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An easy procedure to build up membrane-electrode assemblies for applications dedicated to miniaturized PEMFC using H2 or CH3OH by a two-steps atmospheric plasma process is reported. Firstly, catalyst nanoparticles are grafted on carbon substrates by spraying a Pt colloidal solution in the post-discharge of an RF atmospheric plasma torch. In the second step, the resulting decorated electrodes are covered by plasma synthesized polymeric membranes in the discharge of a DBD. The sulfonated polystyrene membranes are synthesized by injecting simultaneously styrene and trifluoromethanesulfonic acid monomers, in the presence of a carrier gas (Ar or He). The membranes are chemically characterized by XPS, ToF-SIMS, and FTIR (IRRAS) and their deposition rate is investigated by SEM., Comment: 14 pages, 11 figures

The texturization of poly(tetrafluoroethylene) (PTFE) surfaces is achieved at atmospheric pressure by using the post-discharge of a radio-frequency plasma torch supplied in helium and oxygen gases. The surface properties are characterized by contact angle measurement, X-ray photoelectron spectroscopy and atomic force microscopy. We show that the plasma treatment increases the surface hydrophobicity (with water contact angles increasing from 115 to 155{\deg}) only by modifying the PTFE surface morphology and not the stoichiometry. Measurements of sample mass losses correlated to the ejection of CF$_2$ fragments from the PTFE surface evidenced an etching mechanism at atmospheric pressure.

An organometallic powder (platinum (II) acetylacetonate) is decomposed in the post-discharge of an atmospheric RF plasma torch to deposit Pt nanoparticles on carbon black supports. The resulting nanohybrid materials are characterized by FEG-SEM and XPS techniques to highlight their high content in Pt, their oxidation degree, and the dispersion of the Pt nanoparticles on the substrate. ICP-MS and electrochemical characterizations in a single fuel cell (cyclic voltammetry, dynamic polarization curves) are also performed on electrodes realized by treating the powder mixture overlaid on gas diffusion layers. The comparison of the catalytic activity and the Pt loading with commercially available electrodes shows the great potential of this simple innovative, fast, and robust deposition method.

A combination of experiments and extensive modelling, including a chemical kinetics analysis, was performed for a CO$_2$/H$_2$O plasma in a dielectric barrier discharge. This provides a better understanding of the mechanisms related to the reactivity of the plasma and of the conversions into value-added products, such as methanol., Comment: http://www.ispc-conference.org/ispcproc/ispc22/P-II-8-26.pdf

In this paper, we present a new, simple, robust and efficient technique to decorate multi-wall carbon nanotubes (MWCNT) with metal nanoparticles. As case studies, Au, Pt and Rh nanoparticles are grafted onto MWCNTs by spraying a colloidal solution into the post-discharge of an atmospheric argon or argon/oxygen RF plasma. The method that we introduce here is different from those usually described in the literature, since the treatment is operated at atmospheric pressure, allowing the realization in only one step of the surface activation and the deposition processes. We demonstrate experimentally that the addition of oxygen gas in the plasma increases significantly the amount of grafted metal nanoparticles. Moreover, TEM pictures clearly show that the grafted nanoparticles are well controlled in size.

Among various surface modification techniques, plasma can be used as a source for tailoring the surface properties of diverse materials. HDPE and fluoropolymer surfaces have been treated by the post-discharge of an atmospheric RF-plasma torch supplied with helium and oxygen gases. The plasma-treated surfaces were characterized by measurements of mass losses, water contact angles, x-ray photoelectron spectroscopy and atomic force microscopy. This experimental approach correlated with an optical characterization of the plasma phase allowed us to propose etching mechanisms occurring at the post-discharge/polymer interface. We discuss how competitive and synergistic effects can result from the oxidation and/or the roughening of the surface but also from the excimer VUV radiation, the He metastable species and the O radicals reaching the plasma-polymer interface.

High density polyethylene surfaces were exposed to the atmospheric post-discharge of a radiofrequency plasma torch supplied in helium and oxygen. Dynamic water contact angle measurements were performed to evaluate changes in surface hydrophilicity and angle resolved x-ray photoelectron spectroscopy was carried out to identify the functional groups responsible for wettability changes and to study their subsurface depth profiles, up to 9 nm in depth. The reactions leading to the formation of C-O, C=O and O-C=O groups were simulated by molecular dynamics. These simulations demonstrate that impinging oxygen atoms do not react immediately upon impact but rather remain at or close to the surface before eventually reacting. The simulations also explain the release of gaseous species in the ambient environment as well as the ejection of low molecular weight oxidized materials from the surface.

Anionic surfactants based on fatty acids are usually used to modify the particle surface properties of CaCO$_3$ with the aim to enhance its dispersion and compatibility with polymer matrices. In this study sodium oleate was used for the preparation of ultra-hydrophobic CaCO$_3$ nanoparticles using a wet carbonation route. The effect of sodium oleate on the characteristics, particle size, morphology, surface potential, thermal decomposition and hydrophobicity of CaCO$_3$, was investigated using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), Zeta potential, thermogravimetric analysis (TGA) and water contact angle measurement (WCA). The results showed that the addition of 2 wt% sodium oleate helps in reducing the particle size from 2 {\mu}m length scalenohedral particles to 45 nm rhombohedral particles and modifying of the hydrophobic property of CaCO$_3$.

In the present work, multiwalled carbon nanotubes were decorated with rhodium nanoparticles using a colloidal solution in the post-discharge of an RF atmospheric plasma of argon (Ar) or argon/oxygen (Ar:O$_2$). The properties of these hybrid materials towards the room temperature detection of NO$_2$, C$_2$H$_4$, CO, C$_6$H$_6$ and moisture were investigated and discussed in view of compositional and morphological studies. It was found that the presence of oxygen in the plasma treatment is essential to significantly enhance the gas response of Rh-decorated multiwalled carbon nanotubes and to avoid response saturation even at low gas/vapor concentrations. These desirable effects are attributed to the presence of oxygen during the CNT plasma treatment since oxygenated vacancies act both as active adsorption sites for gases and as anchoring sites for Rh nanoparticles (the presence of Rh nanoclusters is nearly doubled in Ar-O$_2$ treated samples as compared to Ar treated samples). The oxygen treatment also makes easier the charge transfer between Rh nanoparticles and carbon nanotubes upon gas adsorption. The method for treating and decorating multiwalled carbon nanotubes used here is simple, fast and scalable for producing gas sensitive nanohybrid materials with uniform and well-controlled properties.

In the context of polymer surface treatment, the afterglow of an atmospheric pressure Ar/O$_2$ radiofrequency plasma is characterized by optical emission spectroscopy, laser induced fluorescence and mass spectrometry. The influence of the O$_2$ gas flow rate and the source power on the plasma properties (gas temperature, Ar excitation temperature, relative concentrations of O atoms and OH radicals) are evaluated. We show that for plasma torch-to-substrate distances lower than 6 mm, the afterglow creates a protective atmosphere, thus the plasma gas composition interacting with the substrate is well controlled. For higher distances, the influence of ambient air can no longer be neglected and gradients in Ar, O$_2$ and N$_2$ concentrations are measured as a function of axial and vertical position., Comment: http://mpserver.pst.qub.ac.uk/sites/icpig2011/301_C10_Duluard.pdf, 30th-ICPIG, Belfast, Northern Ireland, 28th August-2nd September 2011, C10

Plasma processes are an innovative approach for the decomposition of CO2 in O radicals and CO as a valuable carbon source. In this experimental work, a tubular dielectric barrier discharge operating at atmospheric pressure has been used to split CO2 and study its conversion considering the influence of frequency and power, as well as the influence of various electrical regimes (AC, AC pulsed regimes). The CO2 conversion has been measured by mass spectrometry and gas chromatography while gas and walls temperatures have been determined and correlated to evaluate their influence of the CO2 splitting.

The in-depth oxygen diffusion into a low density polyethylene film is performed in the post-discharge of an atmospheric plasma torch, supplied in argon as carrier gas and with or without oxygen as reactive gas. The chemical and structural properties of the polymer surface and bulk are studied in terms of plasma parameters (treatment time, power, and reactive gas flow rate). A good correlation between XPS and Fourier transform infrared spectroscopy analyses is demonstrated. The penetration depth of oxygen into the bulk of the polymer is investigated by angle resolved-XPS and time-of-flight SIMS. It is shown that, depending on the plasma conditions, oxygen could penetrate up to 20--40 nm into the low density polyethylene during the atmospheric plasma treatment.

The reactivity of water vapor introduced in an atmospheric dielectric barrier discharge supplied in argon is investigated through optical emission spectroscopy measurements. This discharge is also used for the treatment of LDPE surfaces. Water contact angles measurements, XPS and AFM techniques are used to study the grafting of oxygen functions on the LDPE surface and increase its hydrophilicity.

The atmospheric pressure PECVD deposition and texturization of hydrophobic coatings using liquid fluorinated C6F12 and C6F14 precursors are investigated. The effect of the carrier gas (argon and helium) is discussed in terms of the behavior of the gas phase and of the characteristics of the deposited film. Mass spectrom-etry measurements indicate that the fragmentation is higher with argon while helium reacts very easily with oxygen impurities leading to the formation of CxFyOz compounds. These observations are consistent with the chemical composition of the films determined by XPS and the variation in the deposition rate. Moreover, the streamers present in the argon discharge affect the morphology of the surface by increasing the roughness, which leads to the increase in the hydrophobicity of the coatings., Comment: arXiv admin note: text overlap with arXiv:1604.08752

In this experimental study, a flowing dielectric barrier discharge operating at atmospheric pressure is used for the splitting of CO2 into O2 and CO. The influence of the applied frequency and plasma power on the microdischarge properties is investigated to understand their role on the CO2 conversion. Electrical measurements are carried out to explain the conversion trends and to characterize the microdischarges through their number, their lifetime, their intensity and the induced electrical charge. Their influence on the gas and electrode temperatures is also evidenced through optical emission spectroscopy and infrared imaging. It is shown that, in our configuration, the conversion depends mostly on the charge delivered in the plasma and not on the effective plasma voltage when the applied power is modified. Similarly, at constant total current, a better conversion is observed at low frequencies, where a less filamentary discharge regime with a higher effective plasma voltage than that at a higher frequency is obtained.

Low density polyethylene (LDPE) surfaces have been plasma modified to improve their nanostructural and wettability properties. These modifications can significantly improve the deposition of subsequent layers such as films with specific barrier properties. For this purpose, we compare the treatments induced by two atmospheric plasma torches with different configurations (showerhead vs. linear). The modifications of LDPE films in terms of chemical surface composition and surface morphology are evidenced by X-ray photoelectron spectro-scopy, water contact angles measurements, and atomic force microscopy. A comparison between the two post-discharge treatments is achieved for several torch-to-substrate distances (gaps), treatment times, and oxygen flow rates in terms of etching rate, roughening rate, diffusion of oxygen into the subsur-face and hydrophilicity. By correlating these results with the chemical composition of the post-discharges, we identify and compare the 'species which are responsible for the chemical surface functionalization, the surface roughening, and etching.