Adhesion energy of single wall carbon nanotube loops on various substrates

The physics of adhesion of one-dimensional nano structures such as nanotubes, nano wires, and biopolymers on different material substrates is of great interest for the study of biological adhesion and the development of nano electronics and nano mechanics. In this paper, we present force spectroscopy experiments of a single wall carbon nanotube loop using our home-made interferometric atomic force microscope. Characteristic force plateaux during the peeling process allows us to access to quantitative values of the adhesion energy per unit length on various substrates: graphite, mica, platinum, gold and silicon. By combining a time-frequency analysis of the deflexion of the cantilever, we access to the dynamic stiffness of the contact, providing more information on the nanotube configurations and its intrinsic mechanical properties

Raman spectra of misoriented bilayer graphene

We compare the main feature of the measured Raman scattering spectra from single layer graphene with a bilayer in which the two layers are arbitrarily misoriented. The profiles of the 2D bands are very similar having only one component, contrary to the four found for commensurate Bernal bilayers. These results agree with recent theoretical calculations and point to the similarity of the electronic structures of single layer graphene and misoriented bilayer graphene. Another new aspect is that the dependance of the 2D frequency on the laser excitation energy is different in these two latter systems

Frequency modulated self-oscillation and phase inertia in a synchronized nanowire mechanical resonator

Synchronization has been reported for a wide range of self-oscillating systems. However, even though it has been predicted theoretically for several decades, the experimental realization of phase self-oscillation, sometimes called phase trapping, in the high driving regime has been studied only recently. We explored in detail the phase dynamics in a synchronized field emission SiC nanoelectromechanical system with intrinsic feedback. A richer variety of phase behavior has been unambiguously identified, implying phase modulation and inertia. This synchronization regime is expected to have implications for the comprehension of the dynamics of interacting self-oscillating networks and for the generation of frequency modulated signals at the nanoscal

Role of fluctuations and nonlinearities on field emission nanomechanical self-oscillators

A theoretical and experimental description of the threshold, amplitude, and stability of a self-oscillating nanowire in a field emission configuration is presented. Two thresholds for the onset of self-oscillation are identified, one induced by fluctuations of the electromagnetic environment and a second revealed by these fluctuations by measuring the probability density function of the current. The ac and dc components of the current and the phase stability are quantified. An ac to dc ratio above 100% and an Allan deviation of 1.3x10-5 at room temperature can be attained. Finally, it is shown that a simple nonlinear model cannot describe the equilibrium effective potential in the self-oscillating regime due to the high amplitude of oscillations

Self-oscillations in field emission nanowire mechanical resonators: a nanometric DC-AC conversion

We report the observation of self-oscillations in a bottom-up nanoelectromechanical system (NEMS) during field emission driven by a constant applied voltage. An electromechanical model is explored that explains the phenomenon and that can be directly used to develop integrated devices. In this first study we have already achieved ~50% DC/AC (direct to alternative current) conversion. Electrical self-oscillations in NEMS open up a new path for the development of high speed, autonomous nanoresonators, and signal generators and show that field emission (FE) is a powerful tool for building new nano-components

Current Saturation in Field Emission from H-Passivated Si Nanowires

International audienceThis paper explores the field emission (FE) properties of highly crystalline Si nanowires (NWs) with controlled surface passivation. The NWs were batch-grown by the vapor_liquid_solid process using Au catalysts with no intentional doping. The FE current_voltage characteristics showed quasi-ideal current saturation that resembles those predicted by the basic theory for emission from semiconductors, even at room temperature. In the saturation region, the currents were extremely sensitive to temperature and also increased linearly with voltage drop along the nanowire. The latter permits the estimation of the doping concentration and the carrier lifetime, which is limited by surface recombination. The conductivity could be tuned over 2 orders of magnitude by in situ hydrogen passivation/desorption cycles. This work highlights the role of dangling bonds in surface leakage currents and demonstrates the use of hydrogen passivation for optimizing the FE characteristics of Si NWs

Field emission measure of the time response of individual semiconducting nanowires to laser excitation

International audienceA simple technique is explored to determine the temporal photo-response, s, of individual semiconducting SiC and Si nanowires (NWs), with a high time resolution. Laser-assisted field emission (LAFE) from the NWs is first shown to be highly sensitive to continuous laser illumination. Pulsed illumination is then combined with measurements of the total energy distributions to determine s which were rather large, 4-200 ls. The time response scaled roughly with the square of the NWs length and could be attributed to laser-induced heating. LAFE is thus a new tool for quantifying rapid thermo-optical effects in such nano-objects

Femtosecond Laser Induced Resonant Tunneling in an Individual Quantum Dot Attached to a Nanotip

Quantized nano-objects offer a myriad of exciting possibilities for manipulating electrons and light that impact photonics, nanoelectronics, and quantum information. In this context, ultrashort laser pulses combined with nanotips and field emission have permitted renewing nano-characterization and control electron dynamics with unprecedented space and time resolution reaching femtosecond and even attosecond regimes. A crucial missing step in these experiments is that no signature of quantized energy levels has yet been observed. We combine in situ nanostructuration of nanotips and ultrashort laser pulse excitation to induce multiphoton excitation and electron emission from a single quantized nano-object attached at the apex of a metal nanotip. Femtosecond induced tunneling through well-defined localized confinement states that are tunable in energy is demonstrated. This paves the way for the development of ultrafast manipulation of electron emission from isolated nano-objects including stereographically fixed individual molecules and high brightness, ultrafast, coherent single electron sources for quantum optics experiments

Nonlinear polarization coupling in freestanding nanowire/nanotube resonators

In this work, we study the nonlinear coupling between the transverse modes of nanoresonators such as nanotubes or nanowires in a singly clamped configuration. We previously showed that at high driving, this coupling could result in a transition from independent planar modes to a locked elliptical motion, with important modifications of the resonance curves. Here, we clarify the physical origins, associated with a 1:1 internal resonance, and study in depth this transition as a function of the relevant parameters. We present simple formulae that permit to predict the emergence of this transition as a function of the frequency difference between the polarizations and the nonlinear coefficients and give the “backbone curves” corresponding to the elliptical regime. We also show that the elliptical regime is associated with the emergence of a new set of solutions of which one branch is stable. Finally, we compare single and double clamped configurations and explain why the elliptical transition appears on different polarizations