Self-consistent theory of molecular switching

Abstract

We study the model of a molecular switch comprised of a molecule with a soft vibrational degree of freedom coupled to metallic leads. In the presence of strong electron-ion interaction, different charge states of the molecule correspond to substantially different ionic configurations, which can lead to very slow switching between energetically close configurations (Franck-Condon blockade). Application of transport voltage, however, can drive the molecule far out of thermal equilibrium and thus dramatically accelerate the switching. The tunneling electrons play the role of a heat bath with an effective temperature dependent on the applied transport voltage. Including the transport-induced "heating" selfconsistently, we determine the stationary current-voltage characteristics of the device, and the switching dynamics for symmetric and asymmetric devices. We also study the effects of an extra dissipative environment and demonstrate that it can lead to enhanced non-linearities in the transport properties of the device and dramatically suppress the switching dynamics.

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• The effect of elastic disorder on single electron transport through a buckled nanotube
• Tunable anharmonicity in cavity optomechanics in the unresolved sideband regime
• Evidence for atomic-scale vibron-mediated electron bunching