In the experiment, a 6√3 x 6√3 structure was first made by MBE on the anisotropic terrace of the Si-terminated surface of a nitrogen-doped 6H-SiC(0001) substrate vicinal to the [1-100] direction. The tilting angle of the substrate was 4 degree, and a well-ordered step-and-terrace structure was made after cleaning the substrate by annealing in hydrogen as confirmed by atomic force microscopy. We optimized the substrate temperature and the carbon deposition rate to make a homogeneous 6√3 x 6√3 structure on the terraces without thermal decomposition of the substrate. The surface structure was in situ monitored by reflection high energy electron diffraction, and the width of the 6√3 x 6√3 area on the terrace was adjusted by monitoring the 6√3 x 6√3 spots. After stopping the growth, the sample was exposed to hydrogen molecules at 600 °C to transform the surface 6√3 x 6√3 layer to single-layer graphene by inserting hydrogen atoms at the interface. [2]

Graphene honeycomb lattice without the 6√3 x 6√3 structure was confirmed by low energy electron diffraction and scanning tunneling microscopy (STM). Few point defects are seen at the graphene on the terrace in the STM images of atomic resolution. The width of graphene nanoribbon on the substrate terrace is 10-15 nm, depending on the growth condition. The electronic states of the graphene nanoribbon were studied using angle-resolved photoemission spectroscopy (ARPES) at 130 K as in the previous report. [3] The top of the π band of the graphene nanoribbon was 0.05 ~ 0.25 eV below the Fermi energy. No signal from the π* band was detected by ARPES above the top of the π band, indicating the gap formation at E_D.

References

1. M. Y. Han et al., Phys. Rev. Lett. 98, 206805 (2007).

2. C. Riedl et al., Phys. Rev. Lett. 103, 246804 (2009).

3. K. Nakatsuji et al., Phys. Rev. B82 045428 (2010).

CNTFETs with a single semiconducting tube yield too low current (25 µA) for useful applications and thus the transistors with thousands tubes in parallel are being fabricated [1][2]. unfortunately, following theory 1/3rd of all tubes are metallic. Carrier scattering is better understood for metallic tubes and it is believed that for semiconducting tubes, despite more complexity, the same scattering mechanisms are applicable: CNTs defect scattering, physical bends and phonon scattering are present. Investigation of CNTFETs with a single semicoducting (ST), single metallic (MT) and metallic+semiconducting (MST) tubes at different lattice temperature environment was never done before and enables a deeper insight of CNT transport properties to further improve the application-oriented device behavior. It was shown that multifinger CNTFETs exhibited a weak temperature dependence of IV, RF and NF indicating a very weak electron-phonon interaction and the absence of charge-carrier freeze-out known for conventional doped semiconductors [3],[4].

In this work transistors with single ST, single MT and double MST were selected. Transistors have 800 nm channel length and features n-type behavior. IV characteristics were measured on wafer for manufacturable CNTFET process selected single CNTs at different lattice temperatures. The investigated structures have a fixed gate length of 0.35 µm and gate width of 40 µm. The source-drain spacing (channel length) is 800 nm. A 20 nm thick HfO2 was used for the gate oxide. The devices were fabricated with the process technology described in [1][2].The CNTFETs were embedded in DC pads for on-wafer measurements. Transfer characteristics of ST and MT transistor structures at ambient temperature T0 = 300 K, are shown in Fig.1 and Fig.2, Fig.3, Fig.4. The drain current show saturation for ST device, typical for MOSFETs. Nevertheless the carrier transport is very different. The dependence of drain current over the temperature will enable the analysis of transport behavior of single ST and MT and coupled MST. As it is seen from Fig.3 and Fig.4 the MT transistor structure behaves as nonlinear resistor.

One route to realizing graphene as a material for digital-type devices is through the lithographic patterning of graphene nanoribbons (GNRs). GNRs enable band gap engineering that is dependent on nanoribbon width and edge state. We employed two complementary AFM-based lithography techniques to pattern GNRs: (1) thermal dip-pen nanolithography (tDPN)¹ and (2) thermochemical nanolithography (TCNL)². Though inverse in approach, both techniques generate GNRs into a larger sheet of insulating chemically-modified graphene. Both lithographies were performed on CVD-grown single-layered graphene (SLG) on SiO₂/Si substrates using heated AFM probes. The first approach, tDPN, used the heated probe to deposit narrow polystyrene (PS) ribbons on pristine graphene. The areas of the graphene not protected by the polymer were then fluorinated, converting them to a highly insulating state, which leaves behind a chemically isolate GNR channel. We show that the PS protected ribbon was the only conductive pathway for active device. Secondly, we use the converse approach by using the heated AFM probe to locally reduce fluorographene back to graphene, leaving behind a conductive GNR channel. Both techniques can generate a wide range of nanoribbon widths while avoiding electron beams which can damage graphene. We discuss the relative merits of each strategy, as well as their impact on electrical properties (e.g., doping).

1. WK Lee et al., Nano Letters, 11, 5461, 2011

2. Z Wei et al., Science, 328, 1371, 2010

Previously reported efforts have identified the potential of vertically oriented graphene nanosheets in electrochemical double-layer capacitors (Miller et. al, Science 2010) for efficient AC line-filtering performance. Continued investigations to improve performance suggest that the availability of a high edge and surface defect density could be the dominant mechanism. Furthermore, charge/discharge profiles over time show that performance can actually increase as the device ages. In an effort to understand these findings, X-ray photoelectron spectroscopy, Auger electron spectroscopy and near edge absorption fine structure spectroscopy have been utilized to study the interaction of the electrolytes and solvents with the graphene-based electrode materials. The EDL capacitance of graphene nanosheets has been measured before and after Ar plasma bombardment for various times and after exposure to water, isopropanol, methanol, NaOH and KOH. Graphene nanosheet electrochemical capacitors have been disassembled and analyzed following short term and long term operation.