Tracking the Complex Dynamics of Electron-Transfer-Mediated Decay in Real Space and Time

When an electronically excited atom or molecule is embedded in a chemical environment as, e.g., in a liquid or a loosely bound cluster, it can de-excite through mechanisms where neighboring atoms or molecules are actively participating in the decay: either by donating or accepting energy or electrons. For such <i>nonlocal</i> decay channels, nuclear dynamics play a crucial role as they have a direct impact on the decay efficiency itself. Here, we present a detailed study of the electron-transfer-mediated decay in a loosely bound triatomic prototype system, combining experimental results from a 5-fold coincidence measurement and theoretical modeling of the decay process. Depending on the decay time, we find that certain classes of molecular geometries are favored for this type of decay. Our findings provide an intuitive picture of how electron-transfer-mediated decay proceeds. In particular, our results confirm a roaming-like behavior of the atoms of the trimer prior to its decay. Our combined theoretical and experimental approach enables a comprehensive tracing of the real-space properties of the decaying system in the time domain.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2026-01-22
DOI
https://doi.org/10.1021/jacs.5c15510
Primary Topic
Molecular Junctions and Nanostructures
Type
article
Field-Weighted Citation Impact
0.00

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article

Tracking the Complex Dynamics of Electron-Transfer-Mediated Decay in Real Space and Time

T. Jahnke, Gregor Kastirke, J. Rist, M. Weller et al.
Journal of the American Chemical Society
Molecular Junctions and Nanostructures
article

Tracking the Complex Dynamics of Electron-Transfer-Mediated Decay in Real Space and Time

T. Jahnke, Gregor Kastirke, J. Rist, M. Weller, Jan Peter Kruse, M. Kunitski, Jaroslav Hofierka, N. Melzer, A. Geyer, Tsveta Miteva, Nicolas Sisourat, M. Kircher, Dimitrios Tsitsonis, Joshua Williams, M. S. Schöffler, R. Dörner, Lorenz S Cederbaum, Florian Trinter
article en

Abstract

When an electronically excited atom or molecule is embedded in a chemical environment as, e.g., in a liquid or a loosely bound cluster, it can de-excite through mechanisms where neighboring atoms or molecules are actively participating in the decay: either by donating or accepting energy or electrons. For such <i>nonlocal</i> decay channels, nuclear dynamics play a crucial role as they have a direct impact on the decay efficiency itself. Here, we present a detailed study of the electron-transfer-mediated decay in a loosely bound triatomic prototype system, combining experimental results from a 5-fold coincidence measurement and theoretical modeling of the decay process. Depending on the decay time, we find that certain classes of molecular geometries are favored for this type of decay. Our findings provide an intuitive picture of how electron-transfer-mediated decay proceeds. In particular, our results confirm a roaming-like behavior of the atoms of the trimer prior to its decay. Our combined theoretical and experimental approach enables a comprehensive tracing of the real-space properties of the decaying system in the time domain.

Journal of the American Chemical SocietyVol. 148(4)
Goethe University Frankfurt (DE), University of Nevada, Reno (US), Heidelberg University (DE), Fritz Haber Institute of the Max Planck Society (DE), Sorbonne Université (FR), Laboratoire de Chimie Physique - Matière et Rayonnement (FR), Max Planck Institute for Nuclear Physics (DE), Laboratoire Médiations (FR), European X-Ray Free-Electron Laser (DE)
Deutsche Forschungsgemeinschaft, Bundesministerium für Bildung und Forschung, Max-Planck-Gesellschaft
Openalex Percentile: Top 79%
Molecular Junctions and Nanostructures
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