The field of single-molecule magnets is very promising, since an individual magnetic molecule represent the ultimate size limit to store and processing information. Magnetic molecules are considered very promising for spintronics since they can store a bit of information in an extremely small volume. However, in order to make magnetic molecules work, one has to find a way to measure their magnetization. Usual approaches are often very invasive and may lead to a strong perturbation of the properties of the molecules. A European research team has now designed and realized a novel hybrid spintronic nanodevice where the state of the molecule is measured 'indirectly', through a sensor coupled with the molecule.
There has been tremendous interest in cloaking technology using metamaterials and there are two exciting possibilities to obtain drastic scattering reduction from moderately-sized objects. One is the concept of plasmonic cloaking, which is based on the use of a thin metamaterial cover to suppress the scattering from a passive object. The second one is the concept of mantle cloaking, which is based on a simple impedance surface to achieve similar effects. Now, new research shows that even a single layer of atoms, with the exciting conductivity properties of graphene, may achieve similar functionality in planar and cylindrical geometries. Once realized, this concept represents the 'thinnest' possible cloak, operating in the THz spectrum.
Graphene has two distinct types of edges produced when it is cut - armchair type or zigzag type - which correspond to the two crystal axis of graphene. These edge types have distinct electronic, magnetic, and chemical properties, and being able to pattern graphene along particular crystallographic directions to leave edges consisting of a single chirality is crucial for the fabrication of graphene nanoribbon and nanoelectronics devices. A widely discussed method for the patterning of graphene is the channelling of graphite by metal nanoparticles in oxidizing or reducing environments. Researchers now report the live nanoscale observation of this channelling process by silver nanoparticles.
Unlike silicon, graphene lacks an electronic band gap - the gap being an energy range that cannot be occupied by electrons - and therefore has no switching capability; which is essential for electronics applications. Opening an energy gap in graphene's electron energy spectrum is therefore a critical prerequisite for instance for creating graphene transistors. That's where strain engineering of graphene comes in. Researchers have discovered that local strain in a graphene sheet can alter its conducting properties. By varying the amount of local strain, transport gaps can be tailored. In new work, researchers present a new and novel mechanism for gap opening in strained graphene via electrostatic gates and show that it can be important also in realistic situations.
Interaction forces between contact surfaces, such as the adhesion and friction forces, are crucial in many applications at the nanoscale because of the high surface-to-volume ratio of nanomaterials and nanodevices. Over the last decade, various solid lubricant materials, micro/nano patterns, and surface treatment processes have been developed for efficient operation and extended lifetime in MEMS/NEMS applications, and for various fabrication processes such as nanoimprint lithography and transfer printing. From a practical viewpoint, large-area CVD-graphene holds the greatest promise as a solid lubricant because of its excellent scalability and transferability. So far, the tribological characteristics of CVD-graphene at the micro- and nanoscale have not been reported yet. Researchers have now demonstrated the feasibility of using large-area CVD-graphene as a solid lubricant.
The extremely high electron mobility of graphene - under ideal conditions electrons move through it with roughly 100 times the mobility they have in silicon - combined with its superior strength and the fact that it is nearly transparent (2.3 % of light is absorbed; 97.7 % transmitted), make it an ideal candidate for photovoltaic applications. Recent research suggests, though, that doping is a necessity to harvest the full potential of graphene. The challenge then for researchers is to find suitable fabrication techniques for high-quality graphene flakes that exhibit high charge mobilities. Researchers now present a chemical approach towards non-covalently functionalized graphene, which is generated from vastly available and low-priced natural graphite.
There are already several technologies that potentially allow mass production of graphene sheets; several of them are processing graphene in solution by exfoliating graphite. The general problem with this approach is however that is has been so far impossible to regenerate the undisturbed graphene lattice which was present prior to oxidation as decarboxylation inevitable takes place in the reduction step. In new work, researchers have now demonstrated the first bulk wet chemical exfoliation of graphite in association with an in situ covalent functionalization of intermediately generated graphene. With this novel chemical method, it is now possible to achieve covalently bonded functionalities without mechanical or sonochemical treatment. The covalent functionalization also protects the single-layer graphene from reaggregation and substrate-induced doping.
In the decades-old quest to build artificial muscles, many materials have been investigated with regard to their suitability for actuator application (the ability of a material to reversibly change dimensions under the influence of various stimuli). Recently, hope in obtaining improved artificial muscles was revitalized by the discovery of the extraordinary mechanical and electrical properties of graphene and its chemical derivatives. A new study shows that electrical heating of graphene oxide nanoribbons mats results in reversible generation of 1.6% stress and maximum work capacity of about 40 J/kg, which is similar to that of natural muscle. Unlike previous studies, the team obtained the graphene material by chemical unzipping of multi-walled carbon nanotubes.