Pohl Marvin N, Richter Clemens, Lugovoy Evgeny, Seidel Robert, Slavíček Petr, Aziz Emad F, Abel Bernd, Winter Bernd, Hergenhahn Uwe
Helmholtz-Zentrum Berlin für Materialien und Energie, Methods for Material Development , Albert-Einstein-Str. 15, 12489 Berlin, Germany.
Department of Physics, Freie Universität Berlin , Arnimallee 14, 14195 Berlin, Germany.
J Phys Chem B. 2017 Aug 17;121(32):7709-7714. doi: 10.1021/acs.jpcb.7b06061. Epub 2017 Aug 2.
Ion pairing in electrolyte solutions remains a topic of discussion despite a long history of research. Very recently, nearest-neighbor mediated electronic de-excitation processes of core hole vacancies (electron transfer mediated decay, ETMD) were proposed to carry a spectral fingerprint of local solvation structure and in particular of contact ion pairs. Here, for the first time, we apply electron-electron coincidence detection to a liquid microjet, and record ETMD spectra of Li 1s vacancies in aqueous solutions of lithium chloride (LiCl) in direct comparison to lithium acetate (LiOAc). A change in the ETMD spectrum dependent on the electrolyte anion identity is observed for 4.5 M salt concentration. We discuss these findings within the framework of the formation and presence of contact ion pairs and the unique sensitivity of ETMD spectroscopy to ion pairing.
尽管电解质溶液中的离子对研究历史悠久,但它仍是一个讨论的话题。最近,有人提出,核心空穴空位的最近邻介导电子去激发过程(电子转移介导衰变,ETMD)携带局部溶剂化结构的光谱指纹,特别是接触离子对的光谱指纹。在这里,我们首次将电子 - 电子符合探测应用于液体微射流,并记录氯化锂(LiCl)和醋酸锂(LiOAc)水溶液中锂1s空位的ETMD光谱,以便直接比较。在4.5 M盐浓度下,观察到ETMD光谱随电解质阴离子特性的变化。我们在接触离子对的形成和存在以及ETMD光谱对离子对的独特敏感性的框架内讨论这些发现。