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Dynamical quenching of field-induced dissociation of H-2(+) in intense infrared lasers

机译:强红外激光中H-2(+)场致离解的动态猝灭

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The dynamics of dissociation of the hydrogen molecular ion H-2(+) in an intense infrared (IR) field is studied by a series of wave packet simulations, In these simulations, the molecular ion is assumed to be instantly prepared at the initial time by a sudden ionization of the ground-state H-2 parent molecule, and a variety of frequency and intensity conditions of the laser field are considered. A new stabilization mechanism, called dynamical dissociation quenching, is found operative in the IR spectral range, In a Lime-resolved picture, this effect is shown to arise when a proper synchronization between the molecular motions and the laser field oscillations is ensured. In the Floquet, dressed molecule picture, the effect is related to interferences between the Floquet resonances that are excited initially by the nonadiabatic, sudden preparation of the ion. The Floquet analysis of the wave packets in this low frequency regime reveals important intersystem couplings between Floquet blocks, reflecting the highly multiphoton character of the dynamics. (C) 1998 American Institute of Physics. [S0021-9606(98)00310-9]. [References: 38]
机译:通过一系列波包模拟研究了氢分子离子H-2(+)在强红外(IR)场中的解离动力学,在这些模拟中,假定分子离子在初始时间即刻制备通过基态H-2母体分子的突然电离,可以考虑激光场的各种频率和强度条件。发现一种新的稳定机制,称为动态解离猝灭,在红外光谱范围内有效。在石灰分辨的照片中,当确保分子运动与激光场振荡之间的适当同步时,就会显示出这种效应。在Floquet穿戴的分子图片中,该效果与Floquet共振之间的干扰有关,这些干扰最初是由非绝热的离子突然激发而激发的。在这种低频状态下对波包进行的Floquet分析揭示了Floquet块之间重要的系统间耦合,反映了动力学的高度多光子特性。 (C)1998美国物理研究所。 [S0021-9606(98)00310-9]。 [参考:38]

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