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一部量子分子影片:一氧化氮(NO)在真空紫外光激发的3pσΣ态下的多聚体预解离动力学

A quantum molecular movie: polyad predissociation dynamics in the VUV excited 3pσΣ state of NO.

作者信息

Makhija Varun, Boguslavskiy Andrey E, Forbes Ruaridh, Veyrinas Kevin, Wilkinson Iain, Lausten Rune, Schuurman Michael S, Grant Edward R, Stolow Albert

机构信息

Department of Chemistry and Physics, University of Mary Washington, Fredericksburg, VA 22401, USA and Department of Physics, University of Ottawa, 150 Louis Pasteur, Ottawa, ON K1N 6N5, Canada.

Department of Physics, University of Ottawa, 150 Louis Pasteur, Ottawa, ON K1N 6N5, Canada.

出版信息

Faraday Discuss. 2021 May 27;228(0):191-225. doi: 10.1039/d0fd00128g.

Abstract

The optical formation of coherent superposition states, a wavepacket, can allow the study of zeroth-order states, the evolution of which exhibit structural and electronic changes as a function of time: this leads to the notion of a molecular movie. Intramolecular vibrational energy redistribution, due to anharmonic coupling between modes, is the molecular movie considered here. There is no guarantee, however, that the formed superposition will behave semi-classically (e.g. Gaussian wavepacket dynamics) or even as an intuitively useful zeroth-order state. Here we present time-resolved photoelectron spectroscopy (TRPES) studies of an electronically excited triatomic molecule wherein the vibrational dynamics must be treated quantum mechanically and the simple picture of population flow between coupled normal modes fails. Specifically, we report on vibronic wavepacket dynamics in the zeroth-order 3pσ2Σu Rydberg state of NO2. This wavepacket exemplifies two general features of excited state dynamics in polyatomic molecules: anharmonic multimodal vibrational coupling (forming polyads); nonadiabatic coupling between nuclear and electronic coordinates, leading to predissociation. The latter suggests that the polyad vibrational states in the zeroth-order 3p Rydberg manifold are quasi-bound and best understood to be scattering resonances. We observed a rapid dephasing of an initially prepared 'bright' valence state into the relatively long-lived 3p Rydberg state whose multimodal vibrational dynamics and decay we monitor as a function of time. Our quantum simulations, based on an effective spectroscopic Hamiltonian, describe the essential features of the multimodal Fermi resonance-driven vibrational dynamics in the 3p state. We also present evidence of polyad-specificity in the state-dependent predissociation rates, leading to free atomic and molecular fragments. We emphasize that a quantum molecular movie is required to visualize wavepacket dynamics in the 3pσ2Σu Rydberg state of NO2.

摘要

相干叠加态(一种波包)的光学形成能够实现对零阶态的研究,其演化随时间呈现出结构和电子变化:这催生了分子电影的概念。分子内振动能量重新分布,源于模式间的非谐耦合,是本文所探讨的分子电影。然而,所形成的叠加态不一定会表现出半经典行为(如高斯波包动力学),甚至不一定是直观上有用的零阶态。在此,我们展示了对一个电子激发的三原子分子的时间分辨光电子能谱(TRPES)研究,其中振动动力学必须用量子力学方法处理,且耦合简正模式之间的简单布居流动图景不再适用。具体而言,我们报告了NO₂的零阶3pσ²Σu里德堡态中的振转波包动力学。这个波包体现了多原子分子激发态动力学的两个普遍特征:非谐多模振动耦合(形成多组振动模式);核坐标与电子坐标之间的非绝热耦合,导致预解离。后者表明零阶3s里德堡流形中的多组振动模式态是准束缚的,最好理解为散射共振。我们观察到一个初始制备的“明亮”价态迅速退相到相对长寿命的3p里德堡态,我们监测其多模振动动力学和衰变随时间的变化。我们基于有效光谱哈密顿量的量子模拟描述了3p态中多模费米共振驱动的振动动力学的基本特征。我们还展示了在与态相关的预解离速率中多组振动模式特异性的证据,这导致了自由原子和分子碎片的产生。我们强调,需要一部量子分子电影来可视化NO₂的3pσ²Σu里德堡态中的波包动力学。

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