论文标题
单原子链中非线性振动模式的灌木料的共振激发
Resonant excitation of the bushes of nonlinear vibrational modes in monoatomic chains
论文作者
论文摘要
许多作者已经研究了一维非线性周期性结构中的Intermode相互作用,从上个世纪中叶Fermi,Pasta和Ulam(FPU)的经典作品开始。然而,未揭示出不同对称性的非线性振动模式之间能量转移的对称选择规则,从而尚未发现这种模式的某些灌木丛的激发。每个灌木丛都确定了被考虑系统的非线性动力学方程的精确解。给定灌木的模式的收集不会随时间变化,而这些模式之间存在连续的能量交换。非线性正常模式(NNM)的灌木是借助群体理论方法构建的,因此对于具有较大振幅原子振动和任何类型的原子间相互作用的情况,它们可以存在。在大多数出版物中,在周期性边界条件下研究了一维系统中NNM或类似动力学对象的灌木。在本文中,我们介绍了固定边界条件的单原子链中NNM的灌木丛的研究,该研究阐明了此类系统中Intermode相互作用的一系列新属性,以及一种通过延续常规正常模式构建NNM的灌木丛的方法。本研究是针对Lennard-Jones间原子潜力进行的,但本文开发的方法对于任意的单元链有效。
Intermode interactions in one-dimensional nonlinear periodic structures have been studied by many authors, starting with the classic work by Fermi, Pasta, and Ulam (FPU) in the middle of the last century. However, symmetry selection rules for the energy transfer between nonlinear vibrational modes of different symmetry, which lead to the possibility of excitation of some bushes of such modes, were not revealed. Each bush determines an exact solution of nonlinear dynamical equations of the considered system. The collection of modes of a given bush does not change in time, while there is a continuous energy exchange between these modes. Bushes of nonlinear normal modes (NNMs) are constructed with the aid of group-theoretical methods and therefore they can exist for cases with large-amplitude atomic vibrations and for any type of interatomic interactions. In most publications, bushes of NNMs or similar dynamical objects in one-dimensional systems are investigated under periodic boundary conditions. In this paper, we present a study of bushes of NNMs in monoatomic chains for the case of fixed boundary conditions, which sheds light on a series of new properties of intermode interactions in such systems, as well as a method for constructing bushes of NNMs by continuation of conventional normal modes to the case of large atomic oscillations. The present study was carried out for the chains with the Lennard-Jones interatomic potential, but methods developed in this paper are valid for arbitrary monoatomic chains.