Two elastically coupled nanomechanical resonators driven independently near their resonance frequencies show intricate nonlinear dynamics. The dynamics provide a scheme for realizing a nanomechanical system with tunable frequency and nonlinear properties. For large vibration amplitudes the system develops spontaneous oscillations of amplitude modulation that also show period doubling transitions and chaos. The complex nonlinear dynamics are quantitatively predicted by a simple theoretical model.
We consider a nanomechanical analogue of a nonlinear interferometer, consisting of two parallel, flexural nanomechanical resonators, each with an intrinsic Duffing nonlinearity and with a switchable beamsplitter-like coupling between them. We calculate the precision with which the strength of the nonlinearity can be estimated and show that it scales as $1/n^{3/2}$, where $n$ is the mean phonon number of the initial state. This result holds even in the presence of dissipation, but assumes the ability to make measurements of the quadrature components of the nanoresonators.
We investigate nonlinear dispersive mode coupling between the flexural in- and out-of-plane modes of two doubly clamped, nanomechanical silicon nitride string resonators. As the amplitude of one mode transitions from the linear response regime into the nonlinear regime, we find a frequency shift of two other modes. The resonators are strongly elastically coupled via a shared clamping point and can be tuned in and out of resonance dielectrically, giving rise to multimode avoided crossings. When the modes start hybridizing, their polarization changes. This affects the nonlinear dispersive coupling in a non-trivial way. We propose a theoretical model to describe the dependence of the dispersive coupling on the mode hybridization.
We investigate theoretically the non-linear dynamics of a coupled nanomechanical oscillator. Under a weak radio frequency excitation, the resonators can be parametrically tuned into a self-sustained oscillatory regime. The transfer of electrons from one contact to the other is then mechanically assisted, generating a rectified current. The direction of the rectified current is, in most unstable regions, determined by the phase shift between the mechanical oscillations and the signal. However, we locate intriguing parametrical regions of uni-directional rectified current, suggesting a practical scheme for the realization of a self-powered device in the nanoscale. In these regions, a dynamical symmetry breaking is induced by the non-linear coupling of the mechanical and electrical degrees of freedom. When operating within the Coulomb blockade limit, we locate bands of instability of enhanced gain.
We present measurements of the dissipation and frequency shift in nanomechanical gold resonators at temperatures down to 10 mK. The resonators were fabricated as doubly-clamped beams above a GaAs substrate and actuated magnetomotively. Measurements on beams with frequencies 7.95 MHz and 3.87 MHz revealed that from 30 mK to 500 mK the dissipation increases with temperature as $T^{0.5}$, with saturation occurring at higher temperatures. The relative frequency shift of the resonators increases logarithmically with temperature up to at least 400 mK. Similarities with the behavior of bulk amorphous solids suggest that the dissipation in our resonators is dominated by two-level systems.
We study resonant response of an underdamped nanomechanical resonator with fluctuating frequency. The fluctuations are due to diffusion of molecules or microparticles along the resonator. They lead to broadening and change of shape of the oscillator spectrum. The spectrum is found for the diffusion confined to a small part of the resonator and where it occurs along the whole nanobeam. The analysis is based on extending to the continuous limit, and appropriately modifying, the method of interfering partial spectra. We establish the conditions of applicability of the fluctuation-dissipation relations between the susceptibility and the power spectrum. We also find where the effect of frequency fluctuations can be described by a convolution of the spectra without these fluctuations and with them as the only source of the spectral broadening.