Proposed imaging of the ultrafast electronic motion in samples using x-ray phase-contrast

TL;DR

This paper proposes using ultrafast x-ray phase-contrast imaging to directly visualize instantaneous electron densities in real-time, overcoming limitations of traditional scattering methods and enabling detailed insights into electron dynamics and bonding in complex systems.

Contribution

It introduces a novel imaging technique that captures real-time electron densities and their Laplacians, avoiding inelastic scattering issues present in previous methods.

Findings

Ultrafast x-ray phase contrast imaging can visualize instantaneous electron densities.

Inelastic scattering does not affect phase contrast imaging due to interference effects.

Potential to image charge distribution topology and bonding in molecular systems.

Abstract

Tracing the motion of electrons has enormous relevance to understanding ubiquitous phenomena in ultrafast science, such as the dynamical evolution of the electron density during complex chemical and biological processes. Scattering of ultrashort x-ray pulses from an electronic wavepacket would appear to be the most obvious approach to image the electronic motion in real-time and real-space with the notion that such scattering patterns, in the far-field regime, encode the instantaneous electron density of the wavepacket. However, recent results by Dixit {\em et al.} [Proc. Natl. Acad. Sci. U.S.A., {\bf 109}, 11636 (2012)] have put this notion into question and shown that the scattering in the far-field regime probes spatio-temporal density-density correlations. Here, we propose a possible way to image the instantaneous electron density of the wavepacket via ultrafast x-ray {\em phase contrast imaging}. Moreover, we show that inelastic scattering processes, which plague ultrafast scattering in the far-field regime, do not contribute in ultrafast x-ray phase contrast imaging as a consequence of an interference effect. We illustrate our general findings by means of a wavepacket that lies in the time and energy range of the dynamics of valence electrons in complex molecular and biological systems. This present work offers a potential to image not only instantaneous snapshots of non-stationary electron dynamics, but also the Laplacian of these snapshots which provide information about the complex bonding and topology of the charge distributions in the systems.