RESUMO
Van der Waals heterostructures formed by stacked 2D materials show exceptional electronic, mechanical, and optical properties. Superlubricity, a condition where atomically flat, incommensurate planes of atoms result in ultra-low friction, is a prime example enabling, for example, self-assembly of optically visible graphene nanostructures in air via a sliding auto-kirigami process. Here, it is demonstrated that a subtle but ubiquitous adsorbate stripe structure found on graphene and graphitic surfaces in ambient conditions remains stable within the interface between twisted graphene layers as they slide over each other. Despite this contamination, the interface retains an exceptional superlubricious state with an estimated upper bound frictional shear strength of 10 kPa, indicating that direct atomic incommensurate contact is not required to achieve ambient superlubricity for 2D materials. The results suggest that any phenomena depending on 2D heterostructure interfaces such as exotic electronic behavior may need to consider the presence of stripe adsorbate structures that remain intercalated.
RESUMO
In the last decade, new potential applications of micro- and nano-products in telecommunication, medical diagnostics, photovoltaic, and optoelectronic systems have increased the interest to develop micro-engineering technologies. Injection molding of polymeric materials is a recent method being adapted for serial manufacturing of optic components and packaging at the micro- and nano-scale. Quality assurance of replication into small cavities is an important but underdeveloped factor that is needed to ensure high production efficiency in any micro-fabrication industry. In this work, we introduce a fiber-based interferometric measurement sensor to monitor the cavity filling of optical microstructures fabricated into a macroscopic molding die. The interferometer was capable of resolving melt front motion into the microcavity to the point of complete filling as verified by atomic force microscopy. Despite the low reflectivity of the transparent polymer and unoptimized reflected light collection optics, this system is capable of monitoring polymer movement during the course of filling and detecting the completion of the process. The simplicity and flexibility of the technology could allow eventual instrumentation of injection molds, embossing, and nanoimprint tooling suitably modified with a small optical window to accommodate light from an optical fiber. This would provide a solution to the challenging problem of monitoring local, nanometer scale filling processes.
RESUMO
Scanning tunneling microscopy (STM) and atomic force microscopy (AFM) images of graphene reveal either a triangular or honeycomb pattern at the atomic scale depending on the imaging parameters. The triangular patterns at the atomic scale are particularly difficult to interpret, as the maxima in the images could be every other carbon atom in the six-fold hexagonal array or even a hollow site. Carbon sites exhibit an inequivalent electronic structure in HOPG or multilayer graphene due to the presence of a carbon atom or a hollow site underneath. In this work, we report small-amplitude, simultaneous STM/AFM imaging using a metallic (tungsten) tip, of the graphene surface as-grown by chemical vapor deposition (CVD) on Cu foils. Truly simultaneous operation is possible only with the use of small oscillation amplitudes. Under a typical STM imaging regime the force interaction is found to be repulsive. Force-distance spectroscopy revealed a maximum attractive force of about 7 nN between the tip and carbon/hollow sites. We obtained different contrast between force and STM topography images for atomic features. A honeycomb pattern showing all six carbon atoms is revealed in AFM images. In one contrast type, simultaneously acquired STM topography revealed hollow sites to be brighter. In another, a triangular array with maxima located in between the two carbon atoms was acquired in STM topography.
