Nitrogen K-Edge X-ray Absorption Spectra of Ammonium and Ammonia in Water Solution: Assessing the Performance of Polarizable Embedding Coupled Cluster Methods

被引:14
作者
Reinholdt, Peter [1 ]
Vidal, Marta L. [2 ]
Kongsted, Jacob [1 ]
Iannuzzi, Marcella [3 ]
Coriani, Sonia [2 ]
Odelius, Michael [4 ]
机构
[1] Univ So Denmark, Inst Fys Kemi & Farmaci, DK-5230 Odense, Denmark
[2] Tech Univ Denmark, DTU Chem, DK-2800 Lyngby, Denmark
[3] Univ Zurich, Phys Chem Inst, CH-8057 Zurich, Switzerland
[4] Stockholm Univ, AlbaNova Univ Ctr, Dept Phys, SE-10691 Stockholm, Sweden
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2021年 / 12卷 / 36期
基金
瑞典研究理事会;
关键词
MOLECULAR-PROPERTIES; ELECTRONIC-STRUCTURE; EXCITED-STATES; SPECTROSCOPY; ENVIRONMENTS; SINGLES; LIQUIDS; SHELL;
D O I
10.1021/acs.jpclett.1c02031
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The recent development of liquid jet and liquid leaf sample delivery systems allows for accurate measurements of soft X-ray absorption spectra in transmission mode of solutes in a liquid environment. As this type of measurement becomes increasingly accessible, there is a strong need for reliable theoretical methods for assisting in the interpretation of the experimental data. Coupled cluster methods have been extensively developed over the past decade to simulate X-ray absorption in the gas phase. Their performance for solvated species, on the contrary, remains largely unexplored. Here, we investigate the current state of the art of coupled cluster modeling of nitrogen K-edge X-ray absorption of aqueous ammonia and ammonium based on quantum mechanics/molecular mechanics, where both the level of coupled cluster calculations and polarizable embedding are scrutinized. The results are compared to existing experimental data as well as simulations based on transition potential density functional theory.
引用
收藏
页码:8865 / 8871
页数:7
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