Computed Tomography, μ-CT), mechanical properties (three-point bending and compression tests), and physical properties (electrochemical impedance spectroscopy, EIS and thermal conductivity measurements). At 28 days, all GNP-modified mortars showed about 12% increased density. Mortars reinforced with high aspect ratio GNPs exhibited the highest compressive and flexural strength: about 14% and 4% improvements compared to control sample, respectively. Conversely, low aspect ratio GNPs led to cementitious nanocomposites characterized by 36% decreased electrical resistivity combined with 60% increased thermal conductivity with respect to the control sample.

Strain monitoring is of great interest in order to check components structural life, to prevent catastrophic failures, and, possibly, to predict residual life in case of unexpected events. In this study, strain sensing epoxy-based coatings containing carbon nanotubes (MWCNTs), graphene nanoplatelets (GNPs), and a mix of the two (MWCNT+GNP) have been produced, with the same initial electrical resistivity, and applied on glass fiber reinforced composites. Morphological, mechanical, and electrical tests have been then performed evaluating the resistance variation and the strain sensing performance of the sensors. A theoretical model to relate the resulting gauge factors to the different types of nanofillers has been applied. The results showed that all systems present a strain sensing performance with different gauge factors (and hence sensitivity) at low strain: GNP samples showed the highest gauge factor (10.3), MWCNT samples the lowest (1.5), and the mixed system lies in the middle (4.3). From analytical analysis, the value of initial distance among conductive particles was found to be 0.3 nm in the case of MWCNT and 1.2 nm for GNP, explaining why the gauge factors of the produced sensors are different.

Recent improvements in additive layer manufacturing (ALM) have provided new designs of geometrically complex structures with lighter materials and low processing costs. The use of additive manufacturing in spacecraft production is opening up many new possibilities in both design and fabrication, allowing for the reduction of the weight of the structure subsystems. In this aim, polymeric ALM structures can become a choice, in terms of lightweight and demisability, as far as good thermomechanical properties. Moreover, provided that fused-deposition modeling (FDM) is used, nanosats and other structures could be easily produced in space. However, the choice of the material is a crucial step of the process, as the final performance of the printed parts is strongly dependent on three pillars: design, material, and printing process. As a high-performance technopolymer, polyether ether ketone (PEEK) has been adopted to fabricate parts via ALM, however, the space compatibility of 3D-printed parts remains not demonstrated. This work aimed to realize a nanosat polymeric structure via FDM, including all the phases of the development process: thermomechanical design, raw material selection, printing process tuning, and manufacturing of a proof of concept of a technological model. The design phase includes the application of topology optimization to maximize mass saving and take full advantage of the ALM capability. 3D-printed parts were characterized via thermomechanical tests, outgassing tests of 3D-printed parts are reported confirming the outstanding performance of polyether ether ketone and its potential as a material for structural space application.

The electrocatalytic nitrogen reduction reaction (NRR) has been deemed a promising and reliable approach to massively produce ammonia under ambient conditions. A high-efficiency electrocatalyst with an excellent selectivity is highly required to reduce the multiple reaction barriers of N2 + 3H2O → 2NH3 + 1.5O2. Here, we report electrospun zirconia nanofibers as a non-noble NRR electrocatalyst to convert nitrogen to ammonia. Theoretical calculations predict that the Zr sites with oxygen vacancies are favorable for nitrogen adsorption and reduction. Experimentally, the larger concentration of oxygen defects in such an electrocatalyst allowed achieving a NH3 formation rate of 9.63 μg h−1 mgcat.−1 and an optimal faradaic efficiency of 12.1% at −0.7 V vs. the reversible hydrogen electrode in 0.1 M Na2SO4.

In this work, porous complex and metal-free cathodes based on a (La0.6Sr0.4) (Cr0.5Mn0.5) O3 (LSCM) screen-printed backbone infiltrated with Ce0.9Gd0.1O2 (GDC) were fabricated for solid oxide electrolyzer cells. GDC infiltration has been optimized by structural and microstructural investigation and tested by electrochemical measurements in CO/CO2 mixtures. Infiltrated electrodes with a non-aqueous GDC solution showed the best electro-catalytic activity towards CO2 reduction, exhibiting a much lower polarization resistance, i.e., Rpol = 0.3 Ω&middot, cm2 at 900 &deg, C. The electrochemical performance of LSCM/GDCE in terms of Rpol is comparable to the best-performing Ni-YSZ cathode in the same operating conditions (Rpol = 0.23 Ω&middot, cm2).

Perovskite oxides such as ferrites have been widely investigated for their remarkable electrochemical activity as SOFC electrodes. However, their phase instability in reducing conditions remains an issue for anode application. The role of Mn substitution into B-site of La0.6Sr0.4FeO3-δ (LSF) perovskite oxide was investigated. New insights on the structural evolution of La0.6Sr0.4Fe0.8Mn0.2O3-δ (LSFMn) upon high temperature reduction were revealed. In oxidizing atmosphere, Mn substitution reduces the oxygen vacancy concentration while, switching to reducing conditions, it drives the transition from rhombohedral perovskite to single Ruddlesden-Popper phase, affecting the Fe0 exsolution. Redox-cycles of LSFMn were investigated and the properties of re-oxidized compounds were highlighted. The effect of Mn substitution on perovskite conductivity was also evaluated both in oxidizing and reducing conditions.

A structured catalyst for the dry reforming of methane (DRM) was investigated as a biogas pre-reformer for indirect internal reforming solid oxide fuel cell (IIR-SOFC). For this purpose, a NiCrAl open-cell foam was chosen as support and Ni-based samarium doped ceria (Ni-SmDC) as catalyst. Ni-SmDC powder is a highly performing catalyst showing a remarkable carbon resistance due to the presence of oxygen vacancies that promote coke gasification by CO2 activation. Ni-SmDC powder was deposited on the metallic support by wash-coating method. The metallic foam, the powder, and the structured catalyst were characterized by several techniques such as: N2 adsorption-desorption technique, X-ray diffraction (XRD), scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDX), focused ion beam (FIB), temperature programmed reduction (H2-TPR), and Raman spectroscopy. Catalytic tests were performed on structured catalysts to evaluate activity, selectivity, and stability at SOFC operating conditions.

In cultural heritage field, significant research efforts have been recently made to improve the efficacy of anti-vegetative treatments and to reduce the environmental impact caused by biocides high concentration. According to the pro-ecological approach, this work reports a novel approach based on the encapsulation/incorporation of environmentally-friendly biocides in different silica nanosystems in order to control the development of biological patinas on outdoor cultural heritage. Two different green biocides have been selected and tested in silica nanosystems: the zosteric acid sodium salt (ZS), a natural antifoulant compound produced by Zostera marina (eelgrass), and the usnic acid (UA), a secondary metabolite produced by some saxicolous lichens. ZS was previously successfully encapsulated but never entrapped in mesoporous silica; instead, UA is, for the first time, encapsulated and in situ entrapped into the silica nanosystems in order to control the release over time. Both silica nanosystems have been characterized as far as their dimensions and superficial properties and loading capability. The antifouling activity was assessed against microorganisms from biopatinas colonising the Aurelian Walls in Rome. Our results have shown that the two nanosystems have complementary properties, thus it is possible to tune the antifouling efficiency by combining the two in different proportions.

Solid oxide photoelectrochemical cells (SOPECs) with inorganic ion-conducting electrolytes provide an alternative solution for light harvesting and conversion. Exploring potential photoelectrodes for SOPECs and understanding their operation mechanisms are crucial for continuously developing this technology. Here, ceria-based thin films were newly explored as photoelectrodes for SOPEC applications. It was found that the photoresponse of ceria-based thin films can be tuned both by Sm-doping-induced defects and by the heating temperature of SOPECs. The whole process was found to depend on the surface electrochemical redox reactions synergistically with the bulk photoelectric effect. Samarium doping level can selectively switch the open-circuit voltages polarity of SOPECs under illumination, thus shifting the potential of photoelectrodes and changing their photoresponse. The role of defect chemistry engineering in determining such a photoelectrochemical process was discussed. Transient absorption and X-ray photoemission spectroscopies, together with the state-of-the-art in operando X-ray absorption spectroscopy, allowed us to provide a compelling explanation of the experimentally observed switching behavior on the basis of the surface reactions and successive charge balance in the bulk.

A thermoresponsive Pluronic/alginate semisynthetic hydrogel is used to bioprint 3D hepatic constructs, with the aim to investigate liver-specific metabolic activity of the 3D constructs compared to traditional 2D adherent cultures. The bioprinting method relies on a bioinert hydrogel and is characterized by high-shape fidelity, mild depositing conditions and easily controllable gelation mechanism. Furthermore, the dissolution of the sacrificial Pluronic templating agent significantly ameliorates the diffusive properties of the printed hydrogel. The present findings demonstrate high viability and liver-specific metabolic activity, as assessed by synthesis of urea, albumin, and expression levels of the detoxifying CYP1A2 enzyme of cells embedded in the 3D hydrogel system. A markedly increased sensitivity to a well-known hepatotoxic drug (acetaminophen) is observed for cells in 3D constructs compared to 2D cultures. Therefore, the 3D model developed herein may represent an in vitro alternative to animal models for investigating drug-induced hepatotoxicity.

In the frame of the HERACLES (HEritage Resilience Against CLimate Events on Site) project, a set of cultural heritage sites was studied to improve their resilience against climate events. The mediaeval Town Walls of Gubbio, in the centre of Italy, are among these. Over the centuries, several factors including environmental actions and structural and material repairs have produced different criticalities, involving both structure and materials. A severe problem consists in the progressive degradation of the mortars binding the masonry. Since the wall body structure behaves/reacts properly only if the cohesion between mortar and stones is sufficiently large, it follows that mortars degradation represents a quite significant issue that deserves a special attention. The present work focuses on the characterization of the mortars sampled in various parts of the Walls, corresponding to different historical periods, restoration measures and interventions. They were characterized to determine the corresponding mineralogical and chemical compositions along with morphological features and to investigate their mechanical properties. For that purpose, penetrometric and sclerometric tests on site and ex situ laboratory techniques, such as X-ray diffraction, polarized light microscopy, scanning electron microscopy, thermogravimetry and differential thermal analysis, were used to examine the weathering effects on mortars and more generally their degradation state, in order to plan appropriate restoration and repair actions.

Several proton conductive ceramic oxides are evaluated for potential application in ceramic-NiO composite anodes for proton-conducting La0.99Ca0.01NbO4 (LNO) electrolyte-based fuel cells. Chemical compatibility tests show that most of the existing proton-conducting oxides are unfavorable for application in LNO electrolyte-based fuel cells because of undesirable reactions at high temperatures. Further considering the chemical compatibility with NiO and the ability to promote the densification of the deposited LNO electrolyte, LNO-NiO composite anode proves to be the only suitable anode candidate. With humidified hydrogen (∼3%H2O) as the fuel and static air as the oxidant, fuel cells based on LNO electrolyte film deposited on LNO-NiO anodes show a peak power density of 24 mW cm−2 at 750 °C, this value being one of the largest ever reported for LNO-based cells. Further investigation reveals that the polarization resistance of the cell is the major contribution to the total cell resistance, limiting the overall cell performance.

An innovative concept of a low-cost pH optode with working volumes of less than 150 µL is presented. The pH monitoring is based on the color changing effect of pH indicators. The optode includes an RGB color sensor patch TCS34725 from Adafruit, a controllable LED and reactor slides and is addressed by a self-written LabVIEW© software. Utilizing the hue value of the HSV color model, it is possible to analyze the color change of the indicator and estimate the pH value of the analyzed samples by exploiting sigmoidal fit models. Measurements carried out with phenol red and DMEM (Dulbecco's Modified Eagle's Medium) reported a standard error of calibration in the physiologic pH range (6.5–7.5) of ±0.04 pH units.

In the present study, morphological and electrical properties of BaZrO3 were investigated as a function of the ionic radii mismatch between Zr and the different B-site dopants (Al, Sc, In, Lu, Tm, Y, Gd, Sm, Nd, and La) for the same solute concentration and valence. Our study highlights the critical role of the ionic radius of the acceptor dopant on stability, sinterability, and proton conductivity of barium zirconate. From our study, Gd-doped barium zirconate emerges as a novel promising material for proton conductor electrolytes.

In this work, hydrophilic silver nanoparticles (AgNPs), bifunctionalized with citrate (Cit) and L-cysteine (L-cys), were synthesized. The typical local surface plasmon resonance (LSPR) at &lambda, max = 400 nm together with Dynamic Light Scattering (DLS) measurements (&lt, 2RH&gt, = 8 &plusmn, 1 nm) and TEM studies (&Oslash, = 5 &plusmn, 2 nm) confirmed the system nanodimension and the stability in water. Molecular and electronic structures of AgNPs were investigated by FTIR, SR-XPS, and NEXAFS techniques. We tested the system as plasmonic sensor in water with 16 different metal ions, finding sensitivity to Hg2+ in the range 1&ndash, 10 ppm. After this first screening, the molecular and electronic structure of the AgNPs-Hg2+ conjugated system was deeply investigated by SR-XPS. Moreover, in view of AgNPs application as sensors in real water systems, environmental safety assessment (ecosafety) was performed by using standardized ecotoxicity bioassay as algal growth inhibition tests (OECD 201, ISO 10253:2006), coupled with determination of Ag+ release from the nanoparticles in fresh and marine aqueous exposure media, by means of ICP-MS. These latest studies confirmed low toxicity and low Ag+ release. Therefore, these ecosafe AgNPs demonstrate a great potential in selective detection of environmental Hg2+, which may attract a great interest for several biological research fields.

High materials costs and low performance are the persisting bottlenecks that significantly affect the microbial fuel cells (MFCs) applications. The membraneless single-chamber MFC with an air-breathing cathode is a simple configuration where the bacteria play a role in both the anodic and cathodic processes. However, the microbial cathodic semi-reaction is the rate-determining step that can impair the advantage of the natural availability of oxygen in the air. In this work, the microbial catalysis was improved adding cerium oxide nanoparticles (nanoceria) in carbon-based cathodes of air-breathing MFCs, boosting their performance. Two kinds of nanoparticles were tested: CeO2 and Sm-doped CeO2 (Sm-CeO2) on carbon powder, using pristine carbon powder cathodes as a control. The energy generated was 113, 65 and 31 mWh m−2, for Sm-CeO2, CeO2 and control MFCs, respectively, during four subsequent fed cycles of 0.036 mol L−1 Na-acetate in carbonate buffer solution. The better performance of MFCs was correlated to the oxygen preferential and controlled entrapping and release via Ce4+/3+ redox reaction at the carbon particle surface, as well as to the increased cathode active specific surface area. The achieved results suggest that nanoceria can act as oxygen storage for bacteria in the anaerobic biofilm colonizing the cathode.

Multilayered heterostructures of Ce0.85Sm0.15O2-delta and Y0.16Zr0.92O2-delta of a high crystallographic quality were fabricated on (001) - oriented MgO single crystal substrates. Keeping the total thickness of the heterostructures constant, the number of ceria-zirconia bilayers was increased while reducing the thickness of each layer. At each interface Ce was found primarily in the reduced, 3+ oxidation state in a layer extending about 2 nm from the interface. Concurrently, the conductivity decreased as the thickness of the layers was reduced suggesting a progressive confinement of the charge transport along the YSZ layers. The comparative analysis of the in-plane electrical characterization suggests that the contribution to the total electrical conductivity of these interfacial regions is negligible. For the smallest layer thickness of 2 nm the doped ceria layers are electrically insulating and the ionic transport only occurs through the zirconia layers. This is explained in terms of a reduced mobility of the oxygen vacancies in the highly reduced ceria.

Copper and gadolinium doped ceria (GDC) anode supported fuel cells were co-sintered at relatively low temperature (900 °C) and successfully tested in the intermediate temperature (IT) range. The GDC electrolyte densification was promoted by a compressive strain induced by increasing the anodic thickness and was evaluated by SEM investigation. Instead of more commonly used La0.8Sr0.2Fe0.6Co0.4O3-δ, strontium and copper-doped lanthanum ferrite La0.8Sr0.2Fe0.8Cu0.2O3-δ (LSFCu) mixed with 30 wt% GDC (LSFCu-GDC) was employed as cathodic material. Preliminary tests on Cu-GDC/GDC/LSFCu-GDC single cells showed promising results at temperature as low as 650 °C using hydrogen as fuel.

© 2019 The Royal Society of Chemistry. A rational design of a high-performance cathode for proton-conducting solid oxide fuel cells (SOFCs) is proposed in this study with the aim of improving the hydration properties of conventional perovskite cathode materials, thus leading to the development of new materials with enhanced proton migration. Herein, potassium is used to dope traditional Ba0.5Sr0.5Co0.8Fe0.2O3-δ (BSCF), which is demonstrated to be a beneficial way for improving hydration, both experimentally and theoretically. The theoretical study was needed to overcome practical limits that hindered direct hydrogen mobility measurements. The novel material Ba0.4K0.1Sr0.5Co0.8Fe0.2O3-δ (BKSCF) shows a lower overall proton migration energy compared with that of the sample without K, suggesting that K-doping enhances proton conduction, which shows an improved performance by extending the catalytic sites to the whole cathode area. As a result, a fuel cell built with the novel BKSCF cathode shows an encouraging fuel cell performance of 441 and 1275 mW cm-2 at 600 and 700 °C, respectively, which is significantly higher than that of the cell using the pristine BSCF cathode. This study provides a new and rational way to design a perovskite cathode for proton-conducting SOFCs with high performance.

Solid oxide fuel cells (SOFCs) represent the most efficient devices for producing electrical power from fuels. The limit in their application is due to the high operation temperature of conventional SOFC materials. Progress is made toward lower operating temperatures using alternative oxygen-ion conducting electrolytes, but problems of stability and electronic conductivity still remain. A promising alternative is the use of chemically stable proton-conducting Y-doped BaZrO3 (BZY) electrolytes, but their practical applications are limited by the BZY's relatively low performance. Herein, it is reported that deposition by impregnation of cathode nanoparticles on BZY backbones provides a powerful strategy to improve the BZY-based SOFC performance below 600 °C, allowing an outstanding power output for this chemically stable electrolyte. Moreover, it is demonstrated that keeping the nanostructure is more important than keeping the desired chemical composition. The proposed scalable processing method can make BZY a competitive electrolyte for SOFC applications.

Proton-conducting oxides offer a promising electrolyte solution for intermediate temperature solid oxide fuel cells (SOFCs) due to their high conductivity and low activation energy. However, the lower operation temperature leads to a reduced cathode activity and thus a poorer fuel cell performance. La0.8Sr0.2MnO3−δ (LSM) is the classical cathode material for high-temperature SOFCs, which lack features as a proper SOFC cathode material at intermediate temperatures. Despite this, we here successfully couple nanostructured LSM cathode with proton-conducting electrolytes to operate below 600°C with desirable SOFC performance. Inkjet printing allows depositing nanostructured particles of LSM on Y-doped BaZrO3 (BZY) backbones as cathodes for proton-conducting SOFCs, which provides one of the highest power output for the BZY-based fuel cells below 600°C. This somehow changes the common knowledge that LSM can be applied as a SOFC cathode materials only at high temperatures (above 700°C).

TiO2 coatings on AA6082 aluminium alloy were obtained at low temperature (80 and 100°C) by the sol-gel dip-coating technique starting from titanium tetra-isopropoxide solution in ethyl alcohol. The preparation was carried out in the presence of acetic acid with both functions of catalyst and chelating agent. The curing temperatures used for these coatings are between 80 and 100°C, low enough to make such coatings suitable to incorporate additives such as organic inhibitors or polymeric nanoparticles. The coated samples were characterised by scanning electron microscopy and energy-dispersive spectroscopy, atomic force microscopy, X-ray diffraction, X-ray photoelectron spectroscopy and electrochemical impedance spectroscopy (EIS). Compact coatings with a thickness of 500 nm, consisting of amorphous and nearly stoichiometric titanium dioxide, were obtained. EIS results revealed an effective corrosion protection of the substrate for more than 120 h of immersion in 3.5 wt-% NaCl aqueous solution.

International audience; Bare and Al2O3-coated austenitic steel samples are exposed to lead-fast-reactor relevant corrosive conditions.Selective leaching of Ni, Mn and Cr is observed in bare samples exposed to high temperature stagnant lead(550 DC, 10et8722;8 wt.percent oxygen, 1000 and 4000 h). By contrast, corrosion is not observed in either pristine (4000 h)or irradiated (1000 h) coated samples. Further characterization and testing methods include SEM, TEM, STEM,EDS, cyclic nanoimpact, microindentation, scratch, and thermal cycling. Overall, the results show that thecoatings retain structural integrity under the conditions investigated, which is a crucial prerogative for corrosionprotection with ceramic coatings.