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电子转移介导衰变对离子配对的敏感性。

Sensitivity of Electron Transfer Mediated Decay to Ion Pairing.

作者信息

Pohl Marvin N, Richter Clemens, Lugovoy Evgeny, Seidel Robert, Slavíček Petr, Aziz Emad F, Abel Bernd, Winter Bernd, Hergenhahn Uwe

机构信息

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.

出版信息

J Phys Chem B. 2017 Aug 17;121(32):7709-7714. doi: 10.1021/acs.jpcb.7b06061. Epub 2017 Aug 2.

Abstract

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.

摘要

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。

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