Watching coherent molecular structural dynamics during photoreaction: beyond kinetic description

TL;DR

This study uses ultrafast X-ray spectroscopy to observe real-time molecular structural dynamics during a photoreaction, revealing coherent oscillations and energy redistribution beyond simple kinetic models.

Contribution

It demonstrates the capability of ultrafast X-ray absorption spectroscopy to directly observe and analyze complex molecular dynamics during photoreactions, going beyond traditional kinetic descriptions.

Findings

Observation of structural breathing oscillations (~265 fs period)

Loss of synchrony in oscillations within ~330 fs

Energy redistribution and vibrational cooling within ~1.6 ps

Abstract

A deep understanding of molecular photo-transformations is challenging because of the complex interaction between the configurations of electrons and nuclei. An initial optical excitation dissipates energy into electronic and structural degrees of freedom, often in less than one trillionth (10^-12) of a second. Molecular dynamics induced by photoexcitation have been very successfully studied with femtosecond optical spectroscopies, but electronic and nuclear dynamics are often very difficult to disentangle. X-ray based spectroscopies can reduce the ambiguity between theoretical models and experimental data, but it is only with the recent development of bright ultrafast X-ray sources, that key information during transient molecular processes can be obtained on their intrinsic timescale. In this letter, Free Electron Laser (FEL) radiation is used to measure ultrafast changes in the X-ray Absorption Near Edge Structure (XANES) during the prototypical photoreaction of a spin crossover compound. We reveal its transformation from the ligand-located electronic photoexcitation to the structural trapping of the high spin state. The results require a description beyond a kinetic model and provide a direct observation of a dynamic breathing of the main structural change. The coherent structural oscillations (period of ~265 fs) in the photoproduct potential lose synchrony within ~330 fs, whereas incoherent motions reveal the energy redistribution and vibrational cooling within ~1.6 ps. We foresee that ultrafast X-ray spectroscopies will provide invaluable insight to understand the complex physics of fundamental light induced phenomena, which are of prime interest in a multitude of chemical, physical and biological processes.