Ultrafast dissociation of molecules studied at BESSY II

The X-ray photons trigger a ‘molecular catapult effect’: light atomic groups are ejected first, similar to projectiles shot from a catapult, while the heavier atoms – bromine and chlorine – separate much more slowly. The image was printed on the cover of "The Journal of Physical Chemistry Letters".

The X-ray photons trigger a ‘molecular catapult effect’: light atomic groups are ejected first, similar to projectiles shot from a catapult, while the heavier atoms – bromine and chlorine – separate much more slowly. The image was printed on the cover of "The Journal of Physical Chemistry Letters". © The Journal of Physical Chemistry Letters

For the first time, an international team has tracked at BESSY II how heavy molecules – in this case bromochloromethane – disintegrate into smaller fragments when they absorb X-ray light. Using a newly developed analytical method, they were able to visualise the ultrafast dynamics of this process. In this process, the X-ray photons trigger a "molecular catapult effect": light atomic groups are ejected first, similar to projectiles fired from a catapult, while the heavier atoms - bromine and chlorine - separate more slowly.

 

When X-rays hit molecules, they can knock electrons out of certain orbitals and into extremely high-energy states, breaking chemical bonds. This often happens ultra rapidly, in just a few femtoseconds (10-15 s). While this phenomenon has been studied in light molecules such as ammonia, oxygen, hydrochloric acid or simple carbon compounds, it has hardly been studied in molecules with heavier atoms.

A team from France and Germany has now studied the rapid decay of molecules containing halogens. They focused on a molecule in which bromine and chlorine atoms are linked by a light bridge - an alkylene group (CH2). The measurements were made at the XUV beamline of BESSY II.

The absorption of the X-rays caused molecular bonds to break, creating ionic fragments that could be analysed. The scientists were able to produce a visualisation from the measurement data. It shows how the atoms move in the fleeting intermediate states just before the bonds break. To do this, the team developed a new method of analysis called IPA (Ion Pair Average) and combined it with ab initio theoretical calculations to reconstruct the processes.

The results show that light groups of atoms such as CH2 are ejected first, while the heavier atoms - bromine and chlorine - are left behind and therefore separate more slowly. Interestingly, this catapult-like behaviour only occurs at certain X-ray energies. Theoretical simulations, in agreement with experimental observations, emphasise the crucial role of vibrations of the lighter groups of atoms in triggering these ultrafast reactions.

“This study highlights the unique dynamics of molecular dissociation upon X-ray irradiation," says Dr Oksana Travnikova (CNRS, Université Sorbonne, France), first author of the study now published in J. Phys. Chem. Lett. In particular, it shows that the catapult-like motion of light groups initiates the separation of heavy fragments, a process that unfolds in a remarkably short time. These findings could deepen our understanding of chemical reactions at the molecular level and how high-energy radiation affects complex molecules.

CCdM/arö

  • Copy link

You might also be interested in

  • BESSY II: How intrinsic oxygen shortens the lifespan of solid-state batteries
    Science Highlight
    08.05.2026
    BESSY II: How intrinsic oxygen shortens the lifespan of solid-state batteries
    Although solid-state batteries (SSBs) demonstrate high performance and are intrinsically safe, their capacity currently declines rapidly. A team from the TU Wien, Humboldt-University Berlin and HZB has now analysed a TiS₂|Li₃YCl₆ solid-state half-cell in operando at BESSY II using a special sample environment that allows for non-destructive investigation under real operating conditions. Data obtained by combination of soft and hard X-ray photoelectron spectroscopy (XPS and HAXPES) revealed a new degradation mechanism that had not previously been identified in solid-state batteries. They have gained some surprising insights, particularly regarding the harmful role played by intrinsic oxygen. This study provides valuable information for improving design and handling of such batteries.
  • Spintronics at BESSY II: Real-time analysis of magnetic bilayer systems
    Science Highlight
    29.04.2026
    Spintronics at BESSY II: Real-time analysis of magnetic bilayer systems
    Spintronic devices enable data processing with significantly lower energy consumption. They are based on the interaction between ferromagnetic and antiferromagnetic layers. Now, a team from Freie Universität Berlin, HZB and Uppsala University has succeeded in tracking, for each layer separately, how the magnetic order changes after a short laser pulse has excited the system. They were also able to identify the main cause of the loss of antiferromagnetic order in the oxide layer: the excitation is transported from the hot electrons in the ferromagnetic metal to the spins in the antiferromagnet.
  • Electrocatalysts: New model for charge separation at the solid-liquid interface
    Science Highlight
    16.04.2026
    Electrocatalysts: New model for charge separation at the solid-liquid interface
    Hydrogen is at the heart of the transition to carbon neutrality, as both an energy carrier and a reagent for green chemistry. However, large-scale production of hydrogen via electrolysis, as well as the production of many other chemical products, requires significantly cheaper and more efficient catalysts. A precise understanding of the electrochemical processes that take place at the interface between the solid catalyst and the liquid medium is highly useful for developing better electrocatalysts. In the journal Nature Communications, an European team has now presented a powerful model that determines charge separation at the interface, the formation of the electric double layer and local electric potential variations, and the resulting influence on the catalytic activity.