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Register a new userObservation of decoherence in a carbon nanotube mechanical resonator
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In physical systems, decoherence can arise from both dissipative and dephasing processes. In mechanical resonators, the driven frequency response measures a combination of both, while time domain techniques such as ringdown measurements can separate the two. Here, we report the first observation of the mechanical ringdown of a carbon nanotube mechanical resonator. Comparing the mechanical quality factor obtained from frequency- and time-domain measurements, we find a spectral quality factor four times smaller than that measured in ringdown, demonstrating dephasing-induced decoherence of the nanomechanical motion. This decoherence is seen to arise at high driving amplitudes, pointing to a non-linear dephasing mechanism. Our results highlight the importance of time-domain techniques for understanding dissipation in nano-mechanical resonators, and the relevance of decoherence mechanisms in nanotube mechanics.
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We report on the nonlinear coupling between the mechanical modes of a nanotube resonator. The coupling is revealed in a pump-probe experiment where a mode driven by a pump force is shown to modify the motion of a second mode measured with a probe force. In a second series of experiments, we actuate the resonator with only one oscillating force. Mechanical resonances feature exotic lineshapes with reproducible dips, peaks, and jumps when the measured mode is commensurate with another mode with a frequency ratio of either 2 or 3. Conventional lineshapes are recovered by detuning the frequency ratio using the voltage on a nearby gate electrode. The exotic lineshapes are attributed to strong coupling between the mechanical modes. The possibility to control the strength of the coupling with the gate voltage holds promise for various experiments, such as quantum manipulation, mechanical signal processing, and the study of the quantum-toclassical transition.
Since the advent of atomic force microscopy, mechanical resonators have been used to study a wide variety of phenomena, such as the dynamics of individual electron spins, persistent currents in normal metal rings, and the Casimir force. Key to these experiments is the ability to measure weak forces. Here, we report on force sensing experiments with a sensitivity of 12 zN Hz^(-1/2) at a temperature of 1.2 K using a resonator made of a carbon nanotube. An ultra-sensitive method based on cross-correlated electrical noise measurements, in combination with parametric downconversion, is used to detect the low-amplitude vibrations of the nanotube induced by weak forces. The force sensitivity is quantified by applying a known capacitive force. This detection method also allows us to measure the Brownian vibrations of the nanotube down to cryogenic temperatures. Force sensing with nanotube resonators offers new opportunities for detecting and manipulating individual nuclear spins as well as for magnetometry measurements.
Graphene and carbon nanotubes represent the ultimate size limit of one and two-dimensional nanoelectromechanical resonators. Because of their reduced dimensionality, graphene and carbon nanotubes display unusual mechanical behavior; in particular, their dynamics is highly nonlinear. Here, we review several types of nonlinear behavior in resonators made from nanotubes and graphene. We first discuss an unprecedented scenario where damping is described by a nonlinear force. This scenario is supported by several experimental facts: (i) the quality factor varies with the amplitude of the motion as a power law whose exponent coincides with the value predicted by the nonlinear damping model, (ii) hysteretic behavior (of the motional amplitude as a function of driving frequency) is absent in some of our resonators even for large driving forces, as expected when nonlinear damping forces are large, and (iii) when we quantify the linear damping force (by performing parametric excitation measurements) we find that it is significantly smaller than the nonlinear damping force. We then review parametric excitation measurements, an alternative actuation method which is based on nonlinear dynamics. Finally, we discuss experiments where the mechanical motion is coupled to electron transport through a nanotube. The coupling can be made so strong that the associated force acting on the nanotube becomes highly nonlinear with displacement and velocity. Overall, graphene and nanotube resonators hold promise for future studies on classical and quantum nonlinear dynamics.
Single electron transistors (SETs) fabricated from single-walled carbon nanotubes (SWNTs) can be operated as highly sensitive charge detectors reaching sensitivity levels comparable to metallic radio frequency SETs (rf-SETs). Here we demonstrate how the charge sensitivity of the device can be improved by using the mechanical oscillations of a single-walled carbon nanotube quantum dot. To optimize the charge sensitivity $delta Q$, we drive the mechanical resonator far into the nonlinear regime and bias it to an operating point where the mechanical third order nonlinearity is cancelled out. This way we enhance $delta Q$, from 6 $mu e/sqrt{textrm{Hz}}$ for the static case, to 0.97 $mu e/sqrt{textrm{Hz}}$, at a probe frequency of $sim$ 1.3 kHz.
Coulomb interactions can have a decisive effect on the ground state of electronic systems. The simplest system in which interactions can play an interesting role is that of two electrons on a string. In the presence of strong interactions the two electrons are predicted to form a Wigner molecule, separating to the ends of the string due to their mutual repulsion. This spatial structure is believed to be clearly imprinted on the energy spectrum, yet to date a direct measurement of such a spectrum in a controllable one-dimensional setting is still missing. Here we use an ultra-clean suspended carbon nanotube to realize this system in a tunable potential. Using tunneling spectroscopy we measure the excitation spectra of two interacting carriers, electrons or holes, and identify seven low-energy states characterized by their spin and isospin quantum numbers. These states fall into two multiplets according to their exchange symmetries. The formation of a strongly-interacting Wigner molecule is evident from the small energy splitting measured between the two multiplets, that is quenched by an order of magnitude compared to the non-interacting value. Our ability to tune the two-electron state in space and to study it for both electrons and holes provides an unambiguous demonstration of the fundamental Wigner molecule state.
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