Diffuse structures and periodic orbits in the photodissociation of small polyatomic molecules

R. Schinke, K. Weide, B. Heumann, V. Engel
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引用次数: 22

Abstract

The relation of diffuse vibrational structures in UV-absorption spectra of (small) polyatomic molecules and internal vibrational motion in excited electronic states are investigated. The method of choice is the propagation of time-dependent wavepackets with the autocorrelation function serving as the link between the energy dependence of the spectrum and the time dependence of the molecular motion in the excited electronic state. For the purpose of this paper we characterize diffuse structures as very short-lived resonances with ‘lifetimes’ of the order of at most one internal vibrational period. In particular, we study a model system for the photodissociation of symmetric triatomic molecules ABA such as H2O, CO2 and O3, the photodissociation of H2O in the second continuum, and the fragmentation of H2S. The existence of unstable periodic orbits and their influence on the dissociation dynamics is especially elucidated. In the case of H2S we demonstrate that the diffuse absorption structures are caused by symmetric stretch motion in a binding state which is strongly coupled to a dissociative state. Diffuse structures can be regarded as very broad resonances in excited electronic states. They manifest transition-state spectroscopy in the original sense of the word.
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小多原子分子光解的扩散结构和周期轨道
研究了(小)多原子分子紫外吸收光谱中的扩散振动结构与激发态内部振动运动的关系。选择的方法是传播时变波包,用自相关函数作为谱的能量依赖性和激发态分子运动的时间依赖性之间的联系。为了本文的目的,我们将扩散结构描述为非常短暂的共振,其“寿命”最多为一个内振动周期的数量级。特别地,我们研究了对称三原子分子ABA如H2O、CO2和O3的光解作用模型系统,H2O在第二连续统中的光解作用,以及H2S的破碎作用。特别阐明了不稳定周期轨道的存在及其对解离动力学的影响。在H2S的情况下,我们证明了扩散吸收结构是由在结合状态下的对称拉伸运动引起的,这种运动与解离状态强耦合。漫射结构可以看作是激发态中非常宽的共振。它们体现了过渡态光谱学这个词的原始意义。
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