Propriétés électriques d'hétérostructures a-GaAs/c-GaAs(n) et de structures de type MIS a-GaAsN/c-GaAs(n)

Heterojunctions were fabricated by deposit of amorphous GaAs and GaAsN on c-GaAs. $I(V)$ and $C(V)$ measurements were performed to determine electrical properties of these structures. The a-GaAs/c-GaAs(n) heterojunctions present a p-n junction like behaviour. The characteristics of the a-GaAsN/c-GaAs(n) heterojunctions present a MIS like structure behaviour with some imperfections. A fixed positive charge was detected and a density of interface states of about $10^{11}$ eV$^{-1}$cm$^{-2}$ was evaluated.L'étude porte sur des couches minces de GaAs et de GaAsN amorphes déposées par pulvérisation cathodique RF réactive sur des substrats de GaAs cristallin. Les caractéristiques électriques $I(V)$ et $C(V)$ ont été mesurées. Les hétérojonctions a-GaAs/c-GaAs(n) présentent un effet redresseur. Cet effet laisse place à une caractéristique symétrique avec une forte atténuation de l'intensité du courant pour les structures a-GaAsN/cGaAs(n). Les structures réalisées ont alors un comportement semblable à celui d'une structure MIS imparfaite. L'existence d'une charge positive fixe dans le a-GaAsN a été mise en évidence. La densité des états d'interface au milieu de la bande interdite est évaluée à quelques $10^{11}$ cm$^{-2}$eV$^{-1}$

Conversion of Argan Nutshells into Novel Porous Carbons in the Scope of Circular Economy: Adsorption Performance of Emerging Contaminants

The present work proposes an experimental strategy to prepare argan nutshell-derived porous carbons using potassium hydroxide (KOH). Several experimental parameters of the activation process were evaluated (temperature, impregnation ratio, and activation time), and an optimized carbon (ACK) was obtained. The surface properties of the ACK sample were determined, and the porous carbon was applied as an adsorbent of diclofenac (DCF) and paroxetine (PARX). A commercial carbon (CC) was used as a benchmark. The ACK porous carbon presented a higher surface area and micropore volume (1624 m2 g−1 and 0.40 cm3 g−1, respectively) than CC carbon (1030 m2 g−1 and 0.30 cm3 g−1, respectively), but the maximum adsorption capacities of DCF (214–217 mg g−1) and PARX (260–275 mg g−1) were comparable among the two carbons. Besides π-π interactions, H-bonds with the electronegative atoms of the adsorbate molecules and the electropositive H of the oxygen functional groups were appointed as the most probable mechanisms for adsorption onto ACK porous carbon. The electrostatic attraction was also considered, particularly for DCF with CC carbon. The pore size might have also been critical, since CC carbon presented more supermicropores (0.7–2 nm), which are usually more favorable toward the adsorption of pharmaceutical molecules. The reusability of the ACK carbon was tested up to four cycles of adsorption–desorption by using ultrasonic washing with water. The results indicated that no more than one cycle of use of ACK should be performed

Cell-Mediated Deposition of Porous Silica on Bacterial Biofilms

Living hybrid materials that respond dynamically to their surrounding environment have important applications in bioreactors. Silica based sol-gels represent appealing matrix materials as they form a mesoporous biocompatible glass lattice that allows for nutrient diffusion while firmly encapsulating living cells. Despite progress in sol-gel cellular encapsulation technologies, current techniques typically form bulk materials and are unable to generate regular silica membranes over complex geometries for large-scale applications. We have developed a novel biomimetic encapsulation technique whereby endogenous extracellular matrix molecules facilitate formation of a cell surface specific biomineral layer. In this study, monoculture Pseudomonas aeruginosa and Nitrosomonas europaea biofilms are exposed to silica precursors under different acid conditions. Scanning electron microscopy (SEM) imaging and electron dispersive X-ray (EDX) elemental analysis revealed the presence of a thin silica layer covering the biofilm surface. Cell survival was confirmed 30 min, 30 days, and 90 days after encapsulation using confocal imaging with a membrane integrity assay and physiological flux measurements of oxygen, glucose, and NH(4)(+). No statistical difference in viability, oxygen flux, or substrate flux was observed after encapsulation in silica glass. Shear induced biofilm detachment was assessed using a particle counter. Encapsulation significantly reduced detachment rate of the biofilms for over 30 days. The results of this study indicate that the thin regular silica membrane permits the diffusion of nutrients and cellular products, supporting continued cellular viability after biomineralization. This technique offers a means of controllably encapsulating biofilms over large surfaces and complex geometries. The generic deposition mechanism employed to form the silica matrix can be translated to a wide range of biological material and represents a platform encapsulation technology. Biotechnol. Bioeng. 2011; 108: 2249-2260. (C) 2011 Wiley Periodicals, Inc