We report that graphene coatings do not significantly disrupt the intrinsic wetting behaviour of surfaces for which surface-water interactions are dominated by van der Waals forces. Our contact angle measurements indicate that a graphene monolayer is wetting-transparent to copper, gold or silicon, but not glass, for which the wettability is dominated by short-range chemical bonding. With increasing number of graphene layers, the contact angle of water on copper gradually transitions towards the bulk graphite value, which is reached for ~6 graphene layers. Molecular dynamics simulations and theoretical predictions confirm our measurements and indicate that graphene's wetting transparency is related to its extreme thinness. We also show a 30-40% increase in condensation heat transfer on copper, as a result of the ability of the graphene coating to suppress copper oxidation without disrupting the intrinsic wettability of the surface. Such an ability to independently tune the properties of surfaces without disrupting their wetting response could have important implications in the design of conducting, conformal and impermeable surface coatings.

Nanostructures are known to be exquisitely sensitive to the chemical environment and offer ultra-high sensitivity for gas-sensing. However, the fabrication and operation of devices that use individual nanostructures for sensing is complex, expensive and suffers from poor reliability due to contamination and large variability from sample-to-sample. By contrast, conventional solid-state and conducting-polymer sensors offer excellent reliability but suffer from reduced sensitivity at room-temperature. Here we report a macro graphene foam-like three-dimensional network which combines the best of both worlds. The walls of the foam are comprised of few-layer graphene sheets resulting in high sensitivity; we demonstrate parts-per-million level detection of NH3 and NO2 in air at room-temperature. Further, the foam is a mechanically robust and flexible macro-scale network that is easy to contact (without Lithography) and can rival the durability and affordability of traditional sensors. Moreover, Joule-heating expels chemisorbed molecules from the foam's surface leading to fully-reversible and low-power operation.

Lithium metal is known to possess a very high theoretical capacity of 3,842 mAh g À 1 in lithium batteries. However, the use of metallic lithium leads to extensive dendritic growth that poses serious safety hazards. Hence, lithium metal has long been replaced by layered lithium metal oxide and phospho-olivine cathodes that offer safer performance over extended cycling, although significantly compromising on the achievable capacities. Here we report the defect-induced plating of metallic lithium within the interior of a porous graphene network. The network acts as a caged entrapment for lithium metal that prevents dendritic growth, facilitating extended cycling of the electrode. The plating of lithium metal within the interior of the porous graphene structure results in very high specific capacities in excess of 850 mAh g À 1 . Extended testing for over 1,000 charge/discharge cycles indicates excellent reversibility and coulombic efficiencies above 99%.

Conventional graphitic anodes in lithium-ion batteries cannot provide high-power densities due to slow diffusivity of lithium ions in the bulk electrode material. Here we report photoflash and laser-reduced free-standing graphene paper as high-rate capable anodes for lithium-ion batteries. Photothermal reduction of graphene oxide yields an expanded structure with micrometer-scale pores, cracks, and intersheet voids. This open-pore structure enables access to the underlying sheets of graphene for lithium ions and facilitates efficient intercalation kinetics even at ultrafast charge/discharge rates of >100 C. Importantly, photothermally reduced graphene anodes are structurally robust and display outstanding stability and cycling ability. At charge/discharge rates of ~40 C, photoreduced graphene anodes delivered a steady capacity of ~156 mAh/g(anode) continuously over 1000 charge/discharge cycles, providing a stable power density of ~10 kW/kg(anode). Such electrodes are envisioned to be mass scalable with relatively simple and low-cost fabrication procedures, thereby providing a clear pathway toward commercialization.

It is well established that pristine multiwalled carbon nanotubes offer poor structural reinforcement in epoxy-based composites. There are several reasons for this which include reduced interfacial contact area since the outermost nanotube shields the internal tubes from the matrix, poor wetting and interfacial adhesion with the heavily cross-linked epoxy chains, and intertube slip within the concentric nanotube cylinders leading to a sword-in-sheath type failure. Here we demonstrate that unzipping such multiwalled carbon nanotubes into graphene nanoribbons results in a significant improvement in load transfer effectiveness. For example, at ∼0.3% weight fraction of nanofillers, the Young's modulus of the epoxy composite with graphene nanoribbons shows ∼30% increase compared to its multiwalled carbon nanotube counterpart. Similarly the ultimate tensile strength for graphene nanoribbons at ∼0.3% weight fraction showed ∼22% improvement compared to multiwalled carbon nanotubes at the same weight fraction of nanofillers in the composite. These results demonstrate that unzipping multiwalled carbon nanotubes into graphene nanoribbons can enable their utilization as high-performance additives for mechanical properties enhancement in composites that rival the properties of singlewalled carbon nanotube composites yet at an order of magnitude lower cost.

The delamination buckling approach provides a facile means to dynamically control the optical transmittance of extremely flexible and stretchable graphene oxide coatings with fast response time. Such graphene oxide coatings can be deposited by scalable solution-processing methods for potential applications in dynamic glazing.

Emerging two-dimensional (2D) materials such as transition metal dichalcogenides offer unique and hitherto unavailable opportunities to tailor the mechanical, thermal, electronic, and optical properties of polymer nanocomposites. In this study, we exfoliated bulk molybdenum disulfide (MoS2) into nanoplatelets, which were then dispersed in epoxy polymers at loading fractions of up to 1% by weight. We characterized the tensile and fracture properties of the composite and show that MoS2 nanoplatelets are highly effective at enhancing the mechanical properties of the epoxy at very low nanofiller loading fractions (below 0.2% by weight). Our results show the potential of 2D sheets of transition metal dichalcogenides as reinforcing additives in polymeric composites. Unlike graphene, transition metal dichalcogenides such as MoS2 are high band gap semiconductors and do not impart significant electrical conductivity to the epoxy matrix. For many applications, it is essential to enhance mechanical properties while also maintaining the electrical insulation properties and the high dielectric constant of the polymer material. In such applications, conductive carbon based fillers such as graphene cannot be utilized. This study demonstrates that 2D transition metal dichalcogenide additives offer an elegant solution to such class of problems.

Previous studies of the interaction of water with graphene-coated surfaces have been limited to flat (smooth) surfaces. Here we created a rough surface by nanopatterning and then draped the surface with a single-layer graphene sheet. We found that the ultrasheer graphene drape prevents the penetration of water into the textured surface thereby drastically reducing the contact angle hysteresis (which is a measure of frictional energy dissipation) and preventing the liquid contact line from getting pinned to the substrate. This has important technological implications since the main obstacle to the motion of liquid drops on rough surfaces is contact angle hysteresis and contact line pinning. Graphene drapes could therefore enable enhanced droplet mobility which is required in a wide range of applications in micro and nanofluidics. Compared to polymer coatings that could fill the cavities between the nano/micropores or significantly alter the roughness profile of the substrate, graphene provides the thinnest (i.e., most sheer) and most conformal drape that is imaginable. Despite its extreme thinness, the graphene drape is mechanically robust, chemically stable, and offers high flexibility and resilience which can enable it to reliably drape arbitrarily complex surface topologies. Graphene drapes may therefore provide a hitherto unavailable ability to tailor the dynamic wettability of surfaces for a variety of applications.