We've updated our Privacy Policy to make it clearer how we use your personal data.

We use cookies to provide you with a better experience. You can read our Cookie Policy here.

Enhancing the Power of Attosecond Spectroscopy

Enhancing the Power of Attosecond Spectroscopy

Enhancing the Power of Attosecond Spectroscopy

Enhancing the Power of Attosecond Spectroscopy

Fingerprints of ultrafast electron-nuclear dynamics obtained with attosecond transient absorption spectroscopy. Credit: N. Golubev, EPFL.
Read time:

Want a FREE PDF version of This News Story?

Complete the form below and we will email you a PDF version of "Enhancing the Power of Attosecond Spectroscopy"

First Name*
Last Name*
Email Address*
Company Type*
Job Function*
Would you like to receive further email communication from Technology Networks?

Technology Networks Ltd. needs the contact information you provide to us to contact you about our products and services. You may unsubscribe from these communications at any time. For information on how to unsubscribe, as well as our privacy practices and commitment to protecting your privacy, check out our Privacy Policy

The last few decades have seen impressive progress in laser-based technologies, which have led to significant advancements in atomic and molecular physics. The development of ultrashort laser pulses now allows scientists to study extremely fast phenomena, like charge transport in molecules and elementary steps of chemical reactions. But beyond that, our ability to observe such processes on the attosecond scale (one quintillionth of a second) means that it is also possible to steer and probe the dynamics of individual electrons on their natural timeframes.

One of the emerging ultrafast technologies is attosecond transient absorption spectroscopy (ATAS), which can track the movement of electrons at a specific site of a molecule. This is a particularly appealing feature of ATAS, because it permits tracing the evolution of the molecular system with spatial resolution at the atomic scale.

Modern lasers can push chemistry into unexplored domains of light-matter interactions, where the role of theory in interpreting the results of ATAS measurements will be more important than ever before. But so far, the theory behind ATAS has been developed only for atoms or for molecules either in the absence of nuclear motion or in the absence of electronic coherence.

Now, a team of physicists from EPFL's Laboratory of Theoretical Physical Chemistry (LCPT) have extended ATAS theory to molecules, including a full account of the correlated electron-nuclear dynamics.

The work, in collaboration with Alexander Kuleff at Heidelberg University, is published in Physical Review Letters.

“We present a simple quasi-analytical expression for the absorption cross-section of molecules, which accounts for the nuclear motion and non-adiabatic dynamics and is composed from physically intuitive terms,” says Nikolay Golubev, a postdoc at LCPT and the study's lead author.

By extending ATAS theory, the scientists also show that this spectroscopy technique has sufficient resolution to “see” the follow-up decoherence of electron motion caused by the molecule’s nuclear rearrangement.

Putting theory into practice, the team tested the polyatomic molecule propiolic acid as an example. “The simulation of X-ray ATAS of the propiolic acid was made possible by combining high-level ab initio electronic structure methods with efficient semiclassical nuclear dynamics,” says Jiří Vaníček, head of the LCPT. By advancing our knowledge of the correlated motion of electrons and nuclei in molecules, the findings of the LCPT researchers could also help our understanding of various other “attochemistry” phenomena.

Reference: Golubev NV, Vaníček J, Kuleff AI. Core-valence attosecond transient absorption spectroscopy of polyatomic molecules. Phys Rev Lett. 2021;127(12):123001. doi: 10.1103/PhysRevLett.127.123001

This article has been republished from the following materials. Note: material may have been edited for length and content. For further information, please contact the cited source.