In the field of bioengineering, depending on the required application, the attachment of various biological entities to the biomaterial is either favored or needs to be prevented. Therefore, different surfaces modification strategies were developed in combination with the characteristics of the materials. The present contribution reports on the use of the specific surface property of a thermoresponsive polymer poly(N-isopropylacrylamide) pNIPAAM obtained by spin coating in combination with plasma treatment for tuning cell behavior on treated polymeric surfaces. Topographical information for the plasma-treated pNIPAAM coatings obtained by Atomic Force Microscopy (AFM) measurements evidenced a more compact surface for Ar treatment due to combined etching and redeposition, while for oxygen, a clear increase of pores diameter is noticed. The chemical surface composition as determined by X-ray Photoelectron Spectroscopy showed the specific modifications induced by plasma treatment, namely strong oxidation for oxygen plasma treatment illustrated by eight times increase of O-C=O contribution and respectively an increase of C-N/O=C-N bonds in the case of ammonia plasma treatment. Structural information provided by FTIR spectroscopy reveals a significant increase of the carboxylic group upon argon and mostly oxygen plasma treatment and the increase in width and intensity of the amide-related groups for the ammonia plasma treatment. The biological investigations evidenced that L929 fibroblast cells viability is increased by 25% upon plasma treatment, while the cell attachment is up to 2.8 times higher for the oxygen plasma-treated surface compared to the initial spin-coated pNIPAAM. Moreover, the cell detachment process proved to be up to 2–3 times faster for the oxygen and argon plasma-treated surfaces and up to 1.5 times faster for the ammonia-treated surface. These results show the versatility of plasma treatment for inducing beneficial chemical modifications of pNIPAAM surfaces that allows the tuning of cellular response for improving the attachment-detachment process in view of tissue engineering.

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.

Control of reactive species generation lies at the core of atmospheric-pressure plasma processing. In this work, we investigate the capability 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 the conventional injection 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.

The high toxicity of hydrogen sulfide combined with poor sensitivity at room operating temperature urge for the development of new sensitive materials for sensors complying with this requirement, as well as a fast response and low cost. In this work, we have successfully developed materials for surface acoustic wave (SAW) sensors sensitive to H₂S gas that provide a reversible response at room temperature. The sensitive materials were created by plasma-enhanced chemical vapor deposition of a-CH films using methane as a precursor with argon and argon admixed with hydrogen or nitrogen and applied on piezoelectric quartz substrates. Smooth films, with an AFM root mean square below 1.5 nm, were obtained in all cases, although slight topographical variations were noted, depending on the gas types. XPS detected varying degrees of oxidation, indicating that the assisting gases played a crucial role in introducing oxygen-containing functional groups, thus influencing the material’s surface chemistry and sensitivity response. A hydrogen plasma treatment was applied on the a-CH deposited sensors as a further sensor preparation step. The hydrogen plasma treatment resulted in significant modifications in the topographical features, including roughness increase and notable variations in the surface aspect ratios, as confirmed through AFM data analysis, which involved advanced pixel height analysis and line profile processing. X-ray photoelectron spectroscopy (XPS) studies indicated the formation of new functional groups, increased defect density, and a significant reduction in electron transitions following hydrogen plasma treatment. The sensors demonstrated a reversible response to H₂S gas within 8 to 20 ppm concentration ranges, effectively detecting these levels. The sensitivity of the sensors was significantly enhanced, up to 39% through hydrogen plasma treatment, reaching an improved overall performance in detecting low concentrations of H₂S down to 0.9 ppm. These findings highlight a-CH thin films as an excellent candidate for next-generation SAW sensors. The study also suggests the potential for experimenting with various assisting gases during plasma deposition and additional plasma treatments to push detection capabilities to below ppm levels.