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Ion time-of-flight and vacuum ultra-violet fluorescence spectroscopy of highly ionized nitrogen.

机译:高电离氮的离子飞行时间和真空紫外荧光光谱。

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This thesis investigates dissociative ionization in ultrafast laser fields. We review a possible mechanism for enhanced excitation that is exclusive to molecular systems and may provide a connection between multiphoton excitation and the phenomenon of enhanced ionization. Following our discussion of the excitation model, we present a study of the vacuum ultraviolet fluorescence produced by molecules in strong laser fields. These results show, that not only is enhanced excitation exclusive to molecules, but also that the excitation is selective, creating only 2s-1(-2) configurations. Such excitations correlate to charge-transfer states that are fundamental to both the electron localization of enhanced ionization and to the multiphoton susceptibility model. To gain a deeper insight into the details of the molecular dissociation we compare the fluorescence with results of an ion time-of-flight study and find that an extension of the excitation model to include odd-charged molecules may be in order. We then show that pump-probe experiments show clear evidence of resonant enhancement of the ionization process.
机译:本文研究了超快激光场中的离解电离。我们审查了分子系统专有的增强激发的可能机制,并可能提供多光子激发与增强电离现象之间的联系。在讨论了激发模型之后,我们对由强激光场中的分子产生的真空紫外荧光进行了研究。这些结果表明,不仅增强了分子专有的激发,而且激发是选择性的,仅产生2s-1(-2)构型。这种激发与电荷转移状态相关,电荷转移状态对于增强电离的电子定位和多光子磁化率模型都是至关重要的。为了更深入地了解分子解离的细节,我们将荧光与离子飞行时间研究的结果进行了比较,发现激发模型的扩展可能包括顺电荷的分子。然后,我们表明,泵浦探针实验显示出电离过程共振增强的明确证据。

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