Time-resolved x-ray scattering from impulsively aligned or oriented molecules

Mats Simmermacher*, Adam Kirrander, Niels Engholm Henriksen

*Corresponding author for this work

Research output: Contribution to journalJournal articleResearchpeer-review

18 Downloads (Pure)

Abstract

Impulsive laser excitation of molecules can create rotational wave packets that lead to transient alignment or orientation. We present a theoretical analysis of the signatures of post-pulse field-free time-dependent alignment and orientation of diatomic molecules in time-resolved nonresonant x-ray scattering. This shows that alignment and its time dependence due to the interference terms of the rotational wave packet are visible in the x-ray scattering signal whereas signatures of orientation and its time dependence are absent. To that end, we discuss the time dependence of the coherent rotational motion associated with electronically resonant one-photon excitations. We illustrate our findings with calculated two-dimensional scattering signals for the sodium fluoride molecule (NaF) in the gas phase.

Original languageEnglish
Article number052825
JournalPhysical Review A
Volume102
Issue number5
ISSN2469-9926
DOIs
Publication statusPublished - 2020

Fingerprint Dive into the research topics of 'Time-resolved x-ray scattering from impulsively aligned or oriented molecules'. Together they form a unique fingerprint.

Cite this