Department of Physical Chemistry, Fritz Haber Institute of the Max Planck Society, Faradayweg 4-6, 14195 Berlin, Germany.
J Chem Phys. 2019 Jan 28;150(4):041702. doi: 10.1063/1.5047033.
The lifetime, coupling, and localization dynamics of electronic states in molecular films near metal electrodes fundamentally determine their propensity to act as precursors or reactants in chemical reactions, crucial for a detailed understanding of charge transport and degradation mechanisms in batteries. In the current study, we investigate the formation dynamics of small polarons and their role as intermediate electronic states in thin films of dimethyl sulfoxide (DMSO) on Cu(111) using time- and angle-resolved two-photon photoemission spectroscopy. Upon photoexcitation, a delocalized DMSO electronic state is initially populated two monolayers from the Cu surface, becoming a small polaron on a 200 fs time scale, consistent with localization due to vibrational dynamics of the DMSO film. The small polaron is a precursor state for an extremely long-lived and weakly coupled multilayer electronic state, with a lifetime of several seconds, thirteen orders of magnitude longer than the small polaron. Although the small polaron in DMSO has a lifetime of 140 fs, its role as a precursor state for long-lived electronic states could make it an important intermediate in multistep battery reactivity.
分子膜中电子态的寿命、耦合和局域动力学从根本上决定了它们在化学反应中作为前体或反应物的倾向,这对于深入了解电池中的电荷输运和降解机制至关重要。在当前的研究中,我们使用时间和角度分辨双光子光发射谱研究了在 Cu(111)上的二甲基亚砜(DMSO)薄膜中形成的小极化子及其作为中间电子态的动力学。光激发后,最初在离 Cu 表面两个单层的位置上填充一个离域的 DMSO 电子态,在 200 fs 的时间尺度上变成一个小极化子,这与由于 DMSO 膜的振动动力学引起的局域化一致。小极化子是一种前体状态,可形成一个极其长寿命和弱耦合的多层电子态,寿命为几秒钟,比小极化子长十三个数量级。尽管 DMSO 中的小极化子的寿命为 140 fs,但它作为长寿命电子态的前体状态,可能使其成为多步电池反应中的重要中间体。