Singh Poonam, Zhang Jia, Ghalgaoui Ahmed, Reimann Klaus, Fingerhut Benjamin P, Woerner Michael, Elsaesser Thomas
Max Born Institut für Nichtlineare Optik und Kurzzeitspektroskopie, Berlin 12489, Germany.
PNAS Nexus. 2022 Jun 7;1(3):pgac078. doi: 10.1093/pnasnexus/pgac078. eCollection 2022 Jul.
An electron solvated in a polar liquid is an elementary quantum system with properties governed by electric interactions with a fluctuating molecular environment. In the prevailing single particle picture, the quantum ground and excited states are determined by a self-consistent potential, as defined by the particular local configuration of the solvation shell. This description neglects collective many-body excitations, which arise from the coupling of electronic degrees of freedom and nuclear motions of the environment. While recent experiments have demonstrated collective nonequilbrium electronic-nuclear motion, i.e. polaron excitations in liquid water, their relevance in the broader context of polar liquids has remained unexplored. Here, we study the nonequilibrium dielectric response of the, compared to water, less polar alcohols isopropanol, and ethylene glycol, that also display a different hydrogen bond pattern. We demonstrate that ultrafast relaxation of photogenerated electrons impulsively induces coherent charge oscillations, which persist for some 10 ps. They emit electric waves in a frequency range from 0.1 to 2 THz, depending on electron concentration. Oscillation frequencies and line shapes are reproduced by a unified polaron picture for alcohols and water, which is based on a Clausius-Mossotti local field approach for the THz dielectric function. The analysis suggests a longitudinal character of many-body polaron excitations and a weak coupling to transverse excitations, supported by the underdamped character of charge oscillations. Polaron dynamics are governed by the long-range Coulomb interaction between an excess electron and several thousands of polar solvent molecules, while local electron solvation geometries play a minor role.
溶解在极性液体中的电子是一个基本量子系统,其性质由与波动分子环境的电相互作用决定。在主流的单粒子图像中,量子基态和激发态由自洽势决定,该自洽势由溶剂化壳层的特定局部构型定义。这种描述忽略了集体多体激发,集体多体激发源于电子自由度与环境核运动的耦合。虽然最近的实验已经证明了集体非平衡电子-核运动,即液态水中的极化子激发,但它们在更广泛的极性液体背景下的相关性仍未得到探索。在这里,我们研究了与水相比极性较小的醇类异丙醇和乙二醇的非平衡介电响应,它们也呈现出不同的氢键模式。我们证明,光生电子的超快弛豫会脉冲式地诱导相干电荷振荡,这种振荡会持续约10皮秒。它们会发射频率范围从0.1到2太赫兹的电波,这取决于电子浓度。醇类和水的统一极化子图像再现了振荡频率和线形,该图像基于用于太赫兹介电函数的克劳修斯-莫索蒂局部场方法。分析表明多体极化子激发具有纵向特性,并且与横向激发的耦合较弱,电荷振荡的欠阻尼特性也支持了这一点。极化子动力学由一个多余电子与数千个极性溶剂分子之间的长程库仑相互作用决定,而局部电子溶剂化几何结构起的作用较小。