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van der Waals heterostructures constitute a new class of artificial materials formed by stacking atomically thin planar crystals. We demonstrated band structure engineering in a van der Waals heterostructure composed of a monolayer graphene flake coupled to a rotationally aligned hexagonal boron nitride substrate. The spatially varying interlayer atomic registry results in both a local breaking of the carbon sublattice symmetry and a long-range moiré superlattice potential in the graphene. In our samples, this interplay between short-and long-wavelength effects resulted in a band structure described by isolated superlattice minibands and an unexpectedly large band gap at charge neutrality. This picture is confirmed by our observation of fractional quantum Hall states at ±5/3 filling and features associated with the Hofstadter butterfly at ultrahigh magnetic fields.

Recent theoretical proposals suggest that strain can be used to engineer graphene electronic states through the creation of a pseudo-magnetic field. This effect is unique to graphene because of its massless Dirac fermion-like band structure and particular lattice symmetry (C₃v). Here, we present experimental spectroscopic measurements by scanning tunneling microscopy of highly strained nanobubbles that form when graphene is grown on a platinum (111) surface. The nanobubbles exhibit Landau levels that form in the presence of strain-induced pseudo-magnetic fields greater than 300 tesla. This demonstration of enormous pseudo-magnetic fields opens the door to both the study of charge carriers in previously inaccessible high magnetic field regimes and deliberate mechanical control over electronic structure in graphene or so-called \"strain engineering.\"

In monolayer graphene, substitutional doping during growth can be used to alter its electronic properties. We used scanning tunneling microscopy, Raman spectroscopy, x-ray spectroscopy, and first principles calculations to characterize individual nitrogen dopants in monolayer graphene grown on a copper substrate. Individual nitrogen atoms were incorporated as graphitic dopants, and a fraction of the extra electron on each nitrogen atom was delocalized into the graphene lattice. The electronic structure of nitrogen-doped graphene was strongly modified only within a few lattice spacings of the site of the nitrogen dopant. These findings show that chemical doping is a promising route to achieving high-quality graphene films with a large carrier concentration.

Silver nanoparticles are susceptible to oxidation and have accordingly received less attention than gold nanoparticles; ultrastable silver nanoparticles are now reported, which can be produced in very large quantities as a single-sized molecular product, and the origins of their enhanced stability are elucidated using a single-crystal X-ray structure and first-principles calculations. Silver nanoparticles as good as gold Noble metals in nanoparticulate form find practical application as catalysts and in optoelectronics, energy conservation and many other fields. Gold nanoparticles, stable and easy to use, have proved much more useful and so have been studied more extensively than silver nanoparticles, which tend to be susceptible to oxidation. Anil Desireddy et al . describe a simple recipe for the large-scale production of single-sized silver nanoclusters, whose electronic structure gives them exceptional chemical stability. With the availability of stable silver nanoparticles, the metal's desirable electrical and physical properties, abundance and comparatively low cost could be harnessed in a wealth of new applications. Noble-metal nanoparticles have had a substantial impact across a diverse range of fields, including catalysis 1 , sensing 2 , photochemistry 3 , optoelectronics 4 , 5 , energy conversion 6 and medicine 7 . Although silver has very desirable physical properties, good relative abundance and low cost, gold nanoparticles have been widely favoured owing to their proved stability and ease of use. Unlike gold, silver is notorious for its susceptibility to oxidation (tarnishing), which has limited the development of important silver-based nanomaterials. Despite two decades of synthetic efforts, silver nanoparticles that are inert or have long-term stability remain unrealized. Here we report a simple synthetic protocol for producing ultrastable silver nanoparticles, yielding a single-sized molecular product in very large quantities with quantitative yield and without the need for size sorting. The stability, purity and yield are substantially better than those for other metal nanoparticles, including gold, owing to an effective stabilization mechanism. The particular size and stoichiometry of the product were found to be insensitive to variations in synthesis parameters. The chemical stability and structural, electronic and optical properties can be understood using first-principles electronic structure theory based on an experimental single-crystal X-ray structure. Although several structures have been determined for protected gold nanoclusters 8 , 9 , 10 , 11 , 12 , none has been reported so far for silver nanoparticles. The total structure of a thiolate-protected silver nanocluster reported here uncovers the unique structure of the silver thiolate protecting layer, consisting of Ag 2 S 5 capping structures. The outstanding stability of the nanoparticle is attributed to a closed-shell 18-electron configuration with a large energy gap between the highest occupied molecular orbital and the lowest unoccupied molecular orbital, an ultrastable 32-silver-atom excavated-dodecahedral 13 core consisting of a hollow 12-silver-atom icosahedron encapsulated by a 20-silver-atom dodecahedron, and the choice of protective coordinating ligands. The straightforward synthesis of large quantities of pure molecular product promises to make this class of materials widely available for further research and technology development 14 , 15 , 16 , 17 , 18 .

The precise location of a solid-state triple point, at which three solid phases coexist in thermal equilibrium, has been determined by controlling the stress and temperature in a nanobeam of vanadium dioxide near its metal–insulator transition. Triple point of the metal–insulator vanadium dioxide Vanadium dioxide (VO 2 ) is of interest in ultrafast optical and electrical switching applications thanks to the material's unique phase transition between metallic and insulating states involving several competing phases. This study of single-crystal VO 2 nanobeams in a system in which the metal–insulator transition is finely controlled by adjusting temperature and strain pinpoints the previously elusive 'triple point' — the transition temperature at which one metallic and two insulating phases can coexist — as 65 °C. Other so-called correlated materials, including manganites and pnictides, also have poorly understood strain-critical phase transitions involving multiple components, and this work demonstrates a method that should be widely applicable in such situations. First-order phase transitions in solids are notoriously challenging to study. The combination of change in unit cell shape, long range of elastic distortion and flow of latent heat leads to large energy barriers resulting in domain structure, hysteresis and cracking. The situation is worse near a triple point, where more than two phases are involved. The well-known metal–insulator transition in vanadium dioxide 1 , a popular candidate for ultrafast optical and electrical switching applications, is a case in point. Even though VO 2 is one of the simplest strongly correlated materials, experimental difficulties posed by the first-order nature of the metal–insulator transition as well as the involvement of at least two competing insulating phases have led to persistent controversy about its nature 1 , 2 , 3 , 4 . Here we show that studying single-crystal VO 2 nanobeams 5 , 6 , 7 , 8 , 9 , 10 , 11 , 12 , 13 , 14 , 15 , 16 in a purpose-built nanomechanical strain apparatus allows investigation of this prototypical phase transition with unprecedented control and precision. Our results include the striking finding that the triple point of the metallic phase and two insulating phases is at the transition temperature, T tr = T c , which we determine to be 65.0 ± 0.1 °C. The findings have profound implications for the mechanism of the metal–insulator transition in VO 2 , but they also demonstrate the importance of this approach for mastering phase transitions in many other strongly correlated materials, such as manganites 17 and iron-based superconductors 18 .

Metals support surface plasmons at optical wavelengths and have the ability to localize light to subwavelength regions. The field enhancements that occur in these regions set the ultimate limitations on a wide range of nonlinear and quantum optical phenomena. We found that the dominant limiting factor is not the resistive loss of the metal, but rather the intrinsic nonlocality of its dielectric response. A semiclassical model of the electronic response of a metal places strict bounds on the ultimate field enhancement. To demonstrate the accuracy of this model, we studied optical scattering from gold nanoparticles spaced a few angstroms from a gold film. The bounds derived from the models and experiments impose limitations on all nanophotonic systems.

Plasmons are directly launched in graphene, and their key parameters — propagation and attenuation — are studied with near-field infrared nano-imaging. Voltage-controlled graphene plasmonics Plasmonic devices, which exploit surface plasmons (electromagnetic waves that propagate along the surface of metals) offer the possibility of controlling and guiding light at subwavelength scales. All eyes are on graphene — atom-thick layers of carbon — as a promising platform for plasmonic applications because it can strongly interact with light and host surface plasmons in the infrared range. Two independent groups reporting in this issue of Nature show that plasmons can be directly launched in graphene, and observed with near-field optical microscopy. Moreover, the wavelengths and amplitudes of the plasmons can be tuned by a gate voltage, a promising capability for the development of on-chip graphene photonics for use in applications including telecommunications and information processing. Surface plasmons are collective oscillations of electrons in metals or semiconductors that enable confinement and control of electromagnetic energy at subwavelength scales 1 , 2 , 3 , 4 , 5 . Rapid progress in plasmonics has largely relied on advances in device nano-fabrication 5 , 6 , 7 , whereas less attention has been paid to the tunable properties of plasmonic media. One such medium—graphene—is amenable to convenient tuning of its electronic and optical properties by varying the applied voltage 8 , 9 , 10 , 11 . Here, using infrared nano-imaging, we show that common graphene/SiO 2 /Si back-gated structures support propagating surface plasmons. The wavelength of graphene plasmons is of the order of 200 nanometres at technologically relevant infrared frequencies, and they can propagate several times this distance. We have succeeded in altering both the amplitude and the wavelength of these plasmons by varying the gate voltage. Using plasmon interferometry, we investigated losses in graphene by exploring real-space profiles of plasmon standing waves formed between the tip of our nano-probe and the edges of the samples. Plasmon dissipation quantified through this analysis is linked to the exotic electrodynamics of graphene 10 . Standard plasmonic figures of merit of our tunable graphene devices surpass those of common metal-based structures.

Heterostructures based on layering of two-dimensional (2D) materials such as graphene and hexagonal boron nitride represent a new class of electronic devices. Realizing this potential, however, depends critically on the ability to make high-quality electrical contact. Here, we report a contact geometry in which we metalize only the ID edge of a 2D graphene layer. In addition to outperforming conventional surface contacts, the edge-contact geometry allows a complete separation of the layer assembly and contact metallization processes. In graphene heterostructures, this enables high electronic performance, including low-temperature ballistic transport over distances longer than 15 micrometers, and room-temperature mobility comparable to the theoretical phonon-scattering limit. The edge-contact geometry provides new design possibilities for multilayered structures of complimentary 2D materials.

We introduce self-assembled nanoantennas to enhance the fluorescence intensity in a plasmonic hotspot of zeptoliter volume. The nanoantennas are prepared by attaching one or two gold nanoparticles (NPs) to DNA origami structures, which also incorporated docking sites for a single fluorescent dye next to one NP or in the gap between two NPs. We measured the dependence of the fluorescence enhancement on NP size and number and compare it to numerical simulations. A maximum of 117-fold fluorescence enhancement was obtained for a dye molecule positioned in the 23-nanometer gap between 100-nanometer gold NPs. Direct visualization of the binding and unbinding of short DNA strands, as well as the conformational dynamics of a DNA Holliday junction in the hotspot of the nanoantenna, show the compatibility with single-molecule assays.