Departamento de Química, Módulo 13, Universidad Autónoma de Madrid, 28049 Madrid, Spain.
Institute for Advanced Research in Chemical Sciences (IAdChem), Universidad Autónoma de Madrid, 28049 Madrid, Spain.
Sci Adv. 2023 Apr 14;9(15):eade3855. doi: 10.1126/sciadv.ade3855. Epub 2023 Apr 12.
Temporal delays extracted from photoionization phases are currently determined with attosecond resolution by using interferometric methods. Such methods require special care when photoionization occurs near Feshbach resonances due to the interference between direct ionization and autoionization. Although theory can accurately handle these interferences in atoms, in molecules, it has to face an additional, so far insurmountable problem: Autoionization is slow, and nuclei move substantially while it happens, i.e., electronic and nuclear motions are coupled. Here, we present a theoretical framework to account for this effect and apply it to evaluate time-resolved and vibrationally resolved photoelectron spectra and photoionization phases of N irradiated by a combination of an extreme ultraviolet (XUV) attosecond pulse train and an infrared pulse. We show that Feshbach resonances lead to unusual non-Franck-Condon vibrational progressions and to ionization phases that strongly vary with photoelectron energy irrespective of the vibrational state of the remaining molecular cation.
目前,通过干涉测量方法,可以以阿秒分辨率确定光电离相中的时间延迟。由于直接电离和自电离之间的干涉,当光电离发生在费什巴赫共振附近时,这些方法需要特别注意。尽管理论可以准确地处理原子中的这些干扰,但在分子中,它必须面对一个额外的、迄今为止无法克服的问题:自电离速度较慢,而在发生自电离时核运动很大,即电子和核运动是耦合的。在这里,我们提出了一个理论框架来考虑这一效应,并将其应用于评估由极紫外(XUV)阿秒脉冲串和红外脉冲组成的辐射照射下 N 的时间分辨和振动分辨光电子能谱和光电离相。我们表明,费什巴赫共振导致了不寻常的非弗朗克-康登振动进展,并导致了与光电子能量强烈变化的电离相,而与剩余分子阳离子的振动状态无关。