Capturing ultrafast molecular motions and lattice dynamics in spin crossover film using femtosecond diffraction methods
Abstract
Abstract A comprehensive insight into ultrafast dynamics of photo-switchable materials is desired for efficient control of material properties through light excitation. Here, we study a polycrystalline spin crossover thin film as a prototypical example and reveal the sequential photo-switching dynamics, from local molecular rearrangement to global lattice deformation. On the earliest femtosecond timescale, the local molecular structural rearrangement occurs within a constant unit-cell volume through a two-step process, involving initial Fe−ligand bond elongation followed by ligand rotation. The highly-oriented structure of the nanocrystalline films and the experimental geometry enables resolving the full anisotropic lattice structural dynamics in and out of the sample plane separately. While both molecular switching and lattice heating influence lattice volume, they exert varying degrees of impact at disparate time scales following photoexcitation. This study highlights the opportunities provided by Mega-electron-volt electron and X-ray free electron laser to advance the understanding of ultrafast dynamics of photo-switchable materials.
Article Details
Authors (26)
Doriana Vinci
European X-ray Free Electron Laser, Holzkoppel 4, 22869 Schenefeld, Germany
Karl Ridier
Fengfeng Qi
Fernando Ardana-Lamas
European X-ray Free Electron Laser, Holzkoppel 4, 22869 Schenefeld, Germany
Peter Zalden
Lai Chung Liu
Tobias Eklund
Mads Sielemann Jakobsen
Robin Schubert
Dmitry Khakhulin
European X-ray Free Electron Laser, Holzkoppel 4, 22869 Schenefeld, Germany
Carsten Deiter
Nicolas Bottin
Hazem Yousef
European X-ray Free Electron Laser, Holzkoppel 4, 22869 Schenefeld, Germany
David von Stetten
Piotr Łaski
Radosław Kamiński
Katarzyna N. Jarzembska
Rachel F. Wallick
Department of Chemistry
Till Stensitzki
Renske M. van der Veen
Department of Chemistry
Henrike M. Müller-Werkmeister
Gábor Molnár
LCC, CNRS and Université de Toulouse, UPS, INP
Dao Xiang
Christopher Milne
Maciej Lorenc
Institut de Physique de Rennes, UMR CNRS 6251, Université de Rennes 1 , 35042 Rennes,
Yifeng Jiang