Deuterium retention and release behavior were investigated in this study, for beryllium, tungsten and mixed beryllium/tungsten thin layers which are of concern for next-generation thermonuclear fusion devices like International Thermonuclear Experimental Reactor. The layers prepared with thermionic vacuum arc technology by using two different ion acceleration voltages 0 V and −700 V respectively were subsequently implanted by exposure to a steady-state deuterium plasma with ion energies of 240 eV/D for D 3 and 360 eV/D for D 2 at a specific fluency of 2.85 × 10 20 m −2 s. Morphology is strongly influenced by layer composition and by the ion acceleration voltage applied in-situ during layer deposition. Crystalline structure analysis shows the presence of a polycrystalline W metallic phase and also highlights a dependence between tungsten crystallite size and Be/W atomic ratio. The amount of deuterium in mixed layers is lower than in pure beryllium layers indicating that W is mitigating D binding states. Results extrapolated for a 'cold chamber and divertor scenario' indicate a limited desorption efficiency (~20%), if the wall baking scenario, for tritium removal procedure in ITER, is to be applied to the investigated layers.

Beryllium-deuterium co-deposited layers were obtained using DC magnetron sputtering technique by varying the Ar/D2 gas mixture composition (10/1; 5/1; 2/1 and 1:1) at a constant deposition rate of 0.06 nm/s, 343 K substrate temperature and 2 Pa gas pressure. The surface morphology of the layers was analyzed using Scanning Electron Microscopy and the layer crystalline structure was analyzed by X-ray diffraction. Rutherford backscattering spectrometry was employed to determine the chemical composition of the layers. D trapping states and inventory quantification were performed using thermal desorption spectroscopy. The morphology of the layers is not influenced by the Ar/D2 gas mixture composition but by the substrate type and roughness. The increase of the D2 content during the deposition leads to the deposition of Be-D amorphous layers and also reduces the layer thickness by decreasing the sputtering yield due to the poisoning of the Be target. The D retention in the layers is dominated by the D trapping in low activation binding states and the increase of D2 flow during deposition leads to a significant build-up of deuterium in these states. Increase of deuterium flow during deposition consequently leads to an increase of D retention in the beryllium layers up to 300%. The resulted Be-D layers release the majority of their D (above 99.99%) at temperatures lower than 700 K.

Autonomous smart natural ventilation systems (SVS) attached to the glass façade of living quarters and office buildings can help reducing the carbon footprint of city buildings in the future, especially during warm seasons and can represent an alternative to the conventional mechanical ventilation systems. The work performed in this manuscript focuses on the investigation of bacteria trapping and killing efficiency of stainless steel grids coated with a mixed layer of Cu-Ag. These grids are to be employed as decontamination filters for a smart natural ventilation prototype that we are currently building in our laboratory. The tested grids were coated with a mixed Cu-Ag layer using thermionic vacuum arc plasma processing technology. The fixed deposition geometry allowed the variation of Cu and Ag atomic concentration in coated layers as a function of substrate position in relation to plasma sources. The test conducted with air contaminated with a pathogen strain of staphylococcus aureus indicated that the filtering efficiency is influenced by two parameters: the pore size dimension and the coating layer composition. The results show that the highest filtering efficiency of 100% was obtained for fine pore (0.5 × 0.5 mm) grids coated with a mixed metallic layer composed of 65 at% Cu and 35 at% Ag. The second test performed only on reference grids and Cu-Ag (65–35 at%) under working conditions, confirm a similar filtering efficiency for the relevant microbiological markers. This particular sample was investigated from morphological, structural, and compositional point of view. The results show that the layer has a high surface roughness with good wear resistance and adhesion to the substrate. The depth profiles presented a uniform composition of Cu and Ag in the layer with small variations caused by changes in deposition rates during the coating process. Identification of the two metallic phases of the Cu and Ag in the layers evidences their crystalline nature. The calculated grain size of the nanocrystalline was in the range 14–21 nm.

Compact and defect-free high melting point oxide strengthened metallic matrix configurations are promising to resolve the hydrogen permeation and brittleness issues relevant to the fusion research community. Previous studies on oxide addition to metallic matrix demonstrated a mitigation in brittleness behavior, while deposition techniques and material configurations are still to be investigated. Thus, here, we report the structural, morphological, and mechanical characterization of metal-oxides thin layers co-deposited by radio frequency (RF)and direct current (DC) magnetron sputtering. A total of six configurations were deposited such as single thin layers of oxides (Al2O3, Er2O3) and co-deposition configurations as metal-oxides (W, Be)—(Al2O3, Er2O3). The study of films roughness by atomic force microscopy (AFM) method show that for Al2O3 metallic-oxides is increased to an extent that could favor gaseous trapping, while co-depositions with Be seem to promote an increased roughness and defects formation probability compared to W co-depositions. Lower elastic modulus on metal-oxide co-depositions was observed, while the indentation hardness increased for Be and decreased for W matrix configurations. These outputs are highly relevant for choosing the proper compact and trap-free configuration that could be categorized as a permeation barrier for hydrogen and furtherly studied in laborious permeation yield campaigns.