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液态水中过量电子的电子能级。

Electronic Levels of Excess Electrons in Liquid Water.

作者信息

Ambrosio Francesco, Miceli Giacomo, Pasquarello Alfredo

机构信息

Chaire de Simulation à l'Echelle Atomique (CSEA), Ecole Polytechnique Fédérale de Lausanne (EPFL) , CH-1015 Lausanne, Switzerland.

出版信息

J Phys Chem Lett. 2017 May 4;8(9):2055-2059. doi: 10.1021/acs.jpclett.7b00699. Epub 2017 Apr 27.

Abstract

We provide a consistent description of the electronic levels associated with localized and delocalized excess electrons in liquid water by combining hybrid-functional molecular dynamics simulations with a grand canonical formulation of solutes in aqueous solution. The excess electron localizes in a cavity with an average radius of 1.8 Å and a majority coordination of five water molecules. The vertical binding energy, the optical s-p transitions, and the adiabatic redox level are found to agree closely with their experimental counterparts. The energy level associated with electron delocalization V is inferred to lie at -0.97 eV with respect to the vacuum level.

摘要

我们通过将混合泛函分子动力学模拟与水溶液中溶质的巨正则公式相结合,对液态水中与局域化和离域化过剩电子相关的电子能级进行了一致的描述。过剩电子定域在一个平均半径为1.8 Å且主要与五个水分子配位的空穴中。发现垂直结合能、光学s-p跃迁和绝热氧化还原能级与相应的实验值非常吻合。推断与电子离域相关的能级V相对于真空能级位于-0.97 eV处。

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