We introduce and analyze a system of two coupled partial differential equations with external noise. The equations are constructed to model transitions of monovalent metallic nanowires with non-axisymmetric intermediate or end states, but also have more general applicability. They provide a rare example of a system for which an exact solution of nonuniform stationary states can be found. We find a transition in activation behavior as the interval length on which the fields are defined is varied. We discuss several applications to physical problems.

Exit times for stochastic Ginzburg-Landau classical field theories with two or more coupled classical fields depend on the interval length on which the fields are defined, the potential in which the fields deterministically evolve, and the relative stiffness of the fields themselves. The latter is of particular importance in that physical applications will generally require different relative stiffnesses, but the effect of varying field stiffnesses has not heretofore been studied. In this paper, we explore the complete phase diagram of escape times as they depend on the various problem parameters. In addition to finding a transition in escape rates as the relative stiffness varies, we also observe a critical slowing down of the string method algorithm as criticality is approached.

We present a theoretical approach for understanding the stability of simple metal nanowires, in particular monovalent metals such as the alkalis and noble metals. Their cross sections are of order one nanometer so that small perturbations from external (usually thermal) noise can cause large geometrical deformations. The nanowire lifetime is defined as the time required for making a transition into a state with a different cross-sectional geometry. This can be a simple overall change in radius, or a change in the cross section shape, or both. We develop a stochastic field theoretical model to describe this noise-induced transition process, in which the initial and final states correspond to locally stable states on a potential surface derived by solving the Schrödinger equation for the electronic structure of the nanowire numerically. The numerical string method is implemented to determine the optimal transition path governing the lifetime. Using these results, we tabulate the lifetimes of sodium and gold nanowires for several different initial geometries.