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Nuclear dynamics of singlet exciton fission in pentacene single crystals

MPS-Authors
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Seiler,  Helene
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

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Krynski,  Marcin
NOMAD, Fritz Haber Institute, Max Planck Society;

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Zahn,  Daniela
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

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Windsor,  Yaov William
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

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Vasileiadis,  Thomas
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

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Ernstorfer,  Ralph
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

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Rossi,  Mariana
NOMAD, Fritz Haber Institute, Max Planck Society;
Max Planck Institute for the Structure and Dynamics of Matter, Max Planck Society;

Schwoerer,  Heinrich
Max Planck Institute for the Structure and Dynamics of Matter, Max Planck Society;

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2011.12016.pdf
(Preprint), 6MB

eabg0869.full.pdf
(Publisher version), 1021KB

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Citation

Seiler, H., Krynski, M., Zahn, D., Hammer, S., Windsor, Y. W., Vasileiadis, T., et al. (2021). Nuclear dynamics of singlet exciton fission in pentacene single crystals. Science Advances, 7(26): eabg0869. doi:10.1126/sciadv.abg0869.


Cite as: https://hdl.handle.net/21.11116/0000-0007-75C9-3
Abstract
Singlet exciton fission (SEF) is a key process in the development of efficient opto-electronic devices. An aspect that is rarely probed directly, and yet has a tremendous impact on SEF properties, is the nuclear structure and dynamics involved in this process. Here we directly observe the nuclear dynamics accompanying the SEF process in single crystal pentacene using femtosecond electron diffraction. The data reveal coherent atomic motions at 1 THz, incoherent motions, and an anisotropic lattice distortion representing the
polaronic character of the triplet excitons. Combining molecular dynamics simulations, time-dependent density functional theory and experimental structure factor analysis, the coherent motions are identified as collective sliding motions of the pentacene molecules along their long axis. Such motions modify the excitonic coupling between adjacent molecules. Our findings reveal that long-range motions play a decisive part in the disintegration of the
electronically correlated triplet pairs, and shed light on why SEF occurs on ultrafast time scales.