155 research outputs found
Incidence of the Tomonaga-Luttinger liquid state on the NMR spin lattice relaxation in Carbon Nanotubes
We report 13C nuclear magnetic resonance measurements on single wall carbon
nanotube (SWCNT) bundles. The temperature dependence of the nuclear
spin-lattice relaxation rate, 1/T1, exhibits a power-law variation, as expected
for a Tomonage-Luttinger liquid (TLL). The observed exponent is smaller than
that expected for the two band TLL model. A departure from the power law is
observed only at low T, where thermal and electronic Zeeman energy merge.
Extrapolation to zero magnetic field indicates gapless spin excitations. The
wide T range on which power-law behavior is observed suggests that SWCNT is so
far the best realization of a one-dimensional quantum metal.Comment: 5 pages, 4 figure
Stabilization of carbon nanotubes by filling with inner tubes: An optical spectroscopy study on double-walled carbon nanotubes under hydrostatic pressure
The stabilization of carbon nanotubes via the filling with inner tubes is
demonstrated by probing the optical transitions in double-walled carbon
nanotube bundles under hydrostatic pressure with optical spectroscopy.
Double-walled carbon nanotube films were prepared from fullerene peapods and
characterized by HRTEM and optical spectroscopy. In comparison to single-walled
carbon nanotubes, the pressure-induced redshifts of the optical transitions in
the outer tubes are significantly smaller below 10 GPa, demonstrating the
enhanced mechanical stability due to the inner tube already at low pressures.
Anomalies at the critical pressure P12 GPa signal the onset of the
pressure-induced deformation of the tubular cross-sections. The value of P
is in very good agreement with theoretical predictions of the pressure-induced
structural transitions in double-walled carbon nanotube bundles with similar
average diameters.Comment: 6 pages, 4 figures; to appear in Phys. Rev.
Synthesis and Characterization of Gadolinium Oxide Nanocrystallites
Lanthanide oxide nanocrystallites have gained a lot of attention due to their diverse use for potential applications and for this reason it is very important to find a suitable preparation method that would be economically inexpensive and easy to implement. The chapter describes the preparation of gadolinium oxide nanocrystallites (nano Gd2O3) through thermal decomposition of a complex formed by Gd(NO3)3·6 H2O and glycine. Decomposition of the complex occurs at temperatures about (250 ± 10)°C. An ultrafine white powder of the gadolinium oxide nanocrystallites was obtained. The resulting nanocrystallites were characterized by X‐ray powder diffraction analysis, which revealed the size of the gadolinium oxide nanocrystallites equal to 10 nm. The morphology of the gadolinium oxide nanocrystallites was examined by scanning electron microscopy. The elemental composition of the product was confirmed by EDS analysis
Linear plasmon dispersion in single-wall carbon nanotubes and the collective excitation spectrum of graphene
We have measured a strictly linear pi-plasmon dispersion along the axis of
individualized single wall carbon nanotubes, which is completely different from
plasmon dispersions of graphite or bundled single wall carbon nanotubes.
Comparative ab initio studies on graphene based systems allow us to reproduce
the different dispersions. This suggests that individualized nanotubes provide
viable experimental access to collective electronic excitations of graphene,
and it validates the use of graphene to understand electronic excitations of
carbon nanotubes. In particular, the calculations reveal that local field
effects (LFE) cause a mixing of electronic transitions, including the 'Dirac
cone', resulting in the observed linear dispersion
Synthesis of carbon nanotubes with and without catalyst particles
The initial development of carbon nanotube synthesis revolved heavily around the use of 3d valence transition metals such as Fe, Ni, and Co. More recently, noble metals (e.g. Au) and poor metals (e.g. In, Pb) have been shown to also yield carbon nanotubes. In addition, various ceramics and semiconductors can serve as catalytic particles suitable for tube formation and in some cases hybrid metal/metal oxide systems are possible. All-carbon systems for carbon nanotube growth without any catalytic particles have also been demonstrated. These different growth systems are briefly examined in this article and serve to highlight the breadth of avenues available for carbon nanotube synthesis
Electron-beam induced synthesis of nanostructures: a review
As the success of nanostructures grows in modern society so does the importance of our ability to control their synthesis in precise manners, often with atomic precision as this can directly affect the final properties of the nanostructures. Hence it is crucial to have both deep insight, ideally with real-time temporal resolution, and precise control during the fabrication of nanomaterials. Transmission electron microscopy offers these attributes potentially providing atomic resolution with near real time temporal resolution. In addition, one can fabricate nanostructures in situ in a TEM. This can be achieved with the use of environmental electron microscopes and/or specialized specimen holders. A rather simpler and rapidly growing approach is to take advantage of the imaging electron beam as a tool for in situ reactions. This is possible because there is a wealth of electron specimen interactions, which, when implemented under controlled conditions, enable different approaches to fabricate nanostructures. Moreover, when using the electron beam to drive reactions no specialized specimen holders or peripheral equipment is required. This review is dedicated to explore the body of work available on electron-beam induced synthesis techniques with in situ capabilities. Particular emphasis is placed on the electron beam-induced synthesis of nanostructures conducted inside a TEM, viz. the e-beam is the sole (or primary) agent triggering and driving the synthesis process
Graphene growth on h-BN by Molecular Beam Epitaxy
The growth of single layer graphene nanometer size domains by solid carbon
source molecular beam epitaxy on hexagonal boron nitride (h-BN) flakes is
demonstrated. Formation of single-layer graphene is clearly apparent in Raman
spectra which display sharp optical phonon bands. Atomic-force microscope
images and Raman maps reveal that the graphene grown depends on the surface
morphology of the h-BN substrates. The growth is governed by the high mobility
of the carbon atoms on the h-BN surface, in a manner that is consistent with
van der Waals epitaxy. The successful growth of graphene layers depends on the
substrate temperature, but is independent of the incident flux of carbon atoms.Comment: Solid State Communications, 201
On the formation process of silicon carbide nanophases via hydrogenated thermally induced templated synthesis
A thermally induced templated synthesis for SiC nanotubes and nanofibers
using ammonia or nitrogen as a carrier gas, single wall carbon nanotubes
(SWCNT) as templates as well as gaseous Si is presented. The bundles of SWCNT
act as both the carbon source and as a nanoframe from which SiC structuctures
form. Depending on the duration of the thermally induced templated reaction,
for a fixed temperature, carrier gas, and gas pressure, various SiC
nanostructures are obtained. These structures include SiC nanorods coated in C,
SiC nanorods, SiC nanotubes, and SiC nanocrytals. From our analysis using
transmission electron microscopy (TEM) and scanning electron microscopy (SEM),
electron energy-loss spectroscopy (EELS), electron diffraction (EDX), optical
absorption spectroscopy and Raman spectroscopy as probes we prove that H has a
key role on the morphology and stochiometry of the different SiC
nanostructures.Comment: 9 pages, 2 Figure
- …