A new approach allows researchers to catch a photocatalyst in action

Scientists used the LCLS at SLAC to uncover how light-driven reactions unfold in a photocatalyst. They observed in space and time how the photocatalyst's structure vibrated and rearranged, capturing the moment when part of it spun off and how atomic motions transitioned from coherent to more random. @ Greg Stewart/SLAC National Accelerator Laboratory

Using SLAC’s X-ray laser, the method revealed atomic motions in a simple catalyst, opening the door to study more complex molecules key to chemical processes in industry and nature. Catalysts facilitate crucial chemical reactions in nature and industry alike. In a subset of them, catalytic activity is triggered by light. For example, when iron pentacarbonyl – a molecule in which a central iron atom is surrounded by five carbon monoxide groups – is exposed to light, the iron sheds its carbon monoxide groups one after another, creating spots for other molecules to dock on to during a catalytic reaction.

Although this process has been studied extensively with spectroscopy, a method that shows how energy moves around in molecules, key details of how the catalyst’s atoms change structure after being hit by light remain unknown.

Now, writing in the journal Nature Communications, a team led by researchers at the Department of Energy’s SLAC National Accelerator Laboratory report how they used ultrafast X-rays from the Linac Coherent Light Source (LCLS), combined with recent theoretical advancements, to reveal those atomic motions on a timescale of femtoseconds, millionths of a billionth of a second. The technique could be used to observe speedy atomic motions in more complex catalysts. “Part of the fun is to make tools that will open new doors,” said Adi Natan, principal investigator and staff scientist at the Stanford PULSE Institute, a joint institute of SLAC and Stanford University. “And being able to see how molecular structures evolve with unprecedented detail will allow us to learn something new about the chemistry of molecules.”

Getting more out of X-ray scattering data

At LCLS, the team shone X-ray pulses on their iron pentacarbonyl sample and analyzed how the X-rays scattered into a detector. Changes in the recorded scattering pattern over time allowed them to determine how the sample’s atomic structure responded to the triggering light flashes. However, the detector’s finite size and other experimental constraints limit the amount of information researchers can glean from these scattering signals. Natan said, “Transforming this restricted scattering data into real-space structural information is like trying to see fine details through a funhouse mirror.”

To overcome these limitations, researchers typically interpret scattering data by matching simulations of possible molecular structures with the data instead of translating the data directly into real space. This also means the analysis becomes harder the more difficult it is to simulate a molecular structure. The metal center in iron pentacarbonyl, for example, makes simulations of atomic motions very challenging.

To get around that, Natan used a theoretical approach he developed previously that relates the observed scattering patterns to the distances between all possible atomic pairs in the molecule. This allows the structure to be extracted directly from the scattering data without simulations. Atomic ‘spectators’ pave the way for more complex analyses

The LCLS study on iron pentacarbonyl was one of the first experimental applications of this new approach, and it allowed the researchers to follow precisely what happened to iron pentacarbonyl as it lost two carbon monoxide groups following a flash of light.

First, the light created vibrations in the molecule that led to the dissociation of one carbon monoxide and a simultaneous rearrangement of the remaining carbon monoxides around the central iron. Then, the second carbon monoxide group was lost with less coordinated movement.

But the research team also observed an effect they hadn’t expected. Although the observed vibrations originated in an iron-carbon pair, the wiggling also occurred in many of the other atomic pairs, which acted as “spectators” that amplified the original motion. Natan said the spectator effect allows tracking of atomic motions throughout the entire molecule by using the motion of the original atomic pair to benchmark the motions of other pairs. And, because the effect does not hinge on the complexity of a molecule, it opens a door to observe much more complex molecules than iron pentacarbonyl.

Combining the structural results with spectroscopy data provides a fuller picture of how chemical reactions unfold – insights that could ultimately allow researchers to tailor the performance of catalysts for different applications.

“Understanding how energy flows through molecules and how atoms move in real space and time brings us one step closer to controlling chemical reactions, helping us design materials,” Natan said. Reference Real-space observation of the dissociation of a transition metal complex and its concurrent energy redistribution

Aviad Schori, Elisa Biasin, Ambar Banerjee, Sébastien Boutet, Philip H. Bucksbaum, Sergio Carbajo, Kelly J. Gaffney, James M. Glownia, Robert Hartsock, Kathryn Ledbetter, Andreas Kaldun, Jason E. Koglin, Kristjan Kunnus, Thomas J. Lane, Mengning Liang, Michael P. Minitti, Jordan T. O’Neal, Robert M. Parrish, Frédéric Poitevin, Jennifer M. Ruddock, Silke Nelson, Brian Stankus, Peter M. Weber, Thomas J. A. Wolf, Michael Odelius & Adi Natan https://www.nature.com/articles/s41467-025-60009-8 SLAC National Accelerator Laboratory