We report the preparation of centimeter‐scale composite membranes formed by monolayer or bilayer graphene and polydimethylsiloxane (PDMS). Graphene was synthesized on copper foils by chemical vapor deposition (CVD), and two methods for transferring the graphene layers from the Cu to the PDMS were tested. The method based on the use of poly(methyl methacrylate) as a sacrificial support layer was more effective in producing membranes with significant gas‐barrier properties, in which the gas permeability values for CO2 and N2 were reduced by up to 30% as compared to blank PDMS membranes. Raman spectroscopy maps and atomic force microscopy revealed that, on the microscopic scale, graphene is preserved upon transfer, but the presence of extended defects such as folds and tears still limits further increases in the composite barrier properties. The deleterious effect of such defects is reduced by using more than one graphene layer. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017, 134, 45521.

Although biofilm formation is a very effective mechanism to sustain bacterial life, it is detrimental in medical and industrial sectors. Current strategies to control biofilm proliferation are typically based on biocides, which exhibit a negative environmental impact. In the search for environmentally friendly solutions, nanotechnology opens the possibility to control the interaction between biological systems and colonized surfaces by introducing nanostructured coatings that have the potential to affect bacterial adhesion by modifying surface properties at the same scale. In this work, we present a study on the performance of graphene and hexagonal boron nitride coatings (h-BN) to reduce biofilm formation. In contraposition to planktonic state, we focused on evaluating the efficiency of graphene and h-BN at the irreversible stage of biofilm formation, where most of the biocide solutions have a poor performance. A wild Enterobacter cloacae strain was isolated, from fouling found in a natural environment, and used in these experiments. According to our results, graphene and h-BN coatings modify surface energy and electrostatic interactions with biological systems. This nanoscale modification determines a significant reduction in biofilm formation at its irreversible stage. No bactericidal effects were found, suggesting both coatings offer a biocompatible solution for biofilm and fouling control in a wide range of applications.

In this work we present a study on the performance of CVD (chemical vapor deposition) graphene coatings grown and transferred on Ni as protection barriers under two scenarios that lead to unwanted metal ion release, microbial corrosion and allergy test conditions. These phenomena have a strong impact in different fields considering nickel (or its alloys) is one of the most widely used metals in industrial and consumer products. Microbial corrosion costs represent fractions of national gross product in different developed countries, whereas Ni allergy is one of the most prevalent allergic conditions in the western world, affecting around 10% of the population. We found that grown graphene coatings act as a protective membrane in biological environments that decreases microbial corrosion of Ni and reduces release of Ni2+ ions (source of Ni allergic contact hypersensitivity) when in contact with sweat. This performance seems not to be connected to the strong orbital hybridization that Ni and graphene interface present, indicating electron transfer might not be playing a main role in the robust response of this nanostructured system. The observed protection from biological environment can be understood in terms of graphene impermeability to transfer Ni2+ ions, which is enhanced for few layers of graphene grown on Ni. We expect our work will provide a new route for application of graphene as a protection coating for metals in biological environments, where current strategies have shown short-term efficiency and have raised health concerns.

Molybdenum disulfide (MoS 2 ) is attractive for use in next-generation nanoelectronic devices and exhibits great potential for humidity sensing applications. Herein, MoS 2 ink was successfully prepared via a simple exfoliation method by sonication. The structural and surface morphology of a deposited ink film was analyzed by scanning electron microscopy (SEM), Raman spectroscopy, and atomic force microscopy (AFM). The aerosol-printed MoS 2 ink sensor has high sensitivity, with a conductivity increase by 6 orders of magnitude upon relative humidity increase from 10 to 95% at room temperature. The sensor also has fast response/recovery times and excellent repeatability. Possible mechanisms for the water-induced conductivity increase are discussed. An analytical model that encompasses two ionic conduction regimes, with a percolation transition to an insulating state below a low humidity threshold, describes the sensor response successfully. In conclusion, our work provides a low-cost and straightforward strategy for fabricating a high-performance humidity sensor and fundamental insights into the sensing mechanism.

Some sub-products from the industrial activity are rich in metals, very often being highly toxic to human health and to the environment. Thus, the development of real-time and ultrasensitive techniques for metals detection is relevant. Herein, we report an ion-sensitive field-effect transistor (ISFET) based on l-phenylalanine functionalized graphene that detects Na+, Co2+, and Al3+ at the nanomolar range and Cu2+ at the picomolar range. Our sensor is prepared using a simple functionalization method and is reusable after a standard HCl cleaning process. Altogether, the ISFET is a promising device for real-time detection of metal ions at low concentrations.