Nuclear dynamical correlation effects in X-ray spectroscopy from a time-domain perspective

TL;DR

This paper introduces a time-correlation method using molecular dynamics to analyze nuclear dynamical effects in X-ray spectra, revealing significant nuclear motion fingerprints especially in second-order resonant inelastic scattering.

Contribution

The authors develop a novel time-correlation approach for X-ray spectral analysis that captures nuclear dynamical effects without relying on specific electronic structure methods.

Findings

Nuclear motions significantly influence second-order resonant inelastic scattering spectra.

The method effectively compares with traditional sampling approaches for gas phase water.

Applicable across various spectroscopic techniques including UV, X-ray photo-electron, and Auger spectroscopies.

Abstract

To date X-ray spectroscopy has become a routine tool that can reveal highly local and element-specific information on the electronic structure of atoms in complex environments. Here, we focus on nuclear dynamical effects in X-ray spectra and develop a rigorous time-correlation method employing ground state molecular dynamics simulations. The importance of nuclear correlation phenomena is demonstrated by comparison against the results from the conventional sampling approach for gas phase water. In contrast to the first-order absorption, second-order resonant inelastic scattering spectra exhibit pronounced fingerprints of nuclear motions. The developed methodology does not depend on the accompanying electronic structure method in principle as well as on the spectral range and, thus, can be applied to, e.g., UV and X-ray photo-electron and Auger spectroscopies.