Recent theoretical calculations and photoemission spectroscopy measurements on the bulk Bi 2 Se 3 material show that it is a three-dimensional topological insulator possessing conductive surface states with nondegenerate spins, attractive for dissipationless electronics and spintronics applications. Nanoscale topological insulator materials have a large surface-to-volume ratio that can manifest the conductive surface states and are promising candidates for devices. Here we report the synthesis and characterization of high quality single crystalline Bi 2 Se 3 nanomaterials with a variety of morphologies. The synthesis of Bi 2 Se 3 nanowires and nanoribbons employs Au-catalyzed vapor-liquid-solid (VLS) mechanism. Nanowires, which exhibit rough surfaces, are formed by stacking nanoplatelets along the axial direction of the wires. Nanoribbons are grown along [11][12][13][14][15][16][17][18][19][20] direction with a rectangular crosssection and have diverse morphologies, including quasi-one-dimensional, sheetlike, zigzag and sawtooth shapes. Scanning tunneling microscopy (STM) studies on nanoribbons show atomically smooth surfaces with 1 nm step edges, indicating single Se-Bi-Se-Bi-Se quintuple layers. STM measurements reveal a honeycomb atomic lattice, suggesting that the STM tip couples not only to the top Se atomic layer, but also to the Bi atomic layer underneath, which opens up the possibility to investigate the contribution of different atomic orbitals to the topological surface states. Transport measurements of a single nanoribbon device (four terminal resistance and Hall resistance) show great promise for nanoribbons as candidates to study topological surface states.Bi 2 Se 3 is a narrow gap semiconductor, previously studied for infrared detectors and thermoelectric applications. 1 Recently, research on Bi2Se3 and related compounds (Bi2Te3 and Sb2Te3) has attracted much interest because they are predicted to be three-dimensional (3D) topological insulators (TIs), a new class of quantum matter possessing conducting surface states with nondegenerate spins. 2 In TIs, the strong spin-orbit coupling dictates robust, nontrivial surface states, which are topologically protected against back scattering from time-reversal invariant defects and impurities. Angleresolved photoemission spectroscopy (ARPES) measurements on bulk single crystals of BixSb1-x, Bi2Se3, and Bi2Te3 have verified the existence of the 3D TI phase. [3][4][5][6][7] In particular, the surface states of Bi2Se3 forms a single Dirac cone inside a large bulk band gap of 0.3 eV, thus being suggested as the reference material for the 3D TIs. 2,4,8 The unique properties of the Bi2Se3 TI may pave the way for dissipationless quantum electronics and room temperature spintronics applications.1 To date, the surface properties of the 3D TIs have been mainly investigated by ARPES measurements on the cleaved surface of bulk crystals. [3][4][5][6][7] Single crystalline nanostructure, on the other hand, offers an attractive alternative system to study the surface sta...

Owing to its unique electronic properties, graphene has recently attracted wide attention in both the condensed matter physics and microelectronic device communities. Despite intense interest in this material, an industrially scalable graphene synthesis process remains elusive. Here, we demonstrate a high-throughput, low-temperature, spatially controlled and scalable epitaxial graphene (EG) synthesis technique based on laser-induced surface decomposition of the Si-rich face of a SiC single-crystal. We confirm the formation of EG on SiC as a result of excimer laser irradiation by using reflection high-energy electron diffraction (RHEED), Raman spectroscopy, synchrotron-based X-ray diffraction, transmission electron microscopy (TEM), and scanning tunneling microscopy (STM). Laser fluence controls the thickness of the graphene film down to a single monolayer. Laser-synthesized graphene does not display some of the structural characteristics observed in EG grown by conventional thermal decomposition on SiC (0001), such as Bernal stacking and surface reconstruction of the underlying SiC surface.

The unimolecular rectifier is a fundamental building block of molecular electronics. Rectification in single molecules can arise from electron transfer between molecular orbitals displaying asymmetric spatial charge distributions, akin to p-n junction diodes in semiconductors. Here we report a novel all-hydrocarbon molecular rectifier consisting of a diamantane-C 60 conjugate. By linking both sp 3 (diamondoid) and sp 2 (fullerene) carbon allotropes, this hybrid molecule opposingly pairs negative and positive electron affinities. The single-molecule conductances of self-assembled domains on Au(111), probed by lowtemperature scanning tunnelling microscopy and spectroscopy, reveal a large rectifying response of the molecular constructs. This specific electronic behaviour is postulated to originate from the electrostatic repulsion of diamantane-C 60 molecules due to positively charged terminal hydrogen atoms on the diamondoid interacting with the top electrode (scanning tip) at various bias voltages. Density functional theory computations scrutinize the electronic and vibrational spectroscopic fingerprints of this unique molecular structure and corroborate the unconventional rectification mechanism.

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Higher harmonic modes in nanoscale silicon cantilevers and microscale quartz tuning forks are detected and characterized using a custom scanning optical homodyne interferometer. Capable of both mass and force sensing, these resonators exhibit high-frequency harmonic motion content with picometer-scale amplitudes detected in a 2.5 MHz bandwidth, driven by ambient thermal radiation. Quartz tuning forks additionally display both in-plane and out-of-plane harmonics. The first six electronically detected resonances are matched to optically detected and mapped fork eigenmodes. Mass sensing experiments utilizing higher tuning fork modes indicate greater than six times sensitivity enhancement over fundamental mode operation.

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