Formation of a Controllable Diffusion Barrier Layer on the Surface of Polydimethylsiloxane Films by Infrared Laser Irradiation.

Developing a diffusion barrier layer on material interfaces has potential applications in various fields such as in packaging materials, pharmaceuticals, chemical filtration, microelectronics, and medical devices. Although numerous physical and chemical methods have been proposed to generate the diffusion barrier layer, the complexity of fabrication techniques and the high manufacturing costs limit their practical utility. Here, we propose an innovative approach to fabricate the diffusion barrier layer by irradiating poly(dimethylsiloxane) (PDMS) with a mid-infrared (λ = 10.6 µm) CO2 laser. This process directly creates a diffusion barrier layer on the PDMS surface by forming a heavily cross-linked network in the polymer matrix. The optimal irradiation conditions were investigated by modulating the defocusing distance, laser power, and number of scanning passes. The barrier thickness can reach up to 70 µm as observed by the scanning electron microscope (SEM). The attenuated total reflectance (ATR), electron dispersive X-ray (EDX), and X-ray photoelectron spectroscopy (XPS) analyses collectively confirmed the formation of the SiOx structure on the modified surface based on the decreased methyl group signal and the increased oxygen/silicon ratio. The diffusion test with the model drugs (rhodamine B and donepezil) demonstrated that the modified surface exhibits effective diffusion barrier properties and the rate of drug diffusion through the modified barrier layer can be controlled by the optimization of the irradiation parameters. This novel approach provides the possibility to develop a controllable diffusion barrier layer in a biocompatible polymer with prospective applications in the fields of pharmaceuticals, packing materials, and medical devices.

Enhanced Performance of KVPO4F0.5O0.5 in Potassium Batteries by Carbon Coating Interfaces.

Potassium vanadium oxyfluoride phosphate of composition KVPO4F0.5O0.5 was modified by a carbon coating to enhance its electrochemical performance. Two distinct methods were used, first, chemical vapor deposition (CVD) using acetylene gas as a carbon precursor and second, an aqueous route using an abundant, cheap, and green precursor (chitosan) followed by a pyrolysis step. The formation of a 5 to 7 nm-thick carbon coating was confirmed by transmission electron microscopy and it was found to be more homogeneous in the case of CVD using acetylene gas. Indeed, an increase of the specific surface area of one order of magnitude, low content of C sp2, and residual oxygen surface functionalities were observed when the coating was obtained using chitosan. Pristine and carbon-coated materials were compared as positive electrode materials in potassium half-cells cycled at a C/5 (C = 26.5 mA g-1) rate within a potential window of 3 to 5 V vs K+/K. The formation by CVD of a uniform carbon coating with the limited presence of surface functions was shown to improve the initial coulombic efficiency up to 87% for KVPFO4F0.5O0.5-C2H2 and to mitigate electrolyte decomposition. Thus, performance at high C-rates such as 10 C was significantly improved, with ∼50% of the initial capacity maintained after 10 cycles, whereas a fast capacity loss is observed for the pristine material.

Tuning the C/N Ratio of C-Rich Graphitic Carbon Nitride (g-C3 N4 ) Materials by the Melamine/Carboxylic Acid Adduct Route.

C-rich graphitic carbonitride materials (CNx ) with a large range of compositions have been prepared thanks to the self-assembly, in different ratios, of melamine (M) and a panel of polycarboxylic acids (A) such as oxalic, tartaric and citric acid. The thermal conversion of the formed adducts (MAy ), led to CNx phases, with x ranging from 0.66 to 1.4 (x=1.33 for g-C3 N4 for comparison). The properties of these materials were examined by different techniques (XRD, Raman spectroscopy, TEM, TGA, XPS and DRIFT). It appears that the increase in the C content is associated with the disappearance of the long-range order of heptazine units and an increase in the sub-nanometer carbon-rich cluster size within the graphitic g-C3 N4 structure. This trend is followed by a significant increase in the interlayer spacing and a lower proportion of N=C-N bonds compared to C=C bonds. The thermal stability under an inert atmosphere of these phases and their UV-Visible absorbance properties were also investigated.

Palladium nanoparticles embedded in mesoporous carbons as efficient, green and reusable catalysts for mild hydrogenations of nitroarenes.

The reduction of nitroarenes is the most efficient route for the preparation of aromatic primary amines. These reductions are generally performed in the presence of heterogeneous transition metal catalysts, which are rather efficient but long and tedious to prepare. In addition, they contain very expensive metals that are in most cases difficult to reuse. Therefore, the development of efficient, easily accessible and reusable Pd catalysts obtained rapidly from safe and non-toxic starting materials was implemented in this report. Two bottom-up synthesis methods were used, the first consisted in the impregnation of a micro/mesoporous carbon support with a Pd salt solution, followed by thermal reduction (at 300, 450 or 600 °C) while the second involved a direct synthesis based on the co-assembly and pyrolysis (600 °C) of a mixture of a phenolic precursor, glyoxal, a surfactant and a Pd salt. The obtained composites possess Pd nanoparticles (NPs) of tunable sizes (ranging from 1-2 to 7.0 nm) and homogeneously distributed in the carbon framework (pores/walls). It turned out that they were successfully used for mild and environment-friendly hydrogenations of nitroarenes at room temperature under H2 (1 atm) in EtOH in the presence of only 5 mequiv. of supported Pd. The determinations of the optimal characteristics of the catalysts constituted a second objective of this study. It was found that the activity of the catalysts was strongly dependent on the Pd NPs sizes, i.e., catalysts bearing small Pd NPs (1.2 nm obtained at 300 °C and 3.4 nm obtained at 450 °C) exhibited an excellent activity, while those containing larger Pd NPs (6.4 nm and 7.0 nm obtained at 600 °C, either by indirect or direct methods) were not active. Moreover, the possibility to reuse the catalysts was shown to be dependent on the surface chemistry of the Pd NPs: the smallest Pd NPs are prone to oxidation by air and their surface was gradually covered by a PdO shell decreasing their activity during reuse. A good compromise between intrinsic catalytic activity (i.e. during first use) and possibility of reuse was found in the catalyst made by impregnation followed by reduction at 450 °C since the hydrogenation could be performed in only 2 h in EtOH or even in water. The catalyst was quantitatively recovered after reaction by filtration, used at least 7 times with no loss of efficiency. Advantageously, almost Pd-free primary aromatic amines were obtained since the Pd leaching was very low (<0.1% of the introduced amount). Compared to numerous reports from the literature, the catalysts described here were both easily accessible from eco-friendly precursors and very active for hydrogenations under mild and "green" reaction conditions.

Use of plasma polymerization to improve adhesion strength in carbon fiber composites cured by electron beam.

Maleic anhydride plasma polymer was deposited at the surface of carbon fibers and functionalized with vinyl and thiol groups to improve its adhesion strength with an acrylate matrix cured by an electron beam. A characterization of the fiber surface properties was done before and after coating (topography, surface chemistry, and surface energy). Sharp improvements of the interfacial shear strength (+ 120%), measured by a micromechanical test derived from the pull-out test, were obtained and, to the best of our knowledge, never reported before. The values were close to the ones obtained with a thermal cure. The comparison of this approach with other types of surface treatments (oxidation, grafting of coupling agents) enabled the establishment of a general strategy for the improvement of the interfacial adhesion in carbon fiber composites cured by an electron beam and potentially the improvement of their mechanical properties. This strategy is based on a high surface density of functionalities that are generating covalent bonding during the polymerization of the matrix and on the insertion of a polymer layer strongly attached to the fiber surface and acting as a buffer between the fiber surface and the matrix to counteract the generation of stress in the interphase.

Characterization of carbon surface chemistry by combined temperature programmed desorption with in situ X-ray photoelectron spectrometry and temperature programmed desorption with mass spectrometry analysis.

The analysis of the surface chemistry of carbon materials is of prime importance in numerous applications, but it is still a challenge to identify and quantify the surface functional groups which are present on a given carbon. Temperature programmed desorption with mass spectrometry analysis (TPD-MS) and X-ray photoelectron spectroscopy with an in situ heating device (TPD-XPS) were combined in order to improve the characterization of carbon surface chemistry. TPD-MS analysis allowed the quantitative analysis of the released gases as a function of temperature, while the use of a TPD device inside the XPS setup enabled the determination of the functional groups that remain on the surface at the same temperatures. TPD-MS results were then used to add constraints on the deconvolution of the O1s envelope of the XPS spectra. Furthermore, a better knowledge of the evolution of oxygen functional groups with temperature during a thermal treatment could be obtained. Hence, we show here that the combination of these two methods allows to increase the reliability of the analysis of the surface chemistry of carbon materials.