Observation of intermolecular Coulombic decay and shake-up satellites in liquid ammonia.

IF 4.7 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2022-07-28 eCollection Date: 2022-07-01 DOI:10.1063/4.0000151
Hanns Christian Schewe, Eva Muchová, Michal Belina, Tillmann Buttersack, Dominik Stemer, Robert Seidel, Stephan Thürmer, Petr Slavíček, Bernd Winter
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Abstract

We report the first nitrogen 1s Auger-Meitner electron spectrum from a liquid ammonia microjet at a temperature of ∼223 K (-50 °C) and compare it with the simultaneously measured spectrum for gas-phase ammonia. The spectra from both phases are interpreted with the assistance of high-level electronic structure and ab initio molecular dynamics calculations. In addition to the regular Auger-Meitner-electron features, we observe electron emission at kinetic energies of 374-388 eV, above the leading Auger-Meitner peak (3a1 2). Based on the electronic structure calculations, we assign this peak to a shake-up satellite in the gas phase, i.e., Auger-Meitner emission from an intermediate state with additional valence excitation present. The high-energy contribution is significantly enhanced in the liquid phase. We consider various mechanisms contributing to this feature. First, in analogy with other hydrogen-bonded liquids (noticeably water), the high-energy signal may be a signature for an ultrafast proton transfer taking place before the electronic decay (proton transfer mediated charge separation). The ab initio dynamical calculations show, however, that such a process is much slower than electronic decay and is, thus, very unlikely. Next, we consider a non-local version of the Auger-Meitner decay, the Intermolecular Coulombic Decay. The electronic structure calculations support an important contribution of this purely electronic mechanism. Finally, we discuss a non-local enhancement of the shake-up processes.

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液氨中分子间库仑衰变和振荡卫星的观测。
我们首次报告了液氨微射流在 ∼223 K (-50 °C)温度下产生的氮1s奥杰-迈特纳电子能谱,并将其与同时测量到的气相氨能谱进行了比较。在高水平电子结构和 ab initio 分子动力学计算的帮助下,对这两相的光谱进行了解释。除了常规的奥杰-迈特纳电子特征外,我们还观察到动能为 374-388 eV 的电子发射,高于奥杰-迈特纳的主峰(3a1 2)。根据电子结构计算,我们将该峰值归因于气相中的震荡卫星,即存在额外价激发的中间态的奥杰-迈特纳发射。在液相中,高能贡献明显增强。我们考虑了导致这一特征的各种机制。首先,与其他氢键液体(尤其是水)类似,高能信号可能是电子衰变前发生的超快质子转移的标志(质子转移介导的电荷分离)。然而,ab initio 动力学计算表明,这种过程比电子衰变慢得多,因此不太可能发生。接下来,我们考虑奥格-迈特纳衰变的非局部版本,即分子间库仑衰变。电子结构计算支持这种纯电子机制的重要贡献。最后,我们讨论震荡过程的非局部增强。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
期刊介绍: ACS Applied Bio Materials is an interdisciplinary journal publishing original research covering all aspects of biomaterials and biointerfaces including and beyond the traditional biosensing, biomedical and therapeutic applications. The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrates knowledge in the areas of materials, engineering, physics, bioscience, and chemistry into important bio applications. The journal is specifically interested in work that addresses the relationship between structure and function and assesses the stability and degradation of materials under relevant environmental and biological conditions.
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