Magneto-plasmonic nanostructures functionalized with cell targeting units are of great interest for nanobiotechnology applications.

Plasma–wall interaction is one of the most important issues that present magnetic confinement devices have to face. In the RFX-mod reversed field pinch experiment plasma–wall interaction has become a hard point increasing plasma current up to the RFX-mod maximum design value of 2 MA, since in this case local power deposition can be as high as 10 MW m⁻². Since the first wall of RFX-mod is entirely covered by graphite tiles different techniques have been tested to control hydrogen wall influx: He glow discharges cleaning, He discharges at high plasma currents, wall boronization and baking. With the best results obtained by boronization, at high plasma currents all such techniques improve the situation but do not allow a complete and stationary hydrogen influx reduction. Furthermore, in the presence of localized high power load the wall still responds providing very high influxes. In order to improve this situation wall conditioning by lithium has been tested. As a first lithization method to deposit a controllable amount of lithium on the wall, a room temperature pellet injector has been used (maximum pellet diameter of 1.8 mm and maximum length of 5 mm). Lithium coatings with a theoretical thickness of about 10 nm have been applied both to clean graphite tiles and over boronized ones. Lithization demonstrated to be effective in lowering hydrogen wall recycling to a value smaller than that of boronized graphite, with the effect lasting 20–30% more than in the boronized case. Compared with boronization, lithization slightly improves (by about 30%) particle confinement time and also clearly affects edge particle transport providing a lower edge density and more peaked density profiles. Lithization also reduces carbon content by about 10% over boronization but still no clear improvement has been observed in terms of energy confinement. Similar results have been obtained performing lithization over boronized graphite.

Some metals belonging to groups IV and V show a high permeability to hydrogen and have been studied as possible alternatives to palladium in membranes for hydrogen purification/separation in order to increase their sustainability and decrease their costs. However, to date, very few alloys among those metals have been investigated, and no membrane studies based on 4–5 element alloys with low or zero Pd content and quasi-amorphous structure have been reported so far. In this work, new membranes based on ZrVTi- and ZrVTiPd alloys were tested for the first time for this application. The unprecedented deposition of micrometric-based multilayers was performed via high-power impulse magnetron sputtering onto porous alumina substrates. Dense Pd/Zr_xV_yTi_zPd_w/Pd multilayers were obtained. The composition of the alloys, morphology and structure, hydrogen permeance, selectivity, and resistance to embrittlement were tested and analyzed depending on the deposition conditions, and the membrane with the enhanced performance was tuned. The environmental impact of these membranes was also investigated to ascertain the sustainability of these alloys relative to more common Pd₇₇Ag₂₃ and V₉₃Pd₇ thin-film membranes using a life cycle assessment analysis. The results showed that the partial substitution of Pd can efficiently lead to a decrease in the environmental impacts of the membranes.