Molybdenum disulfide (MoS2) is an extremely intriguing material because of its unique electrical and optical properties. The preparation of large-area and high-quality MoS2 nanosheets is an important step in a wide range of applications. This study demonstrates that monolayer and few-layer MoS2 nanosheets can be obtained from electrochemical exfoliation of bulk MoS2 crystals. The lateral size of the exfoliated MoS2 nanosheets is in the 5-50 μm range, which is much larger than that of chemically or liquid-phase exfoliated MoS2 nanosheets. The MoS2 nanosheets undergo low levels of oxidation during electrochemical exfoliation. In addition, microscopic and spectroscopic characterizations indicate that the exfoliated MoS2 nanosheets are of high quality and have an intrinsic structure. A back-gate field-effect transistor was fabricated using an exfoliated monolayer MoS2 nanosheet. The on/off current ratio is over 10(6), and the field-effect mobility is approximately 1.2 cm(2) V(-1) s(-1); these values are comparable to the results for micromechanically exfoliated MoS2 nanosheets. The electrochemical exfoliation method is simple and scalable, and it can be applied to exfoliate other transition metal dichalcogenides.
Well-aligned single-crystalline wurzite zinc oxide (ZnO) nanowire array was successfully fabricated on an Al 2 O 3 substrate by a simple physical vapor-deposition method at a low temperature of 450 °C. The diameter and growth rate of ZnO nanowires increased as a function of growth temperature. TEM observation showed that the ZnO nanowires were synthesized along the c-axial direction of the hexagonal crystal structure. We demonstrate that ZnO nanowires followed the self-catalyzed growth mechanism on the ZnO nuclei. Besides high-quality ZnO nanowires, sometimes a fascinating hierarchically ordered ZnO structure was also observed.
Vertically aligned ZnO nanonails and nanopencils are synthesized on a silicon substrate using a modified thermal‐evaporation process, without using a catalyst or predeposited buffer layers. An adiabatic layer is used to provide an abrupt temperature decrease and high gas concentration for the nanostructures growth. The structure and morphology of the as‐synthesized ZnO nanonails and nanopencils are characterized using X‐ray diffraction, and scanning and transmission electron microscopies. Raman and photoluminescence properties are also investigated at room temperature. Field‐emission characterization shows that the turn‐on fields for the vertically aligned ZnO nanonails and nanopencils are 7.9 and 7.2 V μm–1, respectively.
We have investigated nitrogen doping effects on the structure and crystallinity of bamboo-shaped multiwalled carbon nanotubes (BS-MWNTs) by means of x-ray photoemission spectroscopy (XPS) and transmission electron microscopy. By controlling the NH3/C2H2 flow ratio during the chemical vapor deposition, the nitrogen concentrations of 0.4% to 2.4% were obtained. According to the XPS measurements, the increasing nitrogen concentration gave rise to an increase of the N-sp3 C bonds as well as the deterioration of the crystallinity of the BS-MWNTs. Besides, the N-sp3 C bonds were found to prevail over the N-sp2 C bonds above 5% nitrogen concentration. At higher nitrogen concentrations, the BS-MWNTs showed shorter compartment distances, presumably due to the suppressed surface diffusion of carbon on the catalyst particles.
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