Chaire de Simulation à l'Echelle Atomique (CSEA), Ecole Polytechnique Fédérale de Lausanne (EPFL), CH-1015, Lausanne, Switzerland.
Nat Commun. 2023 May 11;14(1):2705. doi: 10.1038/s41467-023-38420-w.
The screening arising from many-body excitations is a crucial quantity for describing absorption and inelastic X-ray scattering (IXS) of materials. Similarly, the electron screening plays a critical role in state-of-the-art approaches for determining the fundamental band gap. However, ab initio studies of the screening in liquid water have remained limited. Here, we use a combined analysis based on the Bethe-Salpeter equation and time-dependent density functional theory. We first show that absorption spectra at near-edge energies are insufficient to assess the accuracy by which the screening is described. Next, when the energy range under scrutiny is extended, we instead find that the IXS spectra are highly sensitive and allow for the selection of the optimal theoretical scheme. This leads to good agreement with experiment over a large range of transferred energies and momenta, and enables establishing the elusive fundamental band gap of liquid water at 9.3 eV.
多体激发引起的筛选是描述材料吸收和非弹性 X 射线散射 (IXS) 的关键量。同样,电子筛选在确定基本能带隙的最先进方法中起着关键作用。然而,液体水中筛选的从头算研究仍然有限。在这里,我们使用基于贝特-萨尔皮特方程和时间相关密度泛函理论的组合分析。我们首先表明,近边缘能量的吸收光谱不足以评估描述筛选的准确性。接下来,当研究的能量范围扩展时,我们发现 IXS 光谱非常敏感,可以选择最佳的理论方案。这导致在很大的转移能量和动量范围内与实验很好地吻合,并能够确定液体水难以捉摸的基本能带隙为 9.3eV。