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Multistep and multiscale electron transfer and localization dynamics at a model electrolyte/metal interface

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King,  Sarah B.
Physical Chemistry, Fritz Haber Institute, Max Planck Society;
Department of Chemistry and James Franck Institute, University of Chicago;

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Broch,  Katharina
Physical Chemistry, Fritz Haber Institute, Max Planck Society;
Institut für Angewandte Physik, Universität Tübingen;

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Demling,  Angelika
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

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Stähler,  Julia
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

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SI_UltrafastDMSO_JCP_revision.pdf
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Citation

King, S. B., Broch, K., Demling, A., & Stähler, J. (2019). Multistep and multiscale electron transfer and localization dynamics at a model electrolyte/metal interface. The Journal of Chemical Physics, 150(4): 041702. doi:10.1063/1.5047033.


Cite as: https://hdl.handle.net/21.11116/0000-0002-9605-F
Abstract
The lifetime, coupling, and localization dynamics of electronic states in molecular films near metal electrodes fundamentally determine their propensity to act as precursors or reactants in chemical reactions, crucial for a detailed understanding of charge transport and degradation mechanisms in batteries. In the current study, we investigate the formation dynamics of small polarons and their role as intermediate electronic states in thin films of dimethyl sulfoxide (DMSO) on Cu(111) using time- and angle-resolved two-photon photoemission spectroscopy. Upon photoexcitation, a delocalized DMSO electronic state is initially populated two monolayers from the Cu surface, becoming a small polaron on a 200 fs time scale, consistent with localization due to vibrational dynamics of the DMSO film. The small polaron is a precursor state for an extremely long-lived and weakly coupled multilayer electronic state, with a lifetime of several seconds, thirteen orders of magnitude longer than the small polaron. Although the small polaron in DMSO has a lifetime of 140 fs, its role as a precursor state for long-lived electronic states could make it an important intermediate in multistep battery reactivity.