Polymer-based nanocomposites have recently received considerable attention due to their unique properties, which makes them feasible for applications in optics, sensors, energy, life sciences, etc. The present work focuses on the synthesis of nanocomposites consisting of a polytetrafluorethylene-like matrix in which metallic nano-silver are embedded, by using multiple magnetron plasmas. By successively exposing the substrate to separate RF magnetrons using as combination of target materials polytetrafluorethylene (PTFE) and silver, individual control of each deposition process is insured, allowing obtaining of structures in which silver nanoparticles are entrapped in-between two PTFE layers with given thicknesses. The topographical and morphological characteristics investigated by means of Scanning Electron Microscopy and Atomic Force Microscopy techniques evidenced the very presence of Ag nanoparticles with typical dimension 7 nm. The chemical composition at various depositing steps was evaluated through X-ray Photoelectron Spectroscopy. We show that the presence of the top PTFE layer prevents silver oxidation, while its thickness allows the tailoring of optical properties, as evidenced by spectroellipsometry. The appearance of chemical bonds between silver atoms and PTFE atoms at interfaces is observed, pointing out that despite of pure physical deposition processes, a chemical interaction between the polymeric matrix and metal is promoted by plasma.

Cellulose is a versatile biopolymer increasingly applied in medicine and industry due to its biodegradability and biocompatibility, along with the renewability and large availability of source materials. However, finding simple, eco-friendly, and effective methods to modify cellulose to provide it with new functionalities remains a challenge. This work presents a new, inexpensive, and eco-friendly method to chemically modify microcrystalline cellulose (MCC) by the submerged cold plasma treatment of an aqueous suspension of MCC containing different oxidizing agents, such as hydrogen peroxide (H₂O₂), sodium hypochlorite (NaClO), or sodium periodate (NaIO₄). Fourier-transform Infrared (FTIR) and X-ray photoelectron spectroscopy (XPS) showed that plasma treatment intensified the oxidizing effect of H₂O₂, NaClO, and NaIO₄, with plasma-assisted NaClO treatment yielding the highest MCC oxidation level. XPS indicated that the plasma-assisted oxidations also resulted in different degrees of chemical degradation of MCC, a finding further supported by the thermogravimetric analysis (TGA) results. X-ray diffraction (XRD) data revealed a different effect of the oxidizing agents on the crystalline and amorphous regions in MCC. Scanning electron microscopy (SEM) images showed that the combined treatment with plasma and chemical oxidizing agents led to MCC fragmentation and varying degrees of defibrillation into nanofibers.

Tungsten erosion and dust occurrence are phenomena of great interest for fusion technology. Herein, we report results concerning the material damage and dust formation in the presence of high temperature and large area or concentrated discharges in helium and argon. In order to generate adequate plasmas, we used tungsten electrodes in two experimental discharge systems, namely a hollow discharge and a microjet discharge. In both exposure cases, we noticed surface modification, which was assigned to sputtering, melting, and vaporization processes, and a significant dust presence. We report the formation on electrode surfaces of tungsten fuzz, nano-cones, nanofibers, and cauliflower- and faced-like particles, depending on the discharge and gas type. Dust with various morphologies and sizes was collected and analyzed with respect to the morphology, size distribution, and chemical composition. We noticed, with respect to erosion and particle formation, common behaviors of W in both laboratory and fusion facilities experiments.

In the current study, bulk tungsten material surfaces are exposed to hydrogen, deuterium, and helium plasmas in the radiofrequency domain (13.56 MHz) at an input power of 250 W using the hollow-cathode configuration. The ejected material is collected on titanium substrates at various distances (from 6 mm up to 40 mm). Therefore, the exposed tungsten materials are investigated for surface changes (blister occurrence, dust formation, or nano-structuration), along with the crystallinity, depending on the plasma’s exposure times (from 30 min up to 120 min for each plasma type). Also, the collected materials are analyzed (morphological, structural, and statistical investigations) for dust and dust film-like appearance. Plasma discharges are analyzed using two methods: optical emission spectroscopy, and single Langmuir probes, to emphasize the nature of the used plasmas (cold discharges, ~2 eV), along with the presence of tungsten emission (e.g., WI 406.31 nm, WI 421.31 nm) during the plasma lifetime. By using a dedicated protocol, a method was established for obtaining fusion-relevant tungsten surfaces in the hydrogen and deuterium plasma discharges. By using the implemented method, the current paper introduces the possibility of obtaining a new tungsten morphology, i.e., the dandelion-like shape, by using helium plasma, in which the W₁₈O₄₉ compound can be found.

Control of reactive species generation lies at the core of atmospheric pressure plasma processing. In this work, we investigate the ability of a cold RF argon plasma jet source to produce reactive oxygen and nitrogen species (RONS) following the injection of a molecular gas (N₂ or O₂), either premixed with the main gas (Ar) or introduced separately into an already generated Ar discharge. We show that, when reactive gases are injected directly into the Ar discharge, the range of operating parameters—particularly the ratio of reactive gas to main gas—is considerably widened compared to conventional injections through the main argon flow. The plasma characteristics at the source exit were analyzed using optical emission spectroscopy (OES), including the determination of electron density, rotational temperature, and the emission intensities of plasma species such as Ar I, NO(A), OH(A), and N₂(C) for both injection types. Overall, the results show that plasmas generated using in-discharge injection are more stable and capable of sustaining enhanced production of reactive radicals such as NO(A) and OH(A), whereas injection through the main gas can be tuned to selectively enhance NO generation. These findings highlight the potential of plasma sources employing premixed or in-discharge reactive gas injection for surface treatment and for the processing of gas and liquid phases.

In this paper, results concerning hydrogen and deuterium plasma (RF, 13.56 MHz) interactions with tungsten surfaces, were reported. We used the Hollow-Cathode (HC) configuration for plasma–tungsten surface interaction experiments, along with the collection of tungsten dust, at different distances. Further on, the plasma-exposed tungsten surfaces and the collected dust were morphologically analyzed by contact profilometry, scanning electron microscopy, and energy dispersive spectroscopy measurements, along with chemical investigations by the X-ray photoelectron spectroscopy technique. The results showed that exposing the tungsten surfaces to the hydrogen plasma induces surface erosion phenomena along with the formation of dust and interconnected W structures. Herein, the mean ejected material volume was ~1.1 × 10⁵ µm³. Deuterium plasma facilitated the formation of blisters at the surface level. For this case, the mean ejected material volume was ~3.3 × 10⁴ µm³. For both plasma types, tungsten dust within nano- and micrometer sizes could be collected. The current study offers a perspective of lab-scaled plasma systems, which are capable of producing tungsten fusion-like surfaces and dust.