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Dynamic Features of the Highly Excited Vibrational States of the HOCl Non-Integrable System Based on the Dynamic Potential and Lyapunov Exponent Approaches

机译:基于动态势和Lyapunov指数方法的HOCl不可积分系统的高振动态的动态特征

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摘要

In this article the dynamic features of the highly excited vibrational states of the hypochlorous acid (HOCl) non-integrable system are studied using the dynamic potential and Lyapunov exponent approaches. On the condition that the 3:1 resonance between the H–O stretching and H–O–Cl bending modes accompany the 2:1 Fermi resonance between the O–Cl stretching and H–O–Cl bending modes, it is found that the dynamic potentials of the highly excited vibrational states vary regularly with different Polyad numbers (P numbers). As the P number increases, the dynamic potentials of the H–O stretching mode remain the same, but those of the H–O–Cl bending mode gradually become complex. In order to investigate the chaotic and stable features of the highly excited vibrational states of the HOCl non-integrable system, the Lyapunov exponents of different energy levels lying in the dynamic potentials of the H–O–Cl bending mode (P = 4 and 5) are calculated. It is shown that the Lyapunov exponents of the energy levels staying in the junction of Morse potential and inverse Morse potential are relative large, which indicates the degrees of chaos for these energy levels is relatively high, but the stabilities of the corresponding states are good. These results could be interpreted as the intramolecular vibrational relaxation (IVR) acting strongly via the HOCl bending motion and causing energy transfers among different modes. Based on the previous studies, these conclusions seem to be generally valid to some extent for non-integrable triatomic molecules.
机译:在本文中,使用动态势和Lyapunov指数方法研究了次氯酸(HOCl)不可积分系统的高激发振动态的动力学特征。在H–O拉伸和H–O–Cl弯曲模式之间的3:1共振伴随O–Cl拉伸和H–O–Cl弯曲模式之间的2:1费米共振的条件下,发现高激发振动态的动态势随不同的Polyad数(P数)而规律地变化。随着P数的增加,H–O拉伸模式的动态电势保持不变,但H–O–Cl弯曲模式的动态电势逐渐变得复杂。为了研究HOCl不可积分系统的高激发振动态的混沌和稳定特征,不同能级的Lyapunov指数位于H–O–Cl弯曲模式的动态势中(P = 4和5 )进行计算。结果表明,停留在莫尔斯电势和莫尔斯逆电势交界处的能级的李雅普诺夫指数相对较大,表明这些能级的混沌程度较高,但相应状态的稳定性较好。这些结果可以解释为分子内振动弛豫(IVR)通过HOC1弯曲运动强烈作用,并导致不同模式之间的能量转移。根据先前的研究,这些结论对于不可整合的三原子分子似乎在一定程度上通常是有效的。

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