| Literature DB >> 24876491 |
Sarah Maria Falke1, Carlo Andrea Rozzi2, Daniele Brida3, Margherita Maiuri4, Michele Amato5, Ephraim Sommer1, Antonietta De Sio1, Angel Rubio6, Giulio Cerullo4, Elisa Molinari7, Christoph Lienau8.
Abstract
Blends of conjugated polymers and fullerene derivatives are prototype systems for organic photovoltaic devices. The primary charge-generation mechanism involves a light-induced ultrafast electron transfer from the light-absorbing and electron-donating polymer to the fullerene electron acceptor. Here, we elucidate the initial quantum dynamics of this process. Experimentally, we observed coherent vibrational motion of the fullerene moiety after impulsive optical excitation of the polymer donor. Comparison with first-principle theoretical simulations evidences coherent electron transfer between donor and acceptor and oscillations of the transferred charge with a 25-femtosecond period matching that of the observed vibrational modes. Our results show that coherent vibronic coupling between electronic and nuclear degrees of freedom is of key importance in triggering charge delocalization and transfer in a noncovalently bound reference system.Entities:
Year: 2014 PMID: 24876491 DOI: 10.1126/science.1249771
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728